- University of Southern California (Los Angeles, CA)
- cGMP Associate Director Process DevelopmentApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP ... in compliance with current Good Manufacturing Practices ( cGMP ). As the Associate Director of Process Development, the individual will be responsible for… more
- University of Rochester (Rochester, NY)
- …and the Upstate Stem Cell cGMP Facility (USCGF) teams. The QC Associate will be responsible for upholding in- process and final release analysis of ... Responsibilities **Position Summary:** The Quality Control (QC) Associate I will be a member of the...are reported in a timely manner to the QA Director of the cGMP Facility, therefore interacting… more
- Merck (Rahway, NJ)
- …job that provides a high degree of technical and project management responsibility. The Associate Director - Process /Facility Lead position will report to ... following: The process /facility lead role at the Associate Director level will serve as a...+ Ability to prepare Standard Operating Procedures (SOP) and cGMP documents. + Experience with quality systems + Effective… more
- BeiGene (Hopewell, NJ)
- **_General Description:_** The Associate Director Site Technical Services is responsible for the day-to-day activities of the Validation team, Metrology, CMMS ... audits and inspections, write and implement Equipment, Facility and Process Installation/Operational/Performance Qualifications (IQ/OQ/PQ), and write deviations, root causes,… more
- Bristol Myers Squibb (Summit, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . BMS is seeking a Associate Director , Regional Procurement Lead for its multi-product Cell-Therapy ... manufacturing facility in Summit, NJ. Reporting to the Director , Cell-Therapy Internal Operational Lead, this role will oversee sourcing for local/regional direct… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director - Site Planning Global Process Leader (GPL) will be ... ini t iatives . Lead the delivery of , digital first , process enhancements to continuously improve core pillar capabilities that will drive enterprise performance… more
- Regeneron Pharmaceuticals (Troy, NY)
- …and drive the development of the new organization and realize our vision. The Associate Director , Procurement Compliance will be responsible for leading a team ... Procurement Compliance Managers and Specialists that support and maintain all cGMP compliance aspects of procurement operations. The major activities include but… more
- Curia (Rensselaer, NY)
- Associate Director of Quality Control in Rensselaer, NY The Associate Director of Quality Control (QC) is responsible for leading the Quality Control ... and compliance to the applicable compendial, regulatory and customer requirements. The Associate Director also ensures compliance of the analytical laboratories… more
- Lilly (Indianapolis, IN)
- …quality oversight of Indianapolis Parenteral Manufacturing's central quality processes. The Associate Director for Site Quality & Compliance is responsible ... & Compliance team. Cross-training to back-up other Site Quality and Compliance Associate Directors is expected. Key Objectives / Deliverables: **Team and Personnel… more
- Takeda Pharmaceuticals (Lexington, MA)
- …true to the best of my knowledge. **Job Description** **Job Title** : Associate Director , US 3PL Operations Management Lead (Operations & Analytics) **Location** ... the "Apply" button, I understand that my employment application process with Takeda will commence and that the information...: Lexington, MA **About the role:** As an Associate Director of US 3PL Operations Management… more