Exciting Opportunity: Part-Time Senior Regulatory and Quality Head
Posted: 26th May 2026 | Viveca Biomed | Medical Devices | UK · Europe · USA
Are you an experienced regulatory and quality leader with strong medical device experience looking for a high-impact, flexible role with a company on the cusp of something truly exciting?
Viveca Biomed is a driven, specialist female health company with an innovative medical device, and we are looking for an exceptional individual to work alongside our existing team, bringing specialist expertise that strengthens our collective capacity as we accelerate our growth.
About Contrelle Activgard & Our Mission
At Viveca Biomed, we are passionate about developing innovative medical devices that make a real difference to patients' lives.
Our flagship product, Contrelle Activgard, is gaining momentum across the UK and Europe, with plans to expand into new European and global markets, including a USA launch.
This is an extraordinary time to join us as we continue to develop the regulatory foundations that will underpin our international expansion and long-term success.
The Role
This is a part-time, senior-level position, approximately 4 to 5 days per month, offering a rare opportunity to make a genuine strategic contribution.
The role can commence immediately.
You will:
What We're Looking For
Location and Flexibility
Our base is in Northumberland, north of Newcastle. In the short term, we envisage a meaningful proportion of your time being spent on site, where you will work alongside the team and immerse yourself in what we are building.
Some work can also be carried out remotely, giving you the flexibility to integrate this role around your wider commitments.
Why Join Viveca Biomed?
Interested?
If this sounds like the opportunity you have been looking for, we would love to hear from you. Please reach out directly via [email protected] or send your CV and a brief note about your experience via LinkedIn.
Are you an experienced regulatory and quality leader with strong medical device experience looking for a high-impact, flexible role with a company on the cusp of something truly exciting?
Viveca Biomed is a driven, specialist female health company with an innovative medical device, and we are looking for an exceptional individual to work alongside our existing team, bringing specialist expertise that strengthens our collective capacity as we accelerate our growth.
About Contrelle Activgard & Our Mission
At Viveca Biomed, we are passionate about developing innovative medical devices that make a real difference to patients' lives.
Our flagship product, Contrelle Activgard, is gaining momentum across the UK and Europe, with plans to expand into new European and global markets, including a USA launch.
This is an extraordinary time to join us as we continue to develop the regulatory foundations that will underpin our international expansion and long-term success.
The Role
This is a part-time, senior-level position, approximately 4 to 5 days per month, offering a rare opportunity to make a genuine strategic contribution.
The role can commence immediately.
You will:
- Work collaboratively alongside our existing skilled team to strengthen and develop our regulatory and quality capabilities as we commercialise Contrelle Activgard across the UK, Europe and the USA
- Ideally contribute expert regulatory guidance to support our US market entry, including navigating FDA requirements, complementing the strengths already within the business
- Partner with our highly capable internal team to uphold and enhance the highest standards of compliance and quality across all markets
- Help lay the groundwork for future exciting product development initiatives, ensuring regulatory excellence is embedded in everything we do from the outset
- Bring specialist expertise that adds real depth to our team, in a role where your contribution will be genuinely valued and immediately felt
What We're Looking For
- Proven experience in regulatory affairs and quality management within the European medical devices sector — this is essential
- Strong working knowledge of UK and European regulatory frameworks (MDR)
- Experience with, or a solid understanding of, FDA requirements for US medical device launches — highly advantageous
- A strategic mindset, with the ability to work autonomously and make an impact in a lean, fast-moving organisation
- A collaborative spirit — you'll be joining a team that is highly capable, deeply committed, and genuinely excited about what we are building
Location and Flexibility
Our base is in Northumberland, north of Newcastle. In the short term, we envisage a meaningful proportion of your time being spent on site, where you will work alongside the team and immerse yourself in what we are building.
Some work can also be carried out remotely, giving you the flexibility to integrate this role around your wider commitments.
Why Join Viveca Biomed?
- Be part of a rapidly growing medical device business with genuine international ambitions
- Work on a product that is already proving its value and changing women’s lives, helping us take it to the world
- Work as a peer alongside a close-knit, highly skilled team where your expertise will complement theirs, your voice will be heard, and your impact felt
- Enjoy a flexible, part-time arrangement that respects your time without compromising on the significance of the role
- Exciting longer-term opportunities as we expand our product portfolio and grow our global footprint
Interested?
If this sounds like the opportunity you have been looking for, we would love to hear from you. Please reach out directly via [email protected] or send your CV and a brief note about your experience via LinkedIn.
