11 Medical Device Regulatory Affairs Jobs in Andover, MA
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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 14 days ago
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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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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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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 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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Sr. Regulatory Affairs Specialist - Endoscopy Boston Scientific - Marlborough, MA, US Research, develop, and implement regulatory strategies for new and modified medical devices Represent Regulatory Affairs on development core teams, providing Regulatory feedback and guidance throughout 18 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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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
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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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Sr Human Factors Engineer, R&D Collins Consulting Inc - Burlington, Massachusetts , biomechanics, human behavior, and physiology. Demonstrated ability to effectively integrate information from to varied disciplines including Engineering, Marketing, Clinical Affairs, and Regulatory Affairs 26 days ago
Top locations
- Boston, MA (5)
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