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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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USF Health Morsani Center AHC (AMGMCAH)
13330 USF Laurel Dr.

Tampa, 33612

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TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

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Please note, the purpose of this posting is to recruit for on-going and future positions. Clinical Laboratory Scientist I - Blood Bank (Full Time, Days) 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 Blood Bank Laboratory opportunity for a Clinical Laboratory Scientist I position at City of Hope, located in Duarte, California. This is a full time 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. 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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" : 900.38837, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a1a5cd658b93c861e80fa69", "title" : "Clinical Laboratory Scientist Lead - Clinical Research", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 115500.0, "max" : 165000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Clinical Laboratory Scientist in Duarte, CA, adjusted for the healthcare industry and company size." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Clinical Laboratory/Pathology", "Onsite, Days, Days" ], "timestamp" : "2026-06-15T11:39:41.135", "fingerprint" : "aff187099fb7c1f1548ce5a27986c9409625e964c1c631b47a6703c20914407b", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=235665", "externalId" : "235665", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Duarte", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.1394513,-117.9772873" } ], "locationText" : "Duarte, California, United States", "minimumEducation" : "Bachelor's Degree", "experienceMinYears" : 8, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "professionalSkills" : [ "Test system analysis", "Troubleshooting", "Regulatory proficiency", "Staff development", "Technical resource" ], "hardSkillsList" : [ "Specimen processing", "Laboratory testing", "Equipment operation", "Result reporting", "Quality control", "Quality assurance", "Performance improvement", "Reagent preparation" ], "hardSkills" : [ { "name" : "Specimen processing", "level" : "intermediate" }, { "name" : "Laboratory testing", "level" : "intermediate" }, { "name" : "Equipment operation", "level" : "intermediate" }, { "name" : "Result reporting", "level" : "intermediate" }, { "name" : "Quality control", "level" : "intermediate" }, { "name" : "Quality assurance", "level" : "intermediate" }, { "name" : "Performance improvement", "level" : "intermediate" }, { "name" : "Reagent preparation", "level" : "intermediate" } ], "majorSkills" : "Clinical laboratory testing, Quality assurance, Regulatory compliance", "majorSkillsList" : [ "Clinical laboratory testing", "Quality assurance", "Regulatory compliance" ], "coreResponsibilities" : "Prepare specimens, Perform clinical laboratory testing, Maintain technical proficiency, Perform quality control, Perform quality assurance, Perform performance improvement, Troubleshoot technical issues, Resolve technical issues, Prepare reagents, Prepare materials, Ensure proper documentation, Follow safety protocols, Uphold integrity standards, Uphold customer service standards, Draft laboratory policies, Revise laboratory policies, Validate laboratory policies, Ensure policy compliance, Draft SOPs, Revise SOPs, Validate SOPs, Ensure SOP compliance, Draft accreditation requirements, Revise accreditation requirements, Validate accreditation requirements, Ensure accreditation compliance, Lead validation of new instruments, Support validation of new instruments, Lead validation of new reagents, Support validation of new reagents, Analyze inspections, Participate in inspections, Analyze proficiency testing, Participate in proficiency testing, Analyze regulatory readiness, Participate in regulatory readiness, Oversee workflow, Oversee scheduling, Oversee staff competency, Oversee quality performance indicators, Identify improvement opportunities, Support departmental operations", "teamCollaboration" : "Laboratory personnel; Laboratory leadership", "domainKnowledge" : "Clinical laboratory testing; FACT; AABB; ACHI; CAP; FDA; Joint Commission; CLIA 1988", "domainList" : [ "clinical-laboratory-testing", "fact", "aabb", "achi", "cap", "fda", "joint-commission", "clia-1988" ], "domainSpecificKnowledge" : [ "Clinical laboratory testing", "FACT", "AABB", "ACHI", "CAP", "FDA", "Joint Commission", "CLIA 1988" ], "documentationSkills" : "Proper documentation", "problemSolvingSkills" : "Troubleshooting", "qualificationsBasic" : "High-complexity clinical laboratory testing, FACT compliance, AABB compliance, ACHI compliance, CAP compliance, FDA compliance, Joint Commission compliance, CLIA 1988 compliance", "qualificationsPreferred" : "Continued growth in test system analysis, Continued growth in troubleshooting, Continued growth in regulatory proficiency", "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. This role involves preparing specimens and performing waived to high‑complexity clinical laboratory testing in full compliance with SOPs and all major regulatory standards, including FACT, AABB, ACHI, CAP, FDA, and Joint Commission requirements. The position supports education by assisting in training students and staff, while also demonstrating continued growth in test system analysis, troubleshooting, and regulatory proficiency. It requires a strong understanding of section operations, contributions to staff development and future testing needs, and serving as a technical resource for laboratory personnel and leadership. All work is performed under the authorization of the Laboratory Director in accordance with CLIA 1988 (CFR 493.1445(a)). As a successful candidate, you will: Maintain strong technical proficiency in specimen processing, laboratory testing, equipment operation, and accurate result reporting. Perform and document quality control, quality assurance, and performance improvement activities, including troubleshooting and resolving complex technical issues. Prepare reagents and materials, ensure proper documentation, follow safety protocols, and uphold high standards of integrity and customer service. Draft, revise, validate, and ensure compliance of laboratory policies, procedures, SOPs, and accreditation requirements. Lead or support validation of new instruments, reagents, and tests; analyze data; and participate in inspections, proficiency testing, and regulatory readiness. Oversee workflow, scheduling, staff competency, and quality performance indicators while identifying improvement opportunities and supporting departmental operations. Your qualifications should include: Bachelor’s Degree Minimum 5 years as a certified or licensed clinical laboratory scientist Clinical Laboratory Scientist 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 Lead - Clinical Research at City of Hope. Skills: Clinical laboratory testing, Quality assurance, Regulatory compliance. Prepare specimens. Perform clinical laboratory testing", "createdAt" : "2026-06-14T06:26:43.012", "lastUpdated" : "2026-06-15T11:39:41.135", "ingestTimestamp" : "2026-06-14T06:26:43.012", "mongoId" : "6a1a5cd658b93c861e80fa69", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 115500, "salaryAnnualMax" : 165000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Specimen processing", "Laboratory testing", "Equipment operation", "Result reporting", "Quality control", "Quality assurance", "Performance improvement", "Reagent preparation", "Clinical laboratory testing", "Regulatory compliance", "Test system analysis", "Troubleshooting", "Regulatory proficiency", "Staff development", "Technical resource", "FACT", "AABB", "ACHI", "CAP", "FDA", "Joint Commission", "CLIA 1988" ], "skillCount" : 22, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Lead", "dataQualityScore" : 0.7777778, "_score" : 889.72266, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c7ea474d8ee00a0953118", "title" : "Laboratory Technician", "company" : "Headlands Research", "industry" : "Healthcare", "salary" : { "min" : 23.0, "max" : 27.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "San Diego, California, United States", "locations" : [ "San Diego", "California", "United States" ], "timestamp" : "2026-06-15T07:06:46.783", "fingerprint" : "a904e8f2dd0621e78737d2ffd318d13e0b98e581b80b6bf006175f96e431f9dc", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/headlandsresearch/jobs/4278330009", "externalId" : "4278330009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "San Diego", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.7174202,-117.1627720" } ], "locationText" : "San Diego, California, United States", "employmentType" : "FULL_TIME", "technicalSkills" : "Phlebotomy", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Specimen collection", "Specimen processing" ], "hardSkills" : [ { "name" : "Specimen collection", "level" : "intermediate" }, { "name" : "Specimen processing", "level" : "intermediate" } ], "majorSkills" : "Lab operations, Clinical research, Patient care", "majorSkillsList" : [ "Lab operations", "Clinical research", "Patient care" ], "coreResponsibilities" : "Lead lab operations, Collect specimens, Process specimens, Organize lab, Maintain lab environment, Manage lab inventory, Manage lab supplies, Prepare kits", "teamCollaboration" : "Coordination with study teams; Interaction with participants; Interaction with providers; Interaction with sponsors", "domainKnowledge" : "Clinical trial delivery; Research protocols; Regulatory standards; Patient care procedures", "domainList" : [ "clinical-trial-delivery", "research-protocols", "regulatory-standards", "patient-care-procedures" ], "domainSpecificKnowledge" : [ "Clinical trial delivery", "Research protocols", "Regulatory standards", "Patient care procedures" ], "toolProficiency" : [ "Excel", "Outlook", "EMRs" ], "continuousLearning" : "Professional development opportunities; Career growth opportunities", "qualificationsBasic" : "Geriatric experience, Medical terminology familiarity, Basic laboratory procedures familiarity, Lab equipment comfort, Regulated processes comfort, Basic computer systems proficiency, Multiple electronic data entry systems comfort", "qualificationsPreferred" : "Clinical research experience, Specimen processing experience, Specimen shipping experience, Lab inventory experience, Interest in Clinical Research Coordinator role, Interest in lab leadership role", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion. Location: San Diego, CA | \uD83C\uDFE5 Site Name: Artemis Institute for Clinical Research | \uD83D\uDD52 Full-Time | \uD83E\uDDEA Clinical Research We’re seeking a Laboratory Technician/Phlebotomist for our clinical research site Artemis Institute for Clinical Research located in San Diego, CA. As a Laboratory Technician, you won’t just be supporting research—you’ll be helping shape the future of healthcare. This is an exciting opportunity for individuals who are ready to grow their skillset and income potential within the clinical research field. \uD83D\uDCBC The Role: If you’re an experienced phlebotomist who enjoys being the go-to person in the lab—and you’re ready for more ownership, variety, and growth—this role is designed for you. This isn’t just a draw-and-go position. You’ll take the lead on lab operations within a clinical research environment, managing everything from specimen collection and processing to lab organization, compliance, and coordination with study teams. You’ll play a critical role in advancing clinical trials while building skills that go far beyond traditional phlebotomy—including exposure to research protocols, regulatory standards, and broader patient care procedures. Type: Regular Full-time Employee Schedule: M/Th 8 AM-5 PM | Tu/W/F: 7AM-3 PM Pay Range: $23-27/hr *Dependent upon relevant experience, certification, and education. Location: Onsite in San Diego, CA (no capabilities for remote or hybrid work) Reports to: Site Director Benefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more. \uD83C\uDF1FWhat We Offer Competitive pay + annual performance incentives Medical, dental, and vision insurance 401(k) plan with company match Paid time off (PTO) and company holidays Opportunities for professional development and career growth A mission-driven culture focused on advancing medicine and improving patient outcomes Responsibilities: Own the Lab Operations: Take the lead on day-to-day lab activities, ensuring everything runs smoothly, safely, and on schedule. Maintain a clean, organized, and inspection-ready lab environment. Manage lab inventory, supplies, and kit preparation across multiple studies. Perform geriatric experience a plus Familiarity with medical terminology and basic laboratory procedures Comfort working with lab equipment, documentation, and regulated processes Strong attention to detail and ability to manage multiple responsibilities at once Proficiency with basic computer systems (Excel, Outlook, EMRs, or similar tools) Comfortable using multiple electronic data entry systems A team-first mindset with a willingness to jump in wherever needed Strong attention to detail, time management, and ability to work in a fast-paced, regulated environment Excellent interpersonal skills—you’ll be interacting with participants, providers, and sponsors Passion for improving patient outcomes through research Bonus points for: Clinical research experience Experience handling specimen processing, shipping, or lab inventory Interest in growing into a Clinical Research Coordinator or lab leadership role Why This Role Stands Out More responsibility than a typical phlebotomy role—you’ll help run the lab, not just support it Exposure to clinical research, opening doors to long-term career growth Skill expansion into patient care, research operations, and regulatory processes Clear path for advancement into coordinator or specialized research roles Ready for What’s Next? If you’re looking to move beyond a traditional phlebotomy role and take on more ownership in a fast-paced, purpose-driven environment, we’d love to connect. Apply today and take the next step in growing your career within clinical research. California Pay Range $23—$27 USD Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind. Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Need Assistance? Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.", "summaryDescription" : "Laboratory Technician at Headlands Research. Skills: Lab operations, Clinical research, Patient care. Lead lab operations. Collect specimens", "postedDate" : "2026-06-13T20:38:05.869", "createdAt" : "2026-06-13T20:38:05.869", "lastUpdated" : "2026-06-15T07:06:46.783", "ingestTimestamp" : "2026-06-13T20:38:05.869", "mongoId" : "6a2c7ea474d8ee00a0953118", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 47840, "salaryAnnualMax" : 56160, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Specimen collection", "Specimen processing", "Lab operations", "Clinical research", "Patient care", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Resource planning", "Continuous improvement", "Clinical trial delivery", "Research protocols", "Regulatory standards", "Patient care procedures", "Excel", "Outlook", "EMRs" ], "skillCount" : 18, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.8888889, "_score" : 889.244, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "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. 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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" : 858.3247, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "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" : 838.4884, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2a8bb974d8ee00a0683a52", "title" : "Laboratory Engineer II", "company" : "University of Rochester", "salary" : { "min" : 60431.0, "max" : 84603.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-13T06:42:33.262", "fingerprint" : "d09eca9b572df30e52aa9a27d2a87a2c1ebd140dcd7af32611569c47e32adc67", "source" : "workday", "language" : "en", "applyUrl" : "https://rochester.wd5.myworkdayjobs.com/UR_Staff/job/Laboratory-for-Laser-Energetics/Laboratory-Engineer-II_R272093", "externalId" : "R272093", "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Rochester", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.1572850,-77.6152140" } ], "locationText" : "Rochester, New York, United States", "employmentType" : "FULL_TIME", "technicalSkills" : "MATLAB, Python, Excel", "professionalSkills" : [ "Technical evaluation", "System performance evaluation", "Laser development" ], "hardSkillsList" : [ "Data analysis", "Technical data processing", "Test planning", "Documentation" ], "softSkillsList" : [ "Adaptability", "Attention to detail", "Organizational skills" ], "hardSkills" : [ { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Technical data processing", "level" : "intermediate" }, { "name" : "Test planning", "level" : "intermediate" }, { "name" : "Documentation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Adaptability" }, { "name" : "Attention to detail" }, { "name" : "Organizational skills" } ], "majorSkills" : "Laser system operation, Data analysis, Laboratory testing", "majorSkillsList" : [ "Laser system operation", "Data analysis", "Laboratory testing" ], "coreResponsibilities" : "Operate FLUX laser system, Perform engineering analysis, Support laser development, Evaluate system performance, Ensure system safety, Collect technical data, Process technical data, Interpret technical data, Identify trends, Identify anomalies, Identify performance improvements, Conduct laboratory testing, Conduct field-testing, Support validation activities, Support verification activities, Develop standard operating procedures, Maintain standard operating procedures, Develop test plans, Maintain test plans, Support laser upgrade projects, Support software development", "teamCollaboration" : "Collaborate with scientists; Collaborate with engineers; Collaborate with technicians; Cross-functional teams", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Laser systems; FLUX laser system", "domainList" : [ "laser-systems", "flux-laser-system" ], "domainSpecificKnowledge" : [ "Laser systems", "FLUX laser system" ], "toolProficiency" : [ "Oscilloscopes", "Diagnostic tools" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Documentation", "problemSolvingSkills" : "Analytical skills; Problem-solving skills", "specialRequirements" : "Work shift assignments, Evening hours", "outcomesObjectives" : "Identify trends; Identify anomalies; Identify performance improvements", "qualificationsBasic" : "Bachelor’s degree in STEM field, 2 years of relevant experience", "qualificationsPreferred" : "Hands-on experience using oscilloscopes, Experience with data analysis tools, Prior experience in a laboratory or manufacturing environment", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive. _**Job Location (Full Address):**_ 250 East River Rd, Rochester, New York, United States of America, 14623 _**Opening:**_ Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 250548 LLE-Laboratory for Laser Energ Work Shift: UR - Day (United States of America) Range: UR URG 110 Compensation Range: $60,431.00 - $84,603.00 _The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job 's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._ _**Responsibilities:**_ LE is seeking a detail-oriented and analytical engineer to support FLUX operations through data-driven analysis, technical evaluation, and hands-on operation and testing. This role is ideal for a candidate with a strong STEM background who enjoys problem-solving, working with technical equipment, and collaborating across engineering teams. The successful candidate must be willing to work shift assignments 1–2 times per week, including evening hours, to support operational needs and testing schedules. **ESSENTIAL FUNCTIONS** * Complete qualification and stand watch in operation of the FLUX laser system * Perform engineering analysis to support laser development, system performance evaluation, operational activities and ensure system safety * Collect, process, and interpret technical data to identify trends, anomalies, and performance improvements * Conduct laboratory and field-testing using equipment such as oscilloscopes and other diagnostic tools * Support validation and verification activities through structured test planning and documentation * Develop and maintain standard operating procedures and test plans to provide clear direction for technicians and operators * Collaborate with cross-functional teams including scientists, engineers, and technicians * Support laser upgrade projects and software development. Will have responsibility over minor aspects under the direction of a project manager. **MINIMUM EDUCATION & EXPERIENCE** * Bachelor’s degree in STEM field and 2 years of relevant experience required * Hands-on experience using oscilloscopes and electronic test equipment preferred * Experience with data analysis tools (e.g., MATLAB, Python, Excel, or similar platforms) preferred * Prior experience in a laboratory or manufacturing environment preferred **KNOWLEDGE, SKILLS AND ABILITIES** * Strong analytical and problem-solving skills required * Ability to interpret technical drawings and schematics required * Willingness and ability to work evening shifts up to 2 times per week required * Strong written and verbal communication skills required * Attention to detail * Strong organizational skills * Ability to work independently and in a team environment * Adaptability to shifting priorities and schedules The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.", "summaryDescription" : "Laboratory Engineer II at University of Rochester. Skills: Laser system operation, Data analysis, Laboratory testing. Operate FLUX laser system. 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Pay: $17.50 - $20.90 per hour DOE Schedule: <20hours per week, as-needed (depending on coverage needs) Benefits: 401(K) with discretionary employer match Free clinical diagnostic laboratory testing performed in house In this role, you will: Coordinate timely and efficient transportation of medical specimens and supplies. Provide excellent customer service to clients and employees. Maintain cleanliness and perform maintenance on company vehicles and transport devices. Ensure compliance with confidentiality and HIPAA regulations. Document operations and complete necessary reports. Assist with training and communication among couriers and relevant departments. Maintain consistent, punctual, and reliable attendance to ensure continuity of operations and support for our team and patients. Education & Certification: High School Diploma or equivalent Experience: Strong preference for candidates with previous driving/courier experience Licensing & Driving Requirements: Valid, unrestricted driver’s license Clean driving record Skills & Competencies: Navigation, punctuality, and ability to follow detailed instructions Ability to drive in inclement weather General Physical Requirements: Frequent lifting up to 30 lbs. Occasional lifting of 30-60 lbs. Ability to enter and exit assigned vehicle. Able to sit in vehicle/drive for up to 4 hours nonstop. Ability to load & unload assigned vehicle, with frequent bending involved. Ability to wear personal protective equipment as needed. Regularly handle potentially infectious samples. Ability to drive assigned vehicle in all types of conditions, including built-up areas, freeway, and rural traffic, hours of darkness, and inclement weather. May be exposed to odorous chemicals and specimens. Occasional-to-regular kneeling, bending, stooping and twisting to perform vehicle inspections and minor operator maintenance, including changing tires. OHSA Category: This position performs tasks that involve exposure to blood, body fluids and/or tissues. All 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 Washington State Pay Range $17.50—$20.90 USD", "summaryDescription" : "Courier (Medical Specimen) at Interpath Laboratory. Skills: Specimen transportation, Customer service, Compliance. Coordinate specimen transportation. Coordinate supply transportation", "postedDate" : "2026-06-14T08:56:38.999", "createdAt" : "2026-06-14T08:56:38.999", "lastUpdated" : "2026-06-15T08:48:30.159", "ingestTimestamp" : "2026-06-14T08:56:38.999", "mongoId" : "6a2ca57374d8ee00a09b68c2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 35360, "salaryAnnualMax" : 41600, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Medical specimen transport", "Vehicle maintenance", "Specimen transportation", "Customer service", "Compliance", "Navigation", "HIPAA regulations" ], "skillCount" : 7, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "_score" : 794.6357, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ae9db74d8ee00a072ce43", "title" : "Medical Laboratory Technician", "company" : "The E-verify Program", "industry" : "Healthcare", "salary" : { "min" : 38000.0, "max" : 55000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Medical Laboratory Technician in the United States, adjusted for part-time employment and the healthcare industry." }, "location" : "United States of America", "locations" : [ "United States of America" ], "certifications" : [ "Medical Laboratory Technician by ASCP Board of Certification (BOC) or equivalent" ], "timestamp" : "2026-06-14T22:55:53.701", "fingerprint" : "f989a05bf0497837f1b2bf213cc89a2a5c78e8514781a860940c3e3dbb561dac", "source" : "workday", "language" : "en", "applyUrl" : "https://musc.wd1.myworkdayjobs.com/MUSC/job/MUSC-Health-Bluffton-Medical-Pavilion/Medical-Laboratory-Technician_R-0000063160-1", "externalId" : "R-0000063160", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "country" : "United States", "continent" : "na", "workMode" : "onsite" } ], "locationText" : "United States", "employmentType" : "PART_TIME", "minimumEducation" : "Associate's", "experienceMinYears" : 1, "hardSkillsList" : [ "Specimen preparation", "Automated laboratory instrumentation", "Quality control", "Quality assurance" ], "hardSkills" : [ { "name" : "Specimen preparation", "level" : "intermediate" }, { "name" : "Automated laboratory instrumentation", "level" : "intermediate" }, { "name" : "Quality control", "level" : "intermediate" }, { "name" : "Quality assurance", "level" : "intermediate" } ], "majorSkills" : "Medical laboratory testing, Specimen preparation, Quality control", "majorSkillsList" : [ "Medical laboratory testing", "Specimen preparation", "Quality control" ], "coreResponsibilities" : "Perform diagnostic medical lab tests, Prepare specimens for testing, Operate laboratory instrumentation, Perform quality control procedures, Record lab results, Follow privacy procedures, Follow safety procedures, Follow biohazard procedures", "domainKnowledge" : "Medical laboratory technology; Diagnostic testing protocols", "domainList" : [ "medical-laboratory-technology", "diagnostic-testing-protocols" ], "domainSpecificKnowledge" : [ "Medical laboratory technology", "Diagnostic testing protocols" ], "toolProficiency" : [ "Automated laboratory instrumentation" ], "documentationSkills" : "Record lab results", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "Associates degree in Medical Laboratory Technology, Certification as a Medical Laboratory Technician by ASCP Board of Certification (BOC) or equivalent, More than one year of clinical experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Job Description Summary** Performs a variety of routine and specialized diagnostic medical lab tests as requested by healthcare staff according to established protocols and procedures. Prepares specimens for microscopic examination or testing procedures. Operates automated laboratory instrumentation and equipment. Performs quality control and assurance procedures. Records lab results in specified system. Follows all required privacy, safety, and biohazard procedures and standards. **Entity** Medical University Hospital Authority (MUHA) **Worker Type** Employee **Worker Sub-Type** Regular **Cost Center** CC005753 CHS – Lab - Bluffton Medical Pavilion (Offsite) **Pay Rate Type** Hourly **Pay Grade** Health-24 **Scheduled Weekly Hours** 24 **Work Shift** **Job Description** Education: Associates degree in Medical Laboratory Technology. Certification as a Medical Laboratory Technician by ASCP Board of Certification (BOC) or equivalent. Work Experience: More than one year of clinical experience. **Additional Job Description** Education: Associates degree in Medical Laboratory Technology. Experience: At least one year of clinical experience. Certification: Certification as a Medical Laboratory Technician by ASCP Board of Certification (BOC) or equivalent. NOTE: _This is a Career Ladder Position. Internal candidates are required to submit and meet Path and Lab ICCE Career Ladder requirements. External candidates are required to complete Path and Lab ICCE Career Ladder requirements within 90 days in position._ _If you like working with energetic enthusiastic individuals, you will enjoy your career with us!