Latest Medical Device Regulatory Affairs jobs in Cambridge, MA

15 Medical Device Regulatory Affairs Jobs in Cambridge, MA

Director of Regulatory Affairs - Software & Systems Philips - Cambridge, MA, US in Regulatory Affairs within FDA regulated medical device/software (SaMD, SiMD) environments (required), with a minimum of 3 years experience in functional/strategic leadership. You have experience More than 30 days ago
Director of Reliability, Availability & Maintainability (RAM) Philips - Cambridge, MA, US , you will collaborate with R&D, Quality Assurance, Regulatory Affairs, and Manufacturing teams to integrate RAM considerations into the product development lifecycle. Provide guidance and training to team members on RAM More than 30 days ago
Quality Regulatory Manager Gabriele & Company - Boston, MA, United States experience in Medical Device industry Regulatory Affairs knowledge Quality Management system knowledge 510K submissions Clinical submissions and trials MDR (Medical Device Rugulation/Reporting) ISO EU 4 days ago
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 18 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 5 days ago
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 16 days ago
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 2 days ago
Hybrid Regulatory Intern Withings - Boston, Massachusetts , 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 20 days ago
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 18 days ago
Regulatory Affairs Manager Pragmatic - Bedford, MA, United States their commitment to excellence in healthcare solutions! The Role As the sole Regulatory Affairs Manager, you'll lead the charge in ensuring compliance with regulatory standards for our medical device products 19 days ago

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