• Head of Site Quality Operations

    Sanofi Group (Swiftwater, PA)
    …Background in manufacturing and development, Quality Assurance, Quality Control, and Regulatory Affairs . + Competencies (LEAD model) - key competencies ... are distributed throughout the world. This position guarantees the Quality and Regulatory compliance of products developed, manufactured and distributed by the site… more
    Sanofi Group (11/05/25)
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  • Principal Design Quality Engineer - Medical Device

    Kelly Services (Peachtree Corners, GA)
    …role partners closely with cross-functional teams, including Operations, R&D, Regulatory Affairs , Marketing, and Quality Assurance. **Qualifications** ... Quality Engineer** **Location:** Norcross, GA **Overview** We are seeking an experienced ** Senior Design Quality Engineer** to join our team in Peachtree Corners,… more
    Kelly Services (11/25/25)
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  • Associate Director, Oncology AI Biomarkers…

    J&J Family of Companies (Spring House, PA)
    …radiomics, etc. across R&D and early and late-stage clinical development, ensuring scientific rigor and regulatory compliance. + Collaborate with internal ... biomarker discovery, translational research, computer vision, clinical development, medical affairs , diagnostics, regulatory , and commercial teams to assess… more
    J&J Family of Companies (10/05/25)
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  • Associate Director, QA Engineering - Combo…

    United Therapeutics (Research Triangle Park, NC)
    …across multiple functional groups (eg, Research and Development, Manufacturing, Validation, Regulatory Affairs , etc.). Negotiate and manage expectations across ... Control, Quality Event, and CAPA programs and supporting management during regulatory agency(ies) inspections, third-party partners, and customer audits. + Work… more
    United Therapeutics (09/26/25)
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  • Lead, HCP Marketer

    Chiesi (Cary, NC)
    …reports. Main Responsibilities + Work directly with the Head of Marketing and other senior leaders to develop go to market strategies and market leading brand plans ... + Work closely with Medical Affairs and Commercial leadership to develop and nurture relationships...and execution of the customer engagement plan. + Attend scientific meetings to stay updated on industry trends, best… more
    Chiesi (11/15/25)
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  • Regional Clinical Study Manager

    BeOne Medicines (San Mateo, CA)
    …in assigned region in close collaboration with regional study start up team and regulatory affairs + Ensures regional and country information in study systems ... the region and provides regular updates on study progress in the region to senior management and Global Clinical Study Manager as required + Represents the regional… more
    BeOne Medicines (10/29/25)
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  • Director, Product Security - MMS Dispensing

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …This role works in close partnership with R&D, Enterprise Security, Quality, Regulatory Affairs , Legal, business leaders and functional authorities at corporate, ... with all levels and geographies within the Dispensing platform, including senior executives, to advance the product security strategy and objectives within… more
    BD (Becton, Dickinson and Company) (10/10/25)
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  • Site Quality Head

    Gilead Sciences, Inc. (La Verne, CA)
    …+ Serve as the site's quality representative to global quality leadership and regulatory agencies. **Compliance & Regulatory Affairs ** + Ensure site-wide ... team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve… more
    Gilead Sciences, Inc. (11/14/25)
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  • Associate Director, US Medical Neuroscience,…

    Bristol Myers Squibb (Princeton, NJ)
    …areas to ensure alignment. The Associate Director will report to the Senior Director, US Medical Neuropsychiatry. Responsibilities + Participate in Medical Matrix ... with stakeholders on medical activities including labeling, safety surveillance, scientific advisory boards, congress support, competitive intelligence, realworld data… more
    Bristol Myers Squibb (10/30/25)
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  • Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Boise, ID)
    …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to ... drug substance and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols and timelines,… more
    Otsuka America Pharmaceutical Inc. (11/25/25)
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