11 Medical Device Regulatory Affairs Jobs in Boston, MA
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Principal Regulatory Specialist Amplitude Vascular Systems - Boston, MA, United States related experience in medical device industry. Regulatory Affairs Certification expected (US) Experience with design controls, including mechanical, software/firmware and risk management review. Experience 9 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 25 days ago
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Hybrid Regulatory Intern Withings - Boston, MA , as assigned. Requirements Qualifications: Student seeking a Bachelors or Masters degree in regulatory affairs Knowledge in US medical device regulations,21 CFR 820 Quality System Regulation and standards 15 - 20 More than 30 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 26 days ago
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Associate Director, US Regulatory Affairs, Advertising & Promotion Proclinical Staffing - Cambridge, MA, United States schedule. Skills & Requirements: At least five (5) years of experience involving the direct implementation of promotional labeling and advertising regulations in the biotech/pharmaceutical/medical device 6 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 14 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 15 days ago
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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 3 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 3 days ago
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Senior Manufacturing Engineer RCM Technologies, Inc. | Life Sciences & IT - Woburn, Massachusetts Job Title: Senior Manufacturing Engineer Job Function: The Manufacturing Engineer will drive Engineering requirements within our medical device client's Operations team and play an active part 20 days ago
Top locations
- Mansfield, MA (3)
- Cambridge, MA (2)
- Marlborough, MA (2)
- Westborough, MA (2)
- Burlington, MA (1)
- Waltham, MA (1)
- Woburn, MA (1)
- Gardner, MA (1)
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