- Legend Biotech USA, Inc. (Raritan, NJ)
- Legend Biotech is seeking an Senior CQV Specialist as part of the Commissioning and Qualification team based in Raritan, NJ. Role OverviewThis position will be ... responsible for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant. This individual… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Sr . Current Good Manufacturing Practices ( cGMP ) Specialist is responsible for adherence to Standard Operating Procedures (SOPs) and ... cGMP regulations pertaining to the manufacture of therapeutics and...proper guidance of junior level team members. As a senior member of the department, this position will actively… more
- University of Southern California (Los Angeles, CA)
- …cell and gene therapy products, identifies equipment and components necessary for cGMP production , implements necessary changes to the process and reagents ... cGMP Process Development (PD) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP -Process-Development--PD-- Specialist \_REQ20159663/apply) Keck School of Medicine Los… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- Regeneron is currently looking for a Drug Production , Senior Manufacturing Specialist in the Global Manufacturing department. In this role, you will focus on ... world while working in a clean room environment. A typical day for a Drug Production , Senior Manufacturing Specialist might include: + Performing all aspects… more
- Boehringer Ingelheim (St. Joseph, MO)
- …using office application software (MS-Word, MS-Excel, MS-Outlook, PowerPoint). **Requirements for a Sr . Specialist Validation** + A BS degree from an accredited ... reflect Boehringer Ingelheim's high regard for our employees. The Principal Specialist , Validation manages all phases of higher level, more complex validation… more
- J&J Family of Companies (Santa Clara, CA)
- …United States of America **Job Description:** Johnson & Johnson is hiring for a ** Sr . Quality Compliance Specialist - Shockwave Medica** l to join our team ... Overview** In compliance with FDA, European MDD/MDR & ISO regulations, the Senior Quality Compliance Specialist will perform work under general supervision.… more
- Cardinal Health (Indianapolis, IN)
- …GMP related documents. + Issuance and reconciliation of product labels for production + Perform AQL testing for visual inspection + Understands technical/release ... (Pharmaceutical or Medical Device) preferred + Possess an understanding of cGMP /compliance requirements for cosmetic and pharmaceutical products + Working knowledge… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …more than 110 countries and regions. **Shift** : 1st - M-F 8:00am - 4:30pm ** Sr . Quality Associate I/II - Summary:** The Sr . Quality Associate I/II will ... primarily serve as a Quality Systems technical specialist as part of the QA Fractionation business unit....medium complexity and developing solutions for defined problems. The Sr . Quality Associate I/II will also perform manufacturing record… more
- Cardinal Health (East Hartford, CT)
- …reliable, safe and effective. This job family provides oversight of production /manufacturing activities, training to operational and quality control personnel, and ... day. Work hours may be subject to change. **_Responsibilities_** + Handles CGMP documentation review related to product release, facilities and equipment, material… more
- Cardinal Health (Dallas, TX)
- …reliable, safe and effective. This job family provides oversight of production /manufacturing activities, training to operational and quality control personnel, and ... improved disease diagnosis, staging, and monitoring. **_Responsibilities_** + Handles cGMP documentation review related to product release, facilities and equipment,… more
