Job Market Guide: Regulatory Affairs Specialist jobs in New York

Competition
Avg
0.484104
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Specialists in New York. Regulatory Affairs Specialists in New York have between ${} and ${} years of experience, averaging $${} years of experience.

7 Regulatory Affairs Specialist jobs in New York

Princeton, NJ
In this role, you will support various types of product studies to gain critical consumer insights for product development and/or to gather and evaluate data in submission activities.
industry
Consumer Goods / Miscellaneous
experience
5 - 7 years

Danbury, CT
In this role, the selected candidate will be responsible to works with regulatory affairs management to determine effective regulatory pathways for a variety of issues.
industry
Business Services
experience
5 - 7 years

$72K - Tarrytown, NY
In this position, you will prepare and support regulatory submissions for in vitro diagnostic products for international registrations.
industry
Consulting
experience
Not Specified

Mahwah, NJ
In this role, the selected candidate will plan, organize and implement strategies and activities required to procure regulatory approval for new and revised product lines.
industry
Business Services
experience
Less than 5 years

Compensation Estimate

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$45K to $75K - Tarrytown, NY
This position prepares regulatory submissions for in vitro diagnostic products for international registrations. Focus will be on new product registration and re-registration of products in China. Must possess good technical writing skills and have a scientific background.
industry
Consulting
experience
Not Specified

Compensation Estimate

What's a Compensation Estimate?

To help you find the most relevant jobs, we've come up with an approximate compensation for this position. This is based on similar jobs with compensation posted.

$45K to $75K - Tarrytown, NY
The candidate will prepares / updates regulatory technical documentation for in vitro diagnostic products.
industry
Consulting
experience
Not Specified

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