Medical Device Regulatory Affairs Jobs

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Regulatory Affairs specialist  

Katalyst Healthcares & Life Sciences - Plainsboro, New Jersey (+2 locations)

for regulatory affairs in supporting changes in the regulatory landscape, including EU MDR. Identify opportunity for regulatory affair processes and drive changes to completion. " Help with our international

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from: - 10 days ago

Senior Regulatory Affairs Specialist  

TalentBurst, Inc. - Plymouth, Minnesota

Regulatory Affairs Skills: Have working knowledge in EU MDR Have working knowledge in Regulatory Change Assessment in Have working knowledge in US and EU medical device submissions Have experience supporting

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from: (+1 source) - 4 days ago

Senior Regulatory Affairs Specialist  

Apex Systems - Plymouth, MN 55441

Job 1349150 Job Description Apex Systems is actively hiring a Senior Regulatory Affairs Specialist near Plymouth, MN for a 12 month contract with an American producer of medical devices, diagnostics

from: - 5 days ago

Senior Regulatory Affairs Specialist  

GTT, LLC - Plymouth, Minnesota

for regulatory affairs processes and drive changes to completion. Required Experience: Must have 3-5 years of experience in Medical Device Regulatory Affairs Required Skills: Have a working knowledge of EU MDR

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from: - 2 days ago

Regulatory Affairs Manager - Global UDI and EU EUDAMED  

Axelon Services Corporation - Parsippany, New Jersey

Regulatory Affairs Manager - Global UDI and EU EUDAMED Remote (Work From Home) 12+ Months Contract Required Skills " Minimum of 2 years Medical Device Regulatory Affairs Experience " US UDI

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from: - 6 days ago

Regulatory Affairs Associate  

DivIHN Integration Inc - Alameda, California 94502

, such as UKCA marking. Requires an advanced degree in science, engineering or related discipline and a minimum of 3 years experience in medical device regulatory affairs. Experience with global regulations

from: (+1 source) - 5 days ago

Regulatory Affairs Associate  

Actalent - Bloomingdale, Illinois

: Regulatory Affairs, Medical Device, Regualtory Documents, FDA, EU MDR, Global Registration, Regulatory Submissions, cGMP, ISO 13485:2016, MDSAP Top Skills Details: Regulatory Affairs,Medical Device,Regualtory

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from: - 4 days ago

Regulatory Affairs Coordinator  

Careerbuilder-US - Franklin Lakes, New Jersey

Our client, a leading medical devices company, is looking for a Regulatory Affairs Coordinator. This is for an initial duration of 8 months and is located in Franklin Lakes, NJ. This is a Hybrid 3

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from: - 9 days ago

Quality Assurance Manager  

CyberCoders - Centennial, CO

Quality Assurance Manager with at least 5 years of relevant experience. You must have a strong knowledge of Medical Device, Regulatory Affairs, Inspection, Test, and Quality Assurance processes 95,000.00 - $110,000.00

from: - 10 days ago

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Manager, Regulatory Affairs  

Thermo Fisher Scientific - Remote, Virginia, United States of America (+1 location)

. Minimum of 6 years of IVD or Medical Device Regulatory Affairs experience or 4 years with advanced degree Hands-on experience with classification of devices; listing, registration, and approval of devices

from: - 11 days ago

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