- Astrix Technology (Indianapolis, IN)
- ** Associate Director , Quality & Compliance** ...15/12/2025 Apply for Job Associate Director , Quality & Compliance, you will **own GMP ... bar + A bias for action, accountability, and pragmatic GMP decision-making + Build quality systems that support **first-in-class cancer therapies** + Join a… more
- Compass Group, North America (Wilmington, MA)
- ESFM **Position Title: GMP UNIT DIRECTOR ** **Salary: $90,000 - $100,000** **Other Forms of Compensation:** None ESFM is the corporate facilities management (FM) ... FAQs and the Compass Employee Referral Policy, email MyReferral@compass-usa.com._** **Job Summary** The ** GMP Unit Director ** will be the on-site leader for our… more
- Merck (Durham, NC)
- **Job Description** The Quality Associate Director / GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, ... Skills:** + Minimum of five (5) years of manufacturing, technology, laboratory, and/or quality operations experience within GMP environment + GMP Compliance… 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 ... as well as drive continuous improvement. **Job Description** + Responsible for directing quality oversight of GMP contract manufacturers of Otsuka clinical and… more
- Catalent Pharma Solutions (Philadelphia, PA)
- ** Associate Director , Quality Assurance** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) ... **This is a full-time salaried position, onsite out of Philadelphia, PA.** The ** Associate Director , Quality Assurance** is responsible for providing… more
- Lilly (Lebanon, IN)
- …facility for both clinical and commercial supply. **Job Position Overview:** The QA Associate Director is responsible for providing leadership and daily support ... operation of the Lilly Advanced Therapies Site (LP2). The Associate Director is also responsible for managing... is also responsible for managing the activities of Quality Assurance personnel with respect to GMP … more
- Lilly (Pleasant Prairie, WI)
- …driving solutions that impact the site and align with corporate objectives. The Associate Director , Quality Assurance, will also provide computer system ... production. This role will leverage a deep understanding of GMP data flows (electronic and paper), the application of...impact the site and align with corporate objectives. The Associate Director , Quality Assurance, will… 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 ... well as drive continuous improvement. **Job Description** + Responsible for directing quality oversight of GMP contract manufacturers of controlled substances… more
- Lilly (Indianapolis, IN)
- …us to develop creative solutions to support communities through philanthropy and volunteerism. The Associate Director - Quality Control leads all aspects of ... fast-paced environment, while delivering on multiple priorities. + Apply knowledge of quality principles and GMPs toward the development of local procedures. +… more
- Fujifilm (Warminster, PA)
- **Position Overview** **Position Description** We are hiring an Associate Director , Quality Assurance. The Associate Director , Quality Assurance ... + Acts as a quality resource with expertise in quality regulations relating to GMP and ISO guidelines. + Direct activities related to the preparation for… more
- Lilly (Lebanon, IN)
- …startup into GMP manufacturing operations. **Position Description:** The ** Associate Director Process Engineering - Peptides Active Pharmaceutical ... used in the manufacturing of peptide products. Additionally, the Associate Director of Process Engineering - Peptides...implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives. + Identify, track,… more
- BD (Becton, Dickinson and Company) (Columbus, NE)
- …a **maker of possible** with us. We are seeking a dynamic and experienced ** Associate Director , Quality Management** to drive organizational change and grow ... BDX Molding Center of Excellence. Reporting to the Senior Director of Quality Operations, you'll serve as...audits + Corrective and preventive action programs (CAPA) + GMP training initiatives + Quality engineering +… more
- Merck (De Soto, KS)
- **Job Description** Join us as the Associate Director , Operations and lead the successful start-up and long-term operation of our state-of-the-art new ... biopharmaceutical facility in Desoto, KS. You will build GMP -compliant operations end to end-people, processes, and plant-while driving cross-functional execution.… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- The Associate Director of Global Supplier Quality will be responsible for the execution of supplier quality audit and monitoring across the company's ... , with 2+ years in supplier or external manufacturing quality . + Strong knowledge of GMP regulations...external manufacturing quality . + Strong knowledge of GMP regulations for small molecules and/or biologics. + Experience… more
- Kemin Industries (Des Moines, IA)
- Overview Kemin Health is hiring an Associate Director of Regulatory/Scientific Affairs and Quality ! In this role, you will be responsible for leading the ... business units' regulatory affairs (RA) and quality assurance (QA) teams by proactively identifying and managing regulatory/ quality risks and opportunities… 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
- Lilly (Lebanon, IN)
- …startup into GMP manufacturing operations._ **Position Description:** The Associate Director - Technical Services/Manufacturing Science (TSMS) is responsible ... for managing the activities of TSMS personnel. The Associate Director TSMS must balance coaching a...implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives. + Interact with… 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 you ... an experienced purification process development professional with experience in GMP manufacturing and technology transfer (TT) to join the...Group located in Waltham, MA in the role of Associate Director . The GMU PPD group operates… more
- Lilly (Indianapolis, IN)
- …for clinical trial medicines, while also reducing costs and environmental impact. The Associate Director of Materials will lead the planning and procurement of ... and regulatory changes. + Ensure all activities comply with GMP , GDP, and site quality standards. +...activities comply with GMP , GDP, and site quality standards. + Develop contingency strategies for critical clinical… more
- Lilly (Lebanon, IN)
- …into GMP manufacturing operations. **Description:** The **Project Engineering Associate Director ** at Lebanon API Manufacturing provides leadership and ... and implement the necessary systems and business processes required to support GMP operations, and build the site culture. This will require significant… more