• Manager, Drug Development Program…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …its lifecycle, by integrating key stakeholders from Discovery, Manufacturing , Preclinical, Global Development and Commercial. Independently manages multiple ... experience required, preferably in the pharmaceutical or related industry and drug development. Specific experience managing the development strategy for a … more
    Regeneron Pharmaceuticals (09/20/25)
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  • Laboratory Technician, CMC Biologics Drug

    US Tech Solutions (North Chicago, IL)
    …preferably in the mornings (around 8am-12pm)** **Job Description:** + The **Biologics Drug Product** Development group develops antibody drug conjugates (Client) ... property through new **formulation** compositions and prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. + We are looking for a person… more
    US Tech Solutions (09/16/25)
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  • Project Engineer- Drug Delivery

    PCI Pharma Services (Rockford, IL)
    …and shape the future of PCI. **Position Summary** As a Project Engineer - Drug Delivery, you'll play a hands-on, critical role in the design, development, and ... for diabetes management-giving you the opportunity to work on cutting-edge drug delivery technology. You'll collaborate with both internal stakeholders and external… more
    PCI Pharma Services (07/18/25)
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  • Scientist III, Technical Project Lead, Drug

    ThermoFisher Scientific (Bend, OR)
    …Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail ... is also considered. **Experience** + Experience of 2-5 years in pharmaceutical development/ manufacturing , with a preference for solid oral dosage forms. + Knowledge… more
    ThermoFisher Scientific (09/07/25)
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  • Project Manager (Client-facing RNA/ Drug

    Danaher Corporation (Fargo, ND)
    …for deliverables while meeting delivery deadlines for development projects and manufacturing campaigns across all service levels for Aldevron clients. This position ... field or CDMO strongly preferred + Understanding of GMP product manufacturing from initiation through release capabilities preferred. ​This role could require… more
    Danaher Corporation (07/18/25)
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  • Verification Scientist IV

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …enable the auditor(s) to conduct a thorough audit of program participants' manufacturing facilities for the manufacture of drug substances, excipients, dietary ... be responsible for conducting and implementing activities related to current Good Manufacturing Practice (cGMP) site audits, quality control and manufacturing more
    The US Pharmacopeial Convention (USP) (08/08/25)
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  • Director, Sustainability Enablement

    Bristol Myers Squibb (Madison, NJ)
    …with ESG disclosure and reporting standards. + Experience with social sustainability, drug development, or pharmaceutical manufacturing a plus. If you come ... Partner closely with cross-functional teams-including supply chain, procurement, R&D, manufacturing , and commercial-to define and implement sustainability programs aligned… more
    Bristol Myers Squibb (09/22/25)
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  • Visual Inspection Technician I

    PCI Pharma Services (Madison, WI)
    …a **Visual Inspection Technician** , you'll be the critical last step in the manufacturing process, ensuring our sterile drug products are free from defects ... + Be part of a **global leader** in pharmaceutical development and manufacturing . + Work in a **clean, safety-focused environment** with purpose-driven colleagues. +… more
    PCI Pharma Services (07/16/25)
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  • Environmental Health Safety & Sustainability…

    Catalent Pharma Solutions (Kansas City, MO)
    …Protection Association), RCRA, ANSI (American National Standards Institute), FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), etc. + All ... Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply… more
    Catalent Pharma Solutions (09/18/25)
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  • Senior Advisor/Director, Global Regulatory Affairs…

    Lilly (Indianapolis, IN)
    …+ Relevant experience in synthetic molecule drug substance and/or drug product development, commercialization, or manufacturing . + Demonstrated deep ... Key responsibilities: + Deep technical knowledge of synthetic molecule CMC drug development science(s). + Knowledge of global CMC regulatory requirements and… more
    Lilly (07/02/25)
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