- Aequor (Thousand Oaks, CA)
- …level of biopharmaceutical experience with responsibility in a quality, analytical development , process development , or manufacturing environment- at ... Control, Quality Assurance, Regulatory, Quality Engineering, International Quality and Process development on projects, issue resolution and investigations.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Operations Support Specialist as part of the Technical Operations team based in Raritan, NJ. ... Role OverviewThe Operations Support Specialist will be part of the Technical Operations team...support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be performed within a… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Operations Support Specialist as part of the Technical Operations team based in Raritan, NJ. ... Role OverviewThe CAR-T Operations Support Specialist will be part of the Technical Operations team...support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be performed within a… more
- Aequor (Davie, FL)
- Description: We are looking for a MS&T Specialist ( Process Engineer) I. Please find the updated job profile below. Looking for candidates with a focus from ... related to critical aspects of products and processes with focus on process engineering. Maintains expertise related to process engineering and chemistry… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …functional requirement specifications, qualification protocols, enterprise or system interface, process development reports, and provide technical assessments, ... process characterization of cell therapy automation technologies, including process development , FATs, SATs, and IQ/OQ/PQ testing.Ensure successful… more
- Houston Methodist (Houston, TX)
- …production or quality control. + Collaborates with cross-functional teams including research, process development , quality assurance and quality control. + Works ... At Houston Methodist, the Sr. Current Good Manufacturing Practices ( cGMP ) Specialist is responsible for adherence to...the department, this position will actively contribute to the development of policies and procedures for the delivery of… 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 ... 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
- 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
- Biomat USA, Inc. (Research Triangle Park, NC)
- …and quality assurance/control documentation. + Assists in the development of cGMP operating procedures that relate to process , computer systems, and ... out of our RTP, NC Office.** Ensures current Good Manufacturing Practices ( cGMP ) and FDA/Grifols Quality Systems are adhered to throughout the evaluation, review… 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
- Bristol Myers Squibb (Indianapolis, IN)
- …with RayzeBio policies, standards, procedures and global current Good Manufacturing Practice ( cGMP ). The Senior Specialist provides Quality support and oversight ... aims to be the global leader in radiopharmaceuticals. **Summary** The Senior Specialist , QA Operations will help support operations through quality oversight in a… more
- Merck (West Point, PA)
- …audits/inspections, and must, therefore, be able to speak knowledgeably about automation, process and cGMP details of the manufacturing operations. + Analyzes ... highest quality of raw materials, intermediates and finished products. The Senior Specialist is Manufacturing Automation, is responsible for: i) management of all… more
- Actalent (Princeton, NJ)
- …Operations support for manufacturing, warehouse, and other technical operations, including in- process checks, deviation identification, and adherence to cGMP ... Job Title: Quality Specialist Job Description We are seeking a dedicated...and drive investigations into deviations, non-conformances, environmental excursions, and process anomalies. + Apply structured root cause analysis tools… more
