Senior Regulatory Affairs Specialist

This range is provided by Connect Life Science. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$80.00/hr - $100.00/hr

We’re partnering with a scaling Class III Med Tech business to hire a Senior Regulatory Affairs Specialist (Contractor). This is a fantastic opportunity to join a brilliant team, with long‑term potential to convert into a permanent role.

The company has developed its technology and is looking to complete first submissions and filings in 2026, which will benefit from extra support on this project.

• Start Date:
  
  January 19
• Hours:
  
  40 per week (full‑time)
• Location:
  
  Remote with some travel to HQ in San Francisco
• Rate:
  Competitive hourly rate
• US‑Based candidates with right to work only

• Supporting the business’ US Regulatory Affairs operations, including submissions to FDA
• Collaborating with both US and global regulatory partners
• Managing a wide variety of RA tasks across Medical Devices
• Ensuring compliance with Class III device regulatory requirements

• 5+ years of Regulatory Affairs experience in Medical Devices, ideally with Class III experience
• Strong knowledge of RA processes across US markets (510(k), PMA, IDE etc.
• High attention to detail, excellent organisation, and ability to manage multiple priorities
• Join an innovative Med Tech scale‑up with exciting projects underway
• Enjoy the flexibility of a remote/hybrid role
• Benefit from the option to go permanent after the contract

If this sounds like the right opportunity for you, apply today and we’ll be in touch to arrange an initial discussion.

Mid‑Senior level

Contract

Quality Assurance and Legal

Medical Equipment Manufacturing