- Lilly (Washington, DC)
- …reduce regulatory risk, and improve efficiency in drug development. The purpose of the Associate Director - Global Regulatory Policy & Strategy is to ... better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees...+ Engage in forums that share regulatory information across GRA components and other Lilly teams and business partners… more
- Lilly (Indianapolis, IN)
- …life better for people around the world. **Purpose:** The Senior Director of Global Regulatory Affairs - CMC ( GRA -CMC) leads and manages the scientific and ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , GRA CMC Small Molecules where you will oversee ... Global Regulatory Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC. **How you will contribute:** + Plan, execute and… more
- Takeda Pharmaceuticals (Boston, MA)
- …what is possible in order to bring life-changing therapies to patients worldwide. As Associate Director , Global Labeling Devices, you will be responsible for ... have the most competitive labeling possible Working within Labeling Team and GRA - Represents Global Labeling Devices at Global Regulatory Team (GRT) -… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... awareness of recent in-class approvals. + Working within Labeling Team and GRA + Represents Global Labeling at Global Regulatory Team (GRT) + Liaises with… more
- Takeda Pharmaceuticals (Boston, MA)
- …bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion ( GRA A&P) Review Lead is ... to prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead you… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **Objective:** Under the direction of the Director or Sr. Director , ODPD, the Assoc. Director is responsible ... regulatory support, validation thru commercialization of oral drug products for global markets. Expertise in drug product manufacturing process optimization, scale… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring ... and clinical trial delivery in partnership with GDO, PSPV, GRA etc. Review the outputs of the safety and...are enterprise-wide (ie Veeva, QMS, Enterprise Audit, etc.) to Global Quality and R&D Quality. Present to CPMQ at… more