• Senior Scientist, MS&T Pharma Drug Product…

    Bristol Myers Squibb (New Brunswick, NJ)
    …and regulatory (current Good Manufacturing Practices (cGMP), filing, + Environmental Health and Safety (EHS)) aspects of API and/or drug product (DP) manufacture ... Active Pharmaceutical Ingredients (APIs), Intermediates and Starting Materials and/or Oral Drug Products, Packaging and artwork, ensuring compliance and security of… more
    Bristol Myers Squibb (09/05/25)
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  • Data Review Assistant

    Charles River Laboratories (Reno, NV)
    …that you can feel passionate about. **Job Summary** We are seeking an experienced Data Review Assistant for our Safety Assessment site located in Reno, Nevada. ... In addition to reviewing all study data , the Data Review Assistant will ensure...is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services,… more
    Charles River Laboratories (09/09/25)
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  • Data Review Assistant I

    Charles River Laboratories (Reno, NV)
    …every day for patients across the globe. **Job Summary** We are seeking a ** Data Review Assistant** for our ** Safety Assessment** site located **in** **Reno, ... River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities… more
    Charles River Laboratories (07/29/25)
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  • PA or CRNP - Hillman Cancer Center - Immunotherapy…

    UPMC (Pittsburgh, PA)
    …Physician Assistant or Nurse Practitioner - Hematology/Oncology - Immunotherapy and Drug Development Center (IDDC) Location: Hillman Cancer Center, 2nd Floor, ... on-call, or hospital rounding. About Us: The Immunotherapy and Drug Development Center (IDDC) is designed to speed the...business unit and health system's goals to improve patient safety , quality, and satisfaction. Formulates a plan of care… more
    UPMC (08/26/25)
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  • Sr Bioprocess Associate I, Antibody Drug…

    Lotte Biologics USA LLC (Syracuse, NY)
    …chromatography skids, filtration operations, isolator operations, aseptic technique, filling of final drug substance, etc.) + Maintains files, records data , logs ... following detailed procedures and batch records ensuring compliance with cGMP and safety requirements. The Senior Bioprocess Associate I works on assignments that… more
    Lotte Biologics USA LLC (07/04/25)
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  • Data Engineer II

    NRG Energy, Inc. (UT)
    …to management on all safety issues._** NRG Energy is committed to a drug and alcohol-free workplace. To the extent permitted by law and any applicable collective ... **Summary:** In this role, you will help drive Vivint's data platform. You will work with a talented team...as computers, phones, photocopiers, filing cabinets and fax machines._** ** SAFETY :** **_Vivint enforces a safety culture whereby… more
    NRG Energy, Inc. (09/09/25)
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  • Quality Control Data Review Scientist

    Cambrex High Point (Charles City, IA)
    …company safety rules and practices. . Reviews raw technical data provided by technicians, chemists and laboratory supervision to ensure accuracy, completeness ... global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire ...as well as our strong commitment to quality and safety , we offer a range of career and growth… more
    Cambrex High Point (09/03/25)
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  • Scientist - Medicinal Chemistry, Integrated…

    Sanofi Group (Cambridge, MA)
    **Job Title:** Scientist - Medicinal Chemistry, Integrated Drug Discovery **Location:** Cambridge, MA **About the Job** Are you ready to shape the future of ... medicine? The race is on to speed up drug discovery and development to find answers for patients...project and able to prioritize work based on emerging data . + Collaborate with other team members to design… more
    Sanofi Group (09/10/25)
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  • Director, Clinical Data Management Medical…

    Takeda Pharmaceuticals (Boston, MA)
    … dictionaries across the drug development spectrum (Phase I through post-marketing safety data management). + Advanced knowledge of broad drug ... activities that support Takeda regulatory commitments including submission of safety data . + Liaise with cross functional...record of strong project management skills and experience managing data management coding activities for large drug … more
    Takeda Pharmaceuticals (08/30/25)
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  • Safety and Training Manager

    Transdev (Jacksonville, FL)
    …be 21 years old; + All Transdev employees must satisfactorily complete a pre-employment drug screen and background check. Safety Sensitive Positions will also be ... autonomous driving technology. We are committed to fostering a culture of safety , professionalism, and inclusivity, with a strong emphasis on Diversity, Equity, and… more
    Transdev (08/23/25)
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