- 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
- 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
- Lilly (Lebanon, IN)
- …enable a successful startup into GMP manufacturing operations. **Position Description:** The ** Associate Director Process Engineering - Peptides Active ... equipment and systems are used in the manufacturing of peptide products. Additionally, the Associate Director of Process Engineering - Peptides leads this … more
- Sanofi Group (Waltham, MA)
- **Job Title:** Associate Director , Genomic Medicine Purification Process Development **Location:** Waltham, MA Work Model: M-F onsite **About the Job** Are ... Group located in Waltham, MA in the role of Associate Director . The GMU PPD group operates...GMP facilities + Strong technical background in AAV purification process + Experience with AAV cGMP Manufacturing,… more
- Bristol Myers Squibb (Indianapolis, IN)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals . The Associate Director of Validation is responsible for leading the validation function ... your application should be directed to Chat with Ripley. R1595528 : Associate Director of Validation **Company:** Bristol-Myers Squibb **Req Number:** R1595528… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …is true to the best of my knowledge. **Job Description** **About the role** As Associate Director , API Process Engineering, you will be Takeda's global ... the "Apply" button, I understand that my employment application process with Takeda will commence and that the information...+ At least 5 years of experience in a cGMP manufacturing environment and at least 5 years of… more
- Lilly (Houston, TX)
- …strives to enable the making of medicine "with safety first and quality always". The Associate Director for MQ Tech@Lilly will be part of the IT Leadership team ... This role will report to the MQ IT Sr Director for LP1. This role will work hand by...+ Provide leadership in the development and execution of cGMP and/or improvement plans within the IT function and… more
- Lilly (Indianapolis, IN)
- …as we achieve drug product manufacturing and commercialization excellence. As the Associate Director of Technical Services/Manufacturing Science (TS/MS) in the ... + **Technical Excellence:** Lead and provide technical and effective process support services for production issue resolution and investigations, ensuring… more
- Merck (Wilson, NC)
- …Description** We are seeking a highly motivated individual for the role of Associate Director , Tech Transfer Leader supporting the Wilson Packaging Technical ... visibility to site deliverables for the device assembly and packaging process , analytical and facility readiness. + Partners with above-site Development and… more
- Lilly (Indianapolis, IN)
- …lead the charge in shaping the future of manufacturing at Eli Lilly? As an Associate Director of Engineering, you'll be at the forefront of this exciting ... 4. Technical Excellence: Lead and provide technical input and effective process support for manufacturing issue resolution and investigations, champion continuous… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director Stability is responsible for stability product strategy and ... preparation, review and approval of stability reports and regulatory filings. The Associate Director is responsible for leading high-performance technical team,… more
- Otsuka America Pharmaceutical Inc. (Honolulu, HI)
- **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight of clinical ... stored, and transported accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role has global responsibility for directing… more
- Otsuka America Pharmaceutical Inc. (Boise, ID)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at ... way that is in accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role will direct Biologics Quality Assurance support,… more
- Catalent Pharma Solutions (Manassas, VA)
- …Engineering, Process Engineering, Utility Systems, and Maintenance functions. The ** Associate Director , Engineering & Maintenance** will direct and lead a ... ** Associate Director , Engineering & Maintenance** **Position...**The Role** + Ensuring full compliance with OSHA and cGMP regulations at all times and working in concert… more