{ "count" : 26984, "data" : [ { "id" : "6a2a91a174d8ee00a068e9ce", "title" : "Calibration Technician", "company" : "LotusWorks", "industry" : "Pharmaceutical", "salary" : { "min" : 34000.0, "max" : 45000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for a Junior Calibration Technician in Dublin, Ireland within the Pharmaceutical industry, adjusted for seniority and company size." }, "location" : "Dublin, Dublin, Ireland", "locations" : [ "Dublin", "Dublin", "Ireland" ], "timestamp" : "2026-06-14T22:15:22.228", "fingerprint" : "a8ca371753424c27155a7afdfa84c8a78a170b598f27e7f411f1385790a081d1", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.eu.greenhouse.io/lotusworks/jobs/4893151101", "externalId" : "4893151101", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Dublin", "state" : "Dublin", "country" : "Ireland", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "53.3437061,-6.2544278" } ], "locationText" : "Dublin, Dublin, Ireland", "minimumEducation" : "Level 7 Degree or Fetac level 6", "experienceMinYears" : 2, "technicalSkills" : "Calibration Systems, Automation, Controls system, Microsoft Windows, Microsoft Word, Microsoft Excel, Microsoft PowerPoint", "professionalSkills" : [ "Documentation", "Interpersonal skills" ], "hardSkillsList" : [ "Process instrumentation calibration", "Temperature calibration", "Pressure calibration", "Flow calibration", "Humidity calibration", "Level calibration", "Density calibration", "Viscosity calibration", "pH analysis", "Conductivity analysis", "Control valve calibration" ], "hardSkills" : [ { "name" : "Process instrumentation calibration", "level" : "intermediate" }, { "name" : "Temperature calibration", "level" : "intermediate" }, { "name" : "Pressure calibration", "level" : "intermediate" }, { "name" : "Flow calibration", "level" : "intermediate" }, { "name" : "Humidity calibration", "level" : "intermediate" }, { "name" : "Level calibration", "level" : "intermediate" }, { "name" : "Density calibration", "level" : "intermediate" }, { "name" : "Viscosity calibration", "level" : "intermediate" }, { "name" : "pH analysis", "level" : "intermediate" }, { "name" : "Conductivity analysis", "level" : "intermediate" }, { "name" : "Control valve calibration", "level" : "intermediate" } ], "majorSkills" : "Process instrumentation, Calibration, Documentation", "majorSkillsList" : [ "Process instrumentation", "Calibration", "Documentation" ], "coreResponsibilities" : "Maintain documentation, Work with operation teams, Carry out calibrations, Report work carried out, Undertake site required training, Update PM schedule, Update site system database", "teamCollaboration" : "Work with operation teams", "domainKnowledge" : "GMP; FDA", "domainList" : [ "gmp", "fda" ], "domainSpecificKnowledge" : [ "GMP", "FDA" ], "toolProficiency" : [ "Maximo" ], "communicationSkills" : "Documentation", "documentationSkills" : "Maintain documentation", "continuousLearning" : "Training And Educational Assistance", "problemSolvingSkills" : "Troubleshooting", "qualificationsBasic" : "2 years industry experience, Calibration Systems knowledge, Automation/Controls system knowledge, Computer Operating Systems literacy, Microsoft Windows literacy, Microsoft Word literacy, Microsoft Excel literacy, Microsoft PowerPoint literacy", "qualificationsPreferred" : "Level 7 Degree in Instrumentation, Level 7 Degree in Calibration, Level 7 Degree in Electrical, Fetac level 6 trade qualification in Instrumentation, Fetac level 6 trade qualification in E&I", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "LotusWorks is an Engineering Services provider specializing in managing Commissioning, Construction Services, Calibration, Operations & Maintenance scopes of work within global manufacturing facilities. LotusWorks operates globally across EMEA and North America partnering with the world's leading manufacturers across the Semiconductor, Pharmaceutical & Biologics, Medical Device and Data Centre sectors. Our team of Engineering and Technical professionals is immersed in cutting-edge technologies and innovations. LotusWorks is committed to a diverse and inclusive workplace, integral to our people-first approach. As a Calibration Technician you will be working with the LotusWorks team, you will join our client site in the pharmaceutical sector. This job is based in a cutting-edge facility in Dublin. Working with the LotusWorks team as a Calibration Technician you will be responsible for the setup, calibration, and troubleshooting of process instrumentation such as temperature, pressure, flow, humidity, level, density, viscosity instrumentation, pH and conductivity analysers and control valves. Responsibilities: Maintain all documentation in an organised and controlled manner in compliance with GMP and FDA. Work with operation teams as required facilitating calibration activities. Carry out calibrations in a safe and timely manner. Report work carried out in compliance with site-based reporting tools. To be available and to undertake any site required training. Update “PM” schedule as required. Update site system database “Maximo” as required. Any other duties or responsibilities that may be assigned to you in your role. Skills Required: Ideally at least 2 years industry experience. A good knowledge of Calibration Systems and Automation/Controls system. Literacy in Computer Operating Systems and applications such as Microsoft Windows, Word, Excel, and PowerPoint etc. Possess excellent Communication / Documentation and Interpersonal skills. Education / Licenses / Certifications: Level 7 Degree qualification in Instrumentation., Calibration or Electrical OR Fetac level 6 trade qualification in Instrumentation or E& I. Proof of education, licenses, and certifications will be required where applicable. Benefits: VHI Healthcare Cover Life Assurance Pension Contribution Training And Educational Assistance Annual GP Check-Up Extra Annual Leave Healthcare Screening Recognition Rewards #INDHP LotusWorks is an equal opportunity employer and prohibits discrimination and harassment of any kind. We are committed to creating a diverse and inclusive workplace where all employees feel valued, respected, and empowered.", "summaryDescription" : "Calibration Technician at LotusWorks. Skills: Process instrumentation, Calibration, Documentation. Maintain documentation. 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Regular, Fixed Term - Regular" ], "timestamp" : "2026-06-15T09:32:20.987", "fingerprint" : "a7d8bfdb1ab16ab28c6d2bbe210385ea7c0452158d73e7a4ae73ea4aa5800650", "source" : "taleo", "language" : "en", "applyUrl" : "https://iaea.taleo.net/careersection/ex/jobdetail.ftl?job=1273036", "externalId" : "1273036", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Monaco", "country" : "Monaco", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "43.7309697,7.4248152" } ], "locationText" : "Monaco, Monaco", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "NAML-Radiometrics Laboratory Monaco-Monaco-Monaco-IAEA Environment Laboratories in Monaco", "summaryDescription" : "Reference Products Assistant (RML)(G6) at IAEA Environment Laboratories", "createdAt" : "2026-06-14T06:40:57.748", "lastUpdated" : "2026-06-15T09:32:20.987", "ingestTimestamp" : "2026-06-14T06:40:57.748", "mongoId" : "694ae67f70f0b99d589af818", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.5555556, "_score" : 825.82916, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Government", "llmIndustryConfidence" : 0.5 }, { "id" : "69164da470f0b99d586f315d", "title" : "Calibration Logistics Lead", "company" : "Amazon Kuiper Manufacturing Enterprises LLC", "industry" : "Operations, IT, Support Engineering, Manufacturing, alexa and amazon devices", "salary" : { "min" : 63400.0, "max" : 104600.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Kirkland, Washington, USA", "locations" : [ "Kirkland, Washington, USA" ], "timestamp" : "2026-06-15T01:50:24.429", "fingerprint" : "75a5dbabd10c5f0e05147c1b37bca154f7582260f3137d67967347bfe080ac95", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3123089/apply", "externalId" : "1333a323-fd89-4996-804f-ed217562facf", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Kirkland", "state" : "Washington", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "47.6765382,-122.2070775" } ], "locationText" : "Kirkland, Washington, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 8, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "professionalSkills" : [ "Supply chain management", "Logistics", "Inventory turn management", "Forecasting", "Operations" ], "hardSkillsList" : [ "Tool calibration", "Risk assessment", "Process documentation" ], "hardSkills" : [ { "name" : "Tool calibration", "level" : "intermediate" }, { "name" : "Risk assessment", "level" : "intermediate" }, { "name" : "Process documentation", "level" : "intermediate" } ], "majorSkills" : "Calibration logistics, Quality systems, Manufacturing quality", "majorSkillsList" : [ "Calibration logistics", "Quality systems", "Manufacturing quality" ], "coreResponsibilities" : "Ensure equipment conform to specifications, Manage intake of tools, Manage return of tools, Manage calibration schedule, Forecast tools for calibration, Forecast equipment for calibration, Coordinate onsite calibration activities, Coordinate risk assessments, Coordinate tool containment, Document records of calibration activities, Perform periodic audits, Define mechanisms to streamline workflows, Implement mechanisms to streamline workflows, Coordinate with quality, Coordinate with manufacturing, Coordinate with engineering", "teamCollaboration" : "Suppliers and internal teams; Quality, manufacturing, and engineering", "projectManagementSkills" : [ "Project management", "Organizing schedules" ], "domainKnowledge" : "Satellite manufacturing; Aerospace quality", "domainList" : [ "satellite-manufacturing", "aerospace-quality" ], "domainSpecificKnowledge" : [ "Satellite manufacturing", "Aerospace quality" ], "documentationSkills" : "Documenting records", "problemSolvingSkills" : "Risk assessment", "specialRequirements" : "Export control requirement", "qualificationsBasic" : "2+ years supply chain management experience, Experience managing projects, Experience organizing schedules, U. S. citizen or national, U. S. permanent resident, Lawfully admitted into the U. S. as refugee, Granted asylum, 18 years or older", "qualificationsPreferred" : "Familiar with regulated industry requirements, Familiar with electrical measurement tools, Familiar with mechanical measurement tools, Familiar with dimensional measurement tools, Familiar with ANSI/NCSL Z540. 1 requirements", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Amazon Leo is an initiative to increase global broadband access through a constellation of 3,236 satellites in low Earth orbit (LEO). Its mission is to bring fast, affordable broadband to unserved and underserved communities around the world. Amazon Leo will help close the digital divide by delivering fast, affordable broadband to a wide range of customers, including consumers, businesses, government agencies, and other organizations operating in places without reliable connectivity. The Quality Team at Amazon Leo is looking for a Calibration Program Lead to join our team and help manage tool compliance within our Manufacturing Quality organization. Export Control Requirement: Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum. Candidates must be 18 years or older with the ability to understand and adhere to all job requirements and safety guidelines. Key job responsibilities The Calibration Logistics Lead will ensure all equipment used in satellite manufacturing conform to manufacturer's specifications. - Manage intake and return of tools to process owners. - Manage calibration schedule and forecasting tools/equipment for upcoming calibrations. - Coordinate onsite calibration activities with suppliers and internal teams. - Coordinate risk assessments and tool containment - Documenting records of calibration activities, including calibration dates, results, relabeling, and any adjustments. - Perform periodic audits of production area for compliance to calibration requirements. - Define and implement mechanisms to streamline too calibration workflows A day in the life This role will work daily to: - Manage intake and return of tools to process owners. - Manage calibration schedule and forecasting tools/equipment for upcoming calibrations. - Coordinate onsite calibration activities with suppliers and internal teams. - Document records of calibration activities, including calibration dates, results, relabeling, and any adjustments. This individual will consistently coordinate with quality, manufacturing, and engineering to understand and ensure compliance to equipment requirements. About the team The Amazon Leo Manufacturing Quality team is driven to develop a Amazon Leo Quality System that is capable of scaling aerospace quality to volume and cost levels to meet end customer needs. This position will join the team at an exciting moment, with an opportunity to own quality system development and contribute to the design of requirements, processes, and systems used across the business. We value data driven decision making, a comfort with dealing in ambiguous situations across multiple projects, and an ability to earn trust of various stakeholders to deliver high quality results. Basic Qualifications: - 2+ years of supply chain management (e.g. logistics, inventory turn management, forecasting, operations) experience - Experience managing projects and organizing schedules Preferred Qualifications: - Familiar with regulated industry requirements (AS9100, ISO13485, or ISO9001) - Familiar with electrical, mechanical, and dimensional measurement tools/systems - Familiar with ANSI/NCSL Z540.1 requirements Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner. Our compensation reflects the cost of labor across several US geographic markets. The base pay for this position ranges from $63,400/year in our lowest geographic market up to $104,600/year in our highest geographic market. Pay is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. Amazon is a total compensation company. Dependent on the position offered, equity, sign-on payments, and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, financial, and/or other benefits. For more information, please visit https://www.aboutamazon.com/workplace/employee-benefits . This position will remain posted until filled. Applicants should apply via our internal or external career site.", "summaryDescription" : "Calibration Logistics Lead at Amazon Kuiper Manufacturing Enterprises LLC. Skills: Calibration logistics, Quality systems, Manufacturing quality. Ensure equipment conform to specifications. Manage intake of tools", "postedDate" : "2026-06-12T23:55:19.199", "createdAt" : "2026-06-12T23:55:19.199", "lastUpdated" : "2026-06-15T01:50:24.429", "ingestTimestamp" : "2026-06-12T23:55:19.199", "mongoId" : "69164da470f0b99d586f315d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3123089/apply", "salaryAnnualMin" : 63400, "salaryAnnualMax" : 104600, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Tool calibration", "Risk assessment", "Process documentation", "Calibration logistics", "Quality systems", "Manufacturing quality", "Supply chain management", "Logistics", "Inventory turn management", "Forecasting", "Operations", "Project management", "Organizing schedules", "Satellite manufacturing", "Aerospace quality" ], "skillCount" : 15, "jobCategory" : "operations", "dataQualityScore" : 1.0, "_score" : 822.0008, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing" }, { "id" : "6a2a64ce74d8ee00a062785b", "title" : "Senior Referent", "company" : "Checkout.com", "industry" : "All cost centres", "salary" : { "min" : 75000.0, "max" : 110000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Referent in FinTech in Paris, France, adjusted for seniority and company size." }, "location" : "Paris", "locations" : [ "Paris" ], "timestamp" : "2026-06-13T08:39:44.844", "fingerprint" : "062a84800aa27b95c11515d2d5e83b37492eafbbee62b1e80de13f196e284219", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/checkout.com/a61b3226-5e35-4718-841c-54224a973409/application", "externalId" : "a61b3226-5e35-4718-841c-54224a973409", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Paris", "country" : "France", "continent" : "eu", "source" : "llm", "workMode" : "hybrid", "geo" : "48.8534951,2.3483915" } ], "locationText" : "Paris, France", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "Machine learning", "professionalSkills" : [ "Operational checks", "Fraud patterns", "Process refinement", "Performance benchmarks", "SOP validation", "High-risk audits", "Data labeling", "Database development", "Detection logic", "Market entries", "Tool migrations", "Fraud cases" ], "hardSkillsList" : [ "Accuracy", "Speed" ], "hardSkills" : [ { "name" : "Accuracy", "level" : "intermediate" }, { "name" : "Speed", "level" : "intermediate" } ], "majorSkills" : "Operational mastery, Excellence oversight, Strategic support", "majorSkillsList" : [ "Operational mastery", "Excellence oversight", "Strategic support" ], "coreResponsibilities" : "Execute operational checks, Act as auditor, Maintain proficiency, Execute MRApp checks, Establish performance benchmarks, Define attainable excellence, Evaluate BPO performance, Stress-test SOPs, Flag unrealistic processes, Conduct deep-dive audits, Label data, Provide labeled datasets, Train machine-learning models, Participate in database development, Create templates, Edit features, Translate audit findings, Improve automated detection logic, Participate in task forces, Ensure technical nuances are captured, Assist Training Managers, Assess fraud case relevance, Assess fraud case complexity", "teamCollaboration" : "Cross-functional teams; Ops-Tech feedback loop; Task Force squads", "domainKnowledge" : "Fintech; Fraud detection; Machine learning models", "domainList" : [ "fintech", "fraud-detection", "machine-learning-models" ], "domainSpecificKnowledge" : [ "Fintech", "Fraud detection", "Machine learning models" ], "toolProficiency" : [ "odash" ], "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "1 to 1.5 days per week execution, Internal gold standard for speed and accuracy, First stress-tester for new SOPs, Final word on accuracy and system integrity, Identify weak signals and emerging fraud trends", "qualificationsPreferred" : "Experience with odash, Experience with new fraud products", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Company Description We’re http://checkout.comCheckout.com http://Checkout.com. You might not know our name, but companies like eBay, Spotify, Klarna, Uber, and Sony do, because we’re behind many of the digital experiences you use every day. We are where the world checks out, enabling over 10 billion transactions daily for more than one billion global shoppers. Whether you want to book a holiday, order food, renew a subscription, or check out online, there’s a good chance our tech powers the payments behind the scenes. Our platform helps the most ambitious businesses deliver effortless digital experiences, at scale. If you want to do career-defining work, you’ve come to the right place. We move fast, think globally, and believe great teams are built by hiring exceptional people with conviction, curiosity, and the desire to make an impact. With 20 offices across six continents and London as our HQ, we’re shaping the future of fintech – and we’re just getting started. MISSION STATEMENT The Senior Referent mission is twofold: to execute the most complex operational checks and to act as a \"Ground Truth\" auditor. The Senior Referents bridge the gap between high-level strategy and floor-level reality, ensuring that our automated systems and human processes are constantly refined based on real-world fraud patterns. 1. OPERATIONAL MASTERY & BENCHMARKING - Expert Execution: Maintain \"Battle-Ready\" proficiency by executing live MRApp checks (allocated 1 to 1.5 days per week). Senior Referents are the internal gold standard for speed and accuracy. - BPO Benchmarking: Use your production time to establish performance benchmarks. Senior Referents define what \"attainable excellence\" looks like, providing a realistic mirror to evaluate BPO performance. - SOP Validation: Act as the first \"stress-tester\" for new Standard Operating Procedures. If a process is unrealistic or creates friction on the floor, you are responsible for flagging it before it is scaled. 2. EXCELLENCE OVERSIGHT & INTELLIGENCE - High-Stakes Auditing: Conduct deep-dive audits on high-risk cases and \"Ground Truth\" labeling. Senior Referents give the final word on accuracy and system integrity. - Fraud Pattern Sensing: Identify \"weak signals\" and emerging fraud trends that automated systems might miss. - Labeling for Data Science: Provide high-quality labeled datasets to the Data Science team to train and refine our machine-learning models. - Database contributor: Participation in the development of the template database by creating templates and editing features. 3. CROSS-FUNCTIONAL STRATEGIC SUPPORT - Ops-Tech Feedback Loop: Translate audit findings into technical requirements to improve automated detection logic. - Project Support: Participate in \"Task Force\" squads for new market entries or tool migrations (e.g., odash, new fraud products), ensuring technical nuances are captured. - Training Calibration: Assist Training Managers in assessing the relevance and complexity of encountered fraud cases. Additional Information Bring all of you to work We create the conditions for high performers to thrive, through real ownership, fewer blockers, and work that makes a difference from day one. Here, you’ll move fast, take on meaningful challenges, and be recognized for the impact you deliver. It’s a place where ambition gets met with opportunity, and where your growth is in your hands. We work as one team, and we back each other to succeed. So whatever your background or identity, if you’re ready to grow and make a difference, you’ll be right at home here. It’s important we set you up for success and make our process as accessible as possible. So let us know in your application, or tell your recruiter directly, if you need anything to make your experience or working environment more comfortable. Life at Checkout.com http://Checkout.com We understand that work is just one part of your life. Our hybrid working model offers flexibility, with three days per week in the office to support collaboration and connection. Curious about what it’s like to be part of our team? Visit our Careers Page https://www.checkout.com/careers to learn more about our culture, open roles, and what drives us. For a closer look at daily life at Checkout.com http://Checkout.com, follow us on LinkedIn https://www.linkedin.com/company/checkout/life/ and Instagram https://www.instagram.com/checkout_com/", "summaryDescription" : "Senior Referent at Checkout.com. Skills: Operational mastery, Excellence oversight, Strategic support. Execute operational checks. 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Skills: Laboratory Operations, Patient Testing, Specimen Collection, Quality Control. 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Support laboratory operations", "createdAt" : "2026-06-14T04:27:48.946", "lastUpdated" : "2026-06-15T07:12:13.584", "ingestTimestamp" : "2026-06-14T04:27:48.946", "mongoId" : "6a15e47758b93c861e7c756a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 38000, "salaryAnnualMax" : 52000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Laboratory Operations", "Patient Testing", "Specimen Collection", "Quality Control", "Healthcare Operations" ], "skillCount" : 5, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.7777778, "_score" : 781.22565, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c7ea474d8ee00a0953118", "title" : "Laboratory Technician", "company" : "Headlands Research", "industry" : "Healthcare", "salary" : { "min" : 23.0, "max" : 27.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "San Diego, California, United States", "locations" : [ "San Diego", "California", "United States" ], "timestamp" : "2026-06-15T07:06:46.783", "fingerprint" : "a904e8f2dd0621e78737d2ffd318d13e0b98e581b80b6bf006175f96e431f9dc", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/headlandsresearch/jobs/4278330009", "externalId" : "4278330009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "San Diego", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.7174202,-117.1627720" } ], "locationText" : "San Diego, California, United States", "employmentType" : "FULL_TIME", "technicalSkills" : "Phlebotomy", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Specimen collection", "Specimen processing" ], "hardSkills" : [ { "name" : "Specimen collection", "level" : "intermediate" }, { "name" : "Specimen processing", "level" : "intermediate" } ], "majorSkills" : "Lab operations, Clinical research, Patient care", "majorSkillsList" : [ "Lab operations", "Clinical research", "Patient care" ], "coreResponsibilities" : "Lead lab operations, Collect specimens, Process specimens, Organize lab, Maintain lab environment, Manage lab inventory, Manage lab supplies, Prepare kits", "teamCollaboration" : "Coordination with study teams; Interaction with participants; Interaction with providers; Interaction with sponsors", "domainKnowledge" : "Clinical trial delivery; Research protocols; Regulatory standards; Patient care procedures", "domainList" : [ "clinical-trial-delivery", "research-protocols", "regulatory-standards", "patient-care-procedures" ], "domainSpecificKnowledge" : [ "Clinical trial delivery", "Research protocols", "Regulatory standards", "Patient care procedures" ], "toolProficiency" : [ "Excel", "Outlook", "EMRs" ], "continuousLearning" : "Professional development opportunities; Career growth opportunities", "qualificationsBasic" : "Geriatric experience, Medical terminology familiarity, Basic laboratory procedures familiarity, Lab equipment comfort, Regulated processes comfort, Basic computer systems proficiency, Multiple electronic data entry systems comfort", "qualificationsPreferred" : "Clinical research experience, Specimen processing experience, Specimen shipping experience, Lab inventory experience, Interest in Clinical Research Coordinator role, Interest in lab leadership role", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion. Location: San Diego, CA | \uD83C\uDFE5 Site Name: Artemis Institute for Clinical Research | \uD83D\uDD52 Full-Time | \uD83E\uDDEA Clinical Research We’re seeking a Laboratory Technician/Phlebotomist for our clinical research site Artemis Institute for Clinical Research located in San Diego, CA. As a Laboratory Technician, you won’t just be supporting research—you’ll be helping shape the future of healthcare. This is an exciting opportunity for individuals who are ready to grow their skillset and income potential within the clinical research field. \uD83D\uDCBC The Role: If you’re an experienced phlebotomist who enjoys being the go-to person in the lab—and you’re ready for more ownership, variety, and growth—this role is designed for you. This isn’t just a draw-and-go position. You’ll take the lead on lab operations within a clinical research environment, managing everything from specimen collection and processing to lab organization, compliance, and coordination with study teams. You’ll play a critical role in advancing clinical trials while building skills that go far beyond traditional phlebotomy—including exposure to research protocols, regulatory standards, and broader patient care procedures. Type: Regular Full-time Employee Schedule: M/Th 8 AM-5 PM | Tu/W/F: 7AM-3 PM Pay Range: $23-27/hr *Dependent upon relevant experience, certification, and education. Location: Onsite in San Diego, CA (no capabilities for remote or hybrid work) Reports to: Site Director Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more. \uD83C\uDF1FWhat We Offer Competitive pay + annual performance incentives Medical, dental, and vision insurance 401(k) plan with company match Paid time off (PTO) and company holidays Opportunities for professional development and career growth A mission-driven culture focused on advancing medicine and improving patient outcomes Responsibilities: Own the Lab Operations: Take the lead on day-to-day lab activities, ensuring everything runs smoothly, safely, and on schedule. Maintain a clean, organized, and inspection-ready lab environment. Manage lab inventory, supplies, and kit preparation across multiple studies. Perform geriatric experience a plus Familiarity with medical terminology and basic laboratory procedures Comfort working with lab equipment, documentation, and regulated processes Strong attention to detail and ability to manage multiple responsibilities at once Proficiency with basic computer systems (Excel, Outlook, EMRs, or similar tools) Comfortable using multiple electronic data entry systems A team-first mindset with a willingness to jump in wherever needed Strong attention to detail, time management, and ability to work in a fast-paced, regulated environment Excellent interpersonal skills—you’ll be interacting with participants, providers, and sponsors Passion for improving patient outcomes through research Bonus points for: Clinical research experience Experience handling specimen processing, shipping, or lab inventory Interest in growing into a Clinical Research Coordinator or lab leadership role Why This Role Stands Out More responsibility than a typical phlebotomy role—you’ll help run the lab, not just support it Exposure to clinical research, opening doors to long-term career growth Skill expansion into patient care, research operations, and regulatory processes Clear path for advancement into coordinator or specialized research roles Ready for What’s Next? If you’re looking to move beyond a traditional phlebotomy role and take on more ownership in a fast-paced, purpose-driven environment, we’d love to connect. Apply today and take the next step in growing your career within clinical research. California Pay Range $23—$27 USD Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind. Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Need Assistance? Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.", "summaryDescription" : "Laboratory Technician at Headlands Research. Skills: Lab operations, Clinical research, Patient care. Lead lab operations. Collect specimens", "postedDate" : "2026-06-13T20:38:05.869", "createdAt" : "2026-06-13T20:38:05.869", "lastUpdated" : "2026-06-15T07:06:46.783", "ingestTimestamp" : "2026-06-13T20:38:05.869", "mongoId" : "6a2c7ea474d8ee00a0953118", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 47840, "salaryAnnualMax" : 56160, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Specimen collection", "Specimen processing", "Lab operations", "Clinical research", "Patient care", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Resource planning", "Continuous improvement", "Clinical trial delivery", "Research protocols", "Regulatory standards", "Patient care procedures", "Excel", "Outlook", "EMRs" ], "skillCount" : 18, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "_score" : 777.098, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a487074d8ee00a05df766", "title" : "Product Manager - Reference Data", "company" : "Addepar", "industry" : "Financial Services", "salary" : { "min" : 75000.0, "max" : 110000.0, "currency" : "GBP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Product Manager in Edinburgh, UK, adjusted for the FinTech industry and manager experience level." }, "location" : "Edinburgh, Scotland, United Kingdom", "locations" : [ "Edinburgh", "Scotland", "United Kingdom" ], "timestamp" : "2026-06-14T04:16:16.489", "fingerprint" : "7284fa3d09e1103e68872b153454df2d5231ac1d024edb9c09c477066fc120b6", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/addepar1/jobs/8576368002", "externalId" : "8576368002", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Edinburgh", "state" : "Scotland", "country" : "United Kingdom", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "55.9533456,-3.1883749" } ], "locationText" : "Edinburgh, Scotland, United Kingdom", "experienceLevel" : "Manager", "technicalSkills" : "pandas, Jupyter", "professionalSkills" : [ "Data quality analysis", "Reporting infrastructure", "Commercial reporting", "Security mastering", "Market data feeds" ], "hardSkillsList" : [ "Data investigations", "Structured analyses", "Querying data systems", "Reconciliation queries", "Validating transformations" ], "softSkillsList" : [ "Rigorous thinking", "Clear communicator" ], "hardSkills" : [ { "name" : "Data investigations", "level" : "intermediate" }, { "name" : "Structured analyses", "level" : "intermediate" }, { "name" : "Querying data systems", "level" : "intermediate" }, { "name" : "Reconciliation queries", "level" : "intermediate" }, { "name" : "Validating transformations", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Rigorous thinking" }, { "name" : "Clear communicator" } ], "majorSkills" : "Reference Data, Data platform, Data quality", "majorSkillsList" : [ "Reference Data", "Data platform", "Data quality" ], "coreResponsibilities" : "Run data investigations, Perform structured analyses, Drive data quality analysis, Profile incoming vendor data, Validate transformations, Identify anomalies, Build reporting infrastructure, Query data systems, Produce views and dashboarding, Support ASM operational workflows, Generate reconciliation queries, Validate node matching, Validate security ID linking, Surface data quality issues, Productise pipeline monitoring, Triage feed errors, Flag issues to operations", "teamCollaboration" : "Cross-functional collaboration; Work with product team", "projectManagementSkills" : [ "Roadmap", "User stories" ], "domainKnowledge" : "Financial data concepts; Asset class concepts; Security level concepts; Reference data; Pricing", "domainList" : [ "financial-data-concepts", "asset-class-concepts", "security-level-concepts", "reference-data", "pricing" ], "domainSpecificKnowledge" : [ "Financial data concepts", "Asset class concepts", "Security level concepts", "Reference data", "Pricing" ], "toolProficiency" : [ "pandas", "Jupyter" ], "communicationSkills" : "Write up findings; Document processes; Present analysis", "documentationSkills" : "Document processes", "problemSolvingSkills" : "Rigorous thinking; Structured analyses; Data investigations", "qualificationsBasic" : "Right to work in UK", "qualificationsPreferred" : "Knowledgeable in financial data concepts, Desire to learn financial data concepts", "rawDescription" : "Who We Are Addepar is a global data and AI platform empowering investment professionals to turn complex financial information into actionable intelligence. Addepar unifies portfolio, market and client data in a total portfolio view and delivers AI-powered insights within investment and client workflows. More than 1,400 firms in nearly 60 countries use Addepar to manage and advise on nearly $9 trillion in assets. Its open platform integrates with nearly 650 software, data and consulting partners to power end-to-end investment operations across firms of all sizes and complexity. Addepar supports clients worldwide with offices in New York City, Salt Lake City, London, Edinburgh, Pune, Dubai, Geneva and São Paulo. The Role We are seeking a Product Manager to join our Reference Data team, based in Edinburgh. Reference Data is part of the Data Enablement team at Addepar. Our mission is to build a scalable, efficient, and high quality data platform that integrates, connects, productionises, and distributes third-party data content across Addepar and to our clients and partners. Our team is organised across two product tracks — Market Data Feeds and Addepar Security Master (ASM). This role will power these tracks. You will be working on projects that focus on turning raw data into the clear, well-structured insights that help our team make better decisions, move faster, and deliver more confidently across feeds, security mastering, and commercial reporting. This role requires deep data skills, rigorous thinking, and the ability to approach tasks with a builder mindset. Applicants must have, and maintain, the right to work in the United Kingdom from the first day of employment. Please note that visa sponsorship is not available for this role. What You'll Do Work on a series of projects that will serve as the analytical foundation across the team, running the data investigations, ad hoc queries, and structured analyses that inform our prioritisation, requirements, and decisions. Drive data quality analysis layer for Market Data Feed builds and our security master: profiling incoming vendor data, validating transformations, identifying anomalies and coverage gaps. Build and maintain the reporting infrastructure that gives the team and leadership visibility into dataset profitability, vendor licensing costs vs. revenue, pipeline health, feed coverage, and commercial activity. Query across our data systems to produce views and dashboarding on profitability by dataset, spend vs. budget, commercial pipeline tracking. Support ASM operational workflows through data by generating output that help us such as running reconciliation queries, validating node matching and security ID linking, and surfacing data quality issues that require attention by our team. Productising our ability to monitor market data pipelines and operational dashboards, triaging feed errors and flagging issues to operations and/or R comfortable with pandas, Jupyter, or similar tools. Able to build reporting that spans multiple data sources with knowledge on how to join pieces of information like Salesforce data with finance data and operational data and produce something coherent and trustworthy. Ideal if knowledgeable in financial data concepts such as asset class and security level concepts, reference data, and pricing or the desire to learn more about these concepts. A builder and self-starter that is dependable in your work. Teammates trust what you produce. A clear communicator who can write up findings, document processes, and present analysis to diverse audiences. Our Values Act Like an Owner - Think and operate with intention, purpose and care. Own outcomes. Build Together - Collaborate to unlock the best solutions. Deliver lasting value. Champion Our Clients - Exceed client expectations. Our clients’ success is our success. Drive Innovation - Be bold and unconstrained in problem solving. Transform the industry. Embrace Learning - Engage our community to broaden our perspective. Bring a growth mindset. In addition to our core values, Addepar is proud to be an equal opportunity employer. We seek to bring together diverse ideas, experiences, skill sets, perspectives, backgrounds and identities to drive innovative solutions. We commit to promoting a welcoming environment where inclusion and belonging are held as a shared responsibility. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. PHISHING SCAM WARNING: Addepar is among several companies recently made aware of a phishing scam involving con artists posing as hiring managers recruiting via email, text and social media. The imposters are creating misleading email accounts, conducting remote “interviews,” and making fake job offers in order to collect personal and financial information from unsuspecting individuals. Please be aware that no job offers will be made from Addepar without a formal interview process. Additionally, Addepar will not ask you to purchase equipment or supplies as part of your onboarding process. If you have any questions, please reach out to ta-operations@addepar.com.", "summaryDescription" : "Product Manager - Reference Data at Addepar. Skills: Reference Data, Data platform, Data quality. Run data investigations. Perform structured analyses", "postedDate" : "2026-06-11T21:02:28.258", "createdAt" : "2026-06-11T21:02:28.258", "lastUpdated" : "2026-06-14T04:16:16.489", "ingestTimestamp" : "2026-06-11T21:02:28.258", "mongoId" : "6a2a487074d8ee00a05df766", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Data investigations", "Structured analyses", "Querying data systems", "Reconciliation queries", "Validating transformations", "Rigorous thinking", "Clear communicator", "Reference Data", "Data platform", "Data quality", "Data quality analysis", "Reporting infrastructure", "Commercial reporting", "Security mastering", "Market data feeds", "Roadmap", "User stories", "Financial data concepts", "Asset class concepts", "Security level concepts", "Reference data", "Pricing", "pandas", "Jupyter" ], "skillCount" : 24, "jobCategory" : "product", "jobSubcategory" : "product-management", "dataQualityScore" : 0.8888889, "_score" : 751.46075, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Financial Services" }, { "id" : "6a2cdcb874d8ee00a0a555d1", "title" : "Laboratory Assistant", "company" : "Luminis Health", "industry" : "Healthcare", "salary" : { "min" : 17.0, "max" : 26.