What are the responsibilities and job description for the Senior Regulatory Affairs Specialist position at Connect Life Science?
We’re partnering with a scaling Class III MedTech 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 have developed their technology and are looking to complete first submissions and filings in 2026, which will benefit from extra support on this project.
📌 Role Overview
- Contract Length: 12 months
- 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
📌 What You’ll Be Doing
- 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
📌 What We’re Looking For
- 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
📌 Why Apply?
- Join a innovative MedTech 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.
Salary : $80 - $100