Medical Device Regulatory Affairs Jobs in Chelmsford, MA
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Aquent - Chelmsford, MA, United States
lifecycle of our Advanced Life Saving Devices, from ideation to launch and beyond. This role requires a deep understanding of the medical device industry, clinical needs, and market trends. The Senior Product
from: linkedin.com - 14 days ago
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Cambridge Interventional - Burlington, MA, United States
Regulatory Affairs and Quality Assurance Manager Cambridge Interventional is seeking a Manager of RA/QA. Cambridge Interventional is a medical device manufacturer committed to advancing
from: linkedin.com - 15 days ago
Medtronic - Boston, MA
affairs experience Nice to Have 7+ years of medical device regulatory affairs experience An advanced degree in regulatory affairs or technical field such as engineering Experience in Pre-Sub, 510(k), De
from: Dice.com - 15 days ago
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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
from: linkedin.com - 13 days ago
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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
from: linkedin.com - 8 days ago
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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
Register your RESUMEfrom: resume-library.com - 17 days ago
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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
from: linkedin.com - 13 days ago
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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
from: linkedin.com - 5 days ago
Boston Scientific - Marlborough, MA, US
Qualifications: Minimum of a Bachelor’s degree with a minimum of 5 years’ experience in Regulatory Affairs or a related discipline (e.g. Quality Systems, R&D, Quality, Post Market) within the medical device, IVD
from: Boston Scientific - 22 days ago
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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
from: linkedin.com - 24 days ago
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