Medical Device Regulatory Affairs Jobs in New Jersey

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Manager, Regulatory Affairs  

Lumicity - , NJ, United States

The ideal candidate will come with a strong background in Regulatory Affairs from within the Medical Device industry. This person will possess strong people management & interpersonal skills

from: linkedin.com - 9 days ago

Associate Director, US Regulatory Affairs, Advertising & Promotion  

Proclinical Staffing - Morristown, NJ, United States

schedule. Skills & Requirements: At least five (5) years of experience involving the direct implementation of promotional labeling and advertising regulations in the biotech/pharmaceutical/medical device

from: linkedin.com - 9 days ago

Regulatory Affairs Specialist  

Katalyst Healthcares & Life Sciences - South Plainfield, New Jersey

: Bachelor's degree in life sciences, regulatory affairs, or a related discipline. Minimum of 5 years of experience in regulatory affairs, preferably in the medical device industry. Proven experience in leading

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from: resume-library.com - 11 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 - 5 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 - 22 days ago

Associate Director, US Advertising and Promotion, Global Regulatory Affairs  

Sanofi EU - Bridgewater, New Jersey

and advertising regulations in the biotech/pharmaceutical/medical device industry; this must include extensive experience providing regulatory input and evaluation as part of a promotional review committee

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from: resume-library.com - 4 days ago

Performance Evaluation Engineer  

Johnson & Johnson - Raritan, NJ

if needed) and prepare technical completion reports. Design fixtures and innovative test methods to measure the physical performance of medical devices such as wound closure devices, breast implants USD 70,000.00 - 112,000.00 per year

from: Dice.com (+1 source) - 9 days ago

Staff Clinical Evaluation Specialist (Hybrid) at Stryker  

Stryker - Mahwah, New Jersey

required; preferably with medical devices. + A minimum of 2 years in a Regulatory Affairs role required. + Strong interest in medical science, clinical research, and scientific communication. + Experience

from: HealtheCareers.com - 16 days ago

Regulatory Affairs Specialist II (Wound Closure & Healing) - Ethicon, Inc.  

Johnson & Johnson - Raritan, NJ

. At least 3+ years of relevant regulatory affairs experience within the healthcare industry required ; MedTech and/or Pharma experience strongly preferred . Knowledge of US (FDA) and OUS (EU Notified Bodies USD 75,000.00 - 105,000.00 per year

from: Dice.com - 16 days ago

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Director, Global Oncology Marketing Digital Pathology (Precision Medicine)  

Merck - Rahway, NJ 07065

. Close collaboration with multiple internal stakeholders across HH, our Research & Development Division, Medical Affairs, Regulatory, Legal etc. as well as external partners (diagnostic & device technology

from: Pharmadiversityjobboard.com - 11 days ago


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