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

Competition
Low
0.032796
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.

11 Regulatory Affairs Specialist jobs in Providence-New Bedford

Raynham, MA
Ability to work with cross-functional team members including R&D, Quality, Labeling, Sterility, Medical and Clinical.
industry
Consulting
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

Mansfield, MA
Participate in overall document management strategies which support the device history file required by FDA regulations and product design dossier required by OUS for obtaining a design examination certificate.
industry
Legal Services
experience
Less than 5 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

Cambridge, MA
Provide truly comprehensive molecular information products that can assess the broadest range of relevant genomic alterations from a patients tumor and distill this complex molecular information into a concise and actionable format that reveals more treatment options for physicians and their patients.
industry
Biotech/Pharma
experience
Less than 5 years

Andover, MA
Advise internal stakeholders (marketing, manufacturing, R&D, etc.) regarding current/pending guidance, regulations, Agency/industry initiatives, etc. to ensure regulatory strategy is in alignment with company objectives.
industry
Manufacturing / Diversified
experience
5 - 7 years

Raynham, MA
Develop label content including IFU(instruction for use) and promotional materials.
industry
Medical Devices & Diagnostics
experience
11 - 15 years

Framingham, MA
Assist in the process for the development and release of labeling materials (Instructions for Use and patient materials) intended for users of HeartWare products. Assist in coordinating and executing all activities necessary.
industry
Medical Devices & Diagnostics
experience
8 - 10 years

Mansfield, MA
The Regulatory Affairs Specialist is responsible for managing all aspects of regulatory affairs associated with the OEM business unit, including but not limited to, technical file review, labeling review, and design control review.
industry
Medical Equipment
experience
Less than 5 years

$70K - $100K - Raynham, MA
Coordinate and prepare premarket application to the US FDA such as 510(k), PMA etc; align technical documentation according to technical documentation structure.
industry
Biotech/Pharma
experience
8 - 10 years

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