PMA Regulatory Affairs Specialist

Job is Expired
Location: Remote
Compensation: Hourly
Reviewed: Mon, Dec 29, 2025

Job Summary

A company is looking for a PMA Contractor Support to handle regulatory affairs for a project.

Key Responsibilities
  • Handle regulatory affairs for medical device PMA submissions
  • Author, draft, and submit all modules for medical device (IVD) PMA
  • Collaborate cross-functionally to gather information for submission documents
Required Qualifications
  • At least 5 years of direct relevant PMA experience
  • Hands-on experience with authoring and submitting PMA documents
  • Experience with tissue-related medical devices is desired
  • Ability to work collaboratively across functions
  • Flexibility in schedule for day shifts (M-F)

COMPLETE JOB DESCRIPTION

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