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Annapolis, MD", "locations" : [ "Annapolis", "MD" ], "timestamp" : "2026-06-15T04:59:58.630", "fingerprint" : "b89082edf78e0b0278297538ba5778f5bdb8b5a2b897b255afd420b65758e4f6", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://boards.greenhouse.io/luminishealth/jobs/5239743008?gh_jid=5239743008", "externalId" : "5239743008", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Annapolis", "state" : "Maryland", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.9786401,-76.4927860" } ], "locationText" : "Annapolis, Maryland, United States", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Process improvement", "Inventory management", "Specimen processing" ], "hardSkillsList" : [ "Venipuncture", "Capillary puncture", "Heel-stick puncture", "Microscopic evaluation", "Quality controls" ], "softSkillsList" : [ "Cooperative" ], "hardSkills" : [ { "name" : "Venipuncture", "level" : "intermediate" }, { "name" : "Capillary puncture", "level" : "intermediate" }, { "name" : "Heel-stick puncture", "level" : "intermediate" }, { "name" : "Microscopic evaluation", "level" : "intermediate" }, { "name" : "Quality controls", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Cooperative" } ], "majorSkills" : "Laboratory support, Specimen collection, Laboratory inventory", "majorSkillsList" : [ "Laboratory support", "Specimen collection", "Laboratory inventory" ], "coreResponsibilities" : "Promote process improvement, Add value to job, Find other work-related tasks, Maintain safe environment, Dispose of biohazard waste, Maintain inter/intradepartmental work flow, Maintain laboratory supplies inventory, Conserve laboratory resources, Provide clinical laboratory information, Participate in training new staff, Determine specimen collection method, Process gynecological specimens, Process non-gynecologic specimens, Perform functions to guidelines, Register patients accurately, Order or accession tests, Respond to requests for results, Send appropriate scheduled reports, Prepare aliquots, Process samples for referral, Distribute specimens, Operate laboratory equipment, Maintain laboratory equipment, Perform preventative maintenance, Troubleshoot problems, Participate in laboratory quality plan, Perform quality controls, Document QC daily, Follow up on issues", "teamCollaboration" : "Foster spirit of cooperation", "domainKnowledge" : "Medical laboratory information; Diagnosis; Treatment; Prevention of diseases; Biohazard waste; Regulatory guidelines; Biological specimens; Gynecological specimens; Non-gynecologic specimens; Lab results; Outside distributes specimens; Laboratory quality plan", "domainList" : [ "medical-laboratory-information", "diagnosis", "treatment", "prevention-of-diseases", "biohazard-waste", "regulatory-guidelines", "biological-specimens", "gynecological-specimens", "non-gynecologic-specimens", "lab-results", "outside-distributes-specimens", "laboratory-quality-plan" ], "domainSpecificKnowledge" : [ "Medical laboratory information", "Diagnosis", "Treatment", "Prevention of diseases", "Biohazard waste", "Regulatory guidelines", "Biological specimens", "Gynecological specimens", "Non-gynecologic specimens", "Lab results", "Outside distributes specimens", "Laboratory quality plan" ], "toolProficiency" : [ "Hospital Information System" ], "communicationSkills" : "Answering questions; Answering requests", "documentationSkills" : "Document QC", "innovationCreativity" : "Innovative ideas", "problemSolvingSkills" : "Troubleshoot problems", "specialRequirements" : "Exposure to blood-borne pathogens, May require travel", "qualificationsBasic" : "High School graduate or equivalent, Six months experience acute care facility", "qualificationsPreferred" : "MLA(ASCP) or PBT(ASCP) preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Position Objective: Provides support to the technical staff in the delivery of medical laboratory information related to diagnosis, treatment, and prevention of diseases. Essential Job Duties: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Creates a work environment that positively promotes process improvement. Explores opportunities to add value to job (innovative ideas) to benefit the organization and taking ownership of the outcome. Proactively finds other work-related tasks during low census. Maintains safe and clean working environment by complying with procedures, rules, and regulations. Labels and disposes of biohazard and/or chemical waste according to regulatory guidelines. Maintains inter- and intradepartmental work flow by fostering a spirit of cooperation (hand offs). Maintains laboratory supplies inventory by checking stock to determine inventory level; anticipating needed supplies; placing and expediting orders for supplies; verifying receipt of supplies; and storing supplies according to manufacturer’s recommended conditions. Conserves laboratory resources by using equipment and supplies as needed to accomplish job results. Provides clinical laboratory information by answering questions and requests. Participates in the training of new staff by serving as a mentor. Determines and executes the best method for obtaining biological specimens from patients of all ages (if required) to include venipuncture, capillary, and heel-stick puncture to ensure quality specimen for testing. Processes gynecological and non-gynecologic specimens for microscopic evaluation (if required), including instrument processing, staining, changing reagents, and cover-slipping. Performs functions to established productivity guidelines with minimal errors. Registers patients accurately in the Hospital Information System. Orders or accessions appropriate tests as requested by an authorized provider by accurately reading and interpreting orders and being familiar with test mnemonics and components. Responds to requests for lab results and sends appropriate scheduled reports. Prepares aliquots and processes samples for referral to outside labs; distributes specimens to testing or processing locations according to established standard work. Operates and maintains laboratory equipment. Performs preventative maintenance and troubleshoots problems to the full extent of ability. Actively participate in the laboratory quality plan/program (ex. investigative reports, notification of delays, etc.). Performs quality controls and documents QC for each lab procedure on a daily basis and follows up on issues (troubleshoots). Educational/Experience Requirements: High School graduate or equivalent Six months experience working in an acute care facility in an equivalent role. Required License/Certifications: N/A MLA(ASCP) or PBT(ASCP), preferred. Knowledge, Skills, Abilities: Ability to work cooperatively with all types of personalities both inside and outside the organization. May require travel to various locations. Working Conditions, Equipment, Physical Demands: There is a reasonable expectation that employees in this position will be exposed to blood-borne pathogens. Physical Demands - The physical demands and work environment that have been described are representative of those an employee encounters while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions in accordance with the Americans with Disabilities Act. The above job description is an overview of the functions and requirements for this position. This document is not intended to be an exhaustive list encompassing every duty and requirement of this position; your supervisor may assign other duties as deemed necessary. Pay Range $17.50—$26 USD Luminis Health Benefits Overview: • Medical, Dental, and Vision Insurance • Retirement Plan (with employer match for employees who work more than 1000 hours in a calendar year) • Paid Time Off • Tuition Assistance Benefits • Employee Referral Bonus Program • Paid Holidays, Disability, and Life/AD&D for full-time employees • Wellness Programs • Employee Assistance Programs and more *Benefit offerings based on employment status Opt-in for text notifications! Luminis Health's two-way SMS texting platform lets you receive notifications and messages from our Talent Acquisition team directly on your phone. To enable this feature, select \"yes\" when asked to \"opt-in to receive text messages\" and to \"Receive updates from a recruiter about this job via SMS\" when completing your application. Once you are opted in, you can easily opt-out at any time. Standard text messaging rates may apply based on the candidate's mobile carrier plan. Luminis Health is not responsible for any charges incurred by the recipient. Candidates are encouraged to review their mobile carrier's plan for applicable text messaging rates and usage charges.", "summaryDescription" : "Laboratory Assistant at Luminis Health. Skills: Laboratory support, Specimen collection, Laboratory inventory. Promote process improvement. Add value to job", "postedDate" : "2026-06-14T05:10:34.175", "createdAt" : "2026-06-14T05:10:34.175", "lastUpdated" : "2026-06-15T04:59:58.630", "ingestTimestamp" : "2026-06-14T05:10:34.175", "mongoId" : "6a2cdcb874d8ee00a0a555d1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 35360, "salaryAnnualMax" : 54080, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Venipuncture", "Capillary puncture", "Heel-stick puncture", "Microscopic evaluation", "Quality controls", "Cooperative", "Laboratory support", "Specimen collection", "Laboratory inventory", "Process improvement", "Inventory management", "Specimen processing", "Medical laboratory information", "Diagnosis", "Treatment", "Prevention of diseases", "Biohazard waste", "Regulatory guidelines", "Biological specimens", "Gynecological specimens", "Non-gynecologic specimens", "Lab results", "Outside distributes specimens", "Laboratory quality plan", "Hospital Information System" ], "skillCount" : 25, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "_score" : 745.1506, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ad31774d8ee00a0714cb7", "title" : "Sr Reference File Maintainer Assoc", "company" : "IQVIA", "industry" : "Healthcare", "salary" : { "min" : 600000.0, "max" : 900000.0, "currency" : "PHP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Sr Reference File Maintainer Assoc in Taguig City, Philippines, adjusted for the healthcare industry and full-time employment." }, "location" : "Taguig City, Philippines", "locations" : [ "Taguig City, Philippines" ], "timestamp" : "2026-06-14T17:57:17.169", "fingerprint" : "a056d4af8b14a4142b25a55c2c0d44cbaced0f6e0a33b6e646d4cf32ef46dfb6", "source" : "workday", "language" : "en", "applyUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Taguig-City-Philippines/Sr-Reference-File-Maintainer-Assoc_R1550629", "externalId" : "R1550629", "industryFunction" : { }, "locationPoint" : "14.5243,121.0792", "structuredLocations" : [ { "city" : "Taguig City", "country" : "Philippines", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "14.5270538,121.0744942" } ], "locationText" : "Taguig City, Philippines", "employmentType" : "FULL_TIME", "experienceMinYears" : 2, "experienceMaxYears" : 5, "experienceLevel" : "Mid", "technicalSkills" : "Windows applications", "professionalSkills" : [ "Healthcare account" ], "hardSkillsList" : [ "Data analysis" ], "softSkillsList" : [ "Critical thinking", "Problem-solving skills" ], "hardSkills" : [ { "name" : "Data analysis", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Critical thinking" }, { "name" : "Problem-solving skills" } ], "majorSkills" : "Reference data maintenance, Data validation, Information gathering", "majorSkillsList" : [ "Reference data maintenance", "Data validation", "Information gathering" ], "coreResponsibilities" : "Complete maintenance of reference data, Perform research to gather information, Validate completeness or accuracy of the data, Perform outbound phone verification of details, Capture client-required details, Perform ad hoc data analysis, Participate on various process improvement, Validate that information gathered represents accurate new data, Result in an update, creation, or deletion in", "domainKnowledge" : "Healthcare organizations; Prescribers", "domainList" : [ "healthcare-organizations", "prescribers" ], "domainSpecificKnowledge" : [ "Healthcare organizations", "Prescribers" ], "toolProficiency" : [ "Excel", "Word" ], "communicationSkills" : "Verbal communication; Written communication", "innovationCreativity" : "Process improvement", "problemSolvingSkills" : "Root cause analysis", "specialRequirements" : "Onsite training", "qualificationsBasic" : "2-year experience in handling voice and healthcare account, College undergraduates with BPO experience, Basic knowledge in Windows applications, Verbal and / or written communication skills in English, Critical thinking and problem-solving skills, Demonstrate understanding of complex concepts and processes, Willing to work in mid shift, Amenable to onsite training in Mckinley, Taguig", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Job Responsibilities:** * Complete maintenance of reference data (healthcare Organizations and Prescribers) as essential for UK Production. * Perform research such as Internet Search, Phone Verification, Database Matches and etc. to gather information from third parties that will validate the completeness or accuracy of the data. * Perform outbound phone verification of details on Organization and Prescriber records to validate accuracy of reference data maintained as well as capture client-required details such as primary office address and primary profession/specialty. * Performs ad hoc data analysis and participates on various process improvement as needed. * Validate that the information gathered from third-party sources represents accurate new data that should result in an update, creation, or deletion in the database existing data. **Job Requirement:** * 2-year experience in handling voice and healthcare account * College undergraduates with BPO experience are also welcome to apply. * Basic knowledge in Windows applications (Excel, Word). * Strong verbal and / or written communication skills in either the language of the country supplied or English. * Critical thinking and problem-solving skills. * Demonstrate strong understanding of complex concepts and processes. * Candidate must be willing to work in mid shift * **Amenable to onsite training in Mckinley, Taguig** IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at [https://jobs.iqvia.com](https://jobs.iqvia.com/) IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.", "summaryDescription" : "Sr Reference File Maintainer Assoc at IQVIA. Skills: Reference data maintenance, Data validation, Information gathering. Complete maintenance of reference data. Perform research to gather information", "postedDate" : "2026-06-12T03:58:43.084", "createdAt" : "2026-06-12T03:58:43.046", "lastUpdated" : "2026-06-14T17:57:17.169", "ingestTimestamp" : "2026-06-12T03:58:43.046", "mongoId" : "6a2ad31774d8ee00a0714cb7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Taguig-City-Philippines/Sr-Reference-File-Maintainer-Assoc_R1550629", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Data analysis", "Critical thinking", "Problem-solving skills", "Reference data maintenance", "Data validation", "Information gathering", "Healthcare account", "Healthcare organizations", "Prescribers", "Excel", "Word" ], "skillCount" : 11, "jobCategory" : "other", "seniorityLevel" : "senior", "dataQualityScore" : 1.0, "_score" : 734.5139, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2cb05874d8ee00a09d9ae9", "title" : "Laboratory Operations & Maintenance Technician", "company" : "Periodic Labs", "industry" : "Atoms: Research Lab, physics, chemistry", "salary" : { "min" : 100000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Menlo Park", "locations" : [ "Menlo Park" ], "timestamp" : "2026-06-15T06:37:43.736", "fingerprint" : "b39c5d93d85ac16b195177f87aeba783159a862441eb60b890b334e57af75a72", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/periodic-labs/b1ad8632-f489-4922-8805-42d84711cda1/application", "externalId" : "b1ad8632-f489-4922-8805-42d84711cda1", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Menlo Park", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.4519671,-122.1779920" } ], "locationText" : "Menlo Park, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "remoteFriendly" : false, "rawDescription" : "ABOUT PERIODIC LABS The most important scientific discoveries of our time won't happen in a traditional lab. We're an AI and physical sciences company building state-of-the-art models to accelerate breakthroughs across materials, energy, and beyond. Backed by world-class investors and growing rapidly, we operate at the pace the frontier requires. Our team brings deep expertise, genuine ownership, and an insatiable drive to push the boundaries of what's scientifically possible. ABOUT THE ROLE Periodic Labs is building an autonomous laboratory for high-throughput materials discovery — combining advanced synthesis, characterization, automation, robotics, and AI to accelerate the development of next-generation materials. We're looking for a highly capable, hands-on Laboratory Operations & Maintenance Technician to help build, maintain, and scale the physical infrastructure that enables our scientific and engineering teams to move quickly. This is an ideal role for someone who enjoys solving practical problems, working with tools, building systems, troubleshooting equipment, and taking ownership of laboratory operations. You'll work across equipment maintenance, gas and vacuum systems, utilities, instrumentation, automation support, machine shop operations, inventory management, and laboratory buildout projects. WHAT YOU'LL DO Equipment Maintenance & Reliability - Execute preventative maintenance programs for laboratory equipment using MaintainX CMMS; develop and improve maintenance procedures, inspection checklists, and work order templates - Perform routine inspections, cleaning, calibration checks, and equipment upkeep across mechanical, electrical, pneumatic, gas, vacuum, and fluid handling systems - Troubleshoot and repair equipment; identify recurring failure modes and implement corrective actions to improve uptime - Coordinate service visits and maintenance activities with equipment vendors - Service vacuum pumps, cooling water systems, chillers, and associated infrastructure; verify equipment meets OEM specifications after maintenance or repairs Asset Management & Documentation - Maintain an accurate asset registry within MaintainX, including equipment records (manuals, schematics, service histories, serial numbers, manufacturer contacts) - Label equipment with asset numbers and QR codes; update equipment layouts, utility matrices, and infrastructure documentation - Track maintenance history and equipment performance metrics Utilities & Infrastructure - Maintain laboratory utility systems including compressed gases, vacuum systems, process cooling water, exhaust systems, gas detection, and general lab infrastructure - Build and modify gas and fluid handling systems from P&IDs and engineering drawings; assemble and install tubing, regulators, valves, gauges, sensors, and associated hardware - Support utility capacity planning and identify infrastructure constraints Equipment Installation & Commissioning - Support installation and startup of new laboratory equipment; coordinate utility hookups including power, water, gas, vacuum, and networking - Procure and install supporting infrastructure including tubing, fittings, pumps, sensors, regulators, and instrumentation - Perform installation verification and commissioning activities; document as-built configurations and equipment changes Automation & Controls Support - Support Controls and Automation Engineers with equipment integration projects - Install and maintain thermocouples, RTDs, pressure transducers, flow meters, solenoid valves, gas sensors, and safety interlocks - Route, terminate, and label instrumentation and communication wiring; assist with sensor replacement, control panel modifications, and field troubleshooting Machine Shop & Fabrication - Fabricate fixtures, brackets, guards, adapters, and experimental hardware using drill press, band saw, chop saw, belt sander, bench grinder, manual mill, and manual lathe - Modify commercial components and support custom equipment builds; maintain machine shop organization and tooling Inventory & Laboratory Operations - Maintain inventories of spare parts, maintenance consumables, PPE, and laboratory supplies; identify critical spare parts and establish appropriate stock levels - Receive and organize incoming equipment, chemicals, gases, and supplies; register chemicals and gas cylinders within laboratory inventory systems - Coordinate gas cylinder replacement and deliveries; support hazardous waste staging and disposal activities - Assist with laboratory organization, equipment moves, and expansion projects Safety & Compliance - Perform all work in accordance with laboratory safety procedures and LOTO requirements; participate in routine safety inspections and identify unsafe conditions - Support safe installation and modification of laboratory equipment and infrastructure - Maintain clean, organized, and professional workspaces; use all appropriate PPE (lab coats, gloves, safety glasses, hearing protection, respirators) YOU WILL THRIVE IN THIS ROLE IF YOU HAVE - 5+ years of experience in laboratory operations, manufacturing, semiconductor, chemical processing, pilot plant, industrial maintenance, or a related environment - The ability to read and interpret P&IDs, mechanical drawings, electrical wiring diagrams, and equipment manuals - Hands-on experience with hand tools, power tools, and mechanical assembly, with strong troubleshooting and problem-solving skills - An associate degree, technical certification, military technical training, trade apprenticeship, or equivalent hands-on experience - Comfort operating in a fast-paced, dynamic startup environment with shifting priorities ESPECIALLY STRONG CANDIDATES MAY ALSO HAVE - Swagelok tubing, fitting, and tube bending experience; gas manifold assembly from P&IDs - Vacuum systems and/or compressed gas systems experience - Semiconductor equipment maintenance experience - Electrical troubleshooting down to PCB/component level using multimeters - MaintainX or other CMMS experience - Forklift or material handling equipment certification - Chemical handling or laboratory operations experience - Process piping and instrumentation experience MECHANICS Minimum education: Bachelor's degree or an equivalent combination of education and training or experience Location: Our lab is located in Menlo Park and we prefer folks to be located in Menlo Park or San Francisco but can be flexible based on role Compensation: The annual compensation range for this role is approximately $100,000 Visa sponsorship: Yes, we sponsor visas and will do everything we can to assist in this process with our legal support. We're building a team of the world's best — the scientists, engineers, and problem-solvers who don't just follow the frontier, they define it. If you're driven to bring AI to life in the physical world and make discoveries that have never been made before, you belong here.", "summaryDescription" : "Laboratory Operations & Maintenance Technician at Periodic Labs", "createdAt" : "2026-06-13T21:49:16.037", "lastUpdated" : "2026-06-15T06:37:43.736", "ingestTimestamp" : "2026-06-13T21:49:16.037", "mongoId" : "6a2cb05874d8ee00a09d9ae9", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 100000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 727.5337, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "id" : "693c2b8470f0b99d5843f9ea", "title" : "System Dev Manager, Antenna Calibration", "company" : "Amazon Kuiper Manufacturing Enterprises LLC", "industry" : "Hardware Development, System Development Engineering, alexa and amazon devices", "salary" : { "min" : 149700.0, "max" : 258800.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Redmond, Washington, USA", "locations" : [ "Redmond, Washington, USA" ], "timestamp" : "2026-06-15T01:14:18.144", "fingerprint" : "769591ec13dfe33bba67d0d98f7455f3eb8af6a0a09b3e6017977b7ce5144da7", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3137681/apply", "externalId" : "6620d191-888c-4cb4-9781-f1d1ea35e933", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Redmond", "state" : "Washington", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "47.6694141,-122.1238767" } ], "locationText" : "Redmond, Washington, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "experienceLevel" : "Manager", "technicalSkills" : "ASIC design, FPGA, RF Hardware, DSP, Digital modulation, Radio architecture, Line-up analysis, RF system design, AWS", "professionalSkills" : [ "Systems architecture", "Hardware engineering", "Software design", "System performance", "Antenna beampattern measurement", "High-volume manufacturing", "Simulation", "Measurement", "Calibration", "Optimization", "Baseband/RF/antenna systems", "System design" ], "hardSkillsList" : [ "Antenna calibration", "Phased array calibration", "Signal processing", "Algorithm development", "Performance analysis", "Design trade-off studies", "End-to-end modeling", "Lab measurement", "System validation" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Antenna calibration", "level" : "intermediate" }, { "name" : "Phased array calibration", "level" : "intermediate" }, { "name" : "Signal processing", "level" : "intermediate" }, { "name" : "Algorithm development", "level" : "intermediate" }, { "name" : "Performance analysis", "level" : "intermediate" }, { "name" : "Design trade-off studies", "level" : "intermediate" }, { "name" : "End-to-end modeling", "level" : "intermediate" }, { "name" : "Lab measurement", "level" : "intermediate" }, { "name" : "System validation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "Antenna calibration, Phased array systems, RF system design, DSP techniques", "majorSkillsList" : [ "Antenna calibration", "Phased array systems", "RF system design", "DSP techniques" ], "coreResponsibilities" : "Design calibration systems, Implement calibration systems, Develop calibration signals, Develop calibration processing, Develop calibration algorithms, Analyze phased array performance, Conduct design trade-off studies, Model baseband/RF/antenna systems, Simulate baseband/RF/antenna systems, Analyze baseband/RF/antenna systems, Measure antenna performance, Validate antenna performance, Measure phased array systems, Validate phased array systems, Measure subsystems, Validate subsystems, Simulate radio designs, Measure radio designs, Fine-tune radio designs", "teamCollaboration" : "Collaborate with systems architects; Collaborate with hardware engineering; Collaborate with FW/SW design teams; Work with multi-disciplinary team; Work with antenna teams; Work with modem teams; Work with RF teams; Work with Digital teams", "projectManagementSkills" : [ "Agile software development", "Agile engineering practices" ], "domainKnowledge" : "Phased array antennas; LEO satellites; Broadband access; Digital divide; ASIC design; Wireless technologies; Medium access procedures; Probability theory; Estimation theory", "domainList" : [ "phased-array-antennas", "leo-satellites", "broadband-access", "digital-divide", "asic-design", "wireless-technologies", "medium-access-procedures", "probability-theory", "estimation-theory" ], "domainSpecificKnowledge" : [ "Phased array antennas", "LEO satellites", "Broadband access", "Digital divide", "ASIC design", "Wireless technologies", "Medium access procedures", "Probability theory", "Estimation theory" ], "toolProficiency" : [ "VSA", "VSG", "VNA", "Oscilloscopes", "CST", "HFSS" ], "problemSolvingSkills" : "Design trade-off studies", "specialRequirements" : "U. S. citizen or national, U. S. permanent resident, Lawfully admitted into the U. S.", "qualificationsBasic" : "5+ years managing system development teams, 7+ years systems engineering experience, Bachelor's degree in Computer Science, Experience in agile software development, 7+ years industry work experience, Experience in DSP techniques, Experience with lab test equipment", "qualificationsPreferred" : "Knowledge of professional software engineering best practices, Knowledge of systems engineering fundamentals, Experience with Agile engineering practices, Experience with AWS platforms, MS in Electrical Engineering, PhD with 5+ years experience, Experience with phased arrays, Experience with antenna simulation tools, Understanding of modern wireless technologies, Familiarity with probability and estimation theory", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Amazon LEO is an initiative to increase global broadband access through a constellation of 3,236 satellites in low Earth orbit (LEO). Its mission is to bring fast, affordable broadband to unserved and underserved communities around the world. Amazon Leo will help close the digital divide by delivering fast, affordable broadband to a wide range of customers, including consumers, businesses, government agencies, and other organizations operating in places without reliable connectivity. The Antenna Calibration team is responsible for the calibration of all of the phased array antennas for Amazon Leo. This includes influence into custom ASIC design, bring-up of hardware, validation of system performance, antenna beampattern measurement, simulation, high-volume manufacturing, as well as the design and development of multiple software applications to carry out our areas of ownership. As a Systems Manager for antenna calibration, you will collaborate with systems architects, hardware engineering design teams & FW/SW design teams to build and test systems containing FPGAs, 1P/3P custom ASICs, and RF Hardware. You will be responsible for key aspects of phased array antenna system design, simulation, measurement, calibration and optimization. You will be working in a collaborative environment with a multi-disciplinary team to deliver advanced high-performance phased array antenna systems. In this role, your responsibilities will include: · Designing and implementing phased array calibration systems, signals, processing and algorithms · Performance analysis and design trade-off studies of phased arrays · End-to-end modeling, simulation and analysis of baseband/RF/antenna systems · Lab measurement and validation of performance of antennas, and phased array systems and subsystems · Working with antenna, modem, RF and Digital teams to simulate, measure and fine-tune radio designs Export Control Requirement: Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum. Basic Qualifications: - 5+ years of managing system or software development teams experience - 7+ years of relevant hands-on systems engineering and administrative work in networking, storage systems, operating systems experience - Bachelor's degree in Computer Science, Engineering, Mathematics, or a related field - Experience in managing system or software development teams - Experience in agile software development methodology - 7+ years of work experience in Aerospace/Semiconductor/Consumer Electronics industry - Experience in DSP techniques, digital modulation, radio architecture, line-up analysis, RF system design - Experience with lab test equipment like VSAs, VSGs, VNAs and Oscilloscopes Preferred Qualifications: - Knowledge of professional software engineering & best practices for full software development life cycle, including coding standards, software architectures, code reviews, source control management, continuous deployments, testing, and operational excellence - Knowledge of systems engineering fundamentals (networking, storage, operating systems) - Experience with Agile engineering practices (Kanban, continuous delivery, etc.) - Experience with AWS platforms, services, and design patterns - MS in Electrical Engineering with 8+ years of work experience or PhD with 5+ years of experience - Experience working with phased arrays, calibration and antenna measurement - Experience with one of the mainstream antenna simulation tools (CST/HFSS) - Good understanding of modern wireless technologies (OFDM/MIMO) and medium access procedures - Familiarity with basics of probability and estimation theory Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner. Our compensation reflects the cost of labor across several US geographic markets. The base pay for this position ranges from $149,700/year in our lowest geographic market up to $258,800/year in our highest geographic market. Pay is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. Amazon is a total compensation company. Dependent on the position offered, equity, sign-on payments, and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, financial, and/or other benefits. For more information, please visit https://www.aboutamazon.com/workplace/employee-benefits . This position will remain posted until filled. Applicants should apply via our internal or external career site.", "summaryDescription" : "System Dev Manager, Antenna Calibration at Amazon Kuiper Manufacturing Enterprises LLC. Skills: Antenna calibration, Phased array systems, RF system design, DSP techniques. Design calibration systems. Implement calibration systems", "postedDate" : "2026-06-13T01:04:15.688", "createdAt" : "2026-06-13T01:04:15.688", "lastUpdated" : "2026-06-15T01:14:18.144", "ingestTimestamp" : "2026-06-13T01:04:15.688", "mongoId" : "693c2b8470f0b99d5843f9ea", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3137681/apply", "salaryAnnualMin" : 149700, "salaryAnnualMax" : 258800, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Antenna calibration", "Phased array calibration", "Signal processing", "Algorithm development", "Performance analysis", "Design trade-off studies", "End-to-end modeling", "Lab measurement", "System validation", "Leadership", "Phased array systems", "RF system design", "DSP techniques", "Systems architecture", "Hardware engineering", "Software design", "System performance", "Antenna beampattern measurement", "High-volume manufacturing", "Simulation", "Measurement", "Calibration", "Optimization", "Baseband/RF/antenna systems", "System design", "Agile software development", "Agile engineering practices", "Phased array antennas", "LEO satellites", "Broadband access", "Digital divide", "ASIC design", "Wireless technologies", "Medium access procedures", "Probability theory", "Estimation theory", "VSA", "VSG", "VNA", "Oscilloscopes", "CST", "HFSS" ], "skillCount" : 42, "jobCategory" : "other", "dataQualityScore" : 1.0, "_score" : 702.60455, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Aerospace" }, { "id" : "693c2b9270f0b99d58440136", "title" : "Software Dev Manager, Antenna Calibration", "company" : "Amazon Kuiper Manufacturing Enterprises LLC", "industry" : "Software Development, alexa and amazon devices", "salary" : { "min" : 166400.0, "max" : 287700.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Redmond, Washington, USA", "locations" : [ "Redmond, Washington, USA" ], "timestamp" : "2026-06-15T05:49:27.587", "fingerprint" : "f4dcfb7b183fdba3b22fcc84f1196a58af26b7efae4e73495d72b088b0897348", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.com/jobs/3137687/apply", "externalId" : "e545ac35-ceb0-4c71-9647-7edbc7ac406f", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Redmond", "state" : "Washington", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "47.6694141,-122.1238767" } ], "locationText" : "Redmond, Washington, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 3, "experienceLevel" : "Manager", "technicalSkills" : "ASIC design, FPGA, ASICs, RF Hardware", "professionalSkills" : [ "System design", "Hardware engineering", "Software design", "System performance", "High-volume manufacturing" ], "hardSkillsList" : [ "Antenna calibration", "Beampattern measurement", "Simulation", "Data storage", "Hardware test automation", "Firmware design", "Application development", "Design automation", "Bring up tools" ], "softSkillsList" : [ "Leadership", "Mentoring", "Coaching" ], "hardSkills" : [ { "name" : "Antenna calibration", "level" : "intermediate" }, { "name" : "Beampattern measurement", "level" : "intermediate" }, { "name" : "Simulation", "level" : "intermediate" }, { "name" : "Data storage", "level" : "intermediate" }, { "name" : "Hardware test automation", "level" : "intermediate" }, { "name" : "Firmware design", "level" : "intermediate" }, { "name" : "Application development", "level" : "intermediate" }, { "name" : "Design automation", "level" : "intermediate" }, { "name" : "Bring up tools", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" }, { "name" : "Coaching" } ], "majorSkills" : "Antenna calibration, Software development, Hardware integration", "majorSkillsList" : [ "Antenna calibration", "Software development", "Hardware integration" ], "coreResponsibilities" : "Influence custom ASIC design, Bring-up hardware, Validate system performance, Measure antenna beampattern, Perform simulation, Oversee high-volume manufacturing, Design software applications, Develop software for manufacturing, Develop calibration software for on-orbit applications, Characterize subsystems and systems related to antennas, Manage complex data storage, Automate hardware tests, Design firmware, Implement firmware, Develop applications, Design automation for 2D and 3D structures, Develop bring up tools for phased array systems, Develop scripts for phased array systems", "teamCollaboration" : "Collaborate with systems architects; Collaborate with hardware engineering design teams; Collaborate with FW/SW design teams", "domainKnowledge" : "Phased array antennas; LEO satellites; Broadband access; ASIC design; RF Hardware; Chip to chip communication", "domainList" : [ "phased-array-antennas", "leo-satellites", "broadband-access", "asic-design", "rf-hardware", "chip-to-chip-communication" ], "domainSpecificKnowledge" : [ "Phased array antennas", "LEO satellites", "Broadband access", "ASIC design", "RF Hardware", "Chip to chip communication" ], "communicationSkills" : "Describe software product features; Describe technical designs; Describe product strategy", "qualificationsBasic" : "3+ years engineering team management, 7+ years working directly within engineering teams, 3+ years designing or architecting systems, 8+ years leading definition and development of multi tier web services, Knowledge of engineering practices for full software/hardware/networks development life cycle, Experience partnering with product or program management teams, Bachelor's degree or foreign equivalent in Computer Science, Engineering, Mathematics, or related field, U. S. citizen or national, U. S. permanent resident, or lawfully admitted into the U. S. as a refugee or granted asylum", "qualificationsPreferred" : "Experience communicating with users, other technical teams, and senior leadership, Experience recruiting, hiring, mentoring/coaching and managing teams of Software Engineers, Experience leading an embedded software team, Experience working with FPGAs, custom ASICs, and high speed chip to chip communication", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Amazon LEO is an initiative to increase global broadband access through a constellation of 3,236 satellites in low Earth orbit (LEO). Its mission is to bring fast, affordable broadband to unserved and underserved communities around the world. Amazon Leo will help close the digital divide by delivering fast, affordable broadband to a wide range of customers, including consumers, businesses, government agencies, and other organizations operating in places without reliable connectivity. The Antenna Calibration team is responsible for the calibration of all of the phased array antennas for Amazon Leo. This includes influence into custom ASIC design, bring-up of hardware, validation of system performance, antenna beampattern measurement, simulation, high-volume manufacturing, as well as the design and development of multiple software applications to carry out our areas of ownership. As a software manager for antenna systems, you will collaborate with systems architects, hardware engineering design teams & FW/SW design teams to build and test systems containing FPGAs, 1P/3P custom ASICs, and RF Hardware. Responsibilities include: - Software design for high-volumn phased array manufacturing - Calibration software for on-orbit applications - Characterizing subsystems and systems related to antennas - Complex data storage - Hardware test automation - Firmware design and implementation - Application development - Design automation for 2D and 3D structures - Develop bring up tools and scripts for phased array systems Export Control Requirement: Due to applicable export control laws and regulations, candidates must be a U.S. citizen or national, U.S. permanent resident (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum. Basic Qualifications: - 3+ years of engineering team management experience - 7+ years of working directly within engineering teams experience - 3+ years of designing or architecting (design patterns, reliability and scaling) of new and existing systems experience - 8+ years of leading the definition and development of multi tier web services experience - Knowledge of engineering practices and patterns for the full software/hardware/networks development life cycle, including coding standards, code reviews, source control management, build processes, testing, certification, and livesite operations - Experience partnering with product or program management teams - Bachelor's degree or foreign equivalent in Computer Science, Engineering, Mathematics, or a related field Preferred Qualifications: - Experience in communicating with users, other technical teams, and senior leadership to collect requirements, describe software product features, technical designs, and product strategy - Experience in recruiting, hiring, mentoring/coaching and managing teams of Software Engineers to improve their skills, and make them more effective, product software engineers - Experience leading an embedded software team, working with FPGAs, custom ASICs, and high speed chip to chip communication. Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner. Our compensation reflects the cost of labor across several US geographic markets. The base pay for this position ranges from $166,400/year in our lowest geographic market up to $287,700/year in our highest geographic market. Pay is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. 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TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

