- Genmab (NJ)
- …feel like a fit? Then we would love to have you join us!The Global Regulatory Labeling , Policy and Intelligence Associate Director will primarily be ... of labeling documents according to internal SOPs and external regulatory requirements.Prepare submission-ready labeling documents; Maintain and track … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and ... applications/supplements & variations (eg, NDA, BLA, MAA). This position authors regulatory documents where necessary with supervision. This position conducts … more
- Merck & Co. (Rahway, NJ)
- …of clinical trial s .- GCS is accountable for the planning, sourcing, labeling , packaging and delivery of clinical supplies to clinical sites globally. The GCS ... as a lead GCS Planning program representative ) such as clinical development, regulatory , quality and other supply chain areas to negotiate timelines ,- strategies… more
- Takeda Pharmaceuticals (Boston, MA)
- …In alignment with TAU/MPD Labeling Lead, coordinates the process to obtain labeling approval by Labeling Senior Management Cross-functional team (Global ... bring life-changing therapies to patients worldwide. Join Takeda as Associate Director, Global Labeling Lead where you...and alignment of the labeling strategy and labeling content. Interface with Senior Management Cross-Functional… more
- Chiesi (Cary, NC)
- …new labeling and changes to existing labeling , and submission of labeling information to regulatory authorities in the United States and Canada. Main ... duties in Canada. + Manage and oversee the submission of promotional labeling materials and supporting documentation to regulatory agencies in accordance… more
- Edwards Lifesciences (Irvine, CA)
- …that we are supporting the needs and interests of the patients we serve. The Senior Director, Corporate & Regulatory Counsel role is a blend of subject matter ... legal expert and strong business acumen. The Senior Director, Corporate & Regulatory Counsel will...the Edwards Headquarters, in Irvine CA and reporting to Senior Vice President, Associate General Counsel, TAVR… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director, Global Regulatory Affairs Advertising and Promotion **Location** : Cambridge, MA Morristown, NJ **About the Job** Are you ... our teams accelerate progress. This individual will be responsible for providing regulatory review and approval of US promotional and other product and… more
- Boehringer Ingelheim (Ridgefield, CT)
- …can support projects of increasing regulatory complexity and/or business impact. The Senior Associate Director, US Product CMC Regulatory Affairs is ... to FDA concerning assigned US investigational and marketed product interactions. The Senior Associate Director position is expected to support projects of… more
- Lilly (Indianapolis, IN)
- …Senior Director-Medical is delegated various responsibilities by the Associate Vice-president or equivalent role to provide leadership, supervision, coordination, ... all necessary regulatory standards. + Provide support for global registrations, labeling and label modifications, and resolution of regulatory issues. +… more
- Amgen (Washington, DC)
- …us and transform the lives of patients while transforming your career. **Global Safety Senior Scientist** **What you will do** Let's do this. Let's change the world. ... management system + Author Safety Assessment Reports and other safety documents and regulatory responses in collaboration with the GSO + Search and review adverse… more
- Allegion (Indianapolis, IN)
- … regulatory submittal. + Perform weekly hazardous waste inspections as per regulatory requirements. + Ensure proper labeling and management of hazardous ... individual to join our team as a Wastewater Treatment Operator or Senior Wastewater Treatment Operator, depending on experience and qualifications. This role is… more
- BioBridge Global (San Antonio, TX)
- …recovery from living and deceased donors._ Job Title: Blood & Tissue Manufacturing Associate I Revision: 0002 Job Code: 700236 Shift: Saturday, Sunday and Monday ... and perform all phases related to blood components production and labeling in accordance with all Standard Operating Procedures (SOPs), organizational policies,… more
- WM (Waco, TX)
- …Other minor duties may be assigned. + Ensure waste types are properly segregated, regulatory shipment windows are met, proper container labeling is adhered to, ... WM?** Stability. Growth. People-First Culture (https://www.wm.com/us/en/inside-wm/who-we-are) . **About the Senior Environmental Technician Role** Supports Sustainability Services onsite program,… more
- Banner Health (Phoenix, AZ)
- …you are looking to leverage your abilities - apply today. As an **Oncology Senior Acute Pharmacy Technician** , you will be responsible for cleanroom procedures, IV ... better as we aim to prevent and cure cancer. As an **Oncology Infusion Senior Acute Pharmacy Technician** , you will be supported by chemotherapy trained Pharmacy… more
- Merck (West Point, PA)
- …portfolio of clinical trials. GCS is accountable for the planning, sourcing, labeling , packaging and delivery of clinical supplies to clinical sites globally. The ... a lead GCS Planning program representative) such as clinical development, regulatory , quality and other supply chain areas to negotiate timelines, strategies… more
- ATS Automation (Souderton, PA)
- …12002 Location: Souderton, PA, US, 18964 Date: Jul 10, 2025 Inventory Control Associate Position Title: Inventory Control Associate , NCC, ATS COMPANY Automated ... expansions, and productivity improvement initiatives. Position Overview: Inventory Control Associate Support production teams by locating, staging, and issuing… more
- J&J Family of Companies (Santa Clara, CA)
- …the treatment of calcified plaque. **Position Overview** The Sr. Clinical Research Associate (Sr. CRA) will be responsible for establishing, managing and meeting ... milestones of clinical studies in compliance with applicable clinical and regulatory standards and in alignment with business needs. They will be accountable for… more
- Bristol Myers Squibb (Madison, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director of WW Medical Neuroscience, Neuro degeneration Medical ... including WW Commercial, Research and Development, Global Drug Development, HEOR, Regulatory Affairs, and other global medical stakeholders. This position reports to… more
- Bristol Myers Squibb (Princeton, NJ)
- …integration points across US functional and commercialization areas to ensure alignment. The Associate Director will report to the Senior Director, US Medical ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , US Medical Neur opsychiatry position works in the US… more
- Grifols Shared Services North America, Inc (San Diego, CA)
- …of translations for documentation and software development. + Ensure compliance of labeling with all applicable regulatory /QSR requirements. + Create and edit ... Diego, CA. This role will be reporting to the Senior Manager, Verification and Validation. This position will provide...documentation in compliance with requirements from applicable regulatory bodies (FDA, IVDR, EUDR) and the European Union… more
