Kenvue 目前正在招聘 a：
我們做什麼
在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。
我們是誰
我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.
Role reports to：
HEAD OF REGULATORY AFFAIRS CEE/R&D SITE LEAD WARSAW位置：
Europe/Middle East/Africa, Poland, Mazowieckie, Warsaw工作地點：
混合你會做什麼
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.
如果您是殘障人士，請查看我們的 殘障人士援助頁面瞭解如何申請便利
