Head of Regulatory Affairs

Corin Group

Bradley Stoke

Hybrid

GBP 85,000 - 90,000

Full time

12 days ago
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Benefits offered by this job

Competitive salary
25 days holiday
Excellent pension
Life assurance
Private medical insurance
Eye tests and flu vaccinations

Job summary

Corin Group is seeking a Head of Regulatory Affairs to lead the Global Regulatory Affairs function. This pivotal leadership role carries responsibility for regulatory strategy, compliance, market access and execution across a diverse product portfolio including orthopaedic implants, software, and robotic devices.

You will oversee a global team, act as PRRC, and drive submissions and registrations across EU/UK/US/Australia, partnering with R&D, Quality, Clinical and Operations to ensure

Qualifications

  • Degree or equivalent in Life Sciences, Engineering, or related field.
  • Extensive Regulatory Affairs experience in the medical device industry.
  • Strong knowledge of EU MDR, UK regulations, FDA requirements and other major frameworks.
  • Experience leading regulatory submissions and engaging with authorities.
  • Broad understanding of regulatory requirements for orthopaedic implants, software, digital and robotic devices.
  • Proven leadership of Regulatory Affairs teams with managing complex workloads.
  • Excellent judgement, decision-making, and stakeholder influencing.
  • Willingness to travel internationally.

Responsibilities

  • Lead and develop the Global Regulatory Affairs team with clear priorities.
  • Act as the organisation's PRRC.
  • Develop and execute global regulatory strategies for development and market access.
  • Ensure timely regulatory submissions and licence maintenance across EU, UK, US, Australia, and others.
  • Provide regulatory leadership across implant/instrument and tech portfolios.
  • Collaborate with R&D, Quality, Clinical, Operations and Product Management.
  • Oversee regulatory impact assessments, documentation and changes.
  • Build interfaces between Regulatory Affairs and wider business functions.
  • Lead interactions with regulators, notified bodies, authorities; manage submissions and audits.
  • Monitor evolving global requirements and implement impact.

Skills

Leadership experience
Global regulatory strategy
People management
Regulatory compliance

Education

Degree in Life Sciences or Engineering

Job description

Head of Regulatory Affairs

Location: Flexible / Hybrid

Travel: Frequent international travel required

Lead Global Regulatory Strategy for Innovative Medical Technologies

Corin is seeking an experienced and strategic Head of Regulatory Affairs to lead our Global Regulatory Affairs function. This is a pivotal leadership role with overall accountability for regulatory strategy, compliance, market access, and regulatory execution across our diverse and innovative product portfolio.

As the single point of accountability for Regulatory Affairs, you will provide direction and oversight across a broad range of medical technologies, including orthopaedic implants and instruments, as well as cutting-edge software, digital and robotic medical devices. You will play a key role in ensuring regulatory excellence throughout the product lifecycle while supporting the successful delivery of Corin's growth ambitions worldwide.

What You'll Be Doing
  • Lead and develop the Global Regulatory Affairs team, ensuring strong performance, clear priorities and effective resource management.
  • Act as the organisation's Person Responsible for Regulatory Compliance (PRRC).
  • Develop and execute global regulatory strategies that support product development, product changes, registrations and continued market access.
  • Ensure timely, high-quality regulatory submissions, registrations and licence maintenance across key global markets including the EU, UK, US, Australia and other international territories.
  • Provide regulatory leadership across both implant/instrument and technical product portfolios, ensuring the appropriate expertise is applied to each area.
  • Serve as the senior Regulatory Affairs representative within cross-functional teams, collaborating closely with R&D, Quality, Clinical, Operations and Product Management.
  • Oversee regulatory impact assessments, technical documentation, manufacturing and product changes, and regulatory commitments.
  • Build effective interfaces and accountability between Regulatory Affairs and wider business functions.
  • Lead significant interactions with regulatory authorities, notified bodies and regulatory organisations, including submissions, responses, audits and meetings.
  • Monitor evolving global regulatory requirements and ensure their impact is effectively assessed and implemented.
  • Provide expert regulatory guidance and risk escalation to senior leadership.
  • Deputise for the Global Director of QA, RA & Clinical on regulatory matters when required.
About You

We're looking for a proven Regulatory Affairs leader who combines deep technical expertise with strong people leadership skills.

You will have:

  • A degree, or equivalent qualification, in Life Sciences, Engineering or a related discipline.
  • Extensive Regulatory Affairs experience within the medical device industry, including leadership responsibility.
  • Strong working knowledge of global medical device regulations, including EU MDR, UK regulations, FDA requirements and other major international frameworks.
  • Experience leading regulatory submissions and engaging directly with regulatory authorities and notified bodies.
  • Broad understanding of regulatory requirements relating to orthopaedic implants and instruments, alongside software, digital and robotic medical devices.
  • Demonstrated success in leading and developing Regulatory Affairs teams while managing complex workloads and competing priorities.
  • Excellent judgement and decision-making capabilities.
  • Strong communication and influencing skills, with the ability to translate complex regulatory matters for senior stakeholders.
  • Flexibility to travel internationally and participate in meetings across multiple global time zones.
Why Join Corin?

At Corin, we're transforming orthopaedics through pioneering technologies that help surgeons improve outcomes and enhance patients' lives. As Head of Regulatory Affairs, you'll have the opportunity to shape global regulatory strategy, influence business decisions at the highest level, and play a key role in bringing innovative medical technologies to markets around the world.

  • A competitive salary £85,000 - £90,000 dependant on experience and a discretionary annual bonus
  • 25 days holiday plus bank holidays
  • Excellent pension – starts at 6%, going up to 9.7% after 18 months.
  • Life assurance – Six times your basic salary
  • Private medical insurance with BUPA for you and your family
  • Free annual eye tests and flu vaccinations
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