Laboratory Manager
$100k - $200kAbbott
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life‑changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution. Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit – an affordable and convenient path to getting a bachelor’s degree. A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune. A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position works out of our San Diego, CA location in the Abbott Infectious Disease Unit. We’re empowering smarter medical and economic decision‑making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people. The person hired in this role will be responsible for managing laboratory operations within a multi‑disciplinary R&D environment supporting development of in‑vitro diagnostic (IVD) products. Ensures laboratories operate safely, efficiently, and in compliance with Abbott Quality System requirements, including FDA Quality System Regulation (21 CFR Part 820) and ISO 13485, as well as applicable biosafety standards. What You’ll Work On Uses professional concepts and company objectives to resolve complex laboratory operational issues in creative and effective ways. Applies comprehensive knowledge of laboratory operations to support R&D objectives in a regulated environment. Ensures compliance with Abbott Quality Systems, FDA QSR, and ISO 13485 requirements. Leads biosafety and laboratory compliance programs consistent with CDC, NIH, and OSHA regulations. Establishes and enforces proper PCR laboratory workflow design (e.g., unidirectional workflow, physical segregation of pre‑ and post‑amplification areas, contamination control practices) to minimize risk of amplicon contamination. Implements and monitors controls such as dedicated equipment, consumables, cleaning protocols, and environmental monitoring to prevent cross‑contamination in molecular workflows. Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors. Maintains laboratories in an inspection‑ready state and supports internal and external audits. Manages lifecycle, calibration, and maintenance of laboratory equipment including freezers, centrifuges, PCR systems, analytical instruments, balances, and pipettes. Coordinates equipment qualification, preventive maintenance, and vendor service contracts. Oversees sample handling, biorepository operations, and chain‑of‑custody controls. Supports compliant shipment and receipt of biological materials per IATA and DOT regulations. Drives 5S implementation to maintain an organized, efficient, and safe lab environment supporting R&D Excellence. May determine methods and procedures on new assignments and provide guidance to staff. Collaborates cross‑functionally with R&D, Quality, Regulatory, EHS, and Facilities. Drives continuous improvement initiatives to enhance operational efficiency and compliance. Required Qualifications Bachelor’s Degree in a related field. 7 years of related experience. Preferred Qualifications Laboratory operations experience in regulated environments such as IVD, medical device, biotechnology, or pharmaceutical industries. Demonstrated knowledge of FDA QSR and ISO 13485 and their application to laboratory operations. 3 years of experience with biosafety programs and laboratory equipment management. Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Abbott is an Equal Opportunity Employer, committed to employee diversity. The base pay for this position is $100,000.00 – $200,000.00. In specific locations, the pay range may vary from the range posted. #J-18808-Ljbffr
- Job Title M-F 8am-5pm Type: Temp to Hire Location: SY King Chavez- 950 S. Euclid Ave. San Diego, CA 92114 Requirements: 5 years of experience as a Senior or Lead CLS Direct experience in point of care testing.SuggestedTemporary work
- Scientific and Laboratory Informatics Manager Our Scientific Informatics practice is where scientific innovation meets leading‑edge technology. We help our clients envision and achieve Digital Laboratory Transformation through co‑creation and application of digital technologies...SuggestedWork at officeLocal area
$85k - $115k
Position Overview Eurofins Advantar Laboratories is seeking a Laboratory Manager - Microbiology to lead microbiology operations at our San Diego site supporting pharmaceutical and medical device clients . This is a people leadership role responsible for overseeing laboratory...SuggestedFull timeMonday to Friday- ...data, processes specimens, and maintains records to ensure regulatory compliance. Under supervision, you will support the Project Manager and Regulatory Manager with study tracking, financial documentation, and trial-related communications across multiple federally funded...Suggested
- ...support community oncologists and patients through various research projects. This full-time role requires coordinating studies, data management, ensuring compliance with regulations, and enhancing patient enrollment strategies. The ideal candidate should hold a BA/BS...SuggestedFull time
- ...the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory... ...product (IP) dispensation and accountability. Coordinate with laboratories to ensure timely testing and reporting. Collect and document...H1bMonday to Friday
$72k - $90k
...compliance with federal regulations, institutional policies, and Good Clinical Practice (GCP) guidelines. This role actively drives and manages relationships with study sponsors and CROs, and serves as the site’s primary point of contact for sponsors, IRB submissions, and...Work at office- ...high unmet medical needs. As the organization continues to grow and expand its clinical pipeline, they are seeking a Clinical Trial Manager to join their Clinical Operations team in San Diego. Position Summary The Clinical Trial Manager will be responsible for overseeing...
