{ "count" : 19921, "data" : [ { "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. 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With a background in warehouse/production environment, you will work along side our technicians to support with the preparation and logging of samples and general housekeeping. #### Step Into the Role Main Responsibilities: * Reception, recording, storage, and retrieval of soil and water samples using LIMS and Regmaster systems. * Preparation of samples including traying out, crushing, drying, weighing, filtering, splitting into separate containers, adding acids, and preparing leachates. * Describing soil types and logging sample descriptions and laboratory data into LIMS and Regmaster. * Preparation, recording, storage, and disposal of water and leachate samples. * Ensuring all health & safety and quality procedures are adhered to at all times. * Maintaining a clean, tidy, and organised laboratory work area. #### Our Offer * £29724.50 per annum * Consett (free onsite parking) * 42.5 hours Mon-Fri between 0600-1800. (1x4hour shift on Sat every 4 weeks with hours gained back the week earlier) Company benefits include… * Company funded 1% benefit allowance * Pension * Enhanced parental leave * 28 days holiday + 2 wellbeing days plus bank holidays #### Your profile Experience required: * A minimum of 2 years’ experience of working in a production/warehouse environment. * Industry experience desired but not essential Qualifications Desired: * A minimum of G.C.S.E grade C or above in Science, Maths and English is desirable. * Forklift Truck Licence Additional skills required: * Proactive approach to work and good organisational skills. * Ability use initiative and work towards targets. * Good communicator. * Basic computer skills. #### Your New Workplace Normec DETS is a leading company providing high-quality analytical testing services for the environmental, construction, waste management, fuels and engineering industries. Based in County Durham and Crayford, our laboratory is accredited to ISO 17025 and MCERTS, ensuring that we meet the highest standards and have the technical expertise required. We offer a wide range of services including asbestos testing, soil contamination testing, water testing and waste analysis. With our efficient logistics, we pick up samples on the same day with our own drivers and vehicles, ensuring rapid sample processing. Our UKAS accredited soil contamination testing lab checks for contaminants, allowing clients to operate safely. We also provide a wide range of UKAS accredited waste testing services to support regulatory compliance, renewable energy qualification, and zero waste to landfill goals. Our knowledgeable team delivers fast turnaround times and precise analysis to help you manage waste effectively and sustainably. #### About Normec Dets is part of Normec, a leading organization in the Testing, Inspection, Certification, and Compliance (TICC) industry. Our expertise covers essential areas such as water, air, and soil quality, fire safety, and food safety, ensuring the highest standards of quality and safety across various sectors. Founded in 2016, Normec is an ambitious, independent, and fast-growing organization with approximately 6,500 colleagues. We offer our colleagues the opportunity to actively contribute to our mission while simultaneously developing their own careers within a dynamic and rapidly growing organization. Together, we work on impactful solutions for our clients and on a sustainable future. The culture within Normec is informal, open, energetic, and entrepreneurial, and is anchored in our GROWTH principles. Through our The Normec Fit program, which brings these principles to life, we ensure that not only our company grows, but also everyone who is part of it. #### Interested? Let’s Talk! [Contact details recruiter + application procedures] Add a contact who they can contact if they have questions and manage expectations by adding insight into the application procedure. This gives clarity and prevents people asking for updates or getting frustrated. Unsolicited contact from recruitment agencies is not appreciated and will not receive a response ## Requirements Don’t fill this box- Only the description above is needed! This information will not be loaded into the Normec website.", "summaryDescription" : "Sample Prep Technician at Normec DETS. Skills: Sample preparation, Laboratory data logging. Receive soil and water samples. Record soil and water samples", "postedDate" : "2026-06-09T15:45:43.000", "createdAt" : "2026-06-14T04:01:55.167", "lastUpdated" : "2026-06-15T08:51:38.023", "ingestTimestamp" : "2026-06-14T04:01:55.167", "mongoId" : "6a2ccee274d8ee00a0a2d0c5", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "<30k", "hasSalary" : false, "allSkills" : [ "Sample preparation", "Soil description", "Data logging", "Proactive approach", "Use initiative", "Laboratory data logging", "Organisational skills", "Process management", "ISO 17025", "MCERTS", "UKAS accredited testing", "LIMS", "Regmaster" ], "skillCount" : 13, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Junior", "dataQualityScore" : 1.0, "_score" : 1040.802, "daysOld" : 5, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Environmental Services", "llmIndustryConfidence" : 0.95 }, { "id" : "6a25966274d8ee00a01a2557", "title" : "Associate Scientist, Sample Preparation", "company" : "Us As We Transform And Accelerate Research", "industry" : "Life Sciences", "salary" : { "min" : 41400.0, "max" : 86100.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "Ithaca, New York, United States of America", "locations" : [ "Ithaca, New York, United States of America" ], "timestamp" : "2026-06-11T19:32:26.981", "fingerprint" : "f08763832ae99ee67a51c6ae044626c7001d9d3597b4f6e7aa8aa131c490b222", "source" : "workday", "language" : "en", "applyUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Ithaca-New-York-United-States-of-America/Associate-Scientist--Sample-Preparation_R1545590", "externalId" : "R1545590", "industryFunction" : { }, "locationPoint" : "43.2917,-84.6075", "structuredLocations" : [ { "city" : "Ithaca", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "42.4374175,-76.5483724" } ], "locationText" : "Ithaca, New York, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's Degree", "experienceMinYears" : 1, "experienceMaxYears" : 2, "experienceLevel" : "Entry", "technicalSkills" : "Microsoft Outlook, Microsoft Word, Microsoft Excel", "professionalSkills" : [ "Laboratory safety", "Infection control", "Hazardous chemical handling" ], "hardSkillsList" : [ "Sample preparation", "Biological sample extraction", "Tissue preparation", "Purification techniques", "Laboratory calculations" ], "hardSkills" : [ { "name" : "Sample preparation", "level" : "intermediate" }, { "name" : "Biological sample extraction", "level" : "intermediate" }, { "name" : "Tissue preparation", "level" : "intermediate" }, { "name" : "Purification techniques", "level" : "intermediate" }, { "name" : "Laboratory calculations", "level" : "intermediate" } ], "majorSkills" : "Sample preparation, Biological sample extraction, Tissue preparation", "majorSkillsList" : [ "Sample preparation", "Biological sample extraction", "Tissue preparation" ], "coreResponsibilities" : "Execute routine techniques, Prepare biological samples, Perform routine sample preparation, Extract from biological matrices, Prepare tissue samples, Perform purification, Document testing, Make observations, Record observations, Perform calculations, Collect data, Prepare data for evaluation, Identify performance errors, Document unusual results, Escalate to senior personnel, Assist with maintaining laboratory equipment, Assist with inventory management, Maintain lab housekeeping, Communicate with stakeholders, Document project work", "teamCollaboration" : "Cross-functional stakeholders; Internal stakeholders", "domainKnowledge" : "Good Laboratory Practices; Laboratory safety practices; Infection control practices; Standard precautions; Hazardous chemical handling; LIMS-enabled workflow", "domainList" : [ "good-laboratory-practices", "laboratory-safety-practices", "infection-control-practices", "standard-precautions", "hazardous-chemical-handling", "lims-enabled-workflow" ], "domainSpecificKnowledge" : [ "Good Laboratory Practices", "Laboratory safety practices", "Infection control practices", "Standard precautions", "Hazardous chemical handling", "LIMS-enabled workflow" ], "documentationSkills" : "Document project work", "problemSolvingSkills" : "Troubleshooting routine experiments", "qualificationsBasic" : "6 months of experience in a regulated laboratory environment, Proficiency with pipetting techniques, Proficiency with routine laboratory calculations", "qualificationsPreferred" : "Experience with automated instrumentation", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "# We are seeking Associate Scientist, Sample Preparation to join IQVIA Laboratories at Ithaca. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. ## Job Summary: Perform routine biological sample preparation to support downstream analysis, including preparing solutions and reagents and troubleshooting routine experiments. Document work in accordance with SOPs and applicable regulatory guidelines while collaborating with cross-functional stakeholders. ## What You'll Be Doing: * Execute routine techniques to prepare biological samples for subsequent analysis * Perform routine sample preparation activities such as extractions from biological matrices, tissue preparation, and purification * Perform and document testing in accordance with SOPs and applicable regulatory guidelines * Make and record observations, perform calculations, and collect and prepare data for evaluation * Identify and document potential performance errors or unusual results and escalate to senior lab personnel * Assist with maintaining laboratory equipment, inventory, and lab housekeeping consistent with 6S standards * Communicate clearly and timely with cross-functional stakeholders and document project work per IQVIA Laboratories processes ## What We Are Looking For: * Bachelor's Degree in a Life Sciences discipline required or High School Diploma or equivalent combination of education and experience required * 6 months of experience in a regulated laboratory environment. * Proficiency with pipetting techniques and routine laboratory calculations regarding batches and specimens * Experience with extractions from biological matrices, tissue preparation, purification, and/or automated instrumentation * Other Equivalent combination of education, training, and experience may be accepted in lieu of degree ## The Knowledge, Skills and Abilities Needed for This Role: * Working knowledge of applicable regulatory standards within area of responsibility, such as Good Laboratory Practices (GLP) * Knowledge of laboratory safety and infection control practices, including standard precautions and hazardous chemical handling * Strong attention to detail and accuracy with the ability to handle multiple tasks simultaneously * Good computer skills using Microsoft Outlook, Word, and Excel and ability to collaborate effectively with internal stakeholders * Ability to support training and onboarding of junior staff and work within a LIMS-enabled workflow environment ## What We Offer You: We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees' physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey. To learn more about our benefits, visit [IQVIA Benefits](https://jobs.iqvia.com/benefits. ). If you're looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at [https://jobs.iqvia.com](https://jobs.iqvia.com/) IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $41,400.00 - $86,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.", "summaryDescription" : "Associate Scientist, Sample Preparation at Us As We Transform And Accelerate Research. Skills: Sample preparation, Biological sample extraction, Tissue preparation. Execute routine techniques. Prepare biological samples", "postedDate" : "2026-06-08T10:16:47.107", "createdAt" : "2026-06-11T10:16:46.932", "lastUpdated" : "2026-06-11T19:32:26.981", "ingestTimestamp" : "2026-06-11T10:16:46.932", "mongoId" : "6a25966274d8ee00a01a2557", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Ithaca-New-York-United-States-of-America/Associate-Scientist--Sample-Preparation_R1545590", "salaryAnnualMin" : 41400, "salaryAnnualMax" : 86100, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Sample preparation", "Biological sample extraction", "Tissue preparation", "Purification techniques", "Laboratory calculations", "Laboratory safety", "Infection control", "Hazardous chemical handling", "Good Laboratory Practices", "Laboratory safety practices", "Infection control practices", "Standard precautions", "LIMS-enabled workflow" ], "skillCount" : 13, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 1.0, "_score" : 1018.98395, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Life Sciences" }, { "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" : 812.609, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a0de91258b93c861eb99057", "title" : "Dermpath Laboratory Histologist", "industry" : "Healthcare", "salary" : { "min" : 45000.0, "max" : 65000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an entry-level Histologist in Tampa, adjusted for the healthcare industry." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
USF Health Morsani Center AHC (AMGMCAH)
13330 USF Laurel Dr.

Tampa, 33612

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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. 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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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We operate in 3 key categories: Animal sports medication and doping control, Human drug testing, and Supplement testing and product certification. We have an exciting opportunity for a highly motivated, proactive laboratory co-ordinator to join our Animal Sports team. As part of our team, you will deliver a high-quality lab support service to the Animal Sports team. This includes: * Acting as the central hub for communication with all teams within Animal Sports * Supporting routine maintenance and operation of analytical instrumentation (including mass spectrometers) * Ownership of and performing the essential tasks needed within the lab (i.e. stock checks, equipment issues, consumable shortages, reference collection management and extracted standard organisation and preparation) * Provide support in our Sample Management team as required We’re looking for a teammate who works flexibly, shows initiative, and brings forward new ideas. You’re hardworking with a positive attitude, manage your time efficiently, and ensure tasks are completed on schedule and to a high standard. This role is well suited to a candidate with laboratory experience, with training and support provided. ## Qualifications * Strong scientific background with practical understanding of biological or chemical laboratory work * Working knowledge of ISO 17025 and the ability to follow accredited quality standards * Excellent laboratory skills with a focus on accuracy, organisation, and safe working practices * Understanding of COSHH assessments within a laboratory environment ## Additional Information Our Values: 1. Passion 2. Curiosity 3. Integrity 4. Brilliance 5. Respect We deliver world-class solutions and foster an inclusive and collaborative environment where every team member can thrive and achieve their full potential! Equal opportunities We are committed to ensuring that every job applicant and employee is valued for their individual talents. We strictly prohibit discrimination on the basis of age, disability, race, colour, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or parental status, religion, or belief. We proudly support an inclusive work environment where everyone can compete and succeed based on their merits. For more information about us, please visit our website www.lgcassure.com/ssas", "summaryDescription" : "Laboratory Co-ordinator at LGC Group. Skills: Lab support service, Analytical instrumentation, Sample management. Act as central hub for communication. 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Diagnosis; Treatment; Prevention of diseases; Biohazard waste; Regulatory guidelines; Biological specimens; Gynecological specimens; Non-gynecologic specimens; Lab results; Outside distributes specimens; Laboratory quality plan", "domainList" : [ "medical-laboratory-information", "diagnosis", "treatment", "prevention-of-diseases", "biohazard-waste", "regulatory-guidelines", "biological-specimens", "gynecological-specimens", "non-gynecologic-specimens", "lab-results", "outside-distributes-specimens", "laboratory-quality-plan" ], "domainSpecificKnowledge" : [ "Medical laboratory information", "Diagnosis", "Treatment", "Prevention of diseases", "Biohazard waste", "Regulatory guidelines", "Biological specimens", "Gynecological specimens", "Non-gynecologic specimens", "Lab results", "Outside distributes specimens", "Laboratory quality plan" ], "toolProficiency" : [ "Hospital Information System" ], "communicationSkills" : "Answering questions; Answering requests", "documentationSkills" : "Document QC", "innovationCreativity" : "Innovative ideas", "problemSolvingSkills" : "Troubleshoot problems", "specialRequirements" : "Exposure to blood-borne pathogens, May require travel", "qualificationsBasic" : "High School graduate or equivalent, Six months experience acute care facility", "qualificationsPreferred" : "MLA(ASCP) or PBT(ASCP) preferred", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Position Objective: Provides support to the technical staff in the delivery of medical laboratory information related to diagnosis, treatment, and prevention of diseases. Essential Job Duties: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Creates a work environment that positively promotes process improvement. Explores opportunities to add value to job (innovative ideas) to benefit the organization and taking ownership of the outcome. Proactively finds other work-related tasks during low census. Maintains safe and clean working environment by complying with procedures, rules, and regulations. Labels and disposes of biohazard and/or chemical waste according to regulatory guidelines. Maintains inter- and intradepartmental work flow by fostering a spirit of cooperation (hand offs). Maintains laboratory supplies inventory by checking stock to determine inventory level; anticipating needed supplies; placing and expediting orders for supplies; verifying receipt of supplies; and storing supplies according to manufacturer’s recommended conditions. Conserves laboratory resources by using equipment and supplies as needed to accomplish job results. Provides clinical laboratory information by answering questions and requests. Participates in the training of new staff by serving as a mentor. Determines and executes the best method for obtaining biological specimens from patients of all ages (if required) to include venipuncture, capillary, and heel-stick puncture to ensure quality specimen for testing. Processes gynecological and non-gynecologic specimens for microscopic evaluation (if required), including instrument processing, staining, changing reagents, and cover-slipping. Performs functions to established productivity guidelines with minimal errors. Registers patients accurately in the Hospital Information System. Orders or accessions appropriate tests as requested by an authorized provider by accurately reading and interpreting orders and being familiar with test mnemonics and components. Responds to requests for lab results and sends appropriate scheduled reports. Prepares aliquots and processes samples for referral to outside labs; distributes specimens to testing or processing locations according to established standard work. Operates and maintains laboratory equipment. Performs preventative maintenance and troubleshoots problems to the full extent of ability. Actively participate in the laboratory quality plan/program (ex. investigative reports, notification of delays, etc.). Performs quality controls and documents QC for each lab procedure on a daily basis and follows up on issues (troubleshoots). Educational/Experience Requirements: High School graduate or equivalent Six months experience working in an acute care facility in an equivalent role. Required License/Certifications: N/A MLA(ASCP) or PBT(ASCP), preferred. Knowledge, Skills, Abilities: Ability to work cooperatively with all types of personalities both inside and outside the organization. May require travel to various locations. Working Conditions, Equipment, Physical Demands: There is a reasonable expectation that employees in this position will be exposed to blood-borne pathogens. Physical Demands - The physical demands and work environment that have been described are representative of those an employee encounters while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions in accordance with the Americans with Disabilities Act. The above job description is an overview of the functions and requirements for this position. This document is not intended to be an exhaustive list encompassing every duty and requirement of this position; your supervisor may assign other duties as deemed necessary. Pay Range $17.50—$26 USD Luminis Health Benefits Overview: • Medical, Dental, and Vision Insurance • Retirement Plan (with employer match for employees who work more than 1000 hours in a calendar year) • Paid Time Off • Tuition Assistance Benefits • Employee Referral Bonus Program • Paid Holidays, Disability, and Life/AD&D for full-time employees • Wellness Programs • Employee Assistance Programs and more *Benefit offerings based on employment status Opt-in for text notifications! Luminis Health's two-way SMS texting platform lets you receive notifications and messages from our Talent Acquisition team directly on your phone. To enable this feature, select \"yes\" when asked to \"opt-in to receive text messages\" and to \"Receive updates from a recruiter about this job via SMS\" when completing your application. Once you are opted in, you can easily opt-out at any time. Standard text messaging rates may apply based on the candidate's mobile carrier plan. Luminis Health is not responsible for any charges incurred by the recipient. Candidates are encouraged to review their mobile carrier's plan for applicable text messaging rates and usage charges.", "summaryDescription" : "Laboratory Assistant at Luminis Health. Skills: Laboratory support, Specimen collection, Laboratory inventory. Promote process improvement. Add value to job", "postedDate" : "2026-06-14T05:10:34.175", "createdAt" : "2026-06-14T05:10:34.175", "lastUpdated" : "2026-06-15T04:59:58.630", "ingestTimestamp" : "2026-06-14T05:10:34.175", "mongoId" : "6a2cdcb874d8ee00a0a555d1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 35360, "salaryAnnualMax" : 54080, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Venipuncture", "Capillary puncture", "Heel-stick puncture", "Microscopic evaluation", "Quality controls", "Cooperative", "Laboratory support", "Specimen collection", "Laboratory inventory", "Process improvement", "Inventory management", "Specimen processing", "Medical laboratory information", "Diagnosis", "Treatment", "Prevention of diseases", "Biohazard waste", "Regulatory guidelines", "Biological specimens", "Gynecological specimens", "Non-gynecologic specimens", "Lab results", "Outside distributes specimens", "Laboratory quality plan", "Hospital Information System" ], "skillCount" : 25, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.8888889, "_score" : 743.2193, "daysOld" : 0, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ebf8074d8ee00a0e9ac8b", "title" : "Clinical Laboratory Technologist", "company" : "LabCorp", "location" : "United States of America", "locations" : [ "United States of America" ], "certifications" : [ "ASCP", "AMT" ], "timestamp" : "2026-06-15T10:13:41.446", "fingerprint" : "31395285e798ac5773952569f072b323184b2b87b1abbc774bcdad1c77b38813", "source" : "workday", "applyUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Bartlesville-OK/Clinical-Laboratory-Technologist_2615389", "externalId" : "2615389", "industryFunction" : { }, "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Bartlesville", "state" : "Oklahoma", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "Bartlesville, Oklahoma, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor", "experienceMinYears" : 1, "experienceMaxYears" : 2, "experienceLevel" : "Junior", "professionalSkills" : [ "Clinical lab science." ], "softSkillsList" : [ "attention to detail, organizational skills" ], "softSkills" : [ { "name" : "attention to detail, organizational skills" } ], "majorSkills" : "clinical laboratory testing, instrumentation, quality control", "majorSkillsList" : [ "clinical laboratory testing, instrumentation, quality control" ], "coreResponsibilities" : "The Clinical Laboratory Technologist determines specimen acceptability, performs routine and complex technical procedures, and operates/troubleshoots instrumentation. This role involves preparing and testing reagents, reporting accurate test results for patient care, and performing preventive maintenance and quality control. The technologist also manages testing bench supplies, maintains a safe work environment, and assists with specimen processing as needed.", "teamCollaboration" : "Ability to work independently and within a team environment.", "toolProficiency" : [ "laboratory information systems" ], "communicationSkills" : "communication skills", "documentationSkills" : "Standard Operating Procedures", "continuousLearning" : "If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!", "problemSolvingSkills" : "technical decisions", "specialRequirements" : "In lieu of education requirements listed above, non-traditional degrees with applicable science credits that meet CLIA standards may meet education requirement.", "qualificationsBasic" : "Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology, or an MLS degree. 1 year or more of clinical laboratory testing experience. Proficient with computers. Able to pass a standardized color blindness test.", "qualificationsPreferred" : "ASCP or AMT certification. Familiarity with laboratory information systems. Flexibility to work overtime or other shifts depending on business needs.", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**LabCorp is seeking a Clinical Lab Professional to join our team at****Ascension St. John Jane Phillips, Bartlesville, OK**. **Work Schedule:** 3 x 12 hour shifts, Monday - Friday, 6:30 PM - 7:00 AM, rotating weekends and holidays. **Job Responsibilities:** * Determine the acceptability of specimens for testing according to established criteria * Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures * Monitor, operate and troubleshoot instrumentation to ensure proper functionality * Demonstrate the ability to make technical decisions regarding testing and problem solving. * Prepare, test and evaluate new reagents or controls * Report accurate and timely test results in order to deliver quality patient care * Perform and document preventive maintenance and quality control procedures * Identify and replenish testing bench supplies as necessary * Assist with processing of specimens when needed * Maintain a safe work environment and wear appropriate personal protective equipment **Minimum Qualifications:** * Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology * 1 year or more of clinical laboratory testing experience OR an MLS degree **Preferred Qualifications:** * ASCP or AMT certification **Additional Job Standards:** * In lieu of education requirements listed above, non-traditional degrees with applicable science credits that meet CLIA standards may meet education requirement * Ability to work independently and within a team environment * Familiarity with laboratory information systems * Proficient with computers * High level of attention detail along with strong communication and organizational skills * Able to pass a standardized color blindness test * Flexibility to work overtime or other shifts depending on business needs At Labcorp we have a passion in helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step!**This role works in a high volume, production based environment performing a vital component of clinical lab science.** **Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please [click here](https://careers.labcorp.com/global/en/us-rewards-and-wellness). _**If you 're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!