- Sumitomo Pharma (St. Paul, MN)
- …(TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations , the specialist ensures accountable functions ... global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused...ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure… more
- Charles River Laboratories (Wilmington, MA)
- …of a global RMS application and other systems supporting RMS operations . Assist with technical and project leadership for the functional implementation of new ... you can feel passionate about. **Job Summary** We are seeking an Applications Specialist Production Support - (Colony Management) in our Research Models and Services… more
- Bristol Myers Squibb (Indianapolis, IN)
- …a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Senior Specialist , External ... procedures and global current Good Manufacturing Practice (cGMP). The Senior Specialist provides Quality support and oversight for CMO operations and… more
- BD (Becton, Dickinson and Company) (Milpitas, CA)
- …product development teams. + Evaluate design, manufacturing, and process changes for global regulatory impact. + Review analytical and clinical protocols to ... **Job Description Summary** We are seeking a Senior International Regulatory Affairs Specialist to join our Regulatory Affairs team. This role is responsible for… more
- BD (Becton, Dickinson and Company) (Denver, CO)
- **Job Description Summary** BD is seeking a Procedural Specialist II to promote our products to customers and potential customers through clinical support and ... makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the...with us. **Job Overview** BD is seeking a Procedural Specialist II to promote our products to customers and… more
- West Pharmaceutical Services (Exton, PA)
- Sr. Specialist Regulatory Affairs, MD Requisition ID: 71773 Date: Nov 21, 2025 Location: Exton, Pennsylvania, US Department: Regulatory Affairs Description: **This ... our sustainability efforts. **Job Summary** The Regulatory Affairs Sr. Specialist is responsible for influencing department regulatory processes and procedures,… more
- Stanford University (Stanford, CA)
- …organizations or committees. + May manage projects related to regulatory activities and clinical operations , develop the regulatory strategy for project teams. + ... Marrow Transplantation and Cellular Therapy (BMT-CT) Divisionis seeking a Clinical Trials Regulatory Specialist II position to...film screening, or listen to a renowned author or global leader speak. + **A caring culture.** We provide… more
- Genentech (South San Francisco, CA)
- …Assistant General Counsel"** role will primarily support Research and Early Development, Clinical Operations , Global Product Development, and Medical Affairs ... legal issues related to the following: + Conducting research through clinical trials (GxP compliance, study participant recruitment and retention, decentralized… more
- Bristol Myers Squibb (Devens, MA)
- …apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of ... team is responsible for 24x7 Quality collaboration and oversight of site operations , including but not limited to Manufacturing, Quality Control laboratories, and… more
- PCI Pharma Services (Bedford, NH)
- …of pharmaceutical or biotech industry + 4+ years of experience in a QA Operations role supporting late stage clinical and/or commercial production + Bachelor's ... Life changing therapies. Global impact. Bridge to thousands of biopharma companies...and shape the future of PCI. The Sr. QA Specialist - Team Lead will work with other departments… more