• Associate Director, CAR-T Manufacturing Operations

    Bristol Myers Squibb (Summit, NJ)
    …strategically. Advanced degree preferred. + Minimum of 10 years of relevant pharmaceutical manufacturing experience with 2-3 years of clean room experience. + ... Minimum of 5 years of direct leadership experiences is required. + 5 years of regulatory audit experience is required. + 2-3 years of working it and managing budgets (to include financial and headcount). + 2-3 years of project management. + Lean leadership… more
    Bristol Myers Squibb (08/02/25)
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  • Coordinator, Individualized Care

    Cardinal Health (Trenton, NJ)
    Cardinal Health Sonexus (TM) Access and Patient Support helps specialty pharmaceutical manufacturers remove barriers to care so that patients can access, afford and ... remain on the therapy they need for a better quality of life. Our diverse expertise in pharma, payer and hub services allows us to deliver best-in-class solutions-driving brand and patient markers of success. We're continuously integrating advanced and… more
    Cardinal Health (08/02/25)
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  • US Medical Director, Dermatology (NextGen…

    Sanofi Group (Morristown, NJ)
    …equivalent advanced medical degree. **Work Experience** : + 5+ years of pharmaceutical industry experience in Medical Affairs + Demonstrated expertise in dermatology ... and/or rheumatology + Proven track record of successful biologic product launches + Advanced knowledge of RWE methodologies, data sources, and applications in US healthcare + Understanding of clinical development and regulatory requirements + Experience… more
    Sanofi Group (08/02/25)
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  • Senior Manager GCO Vendor & Relationship…

    Regeneron Pharmaceuticals (Warren, NJ)
    …minimum of a Bachelor's degree i required with 8+ years' experience in pharmaceutical industry or project management related capacity- preferred. + 5+ years' project ... coordinator or project management experience supporting departments and managing multiple projects simultaneously. + 2+ years SharePoint experience + Clinical Development exposure preferred, but not required Does this sound like you? Apply now to take your… more
    Regeneron Pharmaceuticals (08/02/25)
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  • Scientist Product Development (Solid Dosage)

    Nestle (Bridgewater, NJ)
    …Peptamen(R), Compleat Organic Blends(R), and more. We also have extensive pharmaceutical expertise, offering innovative medicines that aim to prevent, manage, and ... treat gastrointestinal and metabolic-related diseases. At Nestle Health Science, we bring our best for better lives. Our people are challenged to bring fresh, diverse views and make bold moves to empower healthier lives through nutrition. We know brilliant… more
    Nestle (08/02/25)
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  • Sr Manager, Medical Affairs

    Gilead Sciences, Inc. (Parsippany, NJ)
    …MBA **Preferred Qualifications** * 6+ years Medical Affairs (medical device/ pharmaceutical industry), managed care, and HEOR experience, required. Ideally including ... recent experience of a successful launch within Oncology or Hematology * Advanced degree in life sciences in one or more of the following: MD, DO, PharmD, PhD * Significant health outcomes research or medical affairs background in oncology (solid tumor or… more
    Gilead Sciences, Inc. (08/01/25)
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  • Sr Manager National Accounts Sales

    Nestle (Bridgewater, NJ)
    …Peptamen(R), Compleat Organic Blends(R), and more. We also have extensive pharmaceutical expertise, offering innovative medicines that aim to prevent, manage, and ... treat gastrointestinal and metabolic-related diseases. At Nestle Health Science, we bring our best for better lives. Our people are challenged to bring fresh, diverse views and make bold moves to empower healthier lives through nutrition. We know brilliant… more
    Nestle (08/01/25)
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  • Medical Director, Clinical Research

    J&J Family of Companies (Raritan, NJ)
    …years of oncology clinical research experience in clinical development within pharmaceutical industry or equivalent experience in academic or large regional hospital ... is required. + Knowledge of Good Clinical Practices and regulatory requirements for the conduct of high quality oncology clinical trials is required. + Experience in protocol development, medical review, oversight of study conduct, running trials, data quality… more
    J&J Family of Companies (08/01/25)
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  • Director, Clinical Development

    Intra-Cellular Therapies, Inc (Bedminster, NJ)
    …+ Minimum 1 -3 year clinical/research experience in the pharmaceutical industry, relevant governmental organizations, or academic research setting required. ... + Ability to travel at least 30% + Ability to work in a team setting as well as function as an individual contributor + Ability to work efficiently and under tight timelines + Ability to communicate effectively + Ability to be flexible in an ever-changing… more
    Intra-Cellular Therapies, Inc (08/01/25)
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  • Associate Director, Regulatory Labeling Strategy

    Organon & Co. (Jersey City, NJ)
    …discipline required; Master's degree preferred. + Minimum of eight years of pharmaceutical or relevant experience with a focus on product labeling inclusive of ... regulatory product labeling (Core, US and EU labeling) requirements for marketed products. + Knowledgeable about key labeling regulatory requirements worldwide, with a key strength in US regulatory requirements. + Excellent written and verbal communication… more
    Organon & Co. (08/01/25)
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