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Regulatory Affairs Consultant

  • Type Contract
  • Salary competitive
  • Location Monrovia, California
  • Sectors Regulatory Affairs

Title: Regulatory Affairs Consultant

Location: Onsite in Monrovia, CA

Duration: 6 - 12 months, possible conversion

About the Company:

Join my Client's enthusiastic and collaborative regulatory affairs team by contributing to the overall success of regulatory affairs, PMA's, and documentation compliance related activities. The Contractor provides excellent knowledge within Regulatory compliance, PMA's, and ensuring that correct documentation is presented to the FDA.

The Role:

Regulatory Affairs Consultant with class III Medical Device experience, creating and submitting PMA's, and working within Ophthalmology industries.

  • Qualifications:
  • BS in Regulatory or a related field, with 7-15 years of experience in regulatory affairs, class III Medical Devices, and experience within the Ophthalmology industry.
  • Demonstrates advanced experience with PMA submissions, working cross functionally, and ensuring documentation is correct post market.

Sthree US is acting as an Employment Business in relation to this vacancy.

If interested, please apply with your updated resume ASAP.

Sthree US is acting as an Employment Business in relation to this vacancy.