Job Market Guide: Regulatory Affairs Specialist jobs in Harrisburg-Lancaster-Lebanon-York

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

8 Regulatory Affairs Specialist jobs in Harrisburg-Lancaster-Lebanon-York

Falls Church, VA
Coordinate and facilitate the meetings by providing panel members all necessary materials before the meeting, arranging and attending all meetings, and preparing a summary of the meeting proceedings.
industry
Healthcare IT
experience
5 - 7 years

Baltimore, MD
Coordinates timely preparation of requests for Certificates to Foreign Government, Certificates of Manufacture and Free Sale and Certificates of Exportability. Interfaces with applicable regulatory agencies and international consulates.
industry
Financial Services
experience
Less than 5 years

Leesburg, VA
Assists management in evaluating regulatory global impact on proposed products and determining trade issues to anticipate regulatory obstacles.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Gaithersburg, MD
Interact with manufacturing, clinical research and nonclinical research, product development and other related departments.
industry
Biotech/Pharma
experience
5 - 7 years

$40K - $90K - Gaithersburg, MD
The individual is responsible for compiling, publishing, distributing and archiving regulatory submissions for assigned products.
industry
Biotech/Pharma
experience
Less than 5 years

Gaithersburg, MD
The Regulatory Affairs Senior Specialist will be responsible for the management and preparation of regulatory document packages to FDA for our investigational biodefense products, focusing on manufacturing, nonclinical, and clinical development
industry
Biotech/Pharma
experience
5 - 7 years

West Point, PA
The position will be responsible to review Change Control Business Processes and regulatory systems / documentation to generate Regulatory Reports for CMC Conformance group and make recommendations for further actions.
industry
Biotech/Pharma
experience
5 - 7 years

Newtown, PA
Lead a team of multiple SDS authors and serve as primary client point of contact for a consumer goods manufacturing company.
industry
Data Storage
experience
8 - 10 years