- 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
- 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
- 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
- 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 (Phoenix, AZ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** Associate Director responsible for heading up the Engineering Function ... responsibilities including but not limited to electrical, mechanical, and process engineering as well sustainability, reliability and total preventative maintenance… more
- Takeda Pharmaceuticals (Lexington, 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
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Associate Director , Cleaning Validation is responsible for leading and executing Cleaning Validation (CV) activities for a large-scale ... and to mitigate risks associated with the therapeutic product lifecycle. The Associate Director collaborates with cross-functional teams to drive continuous… more
- Novo Nordisk (Boulder, CO)
- …best of both worlds to develop new medicines for patients. The Position The Associate Director of Drug Product Manufacturing is accountable for all clinical drug ... product manufacturing including process characterization activities to support commercialization for nucleic acid programs and will have thorough knowledge of … more
- Lotte Biologics USA LLC (Syracuse, NY)
- …to reliably deliver benefits for patients worldwide. Position Summary The Associate Director of Antibody Drug Conjugate (ADC) Manufacturing Operations ... provides manufacturing services to external customers and internal programs, and the Associate Director will play a critical role in delivering high-quality,… more
- Bristol Myers Squibb (Madison, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The ** Associate Director , Product Technical Steward, Cell Therapy Technical Operations ... + Be the primary owner of the Drug Product process , and leads or participates in process ...above. + Experience should include technical support of a cGMP manufacturing facility, including strong knowledge and engineering leadership… 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
- 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 (Indianapolis, IN)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals . The Associate Director of Validation is responsible for leading the validation function ... execution, manages a cross-functional team, and ensures alignment with regulatory requirements ( cGMP , FDA, USP, and other relevant bodies). The ideal candidate has… 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