{ "count" : 1312, "data" : [ { "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" : 958.3563, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "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. Work with operation teams", "postedDate" : "2026-06-11T20:28:45.502", "createdAt" : "2026-06-11T20:28:45.502", "lastUpdated" : "2026-06-14T22:15:22.228", "ingestTimestamp" : "2026-06-11T20:28:45.502", "mongoId" : "6a2a91a174d8ee00a068e9ce", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Process instrumentation calibration", "Temperature calibration", "Pressure calibration", "Flow calibration", "Humidity calibration", "Level calibration", "Density calibration", "Viscosity calibration", "pH analysis", "Conductivity analysis", "Control valve calibration", "Process instrumentation", "Calibration", "Documentation", "Interpersonal skills", "GMP", "FDA", "Maximo" ], "skillCount" : 18, "jobCategory" : "other", "jobSubcategory" : "calibrations---pharmaceutical-&-biologics-", "dataQualityScore" : 0.7777778, "_score" : 883.2597, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Pharmaceutical" }, { "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" : 861.4182, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "694ae67f70f0b99d589af818", "title" : "Reference Products Assistant (RML)(G6)", "company" : "IAEA Environment Laboratories", "industry" : "Government", "salary" : { "min" : 38000.0, "max" : 52000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level position in Monaco, adjusted for the government industry and the specific company." }, "location" : "Monaco-Monaco-Monaco-IAEA Environment Laboratories in Monaco", "locations" : [ "Monaco-Monaco-Monaco-IAEA Environment Laboratories in Monaco", "2026-01-07, 11:59:00 PM", "36, Fixed Term - 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" : 822.83386, "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" : 810.41895, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Manufacturing" }, { "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" : 742.35913, "daysOld" : 0, "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" : 733.0025, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Financial Services" }, { "id" : "6a15e47758b93c861e7c756a", "title" : "Laboratory Technician", "company" : "Hospitality Health ER", "industry" : "Healthcare", "salary" : { "min" : 38000.0, "max" : 52000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for an Entry-level Laboratory Technician in Longview, United States, within the Healthcare industry, adjusted for company size and full-time employment." }, "location" : "Longview, TX", "locations" : [ "Longview", "TX" ], "timestamp" : "2026-06-15T07:12:13.584", "fingerprint" : "c3d30beef38bdc04819b8a67b4ffcea53a68efbb4bbc71a5f72fb890b9a458f0", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://hospitality-health-er.breezy.hr/p/8f5ab494f357-laboratory-technician", "externalId" : "8f5ab494f357", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Longview", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.5007031,-94.7404900" } ], "locationText" : "Longview, Texas, United States", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Laboratory Operations", "Patient Testing", "Specimen Collection", "Quality Control", "Healthcare Operations" ], "coreResponsibilities" : "Support laboratory operations", "workSiteFlexibility" : "Onsite", "rawDescription" : "Laboratory Technician Location: Longview, TXEmployment Type: Full-TimeLaboratory Operations | Patient Testing | Specimen Collection | Quality Control | Healthcare Operations | Fast-Paced EnvironmentOverviewHospitality Health ER is seeking a Laboratory Technician to support laboratory operations w", "summaryDescription" : "Laboratory Technician at Hospitality Health ER. 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" : 732.22235, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a15e47758b93c861e7c7569", "title" : "Laboratory Technician", "company" : "Hospitality Health ER", "industry" : "Healthcare", "salary" : { "min" : 38000.0, "max" : 52000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for an Entry-level Laboratory Technician in Tyler, United States, within the Healthcare industry, adjusted for company size and specific location." }, "location" : "Tyler, TX", "locations" : [ "Tyler", "TX" ], "timestamp" : "2026-06-15T10:24:20.581", "fingerprint" : "c4f0b354e2b762662e57e0f8a83162a295c55bac831538d73acbeba80dcff99d", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://hospitality-health-er.breezy.hr/p/16d894b82ae7-laboratory-technician", "externalId" : "16d894b82ae7", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tyler", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.3512601,-95.3010624" } ], "locationText" : "Tyler, Texas, United States", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Laboratory Operations", "Patient Testing", "Specimen Collection", "Quality Control", "Healthcare Operations" ], "majorSkills" : "Laboratory Operations, Patient Testing, Specimen Collection, Quality Control", "majorSkillsList" : [ "Laboratory Operations", "Patient Testing", "Specimen Collection", "Quality Control" ], "coreResponsibilities" : "Support laboratory operations", "domainKnowledge" : "Healthcare; Laboratory", "domainList" : [ "healthcare", "laboratory" ], "domainSpecificKnowledge" : [ "Healthcare", "Laboratory" ], "specialRequirements" : "Fast-Paced Environment", "workSiteFlexibility" : "Onsite", "rawDescription" : "Laboratory Technician Location: Tyler, TXEmployment Type: Full-TimeLaboratory Operations | Patient Testing | Specimen Collection | Quality Control | Healthcare Operations | Fast-Paced EnvironmentOverviewHospitality Health ER is seeking a Laboratory Technician to support laboratory operations withi", "summaryDescription" : "Laboratory Technician at Hospitality Health ER. Skills: Laboratory Operations, Patient Testing, Specimen Collection, Quality Control. Support laboratory operations", "createdAt" : "2026-06-13T23:25:08.312", "lastUpdated" : "2026-06-15T10:24:20.581", "ingestTimestamp" : "2026-06-13T23:25:08.312", "mongoId" : "6a15e47758b93c861e7c7569", "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", "Healthcare", "Laboratory" ], "skillCount" : 7, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.7777778, "_score" : 729.6165, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c90fd74d8ee00a0981b02", "title" : "Laboratory Technician", "company" : "CareDx, Inc.", "industry" : "Healthcare", "salary" : { "min" : 345000.0, "max" : 435000.0, "currency" : "SEK", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Junior Laboratory