- Bristol Myers Squibb (Summit, NJ)
- …better place 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 ... to develop expertise in the field of CAR - T Manufacturing and regulatory requirements that pertain CAR T manufacturing. **Resource Management** + Is responsible to… more
- Haleon (Warren, NJ)
- …supplements. In line with a risk-proportionate framework for product vigilance, the ** Associate Director , Consumer Safety Science** is accountable for developing ... related to product defects at manufacturing sites. + Provide safety expertise into regulatory documents and responses to boards of health. + Provide safety inputs in… more
- Bristol Myers Squibb (Princeton, NJ)
- …$160,000-$190,000, plus incentive cash and stock opportunities (based on eligibility). + For Associate Director level, the starting compensation for this job is ... populations, evaluating competitive differentiation, and supporting internal decision-making and regulatory submissions. Experience in virtual population development and qualification,… more
- Ascendis Pharma (Princeton, NJ)
- …develop their skills. Job Overview: We have a dynamic opportunity for an Associate Director , Global Strategic Marketing, who will be responsible for supporting ... and throughout the drug lifecycle. This role will report to the Director , Global Strategic Marketing. This individual is responsible for managing external vendors… more
- Bristol Myers Squibb (Summit, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** Director of Validation, Cell Therapy Technical Operations reports to the ... Senior Director , Cell Therapy Technical Operations within the Cell Therapy...Author or review CMC summaries of validation for worldwide regulatory submissions for initialization and life-cycle changes. + Design… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , HRBP for HOCT and Early Development provides strategic ... experience + Proven leadership effectiveness in followership, innovation, people program /project management, and executive coaching, demonstrating the ability to… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , WW Medical Cell Therapy Autoimmune, LCM/Pan-Indication, will ... an understanding of pharmaceutical drug development including clinical development, regulatory , life cycle management of pharmaceutical products, and knowledge of… more
- Taiho Oncology (Princeton, NJ)
- …the promotional and medical materials review committees. Position Summary: The Associate Director , Promotional Materials will provide guidance to the ... teams regarding communications strategy and planning. + Review and approve the regulatory content of materials created for product promotion, corporate, and other… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Associate Director of Government Pricing is a key leader in the ... ongoing compliance with external and internal requirements and guidance including regulatory , SOX and audit. + Evaluate new and modified contracting proposals,… more
- Bristol Myers Squibb (Princeton, NJ)
- …- $193,900 plus incentive cash and stock opportunities (based on eligibility). For the Associate Director position, the starting compensation for this job is a ... oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external… more