Medical Device Regulatory Affairs Jobs in Mansfield, MA

Aditi Consulting - Mansfield, Massachusetts

or reusable medical devices to support timelines for CE marking and EU commercial release. Lead the submittal of the EU MDR technical documentation for Class III, IIa, or IIb medical devices and collaborate

from: resume-library.com - 6 days ago

Mindlance - Mansfield, Massachusetts

responsibilities are to: " Serves as the Regulatory Affairs lead on cross-functional MDR project teams " Ensures compliance with EU Medical Device Regulations (MDR) and EU guidance throughout the project. " Actively

from: resume-library.com - 6 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 - 26 days ago

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

from: linkedin.com - 12 days ago

Randstad - cambridge, massachusetts

or equivalent internationally-acquired qualifications preferably in Regulatory Affairs and/or a science related field or equivalent experience in the medical device industry Minimum 3 years of regulatory $65 - $80 per hour

from: randstadusa.com - 2 days ago

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

from: linkedin.com - 24 days ago

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

from: linkedin.com - 10 days ago

Olympus Corporation of the Americas - Westborough, MA, US

Required: Regulatory affairs experience in the Medical Device industry is mandatory [minimum 3 years with BS/BA, or 5 years with Associates degree]. Ability to work in small team environment, but also self

from: Olympus Corporation of the Americas - 16 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 - 26 days ago

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

from: snapjobsearch.com - 13 days ago