Technician in Stockholm, Sweden, adjusted for the biotech industry and company size." }, "location" : "Stockholm, Sweden", "locations" : [ "Stockholm", "Sweden" ], "timestamp" : "2026-06-15T21:19:12.890", "fingerprint" : "d4df9c2bc5971028a91d0fb059af8d322f5169508b7d70a3163ab68d5e489501", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/caredxinc/jobs/4265134009", "externalId" : "4265134009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Stockholm", "country" : "Sweden", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "59.3251172,18.0710935" } ], "locationText" : "Stockholm, Sweden", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 1, "experienceMaxYears" : 3, "technicalSkills" : "QPCR, NGS", "professionalSkills" : [ "Molecular biology", "Product development" ], "hardSkillsList" : [ "Molecular biology techniques", "Process optimization" ], "hardSkills" : [ { "name" : "Molecular biology techniques", "level" : "intermediate" }, { "name" : "Process optimization", "level" : "intermediate" } ], "majorSkills" : "HLA typing, Molecular biology", "majorSkillsList" : [ "HLA typing", "Molecular biology" ], "coreResponsibilities" : "Perform in-process reagent qualification, Perform optimization testing, Analyze data, Document results, Perform tasks using molecular biology equipment, Perform tasks using manufacturing equipment, Perform inventory checks, Perform incoming controls", "domainKnowledge" : "Precision medicine; Transplant diagnostics; Genomics; HLA typing; Bone marrow matching; Organ transplantation", "domainList" : [ "precision-medicine", "transplant-diagnostics", "genomics", "hla-typing", "bone-marrow-matching", "organ-transplantation" ], "domainSpecificKnowledge" : [ "Precision medicine", "Transplant diagnostics", "Genomics", "HLA typing", "Bone marrow matching", "Organ transplantation" ], "toolProficiency" : [ "QPCR instrumentations", "NGS sequencers" ], "communicationSkills" : "English proficiency", "documentationSkills" : "Documentation", "problemSolvingSkills" : "Troubleshooting", "qualificationsBasic" : "1-3 years relevant experience, Bachelor's degree, Experience in lab/production, Experience in Molecular Biology, Experience in quality-controlled environment", "qualificationsPreferred" : "Experience in qPCR, Experience in NGS, Knowledge of Swedish, Background within HLA, Experience in GMP or similar, Exposure to molecular biology techniques", "workSiteFlexibility" : "Onsite", "rawDescription" : "CareDx, Inc. is a leading precision medicine solutions company focused on the discovery, development, and commercialization of clinically differentiated, high-value healthcare solutions for transplant patients and caregivers. CareDx offers products, testing services, and digital healthcare solutions along the pre- and post-transplant patient journey, and is the leading provider of genomics-based information for transplant patients. CareDx is looking for a new colleague for permanent employment as Lab technician working on HLA typing reagents in our Stockholm based Operations lab. The CareDx site based in Stockholm develops and manufactures HLA typing products for use with two different methods: qPCR and NGS technologies. The products are developed for both the European and the US markets and are used in transplantation for matching between recipients and donors. HLA typing is a standardized test for bone marrow and organ transplants; the better the match, the lower the complication risk after transplantation. Responsibilities: Main responsibilities will consist of the following laboratory and product line work: In-process reagent qualification Optimization testing, analysis and documentation Perform tasks using specialized molecular biology equipment (e. g. qPCR instrumentations or NGS sequencers) Perform tasks using equipment in the manufacturing facility Perform regular process tasks, such as inventory checks and incoming controls Other duties as assigned Qualifications: Demonstrated experience of working in a quality-controlled environment 1-3 years of relevant laboratory or production experience Bachelor’s degree in Molecular Biology, Biotechnology, or a related field Experience in a lab/production-related environment, specifically within a Molecular Biology field Experience of qPCR and/or NGS is advantageous Excellent knowledge of English and knowledge of Swedish is preferable A background within HLA is highly merited Experience working in a controlled or quality-regulated environment (e. g. GMP or similar), as well as exposure to molecular biology techniques such as qPCR and/or NGS, would be considered advantageous", "summaryDescription" : "Laboratory Technician at CareDx, Inc.. Skills: HLA typing, Molecular biology. Perform in-process reagent qualification. Perform optimization testing", "postedDate" : "2026-06-14T18:37:59.383", "createdAt" : "2026-06-14T18:37:59.383", "lastUpdated" : "2026-06-15T21:19:12.890", "ingestTimestamp" : "2026-06-14T18:37:59.383", "mongoId" : "6a2c90fd74d8ee00a0981b02", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Molecular biology techniques", "Process optimization", "HLA typing", "Molecular biology", "Product development", "Precision medicine", "Transplant diagnostics", "Genomics", "Bone marrow matching", "Organ transplantation", "QPCR instrumentations", "NGS sequencers" ], "skillCount" : 12, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Junior", "dataQualityScore" : 0.8888889, "_score" : 726.47406, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "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" : 719.1555, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2eb32974d8ee00a0e7dd66", "title" : "Reference Data Services Analyst", "company" : "Citi", "salary" : { "min" : 75000.0, "max" : 105000.0, "currency" : "PLN", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Reference Data Services Analyst in Poland, adjusted for the banking industry and entry-level experience." }, "location" : "Poland", "locations" : [ "Poland" ], "timestamp" : "2026-06-15T21:49:50.191", "fingerprint" : "84dce4df11a47d2f1e910d60836ca80f3fffd05e7474b2644eb78c73863aeecb", "source" : "workday", "language" : "en", "applyUrl" : "https://citi.wd5.myworkdayjobs.com/2/job/Olsztyn--Poland/Reference-Data-Services-Analyst_26968000", "externalId" : "26968000", "industryFunction" : { }, "locationPoint" : "51.9194,19.1451", "structuredLocations" : [ { "country" : "Poland", "continent" : "eu", "workMode" : "hybrid" } ], "locationText" : "Poland", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "Entry", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Are you looking for a career move that