- 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
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Associate Director , Microbiology Department: Microbiology Location: Monroe, NC START YOUR APPLICATION ... (https://apply.hrmdirect.com/resumedirect/ApplyOnline/Apply.aspx?req\_id=3090958&source=3090958-CJB-0) The QC Associate Director (AD), Microbiology manages a team of… 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 ... + **Technical Excellence:** Lead and provide technical input and effective process support for manufacturing issue resolution and investigations, champion continuous… more
- United Therapeutics (Durham, NC)
- …diseases, and other orphan diseases. **How you'll contribute** The role of the Associate Director , Fill, Assembly & Pack, Dry Powder Inhalation is responsible ... inhalation product, ensuring adherence to regulatory standards and driving process improvement in RTP, NC. This includes leading a...a related field + 14+ years of experience in cGMP pharmaceutical manufacturing environment with an Associate 's… more
- Bristol Myers Squibb (Bothell, WA)
- …responsible for setting strategy and prioritizing network level initiatives. The Associate Director , Operational Excellence leads and manages an operational ... preferred. Experience: **Basic Qualifications:** + 10+ years' experience in operations, process improvement, or related function. + 5 years of experience in… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- Regeneron is currently seeking an Associate Director / Director for our Quality Control (QC) Technical Resources Chemistry team for in-coming component ... from other internal sites, partners companies, and contract manufacturing companies. As an Associate Director **,** a typical day might include the following: +… more
- Catalent Pharma Solutions (Chelsea, MA)
- ** Associate Director , Facilities** **Position Summary:** Catalent...SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North ... America. Catalent Pharma Solutions is hiring an Associate Director , Facilities who leads the team that manages facility activities and projects, including… more
- Bristol Myers Squibb (Seattle, WA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Title: Associate Director , Cell Therapy Comparability** **Location: Summit, NJ or ... and the ability to help patients are incredible. The ** Associate Director , Cell Therapy Comparability** will lead...vector and cellular product CQAs and control through manufacturing process + Experience with cGMP , ICH guidelines,… more
- Lilly (Indianapolis, IN)
- …Quality Analytical Sciences & QC Operations (AQCO) team is also growing. The Associate Director , Analytical & QC Integrated Services (AQIS), will provide ... and QC Compendial Affairs support to the organization. The Associate Director is accountable for the successful...of study or equivalent experience. + Strong knowledge of cGMP and quality systems. + Minimum of 10 years… more
- Lilly (Indianapolis, IN)
- …twins, computational modeling, edge/IoT, and analytics solutions. **Responsibilities:** The Associate Director - Digital Manufacturing Engineering position has ... streamlining processes, prioritizing work, and supporting the overall DME strategy. The Associate Director role will provide discipline leadership in technology… more
- Lilly (Lebanon, IN)
- …prevent and mitigate variability to deliver a reliable supply of medicine. The Associate Director is primarily responsible to lead TS/MS scientists' team on ... cGMP , applicable global regulatory manufacturing guidance, and the process /cleaning validation in drug substance pharmaceutical manufacturing are a plus.… more