• Machinist 1 - 2nd Shift M-F (3:00 PM - 11:30 PM)

    GE HealthCare (State College, PA)
    …using precision measuring instruments (micrometers, calipers, CMMs). + Maintain documentation in compliance with FDA , ISO 13485, and GMP standards. + Collaborate ... with quality assurance and engineering teams to ensure product conformity. + Maintain a clean and organized work area, adhering to cleanroom protocols when required.… more
    GE HealthCare (08/23/25)
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  • Documentation Clerk

    Mentor Technical Group (Carolina, PR)
    …provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering and technical ... solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With… more
    Mentor Technical Group (08/21/25)
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  • R&D Fellow, Systems Engineering, Interventional…

    Philips (San Diego, CA)
    …and implementing solutions through product development, integration and V&V, ensuring compliance with medical device standards and global regulatory requirements. + ... 60601, IEC 62304, IEC 62366, UL, ANSI, ASTM, ISO, FDA ). + You must be able to successfully perform...won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work… more
    Philips (08/21/25)
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  • Exec Director, Formulation & Process Development

    Gilead Sciences, Inc. (Foster City, CA)
    …cGMP environment (internal and external cGMP manufacturing operations) and compliance requirements. + Provide guidance and strategic directions through interactions ... data management + Lead collaborations with Gilead PDM functions such as Quality Assurance, CMC Reg, Manufacturing and Technical Operations, Product and Portfolio… more
    Gilead Sciences, Inc. (08/20/25)
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  • Associate Engineering Fellow, Combination Product…

    Takeda Pharmaceuticals (Lexington, MA)
    …/ implement contingency plans as required. + Lead the project execution in compliance with design control SOP. Oversee technical aspects of the development process ... **Knowledge and Skills:** + Strong knowledge of developing and commercializing FDA regulated devices / combination products under Design Control regulations and… more
    Takeda Pharmaceuticals (08/20/25)
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  • AD Market Research/Competitive Intelligence - CRM

    Boehringer Ingelheim (Ridgefield, CT)
    …BI personnel in other countries Ensures that corporate standards of excellence and compliance are upheld and performs all Company business in accordance with all ... regulations (eg EEO, FDA , OSHA, PDMA, EPA, PhRMA, SCIP etc.) and Company...Continuous Improvement: Share knowledge of research methodologies and high quality vendors with other managers in the department. Improve… more
    Boehringer Ingelheim (08/19/25)
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  • Customer Fulfilment Manager

    Sanofi Group (Morristown, NJ)
    …packaging, labeling and distribution activities and partnership initiatives + ** Compliance Oversight:** Ensure all outsourced activities and partnerships comply with ... FDA regulations, cGMP requirements, and internal procedures **About You**...a wide range of health and wellbeing benefits including high- quality healthcare, prevention and wellness programs and at least… more
    Sanofi Group (08/17/25)
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  • Patient Delivery Rep, Rx Partners (Casual)

    UPMC (Bridgeville, PA)
    …in timely, safe and accountable manner. + Promote UPMC culture by providing quality , comprehensive services to all customers through a team approach. + Complete ... and/or equipment according to policy. + Maintain accurate and complete records in compliance with State, local, and Federal laws and/or regulations (including FDA more
    UPMC (08/16/25)
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  • Corporate Wellness Manager (Dietitian)

    Compass Group, North America (San Francisco, CA)
    …policies to implement wellness related programs and initiatives and to ensure compliance with FDA nutrition labeling laws. **Key Responsibilities:** + ... Manager I.** The **Wellness Manager** implements corporate nutrition programs, supporting quality assurance in areas of nutrition labeling, food allergies and… more
    Compass Group, North America (08/15/25)
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  • Principal Engineer, Idap TS/MS Product (R3 - R5)

    Lilly (Indianapolis, IN)
    …1 year of experience with design and execution of experimental trials in compliance with SOPs, FDA /ICH guidelines, DEA regulations, and safety requirements for ... site. Provide technical support on non-routine investigations, including on quality and stability. Prepare technical documents including annual product reviews,… more
    Lilly (08/15/25)
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