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Fusion has multiple pipeline programs entering early FIH trials. In addition, Fusion is pursuing combination programs between RCs and other therapeutic modalities including DNA Damage Response Inhibitors (DDRis) and immune-oncology agents. To support execution for these programs, Fusion has a fully operational Good Manufacturing Practice (GMP) compliant state-of-the-art radioconjugate manufacturing facility to meet the demand for our growing pipeline of RCs. **Overview** The Microbiology Supervisor is responsible for leading and supervising all aspects of microbiological control in a regulated aseptic manufacturing environment, with a focus on sterile radiopharmaceutical products. This role combines technical microbiology expertise with hands-on supervisory responsibilities, ensuring robust contamination control, high-quality environmental monitoring, radiological controls and compliance with global regulatory standards (including EU Annex 1 and GMP). Other duties can be assigned as required. **Responsibilities** * Microbiology Leadership: Lead and mentor the microbiology team, supervising daily lab operations and resource planning to meet manufacturing and clinical/commercial supply timelines; manage workload and performance, and drive continuous training to maintain meticulous quality and compliance standards. * Aseptic Process & Risk Assessment: Oversee aseptic process design and simulation, risk assessments, evaluate changes, ensuring compliance with regulatory requirements. * Environmental Monitoring: Establish, maintain, and analyze environmental monitoring programs and EMPQ, perform trend analysis and conduct contamination risk assessments. * Contamination Control: Maintain the site’s Contamination Control Strategy (CCS), including cleanroom zoning, gowning, and disinfectant programs. * Cleanroom Oversight: Monitor cleanroom operations, working cross-functionally with production teams to ensure GMP compliance, best aseptic practices, and effective microbiological controls. * Regulatory Compliance: Act as SME for EU GMP (incl. Annex 1), FDA cGMPs (21 CFR 210/211, Part 11), PIC/S, ICH Q8–Q10/Q9(R1), ISO 14644/13408, relevant sterilization standards (ISO 11135/11137/17665), and compendial requirements (USP/Ph. Eur./JP), ensuring microbiology operations, EM, methods, data integrity, and validations meet internal and external expectations across all markets. * Incident Investigation: Lead contamination event investigations, root cause analysis, CAPA implementation, and process improvements. * Collaboration: Work with cross-functional teams (Quality, Engineering, Production, Validation) on microbiological risk management and regulatory alignment. **Radiopharmaceutical-Specific Responsibilities** * Microbiology Oversight for Radiopharmaceuticals: Adapt and oversee environmental monitoring, bioburden, and sterility assurance strategies for rapid release and short half-life radiopharmaceutical products, including validated parametric/alternative release approaches. * Technical Guidance for Radiopharmaceutical Suites: Advise on interventions in shielded isolators/hot cells. Ensure pragmatic contamination control solutions for frequent setups and short campaigns without compromising quality. * Sampling Plan Design: Design and supervise practical sampling plans tailored for radiopharmaceutical products, ensuring robust data collection and contamination control despite operational constraints. **Qualifications** * Education: Bachelor’s degree (BSc) in Microbiology, Biological Sciences, or a related discipline is required. * Relevant Experience: 5–8 years of experience supervising or leading teams within a laboratory or sterile/aseptic manufacturing environment, including experience with staff training, scheduling, and performance management. * Significant hands-on work with environmental monitoring, contamination control, cleanroom operations, and regulatory compliance (EU Annex 1, cGMP, etc.). * Specialized Experience: previous experience in radiopharmaceutical environments is an asset. * Work in designated labs with radiological controls, contamination monitoring, and PPE requirements. * Willingness and ability to work extended shifts, weekends, or holidays as needed. Occasional after-hours support for investigations, equipment alarms, or urgent testing. * On-site presence in Hamilton, Ontario in classified areas, including work in isolators/hot cells with appropriate PPE and radiation safety protocols * <5% travel required **At AstraZeneca, we foster a collaborative, innovative culture with opportunities to work across teams, functions, and geographies. You’ll join a collaborative, innovative community with opportunities to work across teams, functions, and geographies—where your ideas move fast and your impact is visible. We’re committed to sustainability and equity, taking bold action on climate, access to healthcare, and disease prevention.** **⠀** Annual base salary for this position ranges from 86,266.40 to 113,224.65. AstraZeneca is committed to providing fair and equitable compensation opportunities to all colleagues. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The range provided in this posting represents an offer pay range used in a majority of situations. The base pay offered will vary depending on multiple individualized factors, including the candidate's skills and experience, job-related knowledge, and other specific business and organizational needs. In some cases, offers outside the range may also be considered to address unique circumstances. In addition, our permanent positions offer an annual Variable Pay Bonus/Short Term Incentive opportunity as well as eligibility to participate in our equity-based long-term incentive program (if applicable to role). Benefits offered for permanent roles include a competitive Flex Benefits & Retirement Savings Program, 4 weeks’ paid vacation, and annual Personal Days. Fixed Term Contract/Temporary positions (excluding students) are offered a Contract Benefits Program. We are using AI as part of the recruitment process. This advertisement relates to a current vacancy.", "summaryDescription" : "Microbiology Laboratory Supervisor — Radio Conjugate Laboratory at Fusion Pharmaceuticals. Skills: Microbiological control, Aseptic manufacturing, Regulatory compliance, Radiopharmaceuticals. Lead microbiology team. Supervise daily lab operations", "postedDate" : "2026-06-11T07:00:24.095", "createdAt" : "2026-06-12T07:00:23.916", "lastUpdated" : "2026-06-15T00:36:57.393", "ingestTimestamp" : "2026-06-12T07:00:23.916", "mongoId" : "6a2af78274d8ee00a073d5fb", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Canada--Hamilton--Longwood-Road-South/Microbiology-Laboratory-Supervisor---Radio-Conjugate-Laboratory_R-254267-1", "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Microbiological control", "Environmental monitoring", "Contamination control", "Aseptic process", "Sterility assurance", "Bioburden testing", "Root cause analysis", "CAPA implementation", "Radiation safety", "Leadership", "Mentoring", "Aseptic manufacturing", "Regulatory compliance", "Radiopharmaceuticals", "Risk assessment", "Process design", "Trend analysis", "Resource planning", "Performance management", "Staff training", "Parametric release", "Alternative release", "Radioconjugates", "Precision medicines", "Sterile radiopharmaceutical products", "Radiopharmaceutical suites", "Shielded isolators", "Hot cells", "Short half-life products" ], "skillCount" : 29, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 1.0, "_score" : 675.3297, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Pharmaceuticals" }, { "id" : "6a2a3f5074d8ee00a05c2156", "title" : "ADAS Calibration & Validation Engineer", "company" : "Scout Motors", "salary" : { "min" : 140000.0, "max" : 170000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Charlotte, NC", "locations" : [ "Charlotte", "NC" ], "timestamp" : "2026-06-11T07:37:57.352", "fingerprint" : "502dae6e74af3f667a741ca70e32e758eea033215161e3f789e4536df62e944c", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/scoutmotors/jobs/5155610007", "externalId" : "5155610007", "structuredLocations" : [ { "city" : "Charlotte", "state" : "North Carolina", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "35.2272086,-80.8430827" } ], "locationText" : "Charlotte, North Carolina, United States", "technicalSkills" : "CAN, Ethernet", "professionalSkills" : [ "Calibration configuration", "Release management", "Problem-solving" ], "hardSkillsList" : [ "Data analysis", "Root-cause analysis" ], "hardSkills" : [ { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Root-cause analysis", "level" : "intermediate" } ], "majorSkills" : "ADAS calibration, ADAS validation", "majorSkillsList" : [ "ADAS calibration", "ADAS validation" ], "coreResponsibilities" : "Execute ADAS features calibration and validation, Collaborate with cross functional peers, Meet ADAS calibration and validation deliverables, Develop calibration variants for different vehicles, Participate in ADAS calibration trips, Define trip deliverables, Measure development progress, Provide calibration and validation status, Develop HIL test cases, Stay up-to-date with ADAS technologies, Drive continuous improvement and innovation", "teamCollaboration" : "Cross functional peers; Multidisciplinary teams; Multicultural teams", "domainKnowledge" : "ADAS technologies; Automotive communication protocols; ISO 26262; SAE J3016; FMVSS", "domainList" : [ "adas-technologies", "automotive-communication-protocols", "iso-26262", "sae-j3016", "fmvss" ], "domainSpecificKnowledge" : [ "ADAS technologies", "Automotive communication protocols", "ISO 26262", "SAE J3016", "FMVSS" ], "toolProficiency" : [ "INCA", "Creta", "CANoe", "CANalyzer", "JIRA", "Confluence" ], "communicationSkills" : "Present technical information; Influence decision-making", "innovationCreativity" : "Innovate", "problemSolvingSkills" : "Analytical problem-solving; Root-cause system issues; Implement effective solutions", "specialRequirements" : "4 days per week in the office, Regular in-person meetings, Travel to participate in events", "qualificationsBasic" : "Bachelor's or master’s degree in Electrical Engineering, Mechanical Engineering, Computer Science, or a related field, 8+ years of experience in ADAS feature development or calibration release within the automotive industry, Experience with calibration configuration and release management utilizing calibration tools, Familiarity with automotive communication protocols (CAN and Ethernet), Familiarity with tools for development, simulation, and testing, Analytical problem-solving skills, Ability to operate a vehicle in the US", "qualificationsPreferred" : "Fluency in German is a plus", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Here at Scout Motors, we're carrying forward the heritage of one of the most iconic American vehicles in history. A vehicle dating back to 1960. One that forged the path for future generations of rugged SUVs and trucks and will do so once again. But Scout is more than just a brand, it’s a legacy steeped in a culture of exploration, caretaking, and hard work. The Scout brand is all about respect. Respect for the past and the future by taking an iconic American brand that hasn’t been around for a while, electrifying it, digitizing it, and loading it with American innovation. Respect for communities by creating a company that stands for its people and its customers. Respect for both work and play, with vehicles that are equally at home at a camp site, a job site, or on a Tuesday commute. And respect for our customers by developing two powertrains that meet their requirements — an all-electric powertrain as well as the Harvester™ range extender powertrain which includes a built-in gas-powered generator with an estimated 500 miles of combined range. At Scout Motors, we empower our talented, inclusive, and entrepreneurial teams to innovate. What makes a Scout employee? Someone who is a visionary and a leader, who seeks new paths and shares lessons learned. A knowledgeable doer who collaborates across the company to build better. A go-getter with unrivaled passion. Join us at Scout Motors and be part of shaping the future of transportation. If you're ready to drive change and make history, apply now! What you’ll do At Scout Motors, you don't just design vehicles- you shape the future of the road. Our Engineering team is where bold ideas meet rigorous execution, building machines that are as durable and capable as the people who drive them. You'll work shoulder-to-shoulder with brilliant minds across disciplines, turning complex challenges into elegant, scalable solutions that meet the highest standards of safety, performance, and user experience. This is a place where your fingerprints are found on metal – where what you design gets built, driven, and remembered. If you're hungry to engineer something that matters, Scout Motors is where that ambition finds its highest gear. Become part of an iconic brand that is set to revolutionize the electric pick-up truck & rugged SUV marketplace by achieving the following: Execution of Scout ADAS features calibration and validation in collaboration with cross functional peers in areas like drive, chassis, and steering. Collaborate with Lead ADAS DRE to meet ADAS calibration and validation deliverables for timing and feature maturity based on SW readiness. Work with lead calibration or validation engineer on calibration and validation plans for ADAS features. Develop calibration variants needed for different vehicles and vehicle trim levels for ADAS features. Participate in ADAS calibration trips including defining trip deliverables and measuring development progress for your area of responsibility Work with lead ADAS DRE to provide overall calibration and validation status for program milestones. Work with Virtual testing team to develop HIL test cases to move testing to virtual as much as possible. Stay up-to-date with the latest advancements in ADAS technologies, industry trends, and regulatory requirements to drive continuous improvement and innovation. Location & Travel Expectations: This role may be based out of the Scout Motors corporate headquarters in Charlotte, NC. This role requires 4 days per week in the office, with one day flexible & regular in-person meetings and events. Applicants should expect that the role will require the ability to convene with Scout colleagues in person and travel to participate in events on behalf of the company from time to time. What you’ll bring We expect all Scout employees to have integrity, curiosity, resourcefulness, and strive to exhibit a positive attitude, as well as a growth mindset. You’ll be comfortable with change and flexible in a fast-paced, high-growth environment. You’ll take a collaborative approach to achieve ambitious goals. Here's what else you'll bring: Bachelor's or master’s degree in Electrical Engineering, Mechanical Engineering, Computer Science, or a related field. 8+ years of experience in ADAS feature development or calibration release within the automotive industry. Experience with calibration configuration and release management utilizing calibration tools (e. g. INCA and Creta) Familiarity with automotive communication protocols (CAN and Ethernet) and tools for development, simulation, and testing (e. g. CANoe, CANalyzer, JIRA, and Confluence). Strong analytical problem-solving skills, with the ability to analyze complex data sets, root-cause system issues, and implement effective solutions. Familiarity with relevant safety standards and legislative regulations (e. g. ISO 26262, SAE J3016, FMVSS) Excellent communication and teamwork skills, with the ability to effectively collaborate with multidisciplinary and multicultural teams, present technical information, and influence decision-making processes. Ability to work independently and self-motivated in a dynamic environment. Must have the ability to operate a vehicle in the US. Fluency in German is a plus What you'll gain The benefits of joining Scout include the chance to build products and a company from the ground up. This is a chance to create something new and lasting – with an iconic brand at its foundation. In addition, Scout provides competitive compensation and benefits to support your physical, mental, and financial wellbeing. Program specifics are detailed in company policies and employee benefit guides, select highlights: Competitive insurance including: Medical, dental, vision and income protection plans 401(k) program with: An employer match and immediate vesting Generous Paid Time Off including: 20 days planned PTO, as accrued 40 hours of unplanned PTO and 14 company or floating holidays, annually Up to 16 weeks of paid parental leave for biological and adoptive parents of all genders Paid leave for circumstances related to bereavement, jury duty, voting time, or military leave Pay Transparency This is a full-time, exempt position eligible to receive a base salary and to participate in an annual performance bonus program. Final salary offered will be determined based on factors including but not limited to the candidate's skills and experience. The annual performance bonus program is preset and not candidate dependent. Initial base salary range = $140,000.00 - $170,000.00 Internal leveling code: IC8 Notice to applicants: To be considered for career opportunities at Scout Motors, applicants must be 18 years of age or older. Residing in San Francisco: Pursuant to the San Francisco Fair Chance Ordinance, Scout Motors will consider for employment qualified applicants with arrest and conviction records. Residing in Los Angeles: Scout Motors will consider for employment qualified applicants with criminal histories in a manner consistent with the Los Angeles Fair Chance Initiative for Hiring Ordinance. Residing in New York City: This role is not eligible for remote work in New York City. Equal Opportunity Scout Motors is committed to employing a diverse workforce and is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, veteran status, disability, pregnancy, or any other characteristics protected by law. Scout Motors is committed to compliance with all applicable fair employment practice laws. If you require reasonable accommodation to complete a job application, pre-employment testing, or a job interview or to otherwise participate in the hiring process, please contact ScoutAccommodations@scoutmotors.com.", "summaryDescription" : "ADAS Calibration & Validation Engineer at Scout Motors. Skills: ADAS calibration, ADAS validation. Execute ADAS features calibration and validation. Collaborate with cross functional peers", "postedDate" : "2026-06-11T07:14:46.469", "createdAt" : "2026-06-11T07:14:46.469", "lastUpdated" : "2026-06-11T07:37:57.352", "ingestTimestamp" : "2026-06-11T07:14:46.469", "mongoId" : "6a2a3f5074d8ee00a05c2156", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 140000, "salaryAnnualMax" : 170000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Data analysis", "Root-cause analysis", "ADAS calibration", "ADAS validation", "Calibration configuration", "Release management", "Problem-solving", "ADAS technologies", "Automotive communication protocols", "ISO 26262", "SAE J3016", "FMVSS", "INCA", "Creta", "CANoe", "CANalyzer", "JIRA", "Confluence" ], "skillCount" : 18, "jobCategory" : "engineering", "jobSubcategory" : "vehicle-software-&-electrical-engineering", "dataQualityScore" : 0.7777778, "_score" : 673.0073, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2ca57374d8ee00a09b68c0", "title" : "Chemistry Laboratory Assistant", "company" : "Interpath Laboratory", "industry" : "Healthcare", "salary" : { "min" : 36000.0, "max" : 48000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an Entry-level Chemistry Laboratory Assistant in Pendleton, United States, adjusted for the healthcare industry." }, "location" : "IP Pendleton 1", "locations" : [ "IP Pendleton 1" ], "timestamp" : "2026-06-15T09:05:31.140", "fingerprint" : "d29ffc975f687a417498d1c888a1dd696aa3515ed42bf391309d0ee90bf9e627", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/interpath/jobs/4284045009", "externalId" : "4284045009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Pendleton", "state" : "Oregon", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "45.6720750,-118.7885967" } ], "locationText" : "Pendleton, Oregon, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "High School", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "Entry", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Basic troubleshooting" ], "hardSkills" : [ { "name" : "Basic troubleshooting", "level" : "intermediate" } ], "majorSkills" : "Diagnostic services, Specimen handling, Quality assurance", "majorSkillsList" : [ "Diagnostic services", "Specimen handling", "Quality assurance" ], "coreResponsibilities" : "Perform basic troubleshooting, Participate in proficiency testing, Participate in quality assurance initiatives, Maintain accurate documentation, Answer phones professionally, Ensure compliance with HIPAA guidelines, Follow established safety protocols, Follow infection control protocols, Take on new duties, Gain valuable experience", "teamCollaboration" : "Support for our team; Collaborative setting", "domainKnowledge" : "Clinical laboratory; Diagnostic services; HIPAA guidelines; Infection control", "domainList" : [ "clinical-laboratory", "diagnostic-services", "hipaa-guidelines", "infection-control" ], "domainSpecificKnowledge" : [ "Clinical laboratory", "Diagnostic services", "HIPAA guidelines", "Infection control" ], "communicationSkills" : "Communicate clearly", "documentationSkills" : "Maintain accurate documentation", "continuousLearning" : "Eager to learn new technology; Eager to learn laboratory processes", "problemSolvingSkills" : "Problem-solving", "specialRequirements" : "Exposure to blood, Exposure to body fluids, Exposure to tissues", "qualificationsBasic" : "High School Diploma or equivalent, Reliable attendance and punctuality, Ability to stand and walk, Frequent use of hands, Ability to lift and carry up to 25 pounds, Ability to read and interpret data, Ability to bend, stoop, and reach, Sustained concentration for accurate specimen handling", "qualificationsPreferred" : "Associate's degree or higher", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Start your career with one of the Pacific Northwest’s largest independent clinical and anatomic laboratories. As a Laboratory Assistant, you’ll gain hands-on experience, work alongside skilled professionals, and take your first step toward a rewarding, purpose-driven career in diagnostic services. Pay: $19/hour commensurate with experience and education *This position is eligible for night differential pay (10%)* Schedule: Full-time; Monday - Friday 10:30pm - 7am Benefits Medical, Dental, Vision with In-Network provide basic troubleshooting as needed. Ensure Quality: Participate in proficiency testing and quality assurance initiatives. Administrative Tasks: Maintain accurate documentation, answer phones professionally, and ensure compliance with HIPAA guidelines. Safety First: Follow established safety and infection control protocols. Adapt and Grow: Take on new duties as operational needs evolve and gain valuable experience for future advancement. Reliability: Maintain consistent, punctual, and reliable attendance to ensure continuity of operations and support for our team and patients. Who You Are Dependable, detail-oriented, and committed to accuracy. Skilled in multitasking and problem-solving in a fast-paced environment. A strong team player who thrives in a collaborative setting. Eager to learn new technology and laboratory processes. Familiar with patient confidentiality and HIPAA guidelines. Qualifications High School Diploma or equivalent. Associate's degree or higher preferred. Reliable attendance and punctuality. Physical Requirements Mobility: Ability to stand and walk for extended periods. Manual Dexterity: Frequent use of hands and fingers to handle lab instruments and computer systems. Lifting: Ability to lift and carry up to 25 pounds. Vision & Hearing: Ability to read and interpret data, identify specimens, and communicate clearly in person and by phone. Flexibility: Ability to bend, stoop, and reach to access equipment or supplies. Attention to Detail: Sustained concentration for accurate specimen handling and testing. OSHA Category: This position involves exposure to blood, body fluids, and/or tissues. Employees performing these duties are offered the opportunity to receive the Hepatitis-B vaccination series. About Us: Interpath Laboratory is a family-owned and operated clinical and anatomic pathology laboratory serving communities across Oregon, Washington, Nebraska, and Idaho. With more than 90 locations and over 60 years of steady growth, we are one of the Pacific Northwest’s leading independent laboratories, with plans for continued and strategic expansion into the Midwest. We are known for delivering rapid, reliable, and cost-effective laboratory testing while maintaining the flexibility, innovation, and personal connection that come from remaining independent. Our success is built on strong relationships—with our clients, our patients, and most importantly, our employees. At Interpath, we foster a collaborative, supportive work environment where teamwork, professionalism, and positive attitudes matter. We believe great results start with great people, and we are committed to creating a workplace where employees can build meaningful careers while making a real impact in the communities we serve. We are excited to share with you a short video that shows why the Interpath family is so special. Please click here: https://youtu.be/iMaXUt6s9rg", "summaryDescription" : "Chemistry Laboratory Assistant at Interpath Laboratory. Skills: Diagnostic services, Specimen handling, Quality assurance. Perform basic troubleshooting. Participate in proficiency testing", "postedDate" : "2026-06-14T03:49:37.131", "createdAt" : "2026-06-14T03:49:37.131", "lastUpdated" : "2026-06-15T09:05:31.140", "ingestTimestamp" : "2026-06-14T03:49:37.131", "mongoId" : "6a2ca57374d8ee00a09b68c0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 36000, "salaryAnnualMax" : 48000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Basic troubleshooting", "Diagnostic services", "Specimen handling", "Quality assurance", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Clinical laboratory", "HIPAA guidelines", "Infection control" ], "skillCount" : 14, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 1.0, "_score" : 672.71515, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a16291c58b93c861e95a142", "title" : "Principal Laboratory Planner", "company" : "HDR", "industry" : "Consulting", "salary" : { "min" : 235000.0, "max" : 350000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline data for a Principal Laboratory Planner in Los Angeles, adjusted for executive seniority and the consulting industry." }, "location" : "Multiple Locations", "locations" : [ "Multiple Locations" ], "certifications" : [ "Registered Architect" ], "timestamp" : "2026-06-15T07:54:19.882", "fingerprint" : "4a0de3cd88efa8c4cadeca9d8e975104ebab27974a7ce30bed2fc8d6a9edff1e", "source" : "taleo", "language" : "en", "applyUrl" : "https://hdr.taleo.net/careersection/ex/jobdetail.ftl?job=776711", "externalId" : "776711", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Los Angeles", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.0536909,-118.2427660" } ], "locationText" : "Los Angeles, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 15, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Project management", "Team leadership", "Client presentations" ], "softSkillsList" : [ "Mentoring", "Motivational skills", "Organizational skills", "People skills" ], "softSkills" : [ { "name" : "Mentoring" }, { "name" : "Motivational skills" }, { "name" : "Organizational skills" }, { "name" : "People skills" } ], "majorSkills" : "Laboratory Planning", "majorSkillsList" : [ "Laboratory Planning" ], "teamCollaboration" : "Lead a team", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Local market knowledge; Regional market knowledge", "domainList" : [ "local-market-knowledge", "regional-market-knowledge" ], "domainSpecificKnowledge" : [ "Local market knowledge", "Regional market knowledge" ], "toolProficiency" : [ "Microsoft Word", "Microsoft Excel", "Microsoft Project" ], "communicationSkills" : "Client presentations; Written communication; Verbal communication", "specialRequirements" : "Willing to travel", "qualificationsBasic" : "Bachelor's degree in Architecture, 15 years related experience, 7 years project management experience, Registered Architect, Experience on large-scale projects, Lead a team on projects, Make client presentations, Microsoft Office experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Required Qualifications Bachelor's degree in Architecture 15 years related experience A minimum 7 years project management experience Registered Architect Must have experience on large-scale projects Must be able to lead a team on projects and make client presentations Experience with Microsoft Office (Word, Excel, Project) Extensive knowledge and experience within the local and regional market Strong team leadership, mentoring, motivational/organizational and people skills Excellent written and verbal communication skills Must be willing to travel An attitude and commitment to being an active participant of our employee-owned culture is a must What We Believe HDR is our company. Together, we build on each other's life experiences and perspectives to make great things possible every day. This shapes our collaborative culture, encourages organizational trust and connects us closer to the clients and communities we serve. Our Commitment As employee owners, we all have a role in creating an inclusive environment where each of us is welcomed, valued, respected and empowered to bring our authentic selves to work every day. Our eight Employee Network Groups (Asian Pacific, Black, Hispanic/Latino(a), LGBTQ+, People with Disabilities, Veterans, Women, Young Professionals) help create a sense of belonging and foster a supportive environment where everyone is empowered to engage and contribute. Each group has an executive sponsor and is open to all employees. At At HDR, the health and safety of our employees is of the upmost importance. In accordance with local safety, health, and environmental legislation, HDR is committed to developing, maintaining, and enforcing proactive safe work policies, procedures, and standards. In accordance with the Accessibility for Ontarians with Disabilities Act (AODA) and other applicable legislation, we are committed to meeting the accessibility needs of persons with disabilities. Candidates with disabilities may request reasonable accommodation throughout the recruitment and selection process by contacting our Human Resources team. HDR is a certified Living Wage Employer in Ontario, British Columbia, and Alberta. HDR United States-California-Los Angeles", "summaryDescription" : "Principal Laboratory Planner at HDR. Skills: Laboratory Planning", "createdAt" : "2026-06-14T00:56:48.826", "lastUpdated" : "2026-06-15T07:54:19.882", "ingestTimestamp" : "2026-06-14T00:56:48.826", "mongoId" : "6a16291c58b93c861e95a142", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 235000, "salaryAnnualMax" : 350000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Mentoring", "Motivational skills", "Organizational skills", "People skills", "Laboratory Planning", "Project management", "Team leadership", "Client presentations", "Local market knowledge", "Regional market knowledge", "Registered Architect", "Microsoft Word", "Microsoft Excel", "Microsoft Project" ], "skillCount" : 14, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Executive", "dataQualityScore" : 0.8888889, "_score" : 671.8363, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Consulting", "llmIndustryConfidence" : 0.85 }, { "id" : "6a2a72a674d8ee00a064d12a", "title" : "Manager - Sensor Calibration", "company" : "Zoox", "industry" : "Software Leadership", "salary" : { "min" : 242000.0, "max" : 333000.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "Foster City, CA", "locations" : [ "Foster City, CA" ], "timestamp" : "2026-06-15T00:25:05.690", "fingerprint" : "508be2a1963df488a0048dbd2b4fda1a54194b1680816a6fc610b39117d7f562", "source" : "lever", "language" : "en", "applyUrl" : "https://jobs.lever.co/zoox/bdbdb0cb-0700-4a82-981a-3b7d234db6dd/apply", "externalId" : "bdbdb0cb-0700-4a82-981a-3b7d234db6dd", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Foster City", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.5600336,-122.2688522" } ], "locationText" : "Foster City, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceLevel" : "Manager", "technicalSkills" : "C++, Python, Linear algebra, 3D geometry, Optimization algorithms, Localization, Computer vision, Robotics, AI, Machine learning", "professionalSkills" : [ "Sensor calibration", "Product life-cycle development", "System diagnostics", "Perception systems", "Autonomous operation", "Mobility-as-a-service", "Robotics engineering", "Hardware engineering", "Vehicle engineering", "Field support", "Operations management", "Systems engineering", "Manufacturing", "Service depot maintenance", "Online correction", "Calibration efficiency", "Calibration cost", "Auto-calibration system", "Online sensor calibration" ], "hardSkillsList" : [ "Sensor calibration", "Calibration methodologies", "Intrinsic calibration", "Extrinsic calibration", "Multi-modal sensor suites", "Software engineering fundamentals", "Linear algebra", "3D geometry", "Optimization algorithms", "Localization", "Computer vision" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Sensor calibration", "level" : "intermediate" }, { "name" : "Calibration methodologies", "level" : "intermediate" }, { "name" : "Intrinsic calibration", "level" : "intermediate" }, { "name" : "Extrinsic calibration", "level" : "intermediate" }, { "name" : "Multi-modal sensor suites", "level" : "intermediate" }, { "name" : "Software engineering fundamentals", "level" : "intermediate" }, { "name" : "Linear algebra", "level" : "intermediate" }, { "name" : "3D geometry", "level" : "intermediate" }, { "name" : "Optimization algorithms", "level" : "intermediate" }, { "name" : "Localization", "level" : "intermediate" }, { "name" : "Computer vision", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Sensor calibration, Autonomous vehicles, Robotics, Team management", "majorSkillsList" : [ "Sensor calibration", "Autonomous vehicles", "Robotics", "Team management" ], "coreResponsibilities" : "Build and support a factory, service depot, and, Build scalable and sustainable architecture and software to, Work cross-functionally to shape scalable roles and responsibilities, Optimize calibration efficiency and cost on both the, Work on the next-gen auto-calibration system to support, Lead a specialized team responsible for ensuring the, Develop rigorous testing protocols, Develop system diagnostics, Analyze complex sensor data, Optimize sensor performance across diverse environmental conditions, Ensure perception systems deliver accuracy, Collaborate with cross-functional groups, Overcome complex integration and execution challenges, Maintain robust and accurate sensor calibration", "teamCollaboration" : "Cross-functional groups; Vehicle engineering; Field support team; Operation team; Systems teams; Hardware engineering teams; Perception engineering teams; Systems engineering teams", "projectManagementSkills" : [ "Technical project management" ], "domainKnowledge" : "Autonomous vehicles; Robotics; Advanced driver-assistance systems (ADAS); Sensor calibration; Automobile sensor calibration; Factory manufacturing; Dealership setup; Online setup; Sensor calibration product life-cycle; Intrinsic calibration; Extrinsic calibration; Multi-modal sensor suites; Cameras; Lidars; Radars; Linear algebra; 3D geometry; Optimization algorithms; Localization; Computer vision; Mobility-as-a-service; Cloud-native architecture", "domainList" : [ "autonomous-vehicles", "robotics", "advanced-driver-assistance-systems-adas", "sensor-calibration", "automobile-sensor-calibration", "factory-manufacturing", "dealership-setup", "online-setup", "sensor-calibration-product-life-cycle", "intrinsic-calibration", "extrinsic-calibration", "multi-modal-sensor-suites", "cameras", "lidars", "radars", "linear-algebra", "3d-geometry", "optimization-algorithms", "localization", "computer-vision", "mobility-as-a-service", "cloud-native-architecture" ], "domainSpecificKnowledge" : [ "Autonomous vehicles", "Robotics", "Advanced driver-assistance systems (ADAS)", "Sensor calibration", "Automobile sensor calibration", "Factory manufacturing", "Dealership setup", "Online setup", "Sensor calibration product life-cycle", "Intrinsic calibration", "Extrinsic calibration", "Multi-modal sensor suites", "Cameras", "Lidars", "Radars", "Linear algebra", "3D geometry", "Optimization algorithms", "Localization", "Computer vision", "Mobility-as-a-service", "Cloud-native architecture" ], "communicationSkills" : "Excellent communication", "innovationCreativity" : "R&D", "problemSolvingSkills" : "Complex integration challenges; Execution challenges", "outcomesObjectives" : "Ensure perception systems deliver accuracy; Enable vehicles to safely navigate urban environments; Bring fully autonomous fleet to market", "qualificationsBasic" : "BS, MS, or PhD in Robotics, Computer Science, Electrical Engineering, or a related technical field, 5+ years of industry experience in autonomous vehicles, robotics, or advanced driver-assistance systems (ADAS), Prior working experience in calibration systems from OEM or Tier one, Understanding of automobile sensor calibration in factory manufacturing, dealership, and online setup, Experience with sensor calibration product life-cycle development, Deep technical knowledge of intrinsic and extrinsic calibration methodologies for complex, multi-modal sensor suites, specifically encompassing cameras, lidars, and radars, Proven experience managing, mentoring, and scaling high-performing engineering teams, Ability to guide technical projects from initial research and development through to testing and production deployment, Software engineering fundamentals with proficiency in C++ and Python, Solid foundation in linear algebra, 3D geometry, optimization algorithms, localization, and computer vision, Excellent communication skills, Demonstrated ability to collaborate seamlessly with hardware, perception, and systems engineering teams to resolve complex, system-level integration challenges", "qualificationsPreferred" : "PHD in AI, computer vision, or robotics, Prior 3+ years of working experience from a car manufacturer OEM, tier one", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "## Description As the Sensor Calibration Manager, you will play a critical role in the development and reliability of our purpose-built autonomous vehicles. You will lead a specialized team responsible for ensuring the precise calibration of our core sensor suite, including lidar, radar, and camera systems for factory, service depot, and online. By developing rigorous testing protocols, system diagnostics, analyzing complex sensor data, and optimizing sensor performance across diverse environmental conditions, you will ensure our perception systems deliver the accuracy required for safe and effective autonomous operation. Your leadership will directly impact Zoox's mission to provide the next generation of mobility-as-a-service. Operating at the intersection of robotics and advanced hardware engineering, you will collaborate closely with cross-functional groups—including vehicle engineering, field support team, operation team, and systems teams—to overcome complex integration and execution challenges. Your team's work in maintaining robust and accurate sensor calibration is foundational to enabling our vehicles to safely navigate urban environments and bringing our fully autonomous fleet to market. ## In this role, you will... Build and support a factory, service depot, and online calibration system for all autonomous driving sensors, including camera, lidar, and radar Build scalable and sustainable architecture and software to meet requirements from factory production capacity, service depot maintenance, and online correction use cases Work cross-functionally to shape scalable roles and responsibilities to optimize calibration efficiency and cost on both the manufacturing and service sides Work on the next-gen auto-calibration system to support online sensor calibration capability ## Qualifications Education & Experience: BS, MS, or PhD in Robotics, Computer Science, Electrical Engineering, or a related technical field, with 5+ years of industry experience in autonomous vehicles, robotics, or advanced driver-assistance systems (ADAS). Subject Matter Expertise: Prior working experience in calibration systems from OEM or Tier one. Strong understanding of automobile sensor calibration in factory manufacturing, dealership, and online setup. Experience with sensor calibration product life-cycle development. Deep technical knowledge of intrinsic and extrinsic calibration methodologies for complex, multi-modal sensor suites, specifically encompassing cameras, lidars, and radars. Leadership Track Record: Proven experience managing, mentoring, and scaling high-performing engineering teams, with a strong ability to guide technical projects from initial research and development through to testing and production deployment. Technical Proficiency: Strong software engineering fundamentals with proficiency in C++ and Python, coupled with a solid foundation in linear algebra, 3D geometry, optimization algorithms, localization, and computer vision Cross-Functional Collaboration: Excellent communication skills with a demonstrated ability to collaborate seamlessly with hardware, perception, and systems engineering teams to resolve complex, system-level integration challenges. ## Bonus Qualifications PHD in AI, computer vision, or robotics Prior 3+ years of working experience from a car manufacturer OEM, tier one ## Additional Information About Zoox Zoox is developing the first ground-up, fully autonomous vehicle fleet and the supporting ecosystem required to bring this technology to market. Sitting at the intersection of robotics, machine learning, and design, Zoox aims to provide the next generation of mobility-as-a-service in urban environments. We’re looking for top talent that shares our passion and wants to be part of a fast-moving and highly execution-oriented team. Follow us on LinkedIn Accommodations If you need an accommodation to participate in the application or interview process please reach out to accommodations@zoox.com or your assigned recruiter. A Final Note: You do not need to match every listed expectation to apply for this position. Here at Zoox, we know that diverse perspectives foster the innovation we need to be successful, and we are committed to building a team that encompasses a variety of backgrounds, experiences, and skills.", "summaryDescription" : "Manager - Sensor Calibration at Zoox. Skills: Sensor calibration, Autonomous vehicles, Robotics, Team management. Build and support a factory, service depot, and. Build scalable and sustainable architecture and software to", "postedDate" : "2026-06-09T20:28:21.476", "createdAt" : "2026-06-09T20:28:21.476", "lastUpdated" : "2026-06-15T00:25:05.690", "ingestTimestamp" : "2026-06-12T07:37:39.542", "mongoId" : "6a2a72a674d8ee00a064d12a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 242000, "salaryAnnualMax" : 333000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Sensor calibration", "Calibration methodologies", "Intrinsic calibration", "Extrinsic calibration", "Multi-modal sensor suites", "Software engineering fundamentals", "Linear algebra", "3D geometry", "Optimization algorithms", "Localization", "Computer vision", "Leadership", "Mentoring", "Autonomous vehicles", "Robotics", "Team management", "Product life-cycle development", "System diagnostics", "Perception systems", "Autonomous operation", "Mobility-as-a-service", "Robotics engineering", "Hardware engineering", "Vehicle engineering", "Field support", "Operations management", "Systems engineering", "Manufacturing", "Service depot maintenance", "Online correction", "Calibration efficiency", "Calibration cost", "Auto-calibration system", "Online sensor calibration", "Technical project management", "Advanced driver-assistance systems (ADAS)", "Automobile sensor calibration", "Factory manufacturing", "Dealership setup", "Online setup", "Sensor calibration product life-cycle", "Cameras", "Lidars", "Radars", "Cloud-native architecture" ], "skillCount" : 45, "jobCategory" : "engineering", "dataQualityScore" : 1.0, "_score" : 658.90845, "daysOld" : 5, "hasLocation" : true, "hasGeo" : true }, { "id" : "69fc49814c40e2acd1a81e90", "title" : "Clinical Laboratory Scientist", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 78000.0, "max" : 115000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Clinical Laboratory Scientist in Corona, California, adjusted for the healthcare industry and company size." }, "location" : "United States-California-Corona", "locations" : [ "United States-California-Corona", "Clinical Laboratory/Pathology", "Onsite, Days, Days" ], "timestamp" : "2026-06-15T10:19:54.857", "fingerprint" : "22ce62c07fa4c19b285d73eb4ba365c0536cd03fc693b2f9d2bab10f14630a60", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=238265", "externalId" : "238265", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Corona", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "33.8752945,-117.5664440" } ], "locationText" : "Corona, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's Degree", "professionalSkills" : [ "Laboratory analysis", "Laboratory practices", "Laboratory procedures" ], "hardSkillsList" : [ "Point-of-care testing", "Specimen preparation", "Waived complexity testing", "Moderate complexity testing", "High complexity testing" ], "hardSkills" : [ { "name" : "Point-of-care testing", "level" : "intermediate" }, { "name" : "Specimen preparation", "level" : "intermediate" }, { "name" : "Waived complexity testing", "level" : "intermediate" }, { "name" : "Moderate complexity testing", "level" : "intermediate" }, { "name" : "High complexity testing", "level" : "intermediate" } ], "majorSkills" : "Laboratory procedures, Regulatory compliance", "majorSkillsList" : [ "Laboratory procedures", "Regulatory compliance" ], "coreResponsibilities" : "Perform point-of-care testing, Prepare clinical specimens for analysis, Conduct laboratory procedures, Report laboratory procedures, Ensure testing activities comply, Support training of staff, Support mentorship of staff, Work under Laboratory Director authorization, Comply with CLIA regulations", "teamCollaboration" : "Staff training and mentorship", "domainKnowledge" : "FACT; AABB; ACHI; CAP; FDA; Joint Commission; CLIA regulations", "domainList" : [ "fact", "aabb", "achi", "cap", "fda", "joint-commission", "clia-regulations" ], "domainSpecificKnowledge" : [ "FACT", "AABB", "ACHI", "CAP", "FDA", "Joint Commission", "CLIA regulations" ], "documentationSkills" : "Standard operating procedures", "qualificationsBasic" : "Perform point-of-care testing, Prepare clinical specimens, Conduct laboratory procedures, Report laboratory procedures, Comply with SOPs, Comply with regulatory standards, Support staff training, Support staff mentorship, Work under Laboratory Director", "qualificationsPreferred" : "Training and education of staff", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. a { text-decoration: none; color: #464feb; } tr th, tr td { border: 1px solid #e6e6e6; } tr th { background-color: #f5f5f5; } This full-time role is based in Corona, California and follows a Monday through Friday schedule from 8:00 AM to 4:30 PM. The position is responsible for performing point-of-care testing, preparing clinical specimens for analysis, and conducting as well as reporting waived, moderate, and high-complexity laboratory procedures. All work is carried out in strict compliance with established standard operating procedures and regulatory requirements, including FACT, AABB, ACHI, CAP, FDA, and Joint Commission standards. The role also supports the training and education of staff in laboratory practices and operates under the direction of the Laboratory Director in accordance with Clinical Laboratory Improvement Amendments (CLIA) regulations, CFR Section 493.1445(a). As a successful candidate, you will: a { text-decoration: none; color: #464feb; } tr th, tr td { border: 1px solid #e6e6e6; } tr th { background-color: #f5f5f5; } Perform point-of-care testing and prepare clinical specimens for accurate laboratory analysis Conduct and report waived, moderate, and high-complexity laboratory procedures in accordance with established protocols Ensure all testing activities comply with SOPs and regulatory standards including FACT, AABB, ACHI, CAP, FDA, and Joint Commission Support training and mentorship of staff in laboratory procedures and best practices Work under the authorization of the Laboratory Director in compliance with CLIA regulations (CFR Section 493.1445(a)) Perform other duties as assigned Your qualifications should include: Bachelor’s Degree Clinical Laboratory Scientist Generalist License BLS Certification through the American Heart Association City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Corona", "summaryDescription" : "Clinical Laboratory Scientist at City of Hope. Skills: Laboratory procedures, Regulatory compliance. Perform point-of-care testing. 