11 Medical Device Regulatory Affairs Jobs in Westborough, 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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Global Lead, Medical Affairs, Gastroenterology Olympus Corporation of the Americas - Westborough, MA, US Gastroenterology Fellowship Trained Board Certification Minimum of 10 years of biotechnology/pharmaceutical/medical device industry experience in medical affairs, medical technology, medical strategy with experience More than 30 days ago
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Regional Head of Engineering - Digital Unit Olympus Corporation of the Americas - Westborough, MA, US effectively in cross-functional areas such as R&D, Product Management, Quality, and Regulatory Affairs. Experience working in global, matrixed organizations. Proven experience in creating and managing R&D More than 30 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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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 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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Director of Quality Assurance and Regulatory Affairs Precision Optics Corporation Inc - Gardner , Massachusetts 01440 , United States years of experience in quality assurance & regulatory affairs, preferably in process-oriented manufacturing operations in a regulated environment Minimum 3 years of experience leading quality management 4 days ago
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Manager, Product Quality AbbVie - Worcester, Massachusetts ), Supply Chain, Program Management, Commercial, Medical, Pharmacovigilance, and Regulatory Affairs. Coordinate quality system elements, training, continuous improvement, and tactical support across functions 20 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
- Boston, MA (5)
- Mansfield, MA (3)
- Cambridge, MA (2)
- Marlborough, MA (2)
- Burlington, MA (1)
- Waltham, MA (1)
- Woburn, MA (1)
- Gardner, MA (1)
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