Regulatory Affairs Manager

The industry’s fastest-growing orthopedic solutions company is seeking top-tier Regulatory Affairs professionals to help drive significant technological advancement across a complete suite of surgical products.

What you’ll do: Take initiative and use your knowledge of FDA regulations for Class II and Class III medical devices to assist with preparing and submitting 510(k) and IDE/PMA submissions.

What you’ll get: Gain valuable experience supporting product development and authoring 510(k) submissions for competition-leading, quick-to-market orthopedic devices.

What you bring to the table: A few years of experience in Regulatory Affairs within the medical device industry, experience with 510(k) submissions, and the drive to contribute and advance within a top growing company.

What to do now: Submit your application or email tc@thor-companies.com if you’re interested in learning more…

The industry’s fastest-growing orthopedic solutions company is seeking top-tier Regulatory Affairs professionals to help drive significant technological advancement across a complete suite of surgical products.

Excellent benefits offered, including: 
 

• Stock options
• Medical, Dental and Vision Insurance
• 401k plan with company match
• FSA
• PTO
• Tuition reimbursement
• Lots of everyday/lifestyle perks like pool/ping pong, on-site gym, bball & volleyball courts, access to hiking trails