**_ **Labcorp is proud to be an Equal Opportunity Employer:** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our [accessibility site](https://careers.labcorp.com/global/en/accessibility) or contact us at [Labcorp Accessibility.](mailto:Disability_apply@LabCorp.com) For more information about how we collect and store your personal data, please see our [Privacy Statement](https://www.labcorp.com/about/web-privacy-policy).", "summaryDescription" : "Clinical Laboratory Technologist at LabCorp. Skills: clinical laboratory testing, instrumentation, quality control. The Clinical Laboratory Technologist determines specimen acceptability, performs routine and complex technical procedures, and operates/troubleshoots instrumentation. This role involves preparing and testing reagents, reporting accurate test results for patient care, and performing preventive maintenance and quality control. The technologist also manages testing bench supplies, mai", "postedDate" : "2026-06-10T20:59:08.207", "createdAt" : "2026-06-14T20:59:08.157", "lastUpdated" : "2026-06-15T10:13:41.446", "ingestTimestamp" : "2026-06-14T20:59:08.157", "mongoId" : "6a2ebf8074d8ee00a0e9ac8b", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/Bartlesville-OK/Clinical-Laboratory-Technologist_2615389", "hasSalary" : false, "allSkills" : [ "attention to detail, organizational skills", "clinical laboratory testing, instrumentation, quality control", "Clinical lab science.", "ASCP", "AMT", "laboratory information systems" ], "skillCount" : 6, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 739.26874, "daysOld" : 4, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2caa5574d8ee00a09c9122", "title" : "Specialist Sampling Audit", "company" : "LEONI", "industry" : "Automotive", "salary" : { "min" : 18500.0, "max" : 25500.0, "currency" : "TND", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Tunisia, adjusted for junior seniority and the automotive industry in Sousse." }, "location" : "Sousse, Sousse Governorate, TN", "locations" : [ "Sousse", "Sousse Governorate", "TN" ], "timestamp" : "2026-06-15T10:48:01.456", "fingerprint" : "1e1a0f77477b24b451924d92e5aca3e8cea4792c93cab48a009e26a34848dc8e", "source" : "smartrecruiters", "language" : "en", "applyUrl" : "https://jobs.smartrecruiters.com/LEONI1/744000131951187-specialist-sampling-audit-", "externalId" : "744000131951187", "industryFunction" : { }, "structuredLocations" : [ { "workMode" : "onsite" } ], "locationText" : "", "employmentType" : "FULL_TIME", "minimumEducation" : "University degree", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "entry", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Product audits", "Dimensional conformity", "Functional conformity", "Statistical data", "Quality control" ], "hardSkills" : [ { "name" : "Product audits", "level" : "intermediate" }, { "name" : "Dimensional conformity", "level" : "intermediate" }, { "name" : "Functional conformity", "level" : "intermediate" }, { "name" : "Statistical data", "level" : "intermediate" }, { "name" : "Quality control", "level" : "intermediate" } ], "majorSkills" : "Product audits, Quality control, Continuous improvement", "majorSkillsList" : [ "Product audits", "Quality control", "Continuous improvement" ], "coreResponsibilities" : "Perform product audits, Follow up corrective actions, Verify dimensional conformity, Verify functional conformity, Approve PPAPISIR, Approve initial sample, Register release on customer portal, Ensure compliance with management systems, Ensure compliance with legal requirements, Ensure compliance with regulatory requirements, Check product updates, Check process updates, Check equipment updates, Check tooling updates, Check documentation updates, Approve product processes, Approve production processes, Ensure statistical data availability, Maintain quality control, Maintain technical documents, Ensure continuous improvement implementation, Ensure customer specific requirement compliance, Stop production, Stop dispatch", "domainKnowledge" : "Automotive industry; Wiring systems; Cable harnesses; Integrated management systems; SPC; MSA; CPK; CMK", "domainList" : [ "automotive-industry", "wiring-systems", "cable-harnesses", "integrated-management-systems", "spc", "msa", "cpk", "cmk" ], "domainSpecificKnowledge" : [ "Automotive industry", "Wiring systems", "Cable harnesses", "Integrated management systems", "SPC", "MSA", "CPK", "CMK" ], "documentationSkills" : "Technical documents; Drawing; Drawing complement; Technical change", "problemSolvingSkills" : "Root cause analysis", "qualificationsBasic" : "University degree, 1 year production inspector", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "LEONI is a global leading provider of products, solutions and services for energy and data management in the automotive industry. With around 86,000 employees in 21 countries and consolidated sales of EUR 3.9 billion in 2025 (excluding the former Automotive Cable Solutions division), we are a leading supplier of complex wiring systems and customer‑specific cable harnesses. Since 2025, we have been part of the Luxshare Group, a global technology company headquartered in China. Together, we are shaping the future of mobility. Join us and help drive the transformation of the automotive world. Performs product audits for pre-production phases. - Performs product audits as planned e. g. components, semi-finished goods and finished goods during samples, like A-, B-, C- and D-, and pre-production phases - Follows up corrective actions of product audits non-conformities within the project through QRQC activities in the plant, lead by Industrial Engineering - Verifies the dimensional and functional conformity of the initial samples - Approves PPAPISIR, initial sampling inspection report, german: EMPB, of the initial sample - Registers the release on customer portal if applicable - Ensures compliance with the integrated management systems, legal and regulatory requirements - Checks that products, processes, equipment, tooling and documentation are updated for each technical change - Approves product and production processes according to customer requirements and internal procedures - Ensures that all statistical data SPC, MSA, CPK, CMK, etc. are available during samples, like A-, B-, C- and D-, and pre-production phases - Maintains quality control according to customer requirements and internal procedure during samples, like A-, B-, C- and D-, and pre-production phases - Maintains the technical documents of the customer e.g. drawing, drawing complement, technical change - Ensures implementation of continuous improvement actions of the quality management processes, procedures, policies, activities and reports throughout the segment or area of responsibility - Ensures compliance with customer specific requirement within segment or area of responsibility - Is authorized to stop production and/or dispatch to mitigate risk of non-conforming processes and products ## Qualifications * University degree. * 1 year as a production inspector. ## Additional Information * Drawings. * SpecificationsPrototyping. * Quality Tools and Techniques. * Local Language C2. * English A1. _People of all genders are always meant equally; for linguistic simplification and better readability, only the masculine form is used in the text. LEONI processes your application data in an IT-system that is consistent across the company and uses Foreign Service providers. By sending your application, you agree to this procedure. LEONI ensures the compliance with data protection. _ LEONI Wiring Systems Tunisia SARL", "summaryDescription" : "Specialist Sampling Audit at LEONI. Skills: Product audits, Quality control, Continuous improvement. Perform product audits. Follow up corrective actions", "postedDate" : "2026-06-12T17:41:26.000", "createdAt" : "2026-06-13T23:06:04.879", "lastUpdated" : "2026-06-15T10:48:01.456", "ingestTimestamp" : "2026-06-13T23:06:04.879", "mongoId" : "6a2caa5574d8ee00a09c9122", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "<30k", "hasSalary" : false, "allSkills" : [ "Product audits", "Dimensional conformity", "Functional conformity", "Statistical data", "Quality control", "Continuous improvement", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Automotive industry", "Wiring systems", "Cable harnesses", "Integrated management systems", "SPC", "MSA", "CPK", "CMK" ], "skillCount" : 20, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Junior", "dataQualityScore" : 1.0, "_score" : 737.57404, "daysOld" : 2, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Automotive", "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" : 733.13367, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a15e47758b93c861e7c7569", "title" : "Laboratory Technician", "company" : "Hospitality Health ER", "industry" : "Healthcare", "salary" : { "min" : 38000.0, "max" : 52000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "The estimated salary is based on the market baseline for an Entry-level Laboratory Technician in Tyler, United States, within the Healthcare industry, adjusted for company size and specific location." }, "location" : "Tyler, TX", "locations" : [ "Tyler", "TX" ], "timestamp" : "2026-06-15T10:24:20.581", "fingerprint" : "c4f0b354e2b762662e57e0f8a83162a295c55bac831538d73acbeba80dcff99d", "source" : "breezyhr", "language" : "en", "applyUrl" : "https://hospitality-health-er.breezy.hr/p/16d894b82ae7-laboratory-technician", "externalId" : "16d894b82ae7", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tyler", "state" : "Texas", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "32.3512601,-95.3010624" } ], "locationText" : "Tyler, Texas, United States", "employmentType" : "FULL_TIME", "professionalSkills" : [ "Laboratory Operations", "Patient Testing", "Specimen Collection", "Quality Control", "Healthcare Operations" ], "majorSkills" : "Laboratory Operations, Patient Testing, Specimen Collection, Quality Control", "majorSkillsList" : [ "Laboratory Operations", "Patient Testing", "Specimen Collection", "Quality Control" ], "coreResponsibilities" : "Support laboratory operations", "domainKnowledge" : "Healthcare; Laboratory", "domainList" : [ "healthcare", "laboratory" ], "domainSpecificKnowledge" : [ "Healthcare", "Laboratory" ], "specialRequirements" : "Fast-Paced Environment", "workSiteFlexibility" : "Onsite", "rawDescription" : "Laboratory Technician Location: Tyler, TXEmployment Type: Full-TimeLaboratory Operations | Patient Testing | Specimen Collection | Quality Control | Healthcare Operations | Fast-Paced EnvironmentOverviewHospitality Health ER is seeking a Laboratory Technician to support laboratory operations withi", "summaryDescription" : "Laboratory Technician at Hospitality Health ER. Skills: Laboratory Operations, Patient Testing, Specimen Collection, Quality Control. Support laboratory operations", "createdAt" : "2026-06-13T23:25:08.312", "lastUpdated" : "2026-06-15T10:24:20.581", "ingestTimestamp" : "2026-06-13T23:25:08.312", "mongoId" : "6a15e47758b93c861e7c7569", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 38000, "salaryAnnualMax" : 52000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Laboratory Operations", "Patient Testing", "Specimen Collection", "Quality Control", "Healthcare Operations", "Healthcare", "Laboratory" ], "skillCount" : 7, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.7777778, "_score" : 730.8922, "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" : 720.59094, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2ca57374d8ee00a09b68c0", "title" : "Chemistry Laboratory Assistant", "company" : "Interpath Laboratory", "industry" : "Healthcare", "salary" : { "min" : 36000.0, "max" : 48000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for an Entry-level Chemistry Laboratory Assistant in Pendleton, United States, adjusted for the healthcare industry." }, "location" : "IP Pendleton 1", "locations" : [ "IP Pendleton 1" ], "timestamp" : "2026-06-15T09:05:31.140", "fingerprint" : "d29ffc975f687a417498d1c888a1dd696aa3515ed42bf391309d0ee90bf9e627", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/interpath/jobs/4284045009", "externalId" : "4284045009", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Pendleton", "state" : "Oregon", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "45.6720750,-118.7885967" } ], "locationText" : "Pendleton, Oregon, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "High School", "experienceMinYears" : 0, "experienceMaxYears" : 2, "experienceLevel" : "Entry", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement" ], "hardSkillsList" : [ "Basic troubleshooting" ], "hardSkills" : [ { "name" : "Basic troubleshooting", "level" : "intermediate" } ], "majorSkills" : "Diagnostic services, Specimen handling, Quality assurance", "majorSkillsList" : [ "Diagnostic services", "Specimen handling", "Quality assurance" ], "coreResponsibilities" : "Perform basic troubleshooting, Participate in proficiency testing, Participate in quality assurance initiatives, Maintain accurate documentation, Answer phones professionally, Ensure compliance with HIPAA guidelines, Follow established safety protocols, Follow infection control protocols, Take on new duties, Gain valuable experience", "teamCollaboration" : "Support for our team; Collaborative setting", "domainKnowledge" : "Clinical laboratory; Diagnostic services; HIPAA guidelines; Infection control", "domainList" : [ "clinical-laboratory", "diagnostic-services", "hipaa-guidelines", "infection-control" ], "domainSpecificKnowledge" : [ "Clinical laboratory", "Diagnostic services", "HIPAA guidelines", "Infection control" ], "communicationSkills" : "Communicate clearly", "documentationSkills" : "Maintain accurate documentation", "continuousLearning" : "Eager to learn new technology; Eager to learn laboratory processes", "problemSolvingSkills" : "Problem-solving", "specialRequirements" : "Exposure to blood, Exposure to body fluids, Exposure to tissues", "qualificationsBasic" : "High School Diploma or equivalent, Reliable attendance and punctuality, Ability to stand and walk, Frequent use of hands, Ability to lift and carry up to 25 pounds, Ability to read and interpret data, Ability to bend, stoop, and reach, Sustained concentration for accurate specimen handling", "qualificationsPreferred" : "Associate's degree or higher", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Start your career with one of the Pacific Northwest’s largest independent clinical and anatomic laboratories. As a Laboratory Assistant, you’ll gain hands-on experience, work alongside skilled professionals, and take your first step toward a rewarding, purpose-driven career in diagnostic services. Pay: $19/hour commensurate with experience and education *This position is eligible for night differential pay (10%)* Schedule: Full-time; Monday - Friday 10:30pm - 7am Benefits Medical, Dental, Vision with In-Network provide basic troubleshooting as needed. Ensure Quality: Participate in proficiency testing and quality assurance initiatives. Administrative Tasks: Maintain accurate documentation, answer phones professionally, and ensure compliance with HIPAA guidelines. Safety First: Follow established safety and infection control protocols. Adapt and Grow: Take on new duties as operational needs evolve and gain valuable experience for future advancement. Reliability: Maintain consistent, punctual, and reliable attendance to ensure continuity of operations and support for our team and patients. Who You Are Dependable, detail-oriented, and committed to accuracy. Skilled in multitasking and problem-solving in a fast-paced environment. A strong team player who thrives in a collaborative setting. Eager to learn new technology and laboratory processes. Familiar with patient confidentiality and HIPAA guidelines. Qualifications High School Diploma or equivalent. Associate's degree or higher preferred. Reliable attendance and punctuality. Physical Requirements Mobility: Ability to stand and walk for extended periods. Manual Dexterity: Frequent use of hands and fingers to handle lab instruments and computer systems. Lifting: Ability to lift and carry up to 25 pounds. Vision & Hearing: Ability to read and interpret data, identify specimens, and communicate clearly in person and by phone. Flexibility: Ability to bend, stoop, and reach to access equipment or supplies. Attention to Detail: Sustained concentration for accurate specimen handling and testing. OSHA Category: This position involves exposure to blood, body fluids, and/or tissues. Employees performing these duties are offered the opportunity to receive the Hepatitis-B vaccination series. About Us: Interpath Laboratory is a family-owned and operated clinical and anatomic pathology laboratory serving communities across Oregon, Washington, Nebraska, and Idaho. With more than 90 locations and over 60 years of steady growth, we are one of the Pacific Northwest’s leading independent laboratories, with plans for continued and strategic expansion into the Midwest. We are known for delivering rapid, reliable, and cost-effective laboratory testing while maintaining the flexibility, innovation, and personal connection that come from remaining independent. Our success is built on strong relationships—with our clients, our patients, and most importantly, our employees. At Interpath, we foster a collaborative, supportive work environment where teamwork, professionalism, and positive attitudes matter. We believe great results start with great people, and we are committed to creating a workplace where employees can build meaningful careers while making a real impact in the communities we serve. We are excited to share with you a short video that shows why the Interpath family is so special. Please click here: https://youtu.be/iMaXUt6s9rg", "summaryDescription" : "Chemistry Laboratory Assistant at Interpath Laboratory. Skills: Diagnostic services, Specimen handling, Quality assurance. Perform basic troubleshooting. Participate in proficiency testing", "postedDate" : "2026-06-14T03:49:37.131", "createdAt" : "2026-06-14T03:49:37.131", "lastUpdated" : "2026-06-15T09:05:31.140", "ingestTimestamp" : "2026-06-14T03:49:37.131", "mongoId" : "6a2ca57374d8ee00a09b68c0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 36000, "salaryAnnualMax" : 48000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Basic troubleshooting", "Diagnostic services", "Specimen handling", "Quality assurance", "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Clinical laboratory", "HIPAA guidelines", "Infection control" ], "skillCount" : 14, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 1.0, "_score" : 719.96545, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "69dde45c2beec4dd3d9a3f66", "title" : "Clinical Laboratory Scientist - Blood Bank", "company" : "City of Hope", "industry" : "Healthcare", "salary" : { "min" : 43.0, "max" : 66.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "United States-California-Duarte", "locations" : [ "United States-California-Duarte", "Clinical Laboratory/Pathology" ], "timestamp" : "2026-06-15T08:12:41.271", "fingerprint" : "5a59e0e5be60d037d51bc0b9d676f74cd429abc88bce50985124e60037788123", "source" : "taleo", "language" : "en", "applyUrl" : "https://aa067.taleo.net/careersection/ex/jobdetail.ftl?job=182003", "externalId" : "182003", "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 Degree", "professionalSkills" : [ "Clinical analysis", "Laboratory procedures", "Data entry" ], "hardSkillsList" : [ "Specimen preparation", "Quality control", "Reagent preparation" ], "hardSkills" : [ { "name" : "Specimen preparation", "level" : "intermediate" }, { "name" : "Quality control", "level" : "intermediate" }, { "name" : "Reagent preparation", "level" : "intermediate" } ], "majorSkills" : "Blood Bank, Laboratory Science", "majorSkillsList" : [ "Blood Bank", "Laboratory Science" ], "coreResponsibilities" : "Prepare specimens for analysis, Perform clinical laboratory procedures, Report clinical laboratory procedures, Adhere to SOPs, Adhere to regulatory guidelines, Assist in teaching students, Assist in teaching staff, Maintain knowledge of techniques, Process biological specimens, Demonstrate proficiency in procedures, Perform complex laboratory tests, Perform complex laboratory procedures, Complete tests within turnaround times, Review normal results, Review critical results, Notify supervisors of unusual results, Notify supervisors of discrepancies, Conduct quality control procedures, Perform preventive maintenance, Perform calibrations, Record quality control data, Participate in Quality Assurance, Participate in Performance Improvement, Utilize standard laboratory equipment, Ensure accuracy of recorded results, Ensure completeness of recorded results, Perform data entry, Prepare solutions, Prepare reagents, Prepare culture media, Prepare stains, Label solutions, Label reagents, Label culture media, Label stains, Prioritize work, Provide efficient service, Assist coworkers, Maintain cleanliness, Maintain safety practices, Uphold integrity, Uphold confidentiality, Maintain positive customer service image", "teamCollaboration" : "Interacting with colleagues", "domainKnowledge" : "FACT; AABB; ACHI; CAP; FDA; Joint Commission; Clinical Laboratory Improvement Amendments; Biological specimens; Laboratory equipment", "domainList" : [ "fact", "aabb", "achi", "cap", "fda", "joint-commission", "clinical-laboratory-improvement-amendments", "biological-specimens", "laboratory-equipment" ], "domainSpecificKnowledge" : [ "FACT", "AABB", "ACHI", "CAP", "FDA", "Joint Commission", "Clinical Laboratory Improvement Amendments", "Biological specimens", "Laboratory equipment" ], "qualificationsBasic" : "New licensed clinical laboratory scientists", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Thank you for your interest. 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. 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 Hourly Pay Rate: $43.17 - $66.92 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 - Blood Bank at City of Hope. Skills: Blood Bank, Laboratory Science. Prepare specimens for analysis. Perform clinical laboratory procedures", "createdAt" : "2026-06-14T02:52:32.767", "lastUpdated" : "2026-06-15T08:12:41.271", "ingestTimestamp" : "2026-06-14T02:52:32.767", "mongoId" : "69dde45c2beec4dd3d9a3f66", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 89440, "salaryAnnualMax" : 137280, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Specimen preparation", "Quality control", "Reagent preparation", "Blood Bank", "Laboratory Science", "Clinical analysis", "Laboratory procedures", "Data entry", "FACT", "AABB", "ACHI", "CAP", "FDA", "Joint Commission", "Clinical Laboratory Improvement Amendments", "Biological specimens", "Laboratory equipment" ], "skillCount" : 17, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Entry", "dataQualityScore" : 0.7777778, "_score" : 685.1084, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2c960974d8ee00a098e758", "title" : "Laboratory Director, IVF & ART", "company" : "Di Rezze Family Office", "industry" : "Healthcare", "location" : "Remote", "locations" : [ "Remote" ], "certifications" : [ "HCLD (High-complexity Clinical Laboratory Director)", "ELD" ], "timestamp" : "2026-06-15T07:12:02.198", "fingerprint" : "6d42585f1f35d211f3066596d91203ab34db12556f143c1e3d60c8019ebed6ed", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/dfo/jobs/4281740009", "externalId" : "4281740009", "industryFunction" : { }, "structuredLocations" : [ { "workMode" : "remote" } ], "locationText" : "", "employmentType" : "FULL_TIME", "experienceLevel" : "Director", "technicalSkills" : "EmbryoScope+, RI Witness, Matcher, EIVF, NGS", "professionalSkills" : [ "Process management", "Cross-functional coordination", "Vendor management", "Stakeholder management", "Operational metrics", "Resource planning", "Continuous improvement", "Facility design", "Pre-construction planning", "Construction oversight", "Commissioning", "Equipment installation", "Validation", "Staff recruitment", "Staff onboarding", "SOP authoring", "Quality systems", "QA/QC program", "Regulatory compliance", "Outsourcing relationships", "Automation readiness", "Network expansion" ], "hardSkillsList" : [ "Clinical laboratory management", "Accreditation", "Facility specification", "Equipment planning", "HVAC capacity", "Electrical service", "Medical gas infrastructure", "ISO classification", "Cryostorage capacity", "Andrology workstation", "Robotic IVF deployment", "CLIA", "CAP", "SART membership", "PGT outsourcing", "In-house NGS", "Clinical outcomes", "Technical standard", "Spoke lab integrations", "Acquisition diligence", "Automation partnerships", "Pipeline building" ], "softSkillsList" : [ "Leadership" ], "hardSkills" : [ { "name" : "Clinical laboratory management", "level" : "intermediate" }, { "name" : "Accreditation", "level" : "intermediate" }, { "name" : "Facility specification", "level" : "intermediate" }, { "name" : "Equipment planning", "level" : "intermediate" }, { "name" : "HVAC capacity", "level" : "intermediate" }, { "name" : "Electrical service", "level" : "intermediate" }, { "name" : "Medical gas infrastructure", "level" : "intermediate" }, { "name" : "ISO classification", "level" : "intermediate" }, { "name" : "Cryostorage capacity", "level" : "intermediate" }, { "name" : "Andrology workstation", "level" : "intermediate" }, { "name" : "Robotic IVF deployment", "level" : "intermediate" }, { "name" : "CLIA", "level" : "intermediate" }, { "name" : "CAP", "level" : "intermediate" }, { "name" : "SART membership", "level" : "intermediate" }, { "name" : "PGT outsourcing", "level" : "intermediate" }, { "name" : "In-house NGS", "level" : "intermediate" }, { "name" : "Clinical outcomes", "level" : "intermediate" }, { "name" : "Technical standard", "level" : "intermediate" }, { "name" : "Spoke lab integrations", "level" : "intermediate" }, { "name" : "Acquisition diligence", "level" : "intermediate" }, { "name" : "Automation partnerships", "level" : "intermediate" }, { "name" : "Pipeline building", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" } ], "majorSkills" : "IVF laboratory operations, Accreditation and compliance", "majorSkillsList" : [ "IVF laboratory operations", "Accreditation and compliance" ], "coreResponsibilities" : "Walk candidate sites, Produce technical feasibility memos, Define lab program, Select and brief IVF facility review, Sign off on HVAC, air quality, cryostorage, Build Day 1 equipment plan, Design lab for automation readiness, Oversee construction, Oversee commissioning, Oversee equipment installation, Oversee validation, Recruit senior embryology staff, Onboard senior embryology staff, Recruit senior andrology staff, Onboard senior andrology staff, Author all SOPs, Author quality systems documentation, Author QA/QC program, Drive CLIA accreditation, Drive CAP accreditation, Drive Florida Department of Health accreditation, Lead SART membership application, Establish PGT outsourcing relationships, Direct day-to-day lab operations, Manage clinical outcomes, Manage staffing, Manage quality, Manage regulatory compliance, Manage vendor management, Set technical standard for spoke lab integrations, Set technical standard for acquisition diligence, Lead evaluation of automation partnerships, Lead evaluation of PGT in-sourcing, Mentor junior staff, Build pipeline for network expansion", "teamCollaboration" : "Cross-functional teams; Architects; Engineers; Product teams; Senior staff; Junior staff; Vendors; Stakeholders", "projectManagementSkills" : [ "Feasibility and design engagement", "Construction oversight", "Commissioning", "Accreditation process", "Operations management", "Scale management" ], "domainKnowledge" : "IVF; ART; Embryology; Andrology; Cryostorage; Medical gas infrastructure; ISO classification; PGT; NGS; CLIA; CAP; SART; Robotic IVF; Automation landscape", "domainList" : [ "ivf", "art", "embryology", "andrology", "cryostorage", "medical-gas-infrastructure", "iso-classification", "pgt", "ngs", "clia", "cap", "sart", "robotic-ivf", "automation-landscape" ], "domainSpecificKnowledge" : [ "IVF", "ART", "Embryology", "Andrology", "Cryostorage", "Medical gas infrastructure", "ISO classification", "PGT", "NGS", "CLIA", "CAP", "SART", "Robotic IVF", "Automation landscape" ], "toolProficiency" : [ "EmbryoScope+", "RI Witness", "Matcher", "EIVF", "Conceivable", "AURA", "CHLOE", "Life Whisperer", "ALife" ], "communicationSkills" : "Technical memos; Briefing architects; Briefing engineers; SOP authoring; Quality systems documentation; QA/QC program; Regulatory reporting; SART membership application; Technical standard setting; Acquisition