- Bristol Myers Squibb (Indianapolis, IN)
- …with RayzeBio policies, standards, procedures and global current Good Manufacturing Practice ( cGMP ). The Senior Manager provides Quality support and ... be the global leader in radiopharmaceuticals. **Summary** The Senior Manager , QA for QC is responsible for quality...review, method development, validation , and transfer, equipment validation , and associated projects. The Senior Manager … more
- Endo International (Raleigh, NC)
- …vision of helping everyone we serve live their best life. **Job Description Summary** The Quality Control (QC) Manager serves as a Quality Control technical ... group and compliance activities to achieve key site and corporate objectives. The Quality Control Manager is responsible for overseeing all QC activities to… more
- Reckitt (Salt Lake City, UT)
- Quality Control (QC) Microbiology Manager City: Salt Lake City **We are Reckitt** Home to the world's best loved and trusted hygiene, health, and nutrition ... you to grow in our great organisation. **Reports to:** Quality Control Laboratory Manager **No of Direct...Ensure regulatory compliance with FDA, USP, EU, ISO and cGMP standards. + Day to day implementation, maintenance, and… more
- Fujifilm (Research Triangle Park, NC)
- …or relevant field with 6 years of applicable industry experience; or + Experience in a CGMP Manufacturing, Validation and/or Quality role in a Food & Drug ... **Position Overview** The Quality Assurance (QA) Disposition Manager is...with FUJIFILM Biotechnologies procedures and Current Good Manufacturing Practice ( CGMP ) regulations while making recommendations as needed to release… more
- Nissha Medical Technologies (Panton, VT)
- Quality Manager Summary **Title:** Quality Manager **ID:** 2917 **Department:** Quality **Location:** Paignton, England Description Role Description ... + Follow Employee guidelines and Quality System Regulations as defined by Nissha Medical Technologies...procedures. + Supervisory experience strongly preferred. + Knowledge of cGMP and validation requirements and practices required.… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- Regeneron is currently looking for a Sr. Manager DP (Drug Product) MSAT (Manufacturing Sciences & Technology) to join our Process Sciences Drug Product Engineering ... supporting assembly, labeling and packaging and industrialization, troubleshooting, and validation of drug product processes at manufacturing sites, both… more
- Bausch + Lomb (Clearwater, FL)
- …methods. + Expertise in microbiological principles and applications related to microbial ID, validation and clean room technology. Trained in cGMP for laboratory ... Knowledge in Sterilization Process (Steam, Radiation and EO). + Strong grasp of global quality and regulatory requirements including cGMP , ISO 13485, and 21 CFR… more
- Curia (Albuquerque, NM)
- Manager , Quality Systems in Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development and ... + Education reimbursement + 401k program + Learning platform + And more! Summary: The Quality Systems Manager leads a team that is responsible for ensuring the… more
- Fujifilm (Research Triangle Park, NC)
- …(CAPAs), manages change controls, and ensures compliance with quality and CGMP regulations. This role also supports validation , automation, data integrity, ... **Position Overview** The Senior Manager , Quality Assurance (QA) Technical provides...for you. From our Bioprocess Innovation Center to our cGMP -compliant manufacturing site, we thrive on collaboration, creativity, and… more
- Integra LifeSciences (Princeton, NJ)
- …and set new standards of care. Under direct supervision of Director, Quality Reliability Microbiology, the Sr. Manager , Microbiology Reliability - Tissue ... technical employees is preferred. Responsibilities associated with this Sr. Manager , Microbiology Reliability - Tissue Technology (TT) are directly associated… more