_ The Medical University of South Carolina is an Equal Opportunity Employer. MUSC does not discriminate on the basis of race, color, religion or belief, age, sex, national origin, gender identity, sexual orientation, disability, protected veteran status, family or parental status, or any other status protected by state laws and/or federal regulations. All qualified applicants are encouraged to apply and will receive consideration for employment based upon applicable qualifications, merit and business need. Medical University of South Carolina participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: [http://www.uscis.gov/e-verify/employees](http://www.uscis.gov/e-verify/employees)", "summaryDescription" : "Medical Laboratory Technician at The E-verify Program. Skills: Medical laboratory testing, Specimen preparation, Quality control. Perform diagnostic medical lab tests. Prepare specimens for testing", "postedDate" : "2026-06-09T03:36:19.276", "createdAt" : "2026-06-12T03:36:19.199", "lastUpdated" : "2026-06-14T22:55:53.701", "ingestTimestamp" : "2026-06-12T03:36:19.199", "mongoId" : "6a2ae9db74d8ee00a072ce43", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://musc.wd1.myworkdayjobs.com/MUSC/job/MUSC-Health-Bluffton-Medical-Pavilion/Medical-Laboratory-Technician_R-0000063160-1", "salaryAnnualMin" : 38000, "salaryAnnualMax" : 55000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Specimen preparation", "Automated laboratory instrumentation", "Quality control", "Quality assurance", "Medical laboratory testing", "Medical laboratory technology", "Diagnostic testing protocols", "Medical Laboratory Technician by ASCP Board of Certification (BOC) or equivalent" ], "skillCount" : 8, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 789.0951, "daysOld" : 5, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare" }, { "id" : "6a2ebf8074d8ee00a0e9ac89", "title" : "Specimen Accessioner", "company" : "Labcorp", "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-15T06:49:34.038", "fingerprint" : "cbcc748153347eb03f2884efaa000428c82b28b369a7857e928da9a9ee387ec0", "source" : "workday", "applyUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Salt-Lake-City-UT/Specimen-Accessioner--Part-Time--2nd-Shift_2618192", "externalId" : "2618192", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Salt Lake City", "state" : "Utah", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "Salt Lake City, Utah, United States", "employmentType" : "PART_TIME", "minimumEducation" : "High School", "experienceMinYears" : 1, "experienceMaxYears" : 3, "experienceLevel" : "Junior", "hardSkillsList" : [ "handling human biological specimens", "prepare biological specimens", "verify patient demographic information", "data entry", "pack and ship specimens", "prepare and store excess specimen samples", "resolve and document problem specimens" ], "softSkillsList" : [ "attention to detail, work independently, team environment" ], "hardSkills" : [ { "name" : "handling human biological specimens", "level" : "intermediate" }, { "name" : "prepare biological specimens", "level" : "intermediate" }, { "name" : "verify patient demographic information", "level" : "intermediate" }, { "name" : "data entry", "level" : "intermediate" }, { "name" : "pack and ship specimens", "level" : "intermediate" }, { "name" : "prepare and store excess specimen samples", "level" : "intermediate" }, { "name" : "resolve and document problem specimens", "level" : "intermediate" } ], "softSkills" : [ { "name" : "attention to detail, work independently, team environment" } ], "majorSkills" : "Specimen Processing, Data Entry, Attention to Detail, Specimen Handling", "majorSkillsList" : [ "Specimen Processing, Data Entry, Attention to Detail, Specimen Handling" ], "coreResponsibilities" : "Introduce and prepare biological specimens to the laboratory to ensure accurate processing. Verify patient demographic information matches the test requisition form submitted. Data entry of patient information into the computer system for tracking purposes. Meet key production metrics and quality measures to ensure timely and accurate results. Unpack and route specimens to their respective staging areas. Pack and ship specimens to proper testing facilities when required. Properly prepare and store excess specimen samples. Resolve and document any problem specimens. Operate automated instrumentation under supervision if necessary.", "teamCollaboration" : "Ability to work both independently and in a team environment.", "toolProficiency" : [ "computer skills, typing skills" ], "communicationSkills" : "written communication; verbal communication", "documentationSkills" : "document problem specimens", "problemSolvingSkills" : "problem solve", "specialRequirements" : "Able to pass a standardized color blindness test. Ability to lift up to 30lbs, work in protective equipment and sit/stand for long periods of time. Eye hand coordination in order to accurately identify specimens by touch and sight.", "outcomesObjectives" : "Meet key production metrics and quality measures to ensure timely and accurate results.", "qualificationsBasic" : "High School Diploma or GED equivalent. Proficient computer and typing skills. Able to pass a standardized color blindness test. Comfortable handling human biological specimens including blood, urine and tissue samples. Ability to lift up to 30lbs, work in protective equipment and sit/stand for long periods of time. Eye hand coordination in order to accurately identify specimens by touch and sight.", "qualificationsPreferred" : "Current or prior Labcorp experience. 1 year or more of experience in the healthcare industry, such as a physician's office, clinic or hospital. 1 year of experience in an assembly or manufacturing production environment. 1 year or more of experience in a medical/clinical laboratory experience.", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Labcorp is seeking a Specimen Processor to join our team in Salt Lake City, UT. **Work Schedule:** 8pm-12 am Monday -Friday. 2nd shift differential. **Specimen Processor Responsibilities:** * Introduce and prepare biological specimens to the laboratory to ensure accurate processing * Verify patient demographic information matches the test requisition form submitted * Data entry of patient information into the computer system for tracking purposes * Meet key production metrics and quality measures to ensure timely and accurate results * Unpack and route specimens to their respective staging areas * Pack and ship specimens to proper testing facilities when required * Properly prepare and store excess specimen samples * Resolve and document any problem specimens * Operate automated instrumentation under supervision if necessary **Minimum Qualification:** * High School Diploma or GED equivalent **Preferred Qualification:** * Current or prior Labcorp experience * 1 year or more of experience in the healthcare industry, such as a physician's office, clinic or hospital * 1 year of experience in an assembly or manufacturing production environment * 1 year or more of experience in a medical/clinical laboratory experience **Additional Job Standards:** * Proficient computer and typing skills * Able to pass a standardized color blindness test * Comfortable handling human biological specimens including blood, urine and tissue samples * Ability to lift up to 30lbs, work in protective equipment and sit/stand for long periods of time * Strong eye hand coordination in order to accurately identify specimens by touch and sight * Ability to work both independently and in a team environment * High level of attention to detail with the ability to problem solve * Strong communication skills; both written and verbal At Labcorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step! **Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please [click here](https://careers.labcorp.com/global/en/us-rewards-and-wellness). **Labcorp is proud to be an Equal Opportunity Employer:** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our [accessibility site](https://careers.labcorp.com/global/en/accessibility) or contact us at [Labcorp Accessibility.](mailto:Disability_apply@LabCorp.com) For more information about how we collect and store your personal data, please see our [Privacy Statement](https://www.labcorp.com/about/web-privacy-policy).", "summaryDescription" : "Specimen Accessioner at Labcorp. Skills: Specimen Processing, Data Entry, Attention to Detail, Specimen Handling. Introduce and prepare biological specimens to the laboratory to ensure accurate processing. Verify patient demographic information matches the test requisition form submitted. Data entry of patient information into the computer system for tracking purposes. Meet key production metrics and quality measures to ensure timely and accurate results. Unpack and route specimens to their resp", "postedDate" : "2026-06-10T21:15:11.128", "createdAt" : "2026-06-14T21:15:11.104", "lastUpdated" : "2026-06-15T06:49:34.038", "ingestTimestamp" : "2026-06-14T21:15:11.104", "mongoId" : "6a2ebf8074d8ee00a0e9ac89", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Salt-Lake-City-UT/Specimen-Accessioner--Part-Time--2nd-Shift_2618192", "hasSalary" : false, "allSkills" : [ "handling human biological specimens", "prepare biological specimens", "verify patient demographic information", "data entry", "pack and ship specimens", "prepare and store excess specimen samples", "resolve and document problem specimens", "attention to detail, work independently, team environment", "Specimen Processing, Data Entry, Attention to Detail, Specimen Handling", "computer skills, typing skills" ], "skillCount" : 10, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 785.9816, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ebf8074d8ee00a0e9ac8b", "title" : "Clinical Laboratory Technologist", "company" : "LabCorp", "location" : "United States of America", "locations" : [ "United States of America" ], "certifications" : [ "ASCP", "AMT" ], "timestamp" : "2026-06-15T10:13:41.446", "fingerprint" : "31395285e798ac5773952569f072b323184b2b87b1abbc774bcdad1c77b38813", "source" : "workday", "applyUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Bartlesville-OK/Clinical-Laboratory-Technologist_2615389", "externalId" : "2615389", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Bartlesville", "state" : "Oklahoma", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "Bartlesville, Oklahoma, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor", "experienceMinYears" : 1, "experienceMaxYears" : 2, "experienceLevel" : "Junior", "professionalSkills" : [ "Clinical lab science." ], "softSkillsList" : [ "attention to detail, organizational skills" ], "softSkills" : [ { "name" : "attention to detail, organizational skills" } ], "majorSkills" : "clinical laboratory testing, instrumentation, quality control", "majorSkillsList" : [ "clinical laboratory testing, instrumentation, quality control" ], "coreResponsibilities" : "The Clinical Laboratory Technologist determines specimen acceptability, performs routine and complex technical procedures, and operates/troubleshoots instrumentation. This role involves preparing and testing reagents, reporting accurate test results for patient care, and performing preventive maintenance and quality control. The technologist also manages testing bench supplies, maintains a safe work environment, and assists with specimen processing as needed.", "teamCollaboration" : "Ability to work independently and within a team environment.", "toolProficiency" : [ "laboratory information systems" ], "communicationSkills" : "communication skills", "documentationSkills" : "Standard Operating Procedures", "continuousLearning" : "If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!", "problemSolvingSkills" : "technical decisions", "specialRequirements" : "In lieu of education requirements listed above, non-traditional degrees with applicable science credits that meet CLIA standards may meet education requirement.", "qualificationsBasic" : "Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology, or an MLS degree. 1 year or more of clinical laboratory testing experience. Proficient with computers. Able to pass a standardized color blindness test.", "qualificationsPreferred" : "ASCP or AMT certification. Familiarity with laboratory information systems. Flexibility to work overtime or other shifts depending on business needs.", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**LabCorp is seeking a Clinical Lab Professional to join our team at****Ascension St. John Jane Phillips, Bartlesville, OK**. **Work Schedule:** 3 x 12 hour shifts, Monday - Friday, 6:30 PM - 7:00 AM, rotating weekends and holidays. **Job Responsibilities:** * Determine the acceptability of specimens for testing according to established criteria * Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures * Monitor, operate and troubleshoot instrumentation to ensure proper functionality * Demonstrate the ability to make technical decisions regarding testing and problem solving. * Prepare, test and evaluate new reagents or controls * Report accurate and timely test results in order to deliver quality patient care * Perform and document preventive maintenance and quality control procedures * Identify and replenish testing bench supplies as necessary * Assist with processing of specimens when needed * Maintain a safe work environment and wear appropriate personal protective equipment **Minimum Qualifications:** * Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology * 1 year or more of clinical laboratory testing experience OR an MLS degree **Preferred Qualifications:** * ASCP or AMT certification **Additional Job Standards:** * In lieu of education requirements listed above, non-traditional degrees with applicable science credits that meet CLIA standards may meet education requirement * Ability to work independently and within a team environment * Familiarity with laboratory information systems * Proficient with computers * High level of attention detail along with strong communication and organizational skills * Able to pass a standardized color blindness test * Flexibility to work overtime or other shifts depending on business needs At Labcorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step!**This role works in a high volume, production based environment performing a vital component of clinical lab science.** **Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please [click here](https://careers.labcorp.com/global/en/us-rewards-and-wellness). _**If you 're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!**_ **Labcorp is proud to be an Equal Opportunity Employer:** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our [accessibility site](https://careers.labcorp.com/global/en/accessibility) or contact us at [Labcorp Accessibility.](mailto:Disability_apply@LabCorp.com) For more information about how we collect and store your personal data, please see our [Privacy Statement](https://www.labcorp.com/about/web-privacy-policy).", "summaryDescription" : "Clinical Laboratory Technologist at LabCorp. Skills: clinical laboratory testing, instrumentation, quality control. The Clinical Laboratory Technologist determines specimen acceptability, performs routine and complex technical procedures, and operates/troubleshoots instrumentation. This role involves preparing and testing reagents, reporting accurate test results for patient care, and performing preventive maintenance and quality control. The technologist also manages testing bench supplies, mai", "postedDate" : "2026-06-10T20:59:08.207", "createdAt" : "2026-06-14T20:59:08.157", "lastUpdated" : "2026-06-15T10:13:41.446", "ingestTimestamp" : "2026-06-14T20:59:08.157", "mongoId" : "6a2ebf8074d8ee00a0e9ac8b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Bartlesville-OK/Clinical-Laboratory-Technologist_2615389", "hasSalary" : false, "allSkills" : [ "attention to detail, organizational skills", "clinical laboratory testing, instrumentation, quality control", "Clinical lab science.", "ASCP", "AMT", "laboratory information systems" ], "skillCount" : 6, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 778.71045, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2641b774d8ee00a02140f1", "title" : "Medical Laboratory Technician (MLT)", "company" : "Bon Secours", "industry" : "Healthcare", "salary" : { "min" : 45000.0, "max" : 65000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Medical Laboratory Technician in Emporia, United States, adjusted for the healthcare industry and part-time employment." }, "location" : "Emporia, VA", "locations" : [ "Emporia, VA", "United States of America" ], "certifications" : [ "MLT Medical Laboratory Technician Certification" ], "timestamp" : "2026-06-12T17:05:04.971", "fingerprint" : "e548539aa9e5f55dfe14c1b38262f33e2cc9be47f96ef24c310dbb06a9702ed3", "source" : "workday", "language" : "en", "applyUrl" : "https://wd5.myworkdaysite.com/recruiting/easyservice/BonSecoursCareers/job/Emporia-VA/Medical-Laboratory-Technician-I--MLT----Southern-Virginia-Regional-Medical-Center---PRN_R277116", "externalId" : "R277116", "industryFunction" : { }, "locationPoint" : "36.68598,-77.54248", "structuredLocations" : [ { "city" : "Emporia", "state" : "Virginia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "36.6937606,-77.5357141" } ], "locationText" : "Emporia, Virginia, United States", "employmentType" : "PART_TIME", "minimumEducation" : "Associate's", "professionalSkills" : [ "Laboratory techniques" ], "hardSkillsList" : [ "Performing analytical tests", "Quality control", "Troubleshooting laboratory equipment" ], "hardSkills" : [ { "name" : "Performing analytical tests", "level" : "intermediate" }, { "name" : "Quality control", "level" : "intermediate" }, { "name" : "Troubleshooting laboratory equipment", "level" : "intermediate" } ], "majorSkills" : "Medical laboratory testing, Patient safety", "majorSkillsList" : [ "Medical laboratory testing", "Patient safety" ], "coreResponsibilities" : "Perform analytical tests on biological specimens, Determine acceptability of specimens, Recognize factors that affect measurements and results, Perform quality control for all testing, Maintain a safe and efficient work environment, Perform equipment checks, Clean work area, Monitor temperatures, Troubleshoot laboratory equipment", "domainKnowledge" : "Patient safety; Laboratory techniques", "domainList" : [ "patient-safety", "laboratory-techniques" ], "domainSpecificKnowledge" : [ "Patient safety", "Laboratory techniques" ], "problemSolvingSkills" : "Troubleshoot laboratory equipment", "outcomesObjectives" : "Provide physicians with quality results", "qualificationsBasic" : "MLT Medical Laboratory Technician Certification or eligible", "qualificationsPreferred" : "Two years of technical experience in a clinical laboratory setting", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Thank you for considering a career at Bon Secours!** **Scheduled Weekly Hours:** 0.01 **Work Shift: ** All Work Shifts (United States of America) **Bon Secours** ** __About Us__** As a faith-based and patient-focused organization, Bon Secours exists to enhance the health and well-being of all people in mind, body and spirit through exceptional patient care. Success in this goal requires a culture of compassion, collaboration, excellence and respect. Bon Secours seeks people that are committed to our values of compassion, human dignity, integrity, service and stewardship to create an environment where associates want to work and help communities thrive. **Medical Laboratory Technician I (MLT) – Southern Virginia Regional Medical Center** **Job Summary:** The Medical Laboratory Technician I (MLT) is responsible for performing the routine test on blood, tissues, and other body specimens, as well as providing physicians with quality results using a variety of clinical laboratory equipment. The Medical Laboratory Technician I (MLT) must have a total understanding of patient safety and laboratory techniques necessary to guarantee complete patient safety and anonymity. **Essential Functions:** * Performs analytical tests on biological specimens, in a timely, efficient, and accurate manner in compliance with documented laboratory procedures * Determines acceptability of specimens by performing visual inspections or by recognizing abnormal/ unusual results * Recognizes factors that affect measurements and results by taking the appropriate action according to protocols * Performs quality control for all testing and meets established ranges before patient results are released * Maintains a safe and efficient work environment by performing equipment checks, cleaning work area, monitoring temperatures following hospital policies, and troubleshoots laboratory equipment * Other duties as assigned **Education:** * Must have **one** of the following: * Associates of Science in Medical Lab Technology * Completed 60 semester hours (including six hours of chemistry and six of biology) of academic credit from a college or university accredited by a recognized regional or national accreditation agency and have completed a Medical Lab Technician Program * Completed a 50-week U.S. military medical laboratory training course within the past ten years **Certifications:** * MLT Medical Laboratory Technician Certification or eligible by a nationally recognized certification agency (preferably ASCP) (required) **Experience:** * Two years of technical experience in a clinical laboratory setting (preferred) **Skills & Abilities:** * Ability to provide quality, error-free work in a fast-pasted environment * Engage with staff and patients in a professional manner Bon Secours is an equal opportunity employer. As a [Bon Secours](https://careers.bonsecours.com/us/en/life-at-bon-secours?utm_source=job_description) associate, you’re part of a Mission that matters. We support your well-being – personally and professionally. Our benefits are built to grow with you and meet your unique needs, every step of the way. **What we offer** * Competitive pay, incentives, referral bonuses and 403(b) with employer contributions (when eligible) * Medical, dental, vision, prescription coverage, HSA/FSA options, life insurances, mental health resources and discounts * Paid time off, parental and FMLA leave, short- and long-term disability, backup care for children and elders * Tuition assistance, professional development and continuing education support _Benefits may vary based on the market and employment status._ **Department:** Core Laboratory - Virginia RMC - Richmond _It is our policy to abide by all Federal and State laws, as well as, the requirements of 41 CFR 60-1.4(a), 60-300.5(a) and 60-741.5(a). Accordingly, all applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, sexual orientation, gender identity, age, genetic information, or protected veteran status, and will not be discriminated against on the basis of disability. If you’d like to view a copy of the affirmative action plan or policy statement for Mercy Health– Youngstown, Ohio or Bon Secours – Franklin, Virginia; Petersburg, Virginia; and Emporia, Virginia, which are Affirmative Action and Equal Opportunity Employer, please email[ recruitment@mercy.com](mailto:recruitment@mercy.com). If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact The Talent Acquisition Team at [recruitment@mercy.com](mailto:recruitment@mercy.com). _", "summaryDescription" : "Medical Laboratory Technician (MLT) at Bon Secours. Skills: Medical laboratory testing, Patient safety. 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Nous nous mobilisons pour donner le meilleur de nous-mêmes. Chaque membre de l'équipe a un rôle important à jouer, que vous dirigiez une équipe ou collaboriez avec des coéquipiers sur un projet d’envergure. Quel que soit votre titre, vous faites partie de quelque chose de plus grand que vous. Fondée en 1927, Bauer Hockey a développé le premier patin. Depuis, notre passion pour le jeu, notre volonté d'innover et notre engagement envers la communauté du hockey ont fait de nous la marque la plus digne de confiance de l’industrie. Objectif et valeurs fondamentales: Chez Bauer Hockey, notre raison d’être est d’enrichir les expériences de vie par le sport. Nous avons la responsabilité de cultiver l’avenir de nos marques. Nous agissons toujours en équipe — jamais en solo. Nous aimons ce que nous faisons. Nous croyons que tout est possible et nous nous efforçons de donner le meilleur de nous-mêmes. Nous visons constamment à redéfinir les standards d’excellence dans tout ce que nous entreprenons. Vous souhaitez rejoindre notre équipe en tant qu' Technicien(ne) de Laboratoire? Relevant du gestionnaire du laboratoire de performance, le ou la technicien(ne) de laboratoire sera chargé(e) de tester et d'évaluer les matières premières et les produits finis dans le but d'améliorer continuellement la qualité et la performance des produits. En travaillant avec une équipe de techniciens de laboratoire, vous participerez à la planification quotidienne des tâches, y compris des priorités et des cas spéciaux. *Veuillez fournir votre curriculum vitae en français et en anglais.* Fonctions et responsabilités essentielles de l’emploi: Effectuer des tests de laboratoire sur des échantillons de R&D et des produits finis afin d'évaluer et de valider leurs performances mécaniques. Aider les équipes de développement et de production à prendre des décisions critiques concernant les projets. Évaluer les résultats des tests, préparer des rapports techniques et formuler des recommandations en fonction des résultats. Collaborer avec des chercheurs, des ingénieurs, des développeurs, des designers et d'autres membres de l'équipe afin d'examiner les demandes, d'établir des programmes de test et de fournir des résultats précis ainsi que des recommandations. Être responsable de la gestion de la maintenance, des réparations et de l’étalonnage de l’équipement de laboratoire, ainsi que du développement et de la recommandation de nouvelles méthodologies et de nouveaux équipements de test. Exigences: Posséder un diplôme d’études collégiales (DEC) en sciences, une attestation d’études collégiales (AEC) ou une expérience équivalente. Compétences en communication écrite et verbale en français et en anglais. Capacité à gérer plusieurs projets avec un minimum de supervision. Grande attention aux détails, avec la capacité de lire, de comprendre et de suivre des protocoles et des procédures de test. Connaissance des normes ISO, ASTM ou CSA, un atout. Expérience en étalonnage de l'équipement de laboratoire, un atout. Maîtrise de Microsoft Office. Plus précisément, Microsoft Excel. Doit être en mesure de soulever et/ou de pousser de 20 à 45 lb d’équipement de test ou d’échantillons. Expérience de travail dans un laboratoire d’essais mécaniques. Matériaux composites, un atout. Usinage, CNC ou manuel, un atout. Dessin CAO, un atout. Excellentes compétences en rédaction technique et en analyse. Intéressé(e) ? C'est une bonne chose. Nous le sommes aussi. Nous sommes sûrs que vous voudrez savoir que ce poste est éligible pour participer au plan d'incitation de l'entreprise. Nous offrons également l'un des avantages les plus généreux qui soient, notamment un régime d'épargne-retraite avec contrepartie de l'employeur, un programme de rabais pour les employés sur les vêtements et l'équipement, un environnement de travail décontracté et hybride ainsi qu'une foule d'autres avantages que nous n'avons pas la place de mentionner ici. Nous nous engageons à employer une main-d’œuvre diversifiée et souscrivons au principe de l’accès à l’égalité en emploi. Nous utilisons des outils assistés par l'IA pendant certaines étapes de notre processus de recrutement afin de garantir l'équité et l'efficacité. Toutes les décisions finales d'embauche sont prises par notre équipe de recrutement humaine. *********************************************************** TEAMMATES WANTED Working at Bauer is like playing on a hockey team. We empower each other to be our best. Everyone on the team has an important role to play. You might be leading others or collaborating with teammates on a big project. Whatever your title, you are part of something bigger than yourself. Founded in 1927, Bauer Hockey developed the first skate. Since then, our passion for the game, drive for innovation, and commitment to the hockey community have made us the most trusted brand in hockey. Purpose & Core Values: Our purpose at Bauer Hockey/ Cascade Maverik Lacrosse, is to enrich life experiences through sports. We have the responsibility to cultivate the future of our brands. We are always “we” and never “I”. We love what we do. We believe anything is possible and work to be our best. We strive to always redefine the standard of excellence in all that we do. Want to join our team as a Laboratory Technician? Reporting to the Laboratory Performance Manager, the Laboratory Technician will be responsible for testing and evaluating raw materials and finished products in order to continuously improve product quality and performance. Working with a team of laboratory technicians, you will participate in the daily planning of tasks, including priorities and special cases. *Please provide your resume in French + English* Essential Job Functions & Responsibilities: Perform laboratory tests on R&D samples and finished products to evaluate and validate their mechanical performance. Assist development and production teams in making critical project decisions. Evaluate test results, prepare technical reports and make recommendations based on the results. Collaborate with researchers, engineers, developers, designers and other team members to review requests, establish test programs and provide accurate test results and recommendations. Responsible for managing the maintenance, repair and calibration of laboratory equipment, as well as developing and recommending new test methodologies and equipment. Qualifications: Possess a College Diploma (DEC), College Certificate (AEC) in Sciences, or equivalent experience. French & English written and verbal communication skills. Ability to manage multiple projects with minimal supervision. Extremely detail-oriented, with the ability to read, understand, and follow test protocols and procedures. Knowledge of ISO, ASTM, or CSA standards, an asset. Experience in laboratory equipment calibration, an asset. Proficient in Microsoft Office, specifically Microsoft Excel. Must be able to lift and/or push 20 to 45 lbs of test equipment or samples. Experience working in a mechanical testing laboratory. Knowledge of Composite materials, an asset. Machining, CNC or manual, an asset. CAD drawing, an asset. Excellent technical writing and analytical skills. Interested yet? Good. We are, too. We're pretty sure you’ll want to know this position is eligible to participate in the Company’s annual incentive plan. We also offer one of the most generous benefits packages around including a retirement savings plan with employer match, an employee discount program on apparel and gear, casual & hybrid work environment and a host of other perks we don't have room to mention here. We are committed to employing a diverse workforce and is an equal opportunity employer. We use AI-assisted tools during parts of our recruitment process to help ensure fairness and efficiency. All final hiring decisions are made by our human hiring team.", "summaryDescription" : "Technicien(ne) de Laboratoire/ Laboratory Technician at Bauer Hockey. Skills: Laboratory testing, Mechanical performance, Technical reports. Perform laboratory tests. Evaluate mechanical performance", "postedDate" : "2026-06-14T02:58:10.587", "createdAt" : "2026-06-14T02:58:10.587", "lastUpdated" : "2026-06-15T09:17:53.505", "ingestTimestamp" : "2026-06-14T02:58:10.587", "mongoId" : "6a2c6d1f74d8ee00a091d558", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "50k-75k", "hasSalary" : false, "allSkills" : [ "Mechanical testing", "Laboratory testing", "Mechanical performance", "Technical reports", "Technical writing", "Analytical skills", "Manage multiple projects", "Mechanical testing laboratory", "Composite materials", "Machining", "CNC", "CAD drawing" ], "skillCount" : 12, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "_score" : 743.50934, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Sports & Fitness", "llmIndustryConfidence" : 0.95 }, { "id" : "69cf26132beec4dd3d90b5ce", "title" : "Medical Laboratory Scientist", "company" : "Tampa General Hospital", "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

