- University of Southern California (Los Angeles, CA)
- …in the university's current Good Manufacturing Practices ( cGMP ) facility. The Process Development Specialist is responsible for developing procedures and ... Process Development SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP - Process - Development - Specialist \_REQ20145450/apply) Keck School… more
- University of Southern California (Los Angeles, CA)
- …QC liaison to actively participate in cross-functional meetings with Manufacturing, Process Development , and Quality Assurance to ensure seamless coordination ... make the university what it is. The Senior QC Specialist at the USC/CHLA cGMP Facility will...the planning and performance of complex analytical testing on in- process materials, raw materials, and final products to ensure… more
- Danaher Corporation (Coralville, IA)
- …10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.This ... are provided reasonable accommodation to participate in the job application or interview process , to perform crucial job functions, and to receive other benefits and… more
- Endo International (Rochester, MI)
- …capacity in a fast-paced, cGMP environment and production support areas to process sterile and aseptic products. The specialist works in collaboration with ... are looking for talented individuals to join our team. **Job Description Summary** The Associate Process Engineer, Prep Service Specialist , works in a hands-on… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- Regeneron is looking for a Compliance Specialist to join our Process Sciences Change Management team. This is a non-lab-based position. This position will be ... an opportunity to work on countless aspects of the process and business. As a Compliance Specialist ,...have a Bachelors in life sciences/engineering or related field. cGMP experience is desirable. + Associate Compliance Specialist… more
- Catalent Pharma Solutions (Hanover, MD)
- …and a warehouse._ _The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage ... **Sr. Specialist , QA - Batch Disposition** **Summary:** _Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the… more
- Catalent Pharma Solutions (Harmans, MD)
- …and a warehouse. The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage ... ** Specialist , QA OTF** **Position Summary** Catalent is a...a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide.… more
- Catalent Pharma Solutions (Harmans, MD)
- ** Specialist II, MTO** **Summary:** _Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The ... and a warehouse._ _The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage… more
- Catalent Pharma Solutions (St. Petersburg, FL)
- …teams. Interfaces with Engineering, Procurement, Quality Control, Quality Assurance, Process Development , Project Managers, Validation and Manufacturing ... **Documentation Specialist , Analytical Research & Development ** **Position...of document change control procedures and philosophies within a cGMP environment. Catalent is committed to a Patient First… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Analytical Quality Assurance Specialist (Microbiology) Department: Analytical QA Location: Monroe, NC START YOUR APPLICATION ... New Biological Entities (NBEs'), with eight molecules in various stages of clinical development . Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US… more