Associate Director Medical Affairs Central Europe (m/f/d)

Was wir tun

Bei Kenvue erkennen wir die außergewöhnliche Kraft der täglichen Pflege. Aufbauend auf über einem Jahrhundert Tradition und verwurzelt in der Wissenschaft, sind wir das Haus der ikonischen Marken - darunter NEUTROGENA®, AVEENO®, TYLENOL,® LISTERINE®, JOHNSON'S® und BAND-AID®, die Sie bereits kennen und lieben. Wissenschaft ist unsere Leidenschaft; Fürsorge ist unser Talent.

Wer wir sind

Unser globales Team besteht aus ~ 22.000 brillanten Mitarbeitern mit einer Arbeitsplatzkultur, in der jede Stimme zählt und jeder Beitrag geschätzt wird. Wir sind leidenschaftlich an Erkenntnissen interessiert, Innovation und dem Engagement, unseren Kunden die besten Produkte zu liefern. Mit Fachwissen und Einfühlungsvermögen bedeutet ein Kenvuer zu sein, die Macht zu haben, jeden Tag Millionen von Menschen zu beeinflussen. Wir stellen den Menschen an die erste Stelle, kümmern uns leidenschaftlich, gewinnen Vertrauen in der Wissenschaft und lösen Lösungen mit Mut – und haben brillante Möglichkeiten, die auf Sie warten! Gestalten Sie mit uns unsere Zukunft – und Ihre. Für weitere Informationen , klicken Sie auf hier .

Rollenberichte an:

Senior Director Medical Affairs, EMEA

Standort:

Europe/Middle East/Africa, Germany, North Rhine Westphalia, Rhein-Kreis Neuss

Arbeitsort:

Was Sie tun werden

Associate Director Medical Affairs Central Europe

This position reports into Area Managing Director, Central Europe; Dual-reporting to: Head of Medical Affairs, EMEA and is based at Neuss, Germany.

What we do

At Kenvue , we realize 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 NEUTROGENA®, AVEENO®, TYLENOL®, 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 - and have brilliant opportunities waiting for you! Join us in shaping our future-and yours. For more information, click here .

Role reports to: Area Managing Director, Central Europe with dual reporting to Head of Medical Affairs, EMEA

What you will do

The Associate Director Medical Affairs Central Europe is responsible for managing the design and implementation of medical affairs programs, overseeing budgets, teams, deliverables and vendor activities. You will ensure compliance with regulations, medical excellence and partner with internal and external stakeholders to deliver expert medical and scientific knowledge:

Key Responsibilities

· Lead and inspire medical team colleagues across Central Europe to develop and execute innovative medical affairs strategies and plans that drive scientific excellence, consumer outcomes, and align with organizational goals, standards and external requirements.

· Lead and develop a team of medical affairs professionals, establishing clear accountability and fostering professional development, collaboration, and continuous learning.

· Champion the integration of cutting-edge medical insights, real-world evidence, advanced data analytics and digital solutions into Cluster medical affairs initiatives, ensuring alignment with global standards and local market needs.

· Lead the review and approval of promotional materials to ensure compliance with local regulations, statutory requirements and guidelines.

· Lead the creation, review, and approval of insight-enabled educational and scientific communication materials to ensure accuracy, compliance with local regulations, scientific integrity and impactful delivery to varied stakeholder audiences.

· Manage publication planning and execution, including coordination with internal and external stakeholders to maximize scientific impact.

· Coordinate and support technical training initiatives for internal teams and external partners to enhance product knowledge and compliance.

· Identify and develop effective and lasting organizational relationships with leading HCP experts

· Ensure that assigned clinical data generation activities and registries are designed, implemented and conducted in compliance with applicable Company guidelines, regulations and ethical standards.

· Develop and implement policies and procedures for medical and technical information dissemination related to company products including scientific responses to external enquiries and preparation for internal and external audits and inspections.

· Oversee budget management, contract negotiations, and vendor relationships to optimize resource utilization and project delivery.

· Collaborate cross-functionally with internal stakeholders to provide expert medical support that drives product development and lifecycle management.

What we are looking for

Required Qualifications and Experience

· Master’s degree or equivalent in a relevant scientific or medical discipline.

· 8-10 years of progressive experience in medical affairs or related pharmaceutical/biotech roles with demonstrated growth and leadership responsibilities.

· Proven expertise in managing medical affairs programs, including promotional material review, publication planning, and medical communications.

· Strong knowledge of regulatory requirements, ethical standards, and compliance related to data generation, communication and promotional materials.

· Experience in budget management, contract execution and vendor supervision within a medical affairs context.

· Excellent leadership, communication, and interpersonal skills with the ability to manage and develop high-performing teams.

· Demonstrated ability to collaborate effectively with cross-functional teams and external partners.

· Proficiency in implementing pharmacovigilance and drug safety programs.

Additional Preferred Qualifications

· Exceptional ability to translate complex scientific data into compelling narratives that influence decision-making at multiple levels.

· Proven track record of building and sustaining influential relationships with key stakeholders across diverse healthcare ecosystems.

· Strong strategic mindset combined with agility to navigate evolving regulatory landscapes and market dynamics.

· Advanced proficiency in leveraging digital platforms and data-driven insights to enhance medical affairs impact and innovation.

· Strategic thinking with the capability to influence business outcomes through medical insights and scientific expertise.

What’s in it for you

· Competitive Benefit Package

· Paid Company Holidays, Paid Vacation, Volunteer Time & More!

· Learning & Development Opportunities

· Kenvuer Impact Networks

*Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process.

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

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