diligence; Pipeline building", "documentationSkills" : "Technical memos; SOPs; Quality systems documentation; QA/QC program", "innovationCreativity" : "Automation-ready design; Future robotic IVF deployment", "problemSolvingSkills" : "Feasibility analysis; Technical problem solving; Quality system development; Regulatory compliance; Troubleshooting", "specialRequirements" : "Feasibility and design engagement, Consulting-to-hire path, Transition to full-time Director", "outcomesObjectives" : "Achieve accreditation; Open laboratory; Scale laboratory operations; Meet ISO classification targets; Meet cryostorage capacity targets; Meet andrology room layout targets; Meet procedure room layout targets; Meet Day 1 equipment plan; Achieve CLIA accreditation; Achieve CAP accreditation; Achieve Florida accreditation; Establish PGT outsourcing relationships; Achieve 600+ cycles/year for in-house NGS; Meet clinical outcomes targets; Meet staffing targets; Meet quality targets; Meet regulatory compliance targets; Meet vendor management targets; Set technical standard for spoke lab integrations; Set technical standard for acquisition diligence; Evaluate automation partnerships; Evaluate PGT in-sourcing; Build pipeline for network expansion", "qualificationsBasic" : "HCLD certification through ABB, PhD-track credential with ELD, Commissioned at least one IVF lab, Direct operating experience with time-lapse incubation, Direct operating experience with electronic witnessing, Direct operating experience with modern LIMS, Run a lab through 200-600+ annual cycle inflection, Authored SOPs from scratch, Led CAP inspections, Operated under current witnessing and traceability standards, Familiar with post-Alabama regulatory environment, Familiar with lessons from recent IVF mix-up incidents", "qualificationsPreferred" : "Florida operating experience, Prior tenure at premium-segment network, Direct experience opening or scaling a network lab, Published research, Society leadership (ASRM, SART, ABB)", "remoteFriendly" : true, "workSiteFlexibility" : "Remote", "rawDescription" : "Laboratory Director, IVF transition into operational leadership through accreditation, opening, and scale. Consulting-to-hire. Begin with a paid feasibility and design engagement (typically 8–12 weeks) covering site walk-through, technical memo, facility spec, and equipment plan. Convert to full-time Laboratory Director ahead of construction kickoff. This path is designed for candidates currently in director roles who want to validate the opportunity before transitioning. Both paths lead to the same destination. The recruiter can route candidate preferences. What you will own Phase 1 — Facility design and pre-construction (months 0–6) Walk candidate sites and produce technical feasibility memos covering floor-to-floor height, floor load, HVAC capacity, electrical service, LN2 routing, medical gas infrastructure, and adjacent-tenant risk. Define the lab program: square footage, room adjacencies, ISO classification targets, equipment footprint, cryostorage capacity, andrology and procedure room layout. Select and brief the IVF facility consultant; review schematic and construction documents from the architect of record; sign off on HVAC, air quality, and cryostorage engineering. Build the Day 1 equipment plan, including time-lapse incubation (EmbryoScope+ or equivalent), electronic witnessing (RI Witness or Matcher), LIMS (eIVF or equivalent), and andrology workstation specifications. Design the lab to be automation-ready for future robotic IVF deployment (e.g., Conceivable/AURA) without committing premature capital. Phase 2 — Construction, commissioning, and accreditation (months 6–12) Oversee construction, commissioning, equipment installation, and validation. Recruit and onboard senior embryology and andrology staff (the Laboratory Director chooses these hires). Author all SOPs, quality systems documentation, and the QA/QC program. Drive CLIA, CAP, and Florida licensure; lead the SART membership application. Establish PGT outsourcing relationships for Years 1–2, with a defined pathway to in-house NGS at 600+ cycles/year. Phase 3 — Operations and scale (months 12+) Direct day-to-day lab operations: clinical outcomes, staffing, quality, regulatory compliance, vendor management. Set the technical standard for spoke lab integrations and future acquisition diligence. Lead the Year 2–3 evaluation of automation partnerships and PGT in-sourcing. Mentor junior embryologists; build a pipeline that supports network expansion. Required qualifications Certification: HCLD (High-complexity Clinical Laboratory Director) through ABB, or equivalent PhD-track credential with ELD. Required for CLIA Lab Director of record. Greenfield build experience: Has commissioned at least one IVF lab from shell space through CAP/CLIA accreditation. We will ask for specifics: square footage, cycle volume at launch, lease-to-first-transfer timeline. Technology fluency: Direct operating experience with time-lapse incubation (EmbryoScope+ specifically), electronic witnessing (RI Witness and/or Matcher), and a modern LIMS. Informed opinions on tradeoffs, not brand familiarity. Volume scaling: Has run a lab through the 200 → 600+ annual cycle inflection, with the staffing, equipment redundancy, and quality systems that come with it. Quality systems leadership: Has authored SOPs from scratch, led CAP inspections, and operated under current witnessing and traceability standards. Familiar with post-Alabama regulatory environment and lessons from recent IVF mix-up incidents. Automation literacy: Familiar with the current automation landscape (Conceivable/AURA, CHLOE, Life Whisperer, ALife) without being a true believer. Builds automation-ready, not automation-dependent. Preferred Florida operating experience, including familiarity with Office Surgery Registration pathway. Prior tenure at a premium-segment network (CCRM, Shady Grove, RMA, Boston IVF, Spring Fertility, or equivalent). Direct experience opening or scaling a network lab (multi-site, hub-and-spoke). Published research or society leadership (ASRM, SART, ABB).", "summaryDescription" : "Laboratory Director, IVF & ART at Di Rezze Family Office. Skills: IVF laboratory operations, Accreditation and compliance. Walk candidate sites. Produce technical feasibility memos", "postedDate" : "2026-06-14T04:24:02.840", "createdAt" : "2026-06-14T04:24:02.840", "lastUpdated" : "2026-06-15T07:12:02.198", "ingestTimestamp" : "2026-06-14T04:24:02.840", "mongoId" : "6a2c960974d8ee00a098e758", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "hasSalary" : false, "allSkills" : [ "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", "Leadership", "IVF laboratory operations", "Accreditation and compliance", "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", "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" : 678.1274, "daysOld" : 1, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2a47c974d8ee00a05dc30f", "title" : "Quality Control Specialist I, Sample Management [Contract to Hire]", "company" : "Iovance Biotherapeutics", "industry" : "Biotherapeutics", "salary" : { "min" : 58000.0, "max" : 78000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Junior Quality Control Specialist I in Philadelphia, adjusted for the Biotech industry and contract employment type." }, "location" : "Philadelphia, Pennsylvania, United States", "locations" : [ "Philadelphia", "Pennsylvania", "United States" ], "timestamp" : "2026-06-14T21:12:42.004", "fingerprint" : "b5d43e6ea4a3da24b7986db19a214704ef7539adb498846f272e952d1c078c8b", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/iovancebiotherapeutics/jobs/5248785008", "externalId" : "5248785008", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Philadelphia", "state" : "Pennsylvania", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "39.9527237,-75.1635262" } ], "locationText" : "Philadelphia, Pennsylvania, United States", "employmentType" : "CONTRACT", "minimumEducation" : "Bachelor's", "experienceMinYears" : 2, "professionalSkills" : [ "Sample management", "Inventory management", "Logistics" ], "hardSkillsList" : [ "Mathematical skills", "Packaging samples" ], "softSkillsList" : [ "Judgment", "Problem-solving" ], "hardSkills" : [ { "name" : "Mathematical skills", "level" : "intermediate" }, { "name" : "Packaging samples", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Judgment" }, { "name" : "Problem-solving" } ], "majorSkills" : "Sample management, Inventory tracking, Sample distribution", "majorSkillsList" : [ "Sample management", "Inventory tracking", "Sample distribution" ], "coreResponsibilities" : "Maintain raw material samples, Maintain in-process samples, Maintain final product samples, Track inventory, Reconcile inventory, Ensure timely sample distribution, Support Quality Control activities, Perform internal distribution, Perform external shipping, Ensure proper storage of sample inventory, Ensure proper shipping conditions, Support sample receipt, Support sample documentation, Package samples using temperature controlled dewars, Package samples using cold packs, Package samples using dry ice, Perform Quality Control activities, Perform peer review of logbooks, Adhere to core values, Adhere to policies, Adhere to procedures, Adhere to business ethics, Comply with safety SOPs, Comply with SDS sheets, Comply with laboratory procedures, Complete training sessions, Maintain training documentation, Adhere to GMP, Adhere to SOP procedures, Adhere to GDP, Assist with cycle counts", "teamCollaboration" : "Collaborate with stakeholders", "domainKnowledge" : "Cell therapy; GMP; SOP; GDP; OSHA regulations", "domainList" : [ "cell-therapy", "gmp", "sop", "gdp", "osha-regulations" ], "domainSpecificKnowledge" : [ "Cell therapy", "GMP", "SOP", "GDP", "OSHA regulations" ], "communicationSkills" : "Written communication; Verbal communication", "problemSolvingSkills" : "Creative problem-solving; Troubleshooting; Problem-solving", "specialRequirements" : "Move up to 10 pounds, Repetitive motion, Work in Lab setting, Chemical exposures, Work in cleanroom, Biohazards exposure, Human blood components exposure, Chemicals exposure, Noise exposure, Equipment hazards exposure, Odors exposure", "qualificationsBasic" : "2 years of related experience, Bachelor's degree, Hands-on laboratory experience, Sample handling experience, Inventory experience, Cryo-shipping experience", "qualificationsPreferred" : "Experience with inventory in pharmaceutical industry, Experience with logistics in pharmaceutical industry", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer. Overview The Quality Control Specialist I, Sample Management will ensure time-sensitive distribution of quality control samples in support of QC-related activities. They will be responsible for sample inventory management as well as internal and external sample distribution, including storage and shipping under appropriate conditions, for all the iCTC cell therapy asset. Essential Functions and Responsibilities: Maintain raw material, in-process, and final product samples, including inventory tracking and reconciliation. Ensures timely sample distribution in support of Quality Control activities, including internal distribution and external shipping. Ensures proper storage of sample inventory and proper shipping conditions Support sample receipt and documentation. Maintain current knowledge base of regulations, corporate policies, and industry best practices, trends, and standards to ensure that the function remains in compliance with applicable requirements. Packaging of samples using temperature controlled dewars, cold packs, and dry ice. Perform Quality Control activities Performs peer review of logbooks Must adhere to Iovance Biotherapeutics core values, policies, procedures, and business ethics Comply with safety SOP’s, SDS sheets, and laboratory procedures per company policy and OSHA regulations Complete training sessions and ensure training documentation is maintained Adherence to GMP and SOP procedures including GDP Assist with cycle counts Required Education, Skills, and Knowledge: Bachelor’s degree and a minimum of 2 years of related experience; or an advanced degree without experience; or equivalent work experience. Detail-oriented with strong mathematical skills Excellent written and verbal communication skills Strong collaboration, time management, and organizational skills are required Proven ability to effectively collaborate with a wide range of stakeholders Excellent judgment and creative problem-solving skills Ability to work in a fast-paced and dynamic environment Hands-on laboratory experience with sample handling, inventory, and cryo-shipping Preferred Education, Skills, and Knowledge: Experience with inventory and/or logistics in the pharmaceutical industry The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation. Physical Demands and Activities Required: Must be able to remain in a stationary position standing or sitting for prolonged periods of time. Must be able to move about inside an office and exert up to 10 pounds of force occasionally or a negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects. Must have visual acuity to perform activities such as: preparing and analyzing data and figures, viewing a computer screen, and extensive reading. This position requires repetitive motion, substantial movements (motions) of the wrist, hands, and/or fingers. Must be able to communicate with others to exchange information. Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion Ability to handle work-related stress; ability to handle multiple priorities simultaneously Ability to meet deadlines Work Environment: This position will work in an office, with occasional visits to the Quality Control labs. When in the lab, must be able to work in Lab setting with various chemical/biochemical exposures, including latex and bleach. Able to work in cleanroom with biohazards, human blood components, and chemicals. Potential exposure to noise and equipment hazards and strong odors. #li-onsite The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time. Iovance is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, our employees and applicants will be considered without regard to an individual’s race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law. If you need assistance or accommodation to apply to one of our opportunities, please contact careers@iovance.com. By voluntarily providing information and clicking “Submit Application”, you explicitly consent to the collection and use of your personal information for the purposes described above and in our Candidate Privacy Notice.", "summaryDescription" : "Quality Control Specialist I, Sample Management [Contract to Hire] at Iovance Biotherapeutics. Skills: Sample management, Inventory tracking, Sample distribution. Maintain raw material samples. Maintain in-process samples", "postedDate" : "2026-06-11T22:50:28.114", "createdAt" : "2026-06-11T22:50:28.114", "lastUpdated" : "2026-06-14T21:12:42.004", "ingestTimestamp" : "2026-06-11T22:50:28.114", "mongoId" : "6a2a47c974d8ee00a05dc30f", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 58000, "salaryAnnualMax" : 78000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Mathematical skills", "Packaging samples", "Judgment", "Problem-solving", "Sample management", "Inventory tracking", "Sample distribution", "Inventory management", "Logistics", "Cell therapy", "GMP", "SOP", "GDP", "OSHA regulations" ], "skillCount" : 14, "jobCategory" : "other", "jobSubcategory" : "0082-ictc-quality-control", "dataQualityScore" : 0.8888889, "_score" : 675.57263, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotherapeutics" }, { "id" : "6a2ac4ec74d8ee00a06ffb01", "title" : "Environmental Monitoring & Sample Management Supervisor", "company" : "Legend Biotech EU", "industry" : "Biotechnology", "salary" : { "min" : 75000.0, "max" : 105000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Manager in the Biotech industry in Gent, Belgium, adjusted for seniority and company size." }, "location" : "Gent, East Flanders, Belgium", "locations" : [ "Gent", "East Flanders", "Belgium", "Ghent", "East Flanders", "Belgium" ], "timestamp" : "2026-06-14T19:33:41.882", "fingerprint" : "b8edde2f5e5739d7fc2271216e8741a10ad95cf4a380f049a0af3409d554798e", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/legendcareerseu/jobs/4704951005", "externalId" : "4704951005", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Gent", "state" : "East Flanders", "country" : "Belgium", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "51.0538286,3.7250121" } ], "locationText" : "Gent, East Flanders, Belgium", "minimumEducation" : "Bachelor's", "experienceMinYears" : 3, "experienceLevel" : "Manager", "professionalSkills" : [ "Process coordination", "Operational workflows" ], "hardSkillsList" : [ "Sample management", "Logistics coordination", "GMP documentation" ], "softSkillsList" : [ "Leadership", "Coaching", "Mentoring" ], "hardSkills" : [ { "name" : "Sample management", "level" : "intermediate" }, { "name" : "Logistics coordination", "level" : "intermediate" }, { "name" : "GMP documentation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Coaching" }, { "name" : "Mentoring" } ], "majorSkills" : "Environmental monitoring, Sample management, People management", "majorSkillsList" : [ "Environmental monitoring", "Sample management", "People management" ], "coreResponsibilities" : "Oversee Environmental Monitoring activities, Coordinate batch-related monitoring, Coordinate routine monitoring activities, Ensure timely follow-up of results, Review data, Resolve issues, Monitor sample lifecycle, Track deadlines, Escalate deviations, Resolve issues compliantly, Own collection of QC samples, Own reconciliation of QC samples, Own documentation of QC samples, Own shipment of QC samples, Ensure GMP documentation completeness, Drive workflow optimization, Drive standardization, Contribute to organization of warehouse activities, Contribute to oversight of warehouse activities, Lead a team, Coach team members, Develop team members, Drive engagement, Build trust, Create team culture, Identify opportunities to simplify processes, Identify opportunities to streamline processes, Identify opportunities to scale processes, Lead improvement initiatives, Support improvement initiatives, Collaborate with Operations, Collaborate with Warehouse teams, Collaborate with IPL QC teams, Align priorities, Ensure clear communication, Ensure coordination across departments", "teamCollaboration" : "Cross-functional teams; Operations teams; Warehouse teams; IPL QC teams", "domainKnowledge" : "Pharma; Biotech; Life Sciences; Supply Chain; Logistics; GMP", "domainList" : [ "pharma", "biotech", "life-sciences", "supply-chain", "logistics", "gmp" ], "domainSpecificKnowledge" : [ "Pharma", "Biotech", "Life Sciences", "Supply Chain", "Logistics", "GMP" ], "documentationSkills" : "GMP documentation", "continuousLearning" : "Personal development", "innovationCreativity" : "Process improvement", "problemSolvingSkills" : "Issue resolution", "outcomesObjectives" : "Avoid delays in product release; Ensure timely product release", "qualificationsBasic" : "Bachelor's degree in Life Sciences, Logistics, Supply Chain or equivalent, 3+ years experience in regulated environment, 1+ years experience managing teams, Experience with process coordination, Experience with operational workflows, Fluent English", "qualificationsPreferred" : "Knowledge of Dutch", "workSiteFlexibility" : "Onsite", "rawDescription" : "To support the growth of our Quality Control organization in Ghent, we are looking for a Supervisor Environmental Monitoring (EM) You are responsible for; Environmental Monitoring Oversight: You oversee the coordination and follow-up of Environmental Monitoring activities, including batch-related and routine monitoring activities. You ensure timely follow-up of EM results, data review and issue resulution to avoid delays in product release. You monitor sample lifecycle, track deadlines and ensure deviations or issues are escalated and resolved in a compliant manner. Sample Management & Logistics Coordination: You take ownership of the collection, reconciliation, documentation and shipment of QC samples and ensure all required GMP documentation is complete, accurate and audit-ready. You drive workflow optimization and standardization with a strong focus on scalability and efficiency improvements. You will also contribute to the organization and oversight of warehouse related activities linked to sample handling. People Management & Team Development: You lead a team of 10-15 people with focus on coaching and developing team members, driving engagement in a highly routine based environment while building trust and creating a strong team culture. Operational Excellence & Continuous Improvement: You actively identify opportunities to simplify, streamline and scale processes and lead or support improvement initiatives related to workflow optimization, process standardization and automation. Stakeholder Management & Collaboration: You collaborate closely with Operations, the Warehouse teams and IPL QC teams and align priorities. You ensure clear communication and strong coordination across departments to support timely product release. Who are we looking for? Education A minimum of a bachelor's degree in Life Sciences, Logistics, Supply Chain or equivalent through experience. Experience A minimum of three years of experience in a fast-paced, highly regulated environment, preferably in pharma or biotech. A first experience in managing and leading a team, preferably operational teams. Proven experience with process coordination and operational workflows. Languages Fluent English (written and spoken) is required. Knowledge of Dutch is a strong asset. Strengths You are a hands-on, people focussed leader who enjoys coaching and developing diverse teams. You are a strong communicator who can align stakeholders and manage priorities effectively. You are highly organized and able to manage complex, high-volume workflows. You thrive in a scaling process minded environment and pay attention to detail. You are able to drive structure and efficiency in a scaling environment. You bring a continuous improvement mindset and take ownership of processes. What do we offer you? A meaningful job with an excellent work-life balance. This position falls into our standard Monday to Friday daytime schedule (40h/week) depending on operational needs. A supportive and innovative work environment. We value and encourage learning and personal development. The opportunity to work with people from all over the world. A permanent contract of indefinite duration and an attractive salary package complemented by a wide range of fringe benefits, including additional statutory holidays, meal vouchers, company laptop, smartphone and subscription, net allowance, group and hospitalization insurance, double holiday pay, end-of-year bonus, performance bonus and the possibility to participate in our bicycle lease plan. Many fun and informal events. About Legend Biotech Legend Biotech is a global biotechnology company dedicated to developing, manufacturing, and commercializing innovative and life-saving cell therapies for the treatment of chronic and life-threatening diseases, such as cancer. The company was founded in 2014 and is headquartered in Somerset, New Jersey. Legend Biotech now employs over 2,400 people across six global manufacturing sites. Two of these sites are in Ghent: Obelisc (Technology Park Zwijnaarde) and Tech Lane (Eilandje Zwijnaarde). In Ghent, Legend Biotech focuses on the production of advanced CAR-T cell therapies for the treatment of multiple myeloma, in close collaboration with Johnson & Johnson. Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug-free workplace. For information related to our privacy notice, please review: Legend Biotech Privacy Notice.", "summaryDescription" : "Environmental Monitoring & Sample Management Supervisor at Legend Biotech EU. Skills: Environmental monitoring, Sample management, People management. Oversee Environmental Monitoring activities. Coordinate batch-related monitoring", "postedDate" : "2026-06-11T23:27:04.675", "createdAt" : "2026-06-11T23:27:04.675", "lastUpdated" : "2026-06-14T19:33:41.882", "ingestTimestamp" : "2026-06-11T23:27:04.675", "mongoId" : "6a2ac4ec74d8ee00a06ffb01", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Sample management", "Logistics coordination", "GMP documentation", "Leadership", "Coaching", "Mentoring", "Environmental monitoring", "People management", "Process coordination", "Operational workflows", "Pharma", "Biotech", "Life Sciences", "Supply Chain", "Logistics", "GMP" ], "skillCount" : 16, "jobCategory" : "other", "jobSubcategory" : "quality-&-compliance", "dataQualityScore" : 0.8888889, "_score" : 670.4682, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotechnology" }, { "id" : "6a16291c58b93c861e95a142", "title" : "Principal Laboratory Planner", "company" : "HDR", "industry" : "Consulting", "salary" : { "min" : 235000.0, "max" : 350000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline data for a Principal Laboratory Planner in Los Angeles, adjusted for executive seniority and the consulting industry." }, "location" : "Multiple Locations", "locations" : [ "Multiple Locations" ], "certifications" : [ "Registered Architect" ], "timestamp" : "2026-06-15T07:54:19.882", "fingerprint" : "4a0de3cd88efa8c4cadeca9d8e975104ebab27974a7ce30bed2fc8d6a9edff1e", "source" : "taleo", "language" : "en", "applyUrl" : "https://hdr.taleo.net/careersection/ex/jobdetail.ftl?job=776711", "externalId" : "776711", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Los Angeles", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "34.0536909,-118.2427660" } ], "locationText" : "Los Angeles, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "experienceMinYears" : 15, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Project management", "Team leadership", "Client presentations" ], "softSkillsList" : [ "Mentoring", "Motivational skills", "Organizational skills", "People skills" ], "softSkills" : [ { "name" : "Mentoring" }, { "name" : "Motivational skills" }, { "name" : "Organizational skills" }, { "name" : "People skills" } ], "majorSkills" : "Laboratory Planning", "majorSkillsList" : [ "Laboratory Planning" ], "teamCollaboration" : "Lead a team", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Local market knowledge; Regional market knowledge", "domainList" : [ "local-market-knowledge", "regional-market-knowledge" ], "domainSpecificKnowledge" : [ "Local market knowledge", "Regional market knowledge" ], "toolProficiency" : [ "Microsoft Word", "Microsoft Excel", "Microsoft Project" ], "communicationSkills" : "Client presentations; Written communication; Verbal communication", "specialRequirements" : "Willing to travel", "qualificationsBasic" : "Bachelor's degree in Architecture, 15 years related experience, 7 years project management experience, Registered Architect, Experience on large-scale projects, Lead a team on projects, Make client presentations, Microsoft Office experience", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Required Qualifications Bachelor's degree in Architecture 15 years related experience A minimum 7 years project management experience Registered Architect Must have experience on large-scale projects Must be able to lead a team on projects and make client presentations Experience with Microsoft Office (Word, Excel, Project) Extensive knowledge and experience within the local and regional market Strong team leadership, mentoring, motivational/organizational and people skills Excellent written and verbal communication skills Must be willing to travel An attitude and commitment to being an active participant of our employee-owned culture is a must What We Believe HDR is our company. Together, we build on each other's life experiences and perspectives to make great things possible every day. This shapes our collaborative culture, encourages organizational trust and connects us closer to the clients and communities we serve. Our Commitment As employee owners, we all have a role in creating an inclusive environment where each of us is welcomed, valued, respected and empowered to bring our authentic selves to work every day. Our eight Employee Network Groups (Asian Pacific, Black, Hispanic/Latino(a), LGBTQ+, People with Disabilities, Veterans, Women, Young Professionals) help create a sense of belonging and foster a supportive environment where everyone is empowered to engage and contribute. Each group has an executive sponsor and is open to all employees. At At HDR, the health and safety of our employees is of the upmost importance. In accordance with local safety, health, and environmental legislation, HDR is committed to developing, maintaining, and enforcing proactive safe work policies, procedures, and standards. In accordance with the Accessibility for Ontarians with Disabilities Act (AODA) and other applicable legislation, we are committed to meeting the accessibility needs of persons with disabilities. Candidates with disabilities may request reasonable accommodation throughout the recruitment and selection process by contacting our Human Resources team. HDR is a certified Living Wage Employer in Ontario, British Columbia, and Alberta. HDR United States-California-Los Angeles", "summaryDescription" : "Principal Laboratory Planner at HDR. Skills: Laboratory Planning", "createdAt" : "2026-06-14T00:56:48.826", "lastUpdated" : "2026-06-15T07:54:19.882", "ingestTimestamp" : "2026-06-14T00:56:48.826", "mongoId" : "6a16291c58b93c861e95a142", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 235000, "salaryAnnualMax" : 350000, "salaryBand" : "200k+", "hasSalary" : true, "allSkills" : [ "Mentoring", "Motivational skills", "Organizational skills", "People skills", "Laboratory Planning", "Project management", "Team leadership", "Client presentations", "Local market knowledge", "Regional market knowledge", "Registered Architect", "Microsoft Word", "Microsoft Excel", "Microsoft Project" ], "skillCount" : 14, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Executive", "dataQualityScore" : 0.8888889, "_score" : 669.30597, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Consulting", "llmIndustryConfidence" : 0.85 }, { "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. 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Together, we build on each other's life experiences and perspectives to make great things possible every day. This shapes our collaborative culture, encourages organizational trust and connects us closer to the clients and communities we serve. Our Commitment As employee owners, we all have a role in creating an inclusive environment where each of us is welcomed, valued, respected and empowered to bring our authentic selves to work every day. Our eight Employee Network Groups (Asian Pacific, Black, Hispanic/Latino(a), LGBTQ+, People with Disabilities, Veterans, Women, Young Professionals) help create a sense of belonging and foster a supportive environment where everyone is empowered to engage and contribute. Each group has an executive sponsor and is open to all employees. United States-Washington-Seattle", "summaryDescription" : "Senior Laboratory Planner. Plan laboratories. 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" : 651.6446, "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. 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TGH Brooksville (TGHBRKSV)