" ], "timestamp" : "2026-06-15T10:20:39.368", "fingerprint" : "4b5aa119b4dceeb49053cf3e2e1ef20c7dca7e9ef7fa5f036666f249fc1d0b7d", "source" : "taleo", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=673264", "externalId" : "673264", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tampa", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "Tampa, Florida, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor", "experienceMinYears" : 3, "experienceMaxYears" : 6, "experienceLevel" : "Mid", "professionalSkills" : [ "Esoteric Molecular Laboratory" ], "hardSkillsList" : [ "Medical Technologist" ], "softSkillsList" : [ "independent judgement" ], "hardSkills" : [ { "name" : "Medical Technologist", "level" : "intermediate" } ], "softSkills" : [ { "name" : "independent judgement" } ], "majorSkills" : "Molecular experience", "majorSkillsList" : [ "Molecular experience" ], "coreResponsibilities" : "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.", "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" : 743.0632, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "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" : 732.75226, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "69ce5e3b9bc74574cb6779ea", "title" : "Intern for Testing for Drivability and 48V Operating Strategy", "company" : "Mercedes-Benz AG", "industry" : "Manufacturing", "salary" : { "min" : 21000.0, "max" : 27000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level internship in the automotive industry in Sindelfingen, Germany, adjusted for seniority and company size." }, "location" : "Germany-Baden-Württemberg-Sindelfingen", "locations" : [ "Germany-Baden-Württemberg-Sindelfingen", "Bela-Barenyi-Str Tor 14, , Sindelfingen" ], "timestamp" : "2026-06-15T07:53:41.300", "fingerprint" : "5b0ea176de8f427c55132d1f2c05037521f8d1fea8baf378d3760026e1f439e4", "source" : "taleo", "language" : "de", "applyUrl" : "https://daimler.taleo.net/careersection/ex/jobdetail.ftl?job=889748", "externalId" : "889748", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Sindelfingen", "state" : "Baden-Württemberg", "country" : "Germany", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "48.7084162,9.0035455" } ], "locationText" : "Sindelfingen, Baden-Württemberg, Germany", "employmentType" : "INTERNSHIP", "minimumEducation" : "Bachelor's", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "Entry", "technicalSkills" : "Python, MATLAB, Canape, MDA", "professionalSkills" : [ "Test procedure conception", "Data evaluation", "Measurement data analysis", "Technical documentation", "Project reporting" ], "hardSkillsList" : [ "Powertrain simulation", "Automated data evaluation", "Measurement data analysis" ], "softSkillsList" : [ "Flexibility", "Commitment", "Willingness to learn", "Independent work" ], "hardSkills" : [ { "name" : "Powertrain simulation", "level" : "intermediate" }, { "name" : "Automated data evaluation", "level" : "intermediate" }, { "name" : "Measurement data analysis", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Flexibility" }, { "name" : "Commitment" }, { "name" : "Willingness to learn" }, { "name" : "Independent work" } ], "majorSkills" : "Drivability testing, Operating strategy development, Powertrain development", "majorSkillsList" : [ "Drivability testing", "Operating strategy development", "Powertrain development" ], "coreResponsibilities" : "Develop test procedures, Implement test procedures, Conceive evaluation tools, Develop evaluation tools, Program evaluation tools, Define test methodologies, Coordinate test methodologies, Analyze measurement data, Interpret measurement data, Identify optimization potentials, Support documentation creation, Support project reports", "teamCollaboration" : "Active participation day-to-day business", "domainKnowledge" : "Powertrain development; Drivability; Electrified powertrains; Hybridized powertrains; Automotive engineering; Internal combustion engines; Control engineering", "domainList" : [ "powertrain-development", "drivability", "electrified-powertrains", "hybridized-powertrains", "automotive-engineering", "internal-combustion-engines", "control-engineering" ], "domainSpecificKnowledge" : [ "Powertrain development", "Drivability", "Electrified powertrains", "Hybridized powertrains", "Automotive engineering", "Internal combustion engines", "Control engineering" ], "toolProficiency" : [ "MS Office" ], "communicationSkills" : "German language skills; English language skills", "documentationSkills" : "Technical documentation; Project reports", "continuousLearning" : "Willingness to learn", "innovationCreativity" : "Innovative evaluation tools", "problemSolvingSkills" : "Identify optimization potentials", "qualificationsBasic" : "Completed basic studies, Bachelor's degree, Very good German language skills, Very good English language skills, Proficient in Python, Proficient in MATLAB, Knowledge of automotive engineering, Knowledge of internal combustion engines, Knowledge of control engineering, MS Office proficiency, Driving license class B", "qualificationsPreferred" : "Affinity for programming", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "In powertrain development at Mercedes-Benz, we are leaders in shaping the mobility of tomorrow. A central focus is on drivability, which significantly influences the subjective driving experience – from spontaneous throttle response and smooth gear changes to a harmonious overall vehicle behavior. Simultaneously, through innovative operating strategies, we optimize the interaction of all powertrain components to ensure maximum efficiency, minimal emissions, and superior performance under all conditions. Our work is always close to the product, so our developments directly flow into the vehicles that will inspire our customers worldwide. To master these complex interrelationships and continuously improve them, we are looking for dedicated talents who want to tackle and overcome upcoming challenges with us. As an intern in our team, you will gain comprehensive insights into the forward-looking development of electrified and hybridized vehicle powertrains. You will be actively involved in current development projects to apply your theoretical knowledge directly in practice. Your main tasks will include the conception of test procedures, the development and further development of toolchains for automatic data evaluation, as well as fundamental measurement data analyses. Within these areas of responsibility, you will gain deep insights into the diverse activities of an engineer in powertrain development. Your Tasks: Development and implementation of test procedures in powertrain simulation environments using Python, for the validation of drivability and operating strategy scopes Conception, development, and programming of innovative evaluation tools and toolchains in MATLAB and Python, for the automated analysis and assessment of drivability and operating strategy Definition and coordination of test and evaluation methodologies in comparison with real test resources such as powertrain test benches or prototype vehicles In-depth analysis and interpretation of test bench, simulation, and vehicle measurement data using MATLAB, Canape, MDA, etc., to identify optimization potentials Support in the creation of technical documentation and project reports Active participation in day-to-day business This is a full-time position, limited to 6 months, and can start from mid-May 2026. Field of Study in Technical studies (e.g., Mechanical Engineering / Automotive Engineering / Electrical Engineering / Control Engineering / Mechatronics / Computer Science), completed basic studies / Bachelor's degree Very good German and English language skills, both written and spoken Profound programming knowledge in Python and MATLAB, knowledge in the areas of automotive engineering / internal combustion engines / control engineering, MS Office Communication skills, flexibility, commitment, affinity for programming, team spirit, willingness to learn, independent work Driving license class B Additional Information: We look forward to receiving your online application, including a resume, cover letter, certificates, current certificate of enrollment stating your semester, proof of mandatory internship if applicable, and proof of the standard period of study. Please remember to mark your documents as \"relevant for this application\" in the online form and observe the maximum file size of 5 MB. You can find further information on the hiring criteria here . Severely disabled applicants and applicants with equivalent status are welcome! The representative for severely disabled employees (sbv-sindelfingen@mercedes-benz.com) will gladly support you in the application process. HR Services will be happy to help you with any questions you may have about the application process. You can reach us by email at myhrservice@mercedes-benz.com or by phone at 0711/17-99000 (Mon-Fri 10am-12pm & 1pm-3pm). Mercedes-Benz AG", "summaryDescription" : "Intern for Testing for Drivability and 48V Operating Strategy at Mercedes-Benz AG. Skills: Drivability testing, Operating strategy development, Powertrain development. Develop test procedures. 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true, "hasGeo" : true, "llmIndustry" : "Automotive", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c5d9574d8ee00a08dd0f3", "title" : "Microbiologist Laboratory Reviewer", "company" : "Nivagen Pharmaceuticals", "industry" : "Pharmaceuticals", "salary" : { "min" : 75000.0, "max" : 85000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Pittsburg, California, United States", "locations" : [ "Pittsburg", "California", "United States" ], "timestamp" : "2026-06-14T23:52:56.545", "fingerprint" : "d858ac2fcb6598f28543b0fe71ca320c2480bc342d491553dbf62540046bef77", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/nivagenpharmaceuticals/jobs/5205141008", "externalId" : "5205141008", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Sacramento", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.5810606,-121.4938950" } ], "locationText" : "Sacramento, California, United States", "employmentType" : "FULL_TIME", "technicalSkills" : "Microbiology", "professionalSkills" : [ "Quality control", "Data integrity", "Regulatory compliance" ], "hardSkillsList" : [ "Microbiological testing", "Method validation", "Sterility testing", "Endotoxin testing", "Environmental monitoring", "Microbial limit testing", "Disinfectant qualification", "Container closure integrity" ], "softSkillsList" : [ "Customer Focus", "Optimizes Work Processes", "Resourcefulness", "Manages Complexity", "Ensures Accountability", "Situational Adaptability" ], "hardSkills" : [ { "name" : "Microbiological testing", "level" : "intermediate" }, { "name" : "Method validation", "level" : "intermediate" }, { "name" : "Sterility testing", "level" : "intermediate" }, { "name" : "Endotoxin testing", "level" : "intermediate" }, { "name" : "Environmental monitoring", "level" : "intermediate" }, { "name" : "Microbial limit testing", "level" : "intermediate" }, { "name" : "Disinfectant qualification", "level" : "intermediate" }, { "name" : "Container closure integrity", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Customer Focus" }, { "name" : "Optimizes Work Processes" }, { "name" : "Resourcefulness" }, { "name" : "Manages Complexity" }, { "name" : "Ensures Accountability" }, { "name" : "Situational Adaptability" } ], "majorSkills" : "Microbiological data review, cGMP compliance, Pharmaceutical manufacturing", "majorSkillsList" : [ "Microbiological data review", "cGMP compliance", "Pharmaceutical manufacturing" ], "coreResponsibilities" : "Review laboratory test results, Verify compliance with SOPs, Verify compliance with cGMP, Evaluate method validations, Evaluate method transfers, Evaluate microbiological investigations, Assess environmental monitoring data, Assess sterility testing outcomes, Assess endotoxin testing outcomes, Collaborate with laboratory analysts, Collaborate with quality assurance teams, Resolve discrepancies, Address out-of-specification results, Support investigations related to laboratory deviations, Participate in root cause analysis, Ensure timely review of batch records, Ensure timely release of batch records, Identify trends in laboratory data, Recommend corrective actions, Support process improvements, Support best practices in microbiological testing, Support best practices in documentation, Provide guidance on data integrity, Provide guidance on compliance requirements, Maintain thorough records, Ensure proper documentation, Coordinate calibration, Coordinate maintenance, Participate in internal audits, Participate in external audits, Ensure compliance with safety regulations, Ensure compliance with environmental regulations, Manage workload to meet timelines, Manage workload to meet deadlines, Maintain confidentiality, Handle sensitive information, Update knowledge of regulations, Update knowledge of industry trends, Update knowledge of technological advancements", "teamCollaboration" : "Laboratory analysts; Quality assurance teams", "domainKnowledge" : "Good Manufacturing Practices; cGMP regulations; GLP; Injectable manufacturing; Pharmaceutical supply chain; Generic prescription drugs; Over-the-counter products", "domainList" : [ "good-manufacturing-practices", "cgmp-regulations", "glp", "injectable-manufacturing", "pharmaceutical-supply-chain", "generic-prescription-drugs", "over-the-counter-products" ], "domainSpecificKnowledge" : [ "Good Manufacturing Practices", "cGMP regulations", "GLP", "Injectable manufacturing", "Pharmaceutical supply chain", "Generic prescription drugs", "Over-the-counter products" ], "communicationSkills" : "Effective communication", "documentationSkills" : "Documentation; Data integrity", "continuousLearning" : "Training and development opportunities; Update knowledge of regulations; Update knowledge of industry trends; Update knowledge of technological advancements", "problemSolvingSkills" : "Root cause analysis", "specialRequirements" : "Bend at the waist and knees, Twist at the trunk, Lift up to 25 lbs, Wear laboratory protective gowning, Wear goggles, Wear face shields, Wear respirators, Wear protective gloves", "qualificationsBasic" : "Bachelor's degree in microbiology, Minimum of 3 years of experience in a microbiology laboratory", "qualificationsPreferred" : "Master's degree preferred, Previous experience in a pharmaceutical or compounding environment, Experience with compendia testing, Experience with United States Pharmacopeia, Experience with Food and Drug Administration, Experience with cGMP", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "About the Company: Nivagen is a global company dedicated to enhancing lives by developing and providing cost-effective generic prescription drugs and over-the-counter products for the North American market. For over a decade, we've remained steadfast in our commitment to core values of excellence, integrity, and respect for people. Our team of professionals collaborates tirelessly to pioneer advancements in manufacturing, distribution, and quality control, ensuring a holistic approach to healthcare. Through vertical integration of the pharmaceutical supply chain, cutting-edge technology, and unwavering dedication to excellence, we continually strive to redefine medication accessibility and affordability. We prioritize our employees' well-being by offering competitive pay, comprehensive benefits, and robust training and development opportunities. By investing in our workforce and fostering a culture of growth and support, we empower our team to drive innovation and make a positive impact in the healthcare industry. At Nivagen, our mission is clear: to make a meaningful difference in people's lives by delivering high-quality, affordable medications while upholding the highest standards of integrity and excellence. Job Location: Nivagen Pharmaceuticals, Sacramento, CA 3900 Duckhorn Dr, Sacramento, CA 95834 About the Job: Title of the Position: Microbiologist Laboratory Reviewer (Full Time) At Nivagen as a Microbiologist Laboratory Reviewer you will be responsible for ensuring that pharmaceutical products meet quality standards during the manufacturing process. This role involves real-time monitoring, sampling, testing, and documentation to identify and address any quality issues as they arise, ensuring that all production activities comply with Good Manufacturing Practices (GMP) and regulatory requirements. Position Summary The Microbiology Laboratory Reviewer plays a critical role in ensuring the accuracy and compliance of microbiological data within an injectable manufacturing facility. This position is responsible for reviewing laboratory test results, protocols and reports batch records, and related documentation to verify adherence to standard operating procedures (SOPs), current Good Manufacturing Practices (cGMP) regulations, GLP, and company quality standards. The reviewer works closely with laboratory microbiologist and quality assurance teams to resolve discrepancies, support investigations, and ensure the timely release of products. Key responsibilities include evaluating microbiological method validations, transfers, and investigations, as well as assessing environmental monitoring data, sterility test outcomes, and endotoxin results. The role also involves identifying trends, supporting continuous improvement initiatives, and providing guidance on best practices in documentation and data integrity. Strong attention to detail, effective communication skills, and a commitment to maintaining high standards of safety and compliance are essential for success in this position. Duties and Responsibilities Reviews and verifies laboratory test results, ensuring compliance with SOPs, cGMP, and company policies. Evaluates method validations, transfers, and microbiological investigations for accuracy and completeness. Assesses environmental monitoring data, sterility, and endotoxin testing outcomes for quality and consistency. Collaborates with laboratory analysts and quality assurance teams to resolve discrepancies and address out-of-specification results. Supports investigations related to laboratory deviations and participates in root cause analysis. Ensures timely review and release of batch records and product documentation. Identifies trends or recurring issues in laboratory data and recommends corrective actions. Supports the implementation of process improvements and best practices in microbiological testing and documentation. Provides training and guidance to laboratory staff on data integrity and compliance requirements. Maintains thorough records of all review activities and ensures proper documentation is in place. Calibration and maintenance coordination and record. Participates in internal and external audits as required, providing relevant documentation and expertise. Ensures all work is conducted in accordance with health, safety, and environmental regulations. Demonstrates strong organizational skills and manages workload to meet project timelines and regulatory deadlines. Maintains confidentiality and handles sensitive information with professionalism and integrity. Continuously updates knowledge of relevant regulations, industry trends, and technological advancements in microbiology. Performs other duties as assigned. While performing the responsibilities of the job, the employee is required to talk and hear. Must be able to bend at the waist and knees as well as twist at the trunk. Must be able to lift up to 25 lbs. Must be able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. Personal protective equipment and Respirators are essential for the health and safety of employees. Position requires working in the laboratory as well as sitting Microbiological method development and method validation procedures like BET, Sterility, MLT, Bio Assay and Disinfectant qualification and microbiological hold time validation, Container closure integrity validation. Knowledge and Skills Strong knowledge of microbiological testing techniques, reviewing, methods, and equipment. Key Competencies Customer Focus: Ability to build strong customer relationships and deliver customer centric solutions. Optimizes Work Processes: Know the most effective and efficient processes to get things done, with a focus on continuous improvement. Collaborates: Builds partnerships and works collaboratively with others to meet shared objectives. Resourcefulness: Secures and deploys resources effectively and efficiently. Manages Complexity: Makes sense of complex, high quality, and sometimes contradictory information to effectively solve problems. Ensures Accountability: Holds self and others accountable to meet commitments and objectives. Situational Adaptability: Adapts approach and demeanor in real time to match shifting demands of different situations. Communicates Effectively: Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences. Experience and Qualifications Bachelor’s degree in microbiology, Biology, or related field required; Master's degree preferred. Minimum of 3 years of experience in a microbiology laboratory required. Previous experience in a pharmaceutical or compounding environment preferred. Experience with compendia testing: United States Pharmacopeia, and regulatory requirements (Food and Drug Administration and cGMP) preferred. Experience with microbiological method development and method validation procedures like Sterility Testing, Endotoxin Testing, Disinfectant Efficacy Study, Water Testing, Method Validation, Environment Monitoring, Microbial Limit Testing, PET, and microbiological hold time validation, container closure integrity. Benefits: Pay range $75,000-$85,000 per Year Yearly bonus eligibility Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being Medical, dental and vision coverage Paid time off plan 401k savings plan Additional Information: Nivagen to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors. We are focused on building a diverse and inclusive workforce. If you're excited about this role, but do not meet 100% of the qualifications listed above, we encourage you to apply.", "summaryDescription" : "Microbiologist Laboratory Reviewer at Nivagen Pharmaceuticals. Skills: Microbiological data review, cGMP compliance, Pharmaceutical manufacturing. Review laboratory test results. 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Periods of increased testing", "domainKnowledge" : "Rabies virus; Public health laboratory; Virology; Serology", "domainList" : [ "rabies-virus", "public-health-laboratory", "virology", "serology" ], "domainSpecificKnowledge" : [ "Rabies virus", "Public health laboratory", "Virology", "Serology" ], "toolProficiency" : [ "Fluorescence microscopy" ], "innovationCreativity" : "Implementation of new diagnostic methods", "problemSolvingSkills" : "Troubleshooting laboratory equipment", "specialRequirements" : "On-call rotation, Mandatory reporting during adverse weather, Work with infectious disease agents, Use of personal protective equipment, Ability to manipulate items with fingers, Ability to grasp, Ability to feel/perceive attributes, Periodic serological assessments, Perceive colors normally, Lift up to 35 pounds", "qualificationsBasic" : "Bachelor's degree in medical technology, chemistry, or biological science OR Associate degree in medical technology and two years of experience in a medical laboratory OR Completion of Certified Laboratory Assistant course in medical technology or comparable course and three years of experience in a medical laboratory OR An equivalent combination of education and experience", "qualificationsPreferred" : "Expert-level performance of Direct Fluorescent Antibody–based diagnostic workflows, Demonstrated experience conducting necropsy and tissue dissection procedures, Proficient execution of specimen accessioning processes, Applied experience operating, maintaining, and troubleshooting laboratory equipment, Hands-on experience identifying wildlife species", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Agency** Dept of Health and Human Services **Division** Public Health **Job Classification Title** Medical Laboratory Technologist I (S) **Position Number** 60041369 **Grade** MH14 **About Us** The North Carolina Department of Health and Human Services (DHHS) is one of the largest, most complex agencies in the state, and has approximately 17,000 employees. It is responsible for ensuring the health, safety, and well-being of all North Carolinians, providing human service needs for special populations including individuals who are deaf, blind, developmentally disabled, and mentally ill, and helping poor North Carolinians achieve economic independence. **Description of Work** The Rabies Laboratory Technologist I position functions as a bench technologist in the Rabies Laboratory at the NC State Laboratory of Public Health, performing diagnostic testing of animal specimens for the presence of rabies virus. The role’s primary technical scope includes Direct Fluorescent Antibody testing of necropsied brain tissue, as well as participation in new diagnostic methods introduced in the laboratory. The Rabies Laboratory Technologist I position operates within a high‑throughput public health laboratory environment and performs laboratory procedures ranging from specimen accessioning to slide preparation, staining, and result interpretation. The technologist also conducts necropsy procedures, wildlife species identification, and supports emergency and outbreak‑related testing needs. This role may require participation in an on‑call schedule to ensure timely diagnostics during weekends, holidays, and urgent events. Key Duties Include: \\- Perform Direct Fluorescent Antibody testing of necropsied brain tissue to detect rabies virus. \\- Conduct specimen accessioning, labeling, and controlled handling of animal samples submitted for diagnostic testing. \\- Complete necropsy and dissection procedures to obtain required tissues for laboratory analysis. \\- Prepare laboratory slides through tissue imprinting, fixation, staining, and controlled processing steps. \\- Interpret stained slides using fluorescence microscopy and document results in accordance with laboratory procedures. \\- Perform species identification of bats, foxes, skunks, and other wildlife submitted for rabies investigations. \\- Support validation and implementation of new or updated diagnostic methods introduced in the Rabies Laboratory. \\- Maintain and troubleshoot laboratory equipment and labware required for testing workflows. \\- Participate in on‑call rotations to provide emergency rabies testing during weekends and holidays. \\- Assist additional laboratory units during outbreak responses or periods of increased testing volume. **Knowledge Skills and Abilities/Management Preferences** ## _**Salary Grade Range: $58,265.00 - $87,396.00**_ ## _Candidates now meet the minimum qualifications of a position if they meet the minimum education and experience listed on the vacancy announcement. The Knowledge, Skills, and Abilities (KSAs)/ Management Preferences are not required. Applicants who possess the following skills are preferred: _ * Expert‑level performance of Direct Fluorescent Antibody–based diagnostic workflows, including slide preparation, staining, and interpretation to support rabies virus detection. * Demonstrated experience conducting necropsy and tissue dissection procedures using laboratory‑grade surgical tools for preparation of diagnostic specimens. * Proficient execution of specimen accessioning processes, including controlled handling, labeling, and documentation of animal samples submitted for laboratory testing. * Applied experience operating, maintaining, and troubleshooting laboratory equipment and labware used in virology and serology testing environments. * Hands‑on experience identifying wildlife species such as bats, foxes, and skunks to support accurate classification of specimens submitted for rabies investigations. ## **The Posting Will Close At 11:59 P.M. The Night Before The End Date** ## **This Position Is Designated As Mandatory And Must Report Or Stay Over During Adverse Weather Events** ## **Physical Requirements:** An occupational medical assessment may be required to determine your ability to safely work with biological, chemical, or radiological hazards. This position may also require periodic medical screenings to confirm safety practices are effectively preventing occupational injury or illness. All costs associated with obtaining occupational health services are covered by NCSLPH. This position: * Works frequently with infectious disease agents that require the use of personal protective equipment, such as a respirator. * Uses laboratory equipment requiring ability to manipulate items with fingers, ability to grasp, and ability to feel/perceive the attributes of objects, such as size, shape, temperature, or texture. * Immunization against rabies is a precondition of employment within the rabies laboratory, along with periodic serological assessments of immunization to ensure that the employee maintains an adequate level of immunization. * Mut be able to perceive colors normally. * Must be able to lift up to 35 pounds. **About the NC Division of Public Health (DPH):** The NC Division of Public Health works to promote and contribute to the highest possible level of health for the people of North Carolina. Our entire statewide system of public health has dedicated professionals who carry out our mission every day through a wide range of essential and activities touching the lives of everyone in our state. ## **About the Virology / Serology: Rabies Virus:** Virology/Serology (VS) performs highly complex laboratory tests to identify infections with a variety of bacterial and viral pathogens of public health significance. The majority of reports generated by this Unit are used by state and local health officials in the diagnosis, treatment, surveillance, and control of communicable disease. The mission of VS is to provide quality-assured laboratory services to public and private health provider organizations and to assist other Public Health program partners responsible for communicable disease prevention and control. The Rabies Laboratory at the NCSLPH is the sole source for diagnostic rabies testing in North Carolina. **Compensation and Benefits:** The State of North Carolina offers excellent comprehensive benefits. Employees can participate in health insurance options, standard and supplemental retirement plans, and the NCFlex program (numerous high-quality, low-cost benefits on a pre-tax basis). Employees also receive paid vacation, sick, and community service leave. In addition, paid parental leave is available to eligible employees. Visit the website for State Benefits. ## **Supplemental Contact Information:** The North Carolina Department of Health and Human Services (DHHS) is an Equal Opportunity Employer that embraces an Employment First philosophy, which consists of complying with all federal laws, state laws, and Executive Orders. We are committed to reviewing requests for reasonable accommodation at any time during the hiring process or while on the job. For more information about DHHS: _._ DHHS uses the Merit-Based Recruitment and Selection Plan to fill positions subject to the State Human Resources Act with the most qualified individuals. Hiring salary will be based on relevant qualifications, internal equity, and budgetary considerations pertinent to the advertised position. In accordance with the Governor’s [Executive Order 303](https://gcc02.safelinks.protection.outlook.com/?url=https%3A%2F%2Fgovernor.nc.gov%2Fexecutive-order-no-303%2Fopen&data=05%7C02%7Csamantha.costa%40commerce.nc.gov%7C62856c4dc3364b9449f608dc5b2499a8%7C7a7681dcb9d0449a85c3ecc26cd7ed19%7C0%7C0%7C638485459976214045%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C0%7C%7C%7C&sdata=QMPRMksyCzARBEP8pjuvnhayVBx9Y4Lqv2x7mTq6S%2B4%3D&reserved=0), our agency supports second-chance employment for individuals who were previously incarcerated or justice-involved. We invite all potential applicants to apply for positions for which they may be qualified. ## _Application Process_ **Be sure to complete the application in its entirety.