- 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 ... cGMP Senior Quality Control (QC) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP -Senior-Quality-Control--QC-- Specialist \_REQ20165200/apply) Keck School of Medicine Los… more
- Stanford University (Stanford, CA)
- Process Development Specialist **School of Medicine, Stanford, California, United States** Research Post Date Sep 15, 2025 Requisition # 107283 The Stanford ... Cancer Institute at Stanford University is seeking a Clinical Process Development & Manufacturing Professional 2 to independently conduct major portions of… more
- Belcan (Durham, NC)
- …and quality assurance/control documentation. * Assists in the development of cGMP operating procedures that relate to process , computer systems, and ... Validation Quality Specialist Job Number: 360522 Category: QA /QC Description:...Referral program Responsibilities: * Ensures current Good Manufacturing Practices ( cGMP ) and Quality Systems are adhered to throughout the… more
- J&J Family of Companies (Athens, GA)
- …for all groups onsite. + Identify, design, deliver, and track learning and development activities consistent with a cGMP environment. + Manage all activities ... searching for the best talent for Senior Operations Training Specialist to be onsite in Athens, Georgia! Are you...within the Operations Training Department in compliance with corporate, cGMP , EHS, and other regulatory requirements. + Ensure that… more
- Bristol Myers Squibb (Bothell, WA)
- …more: careers.bms.com/working-with-us . + **Position Summary** The primary focus of the Specialist - MSAT Cell Therapy Engineering Services, Process Support is ... Bristol Myers Squibb's GMP facility in Bothell, WA. The Specialist - MSAT Cell Therapy Engineering Services, Process...relevant experience in biologics or cell therapy manufacturing or development with BS, or 0+ years relevant experience with… more
- PACIV (San Juan, PR)
- …its Puerto Rico office. Job Description: The Computerized System Validation (CSV) Specialist /Engineer will be responsible for development and execution of ... Industry, mainly Bio-Pharma and/or Medical Devices. The resource will be responsible for development and execution of CSV deliverables, as per System Development … more
- Kelly Services (Winston Salem, NC)
- …with incoming material qualification testing and lot release evaluations. + Support process development , validation activities, and data collection for ... **Manufacturing Specialist III - Cell Processing** **Location: Winston Salem...processing techniques, procedures, and regulatory compliance. + Drive continuous process improvement, incident investigations, and deviation resolutions. + Ensure… more
- Actalent (Durham, NC)
- …validation reports. Responsibilities + Assist in the development of cGMP operating procedures related to process , computer systems, and equipment ... Job Title: Quality Specialist - ValidationJob Description We are seeking a...join our team. This role involves developing and maintaining cGMP operating procedures related to process , computer… more
- Takeda Pharmaceuticals (Libertyville, IL)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... the best of my knowledge. **Job Description** **About the Role:** The Learning Specialist , as part of the Site Business Excellence organization, manages the Learning… more
- Catalent Pharma Solutions (Manassas, VA)
- **Quality Assurance Specialist I** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... service to pharma, biotech, and consumer health customers, supporting product development , launch, and full life-cycle supply. With time-tested experience in … more