6 Medical Device Regulatory Affairs Jobs in Somerville, NJ
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Senior Regulatory Affairs Specialist - Medical Devices 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 Yesterday
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Vice President Regulatory Affairs Quality Assurance 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 7 days ago
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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 16 days ago
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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 16 days ago
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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 2 days ago
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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 Yesterday
Top locations
- Edison, NJ (4)
- East Brunswick, NJ (1)
- Florham Park, NJ (1)
- Bridgewater, NJ (1)
- Raritan, NJ (1)
- New York, NY (1)
- Allentown, PA (1)
- New Jersey (4)