** _Resumes will not be accepted in lieu of completing this application._ * Information should be provided in the appropriate areas, to include the following: Education, including high school and all degrees obtained, Work Experience, and Certificates & Licenses. It is critical to our screening and salary determination process that applications contain comprehensive candidate information. * Answers to Supplemental Questions are not a substitute for providing all relevant information within the body of your application. To receive credit for the supplemental questions, you must provide supporting information within the \"Work Experience\" section of the application to support your answers. * If multiple applications are submitted to an individual posting, only the most recent application received prior to the closing date will be accepted. Applications must be submitted by 11:59 PM on the closing date. * Applicants _may_ be subject to a criminal background check. All candidates selected for positions considered \"Positions of Trust\" _will be_ subject to a criminal background check. * Due to the volume of applications received, we are unable to provide information regarding the status of your application over the phone. To check the status of your application, please log in to your account. Upon the closing date, applications are \"Under Review\" and will be screened by Human Resources for qualified applicants. The hiring process may take several weeks. * Degrees must be received from appropriately accredited institutions. Transcripts and degree evaluations may be uploaded with your application. The State of North Carolina/Office of State Human Resources uses the National Association of Credential Evaluation Services (NACES) as a referral resource for applicants who need to have their credentials certified as equivalent. * For a list of organizations that perform this specialized service, please visit the NACES membership website at [https://www.naces.org/members](https://www.naces.org/members) _._ ## _Degree/College Credit Verification_ Degrees must be received from appropriately accredited institutions. _Transcripts, degree evaluations, and cover letters may be uploaded with your application._ ## _Veterans’ and National Guard Preference_ * Applicants seeking Veteran's Preference must attach a DD-214 Member-4 Form (Certificate of Release or Discharge from Active Duty) to their applications. * Applicants seeking National Guard Preference must attach an NGB 23A (RPAS), along with the state application, if they are a current member of the NC National Guard in good standing. * Applicants who are former members of either the NC Army National Guard or the NC Air National Guard, with honorable discharge and six years of creditable service, must attach a copy of the DD 256 or NGB 22, along with the state application. ## _ADA Accommodations_ Consistent with the Americans with Disabilities Act (ADA) and the Pregnant Workers Fairness Act (PWFA), DHHS is committed to the full inclusion of all qualified individuals. As part of this commitment, DHHS will ensure that people with disabilities, or known limitations covered by the PWFA, are provided with reasonable accommodation. If reasonable accommodation is needed to participate in the job application or interview process, please contact the person indicated below. ## _CONTACT INFORMATION_ __ If there are any questions about this posting, please contact Talent Acquisition at [talentacquisition@dhhs.nc.gov](mailto:talentacquisition@dhhs.nc.gov). **_Resumes will not be accepted in lieu of completing this application._ ** **Minimum Education and Experience** Some state job postings say you can qualify by an “equivalent combination of education and experience.” If that language appears below, then you may qualify through EITHER years of education OR years of directly related experience, OR a combination of both. See the Education and Experience Equivalency Guide for details. Bachelor’s degree in medical technology, chemistry, or a biological science from an appropriately accredited institution **OR** Associate degree in medical technology from an appropriately accredited institution and two years of experience in a medical laboratory **OR** Completion of a Certified Laboratory Assistant course in medical technology or a comparable course and three years of experience in a medical laboratory **OR** An equivalent combination of education and experience. **EEO Statement** The State of North Carolina is an Equal Employment Opportunity Employer and dedicated to providing employees with a work environment free from all forms of unlawful employment discrimination, harassment, or retaliation. The state provides reasonable accommodation to employees and applicants with disabilities; known limitations related to pregnancy, childbirth, or related medical conditions; and for religious beliefs, observances, and practices. **Recruiter:** Tresha Walker **Email:** talentacquisition@dhhs.nc.gov", "summaryDescription" : "Rabies Laboratory Technologist at Dept of Health and Human Services. Skills: Rabies virus detection, Diagnostic testing, Laboratory procedures. Perform Direct Fluorescent Antibody testing. Conduct specimen accessioning", "postedDate" : "2026-06-10T04:17:11.820", "createdAt" : "2026-06-12T04:17:11.622", "lastUpdated" : "2026-06-14T23:34:46.931", "ingestTimestamp" : "2026-06-12T04:17:11.622", "mongoId" : "6a2b035474d8ee00a074f298", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://nc.wd108.myworkdayjobs.com/NC_Careers/job/Wake-County-NC/Rabies-Laboratory-Technologist-I_JR-117555", "salaryAnnualMin" : 58265, "salaryAnnualMax" : 87396, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Slide preparation", "Staining", "Result interpretation", "Necropsy procedures", "Tissue dissection", "Rabies virus detection", "Diagnostic testing", "Laboratory procedures", "Wildlife species identification", "Laboratory equipment maintenance", "Rabies virus", "Public health laboratory", "Virology", "Serology", "Immunization against rabies", "Fluorescence microscopy" ], "skillCount" : 16, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 708.67377, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Public Health" }, { "id" : "6a2a409c74d8ee00a05c8297", "title" : "Clinical Laboratory Technologist", "company" : "Montefiore New Rochelle Hospital", "industry" : "Healthcare", "salary" : { "min" : 49.81, "max" : 49.81, "currency" : "USD", "frequency" : "yearly" }, "location" : "16 Guion Place", "locations" : [ "16 Guion Place", "United States of America" ], "certifications" : [ "OHS Annual Assessment", "OHS Fit Test" ], "timestamp" : "2026-06-12T09:42:45.688", "fingerprint" : "555a33b2d1a87be5c39b39786910337f843b8f03a96437514f70d48429fd6fd5", "source" : "workday", "language" : "en", "applyUrl" : "https://montefiore.wd12.myworkdayjobs.com/New_Rochelle/job/16-Guion-Place/Clinical-Laboratory-Technologist_JR230418-1", "externalId" : "JR230418", "industryFunction" : { }, "locationPoint" : "43.35982,5.33421", "structuredLocations" : [ { "city" : "New Rochelle", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "40.9115386,-73.7826363" } ], "locationText" : "New Rochelle, New York, United States", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Laboratory testing" ], "hardSkillsList" : [ "Quality control", "Quality assurance", "Preventative maintenance" ], "hardSkills" : [ { "name" : "Quality control", "level" : "intermediate" }, { "name" : "Quality assurance", "level" : "intermediate" }, { "name" : "Preventative maintenance", "level" : "intermediate" } ], "majorSkills" : "Laboratory testing, Quality control", "majorSkillsList" : [ "Laboratory testing", "Quality control" ], "coreResponsibilities" : "Run tests on patient samples, Provide report to Physician, Identify critical results, Run three levels of controls, Identify QC problems, Remediate QC problems, Stain manual differentials, Read manual differentials, Identify abnormal differentials, Bring abnormal differentials to attention of Physician, Perform daily preventative maintenance, Perform weekly preventative maintenance, Perform monthly preventative maintenance, Draw blood samples from patients, Ensure correct patient, Ensure correct tubes for tests, Dispose of needles and supplies according to standards", "teamCollaboration" : "Provide report to Physician", "domainKnowledge" : "Clinical Laboratory Technologist", "domainList" : [ "clinical-laboratory-technologist" ], "domainSpecificKnowledge" : [ "Clinical Laboratory Technologist" ], "communicationSkills" : "Provide report to Physician", "problemSolvingSkills" : "Remediate QC problems", "outcomesObjectives" : "Results do not have any errors; Equipment runs smoothly; Issues are resolved in a timely manner; Results are provided without errors; Correct samples are collected from the correct patient; All supplies immediately disposed of following each procedure", "qualificationsBasic" : "5 years work experience, Knowledge of laboratory equipment, Knowledge of principles and procedures to run laboratory testing", "qualificationsPreferred" : "BS Preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**City/State:** New Rochelle, New York **Grant Funded:** No **Department:** MNR Lab Operations **Bargaining Unit:** 1199 **Work Shift:** Night **Work Days:** NIGHTS VARY **Scheduled Hours:** 12:30 AM-8:30 AM **Scheduled Daily Hours:** 7.5 HOURS **Hourly Rate:** $49.81 For positions that have only a rate listed, the displayed rate is the hiring rate but could be subject to change based on shift differential, experience, education or other relevant factors. To learn more about the “Montefiore Difference” – who we are at Montefiore and all that we have to offer our associates, please click [here](http://www.mymontebenefits.com/montefiore-difference). **Job Summary** Perform laboratory tests pursuant to established and approved protocols, requiring the exercise of independent judgment and responsibility. Maintain equipment and records; perform quality control and quality assurance related to test performance. **Essential Functions** * 1\\. Run tests on patient samples, provide report to the Physician and identify critical results. * Results do not have any errors. * 2\\. Run three levels of controls, identifying and remediating QC problems. * Equipment runs smoothly, and issues are resolved in a timely manner. * 3\\. Stain and read manual differentials, identify abnormal and bring them to attention of Physician. * Results are provided without errors. * 4\\. Perform daily, weekly and monthly preventative maintenance procedures. * Equipment runs smoothly and issues are resolved in a timely manner. * 5\\. Draw blood samples from patients for analysis in onsite lab or to be sent out to other Montefiore or outside laboratories. Ensures correct patient, correct tubes for required tests, and disposes of needles and other supplies according to standards. * Correct samples are collected from the correct patient with each encounter and all supplies immediately disposed of following each procedure. **Qualifications** * BS Preferred * 4-6 years 5 years work experience * Knowledge of principles and procedures to run laboratory testing. Knowledge of laboratory equipment. * Clinical Laboratory Technologist * OHS Annual Assessment * OHS Fit Test Montefiore New Rochelle Hospital is an equal employment opportunity employer. Montefiore New Rochelle Hospital will recruit, hire, train, transfer, promote, layoff and discharge associates in all job classifications without regard to their race, color, religion, creed, national origin, alienage or citizenship status, age, gender, actual or presumed disability, history of disability, sexual orientation, gender identity, gender expression, genetic predisposition or carrier status, pregnancy, military status, marital status, or partnership status, or any other characteristic protected by law.", "summaryDescription" : "Clinical Laboratory Technologist at Montefiore New Rochelle Hospital. Skills: Laboratory testing, Quality control. Run tests on patient samples. Provide report to Physician", "postedDate" : "2026-06-10T14:21:54.627", "createdAt" : "2026-06-11T14:21:54.455", "lastUpdated" : "2026-06-12T09:42:45.688", "ingestTimestamp" : "2026-06-11T14:21:54.455", "mongoId" : "6a2a409c74d8ee00a05c8297", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://montefiore.wd12.myworkdayjobs.com/New_Rochelle/job/16-Guion-Place/Clinical-Laboratory-Technologist_JR230418-1", "salaryAnnualMin" : 103604, "salaryAnnualMax" : 103604, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Quality control", "Quality assurance", "Preventative maintenance", "Laboratory testing", "Clinical Laboratory Technologist", "OHS Annual Assessment", "OHS Fit Test" ], "skillCount" : 7, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 702.168, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2c94c874d8ee00a098b8f4", "title" : "Electrochemist Lab Scale Testing", "company" : "CMBlu Energy AG", "industry" : "Climate Tech", "salary" : { "min" : 75000.0, "max" : 105000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Electrochemist in Alzenau, Germany, adjusted for the climate tech industry and company size." }, "location" : "Alzenau, Bavaria, Germany", "locations" : [ "Alzenau", "Bavaria", "Germany" ], "timestamp" : "2026-06-15T08:18:15.887", "fingerprint" : "015fc6feac75e59f8a6fa54524fb33bdf13549c5c3293a9bd10f3db92938b3d1", "source" : "greenhouse", "language" : "de", "applyUrl" : "https://boards.eu.greenhouse.io/cmbluenergyag/jobs/4801992101?gh_jid=4801992101", "externalId" : "4801992101", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Alzenau", "state" : "Bavaria", "country" : "Germany", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "50.0858680,9.0813749" } ], "locationText" : "Alzenau, Bavaria, Germany", "minimumEducation" : "Master's", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "technicalSkills" : "EC-Lab, Python, MATLAB", "professionalSkills" : [ "Hypothesis testing", "Data analysis", "Method validation", "Risk identification" ], "hardSkillsList" : [ "Electrochemical interpretation", "Performance analysis", "Degradation analysis", "Transport phenomena", "Kinetics phenomena", "Interface phenomena", "Test design", "Statistical evaluation", "Measurement uncertainty" ], "hardSkills" : [ { "name" : "Electrochemical interpretation", "level" : "intermediate" }, { "name" : "Performance analysis", "level" : "intermediate" }, { "name" : "Degradation analysis", "level" : "intermediate" }, { "name" : "Transport phenomena", "level" : "intermediate" }, { "name" : "Kinetics phenomena", "level" : "intermediate" }, { "name" : "Interface phenomena", "level" : "intermediate" }, { "name" : "Test design", "level" : "intermediate" }, { "name" : "Statistical evaluation", "level" : "intermediate" }, { "name" : "Measurement uncertainty", "level" : "intermediate" } ], "majorSkills" : "Electrochemical testing, Impedance spectroscopy, Cell testing, Data analysis", "majorSkillsList" : [ "Electrochemical testing", "Impedance spectroscopy", "Cell testing", "Data analysis" ], "coreResponsibilities" : "Take overall responsibility for electrochemical interpretation, Analyze performance and degradation behavior, Develop test designs for hypothesis testing, Ensure methodological suitability, Ensure statistical significance, Ensure reproducibility, Review electrochemical results, Ensure plausibility and consistency, Derive action recommendations from test results, Act as technical sparring partner, Identify electrochemical risks", "teamCollaboration" : "Development teams; Electro-Analytics Lab; Cell Testing", "projectManagementSkills" : [ "Experimental design" ], "domainKnowledge" : "SolidFlow batteries; Organic molecules; Half-cell analysis; Full-cell analysis; Impedance spectroscopy; Electrochemical mechanisms", "domainList" : [ "solidflow-batteries", "organic-molecules", "half-cell-analysis", "full-cell-analysis", "impedance-spectroscopy", "electrochemical-mechanisms" ], "domainSpecificKnowledge" : [ "SolidFlow batteries", "Organic molecules", "Half-cell analysis", "Full-cell analysis", "Impedance spectroscopy", "Electrochemical mechanisms" ], "toolProficiency" : [ "EC-Lab", "Python", "MATLAB" ], "communicationSkills" : "Interdisciplinary communication", "continuousLearning" : "Regular training; Exciting projects", "innovationCreativity" : "Prototype development", "problemSolvingSkills" : "Hypothesis testing; Root cause analysis", "outcomesObjectives" : "Develop clear, decision-relevant recommendations", "qualificationsBasic" : "Master's or PhD, 5+ years experience, Master's or PhD in Electrochemistry, Material Science, Chemistry, Half-cell and full-cell analysis, Electrochemical mechanisms understanding, Impedance spectroscopy experience, Modeling experience, Experimental design experience, Data-driven hypothesis testing, Modern evaluation tools, Statistical evaluation experience, Measurement uncertainty understanding, Quality requirements understanding, Excellent German skills, Excellent English skills, Analytical communication skills, Interdisciplinary communication skills", "qualificationsPreferred" : "EC-Lab experience, Python experience, MATLAB experience", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "CMBlu Energy befindet sich auf der spannenden Reise hin zu einem globalen Cleantech-Unternehmen. Unsere Mission: Unbegrenzte Energiespeicherung nach dem Vorbild der Natur ermöglichen – und das für alle, weltweit. Was sind SolidFlow-Batterien?   SolidFlow-Batterien speichern Energie in organischen Molekülen. Der Verzicht auf explosive Materialien macht sie sicher, der Einsatz von sozial und ökologisch konfliktfreien Rohstoffen nachhaltig und die nahezu unbegrenzte Materialverfügbarkeit skalierbar und günstig in der Beschaffung. Das macht unsere patentierte SolidFlow-Technologie zu einem Gamechanger im Aufbau eines globalen klimaneutralen Energiesystems. Vom Start-up zum Scale-up: Gemeinsam packen wir es an   CMBlu Energy entwickelt sich von einem Start-up mit Forschungsschwerpunkt zu einem produzierenden Scale-up, das sich auf dem Sprung in die Serienproduktion befindet. An diesem Ziel arbeiten rund 250 Mitarbeiterinnen und Mitarbeiter bei CMBlu Energy. Unser Hauptsitz ist in Alzenau nähe Frankfurt, mit einer Zweigstelle in Obernburg. Hinzu kommen Tochtergesellschaften in Athen, Griechenland und Petaluma, USA.   Deine Aufgaben Du übernimmst die fachliche Gesamtverantwortung für die elektrochemische Interpretation von Prüfmethoden wie CV, EIS, RDE, GITT/PITT und Zelltests Du analysierst Performance- und Alterungsverhalten mechanistisch, bewertest Transport-, Kinetik- und Grenzflächenphänomene und entwickelst geeignete Testdesigns zur fundierten Hypothesenprüfung Du fungierst als fachliche Gatekeeper-Instanz für Prüfdesigns und stellst die methodische Eignung, statistische Aussagekraft und Reproduzierbarkeit sicher Du prüfst elektrochemische Ergebnisse im Sinne eines unabhängigen 4-Augen-Prinzips und verantwortest die fachliche Plausibilität und Konsistenz von Material-, Halbzell- und Vollzelldaten Du leitest aus Testergebnissen klare, entscheidungsrelevante Handlungsempfehlungen für Entwicklung und Technologie ab Du agierst als technischer Sparringspartner für Entwicklerteams, Electro-Analytics Lab und Cell Testing und identifizierst frühzeitig elektrochemische Risiken Dein Profil Abgeschlossenes Hochschulstudium (Master oder Promotion) in Elektrochemie, Materialwissenschaften, Chemie oder vergleichbar Mindestens 5 Jahre Erfahrung in elektrochemischer Forschung oder industrieller Produktentwicklung mit Schwerpunkt Halb- und Vollzellanalytik Tiefgehendes Verständnis elektrochemischer Mechanismen sowie fundierte Erfahrung in Impedanzspektroskopie und Modellierung Erfahrung in Versuchsplanung (DoE), datenbasierter Hypothesenprüfung und moderner Auswertungstools ( z. B. EC-Lab, Python, MATLAB) Sicherer Umgang mit statistischer Bewertung von Reproduzierbarkeit und Messunsicherheit sowie Grundverständnis relevanter Qualitätsanforderungen Sehr gute Deutsch- und Englischkenntnisse sowie ausgeprägte analytische und interdisziplinäre Kommunikationsfähigkeit Unsere Benefits bei CMBlu Energy AG für Dich: VSOP-Programm: Mit unserem Virtual Stock Option Program (VSOP) kannst du am Erfolg der CMBlu Energy AG teilhaben und vom Wachstum unseres Unternehmens profitieren. Deutschland-Ticket: Wir übernehmen komplett das Deutschland-Bahn-Ticket, damit du nachhaltig und komfortabel reisen kannst. Bedeutungsvolle Arbeit: Arbeite an der Entwicklung unserer innovativen Organic-SolidFlow-Batterie, die einen wichtigen Beitrag zur nachhaltigen Energienutzung und -speicherung leisten. Remote-Arbeit: Abhängig vom Aufgabenbereich bieten wir die Möglichkeit, teilweise remote zu arbeiten, wenn es die Position zulässt. Weiterentwicklungsmöglichkeiten: Wir fördern deine persönliche und berufliche Weiterentwicklung durch regelmäßige Schulungen und spannende Projekte. Faires Gehalt: Wir bieten ein wettbewerbsfähiges und faires Gehalt, das deine Leistung anerkennt. Unsere Werte: Bei CMBlu Energy AG stehen Verlässlichkeit, Innovation und Unermüdlichkeit im Mittelpunkt unserer Zusammenarbeit. Wenn du bereit bist, dich neuen Herausforderungen zu stellen und Innovationen voranzutreiben, wollen wir von dir hören! Bei CMBlu Energy AG arbeitest du mit einem leidenschaftlichen Team zusammen, das sich für Spitzenleistungen und kontinuierliche Verbesserungen einsetzt. Bewirb dich jetzt und sei ein Teil unserer spannenden Reise. Wir freuen uns darauf, dich in unserem Team willkommen zu heißen!", "summaryDescription" : "Electrochemist Lab Scale Testing at CMBlu Energy AG. Skills: Electrochemical testing, Impedance spectroscopy, Cell testing, Data analysis. Take overall responsibility for electrochemical interpretation. Analyze performance and degradation behavior", "postedDate" : "2026-06-13T22:46:40.373", "createdAt" : "2026-06-13T22:46:40.373", "lastUpdated" : "2026-06-15T08:18:15.887", "ingestTimestamp" : "2026-06-13T22:46:40.373", "mongoId" : "6a2c94c874d8ee00a098b8f4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Electrochemical interpretation", "Performance analysis", "Degradation analysis", "Transport phenomena", "Kinetics phenomena", "Interface phenomena", "Test design", "Statistical evaluation", "Measurement uncertainty", "Electrochemical testing", "Impedance spectroscopy", "Cell testing", "Data analysis", "Hypothesis testing", "Method validation", "Risk identification", "Experimental design", "SolidFlow batteries", "Organic molecules", "Half-cell analysis", "Full-cell analysis", "Electrochemical mechanisms", "EC-Lab", "Python", "MATLAB" ], "skillCount" : 25, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.8888889, "_score" : 694.8317, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Climate Tech", "llmIndustryConfidence" : 0.95 }, { "id" : "69ce5e0a9bc74574cb673299", "title" : "Internship - Global Water Analysis Laboratories Network Promotion", "company" : "IAEA", "industry" : "Government", "salary" : { "min" : 20000.0, "max" : 25000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level internship in Vienna, Austria, adjusted for the government industry." }, "location" : "Austria-Vienna-Vienna-IAEA Headquarters", "locations" : [ "Austria-Vienna-Vienna-IAEA Headquarters", "2026-04-03, 6:59:00 AM", "12, Interns, Interns" ], "timestamp" : "2026-06-15T09:44:50.765", "fingerprint" : "a46babcf28aac5e65885a4cb5ab6903fd56222a9af28e0b768982636a6db6eec", "source" : "taleo", "language" : "en", "applyUrl" : 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"Instrumentation calibration", "level" : "intermediate" }, { "name" : "Instrumentation repair", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Highly organized" }, { "name" : "Flexible approach" } ], "majorSkills" : "Materials testing, Geotechnical testing, Laboratory technician", "majorSkillsList" : [ "Materials testing", "Geotechnical testing", "Laboratory technician" ], "coreResponsibilities" : "Conduct materials testing, Perform materials testing on Soils, Perform materials testing on Aggregates, Perform materials testing on Concrete, Perform materials testing on Rock Cores, Coordinate project testing, Report on testing, Communicate test results to Team Lead, Communicate test results to Principal Engineer, Participate in safety activities, Participate in housekeeping activities, Participate in training activities, Order laboratory supplies, Maintain laboratory supplies, Perform other duties as assigned", "teamCollaboration" : "Work as key team member; Work with specialized professionals; Teamwork", "domainKnowledge" : "Geotechnical engineering; Materials engineering; Construction materials; Ontario Provincial Standards; AASHTO; ASTM", "domainList" : [ "geotechnical-engineering", "materials-engineering", "construction-materials", "ontario-provincial-standards", "aashto", "astm" ], "domainSpecificKnowledge" : [ "Geotechnical engineering", "Materials engineering", "Construction materials", "Ontario Provincial Standards", "AASHTO", "ASTM" ], "communicationSkills" : "Verbal communication; Written communication", "continuousLearning" : "Comprehensive training", "problemSolvingSkills" : "Troubleshoot instrumentation; Diagnose instrumentation", "specialRequirements" : "Available to work weekends on short notice, Ability to work and travel throughout Ontario, Ability to adapt to changing work conditions and schedules on short notice, Regularly lifting 25 kg, Clean drivers abstract", "qualificationsBasic" : "College diploma in Civil Engineering, College diploma in Materials Engineering Technology, 2-3 years applicable laboratory experience, Familiarity with Geotechnical and Materials testing protocols, 2-3 years experience conducting testing of Soils & Rock, Experience with Atterberg Limits, Experience with Hydrometers, Experience with Sieves, Experience with Moisture Contents, Experience with Visual Classifications, Experience with advanced lab testing, Experience with Triaxial tests, Experience with Direct Shear, Experience with Consolidation tests, Experience with Permeability tests, Experience with Slake Durability, Experience with Point Load Testing, Capability to calibrate instrumentation, Capability to troubleshoot instrumentation, Capability to diagnose instrumentation, Capability to perform routine repair to instrumentation, Available to work weekends, Ability to work and travel throughout Ontario, Ability to adapt to changing work conditions, Capable of regularly lifting 25 kg, Valid Ontario Class G driver’s license, Clean drivers abstract", "qualificationsPreferred" : "Local Candidates will be preferred", "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "rawDescription" : "### **Job Description** ## **Overview** In this position you will work as a key team member of the Toronto-Vaughan Materials Testing Laboratory team located in Vaughan, ON. The successful candidate will be mentored by a variety of highly specialized professionals and will gain valuable experience in the consulting industry. This intermediate/ senior**** fulltime position will provide comprehensive training in health and safety as well as performing materials testing on various construction materials such as Soils, Aggregates, Concrete & Rock Cores. There is a strong requirement for QA/QC procedures, coordination of project testing, reporting, and teamwork. This opportunity will introduce you to a great team, helping you build key skills that you will need as an **Intermediate Geotechnical Materials Laboratory Technician****,** specifically the application of material properties in construction. ## **Your role** _To perform this role successfully, the candidate will be responsible for but not limited to the following:_ * Conducting materials testing in accordance with OPSS (Ontario Provincial Standards), AASHTO (The American Association of State Highway and Transportation Officials) and ASTM (American Society for Testing and Materials) on various materials such as Soils, Aggregates, Concrete & Rock, etc. * Highly organized, and demonstrate a flexible approach to work assignments. * Effectively communicating test results to the Laboratory Team Lead & Principal Engineer in verbal and written form, timely and effectively. * Participate in functional team activities including safety, housekeeping, training, ordering and maintaining supplies for the laboratory, etc. * Perform other duties as assigned and directed. ## **About you** * College diploma in Civil Engineering or Materials Engineering Technology Programs. * 2-3 years minimum applicable laboratory experience (familiarity with Geotechnical and Materials**** testing protocols). * 2-3 years’ experience conducting testing of Soils & Rock for engineering properties including but not limited to: Atterberg Limits, Hydrometers, Sieves, Moisture Contents, Visual Classifications, advanced lab testing of Various (Triaxial tests, Direct Shear, Consolidation and Permeability tests) Slake Durability, Point Load Testing etc. * Capability to calibrate, troubleshoot, diagnose, and perform routine repair to laboratory instrumentation to ensure they operate at an optimal level. * Available to work weekends on short notice. * Ability to work and travel throughout the Province of Ontario (if required). * Ability to adapt to changing work conditions and schedules on short notice. * Capable of regularly lifting 25 kg test samples as required by the applicable test procedure. * Valid Ontario Class G driver’s license with a clean drivers abstract. * Expected compensation for this role is between Pay Range $56,300- $77,400 annually. Base salaries are determined according to several parameters like skills, experience, and potential impact on the role. Internal and external competitiveness are also taken into account in our offers. Local Candidates will be preferred, and no relocation package will be offered. While AtkinsRéalis Canada Inc., would like to thank all those that apply, only those selected for interviews will be contacted. ## **Rewards & benefits** Explore the rewards and benefits that help you thrive – at every stage of your life and your career at AtkinsRéalis in Canada. Enjoy competitive compensation, employee recognition, and a brilliant range of flexible benefits you can tailor to your health, wellbeing, financial and lifestyle needs. Make the most of diverse opportunities for training and professional development to grow your skills and expertise. And take advantage of our hybrid working culture and generous time-off policies to balance a fulfilling career with your personal life. [Be rewarded. Find out more.](https://careers.atkinsrealis.com/rewards-benefits-canada) ## **About AtkinsRéalis** We're [AtkinsRéalis](https://careers.atkinsrealis.com/), a world-class engineering services and nuclear organization. We connect people, data and technology to transform the world's infrastructure and energy systems. Together, with our industry partners and clients, and our global team of consultants, designers, engineers and project managers, we can change the world. We're committed to leading our clients across our various end markets to engineer a better future for our planet and its people. [Find out more.](https://careers.atkinsrealis.com/) ## **Additional information** AtkinsRéalis cares about your privacy. AtkinsRéalis and other subsidiary or affiliated companies of AtkinsRéalis (referred to throughout as “AtkinsRéalis”) are committed to protecting your privacy. Please consult our [Privacy Notice ](https://careers.atkinsrealis.com/privacy-statement)on our Careers site to know more about how we collect, use, and transfer your Personal Data. By submitting your personal information to AtkinsRéalis, you confirm that you have read and accept our Privacy Notice. _Appropriate accommodation will be provided upon request throughout the recruitment and hiring process as required by Company policy and the Accessibility for Ontarians with Disabilities Act (AODA)._ _Successful applicants will be notified about AtkinsRéalis’ accommodation policies at the time the employment offer is extended, and the information will be shared with new personnel during the onboarding process._ ### **Worker Type** Employee ### **Job Type** Regular _At_ _AtkinsRéalis_ _, we seek to hire individuals with diverse characteristics, backgrounds and perspectives. We strongly believe that world-class talent makes no distinctions based on gender, ethnic or national origin, sexual identity and orientation, age, religion or disability, but enriches itself through these differences._", "summaryDescription" : "Intermediate Geotechnical and Materials Laboratory Technician at Your Privacy. Skills: Materials testing, Geotechnical testing, Laboratory technician. Conduct materials testing. Perform materials testing on Soils", "postedDate" : "2026-06-09T09:51:05.647", "createdAt" : "2026-06-11T09:51:04.969", "lastUpdated" : "2026-06-12T09:28:06.583", "ingestTimestamp" : "2026-06-11T09:51:04.969", "mongoId" : "6a2589c174d8ee00a019a74b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://slihrms.wd3.myworkdayjobs.com/Careers/job/CAONVaughan401-Hanlan-Road/Intermediate-Geotechnical-and-Materials-Laboratory-Technician_R-150181", "salaryAnnualMin" : 56300, "salaryAnnualMax" : 77400, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Materials testing", "Soils testing", "Aggregates testing", "Concrete testing", "Rock cores testing", "Atterberg Limits", "Hydrometers", "Sieves", "Moisture Contents", "Visual Classifications", "Triaxial tests", "Direct Shear", "Consolidation tests", "Permeability tests", "Slake Durability", "Point Load Testing", "Instrumentation calibration", "Instrumentation repair", "Highly organized", "Flexible approach", "Geotechnical testing", "Laboratory technician", "QA/QC procedures", "Project testing coordination", "Laboratory instrumentation", "Geotechnical engineering", "Materials engineering", "Construction materials", "Ontario Provincial Standards", "AASHTO", "ASTM", "Ontario Class G driver’s license" ], "skillCount" : 32, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 1.0, "_score" : 686.2423, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2a8bb974d8ee00a0683a51", "title" : "Laboratory Engineer", "company" : "University of Rochester", "salary" : { "min" : 55955.0, "max" : 78336.