• Software Quality Engineer II

    Abbott (Sylmar, CA)
    …Strong organizational and project management skills. + Ability or aptitude to lead without direct authority. + Programming experience in C/C++/C#, Scripting Language ... Doors, Bugzilla. + Knowledge of FDA 21 CFR part 820, 21 CFR part 11, GMP , IEEE 1012, IEC 62304 and ISO 13485. + Advanced computer skills, including statistical/data… more
    Abbott (11/18/25)
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  • Project Manager

    Takeda Pharmaceuticals (Los Angeles, CA)
    …product development requirements to meet customer and stakeholder expectations. + ** Lead Project Execution:** Establish project strategies, set goals, assign tasks, ... disciplines; PMP certification preferred. + **Regulatory Knowledge:** Familiarity with GMP principles, FDA guidelines, and purchasing practices. + **Analytical &… more
    Takeda Pharmaceuticals (11/16/25)
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  • QA Technician I $23.95

    JBS USA (Manteca, CA)
    …and documentation + Metal Detector calibrations & documentation. + Operational GMP & Sanitation Observations throughout entire plant. + Supervision of proper ... Check bellies at Bacon Press forproper temperature and feel of belly + Lead and document leaker checks + Verifying timeliness and accuracy of production… more
    JBS USA (11/16/25)
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  • QC Associate Scientist - CMC Analytical - Swing…

    LGC Group (Petaluma, CA)
    …closely with its customers to assist the identification and development of lead candidates with a broad suite of bioinformatics, biology, chemistry, manufacturing ... determine accuracy and precision of analysis + Demonstrating a familiarity with GMP guidelines 21 CFR Part 210/211 and ICHQ7 Qualifications Minimum Qualifications: +… more
    LGC Group (11/15/25)
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  • Digital Transformation Program Manager

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …2027._** **Responsibilities:** + Support the implementation of the global strategy and co- lead deployment and execution of the eDHR / other digital technology ... initiatives in Medical Device, Pharmaceutical, or other regulated industry ( GMP , GLP). + Knowledge of Standard Laboratory Practices **Preferred Qualifications:**… more
    BD (Becton, Dickinson and Company) (11/15/25)
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  • Sr. Quality Engineer

    Envista Holdings Corporation (Brea, CA)
    …engineering reviews of design documentation for compliance with stated requirements. + Lead complex technical problems where analysis of situations or data requires ... current process and process changes. + Maintains a working knowledge of FDA GMP , ISO 13485 standards and other applicable standards. + Documents data obtained during… more
    Envista Holdings Corporation (11/15/25)
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  • HVAC Technician

    Amentum (San Diego, CA)
    …to be successful in the assignment. + Performing other duties as assigned by Management or Lead . As the HVAC Technician you will be expected to: + Work in a team ... Requirements** + Technical degree preferred. + Experience working in a GMP or similar regulated environment such as hospitals, biomedical or pharmaceutical… more
    Amentum (11/14/25)
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  • Buyer Associate

    Ferguson Enterprises, LLC. (Novato, CA)
    …working in a fast-paced and highly collaborative team environment to effectively lead and drive process improvements. **Responsibilities:** + Perform a range of ... + Previous experience in a buyer role preferred + Good Manufacturing Practice ( GMP ) experience preferred + Proven ability to follow documented procedures + Knowledge… more
    Ferguson Enterprises, LLC. (11/13/25)
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  • Director, Quality Control Lab

    Herbalife (Lake Forest, CA)
    …Metrics. Leverage data to improve product quality and laboratory efficiency. + Lead laboratory operations and maintain the laboratories in compliance with ISO17025 ... in ISO17025 requirements + Strong proven hands-on experience with variety of both GMP and GLP matters + Strong verbal and written communication skills with ability… more
    Herbalife (11/13/25)
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  • Senior Supplier Quality Engineer

    Abbott (Irvine, CA)
    …experiments for process optimization and/or improvement * Participate in or lead teams in supporting Supplier Development Quality program requirements (eg, represent ... engineering and use of quality tools/methodologies. + Strong knowledge of FDA regulations, GMP , ISO 13485, and ISO 14971. + Experience with SAP and maintaining… more
    Abbott (11/13/25)
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