Medical Device Regulatory Affairs Jobs in Somerville, NJ

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Complaint Specialist, Post-Market Surveillance  

GForce Life Sciences - Parsippany, NJ, United States (+1 location)

Requirements B.S. Degree, preferably in Engineering 2+ years of prior complaint-handling experience with a medical device company Quality experience Nice to Have Prior experience processing medical device

from: linkedin.com - 4 days ago

Senior Pharmacovigilance Associate  

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 - 6 days ago

Regulatory Affairs Specialist II  

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

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from: resume-library.com - 6 days ago

Regulatory Affairs Manager  

Johnson & Johnson Consumer Inc. - Skillman, NJ

and/or Regulatory Affairs Certification (RAC) is desirable * Class I/II Medical Devices and Dietary Supplements, is desirable. What's in it for you * Annual base salary for new hires in this position ranges

from: Johnson & Johnson Consumer Inc. - 9 days ago

Regulatory Affairs Manager  

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 - 24 days ago

Manufacturing Engineer II  

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

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from: resume-library.com - 20 days ago

Associate Principal Scientist, GRACS CMC Regulatory and Quality (Hybrid)  

Merck - Rahway, NJ 07065

for the organization. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory

from: Pharmadiversityjobboard.com - 20 days ago


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