Hiring Now: Regulatory Affairs Department Lead Near You – Apply Today!

Your Next Regulatory Affairs Department Lead Job Starts Here – Apply Now!

Regulatory Affairs Department Lead

Job Posted: 8 days ago

  • Salary: £ Competitive

    Job Type: Permanent

  • Location: Edinburgh

Expire in: 19 days

Job Description

Regulatory Affairs Department Lead (PRRC) Location: Central Scotland with hybrid or remote working available We are recruiting for an experienced Regulatory Affairs Department Lead to join our client, a well-established and respected name in the medical device and in vitro diagnostics (IVD) industry. This is a senior leadership role where you'll oversee a small, capable team and take responsibility for regulatory compliance across multiple global markets, including the US, Canada, and Europe. The focus is on someone who can bring real depth of experience with high-risk Class D devices, and who understands the complexities of IVDR, FDA and Health Canada regulations inside out. You'll need to be comfortable leading from the front, acting as PRRC, and steering technical documentation, submissions, and post-market activities through a constantly evolving regulatory landscape. What you'll be doing: Lead and develop the Regulatory Affairs department, managing a small team Oversee preparation, review and maintenance of technical documentation and submissions for Class D IVD devices (IVDR, FDA 510(k)/PMA, Health Canada) Act as Person Responsible for Regulatory Compliance (PRRC) and ensure compliance with GMP and ISO13485 Support post-market surveillance, vigilance and risk management processes Act as a key point of contact with regulatory bodies and external partners Work closely with other departments to align regulatory work with wider business priorities Maintain a regular on-site presence, with flexibility around hybrid or remote working What you'll need: Extensive regulatory affairs experience within IVD or medical devices Proven track record with regulatory submissions for high-risk Class D devices Strong knowledge of IVDR, FDA and Canadian medical device regulations Hands-on experience of post-market compliance, risk and vigilance activities People management experience, with the ability to lead and mentor a team A collaborative approach and the confidence to work with internal stakeholders and regulatory bodies Fluent English and excellent communication skills Must already have the right to work in the UK What next? If you're looking for a senior role where you can make a real impact and bring your expertise to a high-performing team, we'd love to hear from you. Send your CV or contact us to find out more

Before You Apply

Do not include the following in your job application, CV, or cover letter:

  • Bank details.
  • National Insurance number.
  • Date of birth.

You should not be asked for payment or irrelevant information. If you have concerns about a job advert or employer, seek guidance on how to proceed.

Looking for your next career move? Join a top company hiring Regulatory Affairs Department Lead job near me in Edinburgh! This is your chance to work on exciting projects, grow professionally, and enjoy a rewarding career with competitive pay and excellent benefits. Whether you're an experienced professional or looking to take the next step, this role offers the perfect opportunity to enhance your skills and make an impact. Don’t miss out—apply today via Vita CV and take your career to the next level!

Share This Job

© Vita CV: Registered in England and Wales (16187919).