17240 Cortez Boulevard

Brooksville, 34601

" ], "certifications" : [ "Basic Life Support (BLS)", "Advanced Cardiovascular Life Support (ACLS)", "Pediatric Advance Life Support (PALS)", "National Institutes of Health Stroke Scale (NIHSS)", "STABLE" ], "timestamp" : "2026-06-15T08:51:07.575", "fingerprint" : "b55dd0c1a5fb6eda669ede77088bbb9e6f0006346a2dbf953659849b52929e98", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=676064", "externalId" : "676064", "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 Degree", "professionalSkills" : [ "Nursing care", "Quality improvement" ], "hardSkillsList" : [ "Patient care" ], "hardSkills" : [ { "name" : "Patient care", "level" : "intermediate" } ], "majorSkills" : "Surgical preparation", "majorSkillsList" : [ "Surgical preparation" ], "coreResponsibilities" : "Deliver nursing care, Plan nursing care, Implement nursing care, Document nursing care, Identify situations requiring further action, Report situations requiring further action, Formulate plan of care, Communicate plan of care, Assure patient rights", "domainKnowledge" : "Surgical preparation", "domainList" : [ "surgical-preparation" ], "domainSpecificKnowledge" : [ "Surgical preparation" ], "communicationSkills" : "Communicate plan", "documentationSkills" : "Nursing documentation", "outcomesObjectives" : "Perform job duties per mission", "qualificationsBasic" : "Associate's Degree Nursing, Registered Nurse License", "qualificationsPreferred" : "Unit specific certifications", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision, following established policies, procedures, and professional guidelines, delivers nursing care to patients. Plans and implements nursing care; documents nursing assessments; identifies and reports situations requiring further intervention; formulates and communicates goal-directed plan of care; assures patient rights. Responsible for performing job duties in accordance with the mission, vision and values of Tampa General Hospital and principles of quality improvement. Education Associate's Degree Nursing License Issued by Florida or Compact State Registered Nurse Certifications Basic Life Support (BLS) through American Heart Association or American Red Cross Work Experience Unit specific certifications may be required. May include but not limited to: Advanced Cardiovascular Life Support (ACLS) Pediatric Advance Life Support (PALS) STROKE National Institutes of Health Stroke Scale (NIHSS) STABLE Brooksville", "summaryDescription" : "Clinical Nurse - Surgical Preparation at Tampa General Hospital. Skills: Surgical preparation. Deliver nursing care. Plan nursing care", "createdAt" : "2026-06-14T09:41:38.853", "lastUpdated" : "2026-06-15T08:51:07.575", "ingestTimestamp" : "2026-06-14T09:41:38.853", "mongoId" : "69cf26122beec4dd3d90b4cb", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 70500, "salaryAnnualMax" : 94500, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Patient care", "Surgical preparation", "Nursing care", "Quality improvement", "Basic Life Support (BLS)", "Advanced Cardiovascular Life Support (ACLS)", "Pediatric Advance Life Support (PALS)", "National Institutes of Health Stroke Scale (NIHSS)", "STABLE" ], "skillCount" : 9, "jobCategory" : "healthcare", "jobSubcategory" : "support", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 645.4908, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "id" : "6a2ac4ec74d8ee00a06ffaff", "title" : "Environmental Monitoring & Sample Management Supervisor", "company" : "Legend Biotech", "industry" : "Biotech", "salary" : { "min" : 75000.0, "max" : 105000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market data for a Manager in the Biotech industry in Gent, Belgium, adjusted for seniority and company size." }, "location" : "Gent, East Flanders, Belgium", "locations" : [ "Gent", "East Flanders", "Belgium", "Ghent", "East Flanders", "Belgium" ], "timestamp" : "2026-06-14T21:53:12.510", "fingerprint" : "538ac5f485565442d18ce9b3573769a3f055cb11255a3a883cc7d6a2ba96e7d6", "source" : "greenhouse", "language" : "nl", "applyUrl" : "https://job-boards.greenhouse.io/legendcareerseu/jobs/4704994005", "externalId" : "4704994005", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Gent", "state" : "East Flanders", "country" : "Belgium", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "51.0538286,3.7250121" } ], "locationText" : "Gent, East Flanders, Belgium", "minimumEducation" : "Bachelor's", "experienceMinYears" : 3, "experienceLevel" : "Manager", "professionalSkills" : [ "Sample management", "Logistics coordination", "Process standardization", "Workflow optimization", "Warehouse operations" ], "hardSkillsList" : [ "Data review", "GMP documentation", "Process simplification", "Process streamlining", "Process scaling" ], "softSkillsList" : [ "Leadership", "Coaching", "Development", "Ownership" ], "hardSkills" : [ { "name" : "Data review", "level" : "intermediate" }, { "name" : "GMP documentation", "level" : "intermediate" }, { "name" : "Process simplification", "level" : "intermediate" }, { "name" : "Process streamlining", "level" : "intermediate" }, { "name" : "Process scaling", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Coaching" }, { "name" : "Development" }, { "name" : "Ownership" } ], "majorSkills" : "Environmental monitoring, Sample management, People management, Operational excellence", "majorSkillsList" : [ "Environmental monitoring", "Sample management", "People management", "Operational excellence" ], "coreResponsibilities" : "Coordinate environmental monitoring activities, Follow up on EM results, Review EM data, Solve EM problems, Monitor sample lifecycle, Follow up on deadlines, Escalate deviations, Handle deviations, Collect QC samples, Reconcile QC samples, Document QC samples, Send QC samples, Ensure GMP documentation, Optimize workflows, Standardize workflows, Contribute to warehouse activities, Manage warehouse activities, Coach team members, Develop team members, Stimulate engagement, Build trust, Create team culture, Identify process improvement opportunities, Lead improvement initiatives, Support improvement initiatives, Collaborate with Operations, Collaborate with Warehouse teams, Collaborate with IPL QC teams, Align priorities, Communicate clearly, Ensure strong collaboration", "teamCollaboration" : "Operations teams; Warehouse teams; IPL QC teams", "domainKnowledge" : "Life Sciences; Logistics; Supply Chain; Pharma; Biotech; GMP", "domainList" : [ "life-sciences", "logistics", "supply-chain", "pharma", "biotech", "gmp" ], "domainSpecificKnowledge" : [ "Life Sciences", "Logistics", "Supply Chain", "Pharma", "Biotech", "GMP" ], "communicationSkills" : "Stakeholder alignment; Priority management", "documentationSkills" : "GMP documentation", "problemSolvingSkills" : "Problem-solving", "outcomesObjectives" : "Avoid product release delays; Support timely product release", "qualificationsBasic" : "3+ years experience in regulated environment, Experience managing operational teams, Experience with process coordination, Experience with operational workflows, Fluent English", "qualificationsPreferred" : "Experience in pharma or biotech, Dutch language knowledge", "workSiteFlexibility" : "Onsite", "rawDescription" : "Om de groei van onze Quality Control organisatie in Gent te ondersteunen, zijn we op zoek naar een Environmental Monitoring (EM) Environmental Monitoring (EM) Oversight: Je bent verantwoordelijk voor de coördinatie en opvolging van Environmental Monitoring activiteiten, zowel batch-gerelateerd als routinematig. Je zorgt voor een tijdige opvolging van EM-resultaten, data review en probleemoplossing om vertragingen in product release te vermijden. Je bewaakt de volledige levenscyclus van stalen, volgt deadlines op en zorgt ervoor dat afwijkingen tijdig worden geëscaleerd en correct worden afgehandeld. Sample Management & Logistieke Coördinatie: Je neemt ownership over het verzamelen, reconciliëren, documenteren en verzenden van QC-stalen. Je garandeert dat alle GMP-documentatie volledig, correct en audit-proof is. Je optimaliseert en standaardiseert workflows met een sterke focus op schaalbaarheid en efficiëntie. Daarnaast draag je bij aan de organisatie en opvolging van warehouse-activiteiten gelinkt aan staalbeheer. People Management & Teamontwikkeling: Je stuurt een team van 10–15 medewerkers aan, met focus op coaching en ontwikkeling. Je stimuleert betrokkenheid in een sterk routinematige omgeving, bouwt vertrouwen op en creëert een sterke teamcultuur. Operational Excellence & Continuous Improvement: Je identificeert actief opportuniteiten om processen te vereenvoudigen, stroomlijnen en opschalen. Je leidt of ondersteunt verbeterinitiatieven rond workflow-optimalisatie, standaardisatie en automatisering. Stakeholder Management & Samenwerking: Je werkt nauw samen met Operations, de Warehouse teams en IPL QC teams en stemt prioriteiten af. Je zorgt voor duidelijke communicatie en sterke samenwerking over afdelingen heen om een tijdige product vrijgave te ondersteunen. Naar wie zijn we op zoek? Opleiding Bachelor in Life Sciences, Logistiek, Supply Chain of gelijkwaardig door ervaring. Ervaring Minimum 3 jaar ervaring in een dynamische en sterk gereguleerde omgeving (bij voorkeur pharma of biotech). Eerste ervaring in het aansturen van een team, bij voorkeur operationele teams. Ervaring met procescoördinatie en operationele workflows. Talen Engels op vloeiend niveau is vereist voor deze rol, zowel mondeling als schriftelijk. Kennis van het Nederlands is een voordeel. Sterktes Je bent een hands-on, mensgerichte leider die graag teams coacht en ontwikkelt Je communiceert sterk en kan stakeholders aligneren en prioriteiten managen Je bent zeer georganiseerd en kan complexe, grootschalige workflows beheren Je voelt je thuis in een schaalbare, procesgedreven omgeving en hebt oog voor detail Je kan structuur en efficiëntie brengen in een groeiende organisatie Je hebt een mindset gericht op continue verbetering en neemt ownership Wat wij jou bieden? Een betekenisvolle job met een goede work-life balance Werkregime: maandag tot vrijdag, daguren (40u/week), afhankelijk van de noden Een innovatieve en ondersteunende werkomgeving met focus op ontwikkeling Een internationale werkomgeving met collega’s wereldwijd Een contract van onbepaalde duur en een aantrekkelijk salarispakket, aangevuld met een uitgebreid pakket aan extralegale voordelen, waaronder extra wettelijke vakantiedagen, maaltijdcheques, een bedrijfslaptop, smartphone en abonnement, een nettovergoeding, groeps- en hospitalisatieverzekering, dubbel vakantiegeld, een eindejaarspremie, een prestatiebonus en de mogelijkheid om deel te nemen aan ons fietsleaseplan Veel leuke en informele activiteiten Over Legend Biotech Legend Biotech is een wereldwijd biotechnologiebedrijf dat zicht toelegt op het ontwikkelen, produceren en commercialiseren van innovatieve en levensreddende celtherapieën, waaronder behandelingen voor hardnekkige ziekten zoals kanker. Sinds onze oprichting in 2014 in Somerset, New Jersey, zijn we uitgegroeid tot een bedrijf met meer dan 2400 medewerkers in zes productie-eenheden wereldwijd. In Gent richten we ons op de productie van onze geavanceerde CAR-T-therapie voor de behandeling van multipel myeloom, in samenwerking met Johnson & Johnson. Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug-free workplace. For information related to our privacy notice, please review: Legend Biotech Privacy Notice.", "summaryDescription" : "Environmental Monitoring & Sample Management Supervisor at Legend Biotech. Skills: Environmental monitoring, Sample management, People management, Operational excellence. Coordinate environmental monitoring activities. Follow up on EM results", "postedDate" : "2026-06-11T21:48:16.359", "createdAt" : "2026-06-11T21:48:16.359", "lastUpdated" : "2026-06-14T21:53:12.510", "ingestTimestamp" : "2026-06-11T21:48:16.359", "mongoId" : "6a2ac4ec74d8ee00a06ffaff", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "75k-100k", "hasSalary" : false, "allSkills" : [ "Data review", "GMP documentation", "Process simplification", "Process streamlining", "Process scaling", "Leadership", "Coaching", "Development", "Ownership", "Environmental monitoring", "Sample management", "People management", "Operational excellence", "Logistics coordination", "Process standardization", "Workflow optimization", "Warehouse operations", "Life Sciences", "Logistics", "Supply Chain", "Pharma", "Biotech", "GMP" ], "skillCount" : 23, "jobCategory" : "other", "jobSubcategory" : "quality-&-compliance", "dataQualityScore" : 0.8888889, "_score" : 643.6933, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Biotech" }, { "id" : "6a2c5d9574d8ee00a08dd0f3", "title" : "Microbiologist Laboratory Reviewer", "company" : "Nivagen Pharmaceuticals", "industry" : "Pharmaceuticals", "salary" : { "min" : 75000.0, "max" : 85000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Pittsburg, California, United States", "locations" : [ "Pittsburg", "California", "United States" ], "timestamp" : "2026-06-14T23:52:56.545", "fingerprint" : "d858ac2fcb6598f28543b0fe71ca320c2480bc342d491553dbf62540046bef77", "source" : "greenhouse", "language" : "en", "applyUrl" : "https://job-boards.greenhouse.io/nivagenpharmaceuticals/jobs/5205141008", "externalId" : "5205141008", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Sacramento", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "38.5810606,-121.4938950" } ], "locationText" : "Sacramento, California, United States", "employmentType" : "FULL_TIME", "technicalSkills" : "Microbiology", "professionalSkills" : [ "Quality control", "Data integrity", "Regulatory compliance" ], "hardSkillsList" : [ "Microbiological testing", "Method validation", "Sterility testing", "Endotoxin testing", "Environmental monitoring", "Microbial limit testing", "Disinfectant qualification", "Container closure integrity" ], "softSkillsList" : [ "Customer Focus", "Optimizes Work Processes", "Resourcefulness", "Manages Complexity", "Ensures Accountability", "Situational Adaptability" ], "hardSkills" : [ { "name" : "Microbiological testing", "level" : "intermediate" }, { "name" : "Method validation", "level" : "intermediate" }, { "name" : "Sterility testing", "level" : "intermediate" }, { "name" : "Endotoxin testing", "level" : "intermediate" }, { "name" : "Environmental monitoring", "level" : "intermediate" }, { "name" : "Microbial limit testing", "level" : "intermediate" }, { "name" : "Disinfectant qualification", "level" : "intermediate" }, { "name" : "Container closure integrity", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Customer Focus" }, { "name" : "Optimizes Work Processes" }, { "name" : "Resourcefulness" }, { "name" : "Manages Complexity" }, { "name" : "Ensures Accountability" }, { "name" : "Situational Adaptability" } ], "majorSkills" : "Microbiological data review, cGMP compliance, Pharmaceutical manufacturing", "majorSkillsList" : [ "Microbiological data review", "cGMP compliance", "Pharmaceutical manufacturing" ], "coreResponsibilities" : "Review laboratory test results, Verify compliance with SOPs, Verify compliance with cGMP, Evaluate method validations, Evaluate method transfers, Evaluate microbiological investigations, Assess environmental monitoring data, Assess sterility testing outcomes, Assess endotoxin testing outcomes, Collaborate with laboratory analysts, Collaborate with quality assurance teams, Resolve discrepancies, Address out-of-specification results, Support investigations related to laboratory deviations, Participate in root cause analysis, Ensure timely review of batch records, Ensure timely release of batch records, Identify trends in laboratory data, Recommend corrective actions, Support process improvements, Support best practices in microbiological testing, Support best practices in documentation, Provide guidance on data integrity, Provide guidance on compliance requirements, Maintain thorough records, Ensure proper documentation, Coordinate calibration, Coordinate maintenance, Participate in internal audits, Participate in external audits, Ensure compliance with safety regulations, Ensure compliance with environmental regulations, Manage workload to meet timelines, Manage workload to meet deadlines, Maintain confidentiality, Handle sensitive information, Update knowledge of regulations, Update knowledge of industry trends, Update knowledge of technological advancements", "teamCollaboration" : "Laboratory analysts; Quality assurance teams", "domainKnowledge" : "Good Manufacturing Practices; cGMP regulations; GLP; Injectable manufacturing; Pharmaceutical supply chain; Generic prescription drugs; Over-the-counter products", "domainList" : [ "good-manufacturing-practices", "cgmp-regulations", "glp", "injectable-manufacturing", "pharmaceutical-supply-chain", "generic-prescription-drugs", "over-the-counter-products" ], "domainSpecificKnowledge" : [ "Good Manufacturing Practices", "cGMP regulations", "GLP", "Injectable manufacturing", "Pharmaceutical supply chain", "Generic prescription drugs", "Over-the-counter products" ], "communicationSkills" : "Effective communication", "documentationSkills" : "Documentation; Data integrity", "continuousLearning" : "Training and development opportunities; Update knowledge of regulations; Update knowledge of industry trends; Update knowledge of technological advancements", "problemSolvingSkills" : "Root cause analysis", "specialRequirements" : "Bend at the waist and knees, Twist at the trunk, Lift up to 25 lbs, Wear laboratory protective gowning, Wear goggles, Wear face shields, Wear respirators, Wear protective gloves", "qualificationsBasic" : "Bachelor's degree in microbiology, Minimum of 3 years of experience in a microbiology laboratory", "qualificationsPreferred" : "Master's degree preferred, Previous experience in a pharmaceutical or compounding environment, Experience with compendia testing, Experience with United States Pharmacopeia, Experience with Food and Drug Administration, Experience with cGMP", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "About the Company: Nivagen is a global company dedicated to enhancing lives by developing and providing cost-effective generic prescription drugs and over-the-counter products for the North American market. For over a decade, we've remained steadfast in our commitment to core values of excellence, integrity, and respect for people. Our team of professionals collaborates tirelessly to pioneer advancements in manufacturing, distribution, and quality control, ensuring a holistic approach to healthcare. Through vertical integration of the pharmaceutical supply chain, cutting-edge technology, and unwavering dedication to excellence, we continually strive to redefine medication accessibility and affordability. We prioritize our employees' well-being by offering competitive pay, comprehensive benefits, and robust training and development opportunities. By investing in our workforce and fostering a culture of growth and support, we empower our team to drive innovation and make a positive impact in the healthcare industry. At Nivagen, our mission is clear: to make a meaningful difference in people's lives by delivering high-quality, affordable medications while upholding the highest standards of integrity and excellence. Job Location: Nivagen Pharmaceuticals, Sacramento, CA 3900 Duckhorn Dr, Sacramento, CA 95834 About the Job: Title of the Position: Microbiologist Laboratory Reviewer (Full Time) At Nivagen as a Microbiologist Laboratory Reviewer you will be responsible for ensuring that pharmaceutical products meet quality standards during the manufacturing process. This role involves real-time monitoring, sampling, testing, and documentation to identify and address any quality issues as they arise, ensuring that all production activities comply with Good Manufacturing Practices (GMP) and regulatory requirements. Position Summary The Microbiology Laboratory Reviewer plays a critical role in ensuring the accuracy and compliance of microbiological data within an injectable manufacturing facility. This position is responsible for reviewing laboratory test results, protocols and reports batch records, and related documentation to verify adherence to standard operating procedures (SOPs), current Good Manufacturing Practices (cGMP) regulations, GLP, and company quality standards. The reviewer works closely with laboratory microbiologist and quality assurance teams to resolve discrepancies, support investigations, and ensure the timely release of products. Key responsibilities include evaluating microbiological method validations, transfers, and investigations, as well as assessing environmental monitoring data, sterility test outcomes, and endotoxin results. The role also involves identifying trends, supporting continuous improvement initiatives, and providing guidance on best practices in documentation and data integrity. Strong attention to detail, effective communication skills, and a commitment to maintaining high standards of safety and compliance are essential for success in this position. Duties and Responsibilities Reviews and verifies laboratory test results, ensuring compliance with SOPs, cGMP, and company policies. Evaluates method validations, transfers, and microbiological investigations for accuracy and completeness. Assesses environmental monitoring data, sterility, and endotoxin testing outcomes for quality and consistency. Collaborates with laboratory analysts and quality assurance teams to resolve discrepancies and address out-of-specification results. Supports investigations related to laboratory deviations and participates in root cause analysis. Ensures timely review and release of batch records and product documentation. Identifies trends or recurring issues in laboratory data and recommends corrective actions. Supports the implementation of process improvements and best practices in microbiological testing and documentation. Provides training and guidance to laboratory staff on data integrity and compliance requirements. Maintains thorough records of all review activities and ensures proper documentation is in place. Calibration and maintenance coordination and record. Participates in internal and external audits as required, providing relevant documentation and expertise. Ensures all work is conducted in accordance with health, safety, and environmental regulations. Demonstrates strong organizational skills and manages workload to meet project timelines and regulatory deadlines. Maintains confidentiality and handles sensitive information with professionalism and integrity. Continuously updates knowledge of relevant regulations, industry trends, and technological advancements in microbiology. Performs other duties as assigned. While performing the responsibilities of the job, the employee is required to talk and hear. Must be able to bend at the waist and knees as well as twist at the trunk. Must be able to lift up to 25 lbs. Must be able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. Personal protective equipment and Respirators are essential for the health and safety of employees. Position requires working in the laboratory as well as sitting Microbiological method development and method validation procedures like BET, Sterility, MLT, Bio Assay and Disinfectant qualification and microbiological hold time validation, Container closure integrity validation. Knowledge and Skills Strong knowledge of microbiological testing techniques, reviewing, methods, and equipment. Key Competencies Customer Focus: Ability to build strong customer relationships and deliver customer centric solutions. Optimizes Work Processes: Know the most effective and efficient processes to get things done, with a focus on continuous improvement. Collaborates: Builds partnerships and works collaboratively with others to meet shared objectives. Resourcefulness: Secures and deploys resources effectively and efficiently. Manages Complexity: Makes sense of complex, high quality, and sometimes contradictory information to effectively solve problems. Ensures Accountability: Holds self and others accountable to meet commitments and objectives. Situational Adaptability: Adapts approach and demeanor in real time to match shifting demands of different situations. Communicates Effectively: Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences. Experience and Qualifications Bachelor’s degree in microbiology, Biology, or related field required; Master's degree preferred. Minimum of 3 years of experience in a microbiology laboratory required. Previous experience in a pharmaceutical or compounding environment preferred. Experience with compendia testing: United States Pharmacopeia, and regulatory requirements (Food and Drug Administration and cGMP) preferred. Experience with microbiological method development and method validation procedures like Sterility Testing, Endotoxin Testing, Disinfectant Efficacy Study, Water Testing, Method Validation, Environment Monitoring, Microbial Limit Testing, PET, and microbiological hold time validation, container closure integrity. Benefits: Pay range $75,000-$85,000 per Year Yearly bonus eligibility Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being Medical, dental and vision coverage Paid time off plan 401k savings plan Additional Information: Nivagen to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors. We are focused on building a diverse and inclusive workforce. If you're excited about this role, but do not meet 100% of the qualifications listed above, we encourage you to apply.", "summaryDescription" : "Microbiologist Laboratory Reviewer at Nivagen Pharmaceuticals. Skills: Microbiological data review, cGMP compliance, Pharmaceutical manufacturing. Review laboratory test results. Verify compliance with SOPs", "postedDate" : "2026-06-12T21:36:07.750", "createdAt" : "2026-06-12T21:36:07.750", "lastUpdated" : "2026-06-14T23:52:56.545", "ingestTimestamp" : "2026-06-12T21:36:07.750", "mongoId" : "6a2c5d9574d8ee00a08dd0f3", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 85000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Microbiological testing", "Method validation", "Sterility testing", "Endotoxin testing", "Environmental monitoring", "Microbial limit testing", "Disinfectant qualification", "Container closure integrity", "Customer Focus", "Optimizes Work Processes", "Resourcefulness", "Manages Complexity", "Ensures Accountability", "Situational Adaptability", "Microbiological data review", "cGMP compliance", "Pharmaceutical manufacturing", "Quality control", "Data integrity", "Regulatory compliance", "Good Manufacturing Practices", "cGMP regulations", "GLP", "Injectable manufacturing", "Pharmaceutical supply chain", "Generic prescription drugs", "Over-the-counter products" ], "skillCount" : 27, "jobCategory" : "other", "jobSubcategory" : "qc_-microbiology", "dataQualityScore" : 0.8888889, "_score" : 637.80646, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Pharmaceuticals" }, { "id" : "6a16291c58b93c861e95a147", "title" : "Project Manager- Water Sampling", "salary" : { "min" : 115000.0, "max" : 155000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Senior Project Manager in Engineering in Honolulu, adjusted for seniority and full-time employment." }, "location" : "United States-Hawaii-Honolulu", "locations" : [ "United States-Hawaii-Honolulu" ], "certifications" : [ "Professional Engineer (PE or P. 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Example: Professional Engineer (PE or P.Eng) license. MS Office and MS Project experience is required Demonstrated leadership skills 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. 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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. 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. 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TGH Main Campus (TGHMAIN)