will put you at the heart of a global financial institution? Then bring your skills in analysis, problem solving and communication to Citi’s Corporate Actions Team. By Joining Citi, you will become part of a global organisation whose mission is to serve as a trusted partner to our clients by responsibly providing financial services that enable growth and economic progress. **Team/Role Overview** The Reference Data Services Analyst is a developing professional role responsible for applying specialized knowledge in the monitoring, assessment, analysis, and evaluation of data and operational processes. This individual plays a key part in ensuring data integrity and optimizing organizational procedures. **What you’ll do:** * Complete all mandatory reports in a timely manner and to required standard * Perform daily operations related to the creation, modification, and deletion of reference data (e.g., securities, legal entities, counterparties, market data). * Ensure data accuracy, completeness, and consistency by adhering to established data governance policies and procedures. * Validate data inputs against source documents and internal systems, identifying and resolving discrepancies. * Collaborate with various internal stakeholders, including Front Office, Middle Office, Back Office, Risk Management, and Technology teams, to address reference data requirements and issues. * Participate in testing for system enhancements, upgrades, and new data initiatives. * **Working on shift:** Shift based schedule, 8 hour shifts, starts at 9:00-17:00 and 15:00-23:00**(cover for EMEA and NAM)** **What we’ll need from you:** * Bachelor's degree preferred * 0-2 years of related job experience * Good awareness of client needs/expectations * Proficient in MS Office * Proven success as a team player * **Excellent command of English (both written and spoken) is required, along with strong communication skills** **What we can offer you** By joining Citi Solutions Center Poland, you will not only be part of a business casual workplace with a hybrid working model (up to 2 days working at home per week), but also receive a competitive base salary (which is annually reviewed) and enjoy a whole host of additional benefits such as: * Private Medical Care Program * Life Insurance Program * Pension Plan contribution (PPE Program) * Employee Assistance Program * Paid Parental Leave Program (maternity and paternity leave) * Sport Card * Holidays Allowance * Sport and team recreation activities * Special offers and discounts for employees * Access to an array of learning and development resources * A discretional annual performance related bonus * A chance to make a difference with various affinity networks and charity initiatives Alongside these benefits Citi is committed to ensuring our workplace is where everyone feels comfortable coming to work as their whole self every day. We want the best talent around the world to be energized to join us, motivated to stay, and empowered to thrive. **Sounds like Citi has everything you need? Then apply to discover the true extent of your capabilities.** #LI-KG1 \\------------------------------------------------------ ## **Job Family Group:** Operations - Services \\------------------------------------------------------ ## **Job Family:** Reference Data Services \\------------------------------------------------------ ## **Time Type:** Full time \\------------------------------------------------------ ## **Primary Location Full Time Salary Range:** zł62,070.00 - zł90,630.00 \\------------------------------------------------------ ## **Most Relevant Skills** Please see the requirements listed above. \\------------------------------------------------------ ## **Other Relevant Skills** For complementary skills, please see above and/or contact the recruiter. \\------------------------------------------------------ ## **Automated Processing and AI** We use automated processing, including artificial intelligence, for our legitimate business interests (or our reasonable and appropriate business purposes) to identify and align the candidate's skills and abilities with a specific job opening. Additionally, if you so choose, or consent, we can match your skills and abilities to other suitable roles at Citi. Importantly, all our hiring processes and decisions, including determining your suitability for a role, are conducted, checked, and decided by individuals. Our automated processing and AI do not involve relying on automatic or autonomous decision-making. Please refer to any Jurisdictional Considerations, with specific provisions for your country (where relevant) for further details. \\------------------------------------------------------ _This job opening is for an existing job vacancy._ \\------------------------------------------------------ _Citi is an equal opportunity employer, and qualified candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law._ __ _If you are a person with a disability and need a reasonable accommodation to use our search tools and/or apply for a career opportunity review_ _[Accessibility at Citi](https://www.citigroup.com/citi/accessibility/application-accessibility.htm)._ _View Citi’s[EEO Policy Statement](https://www.citigroup.com/global/eeo-aa-policy) and the [Know Your Rights](https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12ScreenRdr.pdf) poster._", "summaryDescription" : "Reference Data Services Analyst at Citi", "postedDate" : "2026-06-11T21:04:47.335", "createdAt" : "2026-06-14T21:04:47.331", "lastUpdated" : "2026-06-15T21:49:50.191", "ingestTimestamp" : "2026-06-14T21:04:47.331", "mongoId" : "6a2eb32974d8ee00a0e7dd66", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://citi.wd5.myworkdayjobs.com/2/job/Olsztyn--Poland/Reference-Data-Services-Analyst_26968000", "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 705.18756, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Banking", "llmIndustryConfidence" : 0.95 }, { "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. 