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
Kenvue is currently recruiting for:
Regulatory Affairs Trainee
This position reports into HEAD OF REGULATORY AFFAIRS CEE/R&D SITE REGULATORY is based at Warsaw, Poland.
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®, 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.
Job purpose:
Support of activities performed by Regulatory Affairs team related to the products marketed by Kenvue, including medicinal products, medical devices, cosmetics.
Main duties and responsibilities:
- Management of records and databases by keeping these up to date.
- Helping in compiling documentation to be submitted to the relevant authorities.
- Participation in the development of packaging material (Artwork).
- Keeping an up-to-date log on the tasks of the RA department, recording deadlines.
- Performing administrative tasks related to the operation of the RA department (communicating with partner departments, organizing meetings).
- Maintains and archives regulatory documentation (as appropriate).
- Conducts searches of existing files for requested information.
Key Skills & Capabilities:
- University/bachelor’s degree or Equivalent Pharmaceutical, Chemical, Biotech or similar background would be an advantage
- Results driven with a sense of urgency
- Strong organizational skills
- Ability to prioritize
- Confidence to liaise with multiple stakeholders
- Good communication skills
- Thorough attention to detail
- Ability to work in a group and on their own
- Confidence in decision making
- Problem solver
- Proficient in English and Polish language skills
What’s in it for you
- Competitive Benefit Package
- Learning & Development Opportunities
- Kenvuer 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
