- Bristol Myers Squibb (Princeton, NJ)
- …planning, workforce planning, and execution of special projects. The Executive Director , Medical Affairs Strategy and Operations Head is responsible for leading ... + Partner with the WW SVP to design and execute 1-5 year global medical strategies across oncology. + Lead Business Process Management: Overseeing execution of… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Position Summary:** The Associate Director of Global Medical Affairs Omnichannel will be responsible for developing and leading the omnichannel strategy for ... Global Medical Affairs across all therapeutic areas and brands....all omnichannel activities adhere to internal medical, legal, and regulatory standards. + Collaborate with Compliance and Legal to… more
- BeOne Medicines (Pennington, NJ)
- **General Description:** The Senior Director GTS Quality will be the global GTS Business Partner and the primary interface between GTS and Global Quality. ... the manufacturing plants in China & US + Understands the global Quality, risk, and regulatory environment to plan activities for compliance with existing and new… more
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine (TM), the Director will be ... lead responsibilities for assets such as serving as a TM representative on global program teams, biomarker representative on study teams, setting up biomarker plans… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** US Medical Director , Dermatology (NextGen Immunology) **Location** : Cambridge, MA Morristown, NJ **About the Job** A strategic medical leadership ... dermatology and rheumatology therapeutic areas. Reporting to the Senior Medical Director , Dermatology & Rheumatology, this position requires deep expertise in… more
- Western Digital (Trenton, NJ)
- …updates to senior leadership and key stakeholders. + Ensure compliance with global regulatory and sustainability standards throughout the supply chain lifecycle. ... Description** At Western Digital, our vision is to power global innovation and push the boundaries of technology to...**Job Description** We are seeking an experienced and results-driven ** Director of Supply Chain Enabling** to support the Direct… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …10+ Years with MS/MA or MBA **PREFERRED QUALIFICATIONs:** + Proficiency in clinical regulatory requirements ( Global ) is a must. + Expert-level experience working ... improvements in R&D quality processes, systems, and standards to meet regulatory requirements and organizational goals and contribute to the overall quality… more
- Bristol Myers Squibb (Summit, NJ)
- …than here at BMS with our Cell Therapy team. The purpose of the Associate Director , Value Stream CAR T Manufacturing role is to manage and provide oversight of a ... to develop expertise in the field of CAR - T Manufacturing and regulatory requirements that pertain CAR T manufacturing. **Resource Management** + Is responsible to… more
- Bristol Myers Squibb (Princeton, NJ)
- …be the global leader in radiopharmaceuticals . The Senior Medical Director - Clinical Development (GU Cancer/Prostate Renal) has responsibility for the clinical ... development plans in GU cancers. Responsibilities include support for IND preparation, regulatory authority interactions, design and execution of Phase 1 to Phase 3… more
- Bristol Myers Squibb (Princeton, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Associate Director - Operations will oversee the governance, performance, and ... flawless, on-time delivery of campaigns and tactics. The Associate Director will act as the central point of contact,...and Quality Assurance** : Ensure all content adheres to regulatory , MLR, and brand guidelines, maintaining high standards of… more