• Facilities Maintenance Planner (R&D)

    Mentor Technical Group (Redwood City, CA)
    …provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering and technical ... overseeing work order activity compliance with respective regulatory requirements (ie FDA , DEA, OSHA). + Manage Work through the Computerized Maintenance Management… more
    Mentor Technical Group (08/28/25)
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  • Sr. R&D Engineer (Process Development) - Shockwave

    J&J Family of Companies (Santa Clara, CA)
    …in full compliance with the company's Design Control requirements and consistent with FDA , ISO, and MDR requirements + Prototype and develop designs, processes, and ... Support company goals and objectives, policies and procedures, Quality Systems, and FDA regulations + Other duties as assigned **Requirements** + Bachelor's degree… more
    J&J Family of Companies (08/28/25)
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  • Manufacturing Technician - (Graveyard Monday…

    Grifols Shared Services North America, Inc (Los Angeles, CA)
    …plasma derived pharmaceuticals. .Strict adherence to procedures and practices according to FDA regulations. .Strong emphasis on documentation according to FDA ... regulations. .Adhere to departmental corporate safety policies. .Responsible for facility and equipment cleaning. .All work is performed in a clean room (sanitized) manufacturing environment. .Responsible for performing the following daily tasks: cleaning/… more
    Grifols Shared Services North America, Inc (08/28/25)
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  • Validation Associate III

    Wacker Chemical (San Diego, CA)
    …or engineering (Chemical, Mechanical, or related field) + 5-8 years of experience in a FDA and GMP regulated industry. + ISO 7 & ISO 8 gowning experience is ... as well as Microsoft Office Suite. + Knowledge of regulatory requirements, including FDA , GMP, and ISO standards. + Requires good written, verbal, and interpersonal… more
    Wacker Chemical (08/28/25)
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  • Senior Regulatory Labeling Specialist (Ad/Promo)…

    Medtronic (Irvine, CA)
    …and author new process documents + Monitor changes and compliance with applicable FDA and international regulatory laws/standards and the Medtronic Code of Conduct + ... and approval systems + Excellent communication & organizing skills + Knowledge of FDA , EU, and TGA requirements + Knowledge of Neurovascular brain therapies +… more
    Medtronic (08/28/25)
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  • Senior Operations Supervisor

    Biomat USA, Inc. (Bakersfield, CA)
    …all state and federal regulations, US Food and Drug Administration ( FDA )-approved Standard Operating Procedure Manual, Occupational Safety and Health Administration ... highest production standards in accordance with Federal and State regulations, with FDA approved Standard Operating Procedure Manual, OSHA, CLIA and cGMP. + Attends… more
    Biomat USA, Inc. (08/28/25)
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  • Clinical Research Coordinator III - Miriad IBD…

    Cedars-Sinai (Los Angeles, CA)
    …all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board (IRB). **Primary Job Duties and ... with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. + Maintains research practices using Good… more
    Cedars-Sinai (08/27/25)
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  • Quality Operations Specialist

    Astrix Technology (Irvine, CA)
    …teams to drive product and process improvements + Maintain compliance with FDA , ISO 13485, and global quality standards + Assist with manufacturing line ... and documentation skills + Proficient in Microsoft Excel **Preferred:** + Knowledge of FDA regulations (21 CFR 820/803), ISO 13485 + Experience with medical device… more
    Astrix Technology (08/27/25)
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  • Clinical Research Associate I - Miriad IBD Biobank…

    Cedars-Sinai (Los Angeles, CA)
    …study budget and patient research billing. Ensures compliance with all federal, local, FDA , IRB, and HIPAA guidelines and regulations pertaining to the study and ... with all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. + Maintains research practices using Good… more
    Cedars-Sinai (08/27/25)
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  • Senior Director, Operations CIO - Manuf, Quality…

    Medtronic (Northridge, CA)
    …and business impact. + Ensure compliance with all regulatory, audit, and FDA requirements in manufacturing and quality. + Drive accountability and transparency ... leading multi-disciplinary IT teams across multiple sites. + Experience in FDA -regulated or similarly controlled environments strongly preferred. + Proven ability to… more
    Medtronic (08/27/25)
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