Medical Device Regulatory Affairs Jobs in Edison, NJ

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

EPM Scientific - , NY, United States

devices. Role and Responsibilities: As an EMC Test Engineer, you will play a vital role in ensuring our medical devices meet electromagnetic compatibility (EMC) standards. Here are the key responsibilities

from: linkedin.com - 8 days ago

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

from: resume-library.com - 5 days ago

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 - 28 days ago

Johnson and 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

from: Johnson and Johnson - 2 days ago

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 - 5 days ago

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 - 10 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 - More than 30 days ago

Dentsply Sirona - Anywhere, New York, USA

of Experience: • 5(+) years of experience in regulatory affairs, preferably in the medical device industry. • Experience with leading regulatory submissions and managing regulatory projects. • In-depth knowledge

from: Ivyexec.com - 16 days ago

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 - 29 days ago