- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as a Senior Director , GRA CMC Pharmaceuticals Development Portfolio Lead ... CMC team, you will report to the Executive Director and Head, CMC Regulatory Affairs -...you will contribute:** + Leads the Early Development Pharmaceuticals GRA CMC regulatory team in the development… more
- Takeda Pharmaceuticals (Boston, MA)
- …properly manage tasks and work expectations, lead, be influential and effective, collaborate with GRA Liaisons, GRA CMC Leads and other regulatory functions, ... and guidance documents; and acts as an advisor/liaison to senior management to plan, evaluate and recommend implementation strategy...+ Works effectively across a complex matrix environment in GRA with GRLs, CMC RA project leads… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Director , GRA CMC Small Molecules where you will oversee the ... Global Regulatory Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC . **How you will contribute:** + Independently… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. Purpose: The purpose of the Senior Director Global Regulatory Affairs, Global Regulatory Lead (GRL) role is to ... The GRL creates and leads the Global Regulatory Team (inclusive of GRA central functions, GRA - CMC , GRA -Devices, and regional regulatory scientists) and… more
- Takeda Pharmaceuticals (Boston, MA)
- …the company, and to achieve the overall vision and objectives + Engage with GRA CMC & Device Leadership in the talent developmentprocesses to providementoring ... the company on strategictopics. + Builds and managesrelationshipsthroughactivepartnering with key internal ( GRA , GRA CMC , PharmSCi GMS, GQ etc.) and… more
Locations:
Massachusetts,
Indiana