- Sanofi Group (Framingham, MA)
- **Job Title:** Global Quality Lead , GMP , GDP Audit and Inspection - Pipeline Launch **Location:** Framingham, MA or Morristown, NJ **About the Job** We ... in Sanofi. + **Scope:** Manufacturing & Supply, Research & Development, Countries, Digital, Global Quality organizations in Sanofi. And third parties outside of… more
- Eurofins (Cambridge, MA)
- …expectations. + Ensure all activities are conducted in strict accordance with GMP guidelines and quality standards. Leadership Responsibilities: + Supervise and ... are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in… more
- Bristol Myers Squibb (Devens, MA)
- …External Manufacturing, Regulatory Affairs and Brand teams. The individual provides end-to-end global quality oversight of all cell therapy development programs ... for cell therapy commercial, clinical and development products. + Acts as lead Quality management reviewer/approver of regulatory submissions and responses to… more
- Sanofi Group (Waltham, MA)
- …view. **Scope** + Sanofi R&D Sites/ platforms, interactions with CMC, R&D Vaccines, Global Quality , Alliance Management, Global Regulatory Affairs, Clinical ... families. The purpose of this position is to provide quality technical management oversight of Sanofi sponsored GMP... manufacturing and testing of genomic medicines. Specifically, to lead the following activities: + Manage the quality… more
- Fresenius Medical Center (Waltham, MA)
- … and Compliance, Collaboration, No-Limits Mindset and Results Oriented. **PURPOSE AND SCOPE:** Lead Quality Systems Auditor will act as a Subject Matter Expert ... plans, conducts, and leads audits in accordance with the global QS audit program + Lead and...in the interpretation of FDA guidelines, Good Manufacturing Practices ( GMP ) and relevant quality standards for pharmaceuticals… more
- Lilly (Boston, MA)
- …**Summary** We are looking for a proactive, scientifically grounded Director to lead the development and integration of GMP cell banking, cryopreserved ... to scale into future clinical phases. **Roles and Responsibilities** + Establish and lead a unified technical strategy that integrates GMP cell banking,… more
- Bristol Myers Squibb (Devens, MA)
- …as the Global Technical SME for Drug Product and Vector Validation. The lead will develop global technical standards for cell therapy validation and deploy ... providing SME assessment for proposed process life-cycle changes. The lead will serve as the Global Point...global cell therapy validation technical standards via the quality system. + Promote innovative and efficient approaches to… more
- Bristol Myers Squibb (Devens, MA)
- …BioPharma Operating Units, the Sr. Director, BI&T, Devens Digital Plant and Site BI&T Lead will be directly accountable to the US Biologics Leader and Devens Campus ... a standing member of the Devens Campus leadership team. **Key Responsibilities:** + Lead a matrixed organization composed of both site direct reports and groups of… more
- Takeda Pharmaceuticals (North Reading, MA)
- …department is looking for an organized, dedicated, and person with skills in a GMP warehouse environment. You will report to the Supply Chain & Warehouse Lead ... . **How you will contribute:** + Supply and transfer GMP Raw Materials and General Supplies in support of...At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict… more
- Sanofi Group (Framingham, MA)
- …and high- quality responses and support the development and promotion of Global Quality Documentation. + Supports the preparation, execution and closure of ... purposes, and ensuring accurate reporting to Operations Management and Global Quality . . **Core member of critical.... . **Core member of critical governance** + Sanofi's GMP GDP Quality Council to facilitate sharing… more
- Takeda Pharmaceuticals (Lexington, MA)
- …etc. in conjunction with senior staff and global line and function heads + Lead global CMC and Quality key initiatives and represent Pharm Sci to ... my knowledge. **Job Description** **How you will contribute:** + Lead and develop a global team of...Stability and Shelf life; c) Reference Standard Management; d) GMP Quality Systems + Contribute to product… more
- Catalent Pharma Solutions (Chelsea, MA)
- ** Quality Control Analyst IV** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing...in North America. Catalent Pharma Solutions is hiring a Quality Control Analyst IV who is a key analytical… more
- Medtronic (Billerica, MA)
- …and compensation plans (https://www3.benefitsolver.com/benefits/BenefitSolverView?page\_name=signon&co\_num=30601&co\_affid=medtronic) We lead global healthcare ... for this opening will close on - 11 Jun 2025 Position Description: Principal Quality Engineer for Medtronic, Inc located in Billerica, MA. Develop, modify, apply and… more
- Meta (Boston, MA)
- **Summary:** Meta seeks highly engaged and experienced team players for lead roles to join our Design, Engineering & Construction (DEC) organization to direct ... join a high-powered team of industry leaders! **Required Skills:** Lead Contracts Manager - Data Center Design, Engineering &...team, peers, and outside business units to enhance the quality and efficiency of contracting processes. 12. Ensure all… more
- Catalent Pharma Solutions (Chelsea, MA)
- ** Quality Control Analyst II** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing...in North America. Catalent Pharma Solutions is hiring a Quality Control Analyst who is responsible for executing QC… more
- Danaher Corporation (Marlborough, MA)
- …for Cytiva is responsible for supporting the Business and Customers in a global environment by providing quality documents and regulatory support in ongoing ... do: + Support the Business and Customers in a global environment by providing quality documents and...or related field + 3+ years of experience in GMP , quality , product management or a related… more
- Actalent (North Billerica, MA)
- Job Title: Quality InvestigatorJob Description Lead and manage complex investigations related to deviations, non-conformances, and quality events across ... with internal procedures and regulatory expectations. + Facilitate and lead cross-functional team meetings focused on deviation management and investigation… more
- Actalent (Framingham, MA)
- Job Description Lead and manage complex investigations related to deviations, non-conformances, and quality events across manufacturing, packaging, and ... root cause analyses and collaborate cross-functionally with Technical Operations, Manufacturing, Quality Control, and Regulatory Affairs to gather data and ensure… more
- Teleflex (Chelmsford, MA)
- …: Up to 10% **Requisition ID** :12097 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to improve ... the health and quality of people's lives. Through our vision to become...of healthcare. For more information, please visit **teleflex.com** . ** Global Operations -** Global Operations is a… more
- ThermoFisher Scientific (Waltham, MA)
- …**Position summary** The Sr. Director, Compliance will be a valued member of the Global Quality Leadership team, reporting to the Vice President, Global ... implementation of compliance processes and systems in a manner consistent with global quality systems requirements, corporate standards, current regulatory and… more