Job Market Guide: Regulatory Affairs Specialist jobs in NJ

Competition
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Specialists in NJ. Regulatory Affairs Specialists in NJ have between ${} and ${} years of experience, averaging $${} years of experience.

9 Regulatory Affairs Specialist jobs in NJ

MURRAY HILL, NJ
In this role, you will be responsible for develop and implement regulatory strategies for Class III devices through national authorities, physicians, consultants and internal team members.
industry
Industrial Equipment & Supply
experience
5 - 7 years

Allendale, NJ
In this position, you will interpret existing and/or new regulatory requirements as they relate to company products and procedures and also communicate this to appropriate personnel.
industry
Medical Equipment
experience
Less than 5 years

Moorestown, NJ
In this role, you will be responsible for develop US and International regulatory strategies for product submissions, identifying needs for bench, animal and clinical testing.
industry
Aerospace / Defense
experience
5 - 7 years

Hancocks Bridge, NJ
In this role, you will assure all regulatory products prepared are in accordance with applicable procedure, licensing basis, industry codes and all regulatory requirements.
industry
Audio / Video
experience
8 - 10 years

Wayne, NJ
In this role, the selected candidate will review device labeling and advertising materials for compliance with submissions and applicable regulations; analyze and recommend appropriate changes.
industry
Biotech/Pharma
experience
5 - 7 years

$90K - $110K - Skillman, NJ
In this role, the selected candidate will coordinate activities leading up to the generation of information requested by the FDA, through the regulatory review process of drug product applications.
industry
Biotech/Pharma
experience
5 - 7 years

Bridgewater, NJ
In this role you will support regulatory aspects of consumer product development and maintenance of existing products.
industry
Biotech/Pharma
experience
5 - 7 years

Princeton, NJ
In this role, you will evaluate proposed preclinical, clinical and manufacturing changes for regulatory filing strategies, compile, prepare, review and submit regulatory submission to authorities.
industry
Biotech/Pharma
experience
Less than 5 years