- 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
- J&J Family of Companies (Raritan, NJ)
- Associate Director , Autologous Cell Therapy Process Development - 2406176241W **Description** Johnson & Johnson is currently seeking an Associate ... energetic and highly motivated candidate for the role of Associate Director , who possesses proven expertise in..., who possesses proven expertise in autologous cell therapy process development. The ideal candidate will be responsible for… 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
- Amicus Therapeutics (Princeton, NJ)
- …existing products and Continued Process Verification (CPV) activities. The EQL Associate Director will work to build and maintain effective relationships ... with our external partners and ensure the effectiveness of our governance process . The EQL Associate Director will drive performance against agreed… more
- Merck (West Point, PA)
- **Job Description** **Position Description:** ** Associate Director ,** **Technology Transfer** **(TT)** **Systems Group Leader** As part of our Manufacturing ... Operations. We are seeking a highly motivated individual for the role of Associate Director , Technology Transfer (TT) Systems Group Leader in Large Molecule… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and help create possible, together. **Job Description** **Key Responsibilities** Associate Director , Global External Manufacturing Biologics ensures ... global external contract manufacturing network, while ensuring compliance with cGMP , regulatory requirements, and environmental, health, and safety legislations.… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. Responsibilities: The API EM Associate Director (AD) - Quality Control provides analytical leadership for the ... of the regulations applicable to laboratory testing in a cGMP environment. + Identify and resolve laboratory safety issues...to request an accommodation as part of the application process . Any other correspondence will not receive a response.… more
- J&J Family of Companies (Spring House, PA)
- Associate Director , Cell Therapy Decisional Analytics - 2406185128W **Description** Johnson & Johnson is recruiting an Associate Director , Cell Therapy ... at https://www.jnj.com/. We are looking for an energetic and highly motivated Associate Director candidate with demonstrated expertise in the development and… more
- Teva Pharmaceuticals (West Chester, PA)
- …manufacturing process , and process tech transfer to GMP manufacturing sites. Associate Director is a key leadership role in DPD reporting into the head ... Associate Director , Drug Product Development Date:...+ Responsible for biologics drug product development including manufacturing process tech transfer to support PPQ and commercial manufacturing.… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …regulated cGMP environment preferably in Biopharmaceuticals / Plasma Fractionation process and its various capacity constraints. + Detailed experience in supply ... and services in more than 110 countries and regions. ** Director ,Supply Chain** The Director , GTI Supply Chain...significant role as it relates to insuring the proper process controls, reports and systems are in place, allowing… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …professionally to achieve your own career goals. **Job** **Title:** Scientific Associate Director **Location:** New Brunswick **Division:** Global Production & ... at all microbiological testing locations in the BMS network. The Scientific Associate Director will also ensure appropriate strategies for DP-related… more
- Lilly (Lebanon, IN)
- …startup into GMP manufacturing operations. **Position Description:** Reporting to the Senior Director of Operations, Associate Director of the Warehouse ... team of people to operate the state-of-the-art warehouse. The Associate Director of the Warehouse will also...corporate and site goals + Ensure robust inventory management process is developed and maintained + Ensures that all… more
- Bristol Myers Squibb (Trenton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** ** Associate Director Long-Range Supply and Capacity Planning - GPL** ... in their personal lives. Read more: careers.bms.com/working-with-us **Position Summary** The Associate Director , Long Range Supply and Capacity Planning Global… more
- Merck (Durham, NC)
- …the new HPV vaccine drug substance manufacturing facility. As a direct report to the Director of Operations, the Associate ** Director will be accountable for ... in other cross-functional teams to ensure a successful technology transfer, process performance qualification, filing, licensure, and commercial production ramp up… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Associate Director of Drug Substance - EACD will have the primary responsibility to oversight process development and manufacturing ... + Proven track record of solving manufacturing challenges and continuous process improvements + Understanding and knowledge of cGMP /ICH regulations… 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 (Indianapolis, IN)
- …people who are determined to make life better for people around the world. The Associate Director , EPCM Procurement Process Owner in the Development & ... objectives and maintaining compliance with Procurement practices. Continually drive process improvement across projects using metrics. + Provide strategic insights… more
- University of Rochester (Rochester, NY)
- …Unity (CMSU), consisting of approximately 15 team members, with two Directors ( Director Operations and Director Quality Assurance) and the clinical trials ... ensure maximum operational efficiency, resource utilization and overall regulatory and cGMP compliance with all applicable state and federal regulations, licensing… more
- Lilly (Indianapolis, IN)
- …Hub and Product Delivery. In this role, you will lead the sourcing process from strategy development and supplier selection through contract negotiations and ongoing ... relationship management. This role will coordinate and lead the sourcing process to enable competitive selection of suppliers, as well as use market knowledge and… more