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Tracking Code 29-093 Job Description The Regulatory Affairs Specialist must be a talented and highly motivated individual. The position will participate in quality audits and support on-going compliance in the product development process. The position will assist in the5/11/2015 Lexington, MA Save This Job
Santa Monica, CA Full Time Legal Experienced SHARE The Regulatory Affairs Specialist II will provide assistance in the regulatory affairs area to ensure that all domestic and international regulations are met and help maintain established procedures and processes to6/12/2015 Santa Monica, CA Save This Job
Location:USA - CA Company Order Number:339 # of openings:1 Description About the Company TeraRecon is the largest independent provider and a global leader in advanced image processing innovation for CT, MR and PET, advanced imaging-based decision support and 3D visualization5/4/2015 Foster City, CA Save This Job
Santa Monica, CA Full Time Legal Experienced SHARE Provide assistance in the regulatory affairs area to ensure that all domestic and international regulations are met. Help maintain established procedures and processes to assure regulatory compliance. Provide5/13/2015 Santa Monica, CA Save This Job
Job Description: The general responsibilities of the Regulatory Affairs Associate/Specialist will focus on supporting the Regulatory Affairs department in the preparation and submission of regulatory documentation to global regulatory agencies. The level of this position will be5/5/2015 Bothell, WA Save This Job
Description Job Description Title: Credentialing Specialist Grade: Reports To: VP, Contracting & Regulatory Affairs Status: Non Exempt Supervises: N/A Approved By: VP, Contracting & Regulatory Affairs Date Approved: 07/2015 Human Resources: SVP,7/3/2015 Tampa, FL Save This Job
Job ID42 Overview As part of the Quality team, the Quality Systems Specialist supports and maintains site and corporate Quality Systems by performing the duties listed, which include, but are not limited to: Description of Duties Author, revise, and process standard operating5/23/2015 East Windsor, NJ Save This Job
Location: Schaumburg, IL, USA Department: Quality Assurance & Facility Compliance Reports To: Senior Director Quality Assurance Job Summary / Overview: Responsible for the support and approval of change controls for all internal, labeling and external changes involving our5/27/2015 Schaumburg, IL Save This Job
Department: Manufacturing Operations Reports to: Director of Operations and Project Management Scope of Supervision: No Direct Reports EDUCATION, BUSINESS EXPERIENCE, AND PHYSICAL REQUIREMENTS ? Basic computer skills necessary ? Experience in medical device assembly, and working5/10/2015 Minneapolis, MN Save This Job
Location:Headquarters - Pleasanton DESCRIPTION Summary: Coordinates most aspects of company regulatory activities and may interface with domestic and international health authorities. Essential Duties and Responsibilities include the following (other duties may be assigned.): ?6/8/2015 Pleasanton, CA Save This Job