- Oracle (Hartford, CT)
- …driving Oracle's success and competitiveness in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work ... with SaMD in areas such as Regulatory Affairs , Quality Compliance, Product Development, etc. in medical... Affairs , Quality Compliance, Product Development, etc. in medical device industry or equivalent. Experience authoring… 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 ... functions including, but not limited to -- Medical Affairs and Scientific Communications, clinical operations, translational medicine and clinical pharmacology,… more
- Medtronic (North Haven, CT)
- …Have: Minimum Requirements** + Bachelors degree with 4+ years of regulatory affairs experience in the medical device , biotech or pharmaceutical industry ... OR a Masters degree with 2+ years of regulatory affairs experience in the medical device , biotech or pharmaceutical industry. **Nice to Have** +… more
- Bausch + Lomb (Hartford, CT)
- …+ Minimum of 8 years in recent experience in strategic pharmacuetical Regulatory Affairs . This position does not work with medical device , cosmetics or ... and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative...**We offer competitive salary & excellent benefits including:** + Medical , Dental, Eye Health, Disability and Life Insurance begins… more
- Fujifilm (Hartford, CT)
- …**Job Description** **Responsibilities** + Manage and support the day-to-day legal affairs of assigned Medical Device businesses or ... Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with respect to healthcare… more
- Pfizer (Groton, CT)
- …industry, preferably in Drug Development or Clinical Research, ideally within Regulatory Affairs + Subject-matter expertise within assigned therapeutic area ... to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Regulatory Affairs more
- Otsuka America Pharmaceutical Inc. (Hartford, CT)
- …development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and ... in a scientific or technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years' work experience in regulatory… more
- Medtronic (North Haven, CT)
- …with deep knowledge of ISO 14971 to lead risk management strategy for our medical device products (Capital and disposable). This role is pivotal in ensuring ... + Collaborate with cross-functional teams, including R&D, manufacturing, NPD and regulatory affairs , to define and implement systems engineering processes… more
- Adecco US, Inc. (Southington, CT)
- …*Must be familiar with and comfortable using computers. *Working knowledge of the medical device regulatory procedures, lean manufacturing, and manufacturing ... Assembler - Medical Device Assembler, Operations - Adecco...quantity and good manufacturing practices to satisfy customer and Regulatory Affairs requirements. Read and/or understand operating… more
- Medtronic (North Haven, CT)
- …prioritization. * Collaborate with Verification & Validation, Systems Engineering, and Regulatory Affairs to ensure appropriate test coverage and documentation. ... + Knowledge in product development, project management, and commercialization in the medical device industry + Strong communication and teamwork skills; must… more
- Edwards Lifesciences (Hartford, CT)
- …surgery or interventional cardiology are strongly preferred; candidates with other relevant medical device clinical sales support experience will be considered + ... Director and will collaborate with multiple departments including Sales, Clinical Affairs , Marketing, Quality, Regulatory , and Education. After extensive… more
- GE HealthCare (CT)
- …* Work collaboratively with cross functional teams (eg, Engineering, Quality Control, Regulatory Affairs , Technical Support, etc.) to resolve complex product ... experience. * A minimum of three years of relevant experience in medical device industry preferred. * Proficiency in Microsoft Office Suite (Outlook, Word,… more