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：
HEAD OF REGULATORY AFFAIRS CEE/R&D SITE LEAD WARSAW位置：
Europe/Middle East/Africa, Poland, Mazowieckie, Warsaw工作地点：
混合你会做什么
Support of activities performed by RA team related to the products marketed by Kenvue, including medicinal products, medical devices, cosmetics.
Main Duties & Responsibilities
Maintain and update regulatory records, databases, and tracking systems to ensure data accuracy and completeness.
Support the preparation, compilation, and review of documentation for submission to regulatory authorities.
Assist in the development, review, and approval of packaging materials and artwork in compliance with regulatory requirements.
Monitor and maintain Regulatory Affairs project trackers, ensuring deadlines and key milestones are accurately recorded and communicated.
Provide administrative support to the Regulatory Affairs department, including coordinating with cross-functional teams, scheduling meetings, and preparing documentation.
Organize, maintain, and archive regulatory documentation in accordance with internal procedures and applicable regulations.
Conduct searches and retrieve information from regulatory files, databases, and archives as required.
Support ongoing departmental initiatives and contribute to the continuous improvement of Regulatory Affairs processes.
Key Skills & Competencies
Results-oriented with a strong sense of urgency and accountability.
Excellent organizational and time-management skills.
Strong ability to prioritize tasks and manage multiple deadlines effectively.
Confident in collaborating and communicating with a wide range of internal and external stakeholders.
Strong verbal and written communication skills.
Exceptional attention to detail and commitment to accuracy.
Ability to work independently as well as collaboratively within a team environment.
Sound judgment and confidence in decision-making.
Strong analytical and problem-solving abilities.
Proactive, adaptable, and highly motivated approach to work.
Qualifications
Bachelor's degree or equivalent qualification required.
Previous professional experience is not essential; however, experience in a regulated environment would be an advantage.
Academic background in Pharmaceutical Sciences, Chemistry, Biotechnology, Life Sciences, or a related discipline is preferred.
Language Requirements
Fluent Polish and English, both written and spoken.
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