Principal Regulatory Affairs Specialist (UK, IVDR) Remote UK

**Bring more to life**. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cepheid, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you’ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world’s most complex health challenges. Together, we bring MORE change to the world. Learn about the Danaher Business System which makes everything possible. This position is part of Cepheid’s On-Market Sustainment Team and is a UK-based remote position. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. The Principal Regulatory Affairs Specialist (UK, IVDR) plays a critical role in ensuring the continued IVDR compliance for Cepheid’s devices post initial IVDR certification as well as leading the UK regulatory strategy, pre-market and post market. **In this role, you will have the opportunity to:** · Lead the regulatory strategy, implementation and sustainment of IVDs in the UK market. · Liaise with regulatory authorities like the Medicines and Healthcare products Regulatory Agency (MHRA) and act as an administrator for related databases such UK MHRA DORS and EUDAMED. · Recommend regulatory strategy for planned product changes for UKCA and IVDR. · Prepare and maintain UKCA and IVDR Technical Documentation. · Prepare regulatory submissions and submit change notification to the notified body and MHRA · RA lead for notified body technical reviews, surveillance reviews and certificate renewals. Including leading cross functional teams for gathering review responses. · Lead interactions with notified body / MHRA as appropriate. · Monitor the UK and EU IVD regulatory landscape and drive implementation of changes to regulations, standards and guidelines. · Serve as representative in UK and EU associations, gathering regulatory intelligence and advocating to influence regulatory policy. · Collaborate with cross functional teams. Mentor and coach other associates and cross functional teams as needed. **The essential requirements of the job include:** · Bachelor’s degree in Life Science or related field + 8 years’ experience in the IVD or Medical Device industry or Master’s degree in a Life Science or related field + 6 years’ experience in the IVD or Medical Device industry. · 4+ years of Regulatory Affairs experience with in vitro diagnostic and/or medical devices, including hands-on experience with EU IVDR/MDR, UKCA requirements, and technical documentation management. · Strong knowledge of global regulatory requirements and demonstrated ability to interpret regulations, assess compliance impacts, and support regulatory strategies throughout the product lifecycle. · Solid understanding of Quality Management Systems (QMS), including the application of quality principles, risk management, change control, and post-market activities within a regulated environment. · Proven ability to work effectively in cross-functional teams and communicate regulatory requirements to both technical and non-technical stakeholders. · Experience interacting with notified bodies and regulatory authorities, supporting submissions, audits, technical reviews, and compliance activities. · Hands-on experience with MHRA CTDA regulation and submissions is an advantage. Please note that because of summer vacations, there may be a delay in reviewing applications and providin…