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Digital signal processing; RF/Microwave Engineering; Antennas; Electromagnetic theory; Modern wireless technologies; Probability and estimation theory", "domainList" : [ "digital-communication-theory", "digital-signal-processing", "rf-microwave-engineering", "antennas", "electromagnetic-theory", "modern-wireless-technologies", "probability-and-estimation-theory" ], "domainSpecificKnowledge" : [ "Digital communication theory", "Digital signal processing", "RF/Microwave Engineering", "Antennas", "Electromagnetic theory", "Modern wireless technologies", "Probability and estimation theory" ], "toolProficiency" : [ "SystemVue", "ADS", "LabView", "CST", "HFSS", "VSAs", "VSGs", "VNAs", "Oscilloscopes" ], "problemSolvingSkills" : "Root cause analysis; Troubleshooting", "specialRequirements" : "U. S. citizen, U. S. permanent resident, Lawfully admitted into U. S.", "qualificationsBasic" : "Experience leading design, automation, deployment, support, Programming with Python, Ruby, Golang, Java, C++, C#, Rust, Experience with Linux/Unix, Experience with CI/CD pipelines, BS in Electrical Engineering, 7+ years of work experience, Experience in DSP techniques, Experience with lab test equipment, Coding and scripting skills, Experience with simulation tools", "qualificationsPreferred" : "MS in Electrical Engineering with 8+ years experience, PhD with 5+ years experience, Experience working with phased arrays, Experience with calibration, Experience with antenna measurement, Experience with CST/HFSS, Good understanding of wireless technologies, Familiarity with probability and estimation theory", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Amazon LEO is an initiative to increase global broadband access through a constellation of 3,236 satellites in low Earth orbit (LEO). Its mission is to bring fast, affordable broadband to unserved and underserved communities around the world. Amazon Leo will help close the digital divide by delivering fast, affordable broadband to a wide range of customers, including consumers, businesses, government agencies, and other organizations operating in places without reliable connectivity. As Senior Systems Engineer, you will be responsible for key aspects of phased array antenna system design, simulation, measurement, calibration and optimization. You will be working in a collaborative environment with a multi-disciplinary team to deliver advanced high-performance phased array antenna systems. In this role, your responsibilities will include: · Designing and implementing phased array calibration systems, signals, processing and algorithms · Performance analysis and design trade-off studies of phased arrays · End-to-end modeling, simulation and analysis of baseband/RF/antenna systems · Lab measurement and validation of performance of antennas, and phased array systems and subsystems · Working with antenna, modem, RF and Digital teams to simulate, measure and fine-tune radio designs Export Control Requirement: Due to applicable export control laws and regulations, candidates must be U.S. citizens, U.S. permanent residents (i.e., current Green Card holder), or lawfully admitted into the U.S. as a refugee or granted asylum. Basic Qualifications: - Experience leading the design, automation, deployment, and support of large-scale infrastructure - Experience programming with at least one modern language such as Python, Ruby, Golang, Java, C++, C#, Rust - Experience with Linux/Unix - Experience with CI/CD pipelines build processes - BS in Electrical Engineering with relevant coursework in digital communication theory, digital signal processing, RF/Microwave Engineering, Antennas and Electromagnetic theory - 7+ years of work experience in Aerospace/Semiconductor/Consumer Electronics industry - Experience in DSP techniques, digital modulation, radio architecture, line-up analysis, RF system design - Experience with lab test equipment like VSAs, VSGs, VNAs and Oscilloscopes - Coding and scripting skills with demonstrated experience in Matlab/Python/C++ - Experience with simulation tools such as SystemVue, ADS or LabView Preferred Qualifications: - MS in Electrical Engineering with 8+ years of work experience or PhD with 5+ years of experience - Experience working with phased arrays, calibration and antenna measurement - Experience with one of the mainstream antenna simulation tools (CST/HFSS) - Good understanding of modern wireless technologies (OFDM/MIMO) and medium access procedures - Familiarity with basics of probability and estimation theory Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner. Our compensation reflects the cost of labor across several US geographic markets. The base pay for this position ranges from $136,100/year in our lowest geographic market up to $235,200/year in our highest geographic market. Pay is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. Amazon is a total compensation company. Dependent on the position offered, equity, sign-on payments, and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, financial, and/or other benefits. For more information, please visit https://www.aboutamazon.com/workplace/employee-benefits . This position will remain posted until filled. Applicants should apply via our internal or external career site.", "summaryDescription" : "Sr. Systems Dev Engineer, Antenna Calibration at Amazon Kuiper Manufacturing Enterprises LLC. Skills: Phased array antenna, Antenna calibration, RF system design, DSP techniques. Design phased array calibration systems. Implement phased array calibration systems", "postedDate" : "2026-06-13T06:38:22.863", "createdAt" : "2026-06-13T06:38:22.863", "lastUpdated" : "2026-06-15T02:48:20.191", "ingestTimestamp" : "2026-06-13T06:38:22.863", "mongoId" : "693c2b8470f0b99d5843f9e9", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3137686/apply", "salaryAnnualMin" : 136100, "salaryAnnualMax" : 235200, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Digital signal processing", "Phased array calibration", "Phased array signals", "Phased array processing", "Phased array algorithms", "End-to-end modeling", "Lab measurement validation", "Antenna measurement", "Phased array systems", "Subsystem validation", "Radio design tuning", "Digital modulation", "Phased array antenna", "Antenna calibration", "RF system design", "DSP techniques", "Simulation", "Measurement", "Calibration", "Optimization", "Performance analysis", "Design trade-off studies", "Baseband/RF/antenna systems analysis", "Radio architecture", "Line-up analysis", "Digital communication theory", "RF/Microwave Engineering", "Antennas", "Electromagnetic theory", "Modern wireless technologies", "Probability and estimation theory", "SystemVue", "ADS", "LabView", "CST", "HFSS", "VSAs", "VSGs", "VNAs", "Oscilloscopes" ], "skillCount" : 40, "jobCategory" : "other", "dataQualityScore" : 1.0, "_score" : 654.2519, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Aerospace" }, { "id" : "6a16291c58b93c861e95a161", "title" : "Senior Laboratory Planner", "salary" : { "min" : 145000.0, "max" : 205000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Laboratory Planner in Seattle, adjusted for the construction industry and senior experience level." }, "location" : "Multiple Locations", "locations" : [ "Multiple Locations" ], "timestamp" : "2026-06-15T09:07:47.291", "fingerprint" : "b4aaa7a17651bcbebb84910f386cc0f999fce5be7e30232ea03212e051824cb2", "source" : "taleo", "language" : "en", "applyUrl" : "https://hdr.taleo.net/careersection/ex/jobdetail.ftl?job=717350", "externalId" : "717350", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Seattle", "state" : "Washington", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "47.6038321,-122.3300620" } ], "locationText" : "Seattle, Washington, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 12, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Construction planning", "Technical drawing", "Model creation" ], "coreResponsibilities" : "Plan laboratories, Develop construction plans, Create technical drawings, Create models", "teamCollaboration" : "Employee-owned culture", "domainKnowledge" : "Building construction; Precision technical plans", "domainList" : [ "building-construction", "precision-technical-plans" ], "domainSpecificKnowledge" : [ "Building construction", "Precision technical plans" ], "qualificationsBasic" : "Bachelor's degree in Architecture, 12 years related experience, Organizational skills, Knowledge of materials, Knowledge of methods, Knowledge of tools, Understanding of design techniques, Understanding of design tools, Understanding of design principles, Attitude and commitment", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Required Qualifications Bachelor's degree in Architecture or closely related field A minimum of 12 years related experience Strong organizational skills Knowledge of materials, methods and tools involved in the construction of buildings Understanding of design techniques, tools and principles involved in production of precision technical plans, prints, drawings and models An attitude and commitment to being an active participant of our employee-owned culture is a must What We Believe HDR is our company. Together, we build on each other's life experiences and perspectives to make great things possible every day. This shapes our collaborative culture, encourages organizational trust and connects us closer to the clients and communities we serve. Our Commitment As employee owners, we all have a role in creating an inclusive environment where each of us is welcomed, valued, respected and empowered to bring our authentic selves to work every day. Our eight Employee Network Groups (Asian Pacific, Black, Hispanic/Latino(a), LGBTQ+, People with Disabilities, Veterans, Women, Young Professionals) help create a sense of belonging and foster a supportive environment where everyone is empowered to engage and contribute. Each group has an executive sponsor and is open to all employees. United States-Washington-Seattle", "summaryDescription" : "Senior Laboratory Planner. Plan laboratories. Develop construction plans", "createdAt" : "2026-06-14T08:45:06.281", "lastUpdated" : "2026-06-15T09:07:47.291", "ingestTimestamp" : "2026-06-14T08:45:06.281", "mongoId" : "6a16291c58b93c861e95a161", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 145000, "salaryAnnualMax" : 205000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Construction planning", "Technical drawing", "Model creation", "Building construction", "Precision technical plans" ], "skillCount" : 5, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.7777778, "_score" : 652.70917, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Construction", "llmIndustryConfidence" : 0.85 }, { "id" : "6a16471858b93c861e9e5b25", "title" : "Research Laboratory Technician", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 52000.0, "max" : 75000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Research Laboratory Technician in Duarte, California, adjusted for the biotech industry and company size." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Laboratory Research", "Onsite, Days, Days" ], "timestamp" : "2026-06-15T11:50:35.483", "fingerprint" : "793e200c5ca8e5af0c48eed6fbb784fb1eefd320e56c3c3fd4d7442cf99d9a7c", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=239605", "externalId" : "239605", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Duarte", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.1394513,-117.9772873" } ], "locationText" : "Duarte, California, United States", "minimumEducation" : "High School", "experienceMinYears" : 2, "hardSkillsList" : [ "Sterilization techniques", "Prepare simple stains", "Prepare solutions", "Prepare culture media", "Process tissue" ], "hardSkills" : [ { "name" : "Sterilization techniques", "level" : "intermediate" }, { "name" : "Prepare simple stains", "level" : "intermediate" }, { "name" : "Prepare solutions", "level" : "intermediate" }, { "name" : "Prepare culture media", "level" : "intermediate" }, { "name" : "Process tissue", "level" : "intermediate" } ], "majorSkills" : "Scientific data collection, Laboratory maintenance, Laboratory supplies", "majorSkillsList" : [ "Scientific data collection", "Laboratory maintenance", "Laboratory supplies" ], "coreResponsibilities" : "Collect scientific data, Classify scientific data, File scientific data, Prepare solutions, Label tubes, Label specimen containers, Maintain laboratory supplies, Clean laboratory equipment, Maintain required records, Maintain reports, Maintain statistics, Train research aides, Assist research aides, Train research assistants, Assist research assistants, Collect used glassware, Wash used glassware, Clean used glassware, Sterilize used glassware, Collect used equipment, Wash used equipment, Clean used equipment, Sterilize used equipment, Collect used supplies, Wash used supplies, Clean used supplies, Sterilize used supplies, Order laboratory supplies, Receive laboratory supplies, Distribute laboratory supplies, Maintain supply inventories, Process tissue, Collect material for analysis, Deliver material for analysis, Ensure proper labeling, Ensure pertinent information, Assist in care of laboratory work area, Assist in maintenance of laboratory work area, Assist in care of furnishings, Assist in maintenance of furnishings, Assist in care of equipment, Assist in maintenance of equipment", "domainKnowledge" : "Cancer research; Diabetes research; Disease prediction; Disease prevention; Disease cure; Medicine research", "domainList" : [ "cancer-research", "diabetes-research", "disease-prediction", "disease-prevention", "disease-cure", "medicine-research" ], "domainSpecificKnowledge" : [ "Cancer research", "Diabetes research", "Disease prediction", "Disease prevention", "Disease cure", "Medicine research" ], "qualificationsBasic" : "High school diploma or equivalent, Minimum two (2) years of related experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Join the forefront of groundbreaking research at City of Hope where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. Under limited supervision, the Research Laboratory Technician is responsible for the collection, classification and filing of scientific data. The Research Laboratory Technician is also responsible for preparing solutions, labeling tubes/specimen containers and maintaining laboratory supplies. Duties and/or tasks include but are not limited to cleaning of laboratory equipment utilizing proper cleaning protocols and procedures. As a successful candidate, you will: Responsible for the collection, classification and filing of scientific data. Maintains required records, reports and statistics as directed. Trains and assists research aides and assistant in procedures and use of equipment. Collects, washes, cleans and sterilizes used glassware, equipment and supplies using proper sterilization techniques. Orders, Receives, distributes, and maintains supply inventories in laboratories as needed. Prepares simple stains, solutions, culture media, and may process tissue following established procedures. Using appropriate or specified equipment collects and delivers material for analysis. Ensures proper labeling and pertinent information. Assists in the care and maintenance of laboratory work area and furnishings/equipment. Your qualifications should include: High school diploma or equivalent. Minimum two (2) years of related experience or combined education and experience in related field. Additional Information: COH employees may apply for a transfer or promotion to job openings for which they meet the minimum qualifications if they meet the following criteria: Employed at COH in current role for at least 6 months, unless otherwise stipulated in an applicable collective bargaining agreement. Are in good standing and have no current performance issues. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Research Laboratory Technician at City of Hope. Skills: Scientific data collection, Laboratory maintenance, Laboratory supplies. Collect scientific data. Classify scientific data", "createdAt" : "2026-06-14T01:59:53.590", "lastUpdated" : "2026-06-15T11:50:35.483", "ingestTimestamp" : "2026-06-14T01:59:53.590", "mongoId" : "6a16471858b93c861e9e5b25", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 52000, "salaryAnnualMax" : 75000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Sterilization techniques", "Prepare simple stains", "Prepare solutions", "Prepare culture media", "Process tissue", "Scientific data collection", "Laboratory maintenance", "Laboratory supplies", "Cancer research", "Diabetes research", "Disease prediction", "Disease prevention", "Disease cure", "Medicine research" ], "skillCount" : 14, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Junior", "dataQualityScore" : 0.6666667, "_score" : 651.0387, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.85 }, { "id" : "6a2a3f5074d8ee00a05c2155", "title" : "ADAS Calibration and Validation Engineer", "company" : "Scout Motors", "salary" : { "min" : 130000.0, "max" : 160000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Charlotte, NC", "locations" : [ "Charlotte", "NC" ], "timestamp" : "2026-06-11T07:57:46.275", "fingerprint" : "fca0e65e137168d5c52619c451646c1c5c0554196d300c26a546cd320bd2ff65", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/scoutmotors/jobs/5158567007", "externalId" : "5158567007", "structuredLocations" : [ { "city" : "Charlotte", "state" : "North Carolina", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "35.2272086,-80.8430827" } ], "locationText" : "Charlotte, North Carolina, United States", "technicalSkills" : "CAN, Ethernet", "professionalSkills" : [ "Analytical problem-solving" ], "hardSkillsList" : [ "Calibration configuration", "Release management" ], "hardSkills" : [ { "name" : "Calibration configuration", "level" : "intermediate" }, { "name" : "Release management", "level" : "intermediate" } ], "majorSkills" : "ADAS calibration, ADAS validation", "majorSkillsList" : [ "ADAS calibration", "ADAS validation" ], "coreResponsibilities" : "Execute ADAS features calibration, Execute ADAS features validation, Collaborate with peers, Meet calibration deliverables, Meet validation deliverables, Develop calibration variants, Participate in calibration trips, Define trip deliverables, Measure development progress, Provide calibration status, Provide validation status, Develop HIL test cases, Stay up-to-date advancements", "teamCollaboration" : "Cross functional peers; Lead ADAS DRE; Lead calibration engineer; Lead validation engineer; Virtual testing team", "domainKnowledge" : "ADAS technologies; ISO 26262; SAE J3016; FMVSS", "domainList" : [ "adas-technologies", "iso-26262", "sae-j3016", "fmvss" ], "domainSpecificKnowledge" : [ "ADAS technologies", "ISO 26262", "SAE J3016", "FMVSS" ], "toolProficiency" : [ "INCA", "Creta", "CANoe", "CANalyzer", "JIRA", "Confluence" ], "communicationSkills" : "Present technical information; Influence decision-making", "problemSolvingSkills" : "Root-cause system issues; Implement effective solutions", "specialRequirements" : "4 days per week in office, Regular in-person meetings, Travel to participate in events", "qualificationsBasic" : "Bachelor's or master's degree, 8+ years ADAS experience, Operate a vehicle in US", "qualificationsPreferred" : "Fluency in German", "remoteFriendly" : false, "workSiteFlexibility" : "Hybrid", "rawDescription" : "Here at Scout Motors, we're carrying forward the heritage of one of the most iconic American vehicles in history. A vehicle dating back to 1960. One that forged the path for future generations of rugged SUVs and trucks and will do so once again. But Scout is more than just a brand, it’s a legacy steeped in a culture of exploration, caretaking, and hard work. The Scout brand is all about respect. Respect for the past and the future by taking an iconic American brand that hasn’t been around for a while, electrifying it, digitizing it, and loading it with American innovation. Respect for communities by creating a company that stands for its people and its customers. Respect for both work and play, with vehicles that are equally at home at a camp site, a job site, or on a Tuesday commute. And respect for our customers by developing two powertrains that meet their requirements — an all-electric powertrain as well as the Harvester™ range extender powertrain which includes a built-in gas-powered generator with an estimated 500 miles of combined range. At Scout Motors, we empower our talented, inclusive, and entrepreneurial teams to innovate. What makes a Scout employee? Someone who is a visionary and a leader, who seeks new paths and shares lessons learned. A knowledgeable doer who collaborates across the company to build better. A go-getter with unrivaled passion. Join us at Scout Motors and be part of shaping the future of transportation. If you're ready to drive change and make history, apply now! What you’ll do At Scout Motors, you don't just design vehicles- you shape the future of the road. Our Engineering team is where bold ideas meet rigorous execution, building machines that are as durable and capable as the people who drive them. You'll work shoulder-to-shoulder with brilliant minds across disciplines, turning complex challenges into elegant, scalable solutions that meet the highest standards of safety, performance, and user experience. This is a place where your fingerprints are found on metal – where what you design gets built, driven, and remembered. If you're hungry to engineer something that matters, Scout Motors is where that ambition finds its highest gear. Become part of an iconic brand that is set to revolutionize the electric pick-up truck & rugged SUV marketplace by achieving the following: Execution of Scout ADAS features calibration and validation in collaboration with cross functional peers in areas like drive, chassis, and steering. Collaborate with Lead ADAS DRE to meet ADAS calibration and validation deliverables for timing and feature maturity based on SW readiness. Work with lead calibration or validation engineer on calibration and validation plans for ADAS features. Develop calibration variants needed for different vehicles and vehicle trim levels for ADAS features. Participate in ADAS calibration trips including defining trip deliverables and measuring development progress for your area of responsibility Work with lead ADAS DRE to provide overall calibration and validation status for program milestones. Work with Virtual testing team to develop HIL test cases to move testing to virtual as much as possible. Stay up-to-date with the latest advancements in ADAS technologies, industry trends, and regulatory requirements to drive continuous improvement and innovation. Location & Travel Expectations: This role may be based out of the Scout Motors corporate headquarters in Charlotte, NC. This role requires 4 days per week in the office, with regular in-person meetings and events. Applicants should expect that the role will require the ability to convene with Scout colleagues in person and travel to participate in events on behalf of the company from time to time. What you’ll bring We expect all Scout employees to have integrity, curiosity, resourcefulness, and strive to exhibit a positive attitude, as well as a growth mindset. You’ll be comfortable with change and flexible in a fast-paced, high-growth environment. You’ll take a collaborative approach to achieve ambitious goals. Here's what else you'll bring: Bachelor's or master’s degree in Electrical Engineering, Mechanical Engineering, Computer Science, or a related field. 8+ years of experience in ADAS feature development or calibration release within the automotive industry. Experience with calibration configuration and release management utilizing calibration tools (e. g. INCA and Creta) Familiarity with automotive communication protocols (CAN and Ethernet) and tools for development, simulation, and testing (e. g. CANoe, CANalyzer, JIRA, and Confluence). Strong analytical problem-solving skills, with the ability to analyze complex data sets, root-cause system issues, and implement effective solutions. Familiarity with relevant safety standards and legislative regulations (e. g. ISO 26262, SAE J3016, FMVSS) Excellent communication and teamwork skills, with the ability to effectively collaborate with multidisciplinary and multicultural teams, present technical information, and influence decision-making processes. Ability to work independently and self-motivated in a dynamic environment. Must have the ability to operate a vehicle in the US. Fluency in German is a plus What you'll gain The benefits of joining Scout include the chance to build products and a company from the ground up. This is a chance to create something new and lasting – with an iconic brand at its foundation. In addition, Scout provides competitive compensation and benefits to support your physical, mental, and financial wellbeing. Program specifics are detailed in company policies and employee benefit guides, select highlights: Competitive insurance including: Medical, dental, vision and income protection plans 401(k) program with: An employer match and immediate vesting Generous Paid Time Off including: 20 days planned PTO, as accrued 40 hours of unplanned PTO and 14 company or floating holidays, annually Up to 16 weeks of paid parental leave for biological and adoptive parents of all genders Paid leave for circumstances related to bereavement, jury duty, voting time, or military leave Pay Transparency This is a full-time, exempt position eligible to receive a base salary and to participate in an annual performance bonus program. Final salary offered will be determined based on factors including but not limited to the candidate's skills and experience. The annual performance bonus program is preset and not candidate dependent. Initial base salary range = $130,000.00 - $160,000.00 Internal leveling code: IC8 Notice to applicants: To be considered for career opportunities at Scout Motors, applicants must be 18 years of age or older. Residing in San Francisco: Pursuant to the San Francisco Fair Chance Ordinance, Scout Motors will consider for employment qualified applicants with arrest and conviction records. Residing in Los Angeles: Scout Motors will consider for employment qualified applicants with criminal histories in a manner consistent with the Los Angeles Fair Chance Initiative for Hiring Ordinance. Residing in New York City: This role is not eligible for remote work in New York City. Equal Opportunity Scout Motors is committed to employing a diverse workforce and is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, veteran status, disability, pregnancy, or any other characteristics protected by law. Scout Motors is committed to compliance with all applicable fair employment practice laws. If you require reasonable accommodation to complete a job application, pre-employment testing, or a job interview or to otherwise participate in the hiring process, please contact ScoutAccommodations@scoutmotors.com.", "summaryDescription" : "ADAS Calibration and Validation Engineer at Scout Motors. Skills: ADAS calibration, ADAS validation. Execute ADAS features calibration. Execute ADAS features validation", "postedDate" : "2026-06-11T07:18:04.998", "createdAt" : "2026-06-11T07:18:04.998", "lastUpdated" : "2026-06-11T07:57:46.275", "ingestTimestamp" : "2026-06-11T07:18:04.998", "mongoId" : "6a2a3f5074d8ee00a05c2155", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 130000, "salaryAnnualMax" : 160000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Calibration configuration", "Release management", "ADAS calibration", "ADAS validation", "Analytical problem-solving", "ADAS technologies", "ISO 26262", "SAE J3016", "FMVSS", "INCA", "Creta", "CANoe", "CANalyzer", "JIRA", "Confluence" ], "skillCount" : 15, "jobCategory" : "engineering", "jobSubcategory" : "vehicle-software-&-electrical-engineering", "dataQualityScore" : 0.7777778, "_score" : 648.62354, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true }, { "id" : "69dde45c2beec4dd3d9a3f83", "title" : "Manager, Clinical Laboratory - Hematopathology", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 135000.0, "max" : 195000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Manager, Clinical Laboratory - Hematopathology in Duarte, United States, adjusted for seniority and industry." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Clinical Laboratory/Pathology", "Onsite, Days, Days" ], "certifications" : [ "Licensed clinical laboratory professional" ], "timestamp" : "2026-06-15T05:07:45.329", "fingerprint" : "93ed1d499b2dea720095b10fd15c2249455e3d4b7e9213facf6f2fd6ff190453", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=228144", "externalId" : "228144", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Duarte", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.1394513,-117.9772873" } ], "locationText" : "Duarte, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 5, "experienceMaxYears" : 7, "experienceLevel" : "Manager", "professionalSkills" : [ "Fiscal management", "Operational management", "Administrative management" ], "hardSkillsList" : [ "Clinical laboratory" ], "hardSkills" : [ { "name" : "Clinical laboratory", "level" : "intermediate" } ], "majorSkills" : "Hematopathology Laboratory", "majorSkillsList" : [ "Hematopathology Laboratory" ], "coreResponsibilities" : "Direct technical activities, Direct operational activities, Oversee staffing, Oversee performance management, Oversee professional development, Manage budgeting, Manage resource allocation, Manage fiscal planning, Ensure laboratory meets requirements, Promote culture of quality, Promote culture of safety, Promote culture of innovation, Promote culture of continuous improvement", "teamCollaboration" : "Partner with Department Director; Partner with Medical Director", "domainKnowledge" : "Hematopathology testing; Clinical laboratory environment", "domainList" : [ "hematopathology-testing", "clinical-laboratory-environment" ], "domainSpecificKnowledge" : [ "Hematopathology testing", "Clinical laboratory environment" ], "innovationCreativity" : "Innovation", "qualificationsBasic" : "Bachelor's Degree in Science, Five to seven years experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Manager, Clinical Laboratory - Hematopathology Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. We are seeking a licensed clinical laboratory professional to serve as Manager of the Clinical Laboratory , with full responsibility for the Hematopathology Laboratory . This is a key leadership role for a technical expert skilled in operational, administrative, and fiscal management within a complex clinical laboratory environment. The Manager will lead all aspects of the Hematopathology Laboratory's daily operations, ensuring high standards of quality, compliance, and performance. This role partners with the Department Director and the Medical Director of Hematopathology to implement strategic initiatives aligned with department goals and the overall COH enterprise vision. As a successful candidate, you will: Direct the day-to-day technical and operational activities of the Hematopathology Laboratory. Oversee staffing, performance management, and professional development of Hematopathology Laboratory personnel. Manage budgeting, resource allocation, and fiscal planning specific to Hematopathology services. Ensure the laboratory meets all applicable regulatory and accreditation requirements, including CAP, CLIA, the State of California, and The Joint Commission. Promote a culture of quality, safety, innovation, and continuous improvement in Hematopathology testing and processes. Your qualifications should include: Bachelor’s Degree in Science Five to seven years of clinical laboratory technical experience Three to five years of management experience Current Clinical Laboratory Scientist (CLS) license issued by the State of CA City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Manager, Clinical Laboratory - Hematopathology at City of Hope. Skills: Hematopathology Laboratory. Direct technical activities. Direct operational activities", "createdAt" : "2026-06-14T06:09:44.520", "lastUpdated" : "2026-06-15T05:07:45.329", "ingestTimestamp" : "2026-06-14T06:09:44.520", "mongoId" : "69dde45c2beec4dd3d9a3f83", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 135000, "salaryAnnualMax" : 195000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Clinical laboratory", "Hematopathology Laboratory", "Fiscal management", "Operational management", "Administrative management", "Hematopathology testing", "Clinical laboratory environment", "Licensed clinical laboratory professional" ], "skillCount" : 8, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Manager", "dataQualityScore" : 0.8888889, "_score" : 647.6504, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c5d9574d8ee00a08dd0f3", "title" : "Microbiologist Laboratory Reviewer", "company" : "Nivagen Pharmaceuticals", "industry" : "Pharmaceuticals", "salary" : { "min" : 75000.0, "max" : 85000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Pittsburg, California, United States", "locations" : [ "Pittsburg", "California", "United States" ], "timestamp" : "2026-06-14T23:52:56.545", "fingerprint" : "d858ac2fcb6598f28543b0fe71ca320c2480bc342d491553dbf62540046bef77", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/nivagenpharmaceuticals/jobs/5205141008", "externalId" : "5205141008", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Sacramento", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.5810606,-121.4938950" } ], "locationText" : "Sacramento, California, United States", "employmentType" : "FULL_TIME", "technicalSkills" : "Microbiology", "professionalSkills" : [ "Quality control", "Data integrity", "Regulatory compliance" ], "hardSkillsList" : [ "Microbiological testing", "Method validation", "Sterility testing", "Endotoxin testing", "Environmental monitoring", "Microbial limit testing", "Disinfectant qualification", "Container closure integrity" ], "softSkillsList" : [ "Customer Focus", "Optimizes Work Processes", "Resourcefulness", "Manages Complexity", "Ensures Accountability", "Situational Adaptability" ], "hardSkills" : [ { "name" : "Microbiological testing", "level" : "intermediate" }, { "name" : "Method validation", "level" : "intermediate" }, { "name" : "Sterility testing", "level" : "intermediate" }, { "name" : "Endotoxin testing", "level" : "intermediate" }, { "name" : "Environmental monitoring", "level" : "intermediate" }, { "name" : "Microbial limit testing", "level" : "intermediate" }, { "name" : "Disinfectant qualification", "level" : "intermediate" }, { "name" : "Container closure integrity", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Customer Focus" }, { "name" : "Optimizes Work Processes" }, { "name" : "Resourcefulness" }, { "name" : "Manages Complexity" }, { "name" : "Ensures Accountability" }, { "name" : "Situational Adaptability" } ], "majorSkills" : "Microbiological data review, cGMP compliance, Pharmaceutical manufacturing", "majorSkillsList" : [ "Microbiological data review", "cGMP compliance", "Pharmaceutical manufacturing" ], "coreResponsibilities" : "Review laboratory test results, Verify compliance with SOPs, Verify compliance with cGMP, Evaluate method validations, Evaluate method transfers, Evaluate microbiological investigations, Assess environmental monitoring data, Assess sterility testing outcomes, Assess endotoxin testing outcomes, Collaborate with laboratory analysts, Collaborate with quality assurance teams, Resolve discrepancies, Address out-of-specification results, Support investigations related to laboratory deviations, Participate in root cause analysis, Ensure timely review of batch records, Ensure timely release of batch records, Identify trends in laboratory data, Recommend corrective actions, Support process improvements, Support best practices in microbiological testing, Support best practices in documentation, Provide guidance on data integrity, Provide guidance on compliance requirements, Maintain thorough records, Ensure proper documentation, Coordinate calibration, Coordinate maintenance, Participate in internal audits, Participate in external audits, Ensure compliance with safety regulations, Ensure compliance with environmental regulations, Manage workload to meet timelines, Manage workload to meet deadlines, Maintain confidentiality, Handle sensitive information, Update knowledge of regulations, Update knowledge of industry trends, Update knowledge of technological advancements", "teamCollaboration" : "Laboratory analysts; Quality assurance teams", "domainKnowledge" : "Good Manufacturing Practices; cGMP regulations; GLP; Injectable manufacturing; Pharmaceutical supply chain; Generic prescription drugs; Over-the-counter products", "domainList" : [ "good-manufacturing-practices", "cgmp-regulations", "glp", "injectable-manufacturing", "pharmaceutical-supply-chain", "generic-prescription-drugs", "over-the-counter-products" ], "domainSpecificKnowledge" : [ "Good Manufacturing Practices", "cGMP regulations", "GLP", "Injectable manufacturing", "Pharmaceutical supply chain", "Generic prescription drugs", "Over-the-counter products" ], "communicationSkills" : "Effective communication", "documentationSkills" : "Documentation; Data integrity", "continuousLearning" : "Training and development opportunities; Update knowledge of regulations; Update knowledge of industry trends; Update knowledge of technological advancements", "problemSolvingSkills" : "Root cause analysis", "specialRequirements" : "Bend at the waist and knees, Twist at the trunk, Lift up to 25 lbs, Wear laboratory protective gowning, Wear goggles, Wear face shields, Wear respirators, Wear protective gloves", "qualificationsBasic" : "Bachelor's degree in microbiology, Minimum of 3 years of experience in a microbiology laboratory", "qualificationsPreferred" : "Master's degree preferred, Previous experience in a pharmaceutical or compounding environment, Experience with compendia testing, Experience with United States Pharmacopeia, Experience with Food and Drug Administration, Experience with cGMP", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "About the Company: Nivagen is a global company dedicated to enhancing lives by developing and providing cost-effective generic prescription drugs and over-the-counter products for the North American market. For over a decade, we've remained steadfast in our commitment to core values of excellence, integrity, and respect for people. Our team of professionals collaborates tirelessly to pioneer advancements in manufacturing, distribution, and quality control, ensuring a holistic approach to healthcare. Through vertical integration of the pharmaceutical supply chain, cutting-edge technology, and unwavering dedication to excellence, we continually strive to redefine medication accessibility and affordability. We prioritize our employees' well-being by offering competitive pay, comprehensive benefits, and robust training and development opportunities. By investing in our workforce and fostering a culture of growth and support, we empower our team to drive innovation and make a positive impact in the healthcare industry. At Nivagen, our mission is clear: to make a meaningful difference in people's lives by delivering high-quality, affordable medications while upholding the highest standards of integrity and excellence. Job Location: Nivagen Pharmaceuticals, Sacramento, CA 3900 Duckhorn Dr, Sacramento, CA 95834 About the Job: Title of the Position: Microbiologist Laboratory Reviewer (Full Time) At Nivagen as a Microbiologist Laboratory Reviewer you will be responsible for ensuring that pharmaceutical products meet quality standards during the manufacturing process. This role involves real-time monitoring, sampling, testing, and documentation to identify and address any quality issues as they arise, ensuring that all production activities comply with Good Manufacturing Practices (GMP) and regulatory requirements. Position Summary The Microbiology Laboratory Reviewer plays a critical role in ensuring the accuracy and compliance of microbiological data within an injectable manufacturing facility. This position is responsible for reviewing laboratory test results, protocols and reports batch records, and related documentation to verify adherence to standard operating procedures (SOPs), current Good Manufacturing Practices (cGMP) regulations, GLP, and company quality standards. The reviewer works closely with laboratory microbiologist and quality assurance teams to resolve discrepancies, support investigations, and ensure the timely release of products. Key responsibilities include evaluating microbiological method validations, transfers, and investigations, as well as assessing environmental monitoring data, sterility test outcomes, and endotoxin results. The role also involves identifying trends, supporting continuous improvement initiatives, and providing guidance on best practices in documentation and data integrity. Strong attention to detail, effective communication skills, and a commitment to maintaining high standards of safety and compliance are essential for success in this position. Duties and Responsibilities Reviews and verifies laboratory test results, ensuring compliance with SOPs, cGMP, and company policies. Evaluates method validations, transfers, and microbiological investigations for accuracy and completeness. Assesses environmental monitoring data, sterility, and endotoxin testing outcomes for quality and consistency. Collaborates with laboratory analysts and quality assurance teams to resolve discrepancies and address out-of-specification results. Supports investigations related to laboratory deviations and participates in root cause analysis. Ensures timely review and release of batch records and product documentation. Identifies trends or recurring issues in laboratory data and recommends corrective actions. Supports the implementation of process improvements and best practices in microbiological testing and documentation. Provides training and guidance to laboratory staff on data integrity and compliance requirements. Maintains thorough records of all review activities and ensures proper documentation is in place. Calibration and maintenance coordination and record. Participates in internal and external audits as required, providing relevant documentation and expertise. Ensures all work is conducted in accordance with health, safety, and environmental regulations. Demonstrates strong organizational skills and manages workload to meet project timelines and regulatory deadlines. Maintains confidentiality and handles sensitive information with professionalism and integrity. Continuously updates knowledge of relevant regulations, industry trends, and technological advancements in microbiology. Performs other duties as assigned. While performing the responsibilities of the job, the employee is required to talk and hear. Must be able to bend at the waist and knees as well as twist at the trunk. Must be able to lift up to 25 lbs. Must be able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. Personal protective equipment and Respirators are essential for the health and safety of employees. Position requires working in the laboratory as well as sitting Microbiological method development and method validation procedures like BET, Sterility, MLT, Bio Assay and Disinfectant qualification and microbiological hold time validation, Container closure integrity validation. Knowledge and Skills Strong knowledge of microbiological testing techniques, reviewing, methods, and equipment. Key Competencies Customer Focus: Ability to build strong customer relationships and deliver customer centric solutions. Optimizes Work Processes: Know the most effective and efficient processes to get things done, with a focus on continuous improvement. Collaborates: Builds partnerships and works collaboratively with others to meet shared objectives. Resourcefulness: Secures and deploys resources effectively and efficiently. Manages Complexity: Makes sense of complex, high quality, and sometimes contradictory information to effectively solve problems. Ensures Accountability: Holds self and others accountable to meet commitments and objectives. Situational Adaptability: Adapts approach and demeanor in real time to match shifting demands of different situations. Communicates Effectively: Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences. Experience and Qualifications Bachelor’s degree in microbiology, Biology, or related field required; Master's degree preferred. Minimum of 3 years of experience in a microbiology laboratory required. Previous experience in a pharmaceutical or compounding environment preferred. Experience with compendia testing: United States Pharmacopeia, and regulatory requirements (Food and Drug Administration and cGMP) preferred. Experience with microbiological method development and method validation procedures like Sterility Testing, Endotoxin Testing, Disinfectant Efficacy Study, Water Testing, Method Validation, Environment Monitoring, Microbial Limit Testing, PET, and microbiological hold time validation, container closure integrity. Benefits: Pay range $75,000-$85,000 per Year Yearly bonus eligibility Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being Medical, dental and vision coverage Paid time off plan 401k savings plan Additional Information: Nivagen to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors. We are focused on building a diverse and inclusive workforce. If you're excited about this role, but do not meet 100% of the qualifications listed above, we encourage you to apply.", "summaryDescription" : "Microbiologist Laboratory Reviewer at Nivagen Pharmaceuticals. Skills: Microbiological data review, cGMP compliance, Pharmaceutical manufacturing. Review laboratory test results. Verify compliance with SOPs", "postedDate" : "2026-06-12T21:36:07.750", "createdAt" : "2026-06-12T21:36:07.750", "lastUpdated" : "2026-06-14T23:52:56.545", "ingestTimestamp" : "2026-06-12T21:36:07.750", "mongoId" : "6a2c5d9574d8ee00a08dd0f3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 85000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Microbiological testing", "Method validation", "Sterility testing", "Endotoxin testing", "Environmental monitoring", "Microbial limit testing", "Disinfectant qualification", "Container closure integrity", "Customer Focus", "Optimizes Work Processes", "Resourcefulness", "Manages Complexity", "Ensures Accountability", "Situational Adaptability", "Microbiological data review", "cGMP compliance", "Pharmaceutical manufacturing", "Quality control", "Data integrity", "Regulatory compliance", "Good Manufacturing Practices", "cGMP regulations", "GLP", "Injectable manufacturing", "Pharmaceutical supply chain", "Generic prescription drugs", "Over-the-counter products" ], "skillCount" : 27, "jobCategory" : "other", "jobSubcategory" : "qc_-microbiology", "dataQualityScore" : 0.8888889, "_score" : 645.0568, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Pharmaceuticals" }, { "id" : "6a2ebf7d74d8ee00a0e9abaf", "title" : "Clinical Laboratory Operations Site Director", "company" : "Invitae", "salary" : { "min" : 140000.0, "max" : 200000.