- Takeda Pharmaceuticals (Boston, MA)
- …knowledge. **Job Description** **Title: Process Engineer Small Molecules API Process Science ( Associate Director )** **Location: Cambridge, MA (Hybrid)** ... As a Process Engineer Small Molecules API Process Science ( Associate Director ), you...Engineering. + At least 5+ years' experience in a cGMP environment. + At least 5+ years of pharmaceutical… more
- Sanofi Group (Waltham, MA)
- **Job Title:** Associate Director , Genomic Medicine Purification Process Development **Location:** Waltham, MA Work Model: M-F onsite **About the Job** Are ... Group located in Waltham, MA in the role of Associate Director . The GMU PPD group operates...GMP facilities + Strong technical background in AAV purification process + Experience with AAV cGMP Manufacturing,… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …is true to the best of my knowledge. **Job Description** **About the role** As Associate Director , API Process Engineering, you will be Takeda's global ... the "Apply" button, I understand that my employment application process with Takeda will commence and that the information...+ At least 5 years of experience in a cGMP manufacturing environment and at least 5 years of… more
- Bristol Myers Squibb (Devens, MA)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director Stability is responsible for stability product strategy and ... preparation, review and approval of stability reports and regulatory filings. The Associate Director is responsible for leading high-performance technical team,… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight of clinical ... stored, and transported accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role has global responsibility for directing… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at ... way that is in accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role will direct Biologics Quality Assurance support,… more
- Bristol Myers Squibb (Devens, MA)
- …Shop Floor Quality Assurance team to succeed. This position reports to the Associate Director , Shop Floor Quality Assurance. This is an individual contributor ... QASF processes. The incumbent will be considered a local process owner for core QASF systems/processes including but not...the highest quality and the quickest delivery of QA cGMP tasks. + Develop and implement, and continuously improve… more
- Bristol Myers Squibb (Devens, MA)
- …Relationship** This role is stationed in Devens, MA and reports to the Associate Director of Quality Engineering for the Devens Cell Therapy Facility. ... qualification, and validation (CQV), computer systems validation (CSV) and process validation per established local and global standards. **Duties/Responsibilities**… more
- Sanofi Group (Waltham, MA)
- …to join the R&D Automation team in Waltham, MA. Reporting to the Automation Associate Director , this position is responsible for providing day to day and ... project-based automation support for both cGMP and non-GMP groups within the R&D organization located...+ Provide technical solutions to a wide range of process automation related design challenges. + Work collaboratively with… more