Medical Device Regulatory Affairs Jobs in Andover, MA

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

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

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

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

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

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

from: resume-library.com - 6 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

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

Johnson & Johnson - Danvers, MA

for medical devices, considering factors such as product protection, sterility, usability, and regulatory requirements. Collaborate with cross-functional teams, including R&D, Quality, Regulatory Affairs

from: Dice.com - 14 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 - 19 days ago