- ...Description The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring... ...managing the budgets Solid vendor management skills, e.g. CRO, Laboratory, Clinical supply logistics Developing and maintaining standard...Work at officeLocal areaRemote work
$68k - $73k
...independent decisions about how to target and select participants, and whether a potential participant meets eligibility criteria. Manage and coordinate complex biosurveillance. Study Protocol Design and Oversight: Interprets study protocols, assessing feasibility, and...Remote work- ...Research Center (NHRC), Operational Infectious Diseases (OID) Directorate by coordinating and managing clinical research studies. The OID Directorate conducts ongoing, laboratory-based surveillance of US military populations in unique environments to quantify and study...Contract workTemporary workCasual workLocal areaRemote work
- ...to combine the convenience of an oral therapy with the safety and efficacy that patients deserve. About the Role The Clinical Trial Manager (aCTM) is responsible for supporting the day‑to‑day management of clinical studies from startup through closeout. This role is...Contract workWork at office
- ...The Clinical Trial Manager (CTM) is responsible for the day-to-day operational execution and management of assigned clinical studies in the Rare Disease portfolio. This role focuses on planning, initiating, executing, and closing clinical trials with operational excellence...Contract workLocal area
$131k - $163.6k
...a fast-paced environment. Key responsibilities include: Leading study execution across startup, enrollment, conduct, and closeout Managing cross-functional teams and external vendors Owning timelines, budgets, study plans, and operational deliverables Supporting inspection...3 days per week- ...that provides a broad range of consulting services to US Federal Government, US Military, and Commercial clients. Services include Management & IT Consulting, Program & Project Management, and Professional & Admin Services. We can't sponsor H1B. We accept direct hire...Full timeH1bWork at office
$45k - $100k
...day-to-day execution of clinical trials. This includes working directly with patients, coordinating study visits, collecting and managing data, and ensuring studies are conducted in compliance with protocols and regulatory requirements. CRCs work closely with investigators...InternshipLocal area$80k
...related to TBICoE clinical investigations. Communicates with research participants, staff, regulatory affairs and data management groups, laboratory and clinical investigators, management and outside collaborators. Recruits, interviews, and screens TBICoE clinical...Full timeContract workTemporary workWork experience placementLive outWork at officeLocal areaRemote workFlexible hoursWeekend workAfternoon shift$36.31 per hour
...Research Supervisor, the CRC may: provide training, data and chart management, quality assurance check for studies, provide backup to... ...applications such as Velos, Access, Excel and MS Word. Experience with laboratory procedures and values and experience in interpreting them to...Hourly payTemporary workMonday to FridayAfternoon shift$145k - $190k
...Clinical Trial Manager/Sr Clinical Trial Manager Erascais a clinical-stage precision oncology company focused on discovering, developing... .... Experience with managing study vendors (e.g., CRO, IRT, laboratories, core ECG/imaging). Ability to work well with global, multi-disciplinary...Temporary workCasual workLocal areaWorldwideFlexible hours- Platinum Dermatology Partners is seeking a full-time Research Coordinator in San Diego, CA. This role focuses on administering clinical trial research, including patient recruitment, data collection, and compliance with FDA guidelines. Candidates should have a Bachelor’...Full time
- ...Health in San Diego is looking for a Senior Clinical Research Coordinator to lead clinical research trials from start to finish. You'll manage operations, participants, and compliance with regulations while fostering relationships with sponsors. The ideal candidate has over...
$38 - $41 per hour
...guidelines and study protocols, and facilitate daily clinical trial activities (subject recruitment, screening, and enrollment). Collect laboratory specimens, informed consent, and other data from the subject. Maintain source documents, including CRF (case report form)...Hourly payFull timeTemporary workWork at office$70k - $80k
Clinical Research Coordinator The Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed ...Full timeLocal areaShift work$90k - $130k
...Job Overview Labcorp is seeking a Histology Laboratory Supervisor to join our grossing team in San Diego, CA. Work Schedule Monday - Friday 7:30am - 4:00pm Job Responsibilities Manage daily operations of assigned laboratory group to ensure specimens properly shipped and...Work at officeLocal areaMonday to FridayFlexible hours- ...to day operations of the Department/Lab Name department Ensure laboratory tests are accurately performed and results are reported in a... ...state and Federal regulations Responsible for administering and managing policies and procedures Process and maintain payroll and...Hourly payWork at officeAll shiftsMonday to FridayFlexible hoursAfternoon shift
- ...specific conferences as appropriate. Provides support to the Project Manager, Regulatory Manager, or Clinical Research Coordinator with... ..., and weight; scheduling study visits; coordinating clinical, laboratory, and data collection activities; processing and shipping...
- About AbbVie AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. They strive to have a remarkable impact on people’s lives across immunology, oncology, neuroscience...Temporary workLocal area
$125k - $135k
Millennium Health in San Diego seeks a Supervisor for the Analytical Laboratory. This role includes oversight of laboratory processes, supervision of testing personnel, and ensuring compliance with safety and quality standards. The ideal candidate should have a Bachelor...- ...functional teams in writing and verbal presentations as needed. Effectively communicate complex technical topics to collaborators and management. Qualifications PhD in Chemistry, Biochemistry, or Pharmaceutical Sciences with 8+ years related experience in the...Temporary workLocal area
- ...What You Will Do Support the progress of 2-5 hardware‑focused human subjects research studies under the guidance of Research Project Managers and Research Scientists Gain expertise in new and evolving data collection capabilities of the Oura Ring and the research studies...Work at officeLocal areaFlexible hours3 days per week
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