Director, Regulatory Affairs, Pre-Market
5 days ago
Director, Regulatory Affairs, Pre-MarketJob Description SummaryProvides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and postmarket compliance, working closely with healthcare regulatory bodies globally. Interprets simple internal and external business challenges and recommends best practices to improve products, processes or services. Stays informed of industry trends that may influence work.Roles and ResponsibilitiesLeadership & Strategy: Lead and develop the European Regulatory Affairs team, fostering a high-performance and collaborative culture.Define and execute regulatory strategies aligned with GE HealthCare’s global objectives.Represent Regulatory Affairs in cross-functional leadership forums and strategic initiatives.Regulatory Compliance: Ensure compliance with EU MDR and other applicable European regulations.Act as PRRC under MDR, ensuring product conformity and regulatory documentation integrity.Oversee regulatory submissions, CE marking processes, and interactions with Notified Bodies and Competent Authorities.Operational Excellence: Drive continuous improvement in regulatory processes and systems.Monitor regulatory changes and assess impact on GE HealthCare’s product portfolio.Support audits, inspections, and regulatory due diligence activities.Stakeholder Engagement: Collaborate with Quality, Legal, Commercial, and Product teams to ensure regulatory alignment.Provide expert guidance and training on European regulatory requirements.Represent GE HealthCare in industry associations and regulatory forums as needed.Required QualificationsBachelor’s or Master’s degree in Life Sciences, Engineering, or related field.Minimum 10 years of experience in Regulatory Affairs, with significant exposure to European medical device regulations.Proven leadership experience, including team management and strategic planning.Fluent in German and English (written and spoken).Must be based in the European Union and meet the qualifications to act as PRRC under MDR.Strong knowledge of EU MDR, IVDR, and relevant guidance documents.Excellent communication, negotiation, and stakeholder management skills.Desired CharacteristicsExperience working in a global or matrixed organization.Familiarity with digital health technologies and software as a medical device (SaMD).Ability to influence and lead through change.GE HealthCare is an equal opportunities employer and welcomes applications from all qualified candidates. We are committed to diversity and inclusion in the workplace. #J-18808-Ljbffr
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Director of Regulatory Affairs
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london, United Kingdom VRS Regulatory Full timeA unique opportunity to take a key role on the leadership team of a highly successful and award-winning developer of naturally sourced, sustainable ingredients for regulated consumer products. They are the leader in their field, the market is exploding, this position will be paramount to this regulatory centric business’ continued global growth. The...
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Associate Director Regulatory Affairs
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Associate Director, Regulatory Affairs
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City Of London, United Kingdom Shionogi Europe Full timeThis job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board. Description Shape the Future of Regulatory Excellence with Shionogi At Shionogi, we are dedicated to protecting the health and well-being of people worldwide. As a global pharmaceutical leader, we are driven by science, innovation, and a deep sense of...
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Director, Regulatory Affairs, Pre-Market
1 week ago
London, United Kingdom GE HealthCare Full timeJob Description SummaryProvides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch premarket submissions/registrations and postmarket compliance working closely with healthcare regulatory bodies globally. Interprets simple internal and external business challenges and recommends best...
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Senior Director, Regulatory Affairs
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London, Greater London, United Kingdom Beacon Therapeutics (USA) Inc Full time £150,000 - £200,000 per yearJoin Beacon Therapeutics (USA) Inc. as a Full-Time Senior Director of Regulatory Affairs and be at the forefront of transformative biotech innovations. This is a unique opportunity to shape regulatory strategies that directly influence the success of groundbreaking therapeutics in the UK market. Here, you will have the chance to leverage your expertise in a...
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Senior Director, Regulatory Affairs
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London, Greater London, United Kingdom Beacon Therapeutics Full time £120,000 - £200,000 per yearJoin Beacon Therapeutics (USA) Inc. as a Full-Time Senior Director of Regulatory Affairs and be at the forefront of transformative biotech innovations. This is a unique opportunity to shape regulatory strategies that directly influence the success of groundbreaking therapeutics in the UK market. Here, you will have the chance to leverage your expertise in a...
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City Of London, United Kingdom Hanson Search Full timeWe are seeking an experienced Regulatory Affairs Account Director to join a leading global advisory firm. This role suits someone with strong regulatory expertise who is ready to work on high-stakes issues across business, government, and policy. You will advise senior clients, manage key projects, and guide junior colleagues while shaping strategies that...
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City Of London, United Kingdom AIG Full timeRegulatory & Government Affairs Director - 12 Month Contract Join to apply for the Regulatory & Government Affairs Director - 12 Month Contract role at AIG Join us as a Regulatory & Government Affairs Director on a 12 month maternity contract to take your career to the next level with a global market leader. How You Will Create An Impact You will work...