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Act as auditor", "postedDate" : "2026-06-11T16:45:25.971", "createdAt" : "2026-06-11T16:45:25.971", "lastUpdated" : "2026-06-13T08:39:44.844", "ingestTimestamp" : "2026-06-11T16:45:25.971", "mongoId" : "6a2a64ce74d8ee00a062785b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Accuracy", "Speed", "Operational mastery", "Excellence oversight", "Strategic support", "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", "Fintech", "Fraud detection", "Machine learning models", "odash" ], "skillCount" : 21, "jobCategory" : "other", "jobSubcategory" : "idv-ops", "dataQualityScore" : 1.0, "_score" : 705.14716, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true }, { "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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Bring-up hardware", "postedDate" : "2026-06-13T16:05:31.952", "createdAt" : "2026-06-13T16:05:31.952", "lastUpdated" : "2026-06-15T05:49:27.587", "ingestTimestamp" : "2026-06-13T16:05:31.952", "mongoId" : "693c2b9270f0b99d58440136", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.com/jobs/3137687/apply", "salaryAnnualMin" : 166400, "salaryAnnualMax" : 287700, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Antenna calibration", "Beampattern measurement", "Simulation", "Data storage", "Hardware test automation", "Firmware design", "Application development", "Design automation", "Bring up tools", "Leadership", "Mentoring", "Coaching", "Software development", "Hardware integration", "System design", "Hardware engineering", "Software design", "System performance", "High-volume manufacturing", "Phased array antennas", "LEO satellites", "Broadband access", "ASIC design", "RF Hardware", "Chip to chip communication" ], "skillCount" : 25, "jobCategory" : "engineering", "dataQualityScore" : 1.0, "_score" : 694.951, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology" }, { "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. 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TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

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Responsible for performing routine and specialized technical analyses, operating and maintaining instrumentation, and exercising independent judgement in recognizing and solving test related problems.", "problemSolvingSkills" : "test related problems", "specialRequirements" : "Must be currently licensed as a Medical Technologist by the State of Florida Department of Health. 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. Shift differential eligible.", "qualificationsBasic" : "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.", "qualificationsPreferred" : "Molecular experience preferred.", "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. Shift differential eligible 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.   Molecular experience preferred.    Tampa", "summaryDescription" : "Medical Laboratory Scientist at Tampa General Hospital. Skills: Molecular experience. 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, operating and maintaining instrumentation, and exercising independent judgement in recognizing and solving test related problems.", "createdAt" : "2026-06-14T17:30:18.754", "lastUpdated" : "2026-06-15T10:20:39.368", "ingestTimestamp" : "2026-06-14T17:30:18.754", "mongoId" : "69cf26132beec4dd3d90b5ce", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "hasSalary" : false, "allSkills" : [ "Medical Technologist", "independent judgement", "Molecular experience", "Esoteric Molecular Laboratory" ], "skillCount" : 4, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "_score" : 691.62427, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "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" : 669.90063, "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" : 668.2739, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Consulting", "llmIndustryConfidence" : 0.85 }, { "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" : 655.6664, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "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. 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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. 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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. 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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. 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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" : 646.64685, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Aerospace" }, { "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" : 645.0622, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "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. 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: "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" ], 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"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" : 633.2367, "daysOld" : 5, "hasLocation" : true, "hasGeo" : true }, { "id" : "69cf26122beec4dd3d90b40b", "title" : "Laboratory Assistant- Microbiology", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 37000.0, "max" : 48000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level Laboratory Assistant in Tampa, Florida, 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

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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. 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Eur., JP, Sterilization standards", "professionalSkills" : [ "Risk assessment", "Process design", "Trend analysis", "Resource planning", "Performance management", "Staff training", "Parametric release", "Alternative release" ], "hardSkillsList" : [ "Microbiological control", "Environmental monitoring", "Contamination control", "Aseptic process", "Sterility assurance", "Bioburden testing", "Root cause analysis", "CAPA implementation", "Radiation safety" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Microbiological control", "level" : "intermediate" }, { "name" : "Environmental monitoring", "level" : "intermediate" }, { "name" : "Contamination control", "level" : "intermediate" }, { "name" : "Aseptic process", "level" : "intermediate" }, { "name" : "Sterility assurance", "level" : "intermediate" }, { "name" : "Bioburden testing", "level" : "intermediate" }, { "name" : "Root cause analysis", "level" : "intermediate" }, { "name" : "CAPA implementation", "level" : "intermediate" }, { "name" : "Radiation safety", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Microbiological control, Aseptic manufacturing, Regulatory compliance, Radiopharmaceuticals", "majorSkillsList" : [ "Microbiological control", "Aseptic manufacturing", "Regulatory compliance", "Radiopharmaceuticals" ], "coreResponsibilities" : "Lead microbiology team, Supervise daily lab operations, Plan resources, Manage workload, Manage performance, Drive continuous training, Oversee aseptic process design, Oversee aseptic process simulation, Evaluate changes, Establish environmental monitoring, Maintain environmental monitoring, Analyze environmental