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Eur., JP, Sterilization standards", "professionalSkills" : [ "Risk assessment", "Process design", "Trend analysis", "Resource planning", "Performance management", "Staff training", "Parametric release", "Alternative release" ], "hardSkillsList" : [ "Microbiological control", "Environmental monitoring", "Contamination control", "Aseptic process", "Sterility assurance", "Bioburden testing", "Root cause analysis", "CAPA implementation", "Radiation safety" ], "softSkillsList" : [ "Leadership", "Mentoring" ], "hardSkills" : [ { "name" : "Microbiological control", "level" : "intermediate" }, { "name" : "Environmental monitoring", "level" : "intermediate" }, { "name" : "Contamination control", "level" : "intermediate" }, { "name" : "Aseptic process", "level" : "intermediate" }, { "name" : "Sterility assurance", "level" : "intermediate" }, { "name" : "Bioburden testing", "level" : "intermediate" }, { "name" : "Root cause analysis", "level" : "intermediate" }, { "name" : "CAPA implementation", "level" : "intermediate" }, { "name" : "Radiation safety", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Mentoring" } ], "majorSkills" : "Microbiological control, Aseptic manufacturing, Regulatory compliance, Radiopharmaceuticals", "majorSkillsList" : [ "Microbiological control", "Aseptic manufacturing", "Regulatory compliance", "Radiopharmaceuticals" ], "coreResponsibilities" : "Lead microbiology team, Supervise daily lab operations, Plan resources, Manage workload, Manage performance, Drive continuous training, Oversee aseptic process design, Oversee aseptic process simulation, Evaluate changes, Establish environmental monitoring, Maintain environmental monitoring, Analyze environmental monitoring, Perform trend analysis, Conduct contamination risk assessments, Maintain Contamination Control Strategy, Monitor cleanroom operations, Ensure GMP compliance, Ensure best aseptic practices, Ensure effective microbiological controls, Act as SME for regulations, Lead contamination event investigations, Lead root cause analysis, Implement CAPA, Implement process improvements, Work with cross-functional teams, Oversee EM for radiopharmaceuticals, Oversee bioburden for radiopharmaceuticals, Oversee sterility assurance for radiopharmaceuticals, Advise on interventions in isolators/hot cells, Ensure contamination control solutions, Design sampling plans for radiopharmaceuticals, Supervise sampling plans for radiopharmaceuticals", "teamCollaboration" : "Cross-functional teams; Quality; Engineering; Production; Validation", "domainKnowledge" : "Radioconjugates; Precision medicines; Aseptic manufacturing; Sterile radiopharmaceutical products; Radiopharmaceutical suites; Shielded isolators; Hot cells; Short half-life products", "domainList" : [ "radioconjugates", "precision-medicines", "aseptic-manufacturing", "sterile-radiopharmaceutical-products", "radiopharmaceutical-suites", "shielded-isolators", "hot-cells", "short-half-life-products" ], "domainSpecificKnowledge" : [ "Radioconjugates", "Precision medicines", "Aseptic manufacturing", "Sterile radiopharmaceutical products", "Radiopharmaceutical suites", "Shielded isolators", "Hot cells", "Short half-life products" ], "problemSolvingSkills" : "Root cause analysis", "specialRequirements" : "Work extended shifts, Work weekends, Work holidays, After-hours support, On-site presence, <5% travel", "qualificationsBasic" : "Bachelor's degree in Microbiology, 5–8 years supervising laboratory teams, Hands-on environmental monitoring, Contamination control experience, Cleanroom operations experience, Regulatory compliance experience, Work in designated labs, Work in isolators/hot cells", "qualificationsPreferred" : "Experience in radiopharmaceutical environments", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Fusion Pharmaceuticals, a member of the AstraZeneca Group, is a clinical-stage oncology company focused on developing next generation radioconjugates (RCs) as precision medicines. Fusion has multiple pipeline programs entering early FIH trials. In addition, Fusion is pursuing combination programs between RCs and other therapeutic modalities including DNA Damage Response Inhibitors (DDRis) and immune-oncology agents. To support execution for these programs, Fusion has a fully operational Good Manufacturing Practice (GMP) compliant state-of-the-art radioconjugate manufacturing facility to meet the demand for our growing pipeline of RCs. **Overview** The Microbiology Supervisor is responsible for leading and supervising all aspects of microbiological control in a regulated aseptic manufacturing environment, with a focus on sterile radiopharmaceutical products. This role combines technical microbiology expertise with hands-on supervisory responsibilities, ensuring robust contamination control, high-quality environmental monitoring, radiological controls and compliance with global regulatory standards (including EU Annex 1 and GMP). Other duties can be assigned as required. **Responsibilities** * Microbiology Leadership: Lead and mentor the microbiology team, supervising daily lab operations and resource planning to meet manufacturing and clinical/commercial supply timelines; manage workload and performance, and drive continuous training to maintain meticulous quality and compliance standards. * Aseptic Process & Risk Assessment: Oversee aseptic process design and simulation, risk assessments, evaluate changes, ensuring compliance with regulatory requirements. * Environmental Monitoring: Establish, maintain, and analyze environmental monitoring programs and EMPQ, perform trend analysis and conduct contamination risk assessments. * Contamination Control: Maintain the site’s Contamination Control Strategy (CCS), including cleanroom zoning, gowning, and disinfectant programs. * Cleanroom Oversight: Monitor cleanroom operations, working cross-functionally with production teams to ensure GMP compliance, best aseptic practices, and effective microbiological controls. * Regulatory Compliance: Act as SME for EU GMP (incl. Annex 1), FDA cGMPs (21 CFR 210/211, Part 11), PIC/S, ICH Q8–Q10/Q9(R1), ISO 14644/13408, relevant sterilization standards (ISO 11135/11137/17665), and compendial requirements (USP/Ph. Eur./JP), ensuring microbiology operations, EM, methods, data integrity, and validations meet internal and external expectations across all markets. * Incident Investigation: Lead contamination event investigations, root cause analysis, CAPA implementation, and process improvements. * Collaboration: Work with cross-functional teams (Quality, Engineering, Production, Validation) on microbiological risk management and regulatory alignment. **Radiopharmaceutical-Specific Responsibilities** * Microbiology Oversight for Radiopharmaceuticals: Adapt and oversee environmental monitoring, bioburden, and sterility assurance strategies for rapid release and short half-life radiopharmaceutical products, including validated parametric/alternative release approaches. * Technical Guidance for Radiopharmaceutical Suites: Advise on interventions in shielded isolators/hot cells. Ensure pragmatic contamination control solutions for frequent setups and short campaigns without compromising quality. * Sampling Plan Design: Design and supervise practical sampling plans tailored for radiopharmaceutical products, ensuring robust data collection and contamination control despite operational constraints. **Qualifications** * Education: Bachelor’s degree (BSc) in Microbiology, Biological Sciences, or a related discipline is required. * Relevant Experience: 5–8 years of experience supervising or leading teams within a laboratory or sterile/aseptic manufacturing environment, including experience with staff training, scheduling, and performance management. * Significant hands-on work with environmental monitoring, contamination control, cleanroom operations, and regulatory compliance (EU Annex 1, cGMP, etc.). * Specialized Experience: previous experience in radiopharmaceutical environments is an asset. * Work in designated labs with radiological controls, contamination monitoring, and PPE requirements. * Willingness and ability to work extended shifts, weekends, or holidays as needed. Occasional after-hours support for investigations, equipment alarms, or urgent testing. * On-site presence in Hamilton, Ontario in classified areas, including work in isolators/hot cells with appropriate PPE and radiation safety protocols * <5% travel required **At AstraZeneca, we foster a collaborative, innovative culture with opportunities to work across teams, functions, and geographies. You’ll join a collaborative, innovative community with opportunities to work across teams, functions, and geographies—where your ideas move fast and your impact is visible. We’re committed to sustainability and equity, taking bold action on climate, access to healthcare, and disease prevention.** **⠀** Annual base salary for this position ranges from 86,266.40 to 113,224.65. AstraZeneca is committed to providing fair and equitable compensation opportunities to all colleagues. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The range provided in this posting represents an offer pay range used in a majority of situations. The base pay offered will vary depending on multiple individualized factors, including the candidate's skills and experience, job-related knowledge, and other specific business and organizational needs. In some cases, offers outside the range may also be considered to address unique circumstances. In addition, our permanent positions offer an annual Variable Pay Bonus/Short Term Incentive opportunity as well as eligibility to participate in our equity-based long-term incentive program (if applicable to role). Benefits offered for permanent roles include a competitive Flex Benefits & Retirement Savings Program, 4 weeks’ paid vacation, and annual Personal Days. 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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. 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" : 623.7772, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2a8bb974d8ee00a0683a51", "title" : "Laboratory Engineer", "company" : "University of Rochester", "salary" : { "min" : 55955.0, "max" : 78336.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-13T19:14:39.156", "fingerprint" : "0a499374d72c94928e50cfd45f4b307a5fb2db2bbf2ea2fd96819baf49af7603", "source" : "workday", "language" : "en", "applyUrl" : "https://rochester.wd5.myworkdayjobs.com/UR_Staff/job/Laboratory-for-Laser-Energetics/Laboratory-Engineer-I_R272091", "externalId" : "R272091", "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Rochester", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.1572850,-77.6152140" } ], "locationText" : "Rochester, New York, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's degree", "experienceMinYears" : 1, "professionalSkills" : [ "Target assembly", "Manufacturing operations" ], "hardSkillsList" : [ "Metrology hardware", "Manual manipulation" ], "hardSkills" : [ { "name" : "Metrology hardware", "level" : "intermediate" }, { "name" : "Manual manipulation", "level" : "intermediate" } ], "majorSkills" : "Laser laboratory, Component assembly, Data collection", "majorSkillsList" : [ "Laser laboratory", "Component assembly", "Data collection" ], "coreResponsibilities" : "Conduct experiments, tests, and research, Assist in designing experiments, Assist in setting up experiments, Assist in maintaining equipment, Assist in collecting data, Diagnose system components, Perform preventative maintenance, Manage fragile targets, Develop innovative solutions, Manipulate delicate micro-assemblies, Develop manufacturing methods, Develop operation sequences, Develop fabrication processes, Design sequence of operations, Specify procedures for fabrication, Adapt machinery, Maintain records, Maintain reporting systems, Develop documentation of findings, Develop documentation of implemented solutions, Communicate results to staff, Measure completed assemblies, Collect data, Clean lab equipment, Adjust lab equipment, Replace parts on lab equipment, Work in a safe manner", "domainKnowledge" : "Laser laboratory", "domainList" : [ "laser-laboratory" ], "domainSpecificKnowledge" : [ "Laser laboratory" ], "communicationSkills" : "Communicate results", "documentationSkills" : "Develop documentation", "innovationCreativity" : "Develop innovative solutions", "problemSolvingSkills" : "Technical problems", "specialRequirements" : "Work onsite 8:30a-5:30p", "qualificationsBasic" : "Bachelor's degree and 1 year experience, Assemble millimeter-scale components, Work in cleanroom laboratory environment, Operate microscope in cleanroom", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive. _**Job Location (Full Address):**_ 250 East River Rd, Rochester, New York, United States of America, 14623 _**Opening:**_ Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 250548 LLE-Laboratory for Laser Energ Work Shift: UR - Day (United States of America) Range: UR URG 109 Compensation Range: $55,955.00 - $78,336.00 _The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job 's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._ _**Responsibilities:**_ Conducts experiments, tests, and research within a laser laboratory setting. Assists more experienced engineers or scientists in designing and setting up experiments, maintaining equipment, and collecting data. Diagnoses and performs preventative maintenance on system components including recovery, replacement, and reconfiguration of damaged sensitive components. Manages fragile targets for laser exploration. This is an onsite position 8:30a-5:30p. **ESSENTIAL FUNCTIONS** * Required to assemble millimeter-scale components that meet specifications * Expected to develop innovative but practical solutions to technical problems in target assembly to enhance manufacturability * Capable at working in cleanroom laboratory environment, using manual techniques to manipulate delicate micro-assemblies * Ability to operate microscope in cleanroom environment * Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies, and final assemblies. * Designs the sequence of production operations, specifying procedures for the fabrication of applicable tools and equipment, and adapting machinery * Maintains records and reporting systems for coordination of manufacturing operations * Develops appropriate documentation of findings and implemented solutions and communicates results to staff * Measures completed assemblies using metrology hardware and collects data * Cleans, adjusts and replaces parts on lab equipment * Expected to work in a safe manner in accordance with established operating procedures and practices. * Other duties as assigned. **MINIMUM EDUCATION & EXPERIENCE** * Bachelor's degree and 1 year of relevant experience required * Or equivalent combination of education and experience The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.", "summaryDescription" : "Laboratory Engineer at University of Rochester. Skills: Laser laboratory, Component assembly, Data collection. Conduct experiments, tests, and research. 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" : 618.7589, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true }, { "id" : "6a2ebf7d74d8ee00a0e9abaf", "title" : "Clinical Laboratory Operations Site Director", "company" : "Invitae", "salary" : { "min" : 140000.0, "max" : 200000.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "San Francisco, CA", "locations" : [ "San Francisco, CA", "United States of America" ], "timestamp" : "2026-06-15T06:48:10.454", "fingerprint" : "ec0199e6aa224d5c1e20c2bf9dacedf23d030b4fe9459e426f2edb1728348407", "source" : "workday", "applyUrl" : "https://labcorp.wd1.myworkdayjobs.com/External/job/San-Francisco-CA/Clinical-Laboratory-Operations-Site-Director---Invitae_2619979", "externalId" : "2619979", "industryFunction" : { }, "locationPoint" : "19.68044,-99.74877", "structuredLocations" : [ { "city" : "San Francisco", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite" } ], "locationText" : "San Francisco, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor", "experienceMinYears" : 6, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "professionalSkills" : [ "Deep knowledge of CLIA/CAP regulations and inspection readiness. Experience in a commercial diagnostics or precision medicine organization." ], "hardSkillsList" : [ "CLIA/CAP regulations", "regulatory compliance", "workforce planning", "budget management", "capacity planning", "inventory management", "sample accessioning", "wet lab workflows", "post-sequencing processes" ], "softSkillsList" : [ "accountability, engagement, inclusion, collaboration" ], "hardSkills" : [ { "name" : "CLIA/CAP regulations", "level" : "intermediate" }, { "name" : "regulatory compliance", "level" : "intermediate" }, { "name" : "workforce planning", "level" : "intermediate" }, { "name" : "budget management", "level" : "intermediate" }, { "name" : "capacity planning", "level" : "intermediate" }, { "name" : "inventory management", "level" : "intermediate" }, { "name" : "sample accessioning", "level" : "intermediate" }, { "name" : "wet lab workflows", "level" : "intermediate" }, { "name" : "post-sequencing processes", "level" : "intermediate" } ], "softSkills" : [ { "name" : "accountability, engagement, inclusion, collaboration" } ], "majorSkills" : "Clinical Laboratory Operations, People Leadership, Quality & Compliance, Financial Management, Continuous Improvement", "majorSkillsList" : [ "Clinical Laboratory Operations, People Leadership, Quality & Compliance, Financial Management, Continuous Improvement" ], "coreResponsibilities" : "Provide end-to-end operational leadership for a large-scale, high-complexity clinical genetic testing laboratory. Ensure reliable, scalable processing while meeting or exceeding turnaround time and quality targets. Oversee daily laboratory operations including sample accessioning, wet lab workflows, post-sequencing processes, and inventory. Drive capacity planning, strategy, and throughput optimization to support business growth. Maintain full compliance with CLIA, CAP, state, and federal regulations. Serve as the site designee and work closely with the Laboratory Director to ensure regulatory readiness. Support inspections, audits, and corrective/preventive action (CAPA) activities. Champion a culture of quality, safety, and continuous compliance. Lead and develop a multidisciplinary organization. Build a high-performance culture focused on accountability, engagement, inclusion, and professional development. Partner with HR on workforce planning, recruiting, retention, and succession planning. Coach leaders to scale teams effectively in a fast-growing environment. Own site-level operating budgets, staffing models, and cost controls. Identify opportunities to improve cost per test without compromising quality or compliance. Partner with finance and commercial teams to support pricing, capacity forecasting, and margin improvement initiatives. Act as the primary site liaison with R&D, Medical Affairs, Quality, Regulatory, IT, Supply Chain, and Commercial teams. Support assay launches, technology transfers, and process changes from development into production. Provide operational input into new product planning and long-term laboratory strategy. Drive Lean, Six Sigma, or similar continuous improvement initiatives. Support adoption of automation and advanced analytics to improve efficiency and scalability. Promote data-driven decision-making using operational KPIs and quality metrics.", "teamCollaboration" : "Act as the primary site liaison with R&D, Medical Affairs, Quality, Regulatory, IT, Supply Chain, and Commercial teams. Excellent communicator and cross-functional collaborator.", "toolProficiency" : [ "Microsoft Office Suite" ], "communicationSkills" : "communicator", "continuousLearning" : "Support adoption of automation and advanced analytics to improve efficiency and scalability. Promote data-driven decision-making using operational KPIs and quality metrics.", "innovationCreativity" : "Supporting continued growth and innovation in genetic diagnostics. Support adoption of automation and advanced analytics to improve efficiency and scalability.", "problemSolvingSkills" : "process improvement; Lean; Six Sigma; data-driven decision-making", "specialRequirements" : "On-site leadership presence required in a fast-paced, production laboratory environment. Occasional travel for inspections, leadership meetings, or cross-site collaboration.", "outcomesObjectives" : "Ensure excellence in quality, turnaround time, cost, scalability, and regulatory compliance while supporting continued growth and innovation in genetic diagnostics. Build a high-performance culture focused on accountability, engagement, inclusion, and professional development. Identify opportunities to improve cost per test without compromising quality or compliance.", "qualificationsBasic" : "Bachelor’s degree in a Chemical or Biological Science, Clinical Laboratory Science, or Medical Technology. 6 or more years of experience in clinical laboratory operations, with proven leadership responsibilities. 5 or more years experience in leadership, directly managing employees.", "qualificationsPreferred" : "3 or more years experience managing people leaders. 1 year or more experience with Next Generation Sequencing (NGS) based clinical lab testing, bioinformatics workflows, and automation. 1 year or more experience in Lean, Six Sigma, or operational excellence methodologies. 1 year or more experience in a commercial diagnostics or precision medicine organization.", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Invitae, part of Labcorp, is seeking a Clinical Laboratory Operations Site Director for our Genetics laboratory in San Francisco, CA. This position is accountable for the overall leadership, performance, and compliance of a high‑volume clinical genetic testing laboratory. This role provides strategic, operational, and scientific leadership to ensure excellence in quality, turnaround time, cost, scalability, and regulatory compliance while supporting continued growth and innovation in genetic diagnostics. The Site Director is responsible for laboratory operations, people leadership, cross‑functional collaboration, and continuous improvement in a CLIA/CAP‑regulated environment. **Work Schedule:** Monday – Friday, 8am -5pm **Address:** 1400 16th Street, San Francisco, CA 94103 **Job Responsibilities:** **Laboratory Leadership & Operations** * Provide end‑to‑end operational leadership for a large‑scale, high‑complexity clinical genetic testing laboratory. * Ensure reliable, scalable processing while meeting or exceeding turnaround time and quality targets. * Oversee daily laboratory operations including sample accessioning, wet lab workflows, post-sequencing processes, and inventory. * Drive capacity planning, strategy, and throughput optimization to support business growth. **Quality, Compliance & Regulatory** * Maintain full compliance with CLIA, CAP, state, and federal regulations. * Serve as the site designee and work closely with the Laboratory Director to ensure regulatory readiness * Support inspections, audits, and corrective/preventive action (CAPA) activities. * Champion a culture of quality, safety, and continuous compliance. **People & Organizational Leadership** * Lead and develop a multidisciplinary organization. * Build a high‑performance culture focused on accountability, engagement, inclusion, and professional development. * Partner with HR on workforce planning, recruiting, retention, and succession planning. * Coach leaders to scale teams effectively in a fast‑growing environment. **Financial & Business Management** * Own site‑level operating budgets, staffing models, and cost controls. * Identify opportunities to improve cost per test without compromising quality or compliance. * Partner with finance and commercial teams to support pricing, capacity forecasting, and margin improvement initiatives. **Cross‑Functional Collaboration** * Act as the primary site liaison with R&D, Medical Affairs, Quality, Regulatory, IT, Supply Chain, and Commercial teams. * Support assay launches, technology transfers, and process changes from development into production. * Provide operational input into new product planning and long‑term laboratory strategy. **Continuous Improvement & Innovation** * Drive Lean, Six Sigma, or similar continuous improvement initiatives. * Support adoption of automation and advanced analytics to improve efficiency and scalability. * Promote data‑driven decision‑making using operational KPIs and quality metrics. **Minimum Qualifications:** * Bachelor’s degree in a Chemical or Biological Science, Clinical Laboratory Science, or Medical Technology * 6 or more years of experience in clinical laboratory operations, with proven leadership responsibilities * 5 or more years experience in leadership, directly managing employees **Preferred Qualifications:** * 3 or more years experience managing people leaders * 1 year or more experience with Next Generation Sequencing (NGS) based clinical lab testing, bioinformatics workflows, and automation * 1 year or more experience in Lean, Six Sigma, or operational excellence methodologies. * 1 year or more experience in a commercial diagnostics or precision medicine organization. **Additional Job Standards:** * Deep knowledge of CLIA/CAP regulations and inspection readiness. * Proven ability to scale operations in a regulated, production environment. * Strategic and operational thinker with strong execution discipline * Comfortable leading large, complex organizations through change * Data‑driven decision maker with strong financial acumen * Excellent communicator and cross‑functional collaborator * Strong people leader who builds trust and develops talent * On‑site leadership presence required in a fast‑paced, production laboratory environment * Occasional travel for inspections, leadership meetings, or cross‑site collaboration. **Pay Range:** $140,000 - $200,000 per year All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. The position is also eligible for an annual bonus under the Labcorp Bonus Plan. Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers. **Benefits:** Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please [click here](https://careers.labcorp.com/global/en/us-rewards-and-wellness). **Labcorp is proud to be an Equal Opportunity Employer:** Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. **We encourage all to apply** If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our [accessibility site](https://careers.labcorp.com/global/en/accessibility) or contact us at [Labcorp Accessibility.](mailto:Disability_apply@LabCorp.com) For more information about how we collect and store your personal data, please see our [Privacy Statement](https://www.labcorp.com/about/web-privacy-policy).", "summaryDescription" : "Clinical Laboratory Operations Site Director at Invitae. Skills: Clinical Laboratory Operations, People Leadership, Quality & Compliance, Financial Management, Continuous Improvement. Provide end-to-end operational leadership for a large-scale, high-complexity clinical genetic testing laboratory. Ensure reliable, scalable processing while meeting or exceeding turnaround time and quality targets. 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Experience in a commercial diagnostics or precision medicine organization.", "Microsoft Office Suite" ], "skillCount" : 13, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "executive", "dataQualityScore" : 1.0, "_score" : 616.8053, "daysOld" : 3, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.98 }, { "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; 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Carry out hematology examinations", "postedDate" : "2026-06-10T07:27:04.000", "createdAt" : "2026-06-12T03:33:06.094", "lastUpdated" : "2026-06-14T23:30:44.992", "ingestTimestamp" : "2026-06-12T03:33:06.094", "mongoId" : "6a2a4a1b74d8ee00a05e7764", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Laboratory examinations", "Hematology", "Chemistry", "Serology", "Urine analysis", "Feces analysis", "Body fluid analysis", "Data entry", "Data release", "Equipment maintenance", "Reagent procurement", "Health Analyst" ], "skillCount" : 12, "jobCategory" : "other", "jobSubcategory" : "Medical", "dataQualityScore" : 1.0, "_score" : 602.201, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "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. 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], "hardSkillsList" : [ "Sample preparation", "Metallographic sample preparation", "Microstructural assessments", "Metallurgical investigations", "Laboratory equipment operation", "Mechanical testing support", "Technical data preparation", "Record maintenance", "Traceability records", "Failure investigation support", "Process development support", "Assessment technique development", "Customer request support", "On-site inspection", "On-site sample preparation", "Laboratory organisation", "Housekeeping", "6S standards", "Quality standards compliance", "Laboratory audits support" ], "softSkillsList" : [ "Good communication skills", "Organisational skills", "Attention to detail" ], "hardSkills" : [ { "name" : "Sample preparation", "level" : "intermediate" }, { "name" : "Metallographic sample preparation", "level" : "intermediate" }, { "name" : "Microstructural assessments", "level" : "intermediate" }, { "name" : "Metallurgical investigations", "level" : "intermediate" }, { "name" : "Laboratory equipment operation", "level" : "intermediate" }, { "name" : "Mechanical testing support", "level" : "intermediate" }, { "name" : "Technical data preparation", "level" : "intermediate" }, { "name" : "Record maintenance", "level" : "intermediate" }, { "name" : "Traceability records", "level" : "intermediate" }, { "name" : "Failure investigation support", "level" : "intermediate" }, { "name" : "Process development support", "level" : "intermediate" }, { "name" : "Assessment technique development", "level" : "intermediate" }, { "name" : "Customer request support", "level" : "intermediate" }, { "name" : "On-site inspection", "level" : "intermediate" }, { "name" : "On-site sample preparation", "level" : "intermediate" }, { "name" : "Laboratory organisation", "level" : "intermediate" }, { "name" : "Housekeeping", "level" : "intermediate" }, { "name" : "6S standards", "level" : "intermediate" }, { "name" : "Quality standards compliance", "level" : "intermediate" }, { "name" : "Laboratory audits support", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Good communication skills" }, { "name" : "Organisational skills" }, { "name" : "Attention to detail" } ], "majorSkills" : "Materials Laboratory, Metallurgy, Materials Engineering", "majorSkillsList" : [ "Materials Laboratory", "Metallurgy", "Materials Engineering" ], "coreResponsibilities" : "Prepare metallographic samples, Perform visual assessments, Perform microstructural assessments, Support metallurgical investigations, Operate laboratory equipment, Assist with optical microscopy, Assist with scanning electron microscopy, Support mechanical testing activities, Prepare technical data, Prepare records, Prepare reports, Maintain sample logging records, Maintain traceability records, Assist with failure investigations, Assist with Root Cause Analysis, Support process development activities, Support qualification activities, Participate in laboratory process improvement, Assist with development of new assessment techniques, Support customer requests, Assist with on-site inspection, Assist with on-site sample preparation, Support acetate replication activities, Support in-situ metallurgical assessment, Provide support during maintenance outages, Provide support during service execution, Support day-to-day laboratory running, Maintain laboratory organisation, Maintain laboratory housekeeping, Maintain 6S standards, Assist with stock control, Assist with consumables management, Ensure compliance with laboratory procedures, Ensure compliance with quality standards, Ensure compliance with Health & Safety, Support laboratory audits", "teamCollaboration" : "Work with experienced Materials Engineers; Work within a team environment", "domainKnowledge" : "Iron-based alloys; Nickel-based alloys; Power generation industry; Energy sector; Materials engineering sector; Turbine components", "domainList" : [ "iron-based-alloys", "nickel-based-alloys", "power-generation-industry", "energy-sector", "materials-engineering-sector", "turbine-components" ], "domainSpecificKnowledge" : [ "Iron-based alloys", "Nickel-based alloys", "Power generation industry", "Energy sector", "Materials engineering sector", "Turbine components" ], "toolProficiency" : [ "Microsoft Office" ], "communicationSkills" : "Technical information delivery; Technical reports", "documentationSkills" : "Technical data; Records; Reports", "continuousLearning" : "Gain degree-level qualification; Undertake further technical training", "innovationCreativity" : "Process improvement initiatives; Development of new assessment techniques", "problemSolvingSkills" : "Root Cause Analysis; Failure investigations; Technical issue resolution", "specialRequirements" : "3 Year Fixed Term Contract, On-site inspection, On-site sample preparation, Acetate replication, In-situ metallurgical assessment, On-site activities, Maintenance outages support, Service execution support", "outcomesObjectives" : "Deliver high-quality technical information; Deliver high-quality reports", "qualificationsBasic" : "Meet entry requirements for Level 6 Degree Apprenticeship, Interest in Materials Science, Metallurgy, Engineering or Manufacturing, Competent IT skills including Microsoft Office, Fluent in written and spoken Business English, Willingness to learn new techniques, Willingness to undertake further technical training", "qualificationsPreferred" : "Experience with iron and nickel-based alloys", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Mitsubishi Power EMEA is seeking a motivated and enthusiastic Apprentice Laboratory Technician to join our growing Materials Laboratory in Leeds. The Materials Laboratory plays a vital role in supporting engineering activities including materials testing and evaluation, turbine component life assessment, repair development, process improvement initiatives and Root Cause Analysis (RCA) investigations for gas and steam turbine components. Working closely with experienced Materials Engineers, you will be responsible for sample preparation, laboratory operations, metallurgical assessments, technical support activities and assisting with the delivery of high-quality technical information and reports. You will gain practical experience across a broad range of engineering projects involving advanced iron and nickel-based alloys used within the power generation industry. This apprenticeship provides an excellent opportunity to develop specialist knowledge, gain a degree-level qualification and build a long-term career within the energy and materials engineering sector. Key Responsibilities Laboratory and Technical Support * Prepare metallographic samples using cutting, mounting, grinding and polishing equipment. * Perform visual and microstructural assessments of metallic materials. * Support metallurgical investigations involving iron and nickel-based alloys. * Operate laboratory equipment safely and effectively. * Assist with optical microscopy and scanning electron microscopy examinations (training provided). * Support mechanical testing activities both in-house and through approved external laboratories. * Prepare technical data, records and reports to support engineering investigations. * Maintain accurate sample logging and traceability records. Materials Assessment and Engineering Support * Assist Materials Engineers with failure investigations and Root Cause Analysis (RCA) activities. * Support process development and qualification activities for turbine component repairs. * Participate in laboratory process improvement initiatives. * Assist with the development of new assessment techniques for novel materials and manufacturing processes. * Support internal and external customer requests relating to technical issue resolution. On-Site Activities * Assist with on-site inspection and sample preparation activities on gas and steam turbine components. * Support acetate replication and in-situ metallurgical assessment activities (training provided). * Provide support during maintenance outages and service execution activities when required. Laboratory Operations * Support the day-to-day running of the Materials Laboratory. * Maintain laboratory organisation, housekeeping and 6S standards. * Assist with stock control and consumables management. * Ensure compliance with laboratory procedures, quality standards and Health & Safety requirements. * Support internal and external laboratory audits. ## Qualifications * Meet the entry requirements for a relevant Level 6 Degree Apprenticeship programme. * Strong interest in Materials Science, Metallurgy, Engineering or Manufacturing. * Good communication skills and ability to work within a team environment. * Strong organisational skills and attention to detail. * Competent IT skills including Microsoft Office applications. * Fluent in written and spoken Business English. * Willingness to learn new techniques and undertake further technical training. ## Additional Information At Mitsubishi Power EMEA, we are committed to building a workplace where people feel respected, included and able to contribute. Our strength comes from the different experiences, perspectives and expertise of our people. Across our business, we work with colleagues from a wide range of countries, cultures, disciplines and backgrounds, and we believe this diversity helps us make better decisions, solve complex problems and deliver stronger outcomes for our customers. We welcome applications from people of all backgrounds and make recruitment decisions based on skills, knowledge, qualifications, experience and potential. We are committed to providing a fair and consistent recruitment process, giving every candidate the opportunity to demonstrate what they can bring to the role. If you need any reasonable adjustments or support at any stage of the recruitment process, please let us know. We will work with you to understand how we can best support you.", "summaryDescription" : "Apprentice Laboratory Technician (3 Year Fixed Term Contract) at Mitsubishi Power EMEA. Skills: Materials Laboratory, Metallurgy, Materials Engineering. Prepare metallographic samples. Perform visual assessments", "postedDate" : "2026-06-10T10:37:34.000", "createdAt" : "2026-06-12T03:58:52.459", "lastUpdated" : "2026-06-14T23:22:52.905", "ingestTimestamp" : "2026-06-12T03:58:52.459", "mongoId" : "6a2a590a74d8ee00a060c6a2", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryBand" : "<30k", "hasSalary" : false, "allSkills" : [ "Sample preparation", "Metallographic sample preparation", "Microstructural assessments", "Metallurgical investigations", "Laboratory equipment operation", "Mechanical testing support", "Technical data preparation", "Record maintenance", "Traceability records", "Failure investigation support", "Process development support", "Assessment technique development", "Customer request support", "On-site inspection", "On-site sample preparation", "Laboratory organisation", "Housekeeping", "6S standards", "Quality standards compliance", "Laboratory audits support", "Good communication skills", "Organisational skills", "Attention to detail", "Materials Laboratory", "Metallurgy", "Materials Engineering", "Materials testing", "Life assessment", "Repair development", "Process improvement", "Root Cause Analysis", "Metallurgical assessments", "Technical support", "Failure investigations", "Mechanical testing", "Optical microscopy", "Scanning electron microscopy", "Acetate replication", "In-situ assessment", "Stock control", "Consumables management", "Iron-based alloys", "Nickel-based alloys", "Power generation industry", "Energy sector", "Materials engineering sector", "Turbine components", "Microsoft Office" ], "skillCount" : 48, "jobCategory" : "engineering", "jobSubcategory" : "Engineering", "dataQualityScore" : 1.0, "_score" : 596.2863, "daysOld" : 4, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Energy" }, { "id" : "6a2a8bb974d8ee00a0683a52", "title" : "Laboratory Engineer II", "company" : "University of Rochester", "salary" : { "min" : 60431.0, "max" : 84603.0, "currency" : "USD", "frequency" : "yearly" }, "location" : "United States of America", "locations" : [ "United States of America" ], "timestamp" : "2026-06-13T06:42:33.262", "fingerprint" : "d09eca9b572df30e52aa9a27d2a87a2c1ebd140dcd7af32611569c47e32adc67", "source" : "workday", "language" : "en", "applyUrl" : "https://rochester.wd5.myworkdayjobs.com/UR_Staff/job/Laboratory-for-Laser-Energetics/Laboratory-Engineer-II_R272093", "externalId" : "R272093", "locationPoint" : "51.43667,5.97917", "structuredLocations" : [ { "city" : "Rochester", "state" : "New York", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "43.1572850,-77.6152140" } ], "locationText" : "Rochester, New York, United States", "employmentType" : "FULL_TIME", "technicalSkills" : "MATLAB, Python, Excel", "professionalSkills" : [ "Technical evaluation", "System performance evaluation", "Laser development" ], "hardSkillsList" : [ "Data analysis", "Technical data processing", "Test planning", "Documentation" ], "softSkillsList" : [ "Adaptability", "Attention to detail", "Organizational skills" ], "hardSkills" : [ { "name" : "Data analysis", "level" : "intermediate" }, { "name" : "Technical data processing", "level" : "intermediate" }, { "name" : "Test planning", "level" : "intermediate" }, { "name" : "Documentation", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Adaptability" }, { "name" : "Attention to detail" }, { "name" : "Organizational skills" } ], "majorSkills" : "Laser system operation, Data analysis, Laboratory testing", "majorSkillsList" : [ "Laser system operation", "Data analysis", "Laboratory testing" ], "coreResponsibilities" : "Operate FLUX laser system, Perform engineering analysis, Support laser development, Evaluate system performance, Ensure system safety, Collect technical data, Process technical data, Interpret technical data, Identify trends, Identify anomalies, Identify performance improvements, Conduct laboratory testing, Conduct field-testing, Support validation activities, Support verification activities, Develop standard operating procedures, Maintain standard operating procedures, Develop test plans, Maintain test plans, Support laser upgrade projects, Support software development", "teamCollaboration" : "Collaborate with scientists; Collaborate with engineers; Collaborate with technicians; Cross-functional teams", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Laser systems; FLUX laser system", "domainList" : [ "laser-systems", "flux-laser-system" ], "domainSpecificKnowledge" : [ "Laser systems", "FLUX laser system" ], "toolProficiency" : [ "Oscilloscopes", "Diagnostic tools" ], "communicationSkills" : "Written communication; Verbal communication", "documentationSkills" : "Documentation", "problemSolvingSkills" : "Analytical skills; Problem-solving skills", "specialRequirements" : "Work shift assignments, Evening hours", "outcomesObjectives" : "Identify trends; Identify anomalies; Identify performance improvements", "qualificationsBasic" : "Bachelor’s degree in STEM field, 2 years of relevant experience", "qualificationsPreferred" : "Hands-on experience using oscilloscopes, Experience with data analysis tools, Prior experience in a laboratory or manufacturing environment", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive. _**Job Location (Full Address):**_ 250 East River Rd, Rochester, New York, United States of America, 14623 _**Opening:**_ Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 250548 LLE-Laboratory for Laser Energ Work Shift: UR - Day (United States of America) Range: UR URG 110 Compensation Range: $60,431.00 - $84,603.00 _The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job 's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations._ _**Responsibilities:**_ LE is seeking a detail-oriented and analytical engineer to support FLUX operations through data-driven analysis, technical evaluation, and hands-on operation and testing. This role is ideal for a candidate with a strong STEM background who enjoys problem-solving, working with technical equipment, and collaborating across engineering teams. The successful candidate must be willing to work shift assignments 1–2 times per week, including evening hours, to support operational needs and testing schedules. **ESSENTIAL FUNCTIONS** * Complete qualification and stand watch in operation of the FLUX laser system * Perform engineering analysis to support laser development, system performance evaluation, operational activities and ensure system safety * Collect, process, and interpret technical data to identify trends, anomalies, and performance improvements * Conduct laboratory and field-testing using equipment such as oscilloscopes and other diagnostic tools * Support validation and verification activities through structured test planning and documentation * Develop and maintain standard operating procedures and test plans to provide clear direction for technicians and operators * Collaborate with cross-functional teams including scientists, engineers, and technicians * Support laser upgrade projects and software development. Will have responsibility over minor aspects under the direction of a project manager. **MINIMUM EDUCATION & EXPERIENCE** * Bachelor’s degree in STEM field and 2 years of relevant experience required * Hands-on experience using oscilloscopes and electronic test equipment preferred * Experience with data analysis tools (e.g., MATLAB, Python, Excel, or similar platforms) preferred * Prior experience in a laboratory or manufacturing environment preferred **KNOWLEDGE, SKILLS AND ABILITIES** * Strong analytical and problem-solving skills required * Ability to interpret technical drawings and schematics required * Willingness and ability to work evening shifts up to 2 times per week required * Strong written and verbal communication skills required * Attention to detail * Strong organizational skills * Ability to work independently and in a team environment * Adaptability to shifting priorities and schedules The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.", "summaryDescription" : "Laboratory Engineer II at University of Rochester. Skills: Laser system operation, Data analysis, Laboratory testing. Operate FLUX laser system. Perform engineering analysis", "postedDate" : "2026-06-10T19:48:44.471", "createdAt" : "2026-06-11T19:48:44.286", "lastUpdated" : "2026-06-13T06:42:33.262", "ingestTimestamp" : "2026-06-11T19:48:44.286", "mongoId" : "6a2a8bb974d8ee00a0683a52", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://rochester.wd5.myworkdayjobs.com/UR_Staff/job/Laboratory-for-Laser-Energetics/Laboratory-Engineer-II_R272093", "salaryAnnualMin" : 60431, "salaryAnnualMax" : 84603, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Data analysis", "Technical data processing", "Test planning", "Documentation", "Adaptability", "Attention to detail", "Organizational skills", "Laser system operation", "Laboratory testing", "Technical evaluation", "System performance evaluation", "Laser development", "Project management", "Laser systems", "FLUX laser system", "Oscilloscopes", "Diagnostic tools" ], "skillCount" : 17, "jobCategory" : "engineering", "seniorityLevel" : "mid", "dataQualityScore" : 0.8888889, "_score" : 594.3673, "daysOld" : 2, "hasLocation" : true, "hasGeo" : true }, { "id" : "69cf26122beec4dd3d90b3fe", "title" : "Medical Laboratory Scientist - Hematology", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 65000.0, "max" : 95000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Medical Laboratory Scientist in Tampa, FL, adjusted for the Healthcare industry." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

" ], "certifications" : [ "Medical Technologist license" ], "timestamp" : "2026-06-15T08:56:42.298", "fingerprint" : "0bd187ccad73bc0b1896f436a2d0bc273e4ba25e5fca3ca76984f002282f70b4", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=541110", "externalId" : "541110", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tampa", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "27.9449854,-82.4583107" } ], "locationText" : "Tampa, Florida, United States", "minimumEducation" : "Bachelor's", "majorSkills" : "Hematology testing, Laboratory analysis", "majorSkillsList" : [ "Hematology testing", "Laboratory analysis" ], "domainKnowledge" : "CAP Regulations; Hematology", "domainList" : [ "cap-regulations", "hematology" ], "domainSpecificKnowledge" : [ "CAP Regulations", "Hematology" ], "problemSolvingSkills" : "Test problem solving", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision, independently performs all levels of moderate and high complexity testing, following established policies, procedures, and professional guidelines. Responsible for performing routine and specialized technical analyses. Operates and maintains instrumentation according to established laboratory procedures and protocols. Exercises independent judgement in recognizing and solving test related problems. Performs technical job duties as specified in CAP Regulations. Personnel Requirements for Tests of Moderate and High Complexity - Testing. Also responsible for performing job duties in accordance with the mission, vision and values of Tampa General Hospital. Must be currently licensed as a Medical Technologist by the State of Florida Department of Health. Bachelor’s degree in Medical Technology or related area.      Tampa", "summaryDescription" : "Medical Laboratory Scientist - Hematology at Tampa General Hospital. Skills: Hematology testing, Laboratory analysis", "createdAt" : "2026-06-14T00:42:58.318", "lastUpdated" : "2026-06-15T08:56:42.298", "ingestTimestamp" : "2026-06-14T00:42:58.318", "mongoId" : "69cf26122beec4dd3d90b3fe", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 65000, "salaryAnnualMax" : 95000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "Hematology testing", "Laboratory analysis", "CAP Regulations", "Hematology", "Medical Technologist license" ], "skillCount" : 5, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 589.3827, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a0de91358b93c861eb990c4", "title" : "Medical Laboratory Scientist III", "industry" : "Healthcare", "salary" : { "min" : 85000.0, "max" : 125000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Medical Laboratory Scientist III in Brooksville, United States, adjusted for mid-seniority and full-time employment in the healthcare industry." }, "location" : "United States-Florida-Brooksville", "locations" : [ "United States-Florida-Brooksville", "
TGH Brooksville (TGHBRKSV)
17240 Cortez Boulevard

Brooksville, 34601