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-13T19:14:39.156", "fingerprint" : "0a499374d72c94928e50cfd45f4b307a5fb2db2bbf2ea2fd96819baf49af7603", "source" : "workday", "language" : "en", "applyUrl" : "https://rochester.wd5.myworkdayjobs.com/UR_Staff/job/Laboratory-for-Laser-Energetics/Laboratory-Engineer-I_R272091", "externalId" : "R272091", "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Rochester", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.1572850,-77.6152140" } ], "locationText" : "Rochester, New York, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's degree", "experienceMinYears" : 1, "professionalSkills" : [ "Target assembly", "Manufacturing operations" ], "hardSkillsList" : [ "Metrology hardware", "Manual manipulation" ], "hardSkills" : [ { "name" : "Metrology hardware", "level" : "intermediate" }, { "name" : "Manual manipulation", "level" : "intermediate" } ], "majorSkills" : "Laser laboratory, Component assembly, Data collection", "majorSkillsList" : [ "Laser laboratory", "Component assembly", "Data collection" ], "coreResponsibilities" : "Conduct experiments, tests, and research, Assist in designing experiments, Assist in setting up experiments, Assist in maintaining equipment, Assist in collecting data, Diagnose system components, Perform preventative maintenance, Manage fragile targets, Develop innovative solutions, Manipulate delicate micro-assemblies, Develop manufacturing methods, Develop operation sequences, Develop fabrication processes, Design sequence of operations, Specify procedures for fabrication, Adapt machinery, Maintain records, Maintain reporting systems, Develop documentation of findings, Develop documentation of implemented solutions, Communicate results to staff, Measure completed assemblies, Collect data, Clean lab equipment, Adjust lab equipment, Replace parts on lab equipment, Work in a safe manner", "domainKnowledge" : "Laser laboratory", "domainList" : [ "laser-laboratory" ], "domainSpecificKnowledge" : [ "Laser laboratory" ], "communicationSkills" : "Communicate results", "documentationSkills" : "Develop documentation", "innovationCreativity" : "Develop innovative solutions", "problemSolvingSkills" : "Technical problems", "specialRequirements" : "Work onsite 8:30a-5:30p", "qualificationsBasic" : "Bachelor's degree and 1 year experience, Assemble millimeter-scale components, Work in cleanroom laboratory environment, Operate microscope in cleanroom", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive. _**Job Location (Full Address):**_ 250 East River Rd, Rochester, New York, United States of America, 14623 _**Opening:**_ Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 250548 LLE-Laboratory for Laser Energ Work Shift: UR - Day (United States of America) Range: UR URG 109 Compensation Range: $55,955.00 - $78,336.00 _The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job 's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._ _**Responsibilities:**_ Conducts experiments, tests, and research within a laser laboratory setting. Assists more experienced engineers or scientists in designing and setting up experiments, maintaining equipment, and collecting data. Diagnoses and performs preventative maintenance on system components including recovery, replacement, and reconfiguration of damaged sensitive components. Manages fragile targets for laser exploration. This is an onsite position 8:30a-5:30p. **ESSENTIAL FUNCTIONS** * Required to assemble millimeter-scale components that meet specifications * Expected to develop innovative but practical solutions to technical problems in target assembly to enhance manufacturability * Capable at working in cleanroom laboratory environment, using manual techniques to manipulate delicate micro-assemblies * Ability to operate microscope in cleanroom environment * Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies, and final assemblies. * Designs the sequence of production operations, specifying procedures for the fabrication of applicable tools and equipment, and adapting machinery * Maintains records and reporting systems for coordination of manufacturing operations * Develops appropriate documentation of findings and implemented solutions and communicates results to staff * Measures completed assemblies using metrology hardware and collects data * Cleans, adjusts and replaces parts on lab equipment * Expected to work in a safe manner in accordance with established operating procedures and practices. * Other duties as assigned. **MINIMUM EDUCATION & EXPERIENCE** * Bachelor's degree and 1 year of relevant experience required * Or equivalent combination of education and experience The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.", "summaryDescription" : "Laboratory Engineer at University of Rochester. Skills: Laser laboratory, Component assembly, Data collection. Conduct experiments, tests, and research. Assist in designing experiments", "postedDate" : "2026-06-10T18:40:58.891", "createdAt" : "2026-06-11T18:40:58.757", "lastUpdated" : "2026-06-13T19:14:39.156", "ingestTimestamp" : "2026-06-11T18:40:58.757", "mongoId" : "6a2a8bb974d8ee00a0683a51", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://rochester.wd5.myworkdayjobs.com/UR_Staff/job/Laboratory-for-Laser-Energetics/Laboratory-Engineer-I_R272091", "salaryAnnualMin" : 55955, "salaryAnnualMax" : 78336, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Metrology hardware", "Manual manipulation", "Laser laboratory", "Component assembly", "Data collection", "Target assembly", "Manufacturing operations" ], "skillCount" : 7, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 677.85657, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2c960974d8ee00a098e758", "title" : "Laboratory Director, IVF & ART", "company" : "Di Rezze Family Office", "industry" : "Healthcare", "location" : "Remote", "locations" : [ "Remote" ], "certifications" : [ "HCLD (High-complexity Clinical Laboratory Director)", "ELD" ], "timestamp" : "2026-06-15T07:12:02.198", "fingerprint" : "6d42585f1f35d211f3066596d91203ab34db12556f143c1e3d60c8019ebed6ed", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/dfo/jobs/4281740009", "externalId" : "4281740009", "industryFunction" : { }, "structuredLocations" : [ { "workMode" : "remote" } ], "locationText" : "", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "technicalSkills" : "EmbryoScope+, RI Witness, Matcher, EIVF, NGS", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Facility design", "Pre-construction planning", "Construction oversight", "Commissioning", "Equipment installation", "Validation", "Staff recruitment", "Staff onboarding", "SOP authoring", "Quality systems", "QA/QC program", "Regulatory compliance", "Outsourcing relationships", "Automation readiness", "Network expansion" ], "hardSkillsList" : [ "Clinical laboratory management", "Accreditation", "Facility specification", "Equipment planning", "HVAC capacity", "Electrical service", "Medical gas infrastructure", "ISO classification", "Cryostorage capacity", "Andrology workstation", "Robotic IVF deployment", "CLIA", "CAP", "SART membership", "PGT outsourcing", "In-house NGS", "Clinical outcomes", "Technical standard", "Spoke lab integrations", "Acquisition diligence", "Automation partnerships", "Pipeline building" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Clinical laboratory management", "level" : "intermediate" }, { "name" : "Accreditation", "level" : "intermediate" }, { "name" : "Facility specification", "level" : "intermediate" }, { "name" : "Equipment planning", "level" : "intermediate" }, { "name" : "HVAC capacity", "level" : "intermediate" }, { "name" : "Electrical service", "level" : "intermediate" }, { "name" : "Medical gas infrastructure", "level" : "intermediate" }, { "name" : "ISO classification", "level" : "intermediate" }, { "name" : "Cryostorage capacity", "level" : "intermediate" }, { "name" : "Andrology workstation", "level" : "intermediate" }, { "name" : "Robotic IVF deployment", "level" : "intermediate" }, { "name" : "CLIA", "level" : "intermediate" }, { "name" : "CAP", "level" : "intermediate" }, { "name" : "SART membership", "level" : "intermediate" }, { "name" : "PGT outsourcing", "level" : "intermediate" }, { "name" : "In-house NGS", "level" : "intermediate" }, { "name" : "Clinical outcomes", "level" : "intermediate" }, { "name" : "Technical standard", "level" : "intermediate" }, { "name" : "Spoke lab integrations", "level" : "intermediate" }, { "name" : "Acquisition diligence", "level" : "intermediate" }, { "name" : "Automation partnerships", "level" : "intermediate" }, { "name" : "Pipeline building", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "IVF laboratory operations, Accreditation and compliance", "majorSkillsList" : [ "IVF laboratory operations", "Accreditation and compliance" ], "coreResponsibilities" : "Walk candidate sites, Produce technical feasibility memos, Define lab program, Select and brief IVF facility review, Sign off on HVAC, air quality, cryostorage, Build Day 1 equipment plan, Design lab for automation readiness, Oversee construction, Oversee commissioning, Oversee equipment installation, Oversee validation, Recruit senior embryology staff, Onboard senior embryology staff, Recruit senior andrology staff, Onboard senior andrology staff, Author all SOPs, Author quality systems documentation, Author QA/QC program, Drive CLIA accreditation, Drive CAP accreditation, Drive Florida Department of Health accreditation, Lead SART membership application, Establish PGT outsourcing relationships, Direct day-to-day lab operations, Manage clinical outcomes, Manage staffing, Manage quality, Manage regulatory compliance, Manage vendor management, Set technical standard for spoke lab integrations, Set technical standard for acquisition diligence, Lead evaluation of automation partnerships, Lead evaluation of PGT in-sourcing, Mentor junior staff, Build pipeline for network expansion", "teamCollaboration" : "Cross-functional teams; Architects; Engineers; Product teams; Senior staff; Junior staff; Vendors; Stakeholders", "projectManagementSkills" : [ "Feasibility and design engagement", "Construction oversight", "Commissioning", "Accreditation process", "Operations management", "Scale management" ], "domainKnowledge" : "IVF; ART; Embryology; Andrology; Cryostorage; Medical gas infrastructure; ISO classification; PGT; NGS; CLIA; CAP; SART; Robotic IVF; Automation landscape", "domainList" : [ "ivf", "art", "embryology", "andrology", "cryostorage", "medical-gas-infrastructure", "iso-classification", "pgt", "ngs", "clia", "cap", "sart", "robotic-ivf", "automation-landscape" ], "domainSpecificKnowledge" : [ "IVF", "ART", "Embryology", "Andrology", "Cryostorage", "Medical gas infrastructure", "ISO classification", "PGT", "NGS", "CLIA", "CAP", "SART", "Robotic IVF", "Automation landscape" ], "toolProficiency" : [ "EmbryoScope+", "RI Witness", "Matcher", "EIVF", "Conceivable", "AURA", "CHLOE", "Life Whisperer", "ALife" ], "communicationSkills" : "Technical memos; Briefing architects; Briefing engineers; SOP authoring; Quality systems documentation; QA/QC program; Regulatory reporting; SART membership application; Technical standard setting; Acquisition diligence; Pipeline building", "documentationSkills" : "Technical memos; SOPs; Quality systems documentation; QA/QC program", "innovationCreativity" : "Automation-ready design; Future robotic IVF deployment", "problemSolvingSkills" : "Feasibility analysis; Technical problem solving; Quality system development; Regulatory compliance; Troubleshooting", "specialRequirements" : "Feasibility and design engagement, Consulting-to-hire path, Transition to full-time Director", "outcomesObjectives" : "Achieve accreditation; Open laboratory; Scale laboratory operations; Meet ISO classification targets; Meet cryostorage capacity targets; Meet andrology room layout targets; Meet procedure room layout targets; Meet Day 1 equipment plan; Achieve CLIA accreditation; Achieve CAP accreditation; Achieve Florida accreditation; Establish PGT outsourcing relationships; Achieve 600+ cycles/year for in-house NGS; Meet clinical outcomes targets; Meet staffing targets; Meet quality targets; Meet regulatory compliance targets; Meet vendor management targets; Set technical standard for spoke lab integrations; Set technical standard for acquisition diligence; Evaluate automation partnerships; Evaluate PGT in-sourcing; Build pipeline for network expansion", "qualificationsBasic" : "HCLD certification through ABB, PhD-track credential with ELD, Commissioned at least one IVF lab, Direct operating experience with time-lapse incubation, Direct operating experience with electronic witnessing, Direct operating experience with modern LIMS, Run a lab through 200-600+ annual cycle inflection, Authored SOPs from scratch, Led CAP inspections, Operated under current witnessing and traceability standards, Familiar with post-Alabama regulatory environment, Familiar with lessons from recent IVF mix-up incidents", "qualificationsPreferred" : "Florida operating experience, Prior tenure at premium-segment network, Direct experience opening or scaling a network lab, Published research, Society leadership (ASRM, SART, ABB)", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Laboratory Director, IVF transition into operational leadership through accreditation, opening, and scale. Consulting-to-hire. Begin with a paid feasibility and design engagement (typically 8–12 weeks) covering site walk-through, technical memo, facility spec, and equipment plan. Convert to full-time Laboratory Director ahead of construction kickoff. This path is designed for candidates currently in director roles who want to validate the opportunity before transitioning. Both paths lead to the same destination. The recruiter can route candidate preferences. What you will own Phase 1 — Facility design and pre-construction (months 0–6) Walk candidate sites and produce technical feasibility memos covering floor-to-floor height, floor load, HVAC capacity, electrical service, LN2 routing, medical gas infrastructure, and adjacent-tenant risk. Define the lab program: square footage, room adjacencies, ISO classification targets, equipment footprint, cryostorage capacity, andrology and procedure room layout. Select and brief the IVF facility consultant; review schematic and construction documents from the architect of record; sign off on HVAC, air quality, and cryostorage engineering. Build the Day 1 equipment plan, including time-lapse incubation (EmbryoScope+ or equivalent), electronic witnessing (RI Witness or Matcher), LIMS (eIVF or equivalent), and andrology workstation specifications. Design the lab to be automation-ready for future robotic IVF deployment (e.g., Conceivable/AURA) without committing premature capital. Phase 2 — Construction, commissioning, and accreditation (months 6–12) Oversee construction, commissioning, equipment installation, and validation. Recruit and onboard senior embryology and andrology staff (the Laboratory Director chooses these hires). Author all SOPs, quality systems documentation, and the QA/QC program. Drive CLIA, CAP, and Florida licensure; lead the SART membership application. Establish PGT outsourcing relationships for Years 1–2, with a defined pathway to in-house NGS at 600+ cycles/year. Phase 3 — Operations and scale (months 12+) Direct day-to-day lab operations: clinical outcomes, staffing, quality, regulatory compliance, vendor management. Set the technical standard for spoke lab integrations and future acquisition diligence. Lead the Year 2–3 evaluation of automation partnerships and PGT in-sourcing. Mentor junior embryologists; build a pipeline that supports network expansion. Required qualifications Certification: HCLD (High-complexity Clinical Laboratory Director) through ABB, or equivalent PhD-track credential with ELD. Required for CLIA Lab Director of record. Greenfield build experience: Has commissioned at least one IVF lab from shell space through CAP/CLIA accreditation. We will ask for specifics: square footage, cycle volume at launch, lease-to-first-transfer timeline. Technology fluency: Direct operating experience with time-lapse incubation (EmbryoScope+ specifically), electronic witnessing (RI Witness and/or Matcher), and a modern LIMS. Informed opinions on tradeoffs, not brand familiarity. Volume scaling: Has run a lab through the 200 → 600+ annual cycle inflection, with the staffing, equipment redundancy, and quality systems that come with it. Quality systems leadership: Has authored SOPs from scratch, led CAP inspections, and operated under current witnessing and traceability standards. Familiar with post-Alabama regulatory environment and lessons from recent IVF mix-up incidents. Automation literacy: Familiar with the current automation landscape (Conceivable/AURA, CHLOE, Life Whisperer, ALife) without being a true believer. Builds automation-ready, not automation-dependent. Preferred Florida operating experience, including familiarity with Office Surgery Registration pathway. Prior tenure at a premium-segment network (CCRM, Shady Grove, RMA, Boston IVF, Spring Fertility, or equivalent). Direct experience opening or scaling a network lab (multi-site, hub-and-spoke). Published research or society leadership (ASRM, SART, ABB).", "summaryDescription" : "Laboratory Director, IVF & ART at Di Rezze Family Office. Skills: IVF laboratory operations, Accreditation and compliance. Walk candidate sites. 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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", "Feasibility and design engagement", "Accreditation process", "Operations management", "Scale management", "IVF", "ART", "Embryology", "Andrology", "Cryostorage", "PGT", "NGS", "SART", "Robotic IVF", "Automation landscape", "HCLD (High-complexity Clinical Laboratory Director)", "ELD", "EmbryoScope+", "RI Witness", "Matcher", "EIVF", "Conceivable", "AURA", "CHLOE", "Life Whisperer", "ALife" ], "skillCount" : 72, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Director", "dataQualityScore" : 0.8888889, "_score" : 677.7778, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2a660474d8ee00a062b85a", "title" : "Failure Analysis Manager, Product Integrity, Failure Analysis", "company" : "Amazon.com Services LLC", "industry" : "Hardware Development, alexa and amazon devices", "salary" : { "min" : 151000.0, "max" : 204300.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Seattle, Washington, USA", "locations" : [ "Seattle, Washington, USA" ], "timestamp" : "2026-06-15T00:55:59.753", "fingerprint" : "1a7971a01e81b04d5064491f8547a02c700109446edfd1e5fd3ef59a8664aafb", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.jobs/jobs/10443849/apply", "externalId" : "b67eeed8-43a9-424c-a9dd-0469c9b8e3d5", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Seattle", "state" : "Washington", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "47.6038321,-122.3300620" } ], "locationText" : "Seattle, Washington, United States", "employmentType" : "FULL_TIME", "experienceLevel" : "Manager", "technicalSkills" : "Electrical fault isolation, Physical analysis, Accelerated stress testing, Materials selection", "professionalSkills" : [ "Technical strategy", "Root cause analysis", "Risk assessment", "Corrective actions", "Failure risk", "Product decisions", "Design improvements", "Roadmap planning", "Lab capacity scaling", "Cross-functional problem solving", "Design changes", "Process changes", "Manufacturing changes", "Hardware quality", "Risk assessment", "Corrective action plans", "Stakeholder management", "Program management", "Budget planning" ], "hardSkillsList" : [ "Failure analysis", "Reliability testing", "Materials characterization", "Fault isolation", "Stress testing", "Root cause clarity", "Risk assessment", "Corrective actions", "Failure rate modeling", "DFMEA", "DfR" ], "softSkillsList" : [ "Leadership", "Mentorship" ], "hardSkills" : [ { "name" : "Failure analysis", "level" : "intermediate" }, { "name" : "Reliability testing", "level" : "intermediate" }, { "name" : "Materials characterization", "level" : "intermediate" }, { "name" : "Fault isolation", "level" : "intermediate" }, { "name" : "Stress testing", "level" : "intermediate" }, { "name" : "Root cause clarity", "level" : "intermediate" }, { "name" : "Risk assessment", "level" : "intermediate" }, { "name" : "Corrective actions", "level" : "intermediate" }, { "name" : "Failure rate modeling", "level" : "intermediate" }, { "name" : "DFMEA", "level" : "intermediate" }, { "name" : "DfR", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentorship" } ], "majorSkills" : "Failure analysis, Reliability testing, Hardware quality, Root cause analysis", "majorSkillsList" : [ "Failure analysis", "Reliability testing", "Hardware quality", "Root cause analysis" ], "coreResponsibilities" : "Own failure analysis outcomes, Own reliability testing outcomes, Set technical strategy, Identify capability gaps, Prioritize investment, Define roadmap, Drive cross-functional problem solving, Translate failure insights, Serve as escalation point, Deliver risk assessments, Deliver corrective action plans, Cultivate partnerships, Position lab as resource, Build high-performing team, Recruit top talent, Provide technical mentorship, Create growth paths, Oversee investigations, Oversee reliability tests, Ensure timely updates, Ensure rigorous reports, Ensure clear recommendations, Lead special projects, Innovate on behalf of customers, Expand knowledge base, Develop new methodologies, Manage stakeholder relationships, Communicate resource needs, Communicate project progress, Communicate budget planning", "teamCollaboration" : "Cross-functional problem solving; Partnerships with engineering; Partnerships with supply chain; Partnerships with program teams", "projectManagementSkills" : [ "Roadmap planning" ], "domainKnowledge" : "Consumer electronics; Spacecrafts; Drones; Data center infrastructure; Robotics; Hardware quality; Product Integrity; Failure Analysis; Lab126 subsidiary; Prime Air; Mechatronics; AWS; Annapurna; Lab126 Devices; Materials Characterization; High-reliability industries", "domainList" : [ "consumer-electronics", "spacecrafts", "drones", "data-center-infrastructure", "robotics", "hardware-quality", "product-integrity", "failure-analysis", "lab126-subsidiary", "prime-air", "mechatronics", "aws", "annapurna", "lab126-devices", "materials-characterization", "high-reliability-industries" ], "domainSpecificKnowledge" : [ "Consumer electronics", "Spacecrafts", "Drones", "Data center infrastructure", "Robotics", "Hardware quality", "Product Integrity", "Failure Analysis", "Lab126 subsidiary", "Prime Air", "Mechatronics", "AWS", "Annapurna", "Lab126 Devices", "Materials Characterization", "High-reliability industries" ], "toolProficiency" : [ "CT X-ray", "SEM", "EDS", "FTIR", "XRF" ], "communicationSkills" : "Verbal communication; Written communication; Risk assessment communication; Corrective action communication", "documentationSkills" : "Rigorous reports", "continuousLearning" : "Expand knowledge base; Developing new methodologies", "innovationCreativity" : "Innovate on behalf of customers", "problemSolvingSkills" : "Root cause analysis; Structured problem-solving; Failure analysis; Troubleshooting", "outcomesObjectives" : "Deliver root cause clarity; Shape product decisions; Drive corrective action decisions", "qualificationsBasic" : "7+ years hardware development, Master's degree or equivalent, Proven leadership experience, Hands-on capability component/board/system, Extensive experience resolving quality issues, Ability to operate in fast-paced environments", "qualificationsPreferred" : "Expert-level proficiency leading investigations, Hands-on experience physical FA techniques, Knowledge of reliability engineering disciplines, Experience standing up lab safety programs", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "As the Failure Analysis Manager, you will own the technical strategy and execution for a team that investigates why hardware fails and ensures it doesn't fail again. Your team applies electrical fault isolation, physical analysis, and accelerated stress testing to Amazon's most complex hardware, turning ambiguous failures into actionable design improvements. You will lead a team of highly talented engineers through investigations spanning NPI and field returns, delivering root cause clarity that directly shapes product decisions. You will set the vision for the team's growth, build senior-level partnerships across Amazon's hardware portfolio, and serve as the authoritative voice on failure risk, corrective actions, and recovery plans for critical customer escalations. Key job responsibilities - Own root cause failure analysis and reliability testing outcomes across Amazon's hardware portfolio: consumer electronics, spacecrafts, drones, data center infrastructure, robotics, and some others - Set technical strategy for the team: identify capability gaps, prioritize investment in new analytical methods, and define the roadmap for scaling lab capacity - Drive cross-functional problem solving that translates failure insights into upstream design, process, and manufacturing changes - Serve as the primary escalation point for critical hardware quality issues, delivering clear risk assessments and corrective action plans to senior leadership - Cultivate partnerships with engineering, supply chain, and program teams to position the lab as an indispensable resource across the product lifecycle - Build and develop a high-performing team: recruit top talent, provide technical mentorship, and create growth paths for engineers with diverse science and engineering backgrounds A day in the life You will move fluidly between our office and the lab just down the hallway. You'll oversee a portfolio of investigations and reliability tests at various stages, ensuring your team delivers timely updates, rigorous reports, and clear recommendations that drive corrective action decisions. Beyond day-to-day operations, you will lead special projects to innovate on behalf of customers and expand the Product Integrity team's knowledge base, developing new methodologies to advance materials selection, design, and operational improvements. You will also manage stakeholder relationships across the business, communicating resource needs, project progress, and budget planning as you scale the lab's impact. About the team SPICE lab is a Seattle-based R&D team within Amazon's Lab126 subsidiary, partnering with Amazon's most ambitious hardware organizations. We support a growing portfolio of programs including Prime Air, Leo, Mechatronics, AWS, Annapurna, Lab126 Devices, and others. If you are passionate about building the future and want to take part in developing ideas from concept to production, consider joining the SPICE lab team! Our lab operates across three closely integrated functions: Failure Analysis, Reliability Testing, and Materials Characterization. These disciplines reinforce each other — failure investigations inform test planning, reliability testing reproduces mechanisms to validate root cause hypotheses, and shared analytical techniques underpin materials selection decisions. This role will manage both the Failure Analysis and Reliability Testing teams. Basic Qualifications: - 7+ years of new hardware products development experience - Master's degree or equivalent in mechanical engineering, electrical engineering, material science, physics or equivalent - Proven leadership experience scaling technical teams and root cause FA capabilities in high-reliability industries - Strong hands-on capability with established depth across component, board, and system failure domains, and a track record of influencing hardware design decisions at the portfolio level - Extensive experience resolving critical, systemic quality issues across high-performance hardware programs using structured problem-solving methodologies - Ability to operate in fast-paced, ambiguous environments, manage competing priorities under tight deadlines, and redirect efforts as business needs evolve - Excellent verbal and written communication skills Preferred Qualifications: - Expert-level proficiency leading complex investigations from symptom through root cause to verified corrective action, across both NPI and sustained production - Hands-on experience with physical failure analysis techniques: non-destructive (CT X-ray, optical/UV/thermal imaging, TDR) and destructive (SEM, EDS, FTIR, XRF, cross-sectioning) - Knowledge of reliability engineering disciplines including accelerated life testing, failure rate modeling, Design Failure Mode and Effects Analysis (DFMEA), and Design for Reliability (DfR) - Experience standing up or maturing lab safety programs, quality management systems, and compliance with industry standards 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. The base salary range for this position is listed below. Your Amazon package will include sign-on payments and restricted stock units (RSUs). Final compensation will be determined based on factors including experience, qualifications, and location. Amazon also offers comprehensive benefits including health insurance (medical, dental, vision, prescription, Basic Life & AD&D insurance and option for Supplemental life plans, EAP, Mental Health Support, Medical Advice Line, Flexible Spending Accounts, Adoption and Surrogacy Reimbursement coverage), 401(k) matching, paid time off, and parental leave. Learn more about our benefits at https://amazon.jobs/en/benefits . USA, WA, SEATTLE - 151,000.00 - 204,300.00 USD annually", "summaryDescription" : "Failure Analysis Manager, Product Integrity, Failure Analysis at Amazon.com Services LLC. Skills: Failure analysis, Reliability testing, Hardware quality, Root cause analysis. Own failure analysis outcomes. Own reliability testing outcomes", "postedDate" : "2026-06-13T09:51:13.873", "createdAt" : "2026-06-13T09:51:13.873", "lastUpdated" : "2026-06-15T00:55:59.753", "ingestTimestamp" : "2026-06-13T09:51:13.873", "mongoId" : "6a2a660474d8ee00a062b85a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.jobs/jobs/10443849/apply", "salaryAnnualMin" : 151000, "salaryAnnualMax" : 204300, "salaryBand" : "150k-200k", "hasSalary" : true, "allSkills" : [ "Failure analysis", "Reliability testing", "Materials characterization", "Fault isolation", "Stress testing", "Root cause clarity", "Risk assessment", "Corrective actions", "Failure rate modeling", "DFMEA", "DfR", "Leadership", "Mentorship", "Hardware quality", "Root cause analysis", "Technical strategy", "Failure risk", "Product decisions", "Design improvements", "Roadmap planning", "Lab capacity scaling", "Cross-functional problem solving", "Design changes", "Process changes", "Manufacturing changes", "Corrective action plans", "Stakeholder management", "Program management", "Budget planning", "Consumer electronics", "Spacecrafts", "Drones", "Data center infrastructure", "Robotics", "Product Integrity", "Failure Analysis", "Lab126 subsidiary", "Prime Air", "Mechatronics", "AWS", "Annapurna", "Lab126 Devices", "Materials Characterization", "High-reliability industries", "CT X-ray", "SEM", "EDS", "FTIR", "XRF" ], "skillCount" : 49, "jobCategory" : "other", "dataQualityScore" : 1.0, "_score" : 675.4217, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology" }, { "id" : "69ce5e3b9bc74574cb677a2d", "title" : "Chassis Testing Engineer", "company" : "Mercedes-Benz Group China Ltd.", "industry" : "Manufacturing", "salary" : { "min" : 350000.0, "max" : 550000.0, "currency" : "CNY", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Chassis Testing Engineer in Beijing, China, adjusted for the automotive industry and company size." }, "location" : "China (Mainland)-Beijing-Beijing", "locations" : [ "China (Mainland)-Beijing-Beijing", "8 Boxing Road, BDA, Beijing" ], "timestamp" : "2026-06-15T08:16:51.083", "fingerprint" : "9ef2282ef3052f2e87d219f8f73ef21f1cb5635647568c034620109fc9cc3ace", "source" : "taleo", "language" : "en", "applyUrl" : "https://daimler.taleo.net/careersection/ex/jobdetail.ftl?job=887896", "externalId" : "887896", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Beijing", "country" : "China", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "39.9057136,116.3912972" } ], "locationText" : "Beijing, China", "minimumEducation" : "Bachelor's", "technicalSkills" : "Chassis technology, Chassis control systems", "professionalSkills" : [ "Test fixture design", "Test fixture coordination", "Vendor communication", "3D measurements", "Retrofit coordination", "Test procedure development", "Test concept development" ], "hardSkillsList" : [ "Fatigue testing", "Durability testing", "Mechanical design reading", "Software requirement reading", "Electrical drawing reading" ], "softSkillsList" : [ "Analytical thinking", "Goal orientation", "Result orientation" ], "hardSkills" : [ { "name" : "Fatigue testing", "level" : "intermediate" }, { "name" : "Durability testing", "level" : "intermediate" }, { "name" : "Mechanical design reading", "level" : "intermediate" }, { "name" : "Software requirement reading", "level" : "intermediate" }, { "name" : "Electrical drawing reading", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Analytical thinking" }, { "name" : "Goal orientation" }, { "name" : "Result orientation" } ], "majorSkills" : "Chassis durability, Test laboratory", "majorSkillsList" : [ "Chassis durability", "Test laboratory" ], "coreResponsibilities" : "Plan test bench fixtures, Design test bench fixtures, Coordinate test bench fixtures, Ensure fixture readiness, Coordinate external vendors, Track external vendors, Coordinate onsite measurements, Coordinate international stakeholders, Coordinate chassis retrofit, Align demand, Align with workshop, Ensure planning efficiency, Ensure retrofit efficiency, Plan test rig occupancy, Develop test procedures, Develop test concepts, Align with stakeholders Germany, Perform cross-functional tasks", "teamCollaboration" : "Coordination with HQ Germany; Coordination with international stakeholders; Coordination with counterparts; Cross-functional tasks", "projectManagementSkills" : [ "Planning skills", "Organizational skills" ], "domainKnowledge" : "Automotive engineering; Mechanical engineering; Material science; Measurement technology; Fatigue; Durability; Chassis technology; Chassis control systems; Testing lab; Chassis durability lab; Ride handling; Driving safety", "domainList" : [ "automotive-engineering", "mechanical-engineering", "material-science", "measurement-technology", "fatigue", "durability", "chassis-technology", "chassis-control-systems", "testing-lab", "chassis-durability-lab", "ride-handling", "driving-safety" ], "domainSpecificKnowledge" : [ "Automotive engineering", "Mechanical engineering", "Material science", "Measurement technology", "Fatigue", "Durability", "Chassis technology", "Chassis control systems", "Testing lab", "Chassis durability lab", "Ride handling", "Driving safety" ], "toolProficiency" : [ "Siemens NX" ], "communicationSkills" : "Intercultural competence; Communication skills", "documentationSkills" : "Mechanical design documents; Software requirement documents; Electrical drawings", "problemSolvingSkills" : "Analytical thinking", "specialRequirements" : "Travel inside China, Travel to Germany", "outcomesObjectives" : "Ensure on-time readiness; Match test timeline; Ensure high test bench utilization", "qualificationsBasic" : "University degree automotive engineering, University degree mechanical engineering, Fluent English knowledge, Computer skills mandatory, Windows proficiency, Office proficiency, CAx proficiency, Siemens NX proficiency", "qualificationsPreferred" : "Specialization material science beneficial, Specialization measurement technology beneficial, Chinese native speaking skills preferred, German language beneficial", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Primary Project Responsibility 1.      