Associate Manager Medical Affairs CE

Associate Manager Medical Affairs CE

Ce que nous faisons

Chez Kenvue, nous réalisons le pouvoir extraordinaire des soins quotidiens. S'appuyant sur plus d'un siècle d'héritage et enraciné dans la science, nous sommes la maison de marques emblématiques - dont NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® et BAND-AID® que vous connaissez et aimez déjà. La science est notre passion ; Le soin est notre talent.

Qui nous sommes

Notre équipe mondiale est composée de ~ 22 000 personnes brillantes avec une culture d'entreprise où chaque voix compte et chaque contribution est appréciée. Nous sommes passionnés par les idées, l'innovation et l'engagement à fournir les meilleurs produits à nos clients. Avec de l'expertise et de l'empathie, être un Kenvuer signifie avoir le pouvoir d'avoir un impact sur des millions de personnes chaque jour. Nous donnons la priorité aux personnes, nous nous soucions farouchement, nous gagnons la confiance grâce à la science et nous résolvons les problèmes avec courage - et nous vous offrons de brillantes opportunités ! Joignez-vous à nous pour façonner notre avenir et le vôtre. Pour plus d'informations, cliquez sur ici.

Role relève à :

Associate Director, Applied Science & Medical Affairs EMEA

Lieu :

Europe/Middle East/Africa, Poland, Mazowieckie, Warsaw

Lieu de travail :

Hybride

Ce que tu vas faire

What You Will Do

We are looking for an Associate Manager in Medical Affairs to join our team at Kenvue. In this role, you will be responsible for providing medical, scientific, and technical information related to the company’s products and therapeutic areas of interest to both external customers and internal stakeholders. You will collaborate closely with cross-functional colleagues from departments such as Regulatory Affairs, Marketing, and R&D. Your comfort level with Drugs, Cosmetics, Food Supplements, and Medical Devices will be critical to your success.
 

Location: Warsaw, Poland (hybrid working model; ideally 1-2 days in the office, but flexible depending on location)

 

Key Responsibilities:

• Medical Support: Ensure the medical correctness of information on OTC medicines for CEE countries and provide medical support across these regions. Serve as the external and internal contact for medical-scientific concerns on OTC drugs.

• Content Development: Support the development of professional (HCP) strategies and provide medical input/scientific support for medical/HCP content creation. Review and approve medical content for HCP omnichannel assets.

• Compliance: Ensure educational events comply with internal/external regulations and fulfill compliance requirements. Support the Medical Affairs team in ensuring that official product information texts are medically correct and comply with marketing authorization.

• Pharmacovigilance Support: Assist departments in pharmacovigilance and regulatory affairs by preparing relevant medical/clinical texts. Participate in risk procedures to mitigate drug risks in cooperation with local and European regulatory authorities.

• Training and Communication: Execute or support training courses for healthcare professionals and pharmaceutical sales representatives regarding Kenvue products. Respond to inquiries from healthcare professionals and patients concerning the correct use of medicines, their pharmaceutical quality, effectiveness, and safety.

• Documentation and Registration: Participate in the preparation of registration documents and product information texts for submission to national and international registration authorities. Support the Regulatory Affairs Department in preparing necessary scientific information for HCPs and patient information leaflets.

• Stakeholder Engagement: Advise internal and external customers at national and international levels on drug-related issues. Maintain relationships with internal stakeholders to ensure information integrity and collaboration.
   

Required Qualifications:

• Degree in Pharmacy, Life Sciences, or a related field; a higher degree (e.g., PhD) is desirable.
• Minimum of 5 years of professional experience in a medical/pharmaceutical area, ideally in the industrial sector.
• Outstanding interpersonal skills, including proficiency in spoken and written English.
• Strong presentation skills and the ability to innovate and work flexibly within agile processes.
• Demonstrated ability to work effectively within a team and a strong personal initiative.
• Precise, careful, and well-structured working style.
   

What’s in it for you

• Competitive Benefit Package
• Learning & Development Opportunities
• Kenvue Impact Networks
• This list could vary based on location/region
   

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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