- 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
- Bristol Myers Squibb (New Brunswick, NJ)
- …goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Drug Product Development (DPD)** Our Drug Product ... leading the development, execution, and monitoring of externalization strategy for DPD's drug product portfolio and technology platforms. To achieve this… more
- Merck (Rahway, NJ)
- …lifecycle and maintaining programs in harmony with the portfolio. In addition, the Associate Director will be expected to participate in development of tools ... integration of CMC and Clinical strategies. ** ** **Position Description/Summary:** The CIPM Associate Director , Project Manager, is a core member of DCTs,… more
- Ascendis Pharma (Princeton, NJ)
- …governing the promotion of prescription drug and biologic products. The Associate Director Regulatory Affairs, Advertising and Promotion is responsible for ... committed to working together as one team to achieve extraordinary results. The Associate Director Regulatory Affairs, Advertising and Promotion will be an… 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
- Gilead Sciences, Inc. (Parsippany, NJ)
- …and unique opportunity for a medical writer to join our dynamic team at the Associate Director level. You will author a wide range of regulatory documents ... development, and commercial teams. Medical Writing participates in cross-functional drug discovery, development and commercial product lifecycle management… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position: Associate Director , WW Medical Neuropsychiatry Strategy, Schizophrenia** ... **Location: Princeton Pike or Madison, NJ** The Associate Director of Medical Strategy, Schizophrenia will...including US and WW Commercial, Research and Development, Global Drug Development, HEOR, Regulatory Affairs, and other global medical… more
- Sunrise Senior Living (Basking Ridge, NJ)
- …**COMMUNITY NAME** Sunrise of Basking Ridge **Job ID** 2024-220603 **JOB OVERVIEW** The Associate Director of Sales (ADOS) is responsible for supporting and ... duties the ADOS may, under the supervision of the Director of Sales (DOS), Director of Sales...and positive relationship with prospects by understanding the Sunrise product and how Sunrise can meet the customers' needs.… more
- Sumitomo Pharma (Trenton, NJ)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs** . The Associate Director ... functional plan through the research, review and interpretation of related product approvals, current regulatory guidance documents and recent public Advisory… 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
- Lilly (Branchburg, NJ)
- …$111,000 - $162,800 **Position Description:** The Clinical Trial (CT) Supply Management Associate Director will provide operational leadership of clinical supply ... data, systems, and processes to drive operational excellence and meet Clinical Drug Supply business goals. They will be responsible for driving robust, strategic… 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
- Sumitomo Pharma (Trenton, NJ)
- …. **Job Overview** Associate Director , ... Women's Health (including sub-specialty) preferred. + Solid understanding of drug and life-cycle development of a product ....of drug and life-cycle development of a product . + The ability to work effectively with key… 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
- Merck (Rahway, NJ)
- **Job Description** The Associate Director , Comparator Management is responsible for the sourcing and product management (assessment, order, delivery, ... Managers (CSPM) and function as an independent expert in supply planning, product management and buyer of non-Company commercial products. Candidates should have… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - GI2 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
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Join Gilead and help create possible, together. **Job Description** Job Description ** Associate Director , Clinical Pharmacology - Oncology** **_*This is a ... to cross-functional partners. **EXAMPLE RESPONSIBILITIES:** + As a member of a drug development team, routinely provides input into product development… 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