monitoring, Perform trend analysis, Conduct contamination risk assessments, Maintain Contamination Control Strategy, Monitor cleanroom operations, Ensure GMP compliance, Ensure best aseptic practices, Ensure effective microbiological controls, Act as SME for regulations, Lead contamination event investigations, Lead root cause analysis, Implement CAPA, Implement process improvements, Work with cross-functional teams, Oversee EM for radiopharmaceuticals, Oversee bioburden for radiopharmaceuticals, Oversee sterility assurance for radiopharmaceuticals, Advise on interventions in isolators/hot cells, Ensure contamination control solutions, Design sampling plans for radiopharmaceuticals, Supervise sampling plans for radiopharmaceuticals", "teamCollaboration" : "Cross-functional teams; Quality; Engineering; Production; Validation", "domainKnowledge" : "Radioconjugates; Precision medicines; Aseptic manufacturing; Sterile radiopharmaceutical products; Radiopharmaceutical suites; Shielded isolators; Hot cells; Short half-life products", "domainList" : [ "radioconjugates", "precision-medicines", "aseptic-manufacturing", "sterile-radiopharmaceutical-products", "radiopharmaceutical-suites", "shielded-isolators", "hot-cells", "short-half-life-products" ], "domainSpecificKnowledge" : [ "Radioconjugates", "Precision medicines", "Aseptic manufacturing", "Sterile radiopharmaceutical products", "Radiopharmaceutical suites", "Shielded isolators", "Hot cells", "Short half-life products" ], "problemSolvingSkills" : "Root cause analysis", "specialRequirements" : "Work extended shifts, Work weekends, Work holidays, After-hours support, On-site presence, <5% travel", "qualificationsBasic" : "Bachelor's degree in Microbiology, 5–8 years supervising laboratory teams, Hands-on environmental monitoring, Contamination control experience, Cleanroom operations experience, Regulatory compliance experience, Work in designated labs, Work in isolators/hot cells", "qualificationsPreferred" : "Experience in radiopharmaceutical environments", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Fusion Pharmaceuticals, a member of the AstraZeneca Group, is a clinical-stage oncology company focused on developing next generation radioconjugates (RCs) as precision medicines. 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. 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USF Health Morsani Center AHC (AMGMCAH)
13330 USF Laurel Dr.

Tampa, 33612

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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" : 623.2086, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "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" : 623.0626, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "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. 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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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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. Support doctor's diagnosis", "postedDate" : "2026-06-10T07:27:04.000", "createdAt" : "2026-06-14T07:23:38.599", "lastUpdated" : "2026-06-15T09:26:36.265", "ingestTimestamp" : "2026-06-14T07:23:38.599", "mongoId" : "6a2c619b74d8ee00a08f4e9d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Hematology examination", "Chemistry examination", "Serology examination", "Urine examination", "Feces examination", "Body fluid examination", "Laboratory examinations", "Data entry", "Equipment maintenance", "Service standards", "Data release", "Preventive maintenance", "Quality services", "Safety services", "Hematology", "Chemistry", "Serology", "Urine analysis", "Feces analysis", "Body fluid analysis" ], "skillCount" : 20, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Entry", "dataQualityScore" : 1.0, "_score" : 596.7893, "daysOld" : 5, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a4a1b74d8ee00a05e7764", "title" : "Laboratory Technician", "company" : "Siloam Hospitals Group", "industry" : "Hospital And Health Care", "salary" : { "min" : 6.5E7, "max" : 9.5E7, "currency" : "IDR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an Entry-level Laboratory Technician in Bekasi, Indonesia, adjusted for the healthcare industry and company size." }, "location" : "Bekasi, Jawa Barat, ID", "locations" : [ "Bekasi, Jawa Barat", "ID" ], "timestamp" : "2026-06-14T23:30:44.992", "fingerprint" : "eeb31683dd06d5d8ce33f5844053b305c52a45339fba5a7172ef42cb363f998b", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/SiloamCareers/6000000001143945-laboratory-technician", "externalId" : "6000000001143945", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bekasi", "state" : "Jawa Barat", "country" : "Indonesia", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "-6.2349858,106.9945444" } ], "locationText" : "Bekasi, Jawa Barat, Indonesia", "employmentType" : "FULL_TIME", "minimumEducation" : "Vocational High School", "experienceLevel" : "not-applicable", "professionalSkills" : [ "Health Analyst" ], "hardSkillsList" : [ "Laboratory examinations", "Hematology", "Chemistry", "Serology", "Urine analysis", "Feces analysis", "Body fluid analysis", "Data entry", "Data release", "Equipment maintenance", "Reagent procurement" ], "hardSkills" : [ { "name" : "Laboratory examinations", "level" : "intermediate" }, { "name" : "Hematology", "level" : "intermediate" }, { "name" : "Chemistry", "level" : "intermediate" }, { "name" : "Serology", "level" : "intermediate" }, { "name" : "Urine analysis", "level" : "intermediate" }, { "name" : "Feces analysis", "level" : "intermediate" }, { "name" : "Body fluid analysis", "level" : "intermediate" }, { "name" : "Data entry", "level" : "intermediate" }, { "name" : "Data release", "level" : "intermediate" }, { "name" : "Equipment maintenance", "level" : "intermediate" }, { "name" : "Reagent procurement", "level" : "intermediate" } ], "majorSkills" : "Laboratory examinations, Data entry, Equipment maintenance", "majorSkillsList" : [ "Laboratory examinations", "Data entry", "Equipment maintenance" ], "coreResponsibilities" : "Carry out laboratory examinations, Carry out hematology examinations, Carry out chemistry examinations, Carry out serology examinations, Carry out urine examinations, Carry out feces examinations, Carry out body fluid examinations, Perform data entry into system, Carry out data release of examination results, Prioritize reporting of CITO examination results, Prioritize reporting of CCU examination results, Prioritize reporting of critical condition examination results, Record usage of equipment, Make requests for equipment, Carry out preventive maintenance activities, Record storage of examination results, Organize storage of examination results, Record procurement of reagents, Record receipt of reagents, Record use of reagents, Organize procurement of reagents, Organize receipt of reagents, Organize use of reagents, Collect required data for operational activities, Make reports related to operational activities, Implement procedures for quality services, Implement practices for quality services, Implement procedures for safety services, Implement practices for safety services, Attend training, Collect data for hospital indicators, Make reports for hospital indicators, Collect data for department targets, Make reports for department targets", "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" ], "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! 