Medical Device Regulatory Affairs Jobs in Somerville, NJ

ClinChoice - Raritan, NJ, United States

week at Raritan, NJ office). We are looking for Candidates with Proven experience in regulatory affairs in Class III medical devices and PMA submissions in this position. ClinChoice is a global CRO

from: linkedin.com - Yesterday

EPM Scientific - Bridgewater, NJ, United States

of 12 years of experience in regulatory affairs and quality assurance within the medical device industry. Proven track record of successful PMA submissions and approvals for medical devices. Thorough

from: linkedin.com - 7 days ago

Katalyst Healthcares & Life Sciences - Edison, New Jersey

. Working knowledge of industry consensus standards and FDA guidance is required At least 2 years Regulatory Affairs experience in Medical Device regulations Demonstrated success in taking products through

from: resume-library.com - 16 days ago

Tandym Group - Florham Park, NJ, United States

per device safety reporting requirements In-depth knowledge of the Drug Development process, Signal Detection, and Regulatory Affairs In-depth knowledge of Domestic and Global Safety regulations Profound

from: linkedin.com - 16 days ago

Clinical Dynamix, Inc. - East Brunswick, NJ, US

experience in preparing regulatory submissions including IDEs, 510(k)s and/or PMAs is required. Experience in working with medical device software requirements and companion diagnostics is a plus. A minimum

from: jobvertise.com - 2 days ago

Integrated Resources, Inc - Plainsboro, New Jersey

, and error proof manufacturing processes. " Perform timely technical investigations and provide practical manufacturing solutions, under appropriate regulatory guidelines for Medical Device Manufacture

from: resume-library.com - Yesterday