Medical Device Regulatory Affairs Jobs in Boston, MA

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

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

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

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

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

ProClinical - Boston, MA

operational excellence initiatives within the Regulatory Affairs department. If you are having difficulty in applying or if you have any questions, please contact Nicholas Walker at (+1) 646-367-2908

from: careerbuilder.com - 9 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 - 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 - 14 days ago

Biogen - Cambridge, Massachusetts

of experts from regulatory sciences, pre-clinical, safety, clinical development, clinical operations, medical affairs and clin pharm. This team is accountable for the successful integration of the platform

from: resume-library.com - 22 days ago

TransMedics, Inc. - Andover, MA, United States

14971 to make informed decisions related to our processes and products. Collaborate closely with Regulatory Affairs, Operation, Service, and Quality Assurance teams. BACKGROUND AND QUALIFICATIONS

from: linkedin.com - 11 days ago