Job Market Guide: Regulatory Affairs Specialist jobs in Providence-New Bedford

Competition
Low
0.034126
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Specialists in Providence-New Bedford. Regulatory Affairs Specialists in Providence-New Bedford have between ${} and ${} years of experience, averaging $${} years of experience.

6 Regulatory Affairs Specialist jobs in Providence-New Bedford

Marlborough, MA
Reviews technical publications, articles and abstracts to stay abreast of regulatory developments in the industry.
industry
Healthcare IT
experience
5 - 7 years

$100K - $120K - Boston, MA
Draft, assemble, and file original documentation and submission materials for new or existing products to regulatory authorities to assure that all submissions are accurate, of high quality and well supported by literature and regulatory foundations, are presented in a manner to facilitate review, and are in conformance with appropriate statutes, regulations, and guidelines.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Milford, MA
Participate as a core team member on new product development teams providing regulatory guidance.
industry
Healthcare IT
experience
5 - 7 years

Woburn, MA
Communicate with regulatory agencies on administrative and routine matters in addition to pre-clinical, pre-submission, and submission discussions under the direction of management.
industry
Business Services
experience
5 - 7 years

Andover, MA
Review and approve engineering changes, advertising, promotional items and labeling for regulatory compliance.
industry
Energy & Environmental Services
experience
Less than 5 years

Lexington, MA
As a major contributor to the Regulatory Affairs team in a growing Diagnostic Development and Manufacturing company, you will have primary responsibility for ensuring compliance with the regulatory requirements necessary to register and market our IVD products globally. In this role, you will interface with regulatory agencies, prepare submission documents, and work cross functionally to provide compliance guidance.
industry
Medical Devices & Diagnostics
experience
8 - 10 years