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. 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" : 596.39355, "daysOld" : 4, "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" : 596.01544, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "id" : "69dde45b2beec4dd3d9a3ec2", "title" : "Director, Biobank Laboratory Operations", "company" : "City of Hope", "salary" : { "min" : 215000.0, "max" : 315000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Director, Biobank Laboratory Operations in Duarte, CA, adjusted for industry and company size." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Laboratory Research", "Onsite, Days, Days" ], "timestamp" : "2026-06-15T21:15:39.015", "fingerprint" : "ec77a3813f4050f959289e1fc88f962a8e0ed754e89f8610b88bc87e17aafd05", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=231604", "externalId" : "231604", "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" : "PhD", "experienceMinYears" : 7, "experienceLevel" : "Director", "remoteFriendly" : false, "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 Director of Biobank Laboratory Operations opportunity is available at City of Hope. This is a senior leadership role responsible for providing scientific, operational, and strategic direction for the Henderson Biorepository’s laboratory enterprise across City of Hope. This position partners closely with institutional leaders, researchers, and external collaborators to support biorepository growth, ensure operational scalability, and advance biospecimen ‑ based research initiatives. The Director plays a key role in business planning, service expansion, integration of biorepository functions, and fostering a collaborative, high ‑ performance laboratory culture while upholding quality standards and alignment with the Henderson Biorepository’s mission. As a successful candidate, you will: Laboratory Operations Provide scientific and operational leadership for Henderson Biorepository laboratory operations, including biospecimen collection and processing, Standard Operating Procedures (SOPs) and protocol oversight, process validation, quality control, regulatory compliance, and College of American Pathologist (CAP) biobank accreditation efforts. Serve as the laboratory subject matter expert, supporting IRB protocols, integrating biorepository operations across City of Hope, leading capital equipment and automation initiatives, and collaborating with internal stakeholders and external partners. Biospecimen Research and Teaching Partner with the Scientific Director to expand biospecimen research programs, establish external collaborations, support grant funding efforts, and promote Henderson Biorepository services. Contribute to academic and training programs by teaching biospecimen best practices to COH’s graduate students and supporting workforce development. Budget and Revenue Management Oversee laboratory budgets, expenditures, contracts, service pricing, and vendor agreements to ensure financial stewardship and 100% cost recovery. Ensure appropriate Non-Disclosure Agreements (NDAs), Master Service Agreements (MSAs), and contractual frameworks are in place to support external partnerships and revenue ‑ generating services. Informatics and Data Management Collaborate with Research Informatics and leadership to ensure accurate biospecimen data management within LabVantage and other laboratory information systems. Maintain high standards of data integrity and documentation to support research quality, compliance, and operational efficiency. People Leadership and Development Lead, mentor, and develop a high ‑ performing laboratory team, promoting collaboration, technical excellence, and professional growth. Support staff training across a broad range of biospecimen collection, processing, and preservation techniques. Your qualifications should include: PhD degree in biology, immunology, molecular biology, biochemistry, pathology or a related discipline. 7+ years of hands-on industry or academia experience with collecting and processing human whole blood, histology tissue processing, organoid preparation, nuclei acid extraction, peripheral blood mononuclear cells (PBMCs) isolation and cryopreservation, aseptic technique, and automated cell and liquid processing platforms. 5 years of experience at a managerial level. Required certification/licensure: IATA certification (within 6 months of hire) Preferred qualifications: Familiarity with GLP guidelines and CLIA certification 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" : "Director, Biobank Laboratory Operations at City of Hope", "createdAt" : "2026-06-14T21:52:22.708", "lastUpdated" : "2026-06-15T21:15:39.015", "ingestTimestamp" : "2026-06-14T21:52:22.708", "mongoId" : "69dde45b2beec4dd3d9a3ec2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 215000, "salaryAnnualMax" : 315000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.7777778, "_score" : 594.39746, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c5ca574d8ee00a08d8512", "title" : "UK Laboratory Administrator", "company" : "TFP", "industry" : "Admin / Others", "salary" : { "min" : 24000.0, "max" : 30000.0, "currency" : "GBP", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Laboratory Administrator in Nottingham, UK, adjusted for the healthcare industry and company size." }, "location" : "Nottingham, England, United Kingdom", "locations" : [ "Nottingham, England, United Kingdom" ], "timestamp" : "2026-06-15T08:57:36.017", "fingerprint" : "4d1fab335270eec1b1ea6fc46a01bc074ed9ad3edaa399edaac8545bb6fe14f8", "source" : "recruitee", "language" : "en", "applyUrl" : "https://tfpfertilitygroup.recruitee.com/o/uk-laboratory-administrator-1/c/new", "externalId" : "2635789", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Nottingham", "country" : "United