Regulatory Affairs Specialist


Position Id:

Atlanta area Medical Device company is looking for a highly motivated Regulatory Affairs Specialist to join their team.

Do you want to be working with a team who collaborates in a great open-door environment, with a company who is building and driving great products to market? Are you the type that enjoys a challenge and learning consistently, with an opportunity to prove yourself daily?

This private, mid-sized company has an opportunity for someone to be recognized daily for their contributions. They are looking to complete a new team with a RA Specialist who has the following knowledge and experience:

  • RAC certification
  • Regulatory knowledge both domestically and internationally
  • Medical device Class II/III submission and approval success
  • Exposure to and experience with EU MDR, Labeling, MDSAP, CE, FDA, ISO 13485 to 21 CFR part 11
  • Strong in managing multiple projects and prioritizing work
  • Able to effectively communice with team members at every level, fostering cooperation and commitment
  • PMP or proof of strong management skills
  • Excellent written and verbal skills

Please submit your resume to be considered for this opportunity to work for a wonderful organization with a great boss.

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