- Actalent (Cranbury, NJ)
- …or Technical Service. Responsibilities + Follow all policies, SOPs, and regulatory requirements for pharmaceutical manufacturing. + Perform aseptic gowning ... Technician will be responsible for supporting the production of sterile injectable pharmaceutical products in accordance with cGMP, FDA, and quality standards. This… more
- Merck (Rahway, NJ)
- …leverage advanced computational modeling and simulation tools to support pharmaceutical reserachers in predicting drug behavior, improving descision-making, and ... roadblocks and engaging cross-functional experts to maintain progress. + Support regulatory audits and inspections by collaborating with stakeholders and Quality… more
- Bristol Myers Squibb (Princeton, NJ)
- …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... personal lives. Read more: careers.bms.com/working-with-us . **Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:** The selected candidate will… more
- Bristol Myers Squibb (Princeton, NJ)
- …key leadership role ensures that pharmacovigilance (PV) activities align with regulatory requirements and company standards, and drives the strategy and execution ... optimize product benefit-risk profiles. The ED works cross-functionally with clinical, regulatory , medical affairs, quality, and commercial teams to support the safe… more
- Lilly (Branchburg, NJ)
- …SMEs to drive cohesion. Ensure control strategies are robust, consistent with regulatory and compliance expectations, and are continuously improved. + Ensure ... control strategies are robust, consistent with regulatory and compliance expectations, and are continuously improved. + Assume SME leadership role for a specific… more
- Merck (Rahway, NJ)
- …record of increasing responsibility and independence in a similar role in pharmaceutical drug development, regulatory agency, or academia. + Educational ... external vendors and partners, creating an aligned, quantitative and model-informed regulatory framework to impact strategies and decisions of drug discovery and… more
- Sokol Materials & Services (Skillman, NJ)
- …including plans, test protocols, summary reports, and traceability matrices, ensuring regulatory compliance and accuracy. * Investigate and resolve deviations ... Minimum of 3 years of experience in CQV and/or CSV within the pharmaceutical , biotechnology, cell therapy or medical device industries. + Experience with Cell… more
- Sokol Materials & Services (Skillman, NJ)
- …protocols, summary reports, and traceability matrices, ensuring technical accuracy and compliance with regulatory requirements. * Investigate and resolve ... degree is preferred. + Minimum of 7 years of CQV experience in pharmaceutical , biotechnology, cell therapy, or medical device industries, with at least 5 years… more
- Sumitomo Pharma (Trenton, NJ)
- …encounters is considered confidential. ** Compliance ** : Achieve and maintain Compliance with all applicable regulatory , legal and operational rules and ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations...activities in the US adhere to corporate and healthcare compliance guidance in all activities, including those related to… more
- Sysco (Rahway, NJ)
- …Quality Management System (QMS) that ensures product excellence, customer satisfaction, regulatory compliance , and business continuity across the entire supply ... global quality vision and roadmap aligned with company growth objectives and regulatory landscapes. + Lead the design, development, and implementation of global… more