Medical Device Regulatory Affairs Jobs in Bedford, MA
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 - 4 days ago
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 - 27 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 - 4 days ago
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 - 13 days ago
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 - 3 days ago
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 - 6 days ago
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 - 22 days ago
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 - 27 days ago
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
Register your RESUMEfrom: resume-library.com - 10 days ago
TransMedics, Inc. - Andover, MA, United States
targets and objectives are completed effectively and in a timely manner. The ideal candidate is a technically capable, results-oriented leader with experience in successfully executing medical device
from: linkedin.com - 11 days ago
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