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "San Francisco, CA", "locations" : [ "San Francisco, CA", "United States of America" ], "timestamp" : "2026-06-15T06:48:10.454", "fingerprint" : "ec0199e6aa224d5c1e20c2bf9dacedf23d030b4fe9459e426f2edb1728348407", "source" : "workday", "applyUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/San-Francisco-CA/Clinical-Laboratory-Operations-Site-Director---Invitae_2619979", "externalId" : "2619979", "industryFunction" : { }, "locationPoint" : "19.68044,-99.74877", "structuredLocations" : [ { "city" : "San Francisco", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "San Francisco, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor", "experienceMinYears" : 6, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Deep knowledge of CLIA/CAP regulations and inspection readiness. Experience in a commercial diagnostics or precision medicine organization." ], "hardSkillsList" : [ "CLIA/CAP regulations", "regulatory compliance", "workforce planning", "budget management", "capacity planning", "inventory management", "sample accessioning", "wet lab workflows", "post-sequencing processes" ], "softSkillsList" : [ "accountability, engagement, inclusion, collaboration" ], "hardSkills" : [ { "name" : "CLIA/CAP regulations", "level" : "intermediate" }, { "name" : "regulatory compliance", "level" : "intermediate" }, { "name" : "workforce planning", "level" : "intermediate" }, { "name" : "budget management", "level" : "intermediate" }, { "name" : "capacity planning", "level" : "intermediate" }, { "name" : "inventory management", "level" : "intermediate" }, { "name" : "sample accessioning", "level" : "intermediate" }, { "name" : "wet lab workflows", "level" : "intermediate" }, { "name" : "post-sequencing processes", "level" : "intermediate" } ], "softSkills" : [ { "name" : "accountability, engagement, inclusion, collaboration" } ], "majorSkills" : "Clinical Laboratory Operations, People Leadership, Quality & Compliance, Financial Management, Continuous Improvement", "majorSkillsList" : [ "Clinical Laboratory Operations, People Leadership, Quality & Compliance, Financial Management, Continuous Improvement" ], "coreResponsibilities" : "Provide end-to-end operational leadership for a large-scale, high-complexity clinical genetic testing laboratory. Ensure reliable, scalable processing while meeting or exceeding turnaround time and quality targets. Oversee daily laboratory operations including sample accessioning, wet lab workflows, post-sequencing processes, and inventory. Drive capacity planning, strategy, and throughput optimization to support business growth. Maintain full compliance with CLIA, CAP, state, and federal regulations. Serve as the site designee and work closely with the Laboratory Director to ensure regulatory readiness. Support inspections, audits, and corrective/preventive action (CAPA) activities. Champion a culture of quality, safety, and continuous compliance. Lead and develop a multidisciplinary organization. Build a high-performance culture focused on accountability, engagement, inclusion, and professional development. Partner with HR on workforce planning, recruiting, retention, and succession planning. Coach leaders to scale teams effectively in a fast-growing environment. Own site-level operating budgets, staffing models, and cost controls. Identify opportunities to improve cost per test without compromising quality or compliance. Partner with finance and commercial teams to support pricing, capacity forecasting, and margin improvement initiatives. Act as the primary site liaison with R&D, Medical Affairs, Quality, Regulatory, IT, Supply Chain, and Commercial teams. Support assay launches, technology transfers, and process changes from development into production. Provide operational input into new product planning and long-term laboratory strategy. Drive Lean, Six Sigma, or similar continuous improvement initiatives. Support adoption of automation and advanced analytics to improve efficiency and scalability. Promote data-driven decision-making using operational KPIs and quality metrics.", "teamCollaboration" : "Act as the primary site liaison with R&D, Medical Affairs, Quality, Regulatory, IT, Supply Chain, and Commercial teams. Excellent communicator and cross-functional collaborator.", "toolProficiency" : [ "Microsoft Office Suite" ], "communicationSkills" : "communicator", "continuousLearning" : "Support adoption of automation and advanced analytics to improve efficiency and scalability. Promote data-driven decision-making using operational KPIs and quality metrics.", "innovationCreativity" : "Supporting continued growth and innovation in genetic diagnostics. Support adoption of automation and advanced analytics to improve efficiency and scalability.", "problemSolvingSkills" : "process improvement; Lean; Six Sigma; data-driven decision-making", "specialRequirements" : "On-site leadership presence required in a fast-paced, production laboratory environment. Occasional travel for inspections, leadership meetings, or cross-site collaboration.", "outcomesObjectives" : "Ensure excellence in quality, turnaround time, cost, scalability, and regulatory compliance while supporting continued growth and innovation in genetic diagnostics. Build a high-performance culture focused on accountability, engagement, inclusion, and professional development. Identify opportunities to improve cost per test without compromising quality or compliance.", "qualificationsBasic" : "Bachelor’s degree in a Chemical or Biological Science, Clinical Laboratory Science, or Medical Technology. 6 or more years of experience in clinical laboratory operations, with proven leadership responsibilities. 5 or more years experience in leadership, directly managing employees.", "qualificationsPreferred" : "3 or more years experience managing people leaders. 1 year or more experience with Next Generation Sequencing (NGS) based clinical lab testing, bioinformatics workflows, and automation. 1 year or more experience in Lean, Six Sigma, or operational excellence methodologies. 1 year or more experience in a commercial diagnostics or precision medicine organization.", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Invitae, part of Labcorp, is seeking a Clinical Laboratory Operations Site Director for our Genetics laboratory in San Francisco, CA. This position is accountable for the overall leadership, performance, and compliance of a high‑volume clinical genetic testing laboratory. This role provides strategic, operational, and scientific leadership to ensure excellence in quality, turnaround time, cost, scalability, and regulatory compliance while supporting continued growth and innovation in genetic diagnostics. The Site Director is responsible for laboratory operations, people leadership, cross‑functional collaboration, and continuous improvement in a CLIA/CAP‑regulated environment. **Work Schedule:** Monday – Friday, 8am -5pm **Address:** 1400 16th Street, San Francisco, CA 94103 **Job Responsibilities:** **Laboratory Leadership & Operations** * Provide end‑to‑end operational leadership for a large‑scale, high‑complexity clinical genetic testing laboratory. * Ensure reliable, scalable processing while meeting or exceeding turnaround time and quality targets. * Oversee daily laboratory operations including sample accessioning, wet lab workflows, post-sequencing processes, and inventory. * Drive capacity planning, strategy, and throughput optimization to support business growth. **Quality, Compliance & Regulatory** * Maintain full compliance with CLIA, CAP, state, and federal regulations. * Serve as the site designee and work closely with the Laboratory Director to ensure regulatory readiness * Support inspections, audits, and corrective/preventive action (CAPA) activities. * Champion a culture of quality, safety, and continuous compliance. **People & Organizational Leadership** * Lead and develop a multidisciplinary organization. * Build a high‑performance culture focused on accountability, engagement, inclusion, and professional development. * Partner with HR on workforce planning, recruiting, retention, and succession planning. * Coach leaders to scale teams effectively in a fast‑growing environment. **Financial & Business Management** * Own site‑level operating budgets, staffing models, and cost controls. * Identify opportunities to improve cost per test without compromising quality or compliance. * Partner with finance and commercial teams to support pricing, capacity forecasting, and margin improvement initiatives. **Cross‑Functional Collaboration** * Act as the primary site liaison with R&D, Medical Affairs, Quality, Regulatory, IT, Supply Chain, and Commercial teams. * Support assay launches, technology transfers, and process changes from development into production. * Provide operational input into new product planning and long‑term laboratory strategy. **Continuous Improvement & Innovation** * Drive Lean, Six Sigma, or similar continuous improvement initiatives. * Support adoption of automation and advanced analytics to improve efficiency and scalability. * Promote data‑driven decision‑making using operational KPIs and quality metrics. **Minimum Qualifications:** * Bachelor’s degree in a Chemical or Biological Science, Clinical Laboratory Science, or Medical Technology * 6 or more years of experience in clinical laboratory operations, with proven leadership responsibilities * 5 or more years experience in leadership, directly managing employees **Preferred Qualifications:** * 3 or more years experience managing people leaders * 1 year or more experience with Next Generation Sequencing (NGS) based clinical lab testing, bioinformatics workflows, and automation * 1 year or more experience in Lean, Six Sigma, or operational excellence methodologies. * 1 year or more experience in a commercial diagnostics or precision medicine organization. **Additional Job Standards:** * Deep knowledge of CLIA/CAP regulations and inspection readiness. * Proven ability to scale operations in a regulated, production environment. * Strategic and operational thinker with strong execution discipline * Comfortable leading large, complex organizations through change * Data‑driven decision maker with strong financial acumen * Excellent communicator and cross‑functional collaborator * Strong people leader who builds trust and develops talent * On‑site leadership presence required in a fast‑paced, production laboratory environment * Occasional travel for inspections, leadership meetings, or cross‑site collaboration. **Pay Range:** $140,000 - $200,000 per year All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. The position is also eligible for an annual bonus under the Labcorp Bonus Plan. Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers. **Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please [click here](https://careers.labcorp.com/global/en/us-rewards-and-wellness). **Labcorp is proud to be an Equal Opportunity Employer:** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our [accessibility site](https://careers.labcorp.com/global/en/accessibility) or contact us at [Labcorp Accessibility.](mailto:Disability_apply@LabCorp.com) For more information about how we collect and store your personal data, please see our [Privacy Statement](https://www.labcorp.com/about/web-privacy-policy).", "summaryDescription" : "Clinical Laboratory Operations Site Director at Invitae. Skills: Clinical Laboratory Operations, People Leadership, Quality & Compliance, Financial Management, Continuous Improvement. Provide end-to-end operational leadership for a large-scale, high-complexity clinical genetic testing laboratory. Ensure reliable, scalable processing while meeting or exceeding turnaround time and quality targets. 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Experience in a commercial diagnostics or precision medicine organization.", "Microsoft Office Suite" ], "skillCount" : 13, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "executive", "dataQualityScore" : 1.0, "_score" : 644.85504, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c960974d8ee00a098e758", "title" : "Laboratory Director, IVF & ART", "company" : "Di Rezze Family Office", "industry" : "Healthcare", "location" : "Remote", "locations" : [ "Remote" ], "certifications" : [ "HCLD (High-complexity Clinical Laboratory Director)", "ELD" ], "timestamp" : "2026-06-15T07:12:02.198", "fingerprint" : "6d42585f1f35d211f3066596d91203ab34db12556f143c1e3d60c8019ebed6ed", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/dfo/jobs/4281740009", "externalId" : "4281740009", "industryFunction" : { }, "structuredLocations" : [ { "workMode" : "remote" } ], "locationText" : "", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "technicalSkills" : "EmbryoScope+, RI Witness, Matcher, EIVF, NGS", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Facility design", "Pre-construction planning", "Construction oversight", "Commissioning", "Equipment installation", "Validation", "Staff recruitment", "Staff onboarding", "SOP authoring", "Quality systems", "QA/QC program", "Regulatory compliance", "Outsourcing relationships", "Automation readiness", "Network expansion" ], "hardSkillsList" : [ "Clinical laboratory management", "Accreditation", "Facility specification", "Equipment planning", "HVAC capacity", "Electrical service", "Medical gas infrastructure", "ISO classification", "Cryostorage capacity", "Andrology workstation", "Robotic IVF deployment", "CLIA", "CAP", "SART membership", "PGT outsourcing", "In-house NGS", "Clinical outcomes", "Technical standard", "Spoke lab integrations", "Acquisition diligence", "Automation partnerships", "Pipeline building" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Clinical laboratory management", "level" : "intermediate" }, { "name" : "Accreditation", "level" : "intermediate" }, { "name" : "Facility specification", "level" : "intermediate" }, { "name" : "Equipment planning", "level" : "intermediate" }, { "name" : "HVAC capacity", "level" : "intermediate" }, { "name" : "Electrical service", "level" : "intermediate" }, { "name" : "Medical gas infrastructure", "level" : "intermediate" }, { "name" : "ISO classification", "level" : "intermediate" }, { "name" : "Cryostorage capacity", "level" : "intermediate" }, { "name" : "Andrology workstation", "level" : "intermediate" }, { "name" : "Robotic IVF deployment", "level" : "intermediate" }, { "name" : "CLIA", "level" : "intermediate" }, { "name" : "CAP", "level" : "intermediate" }, { "name" : "SART membership", "level" : "intermediate" }, { "name" : "PGT outsourcing", "level" : "intermediate" }, { "name" : "In-house NGS", "level" : "intermediate" }, { "name" : "Clinical outcomes", "level" : "intermediate" }, { "name" : "Technical standard", "level" : "intermediate" }, { "name" : "Spoke lab integrations", "level" : "intermediate" }, { "name" : "Acquisition diligence", "level" : "intermediate" }, { "name" : "Automation partnerships", "level" : "intermediate" }, { "name" : "Pipeline building", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "IVF laboratory operations, Accreditation and compliance", "majorSkillsList" : [ "IVF laboratory operations", "Accreditation and compliance" ], "coreResponsibilities" : "Walk candidate sites, Produce technical feasibility memos, Define lab program, Select and brief IVF facility review, Sign off on HVAC, air quality, cryostorage, Build Day 1 equipment plan, Design lab for automation readiness, Oversee construction, Oversee commissioning, Oversee equipment installation, Oversee validation, Recruit senior embryology staff, Onboard senior embryology staff, Recruit senior andrology staff, Onboard senior andrology staff, Author all SOPs, Author quality systems documentation, Author QA/QC program, Drive CLIA accreditation, Drive CAP accreditation, Drive Florida Department of Health accreditation, Lead SART membership application, Establish PGT outsourcing relationships, Direct day-to-day lab operations, Manage clinical outcomes, Manage staffing, Manage quality, Manage regulatory compliance, Manage vendor management, Set technical standard for spoke lab integrations, Set technical standard for acquisition diligence, Lead evaluation of automation partnerships, Lead evaluation of PGT in-sourcing, Mentor junior staff, Build pipeline for network expansion", "teamCollaboration" : "Cross-functional teams; Architects; Engineers; Product teams; Senior staff; Junior staff; Vendors; Stakeholders", "projectManagementSkills" : [ "Feasibility and design engagement", "Construction oversight", "Commissioning", "Accreditation process", "Operations management", "Scale management" ], "domainKnowledge" : "IVF; ART; Embryology; Andrology; Cryostorage; Medical gas infrastructure; ISO classification; PGT; NGS; CLIA; CAP; SART; Robotic IVF; Automation landscape", "domainList" : [ "ivf", "art", "embryology", "andrology", "cryostorage", "medical-gas-infrastructure", "iso-classification", "pgt", "ngs", "clia", "cap", "sart", "robotic-ivf", "automation-landscape" ], "domainSpecificKnowledge" : [ "IVF", "ART", "Embryology", "Andrology", "Cryostorage", "Medical gas infrastructure", "ISO classification", "PGT", "NGS", "CLIA", "CAP", "SART", "Robotic IVF", "Automation landscape" ], "toolProficiency" : [ "EmbryoScope+", "RI Witness", "Matcher", "EIVF", "Conceivable", "AURA", "CHLOE", "Life Whisperer", "ALife" ], "communicationSkills" : "Technical memos; Briefing architects; Briefing engineers; SOP authoring; Quality systems documentation; QA/QC program; Regulatory reporting; SART membership application; Technical standard setting; Acquisition diligence; Pipeline building", "documentationSkills" : "Technical memos; SOPs; Quality systems documentation; QA/QC program", "innovationCreativity" : "Automation-ready design; Future robotic IVF deployment", "problemSolvingSkills" : "Feasibility analysis; Technical problem solving; Quality system development; Regulatory compliance; Troubleshooting", "specialRequirements" : "Feasibility and design engagement, Consulting-to-hire path, Transition to full-time Director", "outcomesObjectives" : "Achieve accreditation; Open laboratory; Scale laboratory operations; Meet ISO classification targets; Meet cryostorage capacity targets; Meet andrology room layout targets; Meet procedure room layout targets; Meet Day 1 equipment plan; Achieve CLIA accreditation; Achieve CAP accreditation; Achieve Florida accreditation; Establish PGT outsourcing relationships; Achieve 600+ cycles/year for in-house NGS; Meet clinical outcomes targets; Meet staffing targets; Meet quality targets; Meet regulatory compliance targets; Meet vendor management targets; Set technical standard for spoke lab integrations; Set technical standard for acquisition diligence; Evaluate automation partnerships; Evaluate PGT in-sourcing; Build pipeline for network expansion", "qualificationsBasic" : "HCLD certification through ABB, PhD-track credential with ELD, Commissioned at least one IVF lab, Direct operating experience with time-lapse incubation, Direct operating experience with electronic witnessing, Direct operating experience with modern LIMS, Run a lab through 200-600+ annual cycle inflection, Authored SOPs from scratch, Led CAP inspections, Operated under current witnessing and traceability standards, Familiar with post-Alabama regulatory environment, Familiar with lessons from recent IVF mix-up incidents", "qualificationsPreferred" : "Florida operating experience, Prior tenure at premium-segment network, Direct experience opening or scaling a network lab, Published research, Society leadership (ASRM, SART, ABB)", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Laboratory Director, IVF transition into operational leadership through accreditation, opening, and scale. Consulting-to-hire. Begin with a paid feasibility and design engagement (typically 8–12 weeks) covering site walk-through, technical memo, facility spec, and equipment plan. Convert to full-time Laboratory Director ahead of construction kickoff. This path is designed for candidates currently in director roles who want to validate the opportunity before transitioning. Both paths lead to the same destination. The recruiter can route candidate preferences. What you will own Phase 1 — Facility design and pre-construction (months 0–6) Walk candidate sites and produce technical feasibility memos covering floor-to-floor height, floor load, HVAC capacity, electrical service, LN2 routing, medical gas infrastructure, and adjacent-tenant risk. Define the lab program: square footage, room adjacencies, ISO classification targets, equipment footprint, cryostorage capacity, andrology and procedure room layout. Select and brief the IVF facility consultant; review schematic and construction documents from the architect of record; sign off on HVAC, air quality, and cryostorage engineering. Build the Day 1 equipment plan, including time-lapse incubation (EmbryoScope+ or equivalent), electronic witnessing (RI Witness or Matcher), LIMS (eIVF or equivalent), and andrology workstation specifications. Design the lab to be automation-ready for future robotic IVF deployment (e.g., Conceivable/AURA) without committing premature capital. Phase 2 — Construction, commissioning, and accreditation (months 6–12) Oversee construction, commissioning, equipment installation, and validation. Recruit and onboard senior embryology and andrology staff (the Laboratory Director chooses these hires). Author all SOPs, quality systems documentation, and the QA/QC program. Drive CLIA, CAP, and Florida licensure; lead the SART membership application. Establish PGT outsourcing relationships for Years 1–2, with a defined pathway to in-house NGS at 600+ cycles/year. Phase 3 — Operations and scale (months 12+) Direct day-to-day lab operations: clinical outcomes, staffing, quality, regulatory compliance, vendor management. Set the technical standard for spoke lab integrations and future acquisition diligence. Lead the Year 2–3 evaluation of automation partnerships and PGT in-sourcing. Mentor junior embryologists; build a pipeline that supports network expansion. Required qualifications Certification: HCLD (High-complexity Clinical Laboratory Director) through ABB, or equivalent PhD-track credential with ELD. Required for CLIA Lab Director of record. Greenfield build experience: Has commissioned at least one IVF lab from shell space through CAP/CLIA accreditation. We will ask for specifics: square footage, cycle volume at launch, lease-to-first-transfer timeline. Technology fluency: Direct operating experience with time-lapse incubation (EmbryoScope+ specifically), electronic witnessing (RI Witness and/or Matcher), and a modern LIMS. Informed opinions on tradeoffs, not brand familiarity. Volume scaling: Has run a lab through the 200 → 600+ annual cycle inflection, with the staffing, equipment redundancy, and quality systems that come with it. Quality systems leadership: Has authored SOPs from scratch, led CAP inspections, and operated under current witnessing and traceability standards. Familiar with post-Alabama regulatory environment and lessons from recent IVF mix-up incidents. Automation literacy: Familiar with the current automation landscape (Conceivable/AURA, CHLOE, Life Whisperer, ALife) without being a true believer. Builds automation-ready, not automation-dependent. Preferred Florida operating experience, including familiarity with Office Surgery Registration pathway. Prior tenure at a premium-segment network (CCRM, Shady Grove, RMA, Boston IVF, Spring Fertility, or equivalent). Direct experience opening or scaling a network lab (multi-site, hub-and-spoke). Published research or society leadership (ASRM, SART, ABB).", "summaryDescription" : "Laboratory Director, IVF & ART at Di Rezze Family Office. Skills: IVF laboratory operations, Accreditation and compliance. Walk candidate sites. 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true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2b080174d8ee00a0757b11", "title" : "Fragrance Laboratory Lead", "company" : "Unilever", "industry" : "Consumer Goods", "salary" : { "min" : 2250000.0, "max" : 3500000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Fragrance Laboratory Lead in Mumbai, India, adjusted for the Food & Beverage industry and company size." }, "location" : "India", "locations" : [ "India" ], "timestamp" : "2026-06-14T22:57:58.396", "fingerprint" : "b747468654ff2d2ae309b40c0a50b4838bd4ff765d4a5ba6dcb4400842a0ab78", "source" : "workday", "language" : "en", "applyUrl" : "https://unilever.wd3.myworkdayjobs.com/Unilever_Experienced_Professionals/job/Mumbai-HURC/Fragrance-Laboratory-Lead_R-1182197", "externalId" : "R-1182197", "industryFunction" : { }, "locationPoint" : "20.5937,78.9629", "structuredLocations" : [ { "city" : "Mumbai", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "19.0549990,72.8692035" } ], "locationText" : "Mumbai, India", "employmentType" : "FULL_TIME", "experienceMinYears" : 8, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "professionalSkills" : [ "Laboratory management", "Equipment management", "Budgeting" ], "hardSkillsList" : [ "Laboratory safety", "Waste disposal", "Material management" ], "softSkillsList" : [ "Ownership" ], "hardSkills" : [ { "name" : "Laboratory safety", "level" : "intermediate" }, { "name" : "Waste disposal", "level" : "intermediate" }, { "name" : "Material management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Ownership" } ], "majorSkills" : "Laboratory operations, Equipment maintenance, Regulatory compliance", "majorSkillsList" : [ "Laboratory operations", "Equipment maintenance", "Regulatory compliance" ], "coreResponsibilities" : "Lead laboratory environment management, Support formulation work, Support application work, Support evaluation work, Ensure laboratory operates seamlessly, Maintain a clean workspace, Maintain a safe workspace, Maintain well-functioning workspace, Ensure compliance with health standards, Ensure compliance with safety standards, Ensure compliance with laboratory management standards, Oversee safe handling of laboratory waste, Oversee disposal of laboratory waste, Manage laboratory equipment, Perform routine maintenance, Troubleshoot equipment issues, Replace laboratory equipment, Resolve technical issues, Minimize downtime, Oversee planning for new equipment, Oversee budgeting for new equipment, Oversee budgeting for laboratory needs, Ensure availability of materials, Ensure availability of consumables, Keep evaluation booths operational, Keep testing areas operational, Keep evaluation booths available, Keep testing areas available, Maintain accurate records, Maintain up-to-date records", "teamCollaboration" : "Work across diverse technical teams", "domainKnowledge" : "Fragrance development; Personal Care products; Home Care products; Beauty products", "domainList" : [ "fragrance-development", "personal-care-products", "home-care-products", "beauty-products" ], "domainSpecificKnowledge" : [ "Fragrance development", "Personal Care products", "Home Care products", "Beauty products" ], "documentationSkills" : "Record keeping", "continuousLearning" : "Growth opportunities", "innovationCreativity" : "Enabling innovation", "problemSolvingSkills" : "Problem-solving", "outcomesObjectives" : "Deliver products used by millions; Impact quality; Impact safety; Impact speed of innovation", "qualificationsBasic" : "Bachelor's degree or higher in a scientific discipline, Experience working in a laboratory environment, Experience with safe and effective practices, High attention to detail, Proactive approach to problem-solving, Good understanding of laboratory safety processes, Understanding of standard procedures, Understanding of risk assessments, Understanding of safe handling of materials", "qualificationsPreferred" : "Experience in formulation, Experience in application, Experience in evaluation", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Job Title:** Fragrance Laboratory Lead **Location:** Mumbai HURC **Work Level:** 1D **Want to Change The World?** Unilever is one of the world’s leading suppliers of Beauty, Personal and Home Care products selling in over 190 countries and used by 3.7 billion consumers every day. Unilever has more than 400 brands used in homes around the world, including Dove, Sure, TRESemmé, Sunsilk, Vaseline, Comfort, Persil and Surf. As one of the world’s largest users of fragrances, we recognise that creating exceptional fragrances is at the heart of delivering extraordinary consumer experiences and driving desire at scale. To achieve our ambition, Unilever Fragrance House is undertaking a global fragrance transformation, leveraging expert inhouse fragrance teams to craft unmissably superior fragrances for our Personal Care, Beauty & Wellbeing and Home Care Business Groups. **Job Purpose** Make an Impact That Matters! Are you passionate about creating safe, efficient, and high-performing laboratory environments? As Unilever Fragrance House (UFH) Laboratory Lead, you will play a critical role in enabling innovation by ensuring our laboratory operates seamlessly every day. You will lead the management of our India lab, supporting formulation, application, and evaluation work that ultimately helps deliver products used by millions of people around the world. Your work will directly impact the quality, safety, and speed of innovation across our teams. **What You Will Do** In this role, you will take ownership of the laboratory environment and ensure it consistently supports high-quality R&D work for UFH. Key responsibilities include: • Leading the end-to-end management of the laboratory, ensuring it is organized, efficient, and ready to support all activities • Maintaining a clean, safe, and well-functioning workspace, including all equipment and evaluation areas • Ensuring full compliance with health, safety, and laboratory management standards • Overseeiog safe handling and disposal of laboratory waste in line with regulatory requirements • Managing laboratory equipment, including routine maintenance, troubleshooting, and timely replacement • Working closely with operations teams to resolve technical issues and minimize downtime • Overseeing planning and budgeting for new equipment and ongoing laboratory needs • Ensure availability of all materials and consumables required for smooth laboratory operations • Keeping evaluation booths and testing areas fully operational and available according to timelines • Maintaining accurate and up-to-date records of all laboratory activities **What We Are Looking For** We are looking for someone who combines strong technical discipline with ownership and collaboration: • A bachelor’s degree or higher in a scientific discipline • Experience working in a laboratory environment, with a strong focus on safe and effective practices • Strong collaboration and communication skills, with the ability to work across diverse technical teams • High attention to detail and a proactive approach to problem-solving • Good understanding of laboratory safety processes, including standard procedures, risk assessments, and safe handling of materials **What You Can Expect** • You will join a collaborative and purpose-driven team that believes in doing meaningful work - for both people and the planet - supporting innovation that impacts millions of consumers • Collaborative culture: Work with skilled and supportive colleagues across functions • Growth opportunities: Build expertise in laboratory operations, equipment management, and cross-functional collaboration • Ownership and visibility: Play a key role in ensuring operational excellence in a critical facility **NOTES** Please apply via this portal as e-mail applications may not be processed. Should you require additional information or reasonable adjustments to allow you to present your best self during this process, please contact your Talent Partner listed at the right hand side of this vacancy. **What We Offer** We strive to achieve a family-friendly and inclusive workplace and to, above all, create possibilities for all. Diversity at Unilever is about inclusion, embracing differences, creating possibilities and growing together for better business performance. We embrace diversity in our workforce. This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity. We are also more than happy to provide reasonable adjustments during our application and interview process to enable you to be present your best self. To find out more, including about our Employee Resource Groups, please click here Equity, Diversity & Inclusion (unilever.com).", "summaryDescription" : "Fragrance Laboratory Lead at Unilever. Skills: Laboratory operations, Equipment maintenance, Regulatory compliance. Lead laboratory environment management. Support formulation work", "postedDate" : "2026-06-11T04:17:48.786", "createdAt" : "2026-06-12T04:17:48.775", "lastUpdated" : "2026-06-14T22:57:58.396", "ingestTimestamp" : "2026-06-12T04:17:48.775", "mongoId" : "6a2b080174d8ee00a0757b11", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://unilever.wd3.myworkdayjobs.com/Unilever_Experienced_Professionals/job/Mumbai-HURC/Fragrance-Laboratory-Lead_R-1182197", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Laboratory safety", "Waste disposal", "Material management", "Ownership", "Laboratory operations", "Equipment maintenance", "Regulatory compliance", "Laboratory management", "Equipment management", "Budgeting", "Fragrance development", "Personal Care products", "Home Care products", "Beauty products" ], "skillCount" : 14, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 1.0, "_score" : 634.9248, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Consumer Goods" }, { "id" : "6a2642d774d8ee00a02149a3", "title" : "Electronic Calibration Technician", "company" : "Moog", "salary" : { "min" : 29.5, "max" : 40.5, "currency" : "USD", "frequency" : "yearly" }, "location" : "Buffalo, NY", "locations" : [ "Buffalo, NY", "United States of America" ], "timestamp" : "2026-06-12T15:47:01.112", "fingerprint" : "1fdc7e06c29c48a1a335998e36981f24126e13b9b3e7fe7862b773aa226b9194", "source" : "workday", "language" : "en", "applyUrl" : "https://moog.wd5.myworkdayjobs.com/MOOG_External_Career_Site/job/Buffalo-NY/Electronic-Calibration-Technician_R-26-16457", "externalId" : "R-26-16457", "locationPoint" : "37.64393,-93.09241", "structuredLocations" : [ { "city" : "East Aurora", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.7689141,-78.6177611" } ], "locationText" : "East Aurora, New York, United States", "employmentType" : "FULL_TIME", "experienceMinYears" : 5, "technicalSkills" : "Fluke calibrators, Power supply, Encoders, Temperature baths", "professionalSkills" : [ "Metrology", "Electronic calibration" ], "hardSkillsList" : [ "Fault isolation", "Equipment repair" ], "softSkillsList" : [ "Mentoring", "Ownership" ], "hardSkills" : [ { "name" : "Fault isolation", "level" : "intermediate" }, { "name" : "Equipment repair", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Mentoring" }, { "name" : "Ownership" } ], "majorSkills" : "Electronic calibration, Test equipment maintenance, Troubleshooting", "majorSkillsList" : [ "Electronic calibration", "Test equipment maintenance", "Troubleshooting" ], "coreResponsibilities" : "Calibrate electronic test equipment, Maintain electronic test equipment, Repair electronic test equipment, Perform calibrations following procedures, Build documentation, Review daily schedule, Keep calibration work on track, Deliver calibration work on time, Troubleshoot issues, Perform fault isolation, Interpret symptoms, Recommend improvements, Enhance calibration processes, Enhance maintenance practices, Enhance equipment reliability, Provide insight into design, Gather data for proposals, Support initial calibration activities, Mentor junior technicians, Share technical knowledge, Build team capability, Disassemble equipment, Repair components, Replace components, Reassemble equipment, Verify restored accuracy, Verify compliance, Collaborate with engineering, Offer feedback, Recommend updates to procedures, Ensure calibration records are complete, Ensure calibration records are accurate, Ensure calibration records are compliant", "teamCollaboration" : "Collaborate with engineering; Mentor junior technicians", "projectManagementSkills" : [ "Manage multiple tasks" ], "domainKnowledge" : "Electronic calibration; Metrology; Test equipment", "domainList" : [ "electronic-calibration", "metrology", "test-equipment" ], "domainSpecificKnowledge" : [ "Electronic calibration", "Metrology", "Test equipment" ], "toolProficiency" : [ "Fluke calibrators", "Power supply", "Encoders", "Temperature baths" ], "communicationSkills" : "Technical documentation", "documentationSkills" : "Technical documentation", "continuousLearning" : "Mentorship; Coaching opportunities; Personal growth programs", "innovationCreativity" : "Recommend improvements; Provide insight into design", "problemSolvingSkills" : "Troubleshoot issues; Fault isolation; Logical approach", "qualificationsBasic" : "5+ years of experience in electronic calibration, Hands-on knowledge using electronic equipment, Excellent communication skills, Excellent organizational skills, Ability to write clear technical documentation, Background in calibration/metrology, Manage multiple tasks, Adapt quickly to shifting priorities", "qualificationsPreferred" : "Experience with circuitry, Experience with test system startup", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Moog is a performance culture that empowers people to achieve great things. Our people enjoy solving interesting technical challenges in a culture where everyone trusts each other to do the right thing. For you, working with us can mean deeper job satisfaction, better rewards, and a great quality of life inside and outside of work. **Job Title** : Electronic Calibration Technician **Reporting To:** Supervisor, Metrology **Work Schedule:** Onsite – Buffalo, NY Our team in Military Aircraft Group is looking for an Electronic Calibration Technician to join them. You will report to the Supervisor of Metrology and will have an onsite work schedule in East Aurora, NY. As an Electronic Calibration Technician, you'll play a critical role in maintaining the accuracy and performance of both commercial test equipment and custom-built Moog test consoles. Your work ensures safety, consistency, and excellence across our operations. **_As a Calibration Technician, you will:_** * Calibrate, maintain, and repair electronic test equipment to manufacturer specs or internal standards. * Perform calibrations following established procedures and help build documentation (photos, notes) when procedures don’t yet exist. * Review the daily schedule or service requests to keep calibration work on track and delivered on time. * Troubleshoot issues by performing fault isolation and interpreting symptoms with a logical, methodical approach. * Recommend improvements to enhance calibration processes, maintenance practices, and equipment reliability. * Provide insight into the design of calibration and maintenance aids and assist in gathering data for capital expenditure proposals. * Support initial calibration activities for first‑of‑its‑kind Measurement & Test Equipment (M&TE). * Mentor junior technicians, sharing your technical knowledge and expertise to build team capability. * Disassemble, repair/replace components, and reassemble equipment to verify restored accuracy and compliance. * Collaborate closely with engineering, offering feedback and recommending updates to calibration procedures. * Ensure all calibration records are complete, accurate, and compliant with internal requirements. _**To be considered for this role, here’s what you’ll typically bring:**_ * 5+ years of experience in electronic calibration, assembly, repair, or maintenance. * Strong hands‑on knowledge using electronic equipment essential for test console calibration such as fluke calibrators, power supply, encoders, temperature baths and dead weight pressure calibrators. * Excellent communication and organizational skills, with the ability to write clear technical documentation. * Background in calibration/metrology, especially electronic calibration involving circuitry and test system startup. * A self‑motivated learner who can manage multiple tasks, collaborate well, and take ownership with minimal supervision. * Able to adapt quickly to shifting priorities and contribute technical insight to resolve issues affecting M&TE. _**How we care for you:** _ * Financial Rewards: great compensation package, annual profit sharing, matching 401k and the ability to participate in Employee Stock Purchase Plan, Flexible Spending and Health Savings