- Bristol Myers Squibb (Madison, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary:** The Associate Director , Iberdomide marketing will play a critical role ... sales force readiness activities + Coordinate closely with medical affairs and regulatory teams on scientific communications and thought leader engagement. + Partner… more
- Bristol Myers Squibb (Tampa, FL)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Procurement, Secondary Data & Analytics role will focus ... data stewardship practices to ensure data quality, integrity, and compliance with regulatory requirements. + Subject matter expert for Data & Analytics categories. +… more
- Bristol Myers Squibb (Devens, MA)
- …no better place than here at BMS with our Cell Therapy team. The ** Associate Director ,** **Process Implementation Lead l** eads the transition of hybrid ... people manager role drives project milestones, operational readiness, and regulatory compliance, overseeing reports in support of advanced manufacturing automation… more
- Takeda Pharmaceuticals (Brooklyn Park, MN)
- …**Job Description** About the role: As the Environmental, Health and Safety, Associate Director , you will establish and foster strategic partnerships across ... of strong environmental, health and safety programs in alignment with legal, regulatory , corporate requirements and industry best practice. + Support business growth… more
- Lilly (Lebanon, IN)
- …clinical trial medicines, while also reducing costs and environmental impact. The Associate Director Small Molecule Process Engineering provides leadership and ... approval for documents as appropriate, including investigations, change controls, regulatory submissions, expert opinions, validations, annual product reviews, manufacturing… more
- Mount Sinai Health System (New York, NY)
- …clinical care and optimize provider communication to improve the Patient Experience. The Associate Director will work directly with the CMO to develop and ... maintaining compliance with proper infection prevention practices and maintaining regulatory compliance through continuous quality improvement. In addition, the… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …true to the best of my knowledge. **Job Description** About the role: As the Associate Director of Process Engineering, you will be member of the engineering ... time-efficient, innovative design solutions that meet user, safety, quality, and regulatory requirements. + Oversee and review feasibility studies, design packages,… more
- Abbott (Alameda, CA)
- …medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Associate Director , Complaint Handling** **Working at Abbott** At Abbott, you ... (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and FreeU… more
- Takeda Pharmaceuticals (Boston, MA)
- …leadership at LOC level Decision-making and Autonomy + Responsibility in line with Associate Director level position; independently lead HE projects and support ... Access, Global Evidence and Outcomes, Medica Affairs, Clinical Development, Regulatory Affairs, Biostatistics, Global Emerging Markets (GEM; eg, China), Project… more
- Takeda Pharmaceuticals (Boston, MA)
- …DP/PKG** **Location: Cambridge, MA** **About the role:** As a Process Scientist ( Associate Director ) - Global Manufacturing Science GMSci Drug Product (DP), ... and the life cycle management of existing products. You will lead regulatory interactions, including the preparation of Chemistry, Manufacturing, and Controls (CMC)… more