- 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 ... to be the global leader in radiopharmaceuticals. **Summary** The Senior Specialist , External Manufacturing Quality Assurance is responsible for quality oversight of… more
- Takeda Pharmaceuticals (Los Angeles, CA)
- 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 ... Micro projects. This role involves equipment qualification, partnership in the development of and validation of Microbiology methodologies, analyzing complex data,… more
- ADM (Forsyth, MO)
- …during shift. + Works with necessary groups to resolve outstanding issues with process documents / logbooks, cGMP walk through inspection observations and ... **103915BR** **Job Title:** Quality Assurance Specialist - Forsyth, MO **Department/Function:** Operations: Manufacturing, Production, Maintenance, Utilities **Job… more
- ADM (Kennesaw, GA)
- **103184BR** **Job Title:** Quality Assurance Specialist - Kennesaw, GA **Department/Function:** Operations: Manufacturing, Production, Maintenance, Utilities **Job ... Description:** **Quality Assurance Specialist - Kennesaw, GA** **NATURE & SCOPE** The Quality... reports to the QA Manager and provides independent cGMP oversight on the production floor and across manufacturing… more
- Genentech (Hillsboro, OR)
- …improvement and excellence. **The Opportunity** As an Environmental/Sterility Quality Assurance (EQA) Specialist , you will play a pivotal role in shaping and driving ... and approval of CCS and sterility assurance-related systems, ensuring alignment with cGMP , ATMP GMPs, USP, EP, and JP standards. + Collaborate with manufacturing,… more
- Catalent Pharma Solutions (Kansas City, MO)
- **Senior Validation Specialist I, BioAnalytics Computer System Validation (CSV) & Compliance** **Position Summary:** Catalent, Inc. is a leading global contract ... development and manufacturing organization (CDMO) whose mission is to...Kansas City, MO (KCM) is hiring a Senior Validation Specialist I, BioAnalytics CSV & Compliance. The Senior Validation… more
- Catalent Pharma Solutions (Greendale, IN)
- **Quality Specialist I** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... service to pharma, biotech, and consumer health customers, supporting product development , launch, and full life-cycle supply. With time-tested experience in … more
- Gilead Sciences, Inc. (Foster City, CA)
- …Sr Specialist will be responsible for the ideation, planning, development oversight for the Biologics Clinical Manufacturing business capability. Participates in ... member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we… more
- Catalent Pharma Solutions (Chelsea, MA)
- **Quality Assurance Specialist II, Operations (Night shift, on-site)** **Position Summary:** + **Work Schedule:** Night shift 7-day rotating 12-hour shift with hours ... (Chelsea, MA) Catalent, Inc. is a leading global Contract Development and Manufacturing Organization (CDMO), and the Boston-area facility...SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North… more
- Merck (Wilmington, DE)
- …to:** As part of the Global Digital & Data Quality team, the Senior Specialist collaborates with stakeholders (eg, System Owners, Process Owners, Data Owners, ... **Job Description** The Senior Specialist Digital and Data Quality will be responsible for the quality aspects of GMP computerized systems and the supporting… more