" ], "certifications" : [ "Clinical Lab Technologist Certification", "ASCP", "AMT" ], "timestamp" : "2026-06-15T10:02:31.540", "fingerprint" : "f31060dab2a92af3482fbc237f0ffd18478088e3ac42faa28c9b0783fe494198", "source" : "taleo", "language" : "en", "applyUrl" : "https://tas-tgh.taleo.net/careersection/ex/jobdetail.ftl?job=670007", "externalId" : "670007", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Brooksville", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "28.5552719,-82.3878709" } ], "locationText" : "Brooksville, Florida, United States", "minimumEducation" : "Associate's", "experienceMinYears" : 5, "experienceMaxYears" : 10, "experienceLevel" : "Senior", "domainKnowledge" : "Geriatrics; Adults; Pediatrics; Neonates; Microbiology; Serology; Clinical Chemistry; Hematology; Immunohematology", "domainList" : [ "geriatrics", "adults", "pediatrics", "neonates", "microbiology", "serology", "clinical-chemistry", "hematology", "immunohematology" ], "domainSpecificKnowledge" : [ "Geriatrics", "Adults", "Pediatrics", "Neonates", "Microbiology", "Serology", "Clinical Chemistry", "Hematology", "Immunohematology" ], "communicationSkills" : "Report results", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Performs all approved laboratory procedures in assigned licensure specialties, as required to meet workload demands. coordinating lab resources as outlined below. Precisely and accurately performs and evaluates a variety of technical procedures. Utilizes accepted quality control techniques by manual, semi -automated, or automated methodologies and equipment. Essential Functions Perform work according to established laboratory policies and procedures. Demonstrate the ability to work independently in all areas covered by the FL license. Perform quality control for all tests, evaluate results, and take corrective action as necessary before reporting patient results. Assess specimen integrity for appropriateness of ordered tests, including issues like QNS, hemolysis, and clotting. Ensure procedures, methodologies, and patient results correlate with age-specific criteria for geriatrics, adults, pediatrics, and neonates. Repeat and report all panic/critical test results to a licensed caregiver within 5 minutes of completion. Perform calibrations and maintenance as required by instrument manufacturers, CLIA, and TJC. Complete proficiency testing samples within the requested timeframe. Demonstrate competency in using the LIS and HIS computer systems. Ensure adequate supplies are available and promptly notify the supervisor when supplies are low. Education Associate's Degree Medical Technology or Bachelors Biology or Chemistry License Clinical Lab Technologist Certification American Society of Clinical Pathology (ASCP) or American Medical Technologists (AMT) Work Experience Licensed in all 5 specialties, Microbiology, Serology, Clinical Chemistry, Hematology, Immunohematology Brooksville", "summaryDescription" : "Medical Laboratory Scientist III", "createdAt" : "2026-06-14T09:47:04.758", "lastUpdated" : "2026-06-15T10:02:31.540", "ingestTimestamp" : "2026-06-14T09:47:04.758", "mongoId" : "6a0de91358b93c861eb990c4", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 85000, "salaryAnnualMax" : 125000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Geriatrics", "Adults", "Pediatrics", "Neonates", "Microbiology", "Serology", "Clinical Chemistry", "Hematology", "Immunohematology", "Clinical Lab Technologist Certification", "ASCP", "AMT" ], "skillCount" : 12, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 589.16907, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2b080174d8ee00a0757b11", "title" : "Fragrance Laboratory Lead", "company" : "Unilever", "industry" : "Consumer Goods", "salary" : { "min" : 2250000.0, "max" : 3500000.0, "currency" : "INR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Lead Fragrance Laboratory Lead in Mumbai, India, adjusted for the Food & Beverage industry and company size." }, "location" : "India", "locations" : [ "India" ], "timestamp" : "2026-06-14T22:57:58.396", "fingerprint" : "b747468654ff2d2ae309b40c0a50b4838bd4ff765d4a5ba6dcb4400842a0ab78", "source" : "workday", "language" : "en", "applyUrl" : "https://unilever.wd3.myworkdayjobs.com/Unilever_Experienced_Professionals/job/Mumbai-HURC/Fragrance-Laboratory-Lead_R-1182197", "externalId" : "R-1182197", "industryFunction" : { }, "locationPoint" : "20.5937,78.9629", "structuredLocations" : [ { "city" : "Mumbai", "country" : "India", "continent" : "as", "source" : "llm", "workMode" : "onsite", "geo" : "19.0549990,72.8692035" } ], "locationText" : "Mumbai, India", "employmentType" : "FULL_TIME", "experienceMinYears" : 8, "experienceMaxYears" : 15, "experienceLevel" : "Lead", "professionalSkills" : [ "Laboratory management", "Equipment management", "Budgeting" ], "hardSkillsList" : [ "Laboratory safety", "Waste disposal", "Material management" ], "softSkillsList" : [ "Ownership" ], "hardSkills" : [ { "name" : "Laboratory safety", "level" : "intermediate" }, { "name" : "Waste disposal", "level" : "intermediate" }, { "name" : "Material management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Ownership" } ], "majorSkills" : "Laboratory operations, Equipment maintenance, Regulatory compliance", "majorSkillsList" : [ "Laboratory operations", "Equipment maintenance", "Regulatory compliance" ], "coreResponsibilities" : "Lead laboratory environment management, Support formulation work, Support application work, Support evaluation work, Ensure laboratory operates seamlessly, Maintain a clean workspace, Maintain a safe workspace, Maintain well-functioning workspace, Ensure compliance with health standards, Ensure compliance with safety standards, Ensure compliance with laboratory management standards, Oversee safe handling of laboratory waste, Oversee disposal of laboratory waste, Manage laboratory equipment, Perform routine maintenance, Troubleshoot equipment issues, Replace laboratory equipment, Resolve technical issues, Minimize downtime, Oversee planning for new equipment, Oversee budgeting for new equipment, Oversee budgeting for laboratory needs, Ensure availability of materials, Ensure availability of consumables, Keep evaluation booths operational, Keep testing areas operational, Keep evaluation booths available, Keep testing areas available, Maintain accurate records, Maintain up-to-date records", "teamCollaboration" : "Work across diverse technical teams", "domainKnowledge" : "Fragrance development; Personal Care products; Home Care products; Beauty products", "domainList" : [ "fragrance-development", "personal-care-products", "home-care-products", "beauty-products" ], "domainSpecificKnowledge" : [ "Fragrance development", "Personal Care products", "Home Care products", "Beauty products" ], "documentationSkills" : "Record keeping", "continuousLearning" : "Growth opportunities", "innovationCreativity" : "Enabling innovation", "problemSolvingSkills" : "Problem-solving", "outcomesObjectives" : "Deliver products used by millions; Impact quality; Impact safety; Impact speed of innovation", "qualificationsBasic" : "Bachelor's degree or higher in a scientific discipline, Experience working in a laboratory environment, Experience with safe and effective practices, High attention to detail, Proactive approach to problem-solving, Good understanding of laboratory safety processes, Understanding of standard procedures, Understanding of risk assessments, Understanding of safe handling of materials", "qualificationsPreferred" : "Experience in formulation, Experience in application, Experience in evaluation", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Job Title:** Fragrance Laboratory Lead **Location:** Mumbai HURC **Work Level:** 1D **Want to Change The World?** Unilever is one of the world’s leading suppliers of Beauty, Personal and Home Care products selling in over 190 countries and used by 3.7 billion consumers every day. Unilever has more than 400 brands used in homes around the world, including Dove, Sure, TRESemmé, Sunsilk, Vaseline, Comfort, Persil and Surf. As one of the world’s largest users of fragrances, we recognise that creating exceptional fragrances is at the heart of delivering extraordinary consumer experiences and driving desire at scale. To achieve our ambition, Unilever Fragrance House is undertaking a global fragrance transformation, leveraging expert inhouse fragrance teams to craft unmissably superior fragrances for our Personal Care, Beauty & Wellbeing and Home Care Business Groups. **Job Purpose** Make an Impact That Matters! Are you passionate about creating safe, efficient, and high-performing laboratory environments? As Unilever Fragrance House (UFH) Laboratory Lead, you will play a critical role in enabling innovation by ensuring our laboratory operates seamlessly every day. You will lead the management of our India lab, supporting formulation, application, and evaluation work that ultimately helps deliver products used by millions of people around the world. Your work will directly impact the quality, safety, and speed of innovation across our teams. **What You Will Do** In this role, you will take ownership of the laboratory environment and ensure it consistently supports high-quality R&D work for UFH. Key responsibilities include: • Leading the end-to-end management of the laboratory, ensuring it is organized, efficient, and ready to support all activities • Maintaining a clean, safe, and well-functioning workspace, including all equipment and evaluation areas • Ensuring full compliance with health, safety, and laboratory management standards • Overseeiog safe handling and disposal of laboratory waste in line with regulatory requirements • Managing laboratory equipment, including routine maintenance, troubleshooting, and timely replacement • Working closely with operations teams to resolve technical issues and minimize downtime • Overseeing planning and budgeting for new equipment and ongoing laboratory needs • Ensure availability of all materials and consumables required for smooth laboratory operations • Keeping evaluation booths and testing areas fully operational and available according to timelines • Maintaining accurate and up-to-date records of all laboratory activities **What We Are Looking For** We are looking for someone who combines strong technical discipline with ownership and collaboration: • A bachelor’s degree or higher in a scientific discipline • Experience working in a laboratory environment, with a strong focus on safe and effective practices • Strong collaboration and communication skills, with the ability to work across diverse technical teams • High attention to detail and a proactive approach to problem-solving • Good understanding of laboratory safety processes, including standard procedures, risk assessments, and safe handling of materials **What You Can Expect** • You will join a collaborative and purpose-driven team that believes in doing meaningful work - for both people and the planet - supporting innovation that impacts millions of consumers • Collaborative culture: Work with skilled and supportive colleagues across functions • Growth opportunities: Build expertise in laboratory operations, equipment management, and cross-functional collaboration • Ownership and visibility: Play a key role in ensuring operational excellence in a critical facility **NOTES** Please apply via this portal as e-mail applications may not be processed. Should you require additional information or reasonable adjustments to allow you to present your best self during this process, please contact your Talent Partner listed at the right hand side of this vacancy. **What We Offer** We strive to achieve a family-friendly and inclusive workplace and to, above all, create possibilities for all. Diversity at Unilever is about inclusion, embracing differences, creating possibilities and growing together for better business performance. We embrace diversity in our workforce. This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity. We are also more than happy to provide reasonable adjustments during our application and interview process to enable you to be present your best self. To find out more, including about our Employee Resource Groups, please click here Equity, Diversity & Inclusion (unilever.com).", "summaryDescription" : "Fragrance Laboratory Lead at Unilever. Skills: Laboratory operations, Equipment maintenance, Regulatory compliance. Lead laboratory environment management. Support formulation work", "postedDate" : "2026-06-11T04:17:48.786", "createdAt" : "2026-06-12T04:17:48.775", "lastUpdated" : "2026-06-14T22:57:58.396", "ingestTimestamp" : "2026-06-12T04:17:48.775", "mongoId" : "6a2b080174d8ee00a0757b11", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://unilever.wd3.myworkdayjobs.com/Unilever_Experienced_Professionals/job/Mumbai-HURC/Fragrance-Laboratory-Lead_R-1182197", "salaryBand" : "200k+", "hasSalary" : false, "allSkills" : [ "Laboratory safety", "Waste disposal", "Material management", "Ownership", "Laboratory operations", "Equipment maintenance", "Regulatory compliance", "Laboratory management", "Equipment management", "Budgeting", "Fragrance development", "Personal Care products", "Home Care products", "Beauty products" ], "skillCount" : 14, "jobCategory" : "other", "seniorityLevel" : "mid", "dataQualityScore" : 1.0, "_score" : 587.81476, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Consumer Goods" }, { "id" : "6a2176b974d8ee00a0c1aade", "title" : "Work Preparator", "company" : "D. Cloostermans-Huwaert NV", "industry" : "Systems, Quality, Security Engineering, Support Engineering, amazon business", "salary" : { "min" : 33000.0, "max" : 45000.0, "currency" : "EUR", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Work Preparator in Hamme, Belgium, adjusted for the manufacturing industry and part-time employment." }, "location" : "Hamme, Flanders, BEL", "locations" : [ "Hamme, Flanders, BEL" ], "timestamp" : "2026-06-14T22:25:21.945", "fingerprint" : "ec0cfc33a6b0f1e1779cb644ac3948cc4e47c1bf2a364e2a5317f2a3c8bbb2fb", "source" : "amazon", "language" : "en", "applyUrl" : "https://account.amazon.jobs/jobs/10439719/apply", "externalId" : "842f00dd-0528-41f4-b7b5-ead2ddf95f0e", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Hamme", "state" : "Flanders", "country" : "Belgium", "continent" : "eu", "source" : "llm", "workMode" : "onsite", "geo" : "51.0977642,4.1377229" } ], "locationText" : "Hamme, Flanders, Belgium", "employmentType" : "PART_TIME", "technicalSkills" : "CNC Turning, CNC Milling, Welding, Sheet metal, SAP", "professionalSkills" : [ "Production Planning", "Inventory management", "Capacity planning", "Scheduling principles" ], "hardSkillsList" : [ "Machining techniques", "Technical drawings", "Production routings" ], "hardSkills" : [ { "name" : "Machining techniques", "level" : "intermediate" }, { "name" : "Technical drawings", "level" : "intermediate" }, { "name" : "Production routings", "level" : "intermediate" } ], "majorSkills" : "Production planning, Machining processes, Technical drawings", "majorSkillsList" : [ "Production planning", "Machining processes", "Technical drawings" ], "coreResponsibilities" : "Plan internal production, Monitor internal production, Create production routings, Coordinate with external suppliers, Track delivery dates, Align with project timelines, Order raw materials, Manage inventory levels, Assess manufacturability of parts, Identify potential issues, Define solutions, Translate technical drawings, Represent production department, Monitor project planning, Provide production input, Prepare projects for production, Escalate potential bottlenecks, Escalate delivery risks, Perform pre-calculations, Support accurate project planning, Perform post-calculations, Analyze performance, Identify improvement opportunities", "teamCollaboration" : "Cross-functional project teams; Project team", "projectManagementSkills" : [ "Project planning" ], "domainKnowledge" : "Machining production processes; Welding techniques; Production capacity planning", "domainList" : [ "machining-production-processes", "welding-techniques", "production-capacity-planning" ], "domainSpecificKnowledge" : [ "Machining production processes", "Welding techniques", "Production capacity planning" ], "toolProficiency" : [ "Microsoft Office", "ERP systems" ], "communicationSkills" : "Verbal communication; Written communication", "documentationSkills" : "Technical drawings", "innovationCreativity" : "Invention; Problem-solving", "problemSolvingSkills" : "Problem-solving", "qualificationsBasic" : "Knowledge of mechanical production processes, Knowledge of ERP systems, Experience in Microsoft Office, Communication skills in English", "qualificationsPreferred" : "SAP experience is a plus, Ability to work independently, Proactive approach to problem solving, Communication skills in Dutch", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "At our lab in Hamme, Belgium, we are looking for a Work Preparator to join our Production Department. Depending on industry background and regional terminology, this role may also be recognized as a Manufacturing Process Engineer, Manufacturing Engineer, Production Engineer, Process Planning Engineer, or Production Readiness Engineer. The Mechatronics team builds full-stack innovation that ensures fulfillment and delivery network safety, speed, optimization, sustainability and value. We tackle big goals for the Amazon business and work hard to make automation history through invention, problem-solving, and highly-engaged teams. We are a global organization, with research and development labs based in Hamme, Belgium, Boston, MA (US) and Milan, Italy. Our development portfolio is focused on automation solutions in packaging, labeling, sortation and material conveyance that provide broad extensibility across Amazon businesses. At our lab in Hamme, Belgium we are looking for a Work preparator position within our production departement. As a Work Preparator, you are the crucial link between the production department and cross-functional project teams. You are responsible for preparing, planning, and monitoring both internal production processes and external deliveries. You ensure seamless execution of production activities within a machining environment where processes such as turning, milling, welding, and sheet metal are applied to manufacture parts. Key job responsibilities Production Planning & Coordination • Plan and monitor internal production planning for machining processes (turning, milling, welding, sheet metal) • Create detailed production routings that provide the shop floor with correct production steps and specifications • Coordinate with external suppliers to track delivery dates and align with project timelines • Order raw materials for internal production and manage inventory levels Technical Feasibility & Engineering Collaboration • Work closely with engineers from the start of projects to assess the manufacturability of parts • Identify potential issues and define solutions to ensure smooth production • Translate technical drawings into feasible production processes based on thorough knowledge of machining techniques Project Collaboration & Communication • Represent the production department in multiple concurrent projects • Monitor project planning and provide production input to keep the schedule clear for all departments • Work closely with the project team to thoroughly prepare projects before they go into production • Proactively escalate potential bottlenecks or delivery risks Analysis & Calculations • Perform pre-calculations of production times to support accurate project planning • Perform post-calculations to analyze actual versus planned performance • Identify improvement opportunities based on production data Technical Knowledge (Essential) • Thorough knowledge of machining production processes: o CNC Turning o CNC Milling o Welding (various welding techniques) o Sheet metal • Ability to read and interpret technical drawings • Knowledge of ERP systems (SAP experience is a strong plus) • Understanding of production capacity planning and scheduling principles Internal job description Basic Qualifications: - Knowledge of mechanical production processes (e.g., milling, turning, welding…) - Knowledge of ERP systems, SAP is a plus - Experience in Microsoft Office - Communication skills in English, both verbal and written Preferred Qualifications: - Ability to work independently - Proactive approach to problem solving - Communication skills in Dutch, both verbal and written Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice ( https://www.amazon.jobs/en/privacy_page ) to know more about how we collect, use and transfer the personal data of our candidates. 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.", "summaryDescription" : "Work Preparator at D. Cloostermans-Huwaert NV. Skills: Production planning, Machining processes, Technical drawings. Plan internal production. Monitor internal production", "postedDate" : "2026-06-13T02:38:19.742", "createdAt" : "2026-06-13T02:38:19.742", "lastUpdated" : "2026-06-14T22:25:21.945", "ingestTimestamp" : "2026-06-13T02:38:19.742", "mongoId" : "6a2176b974d8ee00a0c1aade", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "sourceUrl" : "https://account.amazon.jobs/jobs/10439719/apply", "salaryBand" : "30k-50k", "hasSalary" : false, "allSkills" : [ "Machining techniques", "Technical drawings", "Production routings", "Production planning", "Machining processes", "Production Planning", "Inventory management", "Capacity planning", "Scheduling principles", "Project planning", "Machining production processes", "Welding techniques", "Production capacity planning", "Microsoft Office", "ERP systems" ], "skillCount" : 15, "jobCategory" : "engineering", "dataQualityScore" : 0.8888889, "_score" : 585.2737, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true }, { "id" : "69fc49954c40e2acd1a829a0", "title" : "Lab Assistant - Laboratory Services", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 34000.0, "max" : 45000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for Entry level Lab Assistant in Tampa, FL, adjusted for the healthcare industry and hospital size." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

" ], "timestamp" : "2026-06-15T13:25:27.217", "fingerprint" : "488ecbada240401e86d81437d5dba777ab40e4ccfa80fe0bead4ca9cd007a76f", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=677864", "externalId" : "677864", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tampa", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "27.9449854,-82.4583107" } ], "locationText" : "Tampa, Florida, United States", "minimumEducation" : "High School", "domainKnowledge" : "Laboratory testing; Biological safety; CAP", "domainList" : [ "laboratory-testing", "biological-safety", "cap" ], "domainSpecificKnowledge" : [ "Laboratory testing", "Biological safety", "CAP" ], "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision and following established policies, procedures and professional guidelines, the Laboratory Assistant is responsible for the receipt, labeling, processing, delivery and storage of specimens destined for laboratory testing. The team member is also responsible for coordinating with the registration department when specimens are collected and delivered to TGH from an outside physician’s office. Assists with various clerical tasks, receptionist duties, data processing and telephone customer service. Using independent judgment and following TGH and departmental procedures, is responsible for collaborating with nursing personnel, Physicians and Pathologists, regarding the applicable specimen requirements and timely collection of the patient sample(s) necessary for the testing that will be sent to the performing laboratory. Adheres to biological and safety policies and licensure requirements for all laboratory testing and testing facilities; maintains CAP readiness; performs troubleshooting and quality assurance monitoring. Responsible for performing job duties in accordance with the mission, vision and values of Tampa General Hospital. High school diploma or GED 1-2 months of on-the-job training and orientation Previous work as a laboratory assistant is preferred Tampa", "summaryDescription" : "Lab Assistant - Laboratory Services at Tampa General Hospital", "createdAt" : "2026-06-14T06:51:58.424", "lastUpdated" : "2026-06-15T13:25:27.217", "ingestTimestamp" : "2026-06-14T06:51:58.424", "mongoId" : "69fc49954c40e2acd1a829a0", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 34000, "salaryAnnualMax" : 45000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Laboratory testing", "Biological safety", "CAP" ], "skillCount" : 3, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.6666667, "_score" : 584.0121, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2c6d1f74d8ee00a091d558", "title" : "Technicien(ne) de Laboratoire/ Laboratory Technician", "company" : "Bauer Hockey", "industry" : "Sports & Fitness", "salary" : { "min" : 52000.0, "max" : 75000.0, "currency" : "CAD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Laboratory Technician in Blainville, Canada, adjusted for the Sports & Fitness industry." }, "location" : "Blainville, Quebec, Canada", "locations" : [ "Blainville", "Quebec", "Canada" ], "timestamp" : "2026-06-15T09:17:53.505", "fingerprint" : "3c0fccafa313e61a5f9481209629195e844ed119d00ae69c21ecc742d5797c66", "source" : "greenhouse", "language" : "fr", "applyUrl" : "https://job-boards.greenhouse.io/bauerhockeycascademaveriklacrosse/jobs/5162611007", "externalId" : "5162611007", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Blainville", "state" : "Quebec", "country" : "Canada", "continent" : "na", "source" : "llm", "workMode" : "hybrid", "geo" : "45.6793200,-73.8761900" } ], "locationText" : "Blainville, Quebec, Canada", "minimumEducation" : "Bachelor's", "technicalSkills" : "Microsoft Office, Microsoft Excel", "professionalSkills" : [ "Technical writing", "Analytical skills" ], "hardSkillsList" : [ "Mechanical testing", "Laboratory testing" ], "hardSkills" : [ { "name" : "Mechanical testing", "level" : "intermediate" }, { "name" : "Laboratory testing", "level" : "intermediate" } ], "majorSkills" : "Laboratory testing, Mechanical performance, Technical reports", "majorSkillsList" : [ "Laboratory testing", "Mechanical performance", "Technical reports" ], "coreResponsibilities" : "Perform laboratory tests, Evaluate mechanical performance, Assist development teams, Assist production teams, Evaluate test results, Prepare technical reports, Make recommendations, Collaborate with researchers, Collaborate with engineers, Collaborate with developers, Collaborate with designers, Review requests, Establish test programs, Provide accurate results, Provide recommendations, Manage equipment maintenance, Manage equipment repair, Manage equipment calibration, Develop test methodologies, Recommend test methodologies, Develop test equipment, Recommend test equipment", "teamCollaboration" : "Working with a team; Collaborate with researchers; Collaborate with engineers; Collaborate with developers; Collaborate with designers", "projectManagementSkills" : [ "Manage multiple projects" ], "domainKnowledge" : "Mechanical testing laboratory; Composite materials; Machining; CNC; CAD drawing", "domainList" : [ "mechanical-testing-laboratory", "composite-materials", "machining", "cnc", "cad-drawing" ], "domainSpecificKnowledge" : [ "Mechanical testing laboratory", "Composite materials", "Machining", "CNC", "CAD drawing" ], "communicationSkills" : "Written communication; Verbal communication; Technical writing", "documentationSkills" : "Technical reports", "problemSolvingSkills" : "Analytical skills", "specialRequirements" : "Lift and/or push 20-45 lbs", "outcomesObjectives" : "Improve product quality; Improve product performance", "qualificationsBasic" : "College Diploma (DEC), College Certificate (AEC), Equivalent experience, French & English communication, Manage multiple projects, Read and follow protocols, Lift and/or push 20-45 lbs", "qualificationsPreferred" : "Knowledge of ISO standards, Knowledge of ASTM standards, Knowledge of CSA standards, Experience in calibration, Composite materials knowledge, Machining experience, CNC experience, Manual machining experience, CAD drawing experience", "workSiteFlexibility" : "Hybrid", "rawDescription" : "COÉQUIPIERS RECHERCHÉS Travailler chez Bauer, c'est comme jouer dans une équipe de hockey. 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" : 583.5591, "daysOld" : 1, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Sports & Fitness", "llmIndustryConfidence" : 0.95 }, { "id" : "69cf26122beec4dd3d90b425", "title" : "Lab Assistant - Laboratory Services", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 35000.0, "max" : 45000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for entry-level Lab Assistant in Tampa, FL, adjusted for the healthcare industry." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

" ], "timestamp" : "2026-06-15T08:01:57.700", "fingerprint" : "e12d1cb8b365720c07c852991fd57a1a2a9fd35eea1a70eff277654225531f3b", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=676770", "externalId" : "676770", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tampa", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "27.9449854,-82.4583107" } ], "locationText" : "Tampa, Florida, United States", "minimumEducation" : "High School", "teamCollaboration" : "Collaborate with nursing; Collaborate with Physicians; Collaborate with Pathologists", "domainKnowledge" : "Laboratory testing; Biological safety; CAP requirements", "domainList" : [ "laboratory-testing", "biological-safety", "cap-requirements" ], "domainSpecificKnowledge" : [ "Laboratory testing", "Biological safety", "CAP requirements" ], "communicationSkills" : "Telephone customer service", "continuousLearning" : "1-2 months on-the-job training", "problemSolvingSkills" : "Troubleshooting", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision and following established policies, procedures and professional guidelines, the Laboratory Assistant is responsible for the receipt, labeling, processing, delivery and storage of specimens destined for laboratory testing. The team member is also responsible for coordinating with the registration department when specimens are collected and delivered to TGH from an outside physician’s office. Assists with various clerical tasks, receptionist duties, data processing and telephone customer service. Using independent judgment and following TGH and departmental procedures, is responsible for collaborating with nursing personnel, Physicians and Pathologists, regarding the applicable specimen requirements and timely collection of the patient sample(s) necessary for the testing that will be sent to the performing laboratory. Adheres to biological and safety policies and licensure requirements for all laboratory testing and testing facilities; maintains CAP readiness; performs troubleshooting and quality assurance monitoring. Responsible for performing job duties in accordance with the mission, vision and values of Tampa General Hospital. High school diploma or GED 1-2 months of on-the-job training and orientation Tampa", "summaryDescription" : "Lab Assistant - Laboratory Services at Tampa General Hospital", "createdAt" : "2026-06-14T02:46:54.505", "lastUpdated" : "2026-06-15T08:01:57.700", "ingestTimestamp" : "2026-06-14T02:46:54.505", "mongoId" : "69cf26122beec4dd3d90b425", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 35000, "salaryAnnualMax" : 45000, "salaryBand" : "30k-50k", "hasSalary" : true, "allSkills" : [ "Laboratory testing", "Biological safety", "CAP requirements" ], "skillCount" : 3, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Entry", "dataQualityScore" : 0.6666667, "_score" : 582.72235, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "69cf26132beec4dd3d90b5e1", "title" : "Medical Laboratory Scientist - Hematology", "company" : "Tampa General Hospital", "industry" : "Healthcare", "salary" : { "min" : 68000.0, "max" : 92000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Mid-level Medical Laboratory Scientist in Tampa, FL, adjusted for the Healthcare industry and a large hospital setting." }, "location" : "United States-Florida-Tampa", "locations" : [ "United States-Florida-Tampa", "
TGH Main Campus (TGHMAIN)
1 Tampa General Circle

Tampa, 33601

