- Gilead Sciences, Inc. (Foster City, CA)
- …aspirations. Join Gilead and help create possible, together. **Job Description** ** Associate Director , Process Technologies and Development** Gilead Sciences, ... are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available… more
- AbbVie (North Chicago, IL)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The ME&C Associate Director is a global program management expert responsible ... and execution of Biologics and/or Toxin industrialization programs with experience in drug substance and/or drug product transfers. The program manager is to… more
- United Therapeutics (Research Triangle Park, NC)
- …individual expertise and mentoring or developing a member of your team. The Associate Director , QA Engineering will provide advanced support and subject matter ... supply, and new product development of active pharmaceutical ingredients (API), drug substances, drug products, and combination product/medical devices. This… more
- Alloy Therapeutics (Waltham, MA)
- …spanning both Alloy and our affiliated venture studio, 82VS. The Role The Associate Director , Strategic Initiatives and Business Operations is a versatile and ... capabilities that are foundational for discovering and developing therapeutic biologics . The company facilitates affordable, non-exclusive access to the entire… more
- Merck (Rahway, NJ)
- …which focuses on the design, development, and commercialization of novel biologic/ drug /vaccine-device combination products for safe and effective delivery to their ... and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will lead the definition and execution of design… more
- Merck (Rahway, NJ)
- …experience. **Required Experience and Skills:** + Experience with small molecule drug substance and/or biologics process development and scale-up, moving ... overall success of the pilot plant. The Facility Lead position reports to the Director of Operations/Head of SSO Pilot Plant and the successful candidate will be an… more
- Fujifilm (College Station, TX)
- …candidates must have a working knowledge of CGMP regulations for the production of drug substance, drug product, biologics , vaccine, and/or advanced therapy ... **Position Overview** The Director Quality Systems is responsible for developing, implementing,...CGMP regulatory requirements for phase-appropriate clinical and commercial bulk drug substance and drug product manufacture. +… more
- Merck (Rahway, NJ)
- …breakthrough science that radically changes the way we approach serious diseases. The Senior Director will report to an Associate Vice President in the Oncology ... Clinical Research Group. Under the guidance of a supervisor, the Senior Director has primary responsibility for the planning and directing of clinical research… more
- Charles River Laboratories (Rockville, MD)
- …GMP materials required for various client projects under the guidance of the Associate Director Materials Management. They will also interact with Charles River ... worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on… more
- University of Maryland, Baltimore (Baltimore, MD)
- …and regulatory agency site visits. This program covers all major areas of drug product and biologics regulatory science, including: Chemistry, Manufacturing, and ... Clinical Research; Pharmacovigilance; Phase IV Research (eg, Pharmacoepidemiology); and Drug and Biologics Discovery. Additionally, responsibilities include a… more