Accounts * Work/Life Balance: Flexible paid time off, holidays and parental leave program, relocation assistance * Health & Welfare: Comprehensive insurance coverage including medical, dental, vision, life, disability, Employee Assistance Plan (“EAP”) and other supplemental benefit coverages * Professional Skills Development: Tuition Assistance, mentorship and coaching opportunities, leadership development and other personal growth programs * Collaborative and Welcoming Workplace: Inclusive culture rooted in our values, enhanced by Employee Resource Groups, and team-building activities. * Additional site-specific benefits may be offered **Salary Range Transparency:** Buffalo, NY $29.50–$40.50 Annually **Salary Range Disclaimer** The base salary range represents the low and high end of the Moog salary range for this position in the given work location. Actual salaries will vary depending on factors including but not limited to location, experience, and performance. The range(s) listed is just one component of Moog's total compensation package for employees. Other rewards may include annual bonuses, employee stock purchase plan, an open paid time off policy, and many region-specific benefits. This position requires access to U.S. export-controlled information. EOE/AA Minority/Female/Sexual Orientation/Gender Identity/Disability/Veteran _Moog is an Equal Opportunity Employer, and as such affirms the right of every person to participate in all aspects of employment without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. If you are interested in applying for employment and need special assistance or an accommodation to apply for a posted position, contact our Human Resources department via phone at 844-367-5787._ No unsolicited agency submittals please. Agency partners must be invited to participate in a search by our Talent Acquisition Team and have signed terms in place prior to any submittal. Absent compliance with these pre-conditions resumes submitted directly to any Moog Inc. employee or affiliate will not qualify for fee payment, and therefore become the property of Moog Inc.", "summaryDescription" : "Electronic Calibration Technician at Moog. Skills: Electronic calibration, Test equipment maintenance, Troubleshooting. Calibrate electronic test equipment. Maintain electronic test equipment", "postedDate" : "2026-06-09T12:29:43.220", "createdAt" : "2026-06-11T12:29:42.942", "lastUpdated" : "2026-06-12T15:47:01.112", "ingestTimestamp" : "2026-06-11T12:29:42.942", "mongoId" : "6a2642d774d8ee00a02149a3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://moog.wd5.myworkdayjobs.com/MOOG_External_Career_Site/job/Buffalo-NY/Electronic-Calibration-Technician_R-26-16457", "salaryAnnualMin" : 61360, "salaryAnnualMax" : 84240, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Fault isolation", "Equipment repair", "Mentoring", "Ownership", "Electronic calibration", "Test equipment maintenance", "Troubleshooting", "Metrology", "Manage multiple tasks", "Test equipment", "Fluke calibrators", "Power supply", "Encoders", "Temperature baths" ], "skillCount" : 14, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 630.4755, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2ad31874d8ee00a0714d56", "title" : "Reference File Maintainer 2", "company" : "IQVIA", "industry" : "Healthcare", "salary" : { "min" : 360000.0, "max" : 540000.0, "currency" : "PHP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level Reference File Maintainer 2 in Taguig City, Philippines, adjusted for the healthcare industry and company size." }, "location" : "Taguig City, Philippines", "locations" : [ "Taguig City, Philippines" ], "timestamp" : "2026-06-14T22:52:05.119", "fingerprint" : "749927fb6cd251405c64b2ad03ae8f53788062971e13e846d8a4b3fbcd521a73", "source" : "workday", "language" : "en", "applyUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Taguig-City-Philippines/XMLNAME-3155---Reference-File-Maintainer-2_R1542954", "externalId" : "R1542954", "industryFunction" : { }, "locationPoint" : "14.5243,121.0792", "structuredLocations" : [ { "city" : "Taguig City", "country" : "Philippines", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "14.5270538,121.0744942" } ], "locationText" : "Taguig City, Philippines", "employmentType" : "FULL_TIME", "minimumEducation" : "High School", "softSkillsList" : [ "Critical thinking", "Problem-solving" ], "softSkills" : [ { "name" : "Critical thinking" }, { "name" : "Problem-solving" } ], "coreResponsibilities" : "Complete maintenance of reference data, Perform research to gather information, Validate completeness or accuracy of data, Perform outbound phone verification, Validate accuracy of reference data, Capture client-required details, Perform ad hoc data analysis, Participate on various process improvement, Validate information gathered from third-party sources, Update, creation, or deletion in the database", "domainKnowledge" : "Healthcare Organizations; Prescribers", "domainList" : [ "healthcare-organizations", "prescribers" ], "domainSpecificKnowledge" : [ "Healthcare Organizations", "Prescribers" ], "communicationSkills" : "Verbal communication; Written communication", "problemSolvingSkills" : "Problem-solving skills; Critical thinking", "specialRequirements" : "Willing to work in night", "qualificationsBasic" : "High School Diploma or equivalent, Basic knowledge in Windows applications, Verbal and/or written communication skills in English, Critical thinking and problem-solving skills, Demonstrate understanding of complex concepts and processes, Initiative and self-motivated, Willing to work in night", "qualificationsPreferred" : "Experience in handling voice account, Experience in handling healthcare account", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Role Purpose:** * Responsible for the daily maintenance of healthcare Organizations and Prescribers in all database of the US Region. * Validates, research & analyses to client data inquiries with the use of the process tool. **Job Responsibilities:** * Complete maintenance of reference data (healthcare Organizations and Prescribers) as essential for US Production. * Perform research such as Internet Search, Phone Verification, Database Matches and etc. to gather information from third parties that will validate the completeness or accuracy of the data. * Perform outbound phone verification of details on Organization and Prescriber records to validate accuracy of reference data maintained as well as capture client-required details such as primary office address and primary profession/specialty. * Performs ad hoc data analysis and participates on various process improvement as needed. * Validate that the information gathered from third-party sources represents accurate new data that should result in an update, creation, or deletion in the database existing data. **Job Requirement:** * High School Diploma or equivalent Req * Experience in handling voice and healthcare account is an advantage but not a requirement. * Basic knowledge in Windows applications (Excel, Word). * Strong verbal and / or written communication skills in either the language of the country supplied or English. * Critical thinking and problem-solving skills. * Demonstrate strong understanding of complex concepts and processes. * Has initiative and is self-motivated to see through until resolution concerns raised by Clients. * Candidate must be willing to work in night. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at [https://jobs.iqvia.com](https://jobs.iqvia.com/) IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.", "summaryDescription" : "Reference File Maintainer 2 at IQVIA. Complete maintenance of reference data. Perform research to gather information", "postedDate" : "2026-06-10T02:05:53.187", "createdAt" : "2026-06-12T02:05:52.853", "lastUpdated" : "2026-06-14T22:52:05.119", "ingestTimestamp" : "2026-06-12T02:05:52.853", "mongoId" : "6a2ad31874d8ee00a0714d56", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Taguig-City-Philippines/XMLNAME-3155---Reference-File-Maintainer-2_R1542954", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Critical thinking", "Problem-solving", "Healthcare Organizations", "Prescribers" ], "skillCount" : 4, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 629.67413, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2a8bb974d8ee00a0683a51", "title" : "Laboratory Engineer", "company" : "University of Rochester", "salary" : { "min" : 55955.0, "max" : 78336.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-13T19:14:39.156", "fingerprint" : "0a499374d72c94928e50cfd45f4b307a5fb2db2bbf2ea2fd96819baf49af7603", "source" : "workday", "language" : "en", "applyUrl" : "https://rochester.wd5.myworkdayjobs.com/UR_Staff/job/Laboratory-for-Laser-Energetics/Laboratory-Engineer-I_R272091", "externalId" : "R272091", "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Rochester", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.1572850,-77.6152140" } ], "locationText" : "Rochester, New York, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's degree", "experienceMinYears" : 1, "professionalSkills" : [ "Target assembly", "Manufacturing operations" ], "hardSkillsList" : [ "Metrology hardware", "Manual manipulation" ], "hardSkills" : [ { "name" : "Metrology hardware", "level" : "intermediate" }, { "name" : "Manual manipulation", "level" : "intermediate" } ], "majorSkills" : "Laser laboratory, Component assembly, Data collection", "majorSkillsList" : [ "Laser laboratory", "Component assembly", "Data collection" ], "coreResponsibilities" : "Conduct experiments, tests, and research, Assist in designing experiments, Assist in setting up experiments, Assist in maintaining equipment, Assist in collecting data, Diagnose system components, Perform preventative maintenance, Manage fragile targets, Develop innovative solutions, Manipulate delicate micro-assemblies, Develop manufacturing methods, Develop operation sequences, Develop fabrication processes, Design sequence of operations, Specify procedures for fabrication, Adapt machinery, Maintain records, Maintain reporting systems, Develop documentation of findings, Develop documentation of implemented solutions, Communicate results to staff, Measure completed assemblies, Collect data, Clean lab equipment, Adjust lab equipment, Replace parts on lab equipment, Work in a safe manner", "domainKnowledge" : "Laser laboratory", "domainList" : [ "laser-laboratory" ], "domainSpecificKnowledge" : [ "Laser laboratory" ], "communicationSkills" : "Communicate results", "documentationSkills" : "Develop documentation", "innovationCreativity" : "Develop innovative solutions", "problemSolvingSkills" : "Technical problems", "specialRequirements" : "Work onsite 8:30a-5:30p", "qualificationsBasic" : "Bachelor's degree and 1 year experience, Assemble millimeter-scale components, Work in cleanroom laboratory environment, Operate microscope in cleanroom", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive. _**Job Location (Full Address):**_ 250 East River Rd, Rochester, New York, United States of America, 14623 _**Opening:**_ Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 250548 LLE-Laboratory for Laser Energ Work Shift: UR - Day (United States of America) Range: UR URG 109 Compensation Range: $55,955.00 - $78,336.00 _The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job 's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._ _**Responsibilities:**_ Conducts experiments, tests, and research within a laser laboratory setting. Assists more experienced engineers or scientists in designing and setting up experiments, maintaining equipment, and collecting data. Diagnoses and performs preventative maintenance on system components including recovery, replacement, and reconfiguration of damaged sensitive components. Manages fragile targets for laser exploration. This is an onsite position 8:30a-5:30p. **ESSENTIAL FUNCTIONS** * Required to assemble millimeter-scale components that meet specifications * Expected to develop innovative but practical solutions to technical problems in target assembly to enhance manufacturability * Capable at working in cleanroom laboratory environment, using manual techniques to manipulate delicate micro-assemblies * Ability to operate microscope in cleanroom environment * Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies, and final assemblies. * Designs the sequence of production operations, specifying procedures for the fabrication of applicable tools and equipment, and adapting machinery * Maintains records and reporting systems for coordination of manufacturing operations * Develops appropriate documentation of findings and implemented solutions and communicates results to staff * Measures completed assemblies using metrology hardware and collects data * Cleans, adjusts and replaces parts on lab equipment * Expected to work in a safe manner in accordance with established operating procedures and practices. * Other duties as assigned. **MINIMUM EDUCATION & EXPERIENCE** * Bachelor's degree and 1 year of relevant experience required * Or equivalent combination of education and experience The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.", "summaryDescription" : "Laboratory Engineer at University of Rochester. Skills: Laser laboratory, Component assembly, Data collection. Conduct experiments, tests, and research. Assist in designing experiments", "postedDate" : "2026-06-10T18:40:58.891", "createdAt" : "2026-06-11T18:40:58.757", "lastUpdated" : "2026-06-13T19:14:39.156", "ingestTimestamp" : "2026-06-11T18:40:58.757", "mongoId" : "6a2a8bb974d8ee00a0683a51", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://rochester.wd5.myworkdayjobs.com/UR_Staff/job/Laboratory-for-Laser-Energetics/Laboratory-Engineer-I_R272091", "salaryAnnualMin" : 55955, "salaryAnnualMax" : 78336, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Metrology hardware", "Manual manipulation", "Laser laboratory", "Component assembly", "Data collection", "Target assembly", "Manufacturing operations" ], "skillCount" : 7, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 629.2045, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a0de91258b93c861eb99057", "title" : "Dermpath Laboratory Histologist", "industry" : "Healthcare", "salary" : { "min" : 45000.0, "max" : 65000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level Histologist in Tampa, adjusted for the healthcare industry." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
USF Health Morsani Center AHC (AMGMCAH)
13330 USF Laurel Dr.

Tampa, 33612

" ], "certifications" : [ "Issued by Florida or Compact State Clinical Lab Technologist" ], "timestamp" : "2026-06-15T10:56:25.873", "fingerprint" : "6208de638396beb77ac053841c495258e873ef2db0c2f0cdca423c975be13195", "source" : "taleo", "language" : "en", "applyUrl" : "https://tas-tgh.taleo.net/careersection/ex/jobdetail.ftl?job=677291", "externalId" : "677291", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tampa", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "27.9449854,-82.4583107" } ], "locationText" : "Tampa, Florida, United States", "minimumEducation" : "Associate's", "hardSkillsList" : [ "Histological tests", "Histological stains" ], "hardSkills" : [ { "name" : "Histological tests", "level" : "intermediate" }, { "name" : "Histological stains", "level" : "intermediate" } ], "majorSkills" : "Tissue specimen preparation, Histology", "majorSkillsList" : [ "Tissue specimen preparation", "Histology" ], "coreResponsibilities" : "Prepare tissue specimens, Perform histological tests, Perform histological stains, Perform special tests, Keep laboratory up to CLIA Standards", "domainKnowledge" : "CLIA regulations; Proficiency testing; Quality assurance; Quality control; Medical terminology", "domainList" : [ "clia-regulations", "proficiency-testing", "quality-assurance", "quality-control", "medical-terminology" ], "domainSpecificKnowledge" : [ "CLIA regulations", "Proficiency testing", "Quality assurance", "Quality control", "Medical terminology" ], "specialRequirements" : "Process slides timely", "qualificationsBasic" : "Associated Degree - Science, Clinical Lab Technologist License", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision following established policies, procedures, and professional guidelines, prepares high quality tissue specimens for microscopic examination and performs a wide variety of standard and non-standard histological tests and stains and a limited number of new, modified, or special tests and examinations. Required: Associated Degree - Science License/Registrations - Issued by Florida or Compact State Clinical Lab Technologist Work Experience and Additional Information Technical Knowledge, Skills, and Abilities Prepare and keep laboratory up to CLIA Standards. Knowledge of CLIA regulations regarding proficiency testing, quality assurance and quality control. Knowledge of medical terminology. Time Management Skills: able to process slides in a timely manner for surgeon/pathologist while patient is waiting. Tampa", "summaryDescription" : "Dermpath Laboratory Histologist. Skills: Tissue specimen preparation, Histology. Prepare tissue specimens. Perform histological tests", "createdAt" : "2026-06-14T02:56:30.840", "lastUpdated" : "2026-06-15T10:56:25.873", "ingestTimestamp" : "2026-06-14T02:56:30.840", "mongoId" : "6a0de91258b93c861eb99057", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 45000, "salaryAnnualMax" : 65000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Histological tests", "Histological stains", "Tissue specimen preparation", "Histology", "CLIA regulations", "Proficiency testing", "Quality assurance", "Quality control", "Medical terminology", "Issued by Florida or Compact State Clinical Lab Technologist" ], "skillCount" : 10, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.5555556, "_score" : 626.20404, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ad06e74d8ee00a07123d6", "title" : "Clinical Laboratory Supervisor", "company" : "Atrium Health", "industry" : "Healthcare", "salary" : { "min" : 41.1, "max" : 61.65, "currency" : "USD", "frequency" : "yearly" }, "location" : "Milledgeville, GA", "locations" : [ "Milledgeville, GA", "United States of America" ], "certifications" : [ "Medical Laboratory Scientist (MLS) certification", "Medical Technologist (MT) certification" ], "timestamp" : "2026-06-14T15:36:01.071", "fingerprint" : "00356410348a831828b4618bd78a4a16804fb0dcbf7e612ade913508ce49882b", "source" : "workday", "language" : "en", "applyUrl" : "https://aah.wd5.myworkdayjobs.com/External/job/Atrium-Health-Navicent-Baldwin---821-N-Cobb-St-Milledgeville-GA/Clinical-Lab-Supervisor_R220381", "externalId" : "R220381", "industryFunction" : { }, "locationPoint" : "41.96336,-89.77456", "structuredLocations" : [ { "city" : "Milledgeville", "state" : "Georgia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "33.0801429,-83.2320991" } ], "locationText" : "Milledgeville, Georgia, United States", "employmentType" : "FULL_TIME", "technicalSkills" : "Laboratory information systems", "professionalSkills" : [ "Project management", "Decision making", "Delegation", "Team building", "Customer service", "Conflict resolution", "Regulatory compliance", "Accrediting agency requirements", "Licensing agency requirements", "Test systems", "Test processes" ], "hardSkillsList" : [ "Clinical laboratory testing", "Proficiency testing", "Fiscal needs analysis", "Performance improvement", "Quality assurance", "Regulatory compliance", "Accreditation compliance", "Competency testing", "Corrective action implementation", "Performance management" ], "softSkillsList" : [ "Leadership", "Coaching", "Guidance", "Development planning", "Mentoring" ], "hardSkills" : [ { "name" : "Clinical laboratory testing", "level" : "intermediate" }, { "name" : "Proficiency testing", "level" : "intermediate" }, { "name" : "Fiscal needs analysis", "level" : "intermediate" }, { "name" : "Performance improvement", "level" : "intermediate" }, { "name" : "Quality assurance", "level" : "intermediate" }, { "name" : "Regulatory compliance", "level" : "intermediate" }, { "name" : "Accreditation compliance", "level" : "intermediate" }, { "name" : "Competency testing", "level" : "intermediate" }, { "name" : "Corrective action implementation", "level" : "intermediate" }, { "name" : "Performance management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Coaching" }, { "name" : "Guidance" }, { "name" : "Development planning" }, { "name" : "Mentoring" } ], "majorSkills" : "Laboratory operations, Team development, Quality management", "majorSkillsList" : [ "Laboratory operations", "Team development", "Quality management" ], "coreResponsibilities" : "Provide work direction, expertise, and guidance to staff, Oversee clinical laboratory testing, Oversee evaluation of results, Oversee proficiency of testing, Participate in projects to meet strategic initiatives, Implement quantitative outcomes, Monitor budget compliance, Analyze laboratory fiscal needs, Analyze departmental performance, Address fiscal variances, Collaborate on performance improvement processes, Implement performance improvement processes, Optimize teammate engagement, Optimize physician satisfaction, Optimize patient satisfaction, Ensure quality standards are met, Ensure regulatory standards are met, Ensure accreditation standards are met, Ensure competency standards are met, Ensure compliance with policies, Ensure compliance with procedures, Ensure compliance with standardization decisions, Coordinate orientation of staff, Coordinate training of staff, Coordinate competency testing of staff, Coordinate orientation of students, Coordinate training of students, Coordinate competency testing of students, Maintain competency in test systems, Maintain competency in test processes, Serve as technical resource for staff, Implement quality plan, Monitor quality indicators, Review laboratory results for quality, Review laboratory results for accuracy, Review laboratory results for validity, Document corrective action, Implement corrective action, Select team members, Coach team members, Develop team members, Set clear expectations, Inspire the team, Motivate the team, Manage performance, Recognize achievement, Provide feedback, Administer progressive discipline, Recommend hiring, Recommend compensation changes, Recommend promotions, Recommend corrective action decisions, Recommend terminations, Adhere to organization's Code of Ethical Conduct, Ensure compliance with policies, Ensure compliance with regulations, Ensure compliance with laws", "teamCollaboration" : "Site leaders collaboration; Cross-functional collaboration", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Clinical laboratory science; Medical technology; Laboratory information systems; Regulatory agency requirements; Accrediting agency requirements; Licensing agency requirements", "domainList" : [ "clinical-laboratory-science", "medical-technology", "laboratory-information-systems", "regulatory-agency-requirements", "accrediting-agency-requirements", "licensing-agency-requirements" ], "domainSpecificKnowledge" : [ "Clinical laboratory science", "Medical technology", "Laboratory information systems", "Regulatory agency requirements", "Accrediting agency requirements", "Licensing agency requirements" ], "communicationSkills" : "Communication skills", "continuousLearning" : "Career development programs; Educational Assistance Program", "innovationCreativity" : "Clinical innovation", "problemSolvingSkills" : "Decision making; Conflict resolution; Corrective action", "specialRequirements" : "Evening shift, Some overnight as necessary, Operates all equipment, Frequently lifts up to 10 lbs, Occasionally lifts up to 50 lbs, Sit, stand, walk, twist, bend, Exposure to infectious agents, Exposure to human blood, Exposure to body fluids, Wear safety protection, Handle stressful situations, May be required to travel", "outcomesObjectives" : "Achieve Advocate Health goals; Achieve Advocate Health objectives", "qualificationsBasic" : "3 years of experience in technical laboratory services and operations, Bachelor's Degree in Clinical Laboratory Sciences or Medical Technology or equivalent, Medical Laboratory Scientist (MLS) certification issued by the American Society for Clinical Pathology Board of Certification (ASCP BOC), Medical Technologist (MT) certification issued by the American Society for Clinical Pathology (ASCP) or equivalent accrediting agency", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Department:** 60901 Navicent Health Medical Center: Baldwin - Lab **Status:** Full time **Benefits Eligible:** Yes **Hou****rs Per Week:** 40 **Schedule Details/Additional Information:** Monday - Friday (no weekends or holidays) Evening shift - 1p - 1030p - some overnight as necessary **Pay Range** $41.10 - $61.65 \"This position is Sign-on Bonus eligible.\" Based on eligibility requirements. **Job Summary:** Responsible for laboratory operations in the technical area(s) of the Hospitals and Clinics within the Advocate Health enterprise, which may include department, discipline and/or shift oversight. Supervises the implementation of enterprise laboratory strategies and standards through close collaboration with site leaders. Ensures peak laboratory operations by driving optimization of resources, financial performance, growth, safety, teammate engagement, and quality in achieving Advocate Health goals and objectives including planning, monitoring, and implementing laboratory operations in a cost effective, quality and service-oriented manner. **Major Responsibilities:** * Assumes responsibility for the day-to-day operations of the department including providing work direction, expertise, and guidance to the staff. Oversees the clinical laboratory testing, evaluation of results, and the proficiency of testing. * Actively participates in projects to meet strategic initiatives including implementation and development of quantitative outcomes. * Monitors budget compliance. Analyzes laboratory fiscal needs, and departmental performance and takes action to address variances. * Collaborates and implements performance improvement processes to optimize teammate engagement, and physician and patient satisfaction. * Ensures quality, regulatory, accreditation, compliance and competency standards are met. Ensures compliance with current policies, procedures, and standardization and/or consolidation decisions. * Coordinates orientation, training, and competency testing of staff and/or students. Maintains competency, as needed, in test systems and processes in defined discipline for area of responsibility. Serves as a technical resource for staff. * Complies with the quality plan by implementing and monitoring quality indicators. Reviews laboratory results for quality, accuracy and validity. Documents and implements corrective action as appropriate. * Selects, coaches, and develops team. Sets clear expectations to inspire and motivate the team. Manages performance by recognizing achievement, providing feedback, and administering progressive discipline when necessary. Recommends hiring, compensation changes, promotions, corrective action decisions, and terminations. * Responsible for understanding and adhering to the organization's Code of Ethical Conduct and for ensuring that people actions, and the actions of employees supervised, comply with the policies, regulations, and laws applicable to the organization's business. **Licensure, Registration, and/or Certification Required:** * Medical Laboratory Scientist (MLS) certification issued by the American Society for Clinical Pathology Board of Certification (ASCP (American Society for Clinical Pathology) BOC), or * Medical Technologist (MT) certification issued by the American Society for Clinical Pathology (ASCP) or equivalent accrediting agency. **Education Required:** * Bachelor's Degree in Clinical Laboratory Sciences or Medical Technology or equivalent **Experience Required:** * Typically requires 3 years of experience in technical laboratory services and operations. **Knowledge, Skills & Abilities Required:** * Demonstrated leadership skills including project management, decision making, delegation, team building, customer service, and conflict resolution. * Ability to grow leaders through coaching, guidance, and development planning. * Advanced knowledge of regulatory compliance, accrediting and licensing agency requirements. * Current knowledge of medical and technical advancements to plan for future growth and development. * Intermediate computer skills including knowledge and experience with laboratory information systems. * Excellent organization and communication skills. **Physical Requirements and Working Conditions:** * Operates all equipment necessary to perform the job. * Frequently lifts up to 10 lbs. Occasionally lifts up to 50 lbs. * Must be able to sit, stand, walk, twist and bend the majority of the workday. * May be exposed to mechanical, electrical, and/or infectious agents. * Will be exposed to human blood and body fluids. * Must wear appropriate safety protection, i.e. laboratory coats, gloves, gowns and/or eye protection. * Must be able to handle stressful situations in a calm and professional manner. * May be required to travel, therefore may be exposed to inclement weather and adverse road conditions. _This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the incumbent. Incumbent may be required to perform other related duties._ **Our Commitment to You:** Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including: **Compensation** * Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training * Premium pay such as shift, on call, and more based on a teammate's job * Incentive pay for select positions * Opportunity for annual increases based on performance **Benefits and more** * Paid Time Off programs * Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability * Flexible Spending Accounts for eligible health care and dependent care expenses * Family benefits such as adoption assistance and paid parental leave * Defined contribution retirement plans with employer match and other financial wellness programs * Educational Assistance Program Note: Eligibility for programs listed above may depend on your FTE or status (e.g., full-time, part-time, per diem, temporary, etc.); please ask a Recruiter for more information during an interview. **About Advocate Health** [Advocate Health](https://www.advocatehealth.org/) is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names [Advocate Health Care](https://www.advocatehealth.com/) in Illinois; [Atrium Health](https://atriumhealth.org/) in the Carolinas, Georgia and Alabama; and [Aurora Health Care](https://www.aurorahealthcare.org/) in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with [Wake Forest University School of Medicine](https://school.wakehealth.edu/) serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation’s largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.", "summaryDescription" : "Clinical Laboratory Supervisor at Atrium Health. Skills: Laboratory operations, Team development, Quality management. Provide work direction, expertise, and guidance to staff. 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Interacting with healthcare professionals", "domainKnowledge" : "Hematology; Chemistry; Serology; Urine analysis; Feces analysis; Body fluid analysis", "domainList" : [ "hematology", "chemistry", "serology", "urine-analysis", "feces-analysis", "body-fluid-analysis" ], "domainSpecificKnowledge" : [ "Hematology", "Chemistry", "Serology", "Urine analysis", "Feces analysis", "Body fluid analysis" ], "documentationSkills" : "Documenting for targets", "continuousLearning" : "Attending training", "problemSolvingSkills" : "Troubleshoot technical issues", "outcomesObjectives" : "Support achievement of hospital indicators; Support department targets; Support unit targets", "qualificationsBasic" : "Vocational High School Graduate, Health Analyst certification, Perform laboratory tests, Operate laboratory equipment, Analyze test results, Troubleshoot technical issues, Effective communication skills", "qualificationsPreferred" : "Experience in clinical laboratory, Experience in hospital laboratory", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "•Carrying out laboratory examinations related to hematology, chemistry, serology, urine, feces and body fluids in accordance with predetermined procedures and service standards to be used to support a doctor's diagnosis •Carrying out hematology, chemistry, serology, urine, feces and body fluid examinations in accordance with predetermined SOPs and carrying out data entry into the system used to ensure the availability of complete and timely examination data •Carry out data entry and data release of hematology, chemistry, serology, urine, feces and body fluid examination results according to needs and requests, either using a computer or manually to ensure the availability of complete and timely examination data •Prioritize reporting of CITO, CCU examination results and examination results related to the patient's critical condition so that they can be conveyed as quickly as possible to the doctor or nurse •Record usage and make requests for equipment, carry out preventive maintenance activities to maintain availability, cleanliness and maintenance of equipment used in hematology, chemistry, serology, urine, feces and body fluid examination services •Record and organize the storage of hematology, chemistry, serology, urine, feces and body fluid examination results to maintain the completeness and availability of examination results according to the needs of doctors and patients •Record and organize the procurement/receipt/use of hematology, chemistry, serology, urine, feces and body fluid examination reagents to ensure the smoothness and continuity of related services •Collect required data and/or make reports related to operational activities as a responsibility to superiors •Implement procedures and practices for quality and safety services, including attending training, collecting data, documenting and/or making reports needed to support the achievement of hospital wide indicators and related department/unit targets •Minimum Vocational High School Graduate from Health Analyst •Health Analyst •Experience in a clinical or hospital laboratory setting is preferred. •Proficiency in performing laboratory tests and operating laboratory equipment. •Ability to analyze test results and troubleshoot technical issues. •Effective communication skills for interacting with patients and healthcare professionals. ## Qualifications •Minimum Vocational High School Graduate from Health Analyst •Experience in a clinical or hospital laboratory setting is preferred. •Proficiency in performing laboratory tests and operating laboratory equipment. •Ability to analyze test results and troubleshoot technical issues. •Effective communication skills for interacting with patients and healthcare professionals. ## Additional Information [HATI-HATI PADA PENIPUAN] Siloam Hospitals Group kembali mengingatkan untuk tetap berwaspada pada modus penipuan yang mengatasnamakan Siloam! Siloam tidak pernah memungut biaya apapun maupun bekerjasama dengan agen perjalanan dalam proses rekrutmen.", "summaryDescription" : "Laboratory Technician at Siloam Hospitals Group. Skills: Laboratory examinations, Data entry, Equipment maintenance. Carry out laboratory examinations. 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Chemistry; Serology; Urine analysis; Feces analysis; Body fluid analysis", "domainList" : [ "hematology", "chemistry", "serology", "urine-analysis", "feces-analysis", "body-fluid-analysis" ], "domainSpecificKnowledge" : [ "Hematology", "Chemistry", "Serology", "Urine analysis", "Feces analysis", "Body fluid analysis" ], "communicationSkills" : "Interacting with patients; Interacting with healthcare professionals", "documentationSkills" : "Documenting reports", "continuousLearning" : "Attending training", "problemSolvingSkills" : "Analyze test results; Troubleshoot technical issues", "qualificationsBasic" : "Vocational High School Graduate from Health Analyst", "qualificationsPreferred" : "Experience in clinical or hospital laboratory setting, Proficiency in performing laboratory tests, Proficiency in operating laboratory equipment, Ability to analyze test results, Ability to troubleshoot technical issues, Effective communication skills for interacting with patients, Effective communication skills for interacting with healthcare professionals", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "•Carrying out laboratory examinations related to hematology, chemistry, serology, urine, feces and body fluids in accordance with predetermined procedures and service standards to be used to support a doctor's diagnosis •Carrying out hematology, chemistry, serology, urine, feces and body fluid examinations in accordance with predetermined SOPs and carrying out data entry into the system used to ensure the availability of complete and timely examination data •Carry out data entry and data release of hematology, chemistry, serology, urine, feces and body fluid examination results according to needs and requests, either using a computer or manually to ensure the availability of complete and timely examination data •Prioritize reporting of CITO, CCU examination results and examination results related to the patient's critical condition so that they can be conveyed as quickly as possible to the doctor or nurse •Record usage and make requests for equipment, carry out preventive maintenance activities to maintain availability, cleanliness and maintenance of equipment used in hematology, chemistry, serology, urine, feces and body fluid examination services •Record and organize the storage of hematology, chemistry, serology, urine, feces and body fluid examination results to maintain the completeness and availability of examination results according to the needs of doctors and patients •Record and organize the procurement/receipt/use of hematology, chemistry, serology, urine, feces and body fluid examination reagents to ensure the smoothness and continuity of related services •Collect required data and/or make reports related to operational activities as a responsibility to superiors •Implement procedures and practices for quality and safety services, including attending training, collecting data, documenting and/or making reports needed to support the achievement of hospital wide indicators and related department/unit targets •Minimum Vocational High School Graduate from Health Analyst •Health Analyst •Experience in a clinical or hospital laboratory setting is preferred. •Proficiency in performing laboratory tests and operating laboratory equipment. •Ability to analyze test results and troubleshoot technical issues. •Effective communication skills for interacting with patients and healthcare professionals. ## Qualifications •Minimum Vocational High School Graduate from Health Analyst •Experience in a clinical or hospital laboratory setting is preferred. •Proficiency in performing laboratory tests and operating laboratory equipment. •Ability to analyze test results and troubleshoot technical issues. •Effective communication skills for interacting with patients and healthcare professionals. ## Additional Information [HATI-HATI PADA PENIPUAN] Siloam Hospitals Group kembali mengingatkan untuk tetap berwaspada pada modus penipuan yang mengatasnamakan Siloam! 