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

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 - 6 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

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 - 4 days ago

Exergen Corporation - Watertown, MA, United States

or MS in scientific discipline with at least 7-10 years of direct experience in Quality Assurance and Regulatory Affairs in the Medical Device industry. · Experience leading projects in the medical device

from: linkedin.com - 8 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) - 8 days ago

Walker Cole International - Boston, MA, United States

Devices (commercial clinical trials) Experience in self-diagnostics is sought after Strong understanding of ICH GCP and Medical Device regulatory guidelines Valid Driving Licence GCP | Clinical Research

from: linkedin.com - 5 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 - 6 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 - 16 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 - 7 days ago