Director, Medical Affairs EMEA in Reading

Kenvue is currently recruiting for the Director Medical Affairs, EMEA. This position reports into Senior Director Medical Affairs EMEA and is based at GB026 One Station Hill Square.

What we do

At Kenvue, we realise the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NICORETTE®, NEUTROGENA®, IMODIUM®, AVEENO®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.

Who we are

Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage.

Role reports to: Senior Director Medical Affairs EMEA

Location: Reading One Station Hill Square

Travel %: Up to 20%

People Reporting: 5-10 Clinicians and Scientists

What you will do

The Director Medical Affairs, EMEA is responsible for directing the operational functions of medical affairs, ensuring alignment with company goals, and overseeing the design and implementation of medical plans and programs. You will lead medical strategy, project planning, manage budgets and vendor relationships, and foster collaboration to support product development and compliance:

• Lead the strategic planning, vision, and execution of medical affairs initiatives and programs across the EMEA region, ensuring alignment with global healthcare trends, regulatory landscapes, and company objectives including innovation projects.
• Drive cross-functional collaboration between Medical Affairs, Translational Science, Regulatory, other R&D Functions and Commercial teams to integrate medical insights and expertise into product development, lifecycle management, and product launch.
• Oversee the development, review, approval, and implementation of medical and scientific communications and education programs that comply with relevant Country Codes and regulatory standards.
• Champion the development, communication, and utilization of real-world evidence, other data and innovative medical education outputs to support clinical decision-making.
• Manage certain clinical data generation projects including protocol development, budgeting, staffing, and timeline adherence.
• Develop professional relationships with External Experts, Scientific Organizations, Regulatory and policy bodies, healthcare stakeholders, and vendors.
• Input to pharmacovigilance activities, including inspections, adverse event reporting, risk management strategies.
• Influence and lead the digital transformation of medical affairs, including expertise in AI.
• Mentor and develop a high-performing medical affairs team, fostering a culture of scientific excellence, creativity, continuous learning, teamwork, and risk management.

What we are looking for

Required Qualifications

• Higher Clinical or Scientific degree or equivalent with broad medical background and expertise in medical affairs.
• Minimum of 10 years of progressive experience in medical affairs or related pharmaceutical/biotech industry roles.
• Demonstrated leadership skills with experience leading cross-functional teams and complex projects.
• Proven ability to design and implement medical affairs strategies supporting development, life-cycle management and product commercialization.
• Strong knowledge of regulatory requirements, pharmacovigilance, and compliance frameworks relevant to medical affairs.
• Excellent communication and interpersonal skills to effectively collaborate with internal stakeholders and external partners.
• Expertise in budget management, contract negotiation, and vendor oversight within a medical or clinical setting.

Desired Qualifications

• Professional Clinical Qualification, such as Physician, Dentist, Pharmacist or equivalent degree preferred.
• Demonstrated expertise in navigating complex regulatory frameworks and healthcare systems.
• Proven track record of leading innovative medical strategies that have driven measurable impact on patient outcomes and business growth.
• Exceptional leadership skills with the ability to inspire multidisciplinary teams and manage high-stakes projects in a dynamic environment.
• Strong technical expertise including digital fluency.
• Outstanding communication and interpersonal abilities to effectively engage with diverse stakeholders.
• A strategic mindset with a passion for advancing medical science and improving healthcare delivery on a regional scale.
• Ability to drive innovation and continuous improvement in a dynamic, fast-paced environment.

What’s in it for you

Competitive Benefit Package, Paid Company Holidays, Paid Vacation, Volunteer Time & More!

Learning & Development Opportunities

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, colour, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.