- Bristol Myers Squibb (Princeton, NJ)
- …line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance ... career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …in which eight (8) years is in procurement or a related domain. + Minimum of three (3) years in pharmaceutical procurement or direct collaboration with such ... line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance… more
- Taiho Oncology (Princeton, NJ)
- …vision allow us to consistently pursue and develop life-changing innovations. As Senior Director of Scientific & Medical Communications, you'll play a pivotal ... (MRC) and Promotional Review Committee (PRC) to ensure accuracy, compliance , and alignment of all scientific publications....working in Medical Affairs, with at least 12 years of pharmaceutical industry experience, preferably within a… more
- Merck (Trenton, NJ)
- **Job Description** **Position Responsibilities** + The Regional Medical Scientific Director (RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and ... disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual,… more
- Sanofi Group (Morristown, NJ)
- …+ Managed Markets contracting knowledge is required, with demonstrated understanding of pharmaceutical contracting. **Soft and technical skills:** + Excellent ... **Job title:** Associate Director , Contract Development **Location:** Morristown, NJ **About the...NJ **About the Job** Ready to push the limits of what's possible? Join Sanofi in one of… more
- Sanofi Group (Morristown, NJ)
- …record with a minimum of 1 year (3+ years preferred) of regulatory experience, preferably within the pharmaceutical /medical device/biotech industry + ... **Job Title:** Associate Director , Global Regulatory Affairs Advertising and Promotion **Location**...scientific subject matter is extremely helpful + Significant understanding of the US pharmaceutical marketplace, especially the… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …This role is responsible for ensuring the robustness, scalability, and compliance of downstream operations through effective technology transfer, validation ... **Job Summary** **** The Associate Director , MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing processes… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …skilled and experienced professional to join our organization as the Assoc. Director of Manufacturing Science and Technology (MSAT) for Upstream processes. ... This role is responsible for ensuring the robustness, scalability, and compliance of upstream operations through effective technology transfer, validation… more
- BeOne Medicines (Pennington, NJ)
- **General Description:** We are seeking a strategic and detail-oriented Director of Inventory and Cost Accounting to oversee our global inventory valuation and ... + Monitor and ensure adherence to internal and external compliance (eg SOX) related to inventory and costing controls.... accounting/financial experience with at least 8 plus years of relevant finance experience in the pharmaceutical … more
- J&J Family of Companies (Raritan, NJ)
- …is essential for enabling the CARVYKTI network's technical, supply chain, and compliance -related objectives. Collaborating across a complex network of internal ... searching for the best talent for a **Technical Fellow ( Director ), Advanced Therapies - MSAT** to be in Raritan,... of overall experience is required; 7+ years of biotech/ pharmaceutical experience or equivalent industry experience… more