• Technical Writer II

    Adecco US, Inc. (Morristown, NJ)
    …organizational templates. + Collaborate with cross-functional teams including Quality, Manufacturing, Global Regulatory Affairs , and Contract Manufacturing ... Adecco Healthcare & Life Sciences is seeking a skilled ** CMC Regulatory Technical Writer II** to support a global pharmaceutical client in lifecycle… more
    Adecco US, Inc. (12/11/25)
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  • Associate Director, Principal Product Quality Lead

    Bristol Myers Squibb (Madison, NJ)
    …Stability, Analytical Development, Process Development, Manufacturing Sciences and Technologies, Regulatory Affairs , and other Cell Therapy Development ... QA, QC, analytical and process development, manufacturing sciences and technology, and regulatory affairs functions. + Supports the overall product quality… more
    Bristol Myers Squibb (12/24/25)
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  • GRA Device Associate

    Sanofi Group (Morristown, NJ)
    …their families. Your skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse ... of products. The team is part of the GRA CMC & GRA Device Department within Global ...team creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional… more
    Sanofi Group (12/19/25)
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  • Sr. Manager, Supply Chain

    Mitsubishi Chemical Group (Jersey City, NJ)
    …by closely working with MTP internal colleagues in various functions (Quality Assurance, Regulatory Affairs , Marketing, Market Access, Medical Affairs , Drug ... effectively with colleagues in Supply Chain, Accounting, Market Access, Quality Assurance, Regulatory Affairs , Finance, etc. of Tanabe Pharma Group, including… more
    Mitsubishi Chemical Group (12/24/25)
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  • Clinical Study Physician

    Teva Pharmaceuticals (Parsippany, NJ)
    …and Teva Standard Operating Procedures + Partners cross-functionally with departments such as Regulatory Affairs , CMC , Biostatistics, GCO, in the execution ... will be a key contributor to INDs, NDAs, BLAs, and other global regulatory filings and publications. The Director will foster relationships with opinion leaders… more
    Teva Pharmaceuticals (01/06/26)
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  • Director, Clinical Pharmacology Lead

    Organon & Co. (Jersey City, NJ)
    …colleagues in preclinical science, data science, clinical operations, regulatory affairs , chemistry, manufacturing and control ( CMC ), project management and ... are sound, based on the most up-to-date literature and regulatory guidance and support the approved early development plans....live their best lives. We are a $6.5 billion global healthcare company focused on making a world of… more
    Organon & Co. (11/25/25)
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