- Cramer (Norwood, MA)
- …you need a keen eye for detail to ensure our work adheres to regulatory , legal, and medical guidelines. Your day-to-day will include researching, creating, ... who can take direction and work independently-a creative thinker who is learning regulatory rules-and excited to work closely with internal and external teams to… more
- Cramer (Norwood, MA)
- …you need a strict eye for detail to ensure our work adheres to regulatory , legal, and medical guidelines. Your day-to-day will include researching, creating, ... who can take direction and work independently-a creative thinker who never forgets regulatory rules-and excited to work closely with internal and external teams to… more
- Abbott (St. Paul, MN)
- …with PMA / IDE submissions + Experience with Class III medical devices + Ability to define regulatory strategy. Able to follow scientific arguments, ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Abbott (Maple Grove, MN)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more… more
- Abbott (Pleasanton, CA)
- …integrate information from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. + Medical device industry ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- J&J Family of Companies (Irvine, CA)
- …experience, including leadership/management role within Clinical Research **required** . + Medical device clinical experience is _highly desired_ with a ... Clinical R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs, Regulatory Affairs, Health Economics and Market Access,… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Clinical Development and Medical Affairs Fellow is a post-doctoral pharmacist position that will obtain broad exposure to BI US Medical ... Communications, clinical operations, translational medicine and clinical pharmacology, and regulatory affairs. This position will require the Fellow to develop… more
- AbbVie (Irvine, CA)
- …set the strategy for key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans + ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Apply current regulatory guidance as appropriate for safety surveillance and authorship… more
- Danaher Corporation (Sunnyvale, CA)
- …Union In Vitro Diagnostic Regulation (IVDR) as well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) ... plus if you also possess previous experience in: + ISO 9001:2015 + Regulatory Intelligence Cepheid, a Danaher operating company, offers a broad array of… more
- Danaher Corporation (Sunnyvale, CA)
- …Union In Vitro Diagnostic Regulation (IVDR) as well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) ... Certification + ISO 9001:2015 process and assessment certification activities + Regulatory Intelligence program + Technical Writing Cepheid, a Danaher operating… more