16 Medical Device Regulatory Affairs Jobs in Mansfield, MA
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Regulatory Affairs Specialist III Aditi Consulting - Mansfield, Massachusetts or reusable medical devices to support timelines for CE marking and EU commercial release. Lead the submittal of the EU MDR technical documentation for Class III, IIa, or IIb medical devices and collaborate 6 days ago
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Regulatory Affairs Specialist III_US Mindlance - Mansfield, Massachusetts responsibilities are to: " Serves as the Regulatory Affairs lead on cross-functional MDR project teams " Ensures compliance with EU Medical Device Regulations (MDR) and EU guidance throughout the project. " Actively 6 days ago
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Director Regulatory Affairs Medical Device Shepherd Regulatory Search - Marlborough, MA, United States approvals to market devices throughout the product development lifecycle while building and managing a regulatory team. Responsibilities: Develop strategies for regulatory approval of medical devices 26 days ago
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Regulatory Project Manager Gabriele & Company - Boston, MA, United States corrective actions Assist with regulatory information management system, QMSR processes, new eQMS Requirements: Bachelor's degree 7+ years of Quality/Regulatory Affairs experience in Medical Device industry 12 days ago
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regulatory affairs specialist (cambridge) Randstad - cambridge, massachusetts or equivalent internationally-acquired qualifications preferably in Regulatory Affairs and/or a science related field or equivalent experience in the medical device industry Minimum 3 years of regulatory $65 - $80 per hour 2 days ago
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QA/RA Specialist Walker Cole International - Boston, MA, United States . The successful Quality Manager will have: 3+ years of experience in Regulatory Affairs within the Medical Devices Industry Strong working knowledge of Quality Management Systems including ISO13485 requirements 24 days ago
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Medical Device Product Manager Exergen Corporation - Watertown, MA, United States manner. The ideal candidate is a technically capable, results-oriented leader with experience in successfully executing medical device product development and marketing programs. Key Responsibilities 10 days ago
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Specialist I, Regulatory Affairs Olympus Corporation of the Americas - Westborough, MA, US Required: Regulatory affairs experience in the Medical Device industry is mandatory [minimum 3 years with BS/BA, or 5 years with Associates degree]. Ability to work in small team environment, but also self 16 days ago
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Regulatory Manager BostonGene - Waltham, MA, United States plus years of experience in Regulatory Affairs, including United States and international medical device and/or IVD/CDx regulations. 8 plus years of experience in medical device and/or IVD/CDx industry 26 days ago
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Senior Contract and Budget Associate Ergomed - Boston, Massachusetts , with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class 13 days ago
Top locations
- Westborough, MA (5)
- Boston, MA (4)
- Cambridge, MA (2)
- Marlborough, MA (2)
- Andover, MA (1)
- Bedford, MA (1)
- Burlington, MA (1)
- Waltham, MA (1)
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