Chassis System Test Fixtures a)      Planning, design & coordination of test bench fixtures for the chassis durability lab in the Mercedes-Benz Tech Center China. b)      Ensuring on-time readiness for all fixtures & adapters to match the test timeline. c)      External vendor communication & tracking. d)      Coordination of onsite 3D measurements. e)      Coordination of co-operation with international stakeholders. 2.      Chassis Planning & Retrofit f)       Coordination of chassis retrofit activities. g)      Alignment of demand with chassis durability, ride/ handling & driving safety Teams. h)      Alignment with Tech Center China workshop. i)        Ensuring planning & retrofit efficiency. 3.      Chassis System Test j)       In coordination with int./ext. counterparts and HQ Germany - occupancy planning of the test rigs to ensure high test bench utilization. k)      Participation in the further development of the test procedures and concepts used in the test laboratory in order to meet the requirements of the product and the current state of technology. General Task Description 4.      Technical alignment with Stakeholders in Germany. 5.      Cross-functional tasks based on business needs. Qualification § University degree for automotive engineering, mechanical engineering or related engineering background. Specialization in material science or measurement technology beneficial. Experience & Specific Knowledge : § Profund knowledge and experience in at least one of the following area: fatigue and durability/ chassis technology/ chassis control systems engineering or testing lab. § Ability to read mechanical design document and software requirement documents including electrical drawings. § Fluent knowledge of English. § Computer skills mandatory, including Windows, Office, CAx (Siemens NX) § Chinese native speaking skills preferred. § Willingness to travel inside China and to Germany German language beneficial. Soft Skills § Strong planning and organizational skills § Self-responsible working attitude and initiative § High commitment for premium vehicles of Mercedes-Benz and quality § Intercultural competence and communication skills with various hierarchy levels § Analytical thinking § Goal and result orientation § Intercultural competence Mercedes-Benz Group China Ltd.", "summaryDescription" : "Chassis Testing Engineer at Mercedes-Benz Group China Ltd.. Skills: Chassis durability, Test laboratory. Plan test bench fixtures. Design test bench fixtures", "createdAt" : "2026-06-14T01:36:40.677", "lastUpdated" : "2026-06-15T08:16:51.083", "ingestTimestamp" : "2026-06-14T01:36:40.677", "mongoId" : "69ce5e3b9bc74574cb677a2d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Fatigue testing", "Durability testing", "Mechanical design reading", "Software requirement reading", "Electrical drawing reading", "Analytical thinking", "Goal orientation", "Result orientation", "Chassis durability", "Test laboratory", "Test fixture design", "Test fixture coordination", "Vendor communication", "3D measurements", "Retrofit coordination", "Test procedure development", "Test concept development", "Planning skills", "Organizational skills", "Automotive engineering", "Mechanical engineering", "Material science", "Measurement technology", "Fatigue", "Durability", "Chassis technology", "Chassis control systems", "Testing lab", "Chassis durability lab", "Ride handling", "Driving safety", "Siemens NX" ], "skillCount" : 32, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 674.8234, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Automotive", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ad06e74d8ee00a071240d", "title" : "Laboratory Assistant PRN", "company" : "Advocate Health", "industry" : "Healthcare", "salary" : { "min" : 19.8, "max" : 29.7, "currency" : "USD", "frequency" : "yearly" }, "location" : "Macon, GA", "locations" : [ "Macon, GA", "United States of America" ], "certifications" : [ "None required" ], "timestamp" : "2026-06-14T22:21:35.593", "fingerprint" : "3b1df50966737a8025095be8cdf1b54c6412486f6f1006f5c4f8b9fb0e4c9b71", "source" : "workday", "language" : "en", "applyUrl" : "https://aah.wd5.myworkdayjobs.com/External/job/Atrium-Health-Navicent-The-Medical-Center---777-Hemlock-St-Macon-GA/Laboratory-Assistant-PRN_R243599", "externalId" : "R243599", "industryFunction" : { }, "locationPoint" : "50.05072,4.20918", "structuredLocations" : [ { "city" : "Macon", "state" : "Georgia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.8406946,-83.6324022" } ], "locationText" : "Macon, Georgia, United States", "employmentType" : "PART_TIME", "minimumEducation" : "High School", "professionalSkills" : [ "Data entry", "Order entry", "Client support" ], "hardSkillsList" : [ "Patient data retrieval", "Specimen processing", "Specimen labeling" ], "hardSkills" : [ { "name" : "Patient data retrieval", "level" : "intermediate" }, { "name" : "Specimen processing", "level" : "intermediate" }, { "name" : "Specimen labeling", "level" : "intermediate" } ], "majorSkills" : "Data entry, Specimen processing, Client service", "majorSkillsList" : [ "Data entry", "Specimen processing", "Client service" ], "coreResponsibilities" : "Operate laboratory and hospital information system, Enter patient demographic data, Enter laboratory test orders, Process outpatient lab specimens, Order tests accurately, Label specimens for testing, Retrieve patient data and results, Operate remote printers and fax, Retrieve archived patient data, Adhere to HIPAA standards, Provide client service, Call stat results to clients, Document client calls and callbacks, Answer and transfer calls, Utilize telephone call queue system, Enter information into client call database, Use computer system for interdepartmental email, Track specimens, Utilize web based orders, Retrieve results, Scan and index lab requisitions, Inform couriers of specimen pickups, Assist with local specimen pickups, Follow universal safety precaution standards, Follow patient safety policies, Provide support for all lab departments, Retrieve information, Assist as needed", "teamCollaboration" : "Partnership with Patient Registration", "domainKnowledge" : "HIPAA standards", "domainList" : [ "hipaa-standards" ], "domainSpecificKnowledge" : [ "HIPAA standards" ], "toolProficiency" : [ "Laboratory information system", "Hospital information system", "Optical disk" ], "communicationSkills" : "Call stat results; Document client calls", "documentationSkills" : "Document client calls", "specialRequirements" : "Weekend Rotation, Holiday Rotation, Use visual acuity, Hear and verbally communicate, Sit for prolonged periods, Functional range of motion, Grip strength 50-60#, Forward reach, Overhead reach, Bend, squat, kneel, Apply proper body mechanics, Lift up to 10#", "outcomesObjectives" : "Ensure quality results reported timely", "qualificationsBasic" : "High School or GED Diploma Graduate", "qualificationsPreferred" : "Previous lab experience, Medical terminology or knowledge, Customer service data entry and computer skills, Phlebotomy skills a plus", "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Department:** 60916 Navicent Health Medical Center - Lab: Reference Lab Testing **Status:** Part time **Benefits Eligible:** No **Hou****rs Per Week:** 0 **Schedule Details/Additional Information:** * Various Shift: Hours 8:00 am to 10:00 pm (Monday-Friday) * (Weekend Rotation—Sat & Sun) 8:00 am to 5:00 pm every six weeks * (Holiday Rotation) 8:00 am to 5:00 pm every six months **Pay Range** $19.80 - $29.70 **Job Summary:** Performs data entry of patient information and laboratory test orders on outpatient laboratory specimens to ensure quality results are reported timely to the clients of Clinical Laboratory and Central Georgia Diagnostics Reference Laboratory Services. Provides client support for physicians and staff as needed. **Major Responsibilities:** * Operates laboratory and hospital information system for entry and retrieval of patient demographic data and order entry. Works in partnership with Patient Registration department to ensure data is obtained and entered into system. * Processes outpatient lab specimens, accurately orders tests and labels specimens for testing in the clinical lab. * Retrieves patient data and results for clients and physicians. Operates remote printers and fax to deliver information as requested. Retrieves archived patient data from optical disk. Adheres to HIPAA standards at all times to ensure patient confidentiality. * Provides client service with customer oriented focus for clients and physicians concerning clinical data. Calls stat results to clients and physicians. Documents client calls and callbacks in computer. * Answers and transfers calls for Clinical Laboratory and Reference Laboratory. Utilizes appropriate login process for telephone call queue system. Enters appropriate information into client call database for add-on tests, recollects, and follow up issues. * Uses computer system for interdepartmental email, to track specimens, utilize web based orders and retrieve results, and scan and index lab requisitions. * Informs couriers of specimen pickups from clients. Assists with local specimen pickups when regular couriers are not available. * Follows universal safety precaution standards and patient safety policies at all times. * Provides support for all lab departments, retrieves information and assists as needed. **Licensure, Registration, and/or Certification Required:** None required **Education Required:** Must be a High School or GED Diploma Graduate. **Experience preferred:** Previous lab experience **Knowledge, Skills & Abilities preferred:** Medical terminology or knowledge Customer service Strong data entry and computer skills Phlebotomy skills a plus **Physical Requirements and Working Conditions:** Must be able to use visual acuity to see monitor screen, computer and hard copy materials. Must be able to hear and verbally communicate in person and over the phone or radio. Must be able to sit for prolonged periods of time (up to 2 hours). Must be able to comprehend and learn operation of various office equipment. Must have functional range of motion of the cervical, thoracic and lumbar spines, upper and lower extremities with a grip strength of 50-60# specific to job evaluation. Must be able to forward reach, overhead reach, bend, squat, kneel and apply proper body mechanics during the transfers and transport supplies and/or equipment using proper body mechanics. Must be able to lift up to 10# specific to job evaluation. _This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the incumbent. Incumbent may be required to perform other related duties._ **Our Commitment to You:** Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including: **Compensation** * Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training * Premium pay such as shift, on call, and more based on a teammate's job * Incentive pay for select positions * Opportunity for annual increases based on performance **Benefits and more** * Paid Time Off programs * Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability * Flexible Spending Accounts for eligible health care and dependent care expenses * Family benefits such as adoption assistance and paid parental leave * Defined contribution retirement plans with employer match and other financial wellness programs * Educational Assistance Program Note: Eligibility for programs listed above may depend on your FTE or status (e.g., full-time, part-time, per diem, temporary, etc.); please ask a Recruiter for more information during an interview. **About Advocate Health** [Advocate Health](https://www.advocatehealth.org/) is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names [Advocate Health Care](https://www.advocatehealth.com/) in Illinois; [Atrium Health](https://atriumhealth.org/) in the Carolinas, Georgia and Alabama; and [Aurora Health Care](https://www.aurorahealthcare.org/) in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with [Wake Forest University School of Medicine](https://school.wakehealth.edu/) serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation’s largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.", "summaryDescription" : "Laboratory Assistant PRN at Advocate Health. Skills: Data entry, Specimen processing, Client service. Operate laboratory and hospital information system. Enter patient demographic data", "postedDate" : "2026-06-11T02:29:09.090", "createdAt" : "2026-06-12T02:29:09.064", "lastUpdated" : "2026-06-14T22:21:35.593", "ingestTimestamp" : "2026-06-12T02:29:09.064", "mongoId" : "6a2ad06e74d8ee00a071240d", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://aah.wd5.myworkdayjobs.com/External/job/Atrium-Health-Navicent-The-Medical-Center---777-Hemlock-St-Macon-GA/Laboratory-Assistant-PRN_R243599", "salaryAnnualMin" : 41184, "salaryAnnualMax" : 61776, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Patient data retrieval", "Specimen processing", "Specimen labeling", "Data entry", "Client service", "Order entry", "Client support", "HIPAA standards", "None required", "Laboratory information system", "Hospital information system", "Optical disk" ], "skillCount" : 12, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 674.38245, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2c8c4574d8ee00a0974f27", "title" : "Specimen Collector II", "company" : "Millennium Health", "industry" : "Hospital & Health Care", "location" : "East Grand Forks, Minnesota, United States", "locations" : [ "East Grand Forks, Minnesota, United States" ], "timestamp" : "2026-06-15T10:05:40.545", "fingerprint" : "eff1d5e57f6a47f5e0030d6553fa10d94fe2174dc46e30aac4e3787af3c7c74c", "source" : "workable", "applyUrl" : "https://apply.workable.com/j/16ED99B28E/apply", "externalId" : "16ED99B28E", "industryFunction" : { }, "locationPoint" : "47.92998,-97.02452", "structuredLocations" : [ { "city" : "East Grand Forks", "state" : "Minnesota", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "East Grand Forks, Minnesota, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "High School", "experienceMinYears" : 1, "experienceMaxYears" : 2, "experienceLevel" : "Junior", "professionalSkills" : [ "Medical insurance billing, medications, diagnostic codes, federal travel regulations, CLIA Certified, CAP Accredited, E-Verify participant." ], "hardSkillsList" : [ "HIPAA", "HiTrust", "Confidentiality", "Compliance policy", "cyber security controls" ], "hardSkills" : [ { "name" : "HIPAA", "level" : "intermediate" }, { "name" : "HiTrust", "level" : "intermediate" }, { "name" : "Confidentiality", "level" : "intermediate" }, { "name" : "Compliance policy", "level" : "intermediate" }, { "name" : "cyber security controls", "level" : "intermediate" } ], "majorSkills" : "Specimen Collection, Customer Service, HIPAA Compliance", "majorSkillsList" : [ "Specimen Collection, Customer Service, HIPAA Compliance" ], "coreResponsibilities" : "Collect patient urine and/or oral fluid (saliva) specimens, process and package collections for shipping, serve as an intermediary between the practice / clinic and the laboratory, record patient information, physician order details, and pertinent laboratory information, resolve specimen concerns with billing or patient information in ordering portal, order and maintain collection supplies inventory onsite, observe collection for Millennium Health specimens.", "toolProficiency" : [ "smart phone, computer" ], "continuousLearning" : "Tuition Assistance", "specialRequirements" : "Female candidates required for observed collections of gender identified female patients. Driving from/to multiple facilities may be required and occasional overnight coverage. Proof of compliant identification will be required prior to the start of employment. All employment offers are contingent upon the successful completion of a background check.", "outcomesObjectives" : "Help make a positive impact in your community!", "qualificationsBasic" : "6+ months of experience as a specimen collector or 1+ years of experience in the medical field, directly supporting patients preferred. 2+ years of customer service experience can be considered in place of medical experience. Demonstrated ability to navigate a smart phone and computer required. Valid driver’s license reliable transportation. Ability to ensure HIPAA, HiTrust, Confidentiality and Compliance policy, procedures, and standards are always adhered to. Ability to ensure administrative, physical and technical cyber security controls are always adhered to. High School diploma or equivalent required. Physical requirements: sitting 60%, walking 20%, standing 20%, lifting up to 20 lbs. This position requires regular travel. In accordance with federal travel regulations, all employees must possess a valid REAL ID or an acceptable alternative form of identification to comply with government travel guidelines.", "qualificationsPreferred" : "Medical insurance billing and/or familiarity with medications/diagnostic codes is a plus.", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Full Time Female Specimen Collector II ** Location: East Grand Forks, MN Schedule: Full-Time | Monday-Friday- 8am-4pm Seeking: Female candidates required for observed collections of gender identified female patients. Help make a positive impact in your community! Millennium Health LLC is an accredited specialty laboratory with more than a decade of experience in medication monitoring and drug testing services, helping clinicians monitor use of prescription medications and illicit drugs supporting improved clinical decision-making as part of treatment for millions of Americans with chronic pain, mental illness, and substance use disorders. The Specimen Collector II is a key role at Millennium Health. As our representative, this position provides exemplary care and exceptional customer service to patients, clinicians, and our laboratory. As a Specimen Collector II: * Collect patient urine and/or oral fluid (saliva) specimens * Process and package collections for shipping * Serve as an intermediary between the practice / clinic and the laboratory * Record patient information, physician order details, and pertinent laboratory information * Resolve specimen concerns with billing or patient information in ordering portal * Order and maintain collection supplies inventory onsite * Observe collection for Millennium Health specimens (when applicable) * Driving from/to multiple facilities may be required and occasional overnight coverage. **Requirements** Ideal Candidate: * 6+ months of experience as a specimen collector or 1+ years of experience in the medical field, directly supporting patients preferred * 2+ years of customer service experience can be considered in place of medical experience * Demonstrated ability to navigate a smart phone and computer required * Valid driver’s license required; reliable transportation * Medical insurance/billing and/or familiarity with medications/diagnostic codes is a plus * Ability to ensure HIPAA, HiTrust, Confidentiality and Compliance policy, procedures, and standards are always adhered to. * Ability to ensure administrative, physical and technical cyber security controls are always adhered to * High School diploma or equivalent required * Physical requirements: sitting 60%, walking 20%, standing 20%, lifting up to 20 lbs. This position requires regular travel. In accordance with federal travel regulations, all employees must possess a valid REAL ID or an acceptable alternative form of identification to comply with government travel guidelines. Proof of compliant identification will be required prior to the start of employment. Millennium Health is a CLIA Certified and CAP Accredited specialty laboratory. We partner with a trusted and accredited background screening provider, to conduct pre-employment background checks. As part of our screening process, we will review the following: • National, federal, and county criminal history • Global watchlist search • Social Security Number (SSN) trace • FACIS (Fraud and Abuse Control Information System) Level 3 search • SAM (System for Award Management) and OIG (Office of Inspector General) exclusions • Education verification • Driving record (Motor Vehicle Report) • 5-panel urine drug screening All employment offers are contingent upon the successful completion of this background check. Offers may be rescinded if the results do not meet the standards established for the position. **Benefits** Benefits Offered: * Medical, Dental, Vision, Disability Insurance * 401k with Company Match * Paid Time off and Holidays * Tuition Assistance * Behavioral and Health Care Resources * Mileage reimbursement * Salary Range: $18-22/hr. * Salary offered is dependent on qualifications, experience, and geographical location. Please note this job posting is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. Millennium Health is an Equal Opportunity/Affirmative Action Employer and E-Verify participant. All qualified applicants will receive consideration for employment without regard to race, color, creed, sex, national origin, disability, gender identity, sexual orientation or protected veteran status.", "summaryDescription" : "Specimen Collector II at Millennium Health. Skills: Specimen Collection, Customer Service, HIPAA Compliance. Collect patient urine and/or oral fluid (saliva) specimens, process and package collections for shipping, serve as an intermediary between the practice / clinic and the laboratory, record patient information, physician order details, and pertinent laboratory information, resolve specimen concerns with billing or patient information in ordering portal, order and maintain collection supplie", "postedDate" : "2026-06-11T00:00:00.000", "createdAt" : "2026-06-14T17:38:27.350", "lastUpdated" : "2026-06-15T10:05:40.545", "ingestTimestamp" : "2026-06-14T17:38:27.350", "mongoId" : "6a2c8c4574d8ee00a0974f27", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://apply.workable.com/j/16ED99B28E", "hasSalary" : false, "allSkills" : [ "HIPAA", "HiTrust", "Confidentiality", "Compliance policy", "cyber security controls", "Specimen Collection, Customer Service, HIPAA Compliance", "Medical insurance billing, medications, diagnostic codes, federal travel regulations, CLIA Certified, CAP Accredited, E-Verify participant.", "smart phone, computer" ], "skillCount" : 8, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "executive", "dataQualityScore" : 0.8888889, "_score" : 670.3973, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "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. 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Please note, the purpose of this posting is to recruit for on-going and future positions.**** Clinical Laboratory Scientist I/II, Generalist – Core Laboratory (Per Diem) ( Chemistry, Hematology, Urinalysis, Coagulation, Microbiology) Eligible for sign-on bonus of $2,500 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 is 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. About City of Hope Orange County City of Hope Orange County is transforming cancer treatment by bringing world-class expertise and specialized care closer to home. Supported by a regional network of care, our 11-acre academic cancer campus in Irvine is home to City of Hope Orange County Lennar Foundation Cancer Center, our outpatient cancer center, and Orange County’s only cancer specialty hospital, opening in late 2025. With the opening of the hospital, the full continuum of advanced cancer care—from prevention through survivorship—will be available in Orange County for the first time, eliminating the need to travel for lifesaving treatment. Seamlessly connected to our outpatient cancer center, the new clinical research hospital will feature 73 inpatient beds, advanced surgical suites, groundbreaking clinical trials, and holistic services such as rehabilitative therapy and spiritual care. This isn’t standard cancer care. This is lifesaving cancer care. This is Hope. In this role, we are seeking a Clinical Laboratory Scientist I/II to join our growing team! You will be responsible for preparing specimens and conducting clinical laboratory procedures, ranging from waived to high complexity, while ensuring strict adherence to regulatory guidelines such as SOPs, FACT, AABB, ACHI, CAP, FDA, and Joint Commission standards. This position offers a sign-on bonus and presents an excellent opportunity for skilled professionals in the field. This is a Night shift position; 10:00pm – 06:30am (hours may vary); initial training hours may be conducted during day shift hours. Eligible for Night shift differential. Additional Note: This position requires flexibility to accommodate varying patient needs. Shifts may include days, evenings, nights, weekends, and holidays. On-call responsibilities and mandatory overtime may also be necessary. As a successful candidate, you will: Perform a variety of complex laboratory tests and procedures according to prescribed protocols and assigned schedules. Completes procedures within established turnaround times Perform quality control procedures including preventive maintenance, calibrations, review of controls, and records data on appropriate forms . Support and participate in the Quality Assurance efforts and Performance Improvement process. Utilize standard laboratory equipment, and records and checks result for completeness and accuracy. Performs data entry of diagnostic information. EPIC Beaker experience (highly preferred) Your qualifications should include: Bachelor’s Degree; Military applicants without a Bachelor’s degree with the approval of CDPH-LFS (California Department of Public Health – Laboratory Field Services) Minimum 2 years as a certified or licensed clinical laboratory scientist California Clinical Laboratory Scientist (Highly Preferred: CA Clinical Laboratory Scientist (Generalist) – MTA) Hourly Per Diem Pay rate for CLS II: $69.29 / hr Note: For candidates with 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.   United States-California-Irvine", "summaryDescription" : "Clinical Laboratory Scientist I/II, Generalist (Per Diem) (Nights) at City of Hope. Skills: Clinical laboratory, Laboratory procedures, Quality control. Prepare specimens. 