- Sanofi Group (Cambridge, MA)
- **Job title: Device Regulatory Lead ( Associate Director)** + Location: Bridgewater, NJ or Swiftwater, PA or Cambridge, MA **About the job** The Global ... thought was possible. Ready to get started? **Main responsibilities** + Serve as Device Regulatory Lead on assigned project teams (early phase, late stage… more
- Sanofi Group (Cambridge, MA)
- …the job** The Associate Director, US Advertising and Promotion serves as the regulatory lead on Review Committees (RCs) for products in the Rare Disease, ... **Job title: Associate Director, US Advertising and Promotion, Global Regulatory Affairs** + Location: Bridgewater, NJ or Cambridge, MA **About… more
- Sanofi Group (Cambridge, MA)
- …the job** The Associate Director, US Advertising and Promotion serves as the regulatory lead on Review Committees (RCs). As the RC Regulatory Affairs ... **Job title: Associate Director, US Advertising and Promotion, Global Regulatory Affairs** + Location: Cambridge, MA or Bridgewater, NJ **About… more
- IQVIA (Boston, MA)
- …to subject/patient recruitment and on time high quality data collection. The Clinical Lead provides leadership of the clinical team, in support of the project ... for Request for Proposals (RFPs). + Participate in bid defense preparations. Lead the Clinical delivery strategy at bid defense presentations in partnership with… more
- Medtronic (Boston, MA)
- …Medical Education, Global Field Training, Clinical Research, Research and Development, Regulatory and Legal. **A DAY IN THE LIFE - POSITION RESPONSIBILITIES:** ... updated best practices within region + Develops therapy and device operational knowledge and applies this knowledge to processes...as the District Expert and function as the District Lead for simulation + Collaborates with the Global Field… more
- Zimmer Biomet (Boston, MA)
- …respected, empowered, and recognized. **What You Can Expect** The Program Associate Director will oversee lifecycle management business processes to enable the ... key functional areas - Research, Business Development, Finance, Clinical, Commercial, Legal and Regulatory . + Analyze the data related to the portfolio as owned by… more
- embecta (Andover, MA)
- …in Engineering or related field + 10+ years of post-educational experience in Medical Device Design highly desired + Experience as lead in the development of ... **The Staff Engineer, R&D - Verification and Validation, is the technical lead in the design verification or design validation of electromechanical medical devices… more
- embecta (Andover, MA)
- …in Engineering or related field. + 10+ years of post-educational experience in Medical Device Design highly desired. + Experience as lead in the development of ... Engineer, R&D - Verification and Validation, is the technical lead in the design verification or design validation of...medical devices developed by embecta. Reporting up to the Associate Director, R&D - Verification and Validation, the successful… more
- J&J Family of Companies (Raynham, MA)
- …and product release for Medical Devices. In addition, the Site Quality Lead of Raynham/Bridgewater will identify and facilitate the implementation of key ... related to compliance, technology investments, regulation, and resource management/optimization. The associate partners with Site and Business Unit leaders to drive… more
- Amgen (Cambridge, MA)
- …colleagues in identification of user needs from market insights. The SMSE will lead a team responsible for the creation and management of system requirements, ... across the interactions, dependencies, and interfaces of subsystems. The SMSE will lead a team responsible for the integration of the system through clinical… more
- Medtronic (Boston, MA)
- …is assigned to the business unit. + Develop and maintain therapeutic and device operation knowledge; apply this knowledge to the development of well-written, clear, ... analyze literature search results + Address deficiencies and or answer questions from regulatory agencies as needed + Create and manage project schedule for each… more
- Element Materials Technology (Acton, MA)
- …for cleanrooms that may be utilized by hospital pharmacies, and/or medical device and biotechnology companies to manufacture products such as parenteral medicines, ... clients with crucial data to be able to maintain regulatory requirements (ie, ISO, A2LA, FDA, EU, USP, etc.)....at least three years of work experience or an associate degree or greater in a Life Sciences discipline… more