- Bristol Myers Squibb (Cambridge, MA)
- …Precision Medicine, Research teams, Global and Regional Regulatory Leads, Global Regulatory Operations , and Quality by delivering timely, strategic ... and strategic influence. Proven ability to lead teams in making timely, high- quality regulatory decisions that balance innovation, compliance, and enterprise… more
- Sumitomo Pharma (Boston, MA)
- …coordinates, authors, and prepares regulatory submissions and works closely with Regulatory Operations in the electronic submission + Ensure compliance with ... a dynamic, highly motivated, and experienced individual for the position of **Associate Director , Regulatory Affairs (Oncology).** The Associate Director is… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Director , Global Regulatory Labeling Strategy where you will be responsible for ... Labeling at Global Regulatory Team (GRT) + Liaises with US Labeling Operations , EU Labeling Operations , Labeling Devices Lead and Labeling Compliance to… more
- Sanofi Group (Framingham, MA)
- … regulatory authorities. You'll collaborate across R&D, Device, Manufacturing, and Quality teams while preparing high- quality regulatory submissions, ... **Job title** : Global Regulatory Affairs Device Lead (Associate Director )...Our department bridges the gap between technical development, manufacturing operations , and global regulatory authorities to ensure… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **OBJECTIVES/PURPOSE:** Reporting to the Head, Global Regulatory Operations (GRO), the Head of Global Regulatory ... globally. This role involves guiding and mentoring a team of experts, driving regulatory data quality confidence, ensuring global system reach and adoption, and… more
- GRAIL (Boston, MA)
- …documentation. The role collaborates cross-functionally with Quality , Lab Operations , and other stakeholders to support regulatory strategy development, ... **Required Qualifications:** + MS or PhD with 10+ years of experience in regulatory , development, clinical affairs, quality , or program management within the… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Job Summary** The Associate Director , Quality Operations will lead initiatives that drive operational excellence, enhance risk management practices, and ... business process design and governance practices. **Compliance & Governance** + Ensure quality operations comply with global regulatory requirements (eg,… more
- Bristol Myers Squibb (Devens, MA)
- …careers.bms.com/working-with-us . **Position Summary** Bristol-Myers Squibb is seeking an Associate Director , Principal Product Quality Leader (PQL), in Global ... (vector, gene editing and cell therapy projects) to ensure regulatory compliance of GMP operations in support...be directed to Chat with Ripley. R1597688 : Associate Director , Principal Product Quality Lead **Company:** Bristol-Myers… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …ACNO of Professional Practice and a member of the DFCI nursing leadership team, the Director , Nursing Quality and Magnet Program Director (MPD) oversees the ... director plans, designs, directs, and evaluates the nursing quality plan and programs that influence and enhance compliance...specialty standards as well as standards set forth by regulatory agencies. The director works collaboratively with… more
- Trinity Health (West Springfield, MA)
- …Quality Improvement Plan for the PACE Organization (PO) and ensure overall CMS regulatory compliance. The Director , Quality Improvement and Compliance, in ... is responsible for developing and implementing the annual QI plan, including leading quality initiatives and projects. In addition, the Director ensures that… more
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