- Bristol Myers Squibb (Summit, NJ)
- …there's no better place than here at BMS with our Cell Therapy team. The Associate Director , Drug Product External Manufacturing QA provides Quality ... Review, Lot disposition to support the clinical and commercial release of Drug Product . This role will also develop and manage the collaboration and governance… more
- Merck (Rahway, NJ)
- …Research & Division organization of our company. ** ** **Position Description/Summary:** The GPAM Associate Director , Project Manager, is a core member of Early ... **Job Description** **Job Description:** The drug development Project Manager is part of Global...& Development pipeline and realize its full potential. The Associate Director is expected to provide project… more
- Bristol Myers Squibb (Princeton, NJ)
- …strategic initiatives. **Position Summary** Support the development and execution of Drug Development's (DD) Innovation strategy in partnership with DD Leaders, ... The role will require experience with Innovation, emerging technologies, product development / roadmaps, transformational / change leadership, and executive… more
- Merck (Rahway, NJ)
- **Job Description** **Position Description:** Reporting to a Technology Director or Associate Director in Global Engineering Solutions (GES), the ... Associate Director will be part of a high performing team,...knowledge transfer. Candidates with significant experience in engineering design ( Drug Substance, Drug Product , Plant… more
- Capital One (New York, NY)
- Sr Director , Experience Design Research - Enterprise Developer, Associate and Accelerator Design Capital One's Experience Design (XD) organization creates ... memorable, meaningful customer and associate experiences that build our brand with humanity and...The goal of Experience Design Research is to accelerate product teams' learning velocity. We do this by conducting… more
- Bristol Myers Squibb (Princeton, NJ)
- …enhance value of the pharmaceutical product profile. BMS is seeking an Associate Director of Diagnostic Sciences to fulfill this critical role. **MAJOR ... diagnostics (CDx) biomarkers in support of the BMS portfolio. **Summary** The Associate Director of Diagnostic Sciences provides subject matter expertise related… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for ... strategy of multiple assigned products in various stages of drug development, which may include one high complexity ...drug development, which may include one high complexity product and updates to or creation of a new… more
- United Therapeutics (Trenton, NJ)
- …cardiovascular and pulmonary diseases, and other orphan diseases. **How you'll contribute** The Associate Global PV Case Management Director plays a key role in ... in vendor management and oversight + 3+ years of product development and/or postmarketing drug experience +...3+ years of product development and/or postmarketing drug experience + 2+ years of previous functional lead/people… more
- WuXi AppTec (Cranbury, NJ)
- **Overview** ** Associate Director , Project Management (Oligo and Peptide)** **Area of focus: Discovery or medicinal chemistry** **Job Location: Remote USA with ... industry experience preferably in API process R&D and manufacturing and/or Drug Product R&D and manufacturing. + Prior experience in project management or… more
- Sanofi Group (Bridgewater, NJ)
- **Job Title:** Associate Director , Non-Alliance Specialty **Location:** Cambridge, MA or Bridgewater, NJ **About the Job** The Associate Director of ... + Meticulous organizational skills and auditable accuracy in work product + Ability to manage multiple priorities and timelines...process and implication on brand P&L + Understanding of drug pricing, including First Databank and / or Medispan… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Agile Sourcing, Research & Development - Data & ... operations within a subset of the Research & Global Drug Development organizations. Specifically, this role will be focused...comfortable with leading change and taking calculated risk. The Associate Director will lead a team of… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small ... such as IDMP ISO standards for identifying medicinal products and WHO Drug Dictionary + Maintain pharmaceutical product reference data (non-company)… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - Neuroscience TAU ... with the program Global Regulatory Lead (GRL), co-lead and facilitate product -specific Global Regulatory Team (GRT) meetings and cross-functional submission working… more
- Merck (Rahway, NJ)
- …production with respect to device component manufacture and final assembly of biologic/ drug product with device constituent part. + Lead/support the development, ... degree is preferred. + Leadership experience with working knowledge of device, biologic/ drug product , and process development including regulatory submission and… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Regulatory Affairs Strategy Princeton, NJ, USA Req #415 Wednesday, November 27, 2024 Looking for a chance to make a meaningful difference in ... directs global regulatory affairs activities and provides regulatory guidance during drug development, approval and post approval processes and commercialization, in… more
- Merck (Rahway, NJ)
- …and accountable for establishing the timelines for bulk manufacturing needs and release of drug product across assigned program(s). + Works directly in the SAP ... visible forecast for all products used within the assigned program(s) (ie Bulk Drug Product ). + Oversees all bulk drug supply management and ensures proper… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …R&D and Business Unit teams within a multi-disciplinary framework to meet product needs. + Development of evidence for COA measurement strategies for development ... post-authorization and commercial research activities supporting patient-centered needs and product value to regulators, HTA/payers, health care providers and… more
- WuXi AppTec (Cranbury, NJ)
- …or CRO/CMO industry experience preferably in API process R&D and manufacturing and/or Drug Product R&D and manufacturing. + Prior experience in project ... worldwide partners efficient, flexible, and high-quality solutions for the drug development of oligonucleotides, peptides and related synthetic conjugates ("TIDES"… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …collaborates closely with data manager to ensure high quality data. - Drug Development Strategy: Provides input to multiple aspects of the development plan ... are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile. - CRO / Vendor Oversight: Review CRO/vendor proposal and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …meet smooth transition with other sub projects with respect to supply, product quality and stakeholder satisfactions. Responsible to communicate and escalate to ... and management to drive strategies and activities for early and late phase drug development candidates within the team to support overall CMC development plan. -… more