Kingdom", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "52.9534193,-1.1496461" } ], "locationText" : "Nottingham, United Kingdom", "employmentType" : "FULL_TIME", "minimumEducation" : "bachelor's degree", "experienceMinYears" : 1, "experienceLevel" : "experienced", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Record-keeping", "Sample transportation administration", "Storage fees management", "Consent management", "Regulatory compliance" ], "hardSkills" : [ { "name" : "Record-keeping", "level" : "intermediate" }, { "name" : "Sample transportation administration", "level" : "intermediate" }, { "name" : "Storage fees management", "level" : "intermediate" }, { "name" : "Consent management", "level" : "intermediate" }, { "name" : "Regulatory compliance", "level" : "intermediate" } ], "majorSkills" : "Process management, Patient support, Regulatory compliance", "majorSkillsList" : [ "Process management", "Patient support", "Regulatory compliance" ], "coreResponsibilities" : "Manage transportation database, Maintain transportation records, Coordinate sample imports, Coordinate sample exports, Process transport invoices, Liaise with patients for transport, Liaise with clinics for transport, Liaise with couriers for transport, Verify consent documentation, Verify infection screening documentation, Verify compliance documentation, Complete transport checklists, Update patient records, Support patients with courier arrangements, Support patients with self-transport, Monitor storage fees, Contact patients regarding storage fees, Contact patients regarding consent expiry, Chase outstanding payments, Chase consent decisions, Issue statutory notices, Process consent documentation, Update records for laboratory teams, Liaise with laboratory teams, Provide sensitive support to patients, Follow SOPs, Follow policies, Follow risk assessments, Report non-conformities, Support audits, Support risk assessments, Contribute to continuous improvement, Contribute to patient-focused service, Ensure confidentiality, Complete internal training, Maintain up-to-date knowledge, Support onboarding new team members, Support training new team members, Communicate professionally with patients, Communicate professionally with stakeholders, Communicate empathetically with patients, Communicate empathetically with stakeholders, Maintain accurate documentation, Maintain timely documentation, Maintain traceable documentation, Collaborate effectively across teams", "teamCollaboration" : "Collaborate across teams", "domainKnowledge" : "HFEA Code of standards; Gamete transportation; Embryo transportation; Fertility treatments; Sample storage", "domainList" : [ "hfea-code-of-standards", "gamete-transportation", "embryo-transportation", "fertility-treatments", "sample-storage" ], "domainSpecificKnowledge" : [ "HFEA Code of standards", "Gamete transportation", "Embryo transportation", "Fertility treatments", "Sample storage" ], "communicationSkills" : "Explain complex information; Explain sensitive information", "documentationSkills" : "Record-keeping; Documentation management", "continuousLearning" : "Internal training; Maintain knowledge", "specialRequirements" : "Weekend working rotation, Satisfactory criminal record check", "qualificationsBasic" : "College-level education, 1 year healthcare administrative experience, Excellent record-keeping skills, High attention to detail, Multitasking and prioritisation abilities, Flexible, self-motivated approach, Excellent communication skills, Ability to explain complex information, Right to work, Satisfactory criminal record check", "qualificationsPreferred" : "Degree in relevant subject, Experience in IVF clinic, Knowledge of gamete/embryo transportation, Ability to review blood results, Ability to review HFEA consent forms, Experience managing consent expiries", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At TFP, we make families. We shape fertility journeys around people’s lives. Our commitment to outstanding customer experience is demonstrated every day; through genuine care, building trust, sharing our expertise, driving innovation, and showing our passion in all that we do. The Role: UK Laboratory Administrators play a vital role in shaping each patient’s fertility journey. This position supports laboratory functions across the UK, helping to coordinate the safe and timely transportation of gametes and embryos between clinics, guiding patients through the annual storage fee process, and ensuring consents for stored samples are managed with absolute care. Every step in this work must be completed in full alignment with TFP’s unified SOPs and the HFEA Code of Practice; standards that protect patients, ensure regulatory compliance, and uphold the integrity of our laboratories. Because these processes directly impact patients’ hopes, plans, and stored reproductive material, exceptional attention to detail is essential. The post holder must be able to self-manage effectively, staying organised, prioritising tasks confidently, and maintaining accuracy even in a busy and sensitive environment. Above all, the role requires clear, compassionate communication. You will guide patients through complex and sometimes emotional decisions, ensuring they feel supported, informed, and cared for at every stage This is a full-time position working 37.5 hours per week Weekend working is required on rotation of 1:4 The Location: Our UK Lab Admin team is based within our TFP Nurture Fertility clinic. Offering a full suite of treatment and diagnostic services, including PGT. Conveniently located on the outskirts of Nottingham, adjacent to junction 25 of the M1, there is ample free parking for staff and patients at the front of the building. Key Responsibilities: Sample Transportation Administration * Manage and maintain transportation database and records * Coordinate sample imports/exports within required timeframes * Ensure transport invoices are processed prior to shipment * Liaise with patients, clinics, and couriers to arrange transport * Verify consent, infection screening, and compliance documentation * Complete transport checklists and update patient records * Support patients with courier arrangements or self-transport * Ensure all activities follow SOPs and regulatory requirements Storage Fees & Consent Management * Monitor and contact patients regarding storage fees and consent expiry * Chase outstanding payments and consent decisions * Issue statutory notices and process consent documentation * Update records and liaise with laboratory teams as needed * Provide sensitive support to patients