Director, Regulatory Affairs, Europe
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Director, Regulatory Affairs, Europe

GE HEALTHCARE -
Chalfont Saint Giles

Apply Now

Job details

Qualifications

Engineering
Master's degree
Bachelor's degree
Team management
Leadership
Communication skills
Negotiation

Full job description

Job Description Summary

This role provides 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.

Job Description

Responsibilities:

Leadership & 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.
Knowledge of PRRC under MDR, and UKRP under UK MDR, ensuring product conformity and regulatory documentation integrity.
Oversee regulatory submissions, CE / UKCA marking processes Importer and Distributor responsibilities, 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 Qualifications:

Bachelor’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.
Strong knowledge of EU MDR, UK MDR, and relevant guidance documents.
EU and UK IVD regulatory expertise desirable.
Excellent communication, negotiation, and stakeholder management skills.

Preferred Characteristics

Experience 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.
Strong growth mindset and proactive approach.

Inclusion and Diversity

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Behaviors

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Total Rewards

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

Additional Information

Relocation Assistance Provided: No

Apply Now

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