" ], "certifications" : [ "Medical Technologist license" ], "timestamp" : "2026-06-15T09:09:50.633", "fingerprint" : "f28f26ab19db96fad202f7b5ee239e30b4d99b2bf4ab58836a0844abb3610e21", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=540910", "externalId" : "540910", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Tampa", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "27.9449854,-82.4583107" } ], "locationText" : "Tampa, Florida, United States", "minimumEducation" : "Bachelor's", "domainKnowledge" : "CAP Regulations; Moderate complexity testing; High complexity testing", "domainList" : [ "cap-regulations", "moderate-complexity-testing", "high-complexity-testing" ], "domainSpecificKnowledge" : [ "CAP Regulations", "Moderate complexity testing", "High complexity testing" ], "remoteFriendly" : true, "workSiteFlexibility" : "Onsite", "rawDescription" : "Under general supervision, independently performs all levels of moderate and high complexity testing, following established policies, procedures, and professional guidelines. Responsible for performing routine and specialized technical analyses. Operates and maintains instrumentation according to established laboratory procedures and protocols. Exercises independent judgement in recognizing and solving test related problems. Performs technical job duties as specified in CAP Regulations. Personnel Requirements for Tests of Moderate and High Complexity - Testing. Also responsible for performing job duties in accordance with the mission, vision and values of Tampa General Hospital. Must be currently licensed as a Medical Technologist by the State of Florida Department of Health. Bachelor’s degree in Medical Technology or related area.      Tampa", "summaryDescription" : "Medical Laboratory Scientist - Hematology at Tampa General Hospital", "createdAt" : "2026-06-14T01:10:10.024", "lastUpdated" : "2026-06-15T09:09:50.633", "ingestTimestamp" : "2026-06-14T01:10:10.024", "mongoId" : "69cf26132beec4dd3d90b5e1", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 68000, "salaryAnnualMax" : 92000, "salaryBand" : "50k-75k", "hasSalary" : true, "allSkills" : [ "CAP Regulations", "Moderate complexity testing", "High complexity testing", "Medical Technologist license" ], "skillCount" : 4, "jobCategory" : "engineering", "jobSubcategory" : "software", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 582.1001, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 }, { "id" : "6a2cb05874d8ee00a09d9ae9", "title" : "Laboratory Operations & Maintenance Technician", "company" : "Periodic Labs", "industry" : "Atoms: Research Lab, physics, chemistry", "salary" : { "min" : 100000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : false }, "location" : "Menlo Park", "locations" : [ "Menlo Park" ], "timestamp" : "2026-06-15T06:37:43.736", "fingerprint" : "b39c5d93d85ac16b195177f87aeba783159a862441eb60b890b334e57af75a72", "source" : "ashby", "language" : "en", "applyUrl" : "https://jobs.ashbyhq.com/periodic-labs/b1ad8632-f489-4922-8805-42d84711cda1/application", "externalId" : "b1ad8632-f489-4922-8805-42d84711cda1", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Menlo Park", "state" : "California", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "37.4519671,-122.1779920" } ], "locationText" : "Menlo Park, California, United States", "employmentType" : "FULL_TIME", "minimumEducation" : "Bachelor's", "remoteFriendly" : false, "rawDescription" : "ABOUT PERIODIC LABS The most important scientific discoveries of our time won't happen in a traditional lab. We're an AI and physical sciences company building state-of-the-art models to accelerate breakthroughs across materials, energy, and beyond. Backed by world-class investors and growing rapidly, we operate at the pace the frontier requires. Our team brings deep expertise, genuine ownership, and an insatiable drive to push the boundaries of what's scientifically possible. ABOUT THE ROLE Periodic Labs is building an autonomous laboratory for high-throughput materials discovery — combining advanced synthesis, characterization, automation, robotics, and AI to accelerate the development of next-generation materials. We're looking for a highly capable, hands-on Laboratory Operations & Maintenance Technician to help build, maintain, and scale the physical infrastructure that enables our scientific and engineering teams to move quickly. This is an ideal role for someone who enjoys solving practical problems, working with tools, building systems, troubleshooting equipment, and taking ownership of laboratory operations. You'll work across equipment maintenance, gas and vacuum systems, utilities, instrumentation, automation support, machine shop operations, inventory management, and laboratory buildout projects. WHAT YOU'LL DO Equipment Maintenance & Reliability - Execute preventative maintenance programs for laboratory equipment using MaintainX CMMS; develop and improve maintenance procedures, inspection checklists, and work order templates - Perform routine inspections, cleaning, calibration checks, and equipment upkeep across mechanical, electrical, pneumatic, gas, vacuum, and fluid handling systems - Troubleshoot and repair equipment; identify recurring failure modes and implement corrective actions to improve uptime - Coordinate service visits and maintenance activities with equipment vendors - Service vacuum pumps, cooling water systems, chillers, and associated infrastructure; verify equipment meets OEM specifications after maintenance or repairs Asset Management & Documentation - Maintain an accurate asset registry within MaintainX, including equipment records (manuals, schematics, service histories, serial numbers, manufacturer contacts) - Label equipment with asset numbers and QR codes; update equipment layouts, utility matrices, and infrastructure documentation - Track maintenance history and equipment performance metrics Utilities & Infrastructure - Maintain laboratory utility systems including compressed gases, vacuum systems, process cooling water, exhaust systems, gas detection, and general lab infrastructure - Build and modify gas and fluid handling systems from P&IDs and engineering drawings; assemble and install tubing, regulators, valves, gauges, sensors, and associated hardware - Support utility capacity planning and identify infrastructure constraints Equipment Installation & Commissioning - Support installation and startup of new laboratory equipment; coordinate utility hookups including power, water, gas, vacuum, and networking - Procure and install supporting infrastructure including tubing, fittings, pumps, sensors, regulators, and instrumentation - Perform installation verification and commissioning activities; document as-built configurations and equipment changes Automation & Controls Support - Support Controls and Automation Engineers with equipment integration projects - Install and maintain thermocouples, RTDs, pressure transducers, flow meters, solenoid valves, gas sensors, and safety interlocks - Route, terminate, and label instrumentation and communication wiring; assist with sensor replacement, control panel modifications, and field troubleshooting Machine Shop & Fabrication - Fabricate fixtures, brackets, guards, adapters, and experimental hardware using drill press, band saw, chop saw, belt sander, bench grinder, manual mill, and manual lathe - Modify commercial components and support custom equipment builds; maintain machine shop organization and tooling Inventory & Laboratory Operations - Maintain inventories of spare parts, maintenance consumables, PPE, and laboratory supplies; identify critical spare parts and establish appropriate stock levels - Receive and organize incoming equipment, chemicals, gases, and supplies; register chemicals and gas cylinders within laboratory inventory systems - Coordinate gas cylinder replacement and deliveries; support hazardous waste staging and disposal activities - Assist with laboratory organization, equipment moves, and expansion projects Safety & Compliance - Perform all work in accordance with laboratory safety procedures and LOTO requirements; participate in routine safety inspections and identify unsafe conditions - Support safe installation and modification of laboratory equipment and infrastructure - Maintain clean, organized, and professional workspaces; use all appropriate PPE (lab coats, gloves, safety glasses, hearing protection, respirators) YOU WILL THRIVE IN THIS ROLE IF YOU HAVE - 5+ years of experience in laboratory operations, manufacturing, semiconductor, chemical processing, pilot plant, industrial maintenance, or a related environment - The ability to read and interpret P&IDs, mechanical drawings, electrical wiring diagrams, and equipment manuals - Hands-on experience with hand tools, power tools, and mechanical assembly, with strong troubleshooting and problem-solving skills - An associate degree, technical certification, military technical training, trade apprenticeship, or equivalent hands-on experience - Comfort operating in a fast-paced, dynamic startup environment with shifting priorities ESPECIALLY STRONG CANDIDATES MAY ALSO HAVE - Swagelok tubing, fitting, and tube bending experience; gas manifold assembly from P&IDs - Vacuum systems and/or compressed gas systems experience - Semiconductor equipment maintenance experience - Electrical troubleshooting down to PCB/component level using multimeters - MaintainX or other CMMS experience - Forklift or material handling equipment certification - Chemical handling or laboratory operations experience - Process piping and instrumentation experience MECHANICS Minimum education: Bachelor's degree or an equivalent combination of education and training or experience Location: Our lab is located in Menlo Park and we prefer folks to be located in Menlo Park or San Francisco but can be flexible based on role Compensation: The annual compensation range for this role is approximately $100,000 Visa sponsorship: Yes, we sponsor visas and will do everything we can to assist in this process with our legal support. We're building a team of the world's best — the scientists, engineers, and problem-solvers who don't just follow the frontier, they define it. If you're driven to bring AI to life in the physical world and make discoveries that have never been made before, you belong here.", "summaryDescription" : "Laboratory Operations & Maintenance Technician at Periodic Labs", "createdAt" : "2026-06-13T21:49:16.037", "lastUpdated" : "2026-06-15T06:37:43.736", "ingestTimestamp" : "2026-06-13T21:49:16.037", "mongoId" : "6a2cb05874d8ee00a09d9ae9", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 100000, "salaryBand" : "100k-150k", "hasSalary" : true, "allSkills" : [ ], "skillCount" : 0, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.6666667, "_score" : 581.6507, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Technology", "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" : 580.6629, "daysOld" : 5, "hasLocation" : true, "hasGeo" : false, "llmIndustry" : "Healthcare" }, { "id" : "6a2ad06e74d8ee00a07123d6", "title" : "Clinical Laboratory Supervisor", "company" : "Atrium Health", "industry" : "Healthcare", "salary" : { "min" : 41.1, "max" : 61.65, "currency" : "USD", "frequency" : "yearly" }, "location" : "Milledgeville, GA", "locations" : [ "Milledgeville, GA", "United States of America" ], "certifications" : [ "Medical Laboratory Scientist (MLS) certification", "Medical Technologist (MT) certification" ], "timestamp" : "2026-06-14T15:36:01.071", "fingerprint" : "00356410348a831828b4618bd78a4a16804fb0dcbf7e612ade913508ce49882b", "source" : "workday", "language" : "en", "applyUrl" : "https://aah.wd5.myworkdayjobs.com/External/job/Atrium-Health-Navicent-Baldwin---821-N-Cobb-St-Milledgeville-GA/Clinical-Lab-Supervisor_R220381", "externalId" : "R220381", "industryFunction" : { }, "locationPoint" : "41.96336,-89.77456", "structuredLocations" : [ { "city" : "Milledgeville", "state" : "Georgia", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "33.0801429,-83.2320991" } ], "locationText" : "Milledgeville, Georgia, United States", "employmentType" : "FULL_TIME", "technicalSkills" : "Laboratory information systems", "professionalSkills" : [ "Project management", "Decision making", "Delegation", "Team building", "Customer service", "Conflict resolution", "Regulatory compliance", "Accrediting agency requirements", "Licensing agency requirements", "Test systems", "Test processes" ], "hardSkillsList" : [ "Clinical laboratory testing", "Proficiency testing", "Fiscal needs analysis", "Performance improvement", "Quality assurance", "Regulatory compliance", "Accreditation compliance", "Competency testing", "Corrective action implementation", "Performance management" ], "softSkillsList" : [ "Leadership", "Coaching", "Guidance", "Development planning", "Mentoring" ], "hardSkills" : [ { "name" : "Clinical laboratory testing", "level" : "intermediate" }, { "name" : "Proficiency testing", "level" : "intermediate" }, { "name" : "Fiscal needs analysis", "level" : "intermediate" }, { "name" : "Performance improvement", "level" : "intermediate" }, { "name" : "Quality assurance", "level" : "intermediate" }, { "name" : "Regulatory compliance", "level" : "intermediate" }, { "name" : "Accreditation compliance", "level" : "intermediate" }, { "name" : "Competency testing", "level" : "intermediate" }, { "name" : "Corrective action implementation", "level" : "intermediate" }, { "name" : "Performance management", "level" : "intermediate" } ], "softSkills" : [ { "name" : "Leadership" }, { "name" : "Coaching" }, { "name" : "Guidance" }, { "name" : "Development planning" }, { "name" : "Mentoring" } ], "majorSkills" : "Laboratory operations, Team development, Quality management", "majorSkillsList" : [ "Laboratory operations", "Team development", "Quality management" ], "coreResponsibilities" : "Provide work direction, expertise, and guidance to staff, Oversee clinical laboratory testing, Oversee evaluation of results, Oversee proficiency of testing, Participate in projects to meet strategic initiatives, Implement quantitative outcomes, Monitor budget compliance, Analyze laboratory fiscal needs, Analyze departmental performance, Address fiscal variances, Collaborate on performance improvement processes, Implement performance improvement processes, Optimize teammate engagement, Optimize physician satisfaction, Optimize patient satisfaction, Ensure quality standards are met, Ensure regulatory standards are met, Ensure accreditation standards are met, Ensure competency standards are met, Ensure compliance with policies, Ensure compliance with procedures, Ensure compliance with standardization decisions, Coordinate orientation of staff, Coordinate training of staff, Coordinate competency testing of staff, Coordinate orientation of students, Coordinate training of students, Coordinate competency testing of students, Maintain competency in test systems, Maintain competency in test processes, Serve as technical resource for staff, Implement quality plan, Monitor quality indicators, Review laboratory results for quality, Review laboratory results for accuracy, Review laboratory results for validity, Document corrective action, Implement corrective action, Select team members, Coach team members, Develop team members, Set clear expectations, Inspire the team, Motivate the team, Manage performance, Recognize achievement, Provide feedback, Administer progressive discipline, Recommend hiring, Recommend compensation changes, Recommend promotions, Recommend corrective action decisions, Recommend terminations, Adhere to organization's Code of Ethical Conduct, Ensure compliance with policies, Ensure compliance with regulations, Ensure compliance with laws", "teamCollaboration" : "Site leaders collaboration; Cross-functional collaboration", "projectManagementSkills" : [ "Project management" ], "domainKnowledge" : "Clinical laboratory science; Medical technology; Laboratory information systems; Regulatory agency requirements; Accrediting agency requirements; Licensing agency requirements", "domainList" : [ "clinical-laboratory-science", "medical-technology", "laboratory-information-systems", "regulatory-agency-requirements", "accrediting-agency-requirements", "licensing-agency-requirements" ], "domainSpecificKnowledge" : [ "Clinical laboratory science", "Medical technology", "Laboratory information systems", "Regulatory agency requirements", "Accrediting agency requirements", "Licensing agency requirements" ], "communicationSkills" : "Communication skills", "continuousLearning" : "Career development programs; Educational Assistance Program", "innovationCreativity" : "Clinical innovation", "problemSolvingSkills" : "Decision making; Conflict resolution; Corrective action", "specialRequirements" : "Evening shift, Some overnight as necessary, Operates all equipment, Frequently lifts up to 10 lbs, Occasionally lifts up to 50 lbs, Sit, stand, walk, twist, bend, Exposure to infectious agents, Exposure to human blood, Exposure to body fluids, Wear safety protection, Handle stressful situations, May be required to travel", "outcomesObjectives" : "Achieve Advocate Health goals; Achieve Advocate Health objectives", "qualificationsBasic" : "3 years of experience in technical laboratory services and operations, Bachelor's Degree in Clinical Laboratory Sciences or Medical Technology or equivalent, Medical Laboratory Scientist (MLS) certification issued by the American Society for Clinical Pathology Board of Certification (ASCP BOC), Medical Technologist (MT) certification issued by the American Society for Clinical Pathology (ASCP) or equivalent accrediting agency", "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "**Department:** 60901 Navicent Health Medical Center: Baldwin - Lab **Status:** Full time **Benefits Eligible:** Yes **Hou****rs Per Week:** 40 **Schedule Details/Additional Information:** Monday - Friday (no weekends or holidays) Evening shift - 1p - 1030p - some overnight as necessary **Pay Range** $41.10 - $61.65 \"This position is Sign-on Bonus eligible.\" Based on eligibility requirements. **Job Summary:** Responsible for laboratory operations in the technical area(s) of the Hospitals and Clinics within the Advocate Health enterprise, which may include department, discipline and/or shift oversight. Supervises the implementation of enterprise laboratory strategies and standards through close collaboration with site leaders. Ensures peak laboratory operations by driving optimization of resources, financial performance, growth, safety, teammate engagement, and quality in achieving Advocate Health goals and objectives including planning, monitoring, and implementing laboratory operations in a cost effective, quality and service-oriented manner. **Major Responsibilities:** * Assumes responsibility for the day-to-day operations of the department including providing work direction, expertise, and guidance to the staff. Oversees the clinical laboratory testing, evaluation of results, and the proficiency of testing. * Actively participates in projects to meet strategic initiatives including implementation and development of quantitative outcomes. * Monitors budget compliance. Analyzes laboratory fiscal needs, and departmental performance and takes action to address variances. * Collaborates and implements performance improvement processes to optimize teammate engagement, and physician and patient satisfaction. * Ensures quality, regulatory, accreditation, compliance and competency standards are met. Ensures compliance with current policies, procedures, and standardization and/or consolidation decisions. * Coordinates orientation, training, and competency testing of staff and/or students. Maintains competency, as needed, in test systems and processes in defined discipline for area of responsibility. Serves as a technical resource for staff. * Complies with the quality plan by implementing and monitoring quality indicators. Reviews laboratory results for quality, accuracy and validity. Documents and implements corrective action as appropriate. * Selects, coaches, and develops team. Sets clear expectations to inspire and motivate the team. Manages performance by recognizing achievement, providing feedback, and administering progressive discipline when necessary. Recommends hiring, compensation changes, promotions, corrective action decisions, and terminations. * Responsible for understanding and adhering to the organization's Code of Ethical Conduct and for ensuring that people actions, and the actions of employees supervised, comply with the policies, regulations, and laws applicable to the organization's business. **Licensure, Registration, and/or Certification Required:** * Medical Laboratory Scientist (MLS) certification issued by the American Society for Clinical Pathology Board of Certification (ASCP (American Society for Clinical Pathology) BOC), or * Medical Technologist (MT) certification issued by the American Society for Clinical Pathology (ASCP) or equivalent accrediting agency. **Education Required:** * Bachelor's Degree in Clinical Laboratory Sciences or Medical Technology or equivalent **Experience Required:** * Typically requires 3 years of experience in technical laboratory services and operations. **Knowledge, Skills & Abilities Required:** * Demonstrated leadership skills including project management, decision making, delegation, team building, customer service, and conflict resolution. * Ability to grow leaders through coaching, guidance, and development planning. * Advanced knowledge of regulatory compliance, accrediting and licensing agency requirements. * Current knowledge of medical and technical advancements to plan for future growth and development. * Intermediate computer skills including knowledge and experience with laboratory information systems. * Excellent organization and communication skills. **Physical Requirements and Working Conditions:** * Operates all equipment necessary to perform the job. * Frequently lifts up to 10 lbs. Occasionally lifts up to 50 lbs. * Must be able to sit, stand, walk, twist and bend the majority of the workday. * May be exposed to mechanical, electrical, and/or infectious agents. * Will be exposed to human blood and body fluids. * Must wear appropriate safety protection, i.e. laboratory coats, gloves, gowns and/or eye protection. * Must be able to handle stressful situations in a calm and professional manner. * May be required to travel, therefore may be exposed to inclement weather and adverse road conditions. _This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the incumbent. Incumbent may be required to perform other related duties._ **Our Commitment to You:** Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including: **Compensation** * Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training * Premium pay such as shift, on call, and more based on a teammate's job * Incentive pay for select positions * Opportunity for annual increases based on performance **Benefits and more** * Paid Time Off programs * Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability * Flexible Spending Accounts for eligible health care and dependent care expenses * Family benefits such as adoption assistance and paid parental leave * Defined contribution retirement plans with employer match and other financial wellness programs * Educational Assistance Program Note: Eligibility for programs listed above may depend on your FTE or status (e.g., full-time, part-time, per diem, temporary, etc.); please ask a Recruiter for more information during an interview. **About Advocate Health** [Advocate Health](https://www.advocatehealth.org/) is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names [Advocate Health Care](https://www.advocatehealth.com/) in Illinois; [Atrium Health](https://atriumhealth.org/) in the Carolinas, Georgia and Alabama; and [Aurora Health Care](https://www.aurorahealthcare.org/) in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with [Wake Forest University School of Medicine](https://school.wakehealth.edu/) serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation’s largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.", "summaryDescription" : "Clinical Laboratory Supervisor at Atrium Health. Skills: Laboratory operations, Team development, Quality management. Provide work direction, expertise, and guidance to staff. 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" : 579.6369, "daysOld" : 3, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare" }, { "id" : "69cf26122beec4dd3d90b4f7", "title" : "Medical Laboratory Technologist III", "salary" : { "min" : 75000.0, "max" : 105000.0, "currency" : "USD", "frequency" : "yearly", "is_estimated" : true, "estimation_basis" : "Market baseline for a Medical Laboratory Technologist III in Spring Hill, United States, adjusted for mid-seniority in the healthcare industry." }, "location" : "United States-Florida-Spring Hill", "locations" : [ "United States-Florida-Spring Hill", "
TGH Spring Hill (TGHSPRGHLL)
10461 Quality Drive

Spring Hill, 34609

" ], "certifications" : [ "Clinical Lab Technologist Certification", "American Society of Clinical Pathology (ASCP)", "American Medical Technologists (AMT)" ], "timestamp" : "2026-06-15T08:42:53.195", "fingerprint" : "c4cb6042cf8c262021cb45ccbd4780160dc2d11b14e3503e84100e8a1f43fa9f", "source" : "taleo", "language" : "en", "applyUrl" : "https://tgh.taleo.net/careersection/ex/jobdetail.ftl?job=675286", "externalId" : "675286", "industryFunction" : { }, "structuredLocations" : [ { "city" : "Spring Hill", "state" : "Florida", "country" : "United States", "continent" : "na", "source" : "llm", "workMode" : "onsite", "geo" : "28.4635266,-82.5363557" } ], "locationText" : "Spring Hill, Florida, United States", "minimumEducation" : "Associate's", "domainKnowledge" : "Laboratory licensure specialties; Microbiology; Serology; Clinical Chemistry; Hematology; Immunohematology; CLIA; TJC", "domainList" : [ "laboratory-licensure-specialties", "microbiology", "serology", "clinical-chemistry", "hematology", "immunohematology", "clia", "tjc" ], "domainSpecificKnowledge" : [ "Laboratory licensure specialties", "Microbiology", "Serology", "Clinical Chemistry", "Hematology", "Immunohematology", "CLIA", "TJC" ], "remoteFriendly" : false, "workSiteFlexibility" : "Onsite", "rawDescription" : "Performs all approved laboratory procedures in assigned licensure specialties, as required to meet workload demands. coordinating lab resources as outlined below. Precisely and accurately performs and evaluates a variety of technical procedures. Utilizes accepted quality control techniques by manual, semi -automated, or automated methodologies and equipment. Essential Functions Perform work according to established laboratory policies and procedures. Demonstrate the ability to work independently in all areas covered by the FL license. Perform quality control for all tests, evaluate results, and take corrective action as necessary before reporting patient results. Assess specimen integrity for appropriateness of ordered tests, including issues like QNS, hemolysis, and clotting. Ensure procedures, methodologies, and patient results correlate with age-specific criteria for geriatrics, adults, pediatrics, and neonates. Repeat and report all panic/critical test results to a licensed caregiver within 5 minutes of completion. Perform calibrations and maintenance as required by instrument manufacturers, CLIA, and TJC. Complete proficiency testing samples within the requested timeframe. Demonstrate competency in using the LIS and HIS computer systems. Ensure adequate supplies are available and promptly notify the supervisor when supplies are low. Education Associate's Degree Medical Technology or Bachelors Biology or Chemistry License Clinical Lab Technologist Certification American Society of Clinical Pathology (ASCP) or American Medical Technologists (AMT) Work Experience Licensed in all 5 specialties, Microbiology, Serology, Clinical Chemistry, Hematology, Immunohematology Spring Hill", "summaryDescription" : "Medical Laboratory Technologist III", "createdAt" : "2026-06-14T08:25:29.788", "lastUpdated" : "2026-06-15T08:42:53.195", "ingestTimestamp" : "2026-06-14T08:25:29.788", "mongoId" : "69cf26122beec4dd3d90b4f7", "processingStatus" : "llm_updated", "llmProcessingStatus" : true, "salaryAnnualMin" : 75000, "salaryAnnualMax" : 105000, "salaryBand" : "75k-100k", "hasSalary" : true, "allSkills" : [ "Laboratory licensure specialties", "Microbiology", "Serology", "Clinical Chemistry", "Hematology", "Immunohematology", "CLIA", "TJC", "Clinical Lab Technologist Certification", "American Society of Clinical Pathology (ASCP)", "American Medical Technologists (AMT)" ], "skillCount" : 11, "jobCategory" : "operations", "jobSubcategory" : "general", "seniorityLevel" : "Mid", "dataQualityScore" : 0.5555556, "_score" : 579.19385, "hasLocation" : true, "hasGeo" : true, "llmIndustry" : "Healthcare", "llmIndustryConfidence" : 0.95 } ], "status" : 200, "message" : "OK", "pagination" : { "page" : 0, "limit" : 50, "totalCount" : 19921, "totalPages" : 399, "hasNext" : true, "hasPrevious" : false } }

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