Job Market Guide: Regulatory Affairs Specialist jobs in New York

Competition
Low
0.236672
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.

14 Regulatory Affairs Specialist jobs in New York

Audubon, PA
The Regulatory Affairs Specialist assists in writing, submitting and gaining clearance for 510(k) submissions and approval for IDE / PMA submissions to the Food and Drug Administration (FDA) for class II and class III products.
industry
Biotech/Pharma
experience
5 - 7 years

Swiftwater, PA
Must have working knowledge of GMPs. Must be well-organized, work with minimal management and meet aggressive timelines; utilizes knowledge of word processing software, strong writing and analytical skills to document software capabilities and functionality.
industry
Biotech/Pharma
experience
Not Specified

New York, NY
Organize, manage and monitor the hospitals continual readiness for unannounced Joint Commission surveys and provide assistance as needed in interactions with onsite surveys, inspections and investigations from any/all federal, state and local regulatory authorities.
industry
Patient Care
experience
Not Specified

Franklin Lakes, NJ
Analyze and interpret current or proposed domestic and international regulations for impact to BD products and processes to help ensure continuous compliance.
industry
Financial Services
experience
5 - 7 years

Franklin Lakes, NJ
This position will be responsible for all aspects of regulatory affairs including development and execution of global regulatory strategies and submissions for medical devices and drug/device combination products. The incumbent will perform essential duties and responsibilities with some supervision while providing guidance to more junior regulatory associates.
industry
Financial Services
experience
Less than 5 years

Bridgewater, NJ
Work with the Pharmaceutical Regulatory Affairs Senior Manager or other staff to make certain product documentation and support meets regulatory requirements; serve as designee as needed.
industry
Manufacturing / Diversified
experience
5 - 7 years

Franklin Lakes, NJ
This position will be responsible for all aspects of regulatory affairs including development and execution of global regulatory strategies and submissions for medical devices and drug/device combination products. The incumbent will perform essential duties and responsibilities with some supervision while providing guidance to more junior regulatory associates.
industry
Financial Services
experience
Less than 5 years

Mahwah, NJ
Assisting in the establishment and maintenance of regulatory information systems both electronically and hard copy.
industry
Medical Devices & Diagnostics
experience
Less than 5 years

Mahwah, NJ
Participate in New Product Development Teams throughout all phases to ensure US, EU, and other international regulatory requirements are incorporated as part of the development process.
industry
Business Services
experience
Less than 5 years

Mahwah, NJ
The Staff Regulatory Affairs Specialist works with minimal supervision to bring medical devices to market and ensure ongoing compliance while mentoring less experienced colleagues in the development of their regulatory skills.
industry
Medical Equipment
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

Rahway, NJ
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

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