Medical Device Regulatory Affairs Jobs in Cambridge, MA

Philips - Cambridge, MA, US

in Regulatory Affairs within FDA regulated medical device/software (SaMD, SiMD) environments (required), with a minimum of 3 years experience in functional/strategic leadership. You have experience

from: jobvertise.com - More than 30 days ago

Philips - Cambridge, MA, US

, you will collaborate with R&D, Quality Assurance, Regulatory Affairs, and Manufacturing teams to integrate RAM considerations into the product development lifecycle. Provide guidance and training to team members on RAM

from: jobvertise.com - More than 30 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 - 5 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 - 19 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 - 6 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 - 17 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 - 3 days ago

Withings - Boston, Massachusetts

, as assigned. Requirements Qualifications: Student seeking a Bachelors or Masters degree in regulatory affairs Knowledge in US medical device regulations,21 CFR 820 Quality System Regulation and standards

from: resume-library.com (+1 source) - 21 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 - 19 days ago

Pragmatic - Bedford, MA, United States

their commitment to excellence in healthcare solutions! The Role As the sole Regulatory Affairs Manager, you'll lead the charge in ensuring compliance with regulatory standards for our medical device products

from: linkedin.com - 20 days ago