making decisions about stored samples * Escalate non-compliance or legal concerns Quality & Compliance * Follow SOPs, policies, and risk assessments to ensure safe practice * Report non-conformities and support audits and risk assessments * Contribute to continuous improvement and patient-focused service * Ensure compliance with regulatory standards and confidentiality requirements Training & Development * Complete internal training and maintain up-to-date knowledge * Support onboarding and training of new team members Communication * Communicate professionally and empathetically with patients and stakeholders * Maintain accurate, timely, and traceable documentation * Collaborate effectively across teams Confidentiality * Handle all patient and company information in line with data protection regulations ## Requirements Qualifications and Experience: Essential * College-level education * Minimum 1 year’s experience in a healthcare administrative role * Excellent record-keeping skills * High attention to detail * Strong multitasking and prioritisation abilities * Flexible, self-motivated approach * Excellent communication skills * Ability to explain complex and sensitive information to patients * Right to work in the country of application * Satisfactory criminal record check Desirable * Degree in a relevant subject * Experience in an IVF clinic * Knowledge of transportation of gametes/embryos * Ability to review blood results and/or HFEA consent forms * Experience managing consent expiries Location: TFP Nurture Fertility - Nottingham Salary: Competitive (Depending on experience) Working Hours: 37.5 Hours per week Monday to Friday between the hours of 08.00-18.00 Saturday working required on 1:4 rotation Pension: Dual contribution pension scheme Holiday Entitlement: 27 Days + Bank holidays (pro rata) Free parking available on site", "summaryDescription" : "UK Laboratory Administrator at TFP. Skills: Process management, Patient support, Regulatory compliance. Manage transportation database. Maintain transportation records", "postedDate" : "2026-06-10T15:56:11.000", "createdAt" : "2026-06-14T05:56:15.953", "lastUpdated" : "2026-06-15T08:57:36.017", "ingestTimestamp" : "2026-06-14T05:56:15.953", "mongoId" : "6a2c5ca574d8ee00a08d8512", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "<30k", "hasSalary" : false, "allSkills" : [ "Record-keeping", "Sample transportation administration", "Storage fees management", "Consent management", "Regulatory compliance", "Process management", "Patient support", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Resource planning", "Continuous improvement", "HFEA Code of standards", "Gamete transportation", "Embryo transportation", "Fertility treatments", "Sample storage" ], "skillCount" : 17, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Junior", "dataQualityScore" : 1.0, "_score" : 592.87646, "daysOld" : 4, "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" : 591.19617, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Automotive", "llmIndustryConfidence" : 0.92 }, { "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" : 588.7684, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "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" : 588.4396, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "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" : 585.82513, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "69fc49954c40e2acd1a829a0", "title" : "Lab Assistant - Laboratory Services", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 34000.0, "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 and hospital size." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

" ], "timestamp" : "2026-06-15T13:25:27.217", "fingerprint" : "488ecbada240401e86d81437d5dba777ab40e4ccfa80fe0bead4ca9cd007a76f", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=677864", "externalId" : "677864", "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", "domainKnowledge" : "Laboratory testing; Biological safety; CAP", "domainList" : [ "laboratory-testing", "biological-safety", "cap" ], "domainSpecificKnowledge" : [ "Laboratory testing", "Biological safety", "CAP" ], "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 Previous work as a laboratory assistant is preferred Tampa", "summaryDescription" : "Lab Assistant - Laboratory Services at Tampa General Hospital", "createdAt" : "2026-06-14T06:51:58.424", "lastUpdated" : "2026-06-15T13:25:27.217", "ingestTimestamp" : "2026-06-14T06:51:58.424", "mongoId" : "69fc49954c40e2acd1a829a0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 34000, "salaryAnnualMax" : 45000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Laboratory testing", "Biological safety", "CAP" ], "skillCount" : 3, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.6666667, "_score" : 583.4407, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "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" : 583.184, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Consumer Goods" }, { "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" : 581.91266, "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" : 581.1969, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "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" : 580.5531, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "llmIndustryConfidence" : 0.95 }, { "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" : 578.71045, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "69cf26132beec4dd3d90b58f", "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 and 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" : "2026-06-15T12:48:09.699", "fingerprint" : "2d8ce820f90296d48be4ad38b879977d883a3b210ffd143789317ae22478c429", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=633111", "externalId" : "633111", "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 Bachelor's Degree Biology Or Bachelor's Degree Chemistry License/Registration- Issued by Florida or Compact State 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" : "2026-06-14T08:25:18.379", "lastUpdated" : "2026-06-15T12:48:09.699", "ingestTimestamp" : "2026-06-14T08:25:18.379", "mongoId" : "69cf26132beec4dd3d90b58f", "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" : 578.70953, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 } ], "status" : 200, "message" : "OK", "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 1312, "totalPages" : 27, "hasNext" : true, "hasPrevious" : false } }

Maintaining Calibration Laboratory Reference Standards Jobs in New York

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