Job Market Guide: Regulatory Affairs Specialist jobs in Philadelphia

Competition
Low
0.129963
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Specialists in Philadelphia. Regulatory Affairs Specialists in Philadelphia have between ${} and ${} years of experience, averaging $${} years of experience.

9 Regulatory Affairs Specialist jobs in Philadelphia

Baltimore, MD
In this role, you will develop regulatory strategies for moderately to highly complex submissions to FDA and other regulatory agencies.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Baltimore, MD
In this role, the selected candidate will coordinate the preparation of additional data/information requested by regulatory agencies and prepares appropriate responses to all such requests.
industry
Medical Devices & Diagnostics
experience
Less than 5 years

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

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

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

$62K - $83K - Newark, DE
This position Maintains technical files for in vitro diagnostic products in compliance with the European In Vitro Diagnostics Directive 98/79/EC (IVDD). Prepares and reviews regulatory documentation to support conformance to the IVDD.
industry
Consulting
experience
Not Specified

$62K - Newark, DE
In this role, you will maintain technical files for in vitro diagnostic products in compliance with the European In Vitro Diagnostics Directive 98/79/EC (IVDD). Prepares and reviews regulatory documentation to support conformance to the IVDD.
industry
Consulting
experience
Not Specified

Hancocks Bridge, NJ
In this role, you will provide initial or complete task management of regulatory issues. Support the regulatory work functions.
industry
Audio / Video
experience
8 - 10 years

Baltimore, MD
In this role, the selected candidate will coordinate the preparation of additional data/information requested by regulatory agencies and prepares appropriate responses to all such requests.
industry
Business Services
experience
Less than 5 years