• Director, Quality Assurance

    Catalent Pharma Solutions (San Diego, CA)
    …with at least five (5) years' of experience in Quality Assurance or Regulatory Affairs with progressive responsibilities; + Experience in managing people, ... Director of Quality Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose...of the Site Leadership Team working with the General Manager to create and sustain a site culture of… more
    Catalent Pharma Solutions (10/11/25)
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  • Sr. Quality Engineer

    Envista Holdings Corporation (Brea, CA)
    …whether to accept the product and future purchases from the vendor. + Supports Regulatory Affairs with their activities related to submissions and notified body ... to develop, implement, and maintain quality assurance protocols that comply with regulatory requirements an industry standard. The Sr. Quality Engineer will possess… more
    Envista Holdings Corporation (11/15/25)
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  • Medical Safety Specialist II

    Olympus Corporation of the Americas (Center Valley, PA)
    …Medical & Scientific Affairs as well as Infection Prevention & Control, Quality Affairs & Regulatory Affairs , Research & Development, Legal, and Health ... an integral role in the day-to-day functioning of the global medical safety organization. In this vital role, you...Olympus therapeutic areas. You will report directly to the Senior Director Medical Safety as a member of the… more
    Olympus Corporation of the Americas (10/23/25)
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  • Regulatory Writing Sr Mgr

    Amgen (Washington, DC)
    …over 10 million patients worldwide. It's time for a career you can be proud of. ** Regulatory Writing Senior Manager ** **Live** **What you will do** Let's do ... Serve as functional area lead on product teams (eg, Global Regulatory Team, Evidence Generation Team, ...of directly related experience **Preferred Qualifications:** + Experience with regulatory documents in Regulatory Affairs ,… more
    Amgen (11/22/25)
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  • Executive Director, Quality Large Molecule…

    Merck (West Point, PA)
    …biologics and vaccines. The role also requires extensive engagement with Manufacturing, QA, Regulatory Affairs , and Supply Chain. The ideal candidate should have ... will report to this position. + Ensure GMP/GLP and global regulatory compliance; prepare for and respond...biologics. Must have at least 5 years as a manager in a supply focused team (ie critical reagents,… more
    Merck (11/22/25)
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  • Quality Assurance Batch Release Lead

    Sanofi Group (Swiftwater, PA)
    …Participating in internal and external audits and inspections + Collaborating with regulatory affairs to ensure compliance with local and international ... **Job Title:** Batch Release Lead **Grade:** L3 **Hiring manager :** Martin Razo **Location:** Swiftwater, PA **About the...a beautiful park like campus. We are an innovative global healthcare company with one purpose: to chase the… more
    Sanofi Group (10/03/25)
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  • Staff Quality Assurance Engineer

    Danaher Corporation (Indianapolis, IN)
    …and ensuring product quality for Beckman's customers. This position reports to the Senior Manager Manufacturing Quality and is part of the Quality & ... for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory. It's all part... Regulatory Affairs organization located in Indianapolis, IN.… more
    Danaher Corporation (10/28/25)
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  • Principal Research Scientist I, Tissue Material…

    AbbVie (Irvine, CA)
    …and engage key stakeholders, including global strategic marketing, medical affairs , regulatory affairs , clinical development, and publication planning ... for purposes of establishing device proof of concept, completing regulatory submission-related studies (ISO 10993), performing life cycle compliance-related… more
    AbbVie (09/23/25)
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  • Specialist - Regulatory Operations…

    Novo Nordisk (Plainsboro, NJ)
    Regulatory Operations and works cross-functionally with internal departments on Regulatory Affairs related issues. Essential Functions + With direction from ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...to FDA and Health Canada. This individual also supports senior staff with required systems and process maintenance. Responsible… more
    Novo Nordisk (11/21/25)
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  • Architectural Practice Lead

    Jacobs (Los Angeles, CA)
    …each project you will directly interface and collaborate with the discipline leads, senior Project Architect and Design Manager . You are accountable for setting ... degree in Architecture from an accredited University * Professional Registered Architect ( RA ) * 15+ years of AEC buildings experience as a client-facing Design… more
    Jacobs (09/27/25)
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