Nonprofit & Public SectorEntry levelOn site
Regulatory Associate
Globus MedicalAudubon, PA
Posted Oct 2, 2026
What you’d do
Draft, submit and help gain FDA clearance for 510(k) submissions and IDE/PMA approvals for class II and III products. Full time role requiring knowledge of products under review and relevant regulations. Found on the employer's careers page on Oct 17, 2026. Apply through the link.
You’ll need
- Bachelor's in health or science-related field, or equivalent
- Knowledge of US Code of Federal Regulations Title 21
- 0-2 years' experience in medical device industry or equivalent
- Regulatory Affairs experience a plus
- Engineering degree a plus
Our summary of the listing. The full listing has the details.