• CSV Engineer

    Sanofi Group (Swiftwater, PA)
    …ways. Within our Sanofi Manufacturing & Supply Ambition, we're redefining our strategy , culture, and processes to make a tangible impact worldwide. In this ... Validation (CSV) lifecycle activities meet Sanofi's quality requirements and fulfil regulatory expectations. + Design and execute validation protocols and testing. +… more
    Sanofi Group (07/02/25)
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  • Senior Manager, Patient Services, Patient…

    Pfizer (Collegeville, PA)
    …support and programs (copay). + Working knowledge of the compliance and regulatory environment for manufacturers in the pharmaceutical space. + Experience ... with the Director, Affordability Solutions and Brand to execute on approved strategy , coordinate program monitoring and vendor management to enabling patients access… more
    Pfizer (08/21/25)
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  • Account Director, Platform Success - IQVIA Digital…

    IQVIA (Wayne, PA)
    …and email. + Familiarity with healthcare marketing and industry dynamics, including regulatory considerations and the unique needs of pharmaceutical clients. + ... a healthcare specific marketing platform trusted by some of the largest pharmaceutical brands and media agencies. We empower media planning, buying, and analytics… more
    IQVIA (07/04/25)
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  • Associate Director - Life Sciences Advisory…

    Guidehouse (Philadelphia, PA)
    **Job Family** **:** Strategy & Transformation Consulting **Travel Required** **:** Up to 50% **Clearance Required** **:** None **What You Will Do** **:** The ... team provides program design, implementation, and monitoring services to pharmaceutical , biotechnology, and medical device, companies. We support our clients… more
    Guidehouse (08/18/25)
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  • Managing Consultant - Life Sciences Advisory…

    Guidehouse (Philadelphia, PA)
    **Job Family** **:** Strategy & Transformation Consulting **Travel Required** **:** Up to 25% **Clearance Required** **:** None Is life sciences in your DNA? ... Guidehouse's Life Sciences practice is an engine of innovation, helping pharmaceutical , biotech, medical device, and diagnostic companies develop custom solutions… more
    Guidehouse (07/04/25)
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  • Oncology Early Stage Clinical Scientist Senior…

    Pfizer (Collegeville, PA)
    …in Early Development + Familiarity with related disciplines (Biostatistics, Regulatory , Pre-Clinical Pharmacology, Pharmaceutical Sciences) + Proven scientific ... + Support the GDL in the execution of the clinical development strategy and plan for the assigned molecule(s)/indication(s) + Depending on experience, may… more
    Pfizer (08/15/25)
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  • Global Development Lead, Medical Director,…

    Pfizer (Collegeville, PA)
    …first-in-human clinical trials with input from Oncology Research Unit, Oncology Regulatory Strategy , Clinical Pharmacology and Precision Medicine, Oncology ... drug development. + Understanding of related disciplines (eg, biostatistics, regulatory , pre-clinical pharmacology, pharmaceutical sciences). + Demonstrated… more
    Pfizer (08/08/25)
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  • Manager, Biostatistics

    Sumitomo Pharma (Harrisburg, PA)
    …Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) strategy for NDA/BLA submissions, ensuring compliance with regulatory expectations. + ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations...maintain the statistical integrity of study conduct. + Support regulatory submissions by preparing responses to agency inquiries and… more
    Sumitomo Pharma (08/02/25)
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  • Sr Associate, Technical Sales- Integrated Systems

    West Pharmaceutical Services (Exton, PA)
    …the customer pipeline and aligning the appropriate Integrated System product. Develop additional strategy to continue to expand the West reach with new accounts as ... serviced. + Understand market trends including relevant competitors, technology and regulatory issues to keep customer informed + Utilize all service platforms,… more
    West Pharmaceutical Services (07/19/25)
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  • Senior Director, MSAT Biologics

    Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
    …partners. **Key Responsibilities:** + Develop and implement the overall MSAT strategy supporting the company's portfolio, focusing on technical oversight of CDMO ... process validation lifecycle (PPQ, CPV, etc.) ensuring compliance with global regulatory standards. + Establish and oversee robust Continued Process Verification… more
    Otsuka America Pharmaceutical Inc. (07/15/25)
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