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Carry out hematology examinations", "postedDate" : "2026-06-10T07:27:04.000", "createdAt" : "2026-06-12T03:33:06.094", "lastUpdated" : "2026-06-14T23:30:44.992", "ingestTimestamp" : "2026-06-12T03:33:06.094", "mongoId" : "6a2a4a1b74d8ee00a05e7764", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Laboratory examinations", "Hematology", "Chemistry", "Serology", "Urine analysis", "Feces analysis", "Body fluid analysis", "Data entry", "Data release", "Equipment maintenance", "Reagent procurement", "Health Analyst" ], "skillCount" : 12, "jobCategory" : "other", "jobSubcategory" : "Medical", "dataQualityScore" : 1.0, "_score" : 618.65173, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2ad06e74d8ee00a071240d", "title" : "Laboratory Assistant PRN", "company" : "Advocate Health", "industry" : "Healthcare", "salary" : { "min" : 19.8, "max" : 29.7, "currency" : "USD", "frequency" : "yearly" }, "location" : "Macon, GA", "locations" : [ "Macon, GA", "United States of America" ], "certifications" : [ "None required" ], "timestamp" : "2026-06-14T22:21:35.593", "fingerprint" : "3b1df50966737a8025095be8cdf1b54c6412486f6f1006f5c4f8b9fb0e4c9b71", "source" : "workday", "language" : "en", "applyUrl" : "https://aah.wd5.myworkdayjobs.com/External/job/Atrium-Health-Navicent-The-Medical-Center---777-Hemlock-St-Macon-GA/Laboratory-Assistant-PRN_R243599", "externalId" : "R243599", "industryFunction" : { }, "locationPoint" : "50.05072,4.20918", "structuredLocations" : [ { "city" : "Macon", "state" : "Georgia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.8406946,-83.6324022" } ], "locationText" : "Macon, Georgia, United States", "employmentType" : "PART_TIME", "minimumEducation" : "High School", "professionalSkills" : [ "Data entry", "Order entry", "Client support" ], "hardSkillsList" : [ "Patient data retrieval", "Specimen processing", "Specimen labeling" ], "hardSkills" : [ { "name" : "Patient data retrieval", "level" : "intermediate" }, { "name" : "Specimen processing", "level" : "intermediate" }, { "name" : "Specimen labeling", "level" : "intermediate" } ], "majorSkills" : "Data entry, Specimen processing, Client service", "majorSkillsList" : [ "Data entry", "Specimen processing", "Client service" ], "coreResponsibilities" : "Operate laboratory and hospital information system, Enter patient demographic data, Enter laboratory test orders, Process outpatient lab specimens, Order tests accurately, Label specimens for testing, Retrieve patient data and results, Operate remote printers and fax, Retrieve archived patient data, Adhere to HIPAA standards, Provide client service, Call stat results to clients, Document client calls and callbacks, Answer and transfer calls, Utilize telephone call queue system, Enter information into client call database, Use computer system for interdepartmental email, Track specimens, Utilize web based orders, Retrieve results, Scan and index lab requisitions, Inform couriers of specimen pickups, Assist with local specimen pickups, Follow universal safety precaution standards, Follow patient safety policies, Provide support for all lab departments, Retrieve information, Assist as needed", "teamCollaboration" : "Partnership with Patient Registration", "domainKnowledge" : "HIPAA standards", "domainList" : [ "hipaa-standards" ], "domainSpecificKnowledge" : [ "HIPAA standards" ], "toolProficiency" : [ "Laboratory information system", "Hospital information system", "Optical disk" ], "communicationSkills" : "Call stat results; Document client calls", "documentationSkills" : "Document client calls", "specialRequirements" : "Weekend Rotation, Holiday Rotation, Use visual acuity, Hear and verbally communicate, Sit for prolonged periods, Functional range of motion, Grip strength 50-60#, Forward reach, Overhead reach, Bend, squat, kneel, Apply proper body mechanics, Lift up to 10#", "outcomesObjectives" : "Ensure quality results reported timely", "qualificationsBasic" : "High School or GED Diploma Graduate", "qualificationsPreferred" : "Previous lab experience, Medical terminology or knowledge, Customer service data entry and computer skills, Phlebotomy skills a plus", "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Department:** 60916 Navicent Health Medical Center - Lab: Reference Lab Testing **Status:** Part time **Benefits Eligible:** No **Hou****rs Per Week:** 0 **Schedule Details/Additional Information:** * Various Shift: Hours 8:00 am to 10:00 pm (Monday-Friday) * (Weekend Rotation—Sat & Sun) 8:00 am to 5:00 pm every six weeks * (Holiday Rotation) 8:00 am to 5:00 pm every six months **Pay Range** $19.80 - $29.70 **Job Summary:** Performs data entry of patient information and laboratory test orders on outpatient laboratory specimens to ensure quality results are reported timely to the clients of Clinical Laboratory and Central Georgia Diagnostics Reference Laboratory Services. Provides client support for physicians and staff as needed. **Major Responsibilities:** * Operates laboratory and hospital information system for entry and retrieval of patient demographic data and order entry. Works in partnership with Patient Registration department to ensure data is obtained and entered into system. * Processes outpatient lab specimens, accurately orders tests and labels specimens for testing in the clinical lab. * Retrieves patient data and results for clients and physicians. Operates remote printers and fax to deliver information as requested. Retrieves archived patient data from optical disk. Adheres to HIPAA standards at all times to ensure patient confidentiality. * Provides client service with customer oriented focus for clients and physicians concerning clinical data. Calls stat results to clients and physicians. Documents client calls and callbacks in computer. * Answers and transfers calls for Clinical Laboratory and Reference Laboratory. Utilizes appropriate login process for telephone call queue system. Enters appropriate information into client call database for add-on tests, recollects, and follow up issues. * Uses computer system for interdepartmental email, to track specimens, utilize web based orders and retrieve results, and scan and index lab requisitions. * Informs couriers of specimen pickups from clients. Assists with local specimen pickups when regular couriers are not available. * Follows universal safety precaution standards and patient safety policies at all times. * Provides support for all lab departments, retrieves information and assists as needed. **Licensure, Registration, and/or Certification Required:** None required **Education Required:** Must be a High School or GED Diploma Graduate. **Experience preferred:** Previous lab experience **Knowledge, Skills & Abilities preferred:** Medical terminology or knowledge Customer service Strong data entry and computer skills Phlebotomy skills a plus **Physical Requirements and Working Conditions:** Must be able to use visual acuity to see monitor screen, computer and hard copy materials. Must be able to hear and verbally communicate in person and over the phone or radio. Must be able to sit for prolonged periods of time (up to 2 hours). Must be able to comprehend and learn operation of various office equipment. Must have functional range of motion of the cervical, thoracic and lumbar spines, upper and lower extremities with a grip strength of 50-60# specific to job evaluation. Must be able to forward reach, overhead reach, bend, squat, kneel and apply proper body mechanics during the transfers and transport supplies and/or equipment using proper body mechanics. Must be able to lift up to 10# specific to job evaluation. _This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the incumbent. Incumbent may be required to perform other related duties._ **Our Commitment to You:** Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including: **Compensation** * Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training * Premium pay such as shift, on call, and more based on a teammate's job * Incentive pay for select positions * Opportunity for annual increases based on performance **Benefits and more** * Paid Time Off programs * Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability * Flexible Spending Accounts for eligible health care and dependent care expenses * Family benefits such as adoption assistance and paid parental leave * Defined contribution retirement plans with employer match and other financial wellness programs * Educational Assistance Program Note: Eligibility for programs listed above may depend on your FTE or status (e.g., full-time, part-time, per diem, temporary, etc.); please ask a Recruiter for more information during an interview. **About Advocate Health** [Advocate Health](https://www.advocatehealth.org/) is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names [Advocate Health Care](https://www.advocatehealth.com/) in Illinois; [Atrium Health](https://atriumhealth.org/) in the Carolinas, Georgia and Alabama; and [Aurora Health Care](https://www.aurorahealthcare.org/) in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with [Wake Forest University School of Medicine](https://school.wakehealth.edu/) serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation’s largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.", "summaryDescription" : "Laboratory Assistant PRN at Advocate Health. Skills: Data entry, Specimen processing, Client service. Operate laboratory and hospital information system. Enter patient demographic data", "postedDate" : "2026-06-11T02:29:09.090", "createdAt" : "2026-06-12T02:29:09.064", "lastUpdated" : "2026-06-14T22:21:35.593", "ingestTimestamp" : "2026-06-12T02:29:09.064", "mongoId" : "6a2ad06e74d8ee00a071240d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://aah.wd5.myworkdayjobs.com/External/job/Atrium-Health-Navicent-The-Medical-Center---777-Hemlock-St-Macon-GA/Laboratory-Assistant-PRN_R243599", "salaryAnnualMin" : 41184, "salaryAnnualMax" : 61776, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Patient data retrieval", "Specimen processing", "Specimen labeling", "Data entry", "Client service", "Order entry", "Client support", "HIPAA standards", "None required", "Laboratory information system", "Hospital information system", "Optical disk" ], "skillCount" : 12, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 612.81036, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2a528e74d8ee00a05faf79", "title" : "Analytical Laboratory Technician", "company" : "Redwood Materials", "salary" : { "min" : 48500.0, "max" : 68500.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Analytical Laboratory Technician in McCarran, United States, adjusted for company size and industry." }, "location" : "McCarran, NV", "locations" : [ "McCarran", "NV" ], "timestamp" : "2026-06-14T20:17:56.443", "fingerprint" : "7e1a9ad834e1b0443d8a1dc989bef1b491a68876e972d0dd95fa8de94ab4805f", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://boards.greenhouse.io/redwoodmaterials/jobs/6016953004?gh_jid=6016953004", "externalId" : "6016953004", "structuredLocations" : [ { "city" : "McCarran", "state" : "Nevada", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "36.0861034,-115.1611002" } ], "locationText" : "McCarran, Nevada, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "technicalSkills" : "ICP-OES, Auto-titration, X-Ray Fluorescence, Total Organic Carbon, Microsoft Office", "professionalSkills" : [ "Chemical analysis", "Metrological analysis", "Metallurgical analysis", "Data entry", "Data management", "Laboratory organization", "Inventory management", "Safety audits" ], "hardSkillsList" : [ "Chemistry math", "Calculations" ], "hardSkills" : [ { "name" : "Chemistry math", "level" : "intermediate" }, { "name" : "Calculations", "level" : "intermediate" } ], "majorSkills" : "Laboratory analysis, Sample preparation, Instrumentation maintenance", "majorSkillsList" : [ "Laboratory analysis", "Sample preparation", "Instrumentation maintenance" ], "coreResponsibilities" : "Prepare samples for analysis, Perform routine chemical analysis, Perform routine laboratory analytical tasks, Execute laboratory procedures, Handle samples accurately, Enter data accurately, Operate basic instruments, Adhere to safety standards, Adhere to documentation standards, Maintain laboratory instrumentation, Maintain laboratory equipment, Troubleshoot instrumentation, Perform instrument verifications, Sample and test physical characteristics, Organize laboratory, Manage inventory, Conduct safety audits, Perform special projects", "teamCollaboration" : "Team environments; Individual environments", "domainKnowledge" : "Battery supply chain; Energy transition; Battery materials; Chemical safety; Laboratory safety", "domainList" : [ "battery-supply-chain", "energy-transition", "battery-materials", "chemical-safety", "laboratory-safety" ], "domainSpecificKnowledge" : [ "Battery supply chain", "Energy transition", "Battery materials", "Chemical safety", "Laboratory safety" ], "toolProficiency" : [ "Microsoft Office" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Good documentation practices", "problemSolvingSkills" : "Troubleshooting", "specialRequirements" : "Comfortable wearing PPE, Wear respirators, Use step ladder, Sit for long periods, Stand for long periods", "qualificationsBasic" : "2+ years related experience, Laboratory settings experience, Quality settings experience, Chemical production facilities experience, Waste handling experience, Safe work practices experience, Data entry and management experience, Good documentation practices experience, Experimental setup and execution experience, Perform basic chemistry math, Perform calculations, Regularly lift 35 lbs", "qualificationsPreferred" : "ICP-OES experience, Auto-titration experience, X-Ray Fluorescence experience, Total Organic Carbon experience, Sample prep experience, Analysis experience, Chemical handling experience, Laboratory hazards experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "About Redwood Materials Redwood is localizing a global battery supply chain that seamlessly integrates recovery, reuse, and recycling — keeping critical minerals in circulation and driving the energy transition. Founded in 2017, we’re delivering low-cost and large-scale energy storage and producing battery materials in the U. S. for the first time, all from batteries we already have. Analytical Laboratory Technician The Analytical Lab Technician performs routine chemical and laboratory analytical tasks in support of production quality and safety at Redwood Materials facilities. Working under supervision for all assigned tasks, this role is responsible for executing established laboratory procedures per written SOPs and TCMs, accurate sample handling and data entry, basic instrument operation, and adherence to all chemical safety and documentation standards. This role develops foundational proficiency in analytical methods, laboratory information systems, and lab safety while building toward independent operation. Responsibilities will include: Prepares samples for analysis using established tests and techniques. Assists with and performs routine chemical, metrological, and/or metallurgical analysis and reporting. Maintains laboratory instrumentation and equipment, including troubleshooting and performing verifications. Works in a production environment, sampling and testing physical characteristics. Performs additional duties as required, including lab organization, inventory, safety audits, and special projects. Works effectively in both team and individual environments. Desired Qualifications: Bachelor’s degree in science or related field or 2+ years of related experience.  Experience in laboratory settings, quality settings, or chemical production facilities.   Experience in typical laboratory practices including waste handling, safe work practices, data entry and management, good documentation practices and experimental setup and execution.  Comfortable wearing personal protective equipment including but not limited to lab coats and respirators.  Experience with relevant test methods such as ICP-OES, auto-titration, X-Ray Fluorescence, Total Organic Carbon, etc.   Experience with sample prep and analysis, chemical handling and laboratory hazards.  Demonstrates ability to perform basic chemistry math and calculations.  Adept with data acquisition and analysis tools including Laboratory Information Management Systems and Microsoft Office.  Excellent written, verbal communication, and collaboration skills  Excellent attitude: understands priorities change with company needs and willing to work to ensure deadlines are met. Ability to execute with a calm and collaborative urgency.  Ability to regularly lift 35 lbs.  Use of a step ladder   Sit and or stand for long periods of time, greater than 2 hours  A passion for sustainability and making the world a better place!  The position is full-time. Compensation will be commensurate with experience. We collect personal information (PI) from you in connection with your application for employment with Redwood Materials, including the following categories of PI: identifiers, personal records, professional or employment information, and inferences drawn from your PI. We collect your PI for our purposes, including performing services and operations related to your potential employment. If you have additional privacy-related questions, please contact us at privacy@redwoodmaterials.com.", "summaryDescription" : "Analytical Laboratory Technician at Redwood Materials. Skills: Laboratory analysis, Sample preparation, Instrumentation maintenance. Prepare samples for analysis. Perform routine chemical analysis", "postedDate" : "2026-06-11T19:06:50.172", "createdAt" : "2026-06-11T19:06:50.172", "lastUpdated" : "2026-06-14T20:17:56.443", "ingestTimestamp" : "2026-06-11T19:06:50.172", "mongoId" : "6a2a528e74d8ee00a05faf79", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 48500, "salaryAnnualMax" : 68500, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Chemistry math", "Calculations", "Laboratory analysis", "Sample preparation", "Instrumentation maintenance", "Chemical analysis", "Metrological analysis", "Metallurgical analysis", "Data entry", "Data management", "Laboratory organization", "Inventory management", "Safety audits", "Battery supply chain", "Energy transition", "Battery materials", "Chemical safety", "Laboratory safety", "Microsoft Office" ], "skillCount" : 19, "jobCategory" : "engineering", "jobSubcategory" : "engineering-&-technology", "dataQualityScore" : 0.8888889, "_score" : 611.15845, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2a8bb974d8ee00a0683a52", "title" : "Laboratory Engineer II", "company" : "University of Rochester", "salary" : { "min" : 60431.0, "max" : 84603.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-13T06:42:33.262", "fingerprint" : "d09eca9b572df30e52aa9a27d2a87a2c1ebd140dcd7af32611569c47e32adc67", "source" : "workday", "language" : "en", "applyUrl" : "https://rochester.wd5.myworkdayjobs.com/UR_Staff/job/Laboratory-for-Laser-Energetics/Laboratory-Engineer-II_R272093", "externalId" : "R272093", "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Rochester", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.1572850,-77.6152140" } ], "locationText" : "Rochester, New York, United States", "employmentType" : "FULL_TIME", "technicalSkills" : "MATLAB, Python, Excel", "professionalSkills" : [ "Technical evaluation", "System performance evaluation", "Laser development" ], "hardSkillsList" : [ "Data analysis", "Technical data processing", "Test planning", "Documentation" ], "softSkillsList" : [ "Adaptability", "Attention to detail", "Organizational skills" ], "hardSkills" : [ { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Technical data processing", "level" : "intermediate" }, { "name" : "Test planning", "level" : "intermediate" }, { "name" : "Documentation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Adaptability" }, { "name" : "Attention to detail" }, { "name" : "Organizational skills" } ], "majorSkills" : "Laser system operation, Data analysis, Laboratory testing", "majorSkillsList" : [ "Laser system operation", "Data analysis", "Laboratory testing" ], "coreResponsibilities" : "Operate FLUX laser system, Perform engineering analysis, Support laser development, Evaluate system performance, Ensure system safety, Collect technical data, Process technical data, Interpret technical data, Identify trends, Identify anomalies, Identify performance improvements, Conduct laboratory testing, Conduct field-testing, Support validation activities, Support verification activities, Develop standard operating procedures, Maintain standard operating procedures, Develop test plans, Maintain test plans, Support laser upgrade projects, Support software development", "teamCollaboration" : "Collaborate with scientists; Collaborate with engineers; Collaborate with technicians; Cross-functional teams", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Laser systems; FLUX laser system", "domainList" : [ "laser-systems", "flux-laser-system" ], "domainSpecificKnowledge" : [ "Laser systems", "FLUX laser system" ], "toolProficiency" : [ "Oscilloscopes", "Diagnostic tools" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Documentation", "problemSolvingSkills" : "Analytical skills; Problem-solving skills", "specialRequirements" : "Work shift assignments, Evening hours", "outcomesObjectives" : "Identify trends; Identify anomalies; Identify performance improvements", "qualificationsBasic" : "Bachelor’s degree in STEM field, 2 years of relevant experience", "qualificationsPreferred" : "Hands-on experience using oscilloscopes, Experience with data analysis tools, Prior experience in a laboratory or manufacturing environment", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive. _**Job Location (Full Address):**_ 250 East River Rd, Rochester, New York, United States of America, 14623 _**Opening:**_ Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 250548 LLE-Laboratory for Laser Energ Work Shift: UR - Day (United States of America) Range: UR URG 110 Compensation Range: $60,431.00 - $84,603.00 _The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job 's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._ _**Responsibilities:**_ LE is seeking a detail-oriented and analytical engineer to support FLUX operations through data-driven analysis, technical evaluation, and hands-on operation and testing. This role is ideal for a candidate with a strong STEM background who enjoys problem-solving, working with technical equipment, and collaborating across engineering teams. The successful candidate must be willing to work shift assignments 1–2 times per week, including evening hours, to support operational needs and testing schedules. **ESSENTIAL FUNCTIONS** * Complete qualification and stand watch in operation of the FLUX laser system * Perform engineering analysis to support laser development, system performance evaluation, operational activities and ensure system safety * Collect, process, and interpret technical data to identify trends, anomalies, and performance improvements * Conduct laboratory and field-testing using equipment such as oscilloscopes and other diagnostic tools * Support validation and verification activities through structured test planning and documentation * Develop and maintain standard operating procedures and test plans to provide clear direction for technicians and operators * Collaborate with cross-functional teams including scientists, engineers, and technicians * Support laser upgrade projects and software development. Will have responsibility over minor aspects under the direction of a project manager. **MINIMUM EDUCATION & EXPERIENCE** * Bachelor’s degree in STEM field and 2 years of relevant experience required * Hands-on experience using oscilloscopes and electronic test equipment preferred * Experience with data analysis tools (e.g., MATLAB, Python, Excel, or similar platforms) preferred * Prior experience in a laboratory or manufacturing environment preferred **KNOWLEDGE, SKILLS AND ABILITIES** * Strong analytical and problem-solving skills required * Ability to interpret technical drawings and schematics required * Willingness and ability to work evening shifts up to 2 times per week required * Strong written and verbal communication skills required * Attention to detail * Strong organizational skills * Ability to work independently and in a team environment * Adaptability to shifting priorities and schedules The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.", "summaryDescription" : "Laboratory Engineer II at University of Rochester. Skills: Laser system operation, Data analysis, Laboratory testing. Operate FLUX laser system. Perform engineering analysis", "postedDate" : "2026-06-10T19:48:44.471", "createdAt" : "2026-06-11T19:48:44.286", "lastUpdated" : "2026-06-13T06:42:33.262", "ingestTimestamp" : "2026-06-11T19:48:44.286", "mongoId" : "6a2a8bb974d8ee00a0683a52", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://rochester.wd5.myworkdayjobs.com/UR_Staff/job/Laboratory-for-Laser-Energetics/Laboratory-Engineer-II_R272093", "salaryAnnualMin" : 60431, "salaryAnnualMax" : 84603, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Data analysis", "Technical data processing", "Test planning", "Documentation", "Adaptability", "Attention to detail", "Organizational skills", "Laser system operation", "Laboratory testing", "Technical evaluation", "System performance evaluation", "Laser development", "Project management", "Laser systems", "FLUX laser system", "Oscilloscopes", "Diagnostic tools" ], "skillCount" : 17, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 610.7892, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2c7a7a74d8ee00a09459bd", "title" : "Laboratory Specialist (Part-Time)", "company" : "DLH", "industry" : "Healthcare", "salary" : { "min" : 35000.0, "max" : 55000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on 2024-2025 market data for a Part-Time Laboratory Specialist in Atlanta, United States, with 3-5 years of experience and mid-level seniority within the Healthcare industry." }, "location" : "Atlanta, Georgia", "locations" : [ "Atlanta", "Georgia" ], "timestamp" : "2026-06-15T03:46:14.219", "fingerprint" : "300a01665bcf45f5b5562ef08735d59e1632aa51f09d0b4c64deb7fce93a4e8b", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/dlhcorporation/jobs/5162308007", "externalId" : "5162308007", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Atlanta", "state" : "Georgia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "33.7544657,-84.3898151" } ], "locationText" : "Atlanta, Georgia, United States", "employmentType" : "PART_TIME", "minimumEducation" : "High School", "experienceMinYears" : 3, "experienceMaxYears" : 5, "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "LC-MS/MS testing", "Quantitative assays", "Qualitative assays" ], "hardSkills" : [ { "name" : "LC-MS/MS testing", "level" : "intermediate" }, { "name" : "Quantitative assays", "level" : "intermediate" }, { "name" : "Qualitative assays", "level" : "intermediate" } ], "majorSkills" : "Quality Management System, ISO implementation, Laboratory practices", "majorSkillsList" : [ "Quality Management System", "ISO implementation", "Laboratory practices" ], "coreResponsibilities" : "Maintain QMS knowledge, Organize hardcopy files, Organize electronic files, Support SOP revision, Prepare quality reports, Prepare progress reports, Prepare equipment reports, Write QMS documents, Communicate QMS requirements, Conduct quality reviews", "teamCollaboration" : "Cross-functional teams; Stakeholder management", "domainKnowledge" : "Clinical laboratory practices; Laboratory accreditation; Quality management systems; ISO implementation; CLSI; CAP; ISO; Antiretroviral drugs; Antimicrobial drugs", "domainList" : [ "clinical-laboratory-practices", "laboratory-accreditation", "quality-management-systems", "iso-implementation", "clsi", "cap", "iso", "antiretroviral-drugs", "antimicrobial-drugs" ], "domainSpecificKnowledge" : [ "Clinical laboratory practices", "Laboratory accreditation", "Quality management systems", "ISO implementation", "CLSI", "CAP", "ISO", "Antiretroviral drugs", "Antimicrobial drugs" ], "communicationSkills" : "Write documents; Communicate requirements", "documentationSkills" : "SOPs; QA/QC manuals; QMS documents", "specialRequirements" : "NAC clearance", "qualificationsBasic" : "Bachelor's in laboratory science, 3-5 years clinical experience, High school diploma, 6 years laboratory experience, Laboratory regulatory skills, Quality management systems, Obtain NAC clearance", "qualificationsPreferred" : "CLIA lab experience, Clinical labo", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "About Us DLH delivers improved health and national security readiness solutions for federal programs through science research and development, systems engineering and integration, and digital transformation. Our experts in public health, performance evaluation, and health operations solve the complex problems faced by civilian and military customers alike by leveraging advanced tools – including digital transformation, artificial intelligence, data analytics, cloud enablement, modeling, and simulation, and more. With over 2,400 employees dedicated to the idea that “Your Mission is Our Passion,” DLH brings a unique combination of government sector experience, proven methodology, and unwavering commitment to innovation to improve the lives of millions. Overview DLH is looking for a part-time Laboratory Specialist to join our talented and innovative team supporting the Centers for Disease Control and Prevention’s (CDC) Division of HIV Prevention (DHP) in Atlanta, GA. This part-time position will be onsite at a CDC laboratory for 24 hours per week, the days are flexible. Core hours are 9:30-11:30 and also 1-3 p. m. The DHP Laboratory Branch (LB) supports DHP goals to reduce new HIV infections through supporting clinical studies, surveillance and implementation research. The LB conducts liquid chromatography tandem mass spectrometry (LC-MS/MS) testing of biological specimens to detect and quantitate antiretroviral and antimicrobial drugs using quantitative and qualitative assays to provide objective measures of drug use for HIV treatment and prevention. In addition, the clinical and research laboratories must follow and comply with safety and quality management systems (QMS), programs, regulatory guidelines, and standards. To conduct these activities, DHP LB needs laboratory assistants’ support. Responsibilities Maintain knowledge of status, issues, training, and progress related to the Quality Management System (QMS) and ISO implementation and maintenance. Organize and store hardcopy and electronic files for SOPs, forms, and QA/QC manuals. Support the review and revision of equipment-related SOPs and forms; ensure revision dates and signatures are current. Prepare branch-level quality/progress reports; prepare equipment qualification and other reports. Effectively write and communicate QMS documents and requirements. Conduct quality reviews according to procedural criteria established in quality review plans for determining adherence to standards outlined for clinical laboratory practices. Qualifications Bachelor’s degree in laboratory science, medical technology, related field and at least 3-5 years in clinical or research laboratory experience OR a high school diploma and 6 years in clinical or research laboratory experience. Demonstrated laboratory regulatory skills/knowledge through work experience implementing, managing and maintaining quality management systems. Developing processes for and monitoring the performance of laboratory standard operating procedures based on laboratory regulatory policies and quality guidelines or standards, such as {the Clinical Laboratory Standards Institute (CLSI), College of American Pathologists (CAP), International Organization for Standardization (ISO), or a similar body for laboratory accreditation). Must be able to obtain a NAC clearance Preferred Qualifications CLIA lab experience. Clinical laboratory experience. Master’s degree in in laboratory science, medical technology, or related field. Previous experience with federal or state health agency laboratory. Knowledge of HIV lab specimen handling or familiarity with testing and ordering. Experience in a CLIA lab. EEO DLH Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment. DLH will provide reasonable accommodation to individuals with disabilities and disabled Veterans who need assistance to apply. DLH is committed to maintaining a fair and authentic interview process", "summaryDescription" : "Laboratory Specialist (Part-Time) at DLH. Skills: Quality Management System, ISO implementation, Laboratory practices. Maintain QMS knowledge. Organize hardcopy files", "postedDate" : "2026-06-13T21:53:24.311", "createdAt" : "2026-06-13T21:53:24.311", "lastUpdated" : "2026-06-15T03:46:14.219", "ingestTimestamp" : "2026-06-13T21:53:24.311", "mongoId" : "6a2c7a7a74d8ee00a09459bd", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 35000, "salaryAnnualMax" : 55000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "LC-MS/MS testing", "Quantitative assays", "Qualitative assays", "Quality Management System", "ISO implementation", "Laboratory practices", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Clinical laboratory practices", "Laboratory accreditation", "Quality management systems", "CLSI", "CAP", "ISO", "Antiretroviral drugs", "Antimicrobial drugs" ], "skillCount" : 21, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "_score" : 603.6449, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a0ab2021663d49372dc7c8a", "title" : "Automotive Mechanical Technician - ADAS Calibrations", "company" : "Bob Weaver Auto", "industry" : "Manufacturing", "salary" : { "min" : 52000.0, "max" : 78000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimation is based on the market baseline for Automotive Mechanical Technicians in the United States, adjusted for mid-seniority, the automotive industry, and the Pottsville, PA location." }, "location" : "Pottsville, PA", "locations" : [ "Pottsville", "PA" ], "timestamp" : "2026-06-15T08:20:17.026", "fingerprint" : "4c92c3988db2eab2081158fa764b85208097995a211ffd133b098e8f6ff44116", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://bob-weaver-auto.breezy.hr/p/10d442cc015f-automotive-mechanical-technician-adas-calibrations", "externalId" : "10d442cc015f", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Pottsville", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.6851324,-76.1953701" } ], "locationText" : "Pottsville, Pennsylvania, United States", "employmentType" : "FULL_TIME", "coreResponsibilities" : "Calibrate Advanced Driver Assistance Systems", "domainKnowledge" : "Advanced Driver Assistance Systems", "domainList" : [ "advanced-driver-assistance-systems" ], "domainSpecificKnowledge" : [ "Advanced Driver Assistance Systems" ], "workSiteFlexibility" : "Onsite", "rawDescription" : "Join Schuylkill County’s #1 Top-Rated collision center and be a part of our innovative collision team! Today’s vehicles are equipped with sophisticated Advanced Driver Assistance Systems (ADAS) that require expert calibration during collision repairs. If you have a love of all things automotive, a", "summaryDescription" : "Automotive Mechanical Technician - ADAS Calibrations at Bob Weaver Auto. Calibrate Advanced Driver Assistance Systems", "createdAt" : "2026-06-14T00:08:39.047", "lastUpdated" : "2026-06-15T08:20:17.026", "ingestTimestamp" : "2026-06-14T00:08:39.047", "mongoId" : "6a0ab2021663d49372dc7c8a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 52000, "salaryAnnualMax" : 78000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Advanced Driver Assistance Systems" ], "skillCount" : 1, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "_score" : 594.4061, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Automotive", "llmIndustryConfidence" : 0.92 }, { "id" : "6a2ac6b374d8ee00a0707102", "title" : "Quality & Laboratory Supervisor", "company" : "BioMar Australia", "industry" : "Aquaculture", "salary" : { "min" : 95000.0, "max" : 135000.0, "currency" : "AUD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Quality & Laboratory Supervisor in the Food & Beverage industry in Australia, adjusted for seniority and location." }, "location" : "Australia", "locations" : [ "Australia" ], "timestamp" : "2026-06-14T23:34:31.914", "fingerprint" : "a37153d0b46f1ee65d6194023f4fc643eb4b86bb40c7f971d22e994fc21721f6", "source" : "workday", "language" : "en", "applyUrl" : "https://biomarpeople.wd3.myworkdayjobs.com/BioMar/job/BioMar-Australia-Wesley-Vale/Quality---Laboratory-Supervisor_R4188", "externalId" : "R4188", "industryFunction" : { }, "locationPoint" : "-25.2744,133.7751", "structuredLocations" : [ { "country" : "Australia", "continent" : "oc", "workMode" : "onsite" } ], "locationText" : "Australia", "employmentType" : "FULL_TIME", "experienceMinYears" : 8, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "technicalSkills" : "NIR, Wet chemistry, Physical testing, Analytical methods", "professionalSkills" : [ "Quality assurance", "Laboratory operations", "Compliance management", "Continuous improvement", "Process optimisation", "Stakeholder management", "Operational oversight" ], "hardSkillsList" : [ "Quality control testing", "Internal quality audits", "Corrective actions", "Preventive actions", "Risk assessments", "Incident investigations", "Data integrity standards", "Laboratory efficiency", "Interpreting laboratory data", "Analytical problem-solving" ], "softSkillsList" : [ "Leadership", "Teamwork" ], "hardSkills" : [ { "name" : "Quality control testing", "level" : "intermediate" }, { "name" : "Internal quality audits", "level" : "intermediate" }, { "name" : "Corrective actions", "level" : "intermediate" }, { "name" : "Preventive actions", "level" : "intermediate" }, { "name" : "Risk assessments", "level" : "intermediate" }, { "name" : "Incident investigations", "level" : "intermediate" }, { "name" : "Data integrity standards", "level" : "intermediate" }, { "name" : "Laboratory efficiency", "level" : "intermediate" }, { "name" : "Interpreting laboratory data", "level" : "intermediate" }, { "name" : "Analytical problem-solving", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Teamwork" } ], "majorSkills" : "Quality assurance, Laboratory operations, Team supervision, Continuous improvement", "majorSkillsList" : [ "Quality assurance", "Laboratory operations", "Team supervision", "Continuous improvement" ], "coreResponsibilities" : "Supervise laboratory operations, Coordinate laboratory activities, Oversee quality assurance processes, Lead laboratory team members, Coach laboratory team members, Develop laboratory team members, Train laboratory team members, Manage laboratory team performance, Plan laboratory team workload, Oversee quality control testing, Monitor production processes, Collaborate with operational teams, Maintain product quality, Resolve quality issues, Conduct internal quality audits, Manage corrective actions, Manage preventive actions, Ensure HACCP compliance, Ensure ISO standards compliance, Ensure quality management systems compliance, Ensure regulatory requirements compliance, Maintain laboratory equipment, Manage calibration schedules, Manage proficiency testing programs, Maintain data integrity standards, Drive continuous improvement initiatives, Improve laboratory efficiency, Optimise processes, Manage laboratory consumables, Manage purchasing activities, Manage budget inputs, Promote safety culture, Conduct risk assessments, Investigate incidents, Comply with WHS requirements, Act as contact for suppliers, Act as contact for auditors, Act as contact for regulators, Act as contact for internal stakeholders", "teamCollaboration" : "Work with production; Work with operations; Work with suppliers; Work with stakeholders", "domainKnowledge" : "Aquaculture feed products; Food safety standards; HACCP; ISO standards; WHS requirements", "domainList" : [ "aquaculture-feed-products", "food-safety-standards", "haccp", "iso-standards", "whs-requirements" ], "domainSpecificKnowledge" : [ "Aquaculture feed products", "Food safety standards", "HACCP", "ISO standards", "WHS requirements" ], "toolProficiency" : [ "Digital quality systems" ], "continuousLearning" : "Professional development; Ongoing learning", "innovationCreativity" : "Innovation", "problemSolvingSkills" : "Analytical problem-solving", "qualificationsBasic" : "Bachelor of Science, Laboratory qualification, 4–5 years quality assurance, 4–5 years laboratory operations, Previous team supervision experience, Previous team leadership experience", "qualificationsPreferred" : "Knowledge of quality systems, Knowledge of food safety standards, Knowledge of HACCP, Knowledge of ISO requirements", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Quality & Laboratory Supervisor ## **Lead Quality. Drive Improvement. Support Sustainable Aquaculture.** Are you an experienced quality professional with a passion for laboratory excellence, continuous improvement, and leading high-performing teams? Do you enjoy balancing hands-on technical expertise with people leadership and operational oversight? BioMar Australia is seeking a **Quality & Laboratory Supervisor** to join our team on Tasmania’s stunning northwest coast. Reporting to the Quality Manager, this role plays a critical part in ensuring the quality, safety, and compliance of our world-class aquaculture feed products while supervising our laboratory operations and team. ## **About the Role** As the Quality & Laboratory Supervisor, you will be responsible for coordinating laboratory activities, overseeing quality assurance processes, and supporting the ongoing development of laboratory personnel. You will work closely with production, operations, suppliers, and other stakeholders to ensure products consistently meet BioMar’s high standards and regulatory requirements. This role combines technical quality expertise, team supervision, compliance management, and continuous improvement leadership. ## **Key Responsibilities** * Supervise and coordinate daily laboratory operations and quality assurance activities. * Lead, coach, and develop laboratory team members, including training, competency development, performance management, and workload planning. * Oversee quality control testing of raw materials, in-process products, and finished feed products using NIR, wet chemistry, physical testing, and advanced analytical methods. * Monitor production processes and collaborate with operational teams to maintain product quality and resolve quality-related issues. * Conduct internal quality audits and manage corrective and preventive actions. * Ensure compliance with HACCP, ISO standards, quality management systems, and regulatory requirements. * Maintain laboratory equipment, calibration schedules, proficiency testing programs, and data integrity standards. * Drive continuous improvement initiatives, including digital quality systems, laboratory efficiency improvements, and process optimisation. * Manage laboratory consumables, purchasing activities, and budget inputs. * Promote a strong safety culture through risk assessments, incident investigations, and compliance with WHS requirements. * Act as a key point of contact for suppliers, auditors, regulators, and internal stakeholders on quality and laboratory matters. ## **About You** To be successful in this role, you will bring: * A Bachelor of Science, laboratory qualification, or equivalent technical qualification. * 4–5 years’ experience in quality assurance, laboratory operations, or a related technical environment. * Previous experience supervising or leading team members. * Strong knowledge of quality systems, food safety standards, HACCP, and ISO requirements. * Experience interpreting laboratory data and applying analytical problem-solving skills. * Excellent communication and stakeholder management abilities. * Strong organisational skills with the ability to manage competing priorities. * A proactive approach to continuous improvement and operational excellence. * A commitment to workplace safety, quality, and teamwork. ## **What We Offer** At BioMar, our people are at the heart of everything we do. We offer: * Competitive salary aligned to your skills and experience. * Additional 0.5% above-award superannuation contribution. * Comprehensive health and wellbeing program, including Employee Assistance Program (EAP), personal accident insurance, onsite occupational physiologist support, and pre-employment health assessments. * Professional development and ongoing learning opportunities. * A collaborative, values-driven culture focused on sustainability and innovation. * The opportunity to work in one of Tasmania’s most beautiful regions while contributing to the future of sustainable aquaculture. ## **About BioMar** BioMar is a world leader in high-performance aquaculture feed, dedicated to supporting sustainable seafood production across the globe. With operations in more than 90 countries and a strong commitment to innovation, sustainability, and partnership, we work closely with our customers to develop feed solutions that improve fish health, performance, and environmental outcomes. At BioMar, our purpose is to create value through responsible and sustainable aquaculture. Guided by our values of **Trust, Passion, Performance and Partnership** , we strive to make a positive impact on the industry, our communities, and the planet. ## **Apply Now** If you are ready to take the next step in your quality and laboratory career and contribute to the future of sustainable aquaculture, we would love to hear from you. Submit your resume and cover letter outlining your experience and suitability for the role. ## **Powered by Partnership. Driven by Innovation.**", "summaryDescription" : "Quality & Laboratory Supervisor at BioMar Australia. Skills: Quality assurance, Laboratory operations, Team supervision, Continuous improvement. Supervise laboratory operations. Coordinate laboratory activities", "postedDate" : "2026-06-10T03:59:16.114", "createdAt" : "2026-06-12T03:59:16.077", "lastUpdated" : "2026-06-14T23:34:31.914", "ingestTimestamp" : "2026-06-12T03:59:16.077", "mongoId" : "6a2ac6b374d8ee00a0707102", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://biomarpeople.wd3.myworkdayjobs.com/BioMar/job/BioMar-Australia-Wesley-Vale/Quality---Laboratory-Supervisor_R4188", "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Quality control testing", "Internal quality audits", "Corrective actions", "Preventive actions", "Risk assessments", "Incident investigations", "Data integrity standards", "Laboratory efficiency", "Interpreting laboratory data", "Analytical problem-solving", "Leadership", "Teamwork", "Quality assurance", "Laboratory operations", "Team supervision", "Continuous improvement", "Compliance management", "Process optimisation", "Stakeholder management", "Operational oversight", "Aquaculture feed products", "Food safety standards", "HACCP", "ISO standards", "WHS requirements", "Digital quality systems" ], "skillCount" : 26, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 1.0, "_score" : 593.5022, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Aquaculture" }, { "id" : "69cf26122beec4dd3d90b3fe", "title" : "Medical Laboratory Scientist - Hematology", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 65000.0, "max" : 95000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Medical Laboratory Scientist in Tampa, FL, adjusted for the Healthcare industry." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

" ], "certifications" : [ "Medical Technologist license" ], "timestamp" : "2026-06-15T08:56:42.298", "fingerprint" : "0bd187ccad73bc0b1896f436a2d0bc273e4ba25e5fca3ca76984f002282f70b4", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=541110", "externalId" : "541110", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tampa", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "27.9449854,-82.4583107" } ], "locationText" : "Tampa, Florida, United States", "minimumEducation" : "Bachelor's", "majorSkills" : "Hematology testing, Laboratory analysis", "majorSkillsList" : [ "Hematology testing", "Laboratory analysis" ], "domainKnowledge" : "CAP Regulations; Hematology", "domainList" : [ "cap-regulations", "hematology" ], "domainSpecificKnowledge" : [ "CAP Regulations", "Hematology" ], "problemSolvingSkills" : "Test problem solving", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision, independently performs all levels of moderate and high complexity testing, following established policies, procedures, and professional guidelines. Responsible for performing routine and specialized technical analyses. Operates and maintains instrumentation according to established laboratory procedures and protocols. Exercises independent judgement in recognizing and solving test related problems. Performs technical job duties as specified in CAP Regulations. Personnel Requirements for Tests of Moderate and High Complexity - Testing. Also responsible for performing job duties in accordance with the mission, vision and values of Tampa General Hospital. Must be currently licensed as a Medical Technologist by the State of Florida Department of Health. Bachelor’s degree in Medical Technology or related area.      Tampa", "summaryDescription" : "Medical Laboratory Scientist - Hematology at Tampa General Hospital. Skills: Hematology testing, Laboratory analysis", "createdAt" : "2026-06-14T00:42:58.318", "lastUpdated" : "2026-06-15T08:56:42.298", "ingestTimestamp" : "2026-06-14T00:42:58.318", "mongoId" : "69cf26122beec4dd3d90b3fe", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 95000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Hematology testing", "Laboratory analysis", "CAP Regulations", "Hematology", "Medical Technologist license" ], "skillCount" : 5, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 591.7177, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a0de91358b93c861eb990c4", "title" : "Medical Laboratory Scientist III", "industry" : "Healthcare", "salary" : { "min" : 85000.0, "max" : 125000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Medical Laboratory Scientist III in Brooksville, United States, adjusted for mid-seniority and full-time employment in the healthcare industry." }, "location" : "United States-Florida-Brooksville", "locations" : [ "United States-Florida-Brooksville", "
