Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
Associate Director, Applied Science & Medical Affairs EMEA位置：
Europe/Middle East/Africa, Poland, Mazowieckie, Warsaw工作地点：
混合你会做什么
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.
如果您是残障人士，请查看我们的 残障人士援助页面了解如何申请便利
