Senior Director of Regulatory Affairs
RealHighlight
Summary
About the Role
About You
- Bachelor's degree in life sciences, engineering, or related field.
- 10+ years of regulatory affairs experience in medical device, biotech, or pharma.
- Proven experience leading FDA and international submissions.
- Strong knowledge of U.S. and EU regulatory frameworks.
- Leadership experience managing regulatory teams.
- Advanced degree (MS, MBA, etc.).
- Experience with global regulatory environments and multiple product lines.
- Strong project management skills and familiarity with electronic submission systems.
Benefits
- Medical, dental, and vision coverage.
- Paid leave where required by applicable law.
Connecting experts with public sector and life sciences organisations Real is a Life Sciences specialist, part of SThree, the global STEM workforce consultancy. With expertise in biotechnology, pharmaceutical and medical technology, Real advises businesses, builds expert teams and delivers project solutions. In the UK, Real is also a specialist in Higher and Further Education, Central & Local Government, NHS and Healthcare services. Our consultants are truly specialised— focusing on regional market requirements. This allows us to provide organisations with market-specific advice, and place the right professionals into the right projects. We deliver a high-quality service that is fully compliant, regularly audited, and meets regulations and standards locally and globally. The organisations and professionals we partner with benefit from our deep sector expertise, our local and global experience, and our dedicated service. This is how we outpace tomorrow, together.