TGH Brooksville (TGHBRKSV)
17240 Cortez Boulevard

Brooksville, 34601

" ], "certifications" : [ "Clinical Lab Technologist Certification", "ASCP", "AMT" ], "timestamp" : "2026-06-15T10:02:31.540", "fingerprint" : "f31060dab2a92af3482fbc237f0ffd18478088e3ac42faa28c9b0783fe494198", "source" : "taleo", "language" : "en", "applyUrl" : "https://tas-tgh.taleo.net/careersection/ex/jobdetail.ftl?job=670007", "externalId" : "670007", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Brooksville", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "28.5552719,-82.3878709" } ], "locationText" : "Brooksville, Florida, United States", "minimumEducation" : "Associate's", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "domainKnowledge" : "Geriatrics; Adults; Pediatrics; Neonates; Microbiology; Serology; Clinical Chemistry; Hematology; Immunohematology", "domainList" : [ "geriatrics", "adults", "pediatrics", "neonates", "microbiology", "serology", "clinical-chemistry", "hematology", "immunohematology" ], "domainSpecificKnowledge" : [ "Geriatrics", "Adults", "Pediatrics", "Neonates", "Microbiology", "Serology", "Clinical Chemistry", "Hematology", "Immunohematology" ], "communicationSkills" : "Report results", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Performs all approved laboratory procedures in assigned licensure specialties, as required to meet workload demands. coordinating lab resources as outlined below. Precisely and accurately performs and evaluates a variety of technical procedures. Utilizes accepted quality control techniques by manual, semi -automated, or automated methodologies and equipment. Essential Functions Perform work according to established laboratory policies and procedures. Demonstrate the ability to work independently in all areas covered by the FL license. Perform quality control for all tests, evaluate results, and take corrective action as necessary before reporting patient results. Assess specimen integrity for appropriateness of ordered tests, including issues like QNS, hemolysis, and clotting. Ensure procedures, methodologies, and patient results correlate with age-specific criteria for geriatrics, adults, pediatrics, and neonates. Repeat and report all panic/critical test results to a licensed caregiver within 5 minutes of completion. Perform calibrations and maintenance as required by instrument manufacturers, CLIA, and TJC. Complete proficiency testing samples within the requested timeframe. Demonstrate competency in using the LIS and HIS computer systems. Ensure adequate supplies are available and promptly notify the supervisor when supplies are low. Education Associate's Degree Medical Technology or Bachelors Biology or Chemistry License Clinical Lab Technologist Certification American Society of Clinical Pathology (ASCP) or American Medical Technologists (AMT) Work Experience Licensed in all 5 specialties, Microbiology, Serology, Clinical Chemistry, Hematology, Immunohematology Brooksville", "summaryDescription" : "Medical Laboratory Scientist III", "createdAt" : "2026-06-14T09:47:04.758", "lastUpdated" : "2026-06-15T10:02:31.540", "ingestTimestamp" : "2026-06-14T09:47:04.758", "mongoId" : "6a0de91358b93c861eb990c4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 85000, "salaryAnnualMax" : 125000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Geriatrics", "Adults", "Pediatrics", "Neonates", "Microbiology", "Serology", "Clinical Chemistry", "Hematology", "Immunohematology", "Clinical Lab Technologist Certification", "ASCP", "AMT" ], "skillCount" : 12, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 589.97253, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ebf8074d8ee00a0e9ac8b", "title" : "Clinical Laboratory Technologist", "company" : "LabCorp", "location" : "United States of America", "locations" : [ "United States of America" ], "certifications" : [ "ASCP", "AMT" ], "timestamp" : "2026-06-15T10:13:41.446", "fingerprint" : "31395285e798ac5773952569f072b323184b2b87b1abbc774bcdad1c77b38813", "source" : "workday", "applyUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Bartlesville-OK/Clinical-Laboratory-Technologist_2615389", "externalId" : "2615389", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Bartlesville", "state" : "Oklahoma", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "Bartlesville, Oklahoma, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor", "experienceMinYears" : 1, "experienceMaxYears" : 2, "experienceLevel" : "Junior", "professionalSkills" : [ "Clinical lab science." ], "softSkillsList" : [ "attention to detail, organizational skills" ], "softSkills" : [ { "name" : "attention to detail, organizational skills" } ], "majorSkills" : "clinical laboratory testing, instrumentation, quality control", "majorSkillsList" : [ "clinical laboratory testing, instrumentation, quality control" ], "coreResponsibilities" : "The Clinical Laboratory Technologist determines specimen acceptability, performs routine and complex technical procedures, and operates/troubleshoots instrumentation. This role involves preparing and testing reagents, reporting accurate test results for patient care, and performing preventive maintenance and quality control. The technologist also manages testing bench supplies, maintains a safe work environment, and assists with specimen processing as needed.", "teamCollaboration" : "Ability to work independently and within a team environment.", "toolProficiency" : [ "laboratory information systems" ], "communicationSkills" : "communication skills", "documentationSkills" : "Standard Operating Procedures", "continuousLearning" : "If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!", "problemSolvingSkills" : "technical decisions", "specialRequirements" : "In lieu of education requirements listed above, non-traditional degrees with applicable science credits that meet CLIA standards may meet education requirement.", "qualificationsBasic" : "Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology, or an MLS degree. 1 year or more of clinical laboratory testing experience. Proficient with computers. Able to pass a standardized color blindness test.", "qualificationsPreferred" : "ASCP or AMT certification. Familiarity with laboratory information systems. Flexibility to work overtime or other shifts depending on business needs.", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**LabCorp is seeking a Clinical Lab Professional to join our team at****Ascension St. John Jane Phillips, Bartlesville, OK**. **Work Schedule:** 3 x 12 hour shifts, Monday - Friday, 6:30 PM - 7:00 AM, rotating weekends and holidays. **Job Responsibilities:** * Determine the acceptability of specimens for testing according to established criteria * Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures * Monitor, operate and troubleshoot instrumentation to ensure proper functionality * Demonstrate the ability to make technical decisions regarding testing and problem solving. * Prepare, test and evaluate new reagents or controls * Report accurate and timely test results in order to deliver quality patient care * Perform and document preventive maintenance and quality control procedures * Identify and replenish testing bench supplies as necessary * Assist with processing of specimens when needed * Maintain a safe work environment and wear appropriate personal protective equipment **Minimum Qualifications:** * Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology * 1 year or more of clinical laboratory testing experience OR an MLS degree **Preferred Qualifications:** * ASCP or AMT certification **Additional Job Standards:** * In lieu of education requirements listed above, non-traditional degrees with applicable science credits that meet CLIA standards may meet education requirement * Ability to work independently and within a team environment * Familiarity with laboratory information systems * Proficient with computers * High level of attention detail along with strong communication and organizational skills * Able to pass a standardized color blindness test * Flexibility to work overtime or other shifts depending on business needs At Labcorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step!**This role works in a high volume, production based environment performing a vital component of clinical lab science.** **Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please [click here](https://careers.labcorp.com/global/en/us-rewards-and-wellness). _**If you 're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!**_ **Labcorp is proud to be an Equal Opportunity Employer:** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our [accessibility site](https://careers.labcorp.com/global/en/accessibility) or contact us at [Labcorp Accessibility.](mailto:Disability_apply@LabCorp.com) For more information about how we collect and store your personal data, please see our [Privacy Statement](https://www.labcorp.com/about/web-privacy-policy).", "summaryDescription" : "Clinical Laboratory Technologist at LabCorp. Skills: clinical laboratory testing, instrumentation, quality control. The Clinical Laboratory Technologist determines specimen acceptability, performs routine and complex technical procedures, and operates/troubleshoots instrumentation. This role involves preparing and testing reagents, reporting accurate test results for patient care, and performing preventive maintenance and quality control. The technologist also manages testing bench supplies, mai", "postedDate" : "2026-06-10T20:59:08.207", "createdAt" : "2026-06-14T20:59:08.157", "lastUpdated" : "2026-06-15T10:13:41.446", "ingestTimestamp" : "2026-06-14T20:59:08.157", "mongoId" : "6a2ebf8074d8ee00a0e9ac8b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Bartlesville-OK/Clinical-Laboratory-Technologist_2615389", "hasSalary" : false, "allSkills" : [ "attention to detail, organizational skills", "clinical laboratory testing, instrumentation, quality control", "Clinical lab science.", "ASCP", "AMT", "laboratory information systems" ], "skillCount" : 6, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 586.8792, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "69fc49814c40e2acd1a81e8d", "title" : "Clinical Laboratory Scientist - Chemistry", "company" : "City of Hope", "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Clinical Laboratory/Pathology", "Onsite, Evenings, Evenings" ], "certifications" : [ "California Clinical Laboratory Scientist (CLS) licensure" ], "timestamp" : "2026-06-15T10:07:28.144", "fingerprint" : "a707e28e00d0a39770841cad15cd48473baed4813eb65c15de1f7beb9865697a", "source" : "taleo", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=231964", "externalId" : "231964", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Duarte", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "Duarte, California, United States", "minimumEducation" : "Bachelor", "experienceMinYears" : 0, "experienceMaxYears" : 1, "experienceLevel" : "Entry", "technicalSkills" : "clinical laboratory procedures", "professionalSkills" : [ "FACT, AABB, ACHI, CAP, FDA, Joint Commission regulations, Clinical Laboratory Improvement Amendments of 1988, CFR Section 493. 1445(a)" ], "hardSkillsList" : [ "preparing specimens", "performing clinical laboratory procedures", "reporting clinical laboratory procedures", "preparing and processing biological specimens", "performing complex laboratory tests", "reviewing results", "conducting quality control", "performing data entry", "preparing solutions", "preparing reagents", "preparing culture media", "preparing stains" ], "softSkillsList" : [ "compassionate, integrity, confidentiality, customer service" ], "hardSkills" : [ { "name" : "preparing specimens", "level" : "intermediate" }, { "name" : "performing clinical laboratory procedures", "level" : "intermediate" }, { "name" : "reporting clinical laboratory procedures", "level" : "intermediate" }, { "name" : "preparing and processing biological specimens", "level" : "intermediate" }, { "name" : "performing complex laboratory tests", "level" : "intermediate" }, { "name" : "reviewing results", "level" : "intermediate" }, { "name" : "conducting quality control", "level" : "intermediate" }, { "name" : "performing data entry", "level" : "intermediate" }, { "name" : "preparing solutions", "level" : "intermediate" }, { "name" : "preparing reagents", "level" : "intermediate" }, { "name" : "preparing culture media", "level" : "intermediate" }, { "name" : "preparing stains", "level" : "intermediate" } ], "softSkills" : [ { "name" : "compassionate, integrity, confidentiality, customer service" } ], "majorSkills" : "Clinical Laboratory Scientist, specimen preparation, laboratory procedures, quality control, regulatory guidelines", "majorSkillsList" : [ "Clinical Laboratory Scientist, specimen preparation, laboratory procedures, quality control, regulatory guidelines" ], "coreResponsibilities" : "Responsible for preparing specimens for analysis and performing and reporting clinical laboratory procedures, ranging from waived to high complexity, all while adhering to strict compliance with written SOPs and various regulatory guidelines, including FACT, AABB, ACHI, CAP, FDA, and Joint Commission regulations. Additionally, will assist in teaching students and staff, working under the authority of the Laboratory Director as per the Clinical Laboratory Improvement Amendments of 1988, CFR Section 493. 1445(a).", "teamCollaboration" : "assist coworkers as needed", "projectManagementSkills" : [ "assigned schedules" ], "toolProficiency" : [ "standard laboratory equipment" ], "communicationSkills" : "promptly notifying supervisors; interacting with colleagues; interacting with patients; interacting with physicians; interacting with vendors", "documentationSkills" : "data recording; data entry", "continuousLearning" : "Maintain knowledge of techniques for preparing and processing biological specimens for clinical analyses using universal precautions.", "problemSolvingSkills" : "unusual results; discrepancies", "specialRequirements" : "per diem evenings position, welcomes new licensed clinical laboratory scientists to apply, sign-on bonus to eligible candidates", "outcomesObjectives" : "deliver the cures of tomorrow to the people who need them today", "qualificationsBasic" : "Bachelor’s Degree, California Clinical Laboratory Scientist (CLS) licensure", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. We have an exciting Clinical Chemistry Laboratory opportunity for a Clinical Laboratory Scientist I position at City of Hope, located in Duarte, California. This is a per diem evenings position that welcomes new licensed clinical laboratory scientists to apply. We offer a sign-on bonus to eligible candidates. In this role, you will be responsible for preparing specimens for analysis and performing and reporting clinical laboratory procedures, ranging from waived to high complexity, all while adhering to strict compliance with written SOPs and various regulatory guidelines, including FACT, AABB, ACHI, CAP, FDA, and Joint Commission regulations. Additionally, you'll have the opportunity to assist in teaching students and staff, working under the authority of the Laboratory Director as per the Clinical Laboratory Improvement Amendments of 1988, CFR Section 493.1445(a). Join our dynamic team at City of Hope and contribute to groundbreaking medical research and patient care. Apply now! As a successful candidate, you will: Maintain knowledge of techniques for preparing and processing biological specimens for clinical analyses using universal precautions. Demonstrate proficiency in manual, semi-automated, and automated laboratory procedures. Perform a variety of complex laboratory tests and procedures according to prescribed protocols and assigned schedules, completing them within established turnaround times. Review normal and critical results for accuracy and completeness before reporting, promptly notifying supervisors of unusual results or discrepancies. Conduct quality control procedures, including preventive maintenance, calibrations, and data recording, to support and participate in Quality Assurance efforts and the Performance Improvement process. Utilize standard laboratory equipment, ensuring accuracy and completeness of recorded results, while also performing data entry of diagnostic information. Prepare and label solutions, reagents, culture media, and stains following standard formulas and procedures. Prioritize work, provide efficient service, assist coworkers as needed, maintain cleanliness and safety practices, and uphold a high level of integrity and confidentiality while maintaining a positive customer service image when interacting with colleagues, patients, physicians, and vendors. Your qualifications should include: Bachelor’s Degree California Clinical Laboratory Scientist (CLS) licensure City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Clinical Laboratory Scientist - Chemistry at City of Hope. Skills: Clinical Laboratory Scientist, specimen preparation, laboratory procedures, quality control, regulatory guidelines. Responsible for preparing specimens for analysis and performing and reporting clinical laboratory procedures, ranging from waived to high complexity, all while adhering to strict compliance with written SOPs and various regulatory guidelines, including FACT, AABB, ACHI, CAP, FDA, and Joint Commission regulations. Ad", "createdAt" : "2026-06-14T19:55:53.103", "lastUpdated" : "2026-06-15T10:07:28.144", "ingestTimestamp" : "2026-06-14T19:55:53.103", "mongoId" : "69fc49814c40e2acd1a81e8d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "hasSalary" : false, "allSkills" : [ "preparing specimens", "performing clinical laboratory procedures", "reporting clinical laboratory procedures", "preparing and processing biological specimens", "performing complex laboratory tests", "reviewing results", "conducting quality control", "performing data entry", "preparing solutions", "preparing reagents", "preparing culture media", "preparing stains", "compassionate, integrity, confidentiality, customer service", "Clinical Laboratory Scientist, specimen preparation, laboratory procedures, quality control, regulatory guidelines", "FACT, AABB, ACHI, CAP, FDA, Joint Commission regulations, Clinical Laboratory Improvement Amendments of 1988, CFR Section 493. 1445(a)", "assigned schedules", "California Clinical Laboratory Scientist (CLS) licensure", "standard laboratory equipment" ], "skillCount" : 18, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Entry", "dataQualityScore" : 0.6666667, "_score" : 585.77594, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "69cf26122beec4dd3d90b425", "title" : "Lab Assistant - Laboratory Services", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 35000.0, "max" : 45000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for entry-level Lab Assistant in Tampa, FL, adjusted for the healthcare industry." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

" ], "timestamp" : "2026-06-15T08:01:57.700", "fingerprint" : "e12d1cb8b365720c07c852991fd57a1a2a9fd35eea1a70eff277654225531f3b", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=676770", "externalId" : "676770", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tampa", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "27.9449854,-82.4583107" } ], "locationText" : "Tampa, Florida, United States", "minimumEducation" : "High School", "teamCollaboration" : "Collaborate with nursing; Collaborate with Physicians; Collaborate with Pathologists", "domainKnowledge" : "Laboratory testing; Biological safety; CAP requirements", "domainList" : [ "laboratory-testing", "biological-safety", "cap-requirements" ], "domainSpecificKnowledge" : [ "Laboratory testing", "Biological safety", "CAP requirements" ], "communicationSkills" : "Telephone customer service", "continuousLearning" : "1-2 months on-the-job training", "problemSolvingSkills" : "Troubleshooting", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision and following established policies, procedures and professional guidelines, the Laboratory Assistant is responsible for the receipt, labeling, processing, delivery and storage of specimens destined for laboratory testing. The team member is also responsible for coordinating with the registration department when specimens are collected and delivered to TGH from an outside physician’s office. Assists with various clerical tasks, receptionist duties, data processing and telephone customer service. Using independent judgment and following TGH and departmental procedures, is responsible for collaborating with nursing personnel, Physicians and Pathologists, regarding the applicable specimen requirements and timely collection of the patient sample(s) necessary for the testing that will be sent to the performing laboratory. Adheres to biological and safety policies and licensure requirements for all laboratory testing and testing facilities; maintains CAP readiness; performs troubleshooting and quality assurance monitoring. Responsible for performing job duties in accordance with the mission, vision and values of Tampa General Hospital. High school diploma or GED 1-2 months of on-the-job training and orientation Tampa", "summaryDescription" : "Lab Assistant - Laboratory Services at Tampa General Hospital", "createdAt" : "2026-06-14T02:46:54.505", "lastUpdated" : "2026-06-15T08:01:57.700", "ingestTimestamp" : "2026-06-14T02:46:54.505", "mongoId" : "69cf26122beec4dd3d90b425", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 35000, "salaryAnnualMax" : 45000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Laboratory testing", "Biological safety", "CAP requirements" ], "skillCount" : 3, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.6666667, "_score" : 584.6871, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "69cf26132beec4dd3d90b5e1", "title" : "Medical Laboratory Scientist - Hematology", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 68000.0, "max" : 92000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Medical Laboratory Scientist in Tampa, FL, adjusted for the Healthcare industry and a large hospital setting." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

" ], "certifications" : [ "Medical Technologist license" ], "timestamp" : "2026-06-15T09:09:50.633", "fingerprint" : "f28f26ab19db96fad202f7b5ee239e30b4d99b2bf4ab58836a0844abb3610e21", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=540910", "externalId" : "540910", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tampa", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "27.9449854,-82.4583107" } ], "locationText" : "Tampa, Florida, United States", "minimumEducation" : "Bachelor's", "domainKnowledge" : "CAP Regulations; Moderate complexity testing; High complexity testing", "domainList" : [ "cap-regulations", "moderate-complexity-testing", "high-complexity-testing" ], "domainSpecificKnowledge" : [ "CAP Regulations", "Moderate complexity testing", "High complexity testing" ], "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision, independently performs all levels of moderate and high complexity testing, following established policies, procedures, and professional guidelines. Responsible for performing routine and specialized technical analyses. Operates and maintains instrumentation according to established laboratory procedures and protocols. Exercises independent judgement in recognizing and solving test related problems. Performs technical job duties as specified in CAP Regulations. Personnel Requirements for Tests of Moderate and High Complexity - Testing. Also responsible for performing job duties in accordance with the mission, vision and values of Tampa General Hospital. Must be currently licensed as a Medical Technologist by the State of Florida Department of Health. Bachelor’s degree in Medical Technology or related area.      Tampa", "summaryDescription" : "Medical Laboratory Scientist - Hematology at Tampa General Hospital", "createdAt" : "2026-06-14T01:10:10.024", "lastUpdated" : "2026-06-15T09:09:50.633", "ingestTimestamp" : "2026-06-14T01:10:10.024", "mongoId" : "69cf26132beec4dd3d90b5e1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 68000, "salaryAnnualMax" : 92000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "CAP Regulations", "Moderate complexity testing", "High complexity testing", "Medical Technologist license" ], "skillCount" : 4, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 584.33154, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a5e5674d8ee00a061c045", "title" : "ATR - Tax Specialist Referent", "company" : "ATR", "industry" : "Aviation", "salary" : { "min" : 52000.0, "max" : 78000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Tax Specialist in the Aerospace industry in France, adjusted for seniority and company size." }, "location" : "France", "locations" : [ "France" ], "timestamp" : "2026-06-12T19:23:06.156", "fingerprint" : "cfcb8e30c4b4fc3e76268d7ba828f589de60944a0062bf54e65fb46041043c4f", "source" : "workday", "language" : "en", "applyUrl" : "https://ag.wd3.myworkdayjobs.com/Airbus/job/Toulouse-Area/ATR---Tax-Specialist-Referent_JR10420033", "externalId" : "JR10420033", "industryFunction" : { }, "locationPoint" : "46.2276,2.2137", "structuredLocations" : [ { "country" : "France", "continent" : "eu", "workMode" : "onsite" } ], "locationText" : "France", "employmentType" : "FULL_TIME", "experienceMinYears" : 3, "experienceMaxYears" : 5, "experienceLevel" : "Professional", "technicalSkills" : "SAP", "professionalSkills" : [ "Tax law", "Accounting", "Tax compliance", "Transfer pricing", "Tax policy", "Tax risk management", "Regulatory compliance" ], "hardSkillsList" : [ "Tax return preparation", "Tax data analysis", "International tax research", "Contract review", "Tax risk assessment", "Tax monitoring", "Regulatory monitoring" ], "softSkillsList" : [ "Autonomy", "Initiative", "Responsibility", "Proactivity" ], "hardSkills" : [ { "name" : "Tax return preparation", "level" : "intermediate" }, { "name" : "Tax data analysis", "level" : "intermediate" }, { "name" : "International tax research", "level" : "intermediate" }, { "name" : "Contract review", "level" : "intermediate" }, { "name" : "Tax risk assessment", "level" : "intermediate" }, { "name" : "Tax monitoring", "level" : "intermediate" }, { "name" : "Regulatory monitoring", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Autonomy" }, { "name" : "Initiative" }, { "name" : "Responsibility" }, { "name" : "Proactivity" } ], "majorSkills" : "Tax law, Tax compliance, International tax", "majorSkillsList" : [ "Tax law", "Tax compliance", "International tax" ], "coreResponsibilities" : "Prepare tax returns, Review tax returns, Coordinate tax returns, Ensure tax data reliability, Improve processes, Conduct tax research, Analyze tax matters, Support transfer pricing documentation, Manage transfer pricing compliance, Define tax policy, Implement tax policy, Draft contract tax aspects, Secure contract tax aspects, Support risk identification, Support risk assessment, Support risk management, Perform tax monitoring, Ensure regulatory compliance, Act as tax contact, Lead external advisor work, Coordinate external advisor work", "teamCollaboration" : "Group subsidiaries; Internal functions; External advisors", "domainKnowledge" : "French tax rules; International tax matters; Permanent establishment; Withholding taxes; VAT; Transfer pricing; Pillar 2", "domainList" : [ "french-tax-rules", "international-tax-matters", "permanent-establishment", "withholding-taxes", "vat", "transfer-pricing", "pillar-2" ], "domainSpecificKnowledge" : [ "French tax rules", "International tax matters", "Permanent establishment", "Withholding taxes", "VAT", "Transfer pricing", "Pillar 2" ], "toolProficiency" : [ "MS Office", "SAP" ], "documentationSkills" : "Transfer pricing documentation", "continuousLearning" : "Development programs", "problemSolvingSkills" : "Data analysis", "qualificationsBasic" : "Degree in tax law, Accounting qualification, 3-5 years in tax", "qualificationsPreferred" : "Italian language proficiency", "remoteFriendly" : true, "workSiteFlexibility" : "Flexible", "rawDescription" : "****Job Description:**** **_About us_** ATR is the **world 's number one aircraft manufacturer in regional aviation** providing a new generation of turboprops. We are a joint venture between **two European aeronautical heavyweights, Airbus and Leonardo.** From the world’s largest cities, to our planet’s most remote regions**, our purpose is to deliver air travel** to people, communities and businesses in an **innovative, sustainable and modern way.** If you strive for excellence, are driven by **ambition** , **trust** and **respect** as we are, then get your career off to a flighting start with ATR! **Our leadership profile:** **People Centric Entrepreneurial Inspiring Exemplary Innovative Humble** **At ATR y****ou will work with passionate colleagues to make a difference in a human size company with attractive advantages!** We are looking for a Tax Specialist to come onboard in our Finance Directorate in Clément’s team: a team of 4 collaborators! [Career Path: Referent ] **_Your Mission_** * Prepare, review and/or coordinate tax returns (VAT, DAS2, CET, tax credits, Pillar 2, etc.) * Ensure the reliability of tax data extracted from information systems (in particular SAP) and contribute to the continuous improvement of processes * Conduct research and analysis on French and international tax matters (permanent establishment, withholding taxes, VAT, etc.) * Support the monitoring and updating of transfer pricing documentation, as well as related compliance obligations * Contribute to the definition and implementation of the Group’s tax policy * Draft and secure tax aspects of contracts (sales, procurement, partnerships, etc.) * Support operational teams in identifying, assessing, and managing tax risks * Perform ongoing tax monitoring and ensure compliance with regulatory developments * Act as a tax point of contact for Group subsidiaries and internal functions * Lead and coordinate work carried out with external advisors (law firms, consultants) * **_About you_** * Educational background: Degree with a major in tax law and/or accounting qualification with a focus on operational tax * Experience: 3 to 5 years in tax (in a firm, corporate environment, or mixed setting) * Technical skills / knowledge: good knowledge of French tax rules and experience in international taxation; solid understanding of main tax compliance obligations (VAT, etc.); understanding of financial and/or operational flows; strong interest in IT tools and data management (SAP or equivalent) * Soft skills: autonomy and ability to take initiative, strong attention to detail, team spirit, sense of responsibility, and proactivity * Fluent in English and French (Italian is a plus) * Good command of MS Office tools and SAP ** _Our Recruitment Process_** * Clément will contact you * Innovative and digital assessment * To get to know you better: interview with Clément then with a Talent Acquisition Partner ** _What we offer_** **Highly competitive compensation package**(profit and success sharing, employee savings plan…) **Work-life balance** (remote working, 6th week of paid leave, additional days off for family events…) **Well-being / health**(supplementary health & welfare coverage…) **Career paths** enabling employees to develop their skills and build a professional project **Wide choice of development programs** for soft and hard skills **CSE:** ATR (family and employee events) and Airbus CSE (travel, vacation camps …) **Diversity** **and inclusion** : Over 1400 men & women with more than 35 different nationalities work together in our teams ! _ATR is committed to achieving workforce diversity and creating an inclusive working environment. We welcome all applications irrespective of social and cultural background, age, gender, disability, sexual orientation or religious belief._ **_A propos d 'ATR _** ATR est le **premier constructeur mondial d 'avions régionaux** et propose une nouvelle génération de turbopropulseurs. Nous sommes une **filiale de deux poids lourds de l 'aéronautique européenne, Airbus et Leonardo. ** Des plus grandes villes du monde aux régions les plus reculées de notre planète, **notre objectif est d 'assurer le transport aérien** des personnes, des communautés et des entreprises d'une manière innovante, durable et moderne. Si vous recherchez l'excellence, si vous êtes animé par **l 'ambition,** la **confiance** et le **respect,** alors faites décoller votre carrière avec ATR **!** **Notre Leadership Profile :** **Centré(e) sur l’humain un esprit entrepreneur inspirant(e) exemplaire innovant(e) humble** **Vous travaillerez avec des collègues passionnés pour faire la différence dans une entreprise à taille humaine avec des avantages attractifs !** Nous recherchons un Fiscaliste pour rejoindre notre Direction Financière au sein de l'équipe de Clément : une équipe de 4 collaborateurs ! [Career Path: Referent ] **_Votre mission_** * Préparer, revoir et/ou coordonner les déclarations fiscales (TVA, DAS2, CET, crédits d’impôt, Pilier 2, etc.) * Fiabiliser les données fiscales issues des systèmes d’information (notamment SAP) et contribuer à l’amélioration continue des processus * Réaliser des analyses et recherches sur des problématiques fiscales françaises et internationales (établissement stable, retenues à la source, TVA, etc.) * Participer au suivi et à la mise à jour de la documentation prix de transfert, ainsi qu’aux obligations déclaratives associées * Contribuer à la définition et à la mise en œuvre de la politique fiscale du Groupe * Rédiger et sécuriser les aspects fiscaux des contrats (ventes, achats, partenariats, etc.) * Accompagner les équipes opérationnelles dans l’identification, l’évaluation et la gestion des risques fiscaux * Assurer une veille fiscale active et veiller à la conformité aux évolutions réglementaires * Intervenir en tant que point de contact fiscal pour les filiales du Groupe et les fonctions internes * Piloter et coordonner les travaux réalisés avec les conseils externes (cabinets d’avocats, consultants) **_A propos de vous_** * Domaine d'études : Formation avec dominante fiscalité / expertise comptable + fiscalité opérationnelle * Expérience en fiscalité : 3 à 5 ans (cabinet, entreprise ou environnement mixte) * Compétences techniques / connaissances : bonnes connaissances en fiscalité française et expérience en fiscalité internationale; maîtrise des principales obligations déclaratives (TVA, etc.) ; connaissance des flux financiers et/ou opérationnels ; appétence pour les outils informatiques et la gestion des données (SAP ou équivalent) * Compétences non techniques : autonomie et esprit d’initiative, rigueur, esprit d’équipe, sens des responsabilités, proactivité * Maîtrise de l'anglais et du français (l'italien est un plus) * Maîtrise des outils bureautiques, SAP ** _Notre processus de recrutement_** * Vous serez contacté(e) par Clément. * Évaluation innovante et numérique * Pour apprendre à vous connaître : entretien avec Clément et ensuite avec notre Talent Acquisition partner ** _Ce que nous vous offrons_** **Une rémunération très compétitive** (prime d’intéressement et de participation, plan d'épargne salariale...) **Un équilibre entre vie personnelle et vie professionnelle**(télétravail, congés évènements familiaux...) **Bien-être / santé** (couverture complémentaire santé & prévoyance...) **Des parcours de carrières** permettant aux salariés de développer leurs compétences et de construire un projet professionnel **Large choix de programmes de développement** pour les soft skills et hard skills **CSE** : ATR (événements familiaux et salariés) et Airbus CSE (voyages, colonies de vacances...) **Diversité** : Environ 1400 hommes et femmes de plus de 35 nationalités différentes travaillent ensemble au sein de nos équipes ! _ATR s 'engage à assurer la diversité de son personnel et à créer un environnement de travail inclusif. Nous accueillons toutes les candidatures sans distinction d'origine sociale et culturelle, d'âge, de sexe, de handicap, d'orientation sexuelle ou de croyance religieuse_ _._ This job requires an awareness of any potential compliance risks and a commitment to act with integrity, as the foundation for the Company’s success, reputation and sustainable growth. ********Company:******** Avions de Transport Regional (ATR) GIE **Contract Type:** Permanent \\----- Classe Emploi (France): Classe G14 **Experience Level:** Professional **Job Family:** Financial Expertise By submitting your CV or application you are consenting to Airbus using and storing information about you for monitoring purposes relating to your application or future employment. This information will only be used by Airbus. Airbus is committed to achieving workforce diversity and creating an inclusive working environment. We welcome all applications irrespective of social and cultural background, age, gender, disability, sexual orientation or religious belief. Airbus is, and always has been, committed to equal opportunities for all. As such, we will never ask for any type of monetary exchange in the frame of a recruitment process. Any impersonation of Airbus to do so should be reported to [emsom@airbus.com](mailto:emsom@airbus.com). At Airbus, we support you to work, connect and collaborate more easily and flexibly. Wherever possible, we foster flexible working arrangements to stimulate innovative thinking.", "summaryDescription" : "ATR - Tax Specialist Referent at ATR. Skills: Tax law, Tax compliance, International tax. Prepare tax returns. Review tax returns", "postedDate" : "2026-06-11T15:10:25.342", "createdAt" : "2026-06-11T15:10:25.302", "lastUpdated" : "2026-06-12T19:23:06.156", "ingestTimestamp" : "2026-06-11T15:10:25.302", "mongoId" : "6a2a5e5674d8ee00a061c045", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://ag.wd3.myworkdayjobs.com/Airbus/job/Toulouse-Area/ATR---Tax-Specialist-Referent_JR10420033", "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Tax return preparation", "Tax data analysis", "International tax research", "Contract review", "Tax risk assessment", "Tax monitoring", "Regulatory monitoring", "Autonomy", "Initiative", "Responsibility", "Proactivity", "Tax law", "Tax compliance", "International tax", "Accounting", "Transfer pricing", "Tax policy", "Tax risk management", "Regulatory compliance", "French tax rules", "International tax matters", "Permanent establishment", "Withholding taxes", "VAT", "Pillar 2", "MS Office", "SAP" ], "skillCount" : 27, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 1.0, "_score" : 584.3002, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Aviation" }, { "id" : "69cf26122beec4dd3d90b4f7", "title" : "Medical Laboratory Technologist III", "salary" : { "min" : 75000.0, "max" : 105000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Medical Laboratory Technologist III in Spring Hill, United States, adjusted for mid-seniority in the healthcare industry." }, "location" : "United States-Florida-Spring Hill", "locations" : [ "United States-Florida-Spring Hill", "
TGH Spring Hill (TGHSPRGHLL)
10461 Quality Drive

Spring Hill, 34609

" ], "certifications" : [ "Clinical Lab Technologist Certification", "American Society of Clinical Pathology (ASCP)", "American Medical Technologists (AMT)" ], "timestamp" : "2026-06-15T08:42:53.195", "fingerprint" : "c4cb6042cf8c262021cb45ccbd4780160dc2d11b14e3503e84100e8a1f43fa9f", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=675286", "externalId" : "675286", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Spring Hill", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "28.4635266,-82.5363557" } ], "locationText" : "Spring Hill, Florida, United States", "minimumEducation" : "Associate's", "domainKnowledge" : "Laboratory licensure specialties; Microbiology; Serology; Clinical Chemistry; Hematology; Immunohematology; CLIA; TJC", "domainList" : [ "laboratory-licensure-specialties", "microbiology", "serology", "clinical-chemistry", "hematology", "immunohematology", "clia", "tjc" ], "domainSpecificKnowledge" : [ "Laboratory licensure specialties", "Microbiology", "Serology", "Clinical Chemistry", "Hematology", "Immunohematology", "CLIA", "TJC" ], "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Performs all approved laboratory procedures in assigned licensure specialties, as required to meet workload demands. coordinating lab resources as outlined below. Precisely and accurately performs and evaluates a variety of technical procedures. Utilizes accepted quality control techniques by manual, semi -automated, or automated methodologies and equipment. Essential Functions Perform work according to established laboratory policies and procedures. Demonstrate the ability to work independently in all areas covered by the FL license. Perform quality control for all tests, evaluate results, and take corrective action as necessary before reporting patient results. Assess specimen integrity for appropriateness of ordered tests, including issues like QNS, hemolysis, and clotting. Ensure procedures, methodologies, and patient results correlate with age-specific criteria for geriatrics, adults, pediatrics, and neonates. Repeat and report all panic/critical test results to a licensed caregiver within 5 minutes of completion. Perform calibrations and maintenance as required by instrument manufacturers, CLIA, and TJC. Complete proficiency testing samples within the requested timeframe. Demonstrate competency in using the LIS and HIS computer systems. Ensure adequate supplies are available and promptly notify the supervisor when supplies are low. Education Associate's Degree Medical Technology or Bachelors Biology or Chemistry License Clinical Lab Technologist Certification American Society of Clinical Pathology (ASCP) or American Medical Technologists (AMT) Work Experience Licensed in all 5 specialties, Microbiology, Serology, Clinical Chemistry, Hematology, Immunohematology Spring Hill", "summaryDescription" : "Medical Laboratory Technologist III", "createdAt" : "2026-06-14T08:25:29.788", "lastUpdated" : "2026-06-15T08:42:53.195", "ingestTimestamp" : "2026-06-14T08:25:29.788", "mongoId" : "69cf26122beec4dd3d90b4f7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 105000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Laboratory licensure specialties", "Microbiology", "Serology", "Clinical Chemistry", "Hematology", "Immunohematology", "CLIA", "TJC", "Clinical Lab Technologist Certification", "American Society of Clinical Pathology (ASCP)", "American Medical Technologists (AMT)" ], "skillCount" : 11, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.5555556, "_score" : 580.225, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 } ], "status" : 200, "message" : "OK", "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 26984, "totalPages" : 540, "hasNext" : true, "hasPrevious" : false } }

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