- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Job Summary** The Associate Director , Quality Operations will lead initiatives that drive operational excellence, enhance risk management practices, ... quality organization. This role is instrumental in ensuring that quality operations are efficient, compliant, and aligned with strategic business goals. **Job… more
- Bristol Myers Squibb (Devens, MA)
- …more: careers.bms.com/working-with-us . **Position Summary** Bristol-Myers Squibb is seeking an Associate Director , Principal Product Quality Leader (PQL), ... cell therapy projects) to ensure regulatory compliance of GMP operations in support of the program.The PQL must drive...should be directed to Chat with Ripley. R1597688 : Associate Director , Principal Product Quality … more
- Bristol Myers Squibb (Devens, MA)
- …of your application should be directed to Chat with Ripley. R1596112 : Associate Director , Quality Risk Specialist **Company:** Bristol-Myers Squibb **Req ... personal lives. Read more: careers.bms.com/working-with-us . Job Description The Associate Director , RBQM - HOCT, ICN will...HOCT, ICN will mainly be responsible for developing the Quality Narrative at the study and/or ASSET and TA… more
- Bristol Myers Squibb (Devens, MA)
- …personal lives. Read more: careers.bms.com/working-with-us . The ** Associate Director , Product Technical Steward, Cell Therapy Technical Operations (CTTO)** ... be directed to Chat with Ripley. R1598138 : Associate Director , Product Technical Steward, Cell Therapy Technical Operations **Company:** Bristol-Myers… 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 ... stored, and transported accordance with regulatory expectations and applicable cGMP/GDP quality standards. This role has global responsibility for directing clinical… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ... design, implementation and advancement of the Clinical and Safety Quality Compliance strategy, model, and operations as...and Safety Quality Compliance strategy, model, and operations as a key member of the Leadership Team.… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- The Associate Director of Global Supplier Quality will be responsible for the execution of supplier quality audit and monitoring across the company's ... Collaboration** + Collaborate with Procurement, Manufacturing, Regulatory Affairs, and Technical Operations to ensure supplier quality is integrated into… 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 ... way that is in accordance with regulatory expectations and applicable cGMP/GDP quality standards. This role will direct Biologics Quality Assurance support,… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- The Associate Director , Strategic Planning & Operations will support the assets of varying lifecycle stages in the relevant therapeutic area portfolio. This ... medical affairs processes are in place. This position reports directly into the Director , Strategic Planning Lead, who in turn reports into the Medical Excellence &… more
- Philips (Cambridge, MA)
- …member of our talented Hospital Patient Monitoring (HPM) Clinical Affairs team, the Associate Director - Clinical Operations , is responsible for day-to-day ... initiatives. + Assists in the updates and enhancement of quality system processes for Clinical & Medical Affairs, aligning...+ You have a minimum of 10+ years' Clinical Operations experience within Medical Device Clinical Research and FDA… more