- J&J Family of Companies (Raritan, NJ)
- …We are searching for the best talent for a **Technical Fellow ( Director ), Advanced Therapies - MSAT** to be in Raritan, NJ, Titusville, NJ, ... site escalations. In this capacity, they contribute to the development of robust strategies that maintain the validated state...lead to drive down patient related contributions to non-conforming product . Engage with new markets to set up for… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …but not limited to Clinical Supply Chain, other Global Supply Chain teams, Global Product Development and Supply (GPS) and R&D, IT, Business Insights & Analytics ... their personal lives. Read more: careers.bms.com/working-with-us . **Position** : Director Clinical Logistics Global Capability Owner (GCO) **Location** :… more
- Glenmark Pharmaceuticals Inc., USA (Elmwood Park, NJ)
- Associate Director , Regulatory Affairs Department: Regulatory Affairs Location: Elmwood Park, NJ START YOUR APPLICATION ... which includes Commercial Division Heads, R&D, QA, Legal, Business Development , Project Management, Demand Planning, Marketing and others identified on… 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 ... appropriate level of training necessary for CAR-T GMP manufacturing in a multi- product commercial facility. + Is responsible to maintain their Manufacturing Sr.… more
- Sanofi Group (Bridgewater, NJ)
- …4 years in pharmaceutical industry or CRO, previous experience in clinical development **Why Choose Us?** + Bring the miracles of science to life alongside a ... of what you thought was possible. Ready to get started? The Senior Clinical Research Director (Sr CRD) is noted as the **primary clinical lead for programs** . The… more
- Organon & Co. (Jersey City, NJ)
- …of eight years of pharmaceutical or relevant experience with a focus on product labeling inclusive of regulatory product labeling (Core, US and EU labeling) ... The Label Strategist is accountable for developing and maintaining the target product labeling for developmental products, the core labeling documents (CCDS) and US… more
- Bristol Myers Squibb (Princeton, NJ)
- …payer and market access challenges including US market. + Strong knowledge of pharmaceutical development process. + Very strong written and verbal communication ... Medical, Marketing, Market Access, Statistics and Regulatory. **Responsibilities:** + Lead the development of an aligned strategy for GHEOR to demonstrate the value… more
- Organon & Co. (Jersey City, NJ)
- …in-markets, regulatory history, historical performance (production and compliance), new product or market launches, historical relationship between Organon and the ... + Provide support to the contract manufacturer to facilitate and validate new product introductions and/or transfers. + Assist with and/or lead the development ,… more
- Amneal Pharmaceuticals (Bridgewater, NJ)
- …a broad array of issues relating to the marketing and promotion of pharmaceutical products and actively represent Legal on the company PARC to review ... + Negotiate, draft, and review market access/customer-facing contracts including product purchase, supply, distribution, PBM, GPO, wholesaler/distribution, rebate/discount, and… more
- Dr. Reddy's Laboratories (Princeton, NJ)
- …success and with multiple biosimilars and a rare disease innovative biologic in our product development pipeline. This is an exciting time to join an ... would impact Brand financials, and share with internal stakeholders. + Supports development of the pricing and contracting strategy, playbook, and guidelines for all… more