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Build confidence independently", "domainKnowledge" : "GMP", "domainList" : [ "gmp" ], "domainSpecificKnowledge" : [ "GMP" ], "documentationSkills" : "Document work clearly; Follow established procedures", "continuousLearning" : "Progress education while paid; Build skills for career; Participate in training activities; Apply learning during studies; Continuous learning", "innovationCreativity" : "AI-powered biopharma company", "outcomesObjectives" : "Ensure safe medicines reach patients", "qualificationsBasic" : "Pass 5 Leaving Certificate subjects, Maths and science subject required, 250 CAO points, Level 6 Qualification related discipline, Eligibility mature student", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "* **Location:** Waterford * **Start date:** 1st September 2026 * **Duration:** 3 years * **Work Model:** Onsite – During term time, apprentices spend 3 days per week learning on the job at Sanofi Waterford and 2 days per week studying with our education partner, South East Technological University (SETU). **About the job** Are you looking to kick start a career in science working for a world leader in the Biopharmaceutical Industry, and get an opportunity to progress your education while getting paid? Join Sanofi's Quality Control (QC) Laboratory Apprenticeship in Waterford and gain hands-on laboratory experience while building the skills needed for a successful career in the biopharmaceutical industry. The programme is designed for those who wish to develop a career in a laboratory environment where employment is set to grow significantly over the next 3-5 years. Sanofi Waterford is ideally placed to facilitate, mentor and nurture new talent. During term time you would work 3 days per week in our laboratory learning on the job while spending 2 days per week with our education partner, SETU. **Our Team** You will join the QC Device and Incoming Inspection team, responsible for testing devices and inspecting materials to ensure they meet quality standards. This work plays an important role in helping to ensure that safe and effective medicines reach patients around the world. **About Sanofi** We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. **Main responsibilities:**__ * Learn how to carry out device functional testing and incoming component inspection in a laboratory environment * Support the team in performing functional tests on devices and components and recording results accurately * Follow safe working practices to protect yourself, others, and the environment * Assist with maintaining laboratory equipment and keeping the workspace organised * Learn how to document your work clearly and follow established procedures (including GMP) * Work closely with team members while also building confidence to complete tasks independently * Participate in training activities and apply your learning both in the laboratory and during your studies **About you** No previous laboratory experience is required. We're looking for people with curiosity, enthusiasm, and a willingness to learn. To excel in this role, you will need one of the following: * Pass (minimum Grade 06) in 5 Leaving Certificate subjects one of which must be maths and a science subject 250 CAO points or * Level 6 Qualification in a related discipline or * Eligibility to apply as a mature student What will help you succeed: * Be curious about science and interested in how things work * Be motivated to learn and open to trying new things * Be organised and able to manage your time between work and study * Feel comfortable working both independently and as part of a team * Pay attention to detail and take pride in doing things carefully **Why choose us?** * Stretch your skills through apprenticeships, internships, graduate programs, and international experiences that grow with you. * Learn from inspiring mentors and collaborative teams while contributing to real projects that shape the future of healthcare. * Build your future with access to the latest tools, digital innovation, and continuous learning that keep you ahead of the curve. * Explore more with personalized development plans, short-term gigs, and internal mobility across functions and countries. * Grow in a purpose-driven company where your voice matters and your work helps improve millions of lives. * Thrive in inclusive, flexible workplaces that support your personal and professional well-being. * Launch your career with a company that invests in you — and empowers you to reimagine what’s possible. We reserve the right to close this vacancy earlier than the advertised closing date should we receive a sufficient number of applications. #LI-EUR #LI-Onsite # Pursue _progress_ , discover _extraordinary_ Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our [ALL IN video](https://www.youtube.com/watch?v=SkpDBZ-CJKw&t=67s) and check out our Diversity Equity and Inclusion actions at [sanofi.com](https://www.sanofi.com/en/our-responsibility/equality-and-inclusiveness)!", "summaryDescription" : "Quality Control (QC) Laboratory Apprenticeship at Sanofi. 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"Provide work direction, expertise, and guidance to staff, Oversee clinical laboratory testing, Oversee evaluation of results, Oversee proficiency of testing, Participate in projects to meet strategic initiatives, Implement quantitative outcomes, Monitor budget compliance, Analyze laboratory fiscal needs, Analyze departmental performance, Address fiscal variances, Collaborate on performance improvement processes, Implement performance improvement processes, Optimize teammate engagement, Optimize physician satisfaction, Optimize patient satisfaction, Ensure quality standards are met, Ensure regulatory standards are met, Ensure accreditation standards are met, Ensure competency standards are met, Ensure compliance with policies, Ensure compliance with procedures, Ensure compliance with standardization decisions, Coordinate orientation of staff, Coordinate training of staff, Coordinate competency testing of staff, Coordinate orientation of students, Coordinate training of students, Coordinate competency testing of students, Maintain competency in test systems, Maintain competency in test processes, Serve as technical resource for staff, Implement quality plan, Monitor quality indicators, Review laboratory results for quality, Review laboratory results for accuracy, Review laboratory results for validity, Document corrective action, Implement corrective action, Select team members, Coach team members, Develop team members, Set clear expectations, Inspire the team, Motivate the team, Manage performance, Recognize achievement, Provide feedback, Administer progressive discipline, Recommend hiring, Recommend compensation changes, Recommend promotions, Recommend corrective action decisions, Recommend terminations, Adhere to organization's Code of Ethical Conduct, Ensure compliance with policies, Ensure compliance with regulations, Ensure compliance with laws", "teamCollaboration" : "Site leaders collaboration; Cross-functional collaboration", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Clinical laboratory science; Medical technology; Laboratory information systems; Regulatory agency requirements; Accrediting agency requirements; Licensing agency requirements", "domainList" : [ "clinical-laboratory-science", "medical-technology", "laboratory-information-systems", "regulatory-agency-requirements", "accrediting-agency-requirements", "licensing-agency-requirements" ], "domainSpecificKnowledge" : [ "Clinical laboratory science", "Medical technology", "Laboratory information systems", "Regulatory agency requirements", "Accrediting agency requirements", "Licensing agency requirements" ], "communicationSkills" : "Communication skills", "continuousLearning" : "Career development programs; Educational Assistance Program", "innovationCreativity" : "Clinical innovation", "problemSolvingSkills" : "Decision making; Conflict resolution; Corrective action", "specialRequirements" : "Evening shift, Some overnight as necessary, Operates all equipment, Frequently lifts up to 10 lbs, Occasionally lifts up to 50 lbs, Sit, stand, walk, twist, bend, Exposure to infectious agents, Exposure to human blood, Exposure to body fluids, Wear safety protection, Handle stressful situations, May be required to travel", "outcomesObjectives" : "Achieve Advocate Health goals; Achieve Advocate Health objectives", "qualificationsBasic" : "3 years of experience in technical laboratory services and operations, Bachelor's Degree in Clinical Laboratory Sciences or Medical Technology or equivalent, Medical Laboratory Scientist (MLS) certification issued by the American Society for Clinical Pathology Board of Certification (ASCP BOC), Medical Technologist (MT) certification issued by the American Society for Clinical Pathology (ASCP) or equivalent accrediting agency", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Department:** 60901 Navicent Health Medical Center: Baldwin - Lab **Status:** Full time **Benefits Eligible:** Yes **Hou****rs Per Week:** 40 **Schedule Details/Additional Information:** Monday - Friday (no weekends or holidays) Evening shift - 1p - 1030p - some overnight as necessary **Pay Range** $41.10 - $61.65 \"This position is Sign-on Bonus eligible.\" Based on eligibility requirements. **Job Summary:** Responsible for laboratory operations in the technical area(s) of the Hospitals and Clinics within the Advocate Health enterprise, which may include department, discipline and/or shift oversight. Supervises the implementation of enterprise laboratory strategies and standards through close collaboration with site leaders. Ensures peak laboratory operations by driving optimization of resources, financial performance, growth, safety, teammate engagement, and quality in achieving Advocate Health goals and objectives including planning, monitoring, and implementing laboratory operations in a cost effective, quality and service-oriented manner. **Major Responsibilities:** * Assumes responsibility for the day-to-day operations of the department including providing work direction, expertise, and guidance to the staff. Oversees the clinical laboratory testing, evaluation of results, and the proficiency of testing. * Actively participates in projects to meet strategic initiatives including implementation and development of quantitative outcomes. * Monitors budget compliance. Analyzes laboratory fiscal needs, and departmental performance and takes action to address variances. * Collaborates and implements performance improvement processes to optimize teammate engagement, and physician and patient satisfaction. * Ensures quality, regulatory, accreditation, compliance and competency standards are met. Ensures compliance with current policies, procedures, and standardization and/or consolidation decisions. * Coordinates orientation, training, and competency testing of staff and/or students. Maintains competency, as needed, in test systems and processes in defined discipline for area of responsibility. Serves as a technical resource for staff. * Complies with the quality plan by implementing and monitoring quality indicators. Reviews laboratory results for quality, accuracy and validity. Documents and implements corrective action as appropriate. * Selects, coaches, and develops team. Sets clear expectations to inspire and motivate the team. Manages performance by recognizing achievement, providing feedback, and administering progressive discipline when necessary. Recommends hiring, compensation changes, promotions, corrective action decisions, and terminations. * Responsible for understanding and adhering to the organization's Code of Ethical Conduct and for ensuring that people actions, and the actions of employees supervised, comply with the policies, regulations, and laws applicable to the organization's business. **Licensure, Registration, and/or Certification Required:** * Medical Laboratory Scientist (MLS) certification issued by the American Society for Clinical Pathology Board of Certification (ASCP (American Society for Clinical Pathology) BOC), or * Medical Technologist (MT) certification issued by the American Society for Clinical Pathology (ASCP) or equivalent accrediting agency. **Education Required:** * Bachelor's Degree in Clinical Laboratory Sciences or Medical Technology or equivalent **Experience Required:** * Typically requires 3 years of experience in technical laboratory services and operations. **Knowledge, Skills & Abilities Required:** * Demonstrated leadership skills including project management, decision making, delegation, team building, customer service, and conflict resolution. * Ability to grow leaders through coaching, guidance, and development planning. * Advanced knowledge of regulatory compliance, accrediting and licensing agency requirements. * Current knowledge of medical and technical advancements to plan for future growth and development. * Intermediate computer skills including knowledge and experience with laboratory information systems. * Excellent organization and communication skills. **Physical Requirements and Working Conditions:** * Operates all equipment necessary to perform the job. * Frequently lifts up to 10 lbs. Occasionally lifts up to 50 lbs. * Must be able to sit, stand, walk, twist and bend the majority of the workday. * May be exposed to mechanical, electrical, and/or infectious agents. * Will be exposed to human blood and body fluids. * Must wear appropriate safety protection, i.e. laboratory coats, gloves, gowns and/or eye protection. * Must be able to handle stressful situations in a calm and professional manner. * May be required to travel, therefore may be exposed to inclement weather and adverse road conditions. _This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the incumbent. Incumbent may be required to perform other related duties._ **Our Commitment to You:** Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including: **Compensation** * Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training * Premium pay such as shift, on call, and more based on a teammate's job * Incentive pay for select positions * Opportunity for annual increases based on performance **Benefits and more** * Paid Time Off programs * Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability * Flexible Spending Accounts for eligible health care and dependent care expenses * Family benefits such as adoption assistance and paid parental leave * Defined contribution retirement plans with employer match and other financial wellness programs * Educational Assistance Program Note: Eligibility for programs listed above may depend on your FTE or status (e.g., full-time, part-time, per diem, temporary, etc.); please ask a Recruiter for more information during an interview. **About Advocate Health** [Advocate Health](https://www.advocatehealth.org/) is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names [Advocate Health Care](https://www.advocatehealth.com/) in Illinois; [Atrium Health](https://atriumhealth.org/) in the Carolinas, Georgia and Alabama; and [Aurora Health Care](https://www.aurorahealthcare.org/) in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with [Wake Forest University School of Medicine](https://school.wakehealth.edu/) serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation’s largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.", "summaryDescription" : "Clinical Laboratory Supervisor at Atrium Health. Skills: Laboratory operations, Team development, Quality management. Provide work direction, expertise, and guidance to staff. Oversee clinical laboratory testing", "postedDate" : "2026-06-11T03:18:07.491", "createdAt" : "2026-06-12T03:18:07.402", "lastUpdated" : "2026-06-14T15:36:01.071", "ingestTimestamp" : "2026-06-12T03:18:07.402", "mongoId" : "6a2ad06e74d8ee00a07123d6", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://aah.wd5.myworkdayjobs.com/External/job/Atrium-Health-Navicent-Baldwin---821-N-Cobb-St-Milledgeville-GA/Clinical-Lab-Supervisor_R220381", "salaryAnnualMin" : 85488, "salaryAnnualMax" : 128232, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Clinical laboratory testing", "Proficiency testing", "Fiscal needs analysis", "Performance improvement", "Quality assurance", "Regulatory compliance", "Accreditation compliance", "Competency testing", "Corrective action implementation", "Performance management", "Leadership", "Coaching", "Guidance", "Development planning", "Mentoring", "Laboratory operations", "Team development", "Quality management", "Project management", "Decision making", "Delegation", "Team building", "Customer service", "Conflict resolution", "Accrediting agency requirements", "Licensing agency requirements", "Test systems", "Test processes", "Clinical laboratory science", "Medical technology", "Laboratory information systems", "Regulatory agency requirements", "Medical Laboratory Scientist (MLS) certification", "Medical Technologist (MT) certification" ], "skillCount" : 34, "jobCategory" : "healthcare", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 662.2574, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a2b0ce974d8ee00a075f6c7", "title" : "Medical Laboratory Scientist (MLS) - Core Lab", "company" : "Endeavor Health", "industry" : "Healthcare", "salary" : { "min" : 30.46, "max" : 45.69, "currency" : "USD", "frequency" : "yearly" }, "location" : "United States of America", "locations" : [ "United States of America" ], "certifications" : [ "MLS (ASCP)" ], "timestamp" : "2026-06-14T23:21:12.801", "fingerprint" : "a4a21b7886f06c9899a230148fbdac289a9cbfdc281f7c94b91115758eb1a3e4", "source" : "workday", "language" : "en", "applyUrl" : "https://nshs.wd1.myworkdayjobs.com/ns-eeh/job/EVH-Evanston-Hospital/Medical-Laboratory-Scientist--MLS----Core-Lab_R43534", "externalId" : "R43534", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Evanston", "state" : "Illinois", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.0693991,-87.6829320" } ], "locationText" : "Evanston, Illinois, United States", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Clinical lab testing", "Patient satisfaction", "Customer service" ], "hardSkillsList" : [ "Clinical testing", "Quality control", "Instrument maintenance", "Troubleshooting", "Computer functions" ], "hardSkills" : [ { "name" : "Clinical testing", "level" : "intermediate" }, { "name" : "Quality control", "level" : "intermediate" }, { "name" : "Instrument maintenance", "level" : "intermediate" }, { "name" : "Troubleshooting", "level" : "intermediate" }, { "name" : "Computer functions", "level" : "intermediate" } ], "majorSkills" : "Clinical laboratory, Laboratory testing, Quality control", "majorSkillsList" : [ "Clinical laboratory", "Laboratory testing", "Quality control" ], "coreResponsibilities" : "Perform clinical lab testing, Promote patient satisfaction, Instruct coworkers courteously, Perform patient tests manually, Perform patient tests automated, Review patient test results, Notify clinical personnel, Document notification, Perform quality control, Record QC, Take corrective action, Document corrective action, Perform instrument checks, Perform instrument maintenance, Perform instrument troubleshooting, Maintain competencies, Recognize abnormal results, Make decisions releasing results, Notify supervisor, Notify pathologist, Participate in continuing education, Participate in in-services, Participate in lab meetings, Participate in committees, Maintain safe work environment, Use required PPE, Handle biohazardous materials, Handle chemicals, Maintain inventory, Maintain supplies, Perform computer functions, Manage workload, Manage turnaround times, Assist in orientation, Assist in training employees, Assist in training students, Assist in competency assessment, Maintain broad knowledge, Cross-train into other areas, Read emails, Respond to emails, Perform other duties", "teamCollaboration" : "Instruct coworkers; Assist in training", "domainKnowledge" : "Chemistry; Hematology; Urinalysis; Coagulation; Immunology; Bone Marrow; Flow Cytometry; Biohazardous materials; Chemicals", "domainList" : [ "chemistry", "hematology", "urinalysis", "coagulation", "immunology", "bone-marrow", "flow-cytometry", "biohazardous-materials", "chemicals" ], "domainSpecificKnowledge" : [ "Chemistry", "Hematology", "Urinalysis", "Coagulation", "Immunology", "Bone Marrow", "Flow Cytometry", "Biohazardous materials", "Chemicals" ], "communicationSkills" : "Notify clinical personnel; Notify supervisor; Notify pathologist; Read emails; Respond to emails", "documentationSkills" : "Document notification; Document corrective action", "continuousLearning" : "Continuing education programs; In-services", "problemSolvingSkills" : "Troubleshooting; Recognize abnormal results; Make decisions releasing results; Take corrective action", "specialRequirements" : "Rotating holidays, e/o weekend", "qualificationsBasic" : "Bachelor of Science Biology or Chemistry, MLS (ASCP) or equivalent certification, Any experience", "qualificationsPreferred" : "Chemistry, Hematology, UA, Body Fluids, Coagulation", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Hourly Pay Range:** $30.46 - $45.69 - The hourly pay rate offered is determined by a candidate's expertise and years of experience, among other factors. **Position Highlights:** * Position: Medical Laboratory Scientist (MLS) - Core Lab * Location: Evanston Hospital * Full Time/Part Time: Full Time * Hours: Monday-Friday, 3pm-11:30pm, e/o weekend and rotating holidays **What you will do:** Performs clinical lab testing in Chemistry, Hematology, Urinalysis, Coagulation. Special Coagulation, Immunology Bone Marrow and Flow Cytometry testing are performed on the day shift. Actively promotes patient satisfaction and customer service values with all staff members. Instructs and encourages coworkers to treat patients and customers (nurses, physicians, visitors, vendors etc.) courteously. Performs patient tests, manually and with automated clinical laboratory equipment, reagents and/or test methodologies. Reviews patient test results for accuracy and notifies appropriate clinical personnel or all critical results. Documents this notification per established protocols. Performs quality control per established departmental protocols. Records QC appropriately and takes corrective action when QC is not within established guidelines. Documents corrective action taken. Performs instrument checks, maintenance and troubleshooting per department protocols. Maintains competencies in accordance with policy and procedures of the hospital and laboratory department. Recognizes abnormal or unusual test results and makes appropriate decisions before releasing results. Notifies supervisor and pathologist if necessary. Participates in continuing education programs, in-services, lab meetings and various committees. Maintains a safe work environment by using required PPE and protective devices. Handles biohazardous materials and chemicals according to established protocols. Maintains inventory and supplies within respective departments. Performs computer functions efficiently, manages workload and established turnaround times. Assists in orientation and training of new employees and students. May assist in competency assessment of moderate and high complexity testing. Maintains a broad knowledge of all laboratory departments. May cross-train into other areas of the lab as needed. Reads emails and responds in a timely manner. Other projects or duties as assigned. **What you will need:** * Education: Bachelor of Science, Biology or Chemistry * Certification: MLS (ASCP) or equivalent * Experience: Any * Unique or Preferred Skills: Chemistry, Hematology, UA, Body Fluids, Coagulation **Benefits:** * Premium pay such as shift, on call, holiday and more based on an employee’s job * Incentive pay for select positions * Opportunity for annual increases based on performance * Career Pathways to Promote Professional Growth and Development * Various Medical, Dental, Pet and Vision options * Tuition Reimbursement * Free Parking * Wellness Program Savings Plan * Health Savings Account Options * Retirement Options with Company Match * Paid Time Off and Holiday Pay * Community Involvement Opportunities Endeavor Health is a fully integrated healthcare delivery system committed to providing access to quality, vibrant, community-connected care, serving an area of more than 4.2 million residents across six northeast Illinois counties. Our more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals – Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) – all recognized as Magnet hospitals for nursing excellence. For more information, visit [www.endeavorhealth.org](http://www.endeavorhealth.org). When you work for Endeavor Health, you will be part of an organization that encourages its employees to achieve career goals and maximize their professional potential. Please explore our website ([www.endeavorhealth.org](http://www.endeavorhealth.org)) to better understand how Endeavor Health delivers on its mission to “help everyone in our communities be their best”. Endeavor Health is committed to working with and providing reasonable accommodation to individuals with disabilities. Please refer to the main career page for more information. At Endeavor Health, we are united by a shared commitment to working together to create a culture of connection and belonging—each of us bringing different skills and experiences as we deliver safe, seamless, and personal care. Every person, every time. We are committed to fostering an environment where all team members can be their best, learn, and pursue excellence together. EOE: Race/Color/Sex/Sexual Orientation/ Gender Identity/Religion/National Origin/Disability/Vets, VEVRRA Federal Contractor.", "summaryDescription" : "Medical Laboratory Scientist (MLS) - Core Lab at Endeavor Health. Skills: Clinical laboratory, Laboratory testing, Quality control. Perform clinical lab testing. Promote patient satisfaction", "postedDate" : "2026-06-10T05:02:30.359", "createdAt" : "2026-06-12T05:02:30.261", "lastUpdated" : "2026-06-14T23:21:12.801", "ingestTimestamp" : "2026-06-12T05:02:30.261", "mongoId" : "6a2b0ce974d8ee00a075f6c7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://nshs.wd1.myworkdayjobs.com/ns-eeh/job/EVH-Evanston-Hospital/Medical-Laboratory-Scientist--MLS----Core-Lab_R43534", "salaryAnnualMin" : 63356, "salaryAnnualMax" : 95035, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Clinical testing", "Quality control", "Instrument maintenance", "Troubleshooting", "Computer functions", "Clinical laboratory", "Laboratory testing", "Clinical lab testing", "Patient satisfaction", "Customer service", "Chemistry", "Hematology", "Urinalysis", "Coagulation", "Immunology", "Bone Marrow", "Flow Cytometry", "Biohazardous materials", "Chemicals", "MLS (ASCP)" ], "skillCount" : 20, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 655.3134, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "6a16291c58b93c861e95a161", "title" : "Senior Laboratory Planner", "salary" : { "min" : 145000.0, "max" : 205000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Laboratory Planner in Seattle, adjusted for the construction industry and senior experience level." }, "location" : "Multiple Locations", "locations" : [ "Multiple Locations" ], "timestamp" : "2026-06-15T09:07:47.291", "fingerprint" : "b4aaa7a17651bcbebb84910f386cc0f999fce5be7e30232ea03212e051824cb2", "source" : "taleo", "language" : "en", "applyUrl" : "https://hdr.taleo.net/careersection/ex/jobdetail.ftl?job=717350", "externalId" : "717350", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Seattle", "state" : "Washington", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "47.6038321,-122.3300620" } ], "locationText" : "Seattle, Washington, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 12, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Construction planning", "Technical drawing", "Model creation" ], "coreResponsibilities" : "Plan laboratories, Develop construction plans, Create technical drawings, Create models", "teamCollaboration" : "Employee-owned culture", "domainKnowledge" : "Building construction; Precision technical plans", "domainList" : [ "building-construction", "precision-technical-plans" ], "domainSpecificKnowledge" : [ "Building construction", "Precision technical plans" ], "qualificationsBasic" : "Bachelor's degree in Architecture, 12 years related experience, Organizational skills, Knowledge of materials, Knowledge of methods, Knowledge of tools, Understanding of design techniques, Understanding of design tools, Understanding of design principles, Attitude and commitment", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Required Qualifications Bachelor's degree in Architecture or closely related field A minimum of 12 years related experience Strong organizational skills Knowledge of materials, methods and tools involved in the construction of buildings Understanding of design techniques, tools and principles involved in production of precision technical plans, prints, drawings and models An attitude and commitment to being an active participant of our employee-owned culture is a must What We Believe HDR is our company. Together, we build on each other's life experiences and perspectives to make great things possible every day. This shapes our collaborative culture, encourages organizational trust and connects us closer to the clients and communities we serve. Our Commitment As employee owners, we all have a role in creating an inclusive environment where each of us is welcomed, valued, respected and empowered to bring our authentic selves to work every day. Our eight Employee Network Groups (Asian Pacific, Black, Hispanic/Latino(a), LGBTQ+, People with Disabilities, Veterans, Women, Young Professionals) help create a sense of belonging and foster a supportive environment where everyone is empowered to engage and contribute. Each group has an executive sponsor and is open to all employees. United States-Washington-Seattle", "summaryDescription" : "Senior Laboratory Planner. Plan laboratories. Develop construction plans", "createdAt" : "2026-06-14T08:45:06.281", "lastUpdated" : "2026-06-15T09:07:47.291", "ingestTimestamp" : "2026-06-14T08:45:06.281", "mongoId" : "6a16291c58b93c861e95a161", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 145000, "salaryAnnualMax" : 205000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ "Construction planning", "Technical drawing", "Model creation", "Building construction", "Precision technical plans" ], "skillCount" : 5, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Senior", "dataQualityScore" : 0.7777778, "_score" : 651.41315, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Construction", "llmIndustryConfidence" : 0.85 }, { "id" : "6a16471858b93c861e9e5b25", "title" : "Research Laboratory Technician", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 52000.0, "max" : 75000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Research Laboratory Technician in Duarte, California, adjusted for the biotech industry and company size." }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Laboratory Research", "Onsite, Days, Days" ], "timestamp" : "2026-06-15T11:50:35.483", "fingerprint" : "793e200c5ca8e5af0c48eed6fbb784fb1eefd320e56c3c3fd4d7442cf99d9a7c", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=239605", "externalId" : "239605", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Duarte", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.1394513,-117.9772873" } ], "locationText" : "Duarte, California, United States", "minimumEducation" : "High School", "experienceMinYears" : 2, "hardSkillsList" : [ "Sterilization techniques", "Prepare simple stains", "Prepare solutions", "Prepare culture media", "Process tissue" ], "hardSkills" : [ { "name" : "Sterilization techniques", "level" : "intermediate" }, { "name" : "Prepare simple stains", "level" : "intermediate" }, { "name" : "Prepare solutions", "level" : "intermediate" }, { "name" : "Prepare culture media", "level" : "intermediate" }, { "name" : "Process tissue", "level" : "intermediate" } ], "majorSkills" : "Scientific data collection, Laboratory maintenance, Laboratory supplies", "majorSkillsList" : [ "Scientific data collection", "Laboratory maintenance", "Laboratory supplies" ], "coreResponsibilities" : "Collect scientific data, Classify scientific data, File scientific data, Prepare solutions, Label tubes, Label specimen containers, Maintain laboratory supplies, Clean laboratory equipment, Maintain required records, Maintain reports, Maintain statistics, Train research aides, Assist research aides, Train research assistants, Assist research assistants, Collect used glassware, Wash used glassware, Clean used glassware, Sterilize used glassware, Collect used equipment, Wash used equipment, Clean used equipment, Sterilize used equipment, Collect used supplies, Wash used supplies, Clean used supplies, Sterilize used supplies, Order laboratory supplies, Receive laboratory supplies, Distribute laboratory supplies, Maintain supply inventories, Process tissue, Collect material for analysis, Deliver material for analysis, Ensure proper labeling, Ensure pertinent information, Assist in care of laboratory work area, Assist in maintenance of laboratory work area, Assist in care of furnishings, Assist in maintenance of furnishings, Assist in care of equipment, Assist in maintenance of equipment", "domainKnowledge" : "Cancer research; Diabetes research; Disease prediction; Disease prevention; Disease cure; Medicine research", "domainList" : [ "cancer-research", "diabetes-research", "disease-prediction", "disease-prevention", "disease-cure", "medicine-research" ], "domainSpecificKnowledge" : [ "Cancer research", "Diabetes research", "Disease prediction", "Disease prevention", "Disease cure", "Medicine research" ], "qualificationsBasic" : "High school diploma or equivalent, Minimum two (2) years of related experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Join the forefront of groundbreaking research at City of Hope where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. Under limited supervision, the Research Laboratory Technician is responsible for the collection, classification and filing of scientific data. The Research Laboratory Technician is also responsible for preparing solutions, labeling tubes/specimen containers and maintaining laboratory supplies. Duties and/or tasks include but are not limited to cleaning of laboratory equipment utilizing proper cleaning protocols and procedures. As a successful candidate, you will: Responsible for the collection, classification and filing of scientific data. Maintains required records, reports and statistics as directed. Trains and assists research aides and assistant in procedures and use of equipment. Collects, washes, cleans and sterilizes used glassware, equipment and supplies using proper sterilization techniques. Orders, Receives, distributes, and maintains supply inventories in laboratories as needed. Prepares simple stains, solutions, culture media, and may process tissue following established procedures. Using appropriate or specified equipment collects and delivers material for analysis. Ensures proper labeling and pertinent information. Assists in the care and maintenance of laboratory work area and furnishings/equipment. Your qualifications should include: High school diploma or equivalent. Minimum two (2) years of related experience or combined education and experience in related field. Additional Information: COH employees may apply for a transfer or promotion to job openings for which they meet the minimum qualifications if they meet the following criteria: Employed at COH in current role for at least 6 months, unless otherwise stipulated in an applicable collective bargaining agreement. Are in good standing and have no current performance issues. City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE . United States-California-Duarte", "summaryDescription" : "Research Laboratory Technician at City of Hope. Skills: Scientific data collection, Laboratory maintenance, Laboratory supplies. Collect scientific data. Classify scientific data", "createdAt" : "2026-06-14T01:59:53.590", "lastUpdated" : "2026-06-15T11:50:35.483", "ingestTimestamp" : "2026-06-14T01:59:53.590", "mongoId" : "6a16471858b93c861e9e5b25", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 52000, "salaryAnnualMax" : 75000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Sterilization techniques", "Prepare simple stains", "Prepare solutions", "Prepare culture media", "Process tissue", "Scientific data collection", "Laboratory maintenance", "Laboratory supplies", "Cancer research", "Diabetes research", "Disease prediction", "Disease prevention", "Disease cure", "Medicine research" ], "skillCount" : 14, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Junior", "dataQualityScore" : 0.6666667, "_score" : 648.30524, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech", "llmIndustryConfidence" : 0.85 }, { "id" : "69ce5e3b9bc74574cb6779c7", "title" : "Infotainment Testing", "company" : "MBRDI", "industry" : "Manufacturing", "salary" : { "min" : 1200000.0, "max" : 1800000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an Infotainment Testing role in Bangalore, India, adjusted for mid-seniority and full-time employment in the automotive industry." }, "location" : "India-Karnataka-Bangalore", "locations" : [ "India-Karnataka-Bangalore", "Brigade Tech Gardens, Katha No. 119, Kundalahalli Village, K.R. Puram Hobli, Ward No. 85, Bangalore" ], "timestamp" : "2026-06-15T10:31:09.173", "fingerprint" : "1b44c4505e6daa85c21a10650fc3263192050d7219bf25abb1cb9891d1ea289b", "source" : "taleo", "language" : "en", "applyUrl" : "https://daimler.taleo.net/careersection/ex/jobdetail.ftl?job=885533", "externalId" : "885533", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Bangalore", "state" : "Karnataka", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "12.9767936,77.5900820" } ], "locationText" : "Bangalore, Karnataka, India", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 2, "experienceMaxYears" : 6, "experienceLevel" : "Mid", "technicalSkills" : "Python, Robot Framework", "professionalSkills" : [ "Problem-solving", "Analytical skills" ], "hardSkillsList" : [ "Test case creation", "Test case execution", "Defect management" ], "softSkillsList" : [ "Communication skills" ], "hardSkills" : [ { "name" : "Test case creation", "level" : "intermediate" }, { "name" : "Test case execution", "level" : "intermediate" }, { "name" : "Defect management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Communication skills" } ], "majorSkills" : "Manual testing, Test automation", "majorSkillsList" : [ "Manual testing", "Test automation" ], "coreResponsibilities" : "Perform manual testing, Write test cases, Review test cases, Maintain test cases, Write test plans, Review test plans, Maintain test plans, Identify defects, Log defects, Track defects, Collaborate with developers, Collaborate with stakeholders, Support automation efforts, Participate in test strategy discussions, Participate in test reviews, Participate in risk assessments, Validate application behavior", "teamCollaboration" : "Collaborate with developers; Collaborate with stakeholders", "projectManagementSkills" : [ "Agile methodologies" ], "domainKnowledge" : "Infotainment systems", "domainList" : [ "infotainment-systems" ], "domainSpecificKnowledge" : [ "Infotainment systems" ], "toolProficiency" : [ "Jira", "TestRail" ], "communicationSkills" : "Communication skills", "documentationSkills" : "Test case documentation", "continuousLearning" : "Learning opportunities", "innovationCreativity" : "Drive innovation", "problemSolvingSkills" : "Problem-solving skills; Analytical skills", "outcomesObjectives" : "Ensure quality standards", "qualificationsBasic" : "2–6 years manual testing experience, Understanding of SDLC, Understanding of STLC, Understanding of Agile methodologies, Hands-on test case creation, Hands-on test case execution, Hands-on defect management", "qualificationsPreferred" : "Python automation experience, Robot Framework automation experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "About MBRDI: Mercedes-Benz Research and Development India (MBRDI), headquartered in Bengaluru with a satellite office in Pune, is the largest R&D center for Mercedes-Benz Group AG outside of Germany. Our mission is to drive innovation and excellence in automotive engineering, digitalization, and sustainable mobility solutions, shaping the future of mobility. Key responsibilities Perform manual testing of functional, regression, integration, and exploratory test scenarios. Write, review, and maintain test cases and test plans. Identify, log, and track defects using bug tracking tools. Collaborate with developers and stakeholders to ensure quality standards. Support automation efforts using Python and Robot Framework where applicable. Participate in test strategy discussions, reviews, and risk assessments. Validate application behavior across different environments and platforms. Contribute to continuous improvement of QA processes and best practices. Required Skills & Qualifications: 2–6 years of manual testing experience in enterprise or large-scale applications. Strong understanding of SDLC, STLC, and Agile methodologies. Hands-on experience with test case creation, execution, and defect management. Experience with Python and Robot Framework automation is a plus. Knowledge of bug tracking and test management tools (e.g., Jira, TestRail). Excellent analytical, problem-solving, and communication skills. Educational Qualifications: Bachelor’s degree in Computer Science, Information Technology, or related field. Why Join Us? Be part of a purpose-driven organization that’s shaping the future of mobility. Work on cutting-edge technologies and global projects. Thrive in a collaborative, diverse, and inclusive environment. Access world-class infrastructure and learning opportunities. Equal Opportunity Statement: At MBRDI, we are committed to diversity and inclusion. We welcome applications from all qualified individuals, regardless of gender, background, or ability. Mercedes-Benz Research and Development India Private Limited", "summaryDescription" : "Infotainment Testing at MBRDI. Skills: Manual testing, Test automation. Perform manual testing. 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TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

" ], "timestamp" : "2026-06-15T13:45:56.776", "fingerprint" : "566c744c6065e39c2e7fa6a753833ca819d84e607e05c938f0615fda9367d5fe", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=675257", "externalId" : "675257", "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", "documentationSkills" : "Patient charting", "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision and following established policies, procedures and professional guidelines, the Laboratory Assistant is responsible for the receipt, delivery and charting of specimens and reports. Assists with various clerical tasks, such as receptionist duties and date processing. 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" : "Laboratory Assistant- Microbiology at Tampa General Hospital", "createdAt" : "2026-06-14T07:20:58.243", "lastUpdated" : "2026-06-15T13:45:56.776", "ingestTimestamp" : "2026-06-14T07:20:58.243", "mongoId" : "69cf26122beec4dd3d90b40b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 37000, "salaryAnnualMax" : 48000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.5555556, "_score" : 631.7765, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.92 }, { "id" : "6a2af78274d8ee00a073d5fb", "title" : "Microbiology Laboratory Supervisor — Radio Conjugate Laboratory", "company" : "Fusion Pharmaceuticals", "industry" : "Pharmaceuticals", "salary" : { "min" : 86266.0, "max" : 113224.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Canada", "locations" : [ "Canada" ], "timestamp" : "2026-06-15T00:36:57.393", "fingerprint" : "2cdac0a53e1df127e99693046b2724d2c30f024b946902dde0f81b0daa5a9a3a", "source" : "workday", "language" : "en", "applyUrl" : "https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Canada--Hamilton--Longwood-Road-South/Microbiology-Laboratory-Supervisor---Radio-Conjugate-Laboratory_R-254267-1", "externalId" : "R-254267", "industryFunction" : { }, "locationPoint" : "56.1304,-106.3468", "structuredLocations" : [ { "city" : "Hamilton", "state" : "Ontario", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.2560802,-79.8728583" } ], "locationText" : "Hamilton, Ontario, Canada", "employmentType" : "FULL_TIME", "experienceLevel" : "Supervisor", "technicalSkills" : "Microbiology, GMP, EU Annex 1, FDA cGMPs, PIC/S, ICH Q8, ICH Q9, ICH Q10, ISO 14644, ISO 13408, ISO 11135, ISO 11137, ISO 17665, USP, Ph. 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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"fingerprint" : "a38621ce850ec7e0b2318fd108ddc47afc3978d10eae2b15d22994db27d169b7", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/designedconveyorsystems/jobs/7584388003", "externalId" : "7584388003", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Franklin", "state" : "Tennessee", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "35.9252060,-86.8689419" } ], "locationText" : "Franklin, Tennessee, United States", "technicalSkills" : "PLC, WES, WCS", "professionalSkills" : [ "Data analysis", "Statistical methods" ], "hardSkillsList" : [ "Testing engineering", "Material handling equipment", "Industrial products", "System management", "Program management", "Automation go-lives", "Data acquisition", "Safety standards", "Regulatory requirements" ], "hardSkills" : [ { "name" : "Testing engineering", "level" : "intermediate" }, { "name" : "Material handling equipment", "level" : 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Prepare detailed test reports, Present findings to engineering team and management, Identify root causes of failures or performance issues, Collaborate with design engineers to develop solutions, Collaborate with design engineers to test solutions, Implement corrective actions, Ensure material handling equipment meets standards, Ensure material handling equipment meets quality criteria, Ensure material handling equipment meets customer expectations, Participate in development of quality assurance policies, Participate in revision of quality assurance policies, Maintain up-to-date knowledge of industry safety standards, Maintain up-to-date knowledge of regulatory requirements, Ensure all tests are conducted in compliance with, Prioritize safety of personnel and equipment, Work closely with equipment suppliers, Work closely with procurement teams, Work closely with quality assurance teams, Integrate testing results into product lifecycle, Provide technical support to manufacturing teams, Provide technical support to field service teams, Provide training to manufacturing teams, Provide training to field service teams, Contribute to continuous improvement of testing processes, Contribute to continuous improvement of testing methodologies, Stay informed about latest testing technologies, Stay informed about industry trends", "teamCollaboration" : "Multidisciplinary teams; Sales teams; Project management teams; Engineering teams; Consulting teams; Site analysts; Super-users; External OEM vendors; Equipment suppliers; Procurement teams; Quality assurance teams; Manufacturing teams; Field service teams", "projectManagementSkills" : [ "Project management", "Systems engineering", "Site management", "Automation installs" ], "domainKnowledge" : "Material handling equipment; Conveyors; Sorters; Singulators; AS/RS; Robotic handling systems; Lift equipment; Warehouse operations; Industry safety standards; Regulatory requirements", "domainList" : [ "material-handling-equipment", "conveyors", "sorters", "singulators", "as-rs", "robotic-handling-systems", "lift-equipment", "warehouse-operations", "industry-safety-standards", "regulatory-requirements" ], "domainSpecificKnowledge" : [ "Material handling equipment", "Conveyors", "Sorters", "Singulators", "AS/RS", "Robotic handling systems", "Lift equipment", "Warehouse operations", "Industry safety standards", "Regulatory requirements" ], "toolProficiency" : [ "Testing equipment", "Data acquisition systems", "Related software tools" ], "communicationSkills" : "Present technical information", "documentationSkills" : "Test reports", "continuousLearning" : "Latest testing technologies; Industry trends", "problemSolvingSkills" : "Problem-solving; Root cause analysis; Troubleshooting", "specialRequirements" : "75% travel required, Onsite during testing, Exposure to machinery, noise, and dust", "outcomesObjectives" : "Ensure product quality; Ensure compliance with industry standards; Support successful launches; Support 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"workSiteFlexibility" : "Hybrid", "rawDescription" : "Position Overview: As a Material Handling Testing Engineer, you will play a critical role in ensuring the reliability, efficiency, and safety of our material handling equipment solutions. You will be responsible for designing and conducting tests on various types of material handling equipment, analyzing test data, and recommending improvements to ensure product quality and compliance with industry standards. In this position, you will lead all development teams in launching Greenfield/Retrofit automated sites, working side by side with the Project Manager, the Systems Engineer, the Site Manager, automation and software suppliers, and external systems teams managing all facets of the interior automation installs within our customers’ warehouses. They will support DCS’s teams pre- and post- go-live to ensure a smooth transition. Key Responsibilities: Test Planning and Execution: Work with sales, project management, engineering and consulting to design and implement comprehensive test plans to evaluate the performance, durability, and safety of material handling equipment, including conveyors, sorters, singulators, automated storage and retrieval systems (AS/RS), robotic handling systems, and lift equipment. Augment User Acceptance Testing (UAT) and Operational Readiness Tests, working with site analysts, project managers, and super-users internal and from external OEM vendors to run all simulations and scripts required to support successful launches and turnovers. Data Analysis and Reporting: Collect, analyze, and interpret test data, using statistical tools to identify trends, anomalies, or areas for improvement. Prepare detailed test reports and present findings to the engineering team and management. Problem-Solving: Identify root causes of failures or performance issues and collaborate with design engineers to develop and test solutions. Implement corrective actions to improve product quality and performance. Quality Assurance: Ensure all material handling equipment meets or exceeds industry standards, company quality criteria, and customer expectations. Participate in the development and revision of quality assurance policies and procedures. Safety and Compliance: Maintain up-to-date knowledge of industry safety standards and regulatory requirements. Ensure all tests are conducted in compliance with customer standards, prioritizing the safety of personnel and equipment. Collaboration and Support: Work closely with equipment suppliers, procurement, and quality assurance teams to integrate testing results into all phases of the product lifecycle. Provide technical support and training to manufacturing and field service teams as needed. Continuous Improvement: Contribute to the continuous improvement of testing processes and methodologies. Stay informed about the latest testing technologies and industry trends to enhance testing efficiency and effectiveness. Qualifications: Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Industrial Engineering, or a related field. 5+ years of experience in testing engineering, specifically with material handling equipment or similar industrial products. Experience managing large systems and physical programs including PLC/WES/WCS conversions, launches, and automation go-lives. Strong analytical skills with experience in data analysis and statistical methods. Proficient in using testing equipment, data acquisition systems, and related software tools. Excellent problem-solving abilities and attention to detail. Effective communication skills, capable of working in multidisciplinary teams and presenting technical information clearly. Knowledge of industry safety standards and regulations related to material handling equipment. Ability to manage multiple projects simultaneously and work in a fast-paced environment. Working Conditions: This role is remote and involves working onsite during testing. Hands-on testing may require exposure to machinery, noise, and dust. Safety protocols must be strictly followed. Travel is required for field testing or to visit manufacturing sites and is estimated at 75%. About Us:    Conveyor may be in our name, but it’s only part of what we do. DCS was founded in 1982 and has grown to serve major clients in multiple industries by providing material handling, full-scale warehouse operations and conveyor design solutions that are custom crafted for their need. We don’t sell ready-made systems - we build relationships that empower us to craft custom solutions together. It’s the teamwork approach, sharing ideas and building upon them, that produces the best results.    And DCS is committed to creating an extraordinary employment experience for our team. We work like crazy to hire and develop great people, build relationships, and ensure that the programs and services we offer our team are among the best in the business- from a killer snack wall and casual work environment to flexible PTO and opportunities to give back within the community. More reasons to join our team:    We pride ourselves in our family-like culture and casual, but focused, work environment    We offer competitive salaries and health benefits    Our 401K program includes a 100% match up to 5%    Participation in our Discretionary Profit-Sharing Program    We offer our employees flexibility and autonomy    We do community outreach projects throughout the year    We know how to throw company events    We work hard, but we also know how to have fun - darts, anyone? Individuals seeking employment at Designed Conveyor Systems are considered without regards to race, color, religion, national origin, age, sex, marital status, ancestry, physical or mental disability, veteran status, gender identity, or sexual orientation. Accommodation is available to applicants with a disability condition, when applying, testing, or interviewing for a position. Please let us know if you need accommodation. ", "summaryDescription" : "Testing Engineer at Designed Conveyor Systems. Skills: Testing engineering, Material handling, Automation, Data analysis. Design and implement comprehensive test plans. Evaluate performance, durability, and safety of material handling", "postedDate" : "2026-06-11T17:29:08.090", "createdAt" : "2026-06-11T17:29:08.090", "lastUpdated" : "2026-06-14T21:31:55.099", "ingestTimestamp" : "2026-06-11T17:29:08.090", "mongoId" : "6a2a472574d8ee00a05d848a", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 95000, "salaryAnnualMax" : 135000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Testing engineering", "Material handling equipment", "Industrial products", "System management", "Program management", "Automation go-lives", "Data acquisition", "Safety standards", "Regulatory requirements", "Material handling", "Automation", "Data analysis", "Statistical methods", "Project management", "Systems engineering", "Site management", "Automation installs", "Conveyors", "Sorters", "Singulators", "AS/RS", "Robotic handling systems", "Lift equipment", "Warehouse operations", "Industry safety standards", "Testing equipment", "Data acquisition systems", "Related software tools" ], "skillCount" : 28, "jobCategory" : "other", "jobSubcategory" : "project-management,-d&f", "dataQualityScore" : 0.7777778, "_score" : 624.569, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Material Handling" }, { "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" : 623.4973, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c94e874d8ee00a098bdf5", "title" : "Financial Performance and Analysis", "company" : "Getnet", "industry" : "FinTech", "salary" : { "min" : 45000.0, "max" : 65000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Financial Performance and Analysis role in Madrid, Spain, adjusted for the FinTech industry." }, "location" : "Madrid, Madrid, Spain", "locations" : [ "Madrid", "Madrid", "Spain" ], "timestamp" : "2026-06-15T09:26:43.034", "fingerprint" : "d7381340f9999217e17b528557279df139e22bc370b91841aa7b793c17934513", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.eu.greenhouse.io/getnet/jobs/4751604101", "externalId" : "4751604101", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Madrid", "state" : "Madrid", "country" : "Spain", "continent" : "eu", "source" : "llm", "workMode" : "hybrid", "geo" : "40.4237276,-3.6899043" } ], "locationText" : "Madrid, Madrid, Spain", "minimumEducation" : "Bachelor's", "softSkillsList" : [ "Clear communication", "Analytical mindset" ], "softSkills" : [ { "name" : "Clear communication" }, { "name" : "Analytical mindset" } ], "teamCollaboration" : "FP&A teams; Finance & Accounting teams; Finance Tech teams; Regional teams", "domainKnowledge" : "Payment solutions; Fintech; Acquiring hub", "domainList" : [ "payment-solutions", "fintech", "acquiring-hub" ], "domainSpecificKnowledge" : [ "Payment solutions", "Fintech", "Acquiring hub" ], "communicationSkills" : "Clear communication", "continuousLearning" : "Self-development programmes", "problemSolvingSkills" : "Identify data inconsistencies; Identify structural effects; Identify model-related issues", "remoteFriendly" : true, "workSiteFlexibility" : "Hybrid", "rawDescription" : "✨ Your talent drives our future Getnet is a global technology company specializing in payment solutions for commerce. Founded in Brazil and operating across Latin America and the Iberian Peninsula, we support over 1.3 million merchants with end-to-end services — from POS terminals to e-commerce platforms. We are part of PagoNxt, the global fintech of the Santander Group, and operate as an acquiring hub with a strong presence in Spain, Portugal, Brazil, Mexico, Chile, Argentina, and Uruguay. Our mission is clear: to simplify payments with innovation, security, and scale, helping businesses of all sizes grow with agility. We offer a unified platform that integrates hardware, software, fraud prevention, acquiring, reconciliation, and financial services — all in a single ecosystem, so our clients can focus on growing their business. Being part of Getnet means joining a company that combines the innovation of a fintech with the solidity of a global bank. Imagine your future. Care for your career. Simplify your journey. This means you'll have the chance to build impactful solutions, grow with real development opportunities, and thrive in a culture that values well-being, inclusion, and clarity. We combine flexibility, autonomy, and global collaboration — so you can focus on what matters, connect with purpose, and help shape the future. Here, you'll find space to grow, real opportunities to lead, and a culture where everyone belongs and contributes. ✨ If you want to be part of the next generation of financial solutions, this is the place. At Getnet, we are looking for a Financial Performance and Analysis to join our team in Madrid. \uD83D\uDCCCWhat you'll do Financial Model Architecture: maintain and evolve the financial model structure and driver logic used for performance analysis, forecasting and planning. Data Integrity & Consistency: ensure consistency and reliability of data across actuals, forecast and planning cycles through validation and reconciliation. Assumptions & Calculations Validation: review and validate assumptions, calculations and model behaviour to ensure financial coherence. Regional Coordination & Consolidation: coordinate and consolidate financial inputs from countries and regions, applying and explaining consolidation rules. Performance: contribute to financial performance activities by clarifying model-related drivers and structural effects behind deviations. Forecast & Planning: work closely with planning to reflect planning assumptions and scenarios accurately within the financial model. Process & Tool Improvement: collaborate with Finance Tech to improve data quality, automation and robustness across FP&A processes. What we are looking for Experience Strong track record in FP&A, financial modelling, controlling or planning roles. Exposure to actuals, forecast and planning cycles. Experience using planning tools (Oracle EPM or similar) is a plus Experience working with financial data from multiple countries or business units. Education, knowledge and skills Bachelor’s degree in Finance, Economics, Business Administration, Engineering or a related field. A Master’s degree in Finance, Corporate Finance, Business Analytics or similar is a plus. Knowledge of Power BI, Power Query, SQL, Oracle, Databricks or similar tools is an advantage. Solid financial modelling skills and understanding of P&L structure and key drivers. Strong skills and ability to work with structured financial data. Understanding of forecasting logic, assumptions and sensitivities. Ability to identify data inconsistencies, structural effects and model-related issues. Clear communication skills and ability to work with FP&A, Finance & Accounting, Finance Tech and regional teams. Proactive attitude, attention to detail and analytical mindset. \uD83C\uDFAF What we offer \uD83E\uDE7A Medical insurance \uD83D\uDCAA Wellhub \uD83D\uDE91 Life insurance \uD83D\uDC89 Annual healthcare \uD83D\uDE8C Transportation allowance \uD83C\uDF55 Meal voucher/food voucher \uD83D\uDCDA Access to self-development programmes \uD83C\uDFE2 Hybrid Collaborative environment: Successful candidate must be prepared to work 60% on site \uD83D\uDCEC Next step Apply and if you know someone who might be looking for this opportunity, share it.", "summaryDescription" : "Financial Performance and Analysis at Getnet", "postedDate" : "2026-06-14T04:54:16.069", "createdAt" : "2026-06-14T04:54:16.069", "lastUpdated" : "2026-06-15T09:26:43.034", "ingestTimestamp" : "2026-06-14T04:54:16.069", "mongoId" : "6a2c94e874d8ee00a098bdf5", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Clear communication", "Analytical mindset", "Payment solutions", "Fintech", "Acquiring hub" ], "skillCount" : 5, "jobCategory" : "finance", "jobSubcategory" : "accounting", "seniorityLevel" : "Mid", "dataQualityScore" : 0.7777778, "_score" : 612.96075, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "FinTech", "llmIndustryConfidence" : 0.98 }, { "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" : 600.39813, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c619b74d8ee00a08f4e9d", "title" : "Laboratory Technician", "company" : "Siloam Hospitals Group", "industry" : "Hospital And Health Care", "salary" : { "min" : 5400000.0, "max" : 8400000.0, "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" : "2026-06-15T09:26:36.265", "fingerprint" : "3164ca6fa9a847a80907269bf890bee956ddd83bb75c879a51a861428e9173c3", "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" : "High School", "experienceLevel" : "not-applicable", "professionalSkills" : [ "Service standards", "Data entry", "Data release", "Preventive maintenance", "Quality services", "Safety services" ], "hardSkillsList" : [ "Hematology examination", "Chemistry examination", "Serology examination", "Urine examination", "Feces examination", "Body fluid examination" ], "hardSkills" : [ { "name" : "Hematology examination", "level" : "intermediate" }, { "name" : "Chemistry examination", "level" : "intermediate" }, { "name" : "Serology examination", "level" : "intermediate" }, { "name" : "Urine examination", "level" : "intermediate" }, { "name" : "Feces examination", "level" : "intermediate" }, { "name" : "Body fluid examination", "level" : "intermediate" } ], "majorSkills" : "Laboratory examinations, Data entry, Equipment maintenance", "majorSkillsList" : [ "Laboratory examinations", "Data entry", "Equipment maintenance" ], "coreResponsibilities" : "Carry out laboratory examinations, Support doctor's diagnosis, Carry out data entry, Ensure data availability, Ensure timely data, Carry out data release, Prioritize reporting CITO, Prioritize reporting CCU, Convey results quickly, Record equipment usage, Make equipment requests, Maintain equipment availability, Maintain equipment cleanliness, Maintain equipment maintenance, Record storage results, Organize storage results, Record reagent procurement, Record reagent receipt, Record reagent use, Ensure service continuity, Collect required data, Make operational reports, Implement quality procedures, Implement safety procedures, Attend training, Collect data for targets, Document for targets, Make reports for targets", "teamCollaboration" : "Interacting with patients; 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" : 600.3158, "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" : 599.918, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "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" : 588.98047, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 } ], "status" : 200, "message" : "OK", "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 26165, "totalPages" : 524, "hasNext" : true, "hasPrevious" : false } }

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