Senior Regulatory Affairs Specialist - Medical Devices
Listed on 2026-10-06
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Pharmaceutical
Healthcare Compliance, Medical Science Liaison, Regulatory Compliance Specialist
Kelly Science is seeking an experienced Regulatory Affairs Specialist to support regulatory strategy, submissions, and ongoing compliance for a medical device organization in Goose Creek, SC. The role targets hands‑on professionals with 5–10+ years of regulatory experience for Class II/III devices across the product lifecycle.
Responsibilities include developing regulatory pathways, preparing submissions, maintaining technical documentation, and ensuring adherence to 21 CFR Part 820, ISO 13485,
We are currently recruiting a Senior Regulatory Affairs Specialist - Medical Devices for our team in Goose Creek, SC, United States.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Goose Creek, SC, United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 95..
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