• Senior Director of API Manufacturing

    Kelly Services (South San Francisco, CA)
    …manufacturing relationships. + Track record of authoring, reviewing, and supporting regulatory documentation for global drug development. + Outstanding ... Kelly(R) Science & Clinical is seeking an Associate Director/Director of Drug Substance Manufacturing for a direct hire opportunity with a leading biopharmaceutical… more
    Kelly Services (08/29/25)
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  • Process Development Associate - Pre-Pivotal…

    Amgen (Thousand Oaks, CA)
    …lives of patients while transforming your career. **Process Development Associate - Pre-Pivotal Drug Product** **What you will do** Let's do this! Let's change the ... and clinical development programs. In doing so they will contribute to regulatory filings and to Amgen's intellectual property. In addition, you will have… more
    Amgen (09/14/25)
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  • Finance/Budget Analyst

    University of North Carolina- Chapel Hill (Chapel Hill, NC)
    …specimen banking, clinical trials design, clinical trials data management, and new drug and laboratory testing regulatory affairs. Additionally, as the direction ... of NIAID , the Network responds to emergent clinical research needs. The Finance & Budget Analyst will provide leadership, oversight, and support for fiscal activities for monthly reporting to Operations and Finance Manager. This position will review and… more
    University of North Carolina- Chapel Hill (09/12/25)
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  • Registered Dietitian - Research

    University of Miami (Miami, FL)
    …and their families regarding various topics in medical nutrition therapy and drug nutrient interaction. Ensures regulatory compliance including federal, state ... and accrediting agencies. Adheres to University and unit-level policies and procedures and safeguards University assets. This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or… more
    University of Miami (09/09/25)
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  • Changeover Technician I (3rd shift)

    Herbalife (Winston Salem, NC)
    …degree in Automation/Electronics or Industrial Maintenance Technology/Mechatronics * Food and Drug Administration (FDA) or other regulatory experience * 5+ ... years of work experience in a high-speed manufacturing environment * Food manufacturing or packaging experience, and/or blending equipment, batching operation systems **PHYSICAL DEMANDS:** In general, the following physical demands are representative of those… more
    Herbalife (08/29/25)
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  • 2nd shift Industrial Automation Technician

    Herbalife (Winston Salem, NC)
    …degree in Automation/Electronics or Industrial Maintenance Technology/Mechatronics * Food and Drug Administration (FDA) or other regulatory experience * 5+ ... years of work experience in a high-speed manufacturing environment * Food manufacturing or packaging experience, and/or blending equipment, batching operation systems **PHYSICAL DEMANDS:** In general, the following physical demands are representative of those… more
    Herbalife (08/28/25)
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  • Clinical Dietitian 1 - Specialty, Full Time

    University of Miami (Miami, FL)
    …and their families regarding various topics in medical nutrition therapy and drug nutrient interaction. + Ensures regulatory compliance including federal, state ... and accrediting agencies. + Adheres to University and unit-level policies and procedures and safeguards University assets. This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or… more
    University of Miami (07/24/25)
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  • Associate Director, Global Regulator Strategy,…

    Bristol Myers Squibb (Princeton, NJ)
    …+ Understanding of policy, laws, regulations and guidelines as they apply to Regulatory Agencies globally for drug development and approval. + Understanding of ... personal lives. Read more: careers.bms.com/working-with-us . **Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:** The selected candidate will… more
    Bristol Myers Squibb (08/30/25)
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  • Sr. Scientist, Drug /Device Combination…

    Merck (Rahway, NJ)
    …+ Prepare materials for program presentations for management review and regulatory submissions, ensuring clarity and thoroughness. + Lead the implementation and/or ... within Device Development and with external suppliers. + Understand and apply regulatory / compliance requirements relative to design controls and risk management… more
    Merck (09/06/25)
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  • Inpatient Clinical Pharmacist--full-time, nights…

    Penn Medicine (Philadelphia, PA)
    …and dispenses medications using appropriate techniques to ensure positive outcomes of drug therapies and compliance with regulatory requirements and the ... dispensing medications, providing concise, applicable, and timely responses to requests for drug information to ensure optimal drug use and medication-use… more
    Penn Medicine (08/07/25)
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