- University of Southern California (Los Angeles, CA)
- …gene therapies and other biological products for internal/external users. The Associate Director of Process Development ( cGMP ) is responsible for all ... aspects of operations related to the current Good Manufacturing Practices ( cGMP ) laboratory, including manufacturing and process development activities, in order… more
- Merck (Rahway, NJ)
- …utilities. As we prepare to bring this asset online, we are seeking an Associate Director , Operations to lead the end-to-end operational strategy, execution, and ... meet cGMP , aseptic processing, and safety requirements. In parallel, the Associate Director , Operations will design and execute a comprehensive hiring and… more
- Bristol Myers Squibb (Manati, PR)
- …of your application should be directed to Chat with Ripley. R1596585 : Associate Director , BI&T Design and Optimization **Company:** Bristol-Myers Squibb **Req ... standards, as well as, compliance requirements. Delegation authority to represent Director during planned/unplanned events in the Manati Leadership Team. Member of… more
- Mallinckrodt Pharmaceuticals (Horsham, PA)
- Job Title Associate Director , Manufacturing Operations Requisition JR000015470 Associate Director , Manufacturing Operations (Open) Location Horsham, PA ... Additional Locations Job Description Summary Job Description The Associate Director , Manufacturing Operations will provide leadership and management of… 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 ... technical expertise and utilize industry best practices to maintain cGMP compliance for UTC combination products, clinical materials supply, and new product… more
- Lotte Biologics USA LLC (Syracuse, NY)
- …innovation, to reliably deliver benefits for patients worldwide. Position Summary The Associate Director , Project Management Office (PMO) will play a key ... strong business acumen, and hands-on leadership in technical transfer, cGMP operations, and stakeholder management. Duties & Responsibilities Leadership &… more
- Lilly (Pleasant Prairie, WI)
- …solutions to support communities through philanthropy and volunteerism. **Responsibilities:** The Associate Director TS/MS - Sterility Assurance is responsible ... product manufacturing, specifically the formulation/filling/inspection of pharmaceutical products. The Associate Director will provide guidance on time… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …activities related to process and support to business demands. The ** Associate Director , Quality Assurance** is responsible for directing the QA teams ... ** Associate Director , Quality Assurance** **Position Summary:**...and procedures. Responsible for ensuring the site is following cGMP guidelines, adherence to Catalent Corporate Quality Policies and… more
- Takeda Pharmaceuticals (Boston, MA)
- …knowledge. **Job Description** **Title: Process Engineer Small Molecules API Process Science ( Associate Director )** **Location: Cambridge, MA (Hybrid)** ... As a Process Engineer Small Molecules API Process Science ( Associate Director ), you...Engineering. + At least 5+ years' experience in a cGMP environment. + At least 5+ years of pharmaceutical… more
- Lilly (Indianapolis, IN)
- …groups such as Global Facilities Delivery (GFD) and Global Quality. **Responsibilities:** The Associate Director - Global Process Automation & Control ... improvement, and overall customer service for the team. The Associate Director role will provide process...Technical expertise in one or more automation platforms. + cGMP Regulatory knowledge in process or automation… more