Sr. International Regulatory Affairs Specialist Job at Custom Search, Minneapolis, MN

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  • Custom Search
  • Minneapolis, MN

Job Description

Our mid-sized medical client is adding a Sr. Regulatory Affairs Specialist to their team! The Sr. Regulatory Specialist will support international registrations and renewals. This individual is responsible for ensuring product approvals are properly maintained, and product re-registrations are properly managed. The Sr. Regulatory Affairs Specialist will perform regulatory submission/approval activities for all products and ensures compliance with required regulations and established corporate standards.

Your role with the company:

  • Preparing documentation for international regulatory registrations
  • Preparing technical documentation compliant with regulations
  • Defining worldwide regulatory requirements necessary for regulatory approval of products
  • Participating on cross-functional teams as regulatory lead
  • Maintaining regulatory documentation to ensure availability for external audits and preparation of submission packages
  • Authoring submissions, researching requirements, setting priorities, and maintaining project schedules
  • Providing guidance and oversight to team members related to regulatory compliance
  • Act as a Subject Matter Expert (SME) to support internal and external audits
Desired Profile:
  • Bachelor's Degree in Science, Engineering, or other relevant discipline
  • Minimum 8 years' experience in Regulatory Affairs in the medical device industry
  • FDA, EU, Health Canada, and international registrations experience
  • Working knowledge of quality system regulations and guidelines
  • Ability to develop clear, concise, and timely oral and written reports
  • Great communication skills with all levels of personnel
  • High level of organization and planning skills
  • Working knowledge of medical devices, procedures, and terminology
Custom Search

Job Tags

Worldwide,

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