- Regeneron Pharmaceuticals (Troy, NY)
- We are currently looking to fill an Associate Director of Quality Auditing position. This position will be responsible for providing professional expertise, ... leadership, oversight and planning for the Regeneron Quality Auditing function, with primary emphasis on GMP , IT and Quality audits that may impact GMP … more
- ThermoFisher Scientific (Boston, MA)
- …biopharmaceutical company, all while maintaining full-time benefits. Reporting to the Associate Director , CMC QC Stability, will be responsible for ... addition, this role will be responsible for supporting various GMP stability testing programs and Quality Systems,...supporting various GMP stability testing programs and Quality Systems, including handling stability Quality Events,… more
- Fujifilm (College Station, TX)
- …Biotechnologies Texas (FDBT) is seeking ** Quality Assurance (QA) Validation - Associate Director ** to oversee the review and approval of commissioning, ... providing strategic leadership to the validation team. **Job Title:** Quality Assurance (QA) Validation, Associate Director...with cross functional teams and management to instill a " Quality Culture" by coaching personnel on GMP … more
- BD (Becton, Dickinson and Company) (El Paso, TX)
- …pharmacovigilance, post market surveillance, GMP Auditing and Supplier Management. The Associate Director , Quality Management and QA Site Leader ensures ... audits/inspections and provides leadership during regulatory authority visits. The Assoc. Director leads quality programs, continuous improvement efforts, and… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- The Associate Director Quality System is responsible for monitoring the effectiveness of the GxP Quality Management Systems regarding CAPA, Deviations, ... support eQCMS (TrackWise or similar system) enhancements in collaboration with Global Quality Systems. Provide guidance and perform a risk assessment for global CAPA… more
- Catalent Pharma Solutions (Manassas, VA)
- ** Associate Director , Quality ** **Job Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... as a member of the Site Leadership Team the ** Associate Director , Quality ** is accountable...as needed. + Review and ensure compliance with plant GMP 's, HACCP, sanitation and pest control procedures and standards.… more
- Bristol Myers Squibb (Indianapolis, IN)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Associate Director of Chemistry, Manufacturing & Controls (CMC) - Quality ... other tasks as assigned (eg, final Quality reviewer/approver of Quality events and/or GMP documentation, actively contributes to ongoing investigations… more
- BeiGene (Hopewell, NJ)
- **_General Description:_** Establish a stability program in Quality Control for clinical and commercial phase biologics products in accordance to FDA/EU regulations, ... and procedures. Oversee and manage stability studies to deliver scientifically sound GMP test data in accordance to predefined protocols. Oversee the Quality… 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
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Associate Director (AD), Program Quality is responsible for building and sustaining the quality relationship with partners ... customer relationship management or alliance management * Experience in quality assurance in a GMP environment *...* Experience in quality assurance in a GMP environment * Experience in developing and implementing regulatory… more