- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... labeling approval by Labeling Senior Management Cross-functional team ( Global Labeling Oversight Committee - GLOC) driving cross-functional collaboration… more
- Takeda Pharmaceuticals (Boston, MA)
- …of what is possible in order to bring life-changing therapies to patients worldwide. As Associate Director , Global Labeling Devices, you will be ... labeling content for the Information For Use (IFU) and key global labeling documents. -Collaborates cross-functionally to provide input into Clinical IFU,… more
- Chewy (Boston, MA)
- …highest standards of regulatory compliance, quality assurance, and ethical sourcing. The ** Associate Director , Global Compliance & Ethical Sourcing** will ... with R&D, Supply Chain, Operations, Legal, Marketing, and Quality. The Associate Director will also drive compliance investigations, supplier accountability,… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …that will inspire you and empower you to shine? Join us as an Associate Medical Director , Clinical Science in our Gastrointestinal & Inflammation Therapeutic ... be a vital contributor to our inspiring, bold mission **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for the overall … more
- Rhythm Pharmaceuticals (Boston, MA)
- …experienced and highly motivated individual to join its team in Boston, Massachusetts. The Associate Director will be the technical lead for Drug Product small ... Company Overview Rhythm is a global , commercial-stage biopharmaceutical company committed to transforming the...GMP and ICH guidelines related to clinical and commercial labeling , and packaging operations and the overall drug development… more
- Takeda Pharmaceuticals (Boston, MA)
- …development to life cycle management + This individual will act as the global clinical pharmacology lead on PDT projects and contribute to regulatory submissions and ... project. + Contribute to regulatory documents including Investigator Brochures, Labeling and those required for regulatory strategies, interactions, and regulatory… more