- Sanofi Group (Cambridge, MA)
- …year (3+ years preferred) of regulatory experience, preferably within the pharmaceutical/ medical device /biotech industry + Knowledge and understanding of complex ... **Job Title:** Associate Director , Global Regulatory Affairs Advertising and Promotion **Location**...and maintains strong collaborative relationships with Regulatory and other R&D colleagues, as well as other stakeholders (eg, Legal,… more
- Sanofi Group (Cambridge, MA)
- …**About You** **Experience:** + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record of **relevant ... **Job Title:** Director , US Regulatory Affairs - Advertising and Promotion...develops key internal relationships with therapeutic product leaders in R&D and Corporate to foster open communication and teamwork.… more
- Philips (Cambridge, MA)
- …You've acquired 10+ years of experience working in Regulatory Affairs within the medical device industry; Experience with software-enabled medical devices, ... ** Director , Regulatory Affairs- Software and Artificial Intelligence (Ultrasound)**...partnerships between Regulatory Affairs and all key stakeholders including R&D , Product Management, Quality, Medical & Clinical… more
- Medtronic (Boston, MA)
- …and/or Sales Operations) + 6+ years of experience in the pharmaceutical, biotech, medical device , and/or healthcare industries + Minimum 5+ yrs experience in ... brand goals and objectives + Partner with Clinical Marketing, Medical Affairs to provide commercial perspective on publications, scientific...to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference… more
- Fujifilm (Boston, MA)
- …senior product manager, product/technical director ). + Minimum 8 years of medical device experience with strong clinical background. + Prior experience in ... R&D , operations, regulatory, global marketing, infection control, other companies/ device manufacturers, etc.) + Build and maintain strong relationships with Key… more
- Tecomet (Woburn, MA)
- …is completed for identified issues. + Manage the Complaint Handling process and Medical Device Reporting activities. + Oversee the performance of internal and ... and facilitate the development of quality systems for a highly regulated medical device , aerospace, defense industries to achieve customer satisfaction,… more
- Danaher Corporation (Boston, MA)
- …innovation and excellence in the Biopharma sector. This position reports to the Director , Regulatory Affairs and is part of the Global Regulatory Affairs and will ... regulations on the development and registration activities for the respective medical products + Develop and manage regulatory submissions (eg, 510(k), PMA,… more
- ConvaTec (Lexington, MA)
- …a research emphasis on biointerfaces and regenerative engineering + Experience in medical device developing and testing **Travel Requirements** Position requires ... Pioneering trusted medical solutions to improve the lives we touch:...science and our four business units. Reporting to the Director of Biomedical Sciences, this role requires a blend… more
- Norstella (Boston, MA)
- …leading providers of data and intelligence on clinical trials, drug treatments, medical devices and what's new in the regulatory and commercial landscape. Relying ... on us to deliver vital advantage when making critical R&D and commercial decisions, our customers come from over 3000 of the world's leading pharmaceutical, contract… more
- Norstella (Boston, MA)
- …leading providers of data and intelligence on clinical trials, drug treatments, medical devices and what's new in the regulatory and commercial landscape. Relying ... on us to deliver vital advantage when making critical R&D and commercial decisions, our customers come from over 3000 of the world's leading pharmaceutical, contract… more