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：
Senior Regulatory Affairs Manager位置：
Europe/Middle East/Africa, Turkey, Istanbul, Istanbul工作地點：
混合你會做什麼
Kenvue Türkiye is looking for a Regulatory and Medical Affairs Intern to join our team for a 1-year fixed-term contract. This internship offers hands-on exposure to the daily operations of a global FMCG business, assisting Regulatory Affairs department operational activities.
Key Responsibilities:
Daily check the Health Authority website and related Government pages to inform the department about new announcements, laws, guidelines etc.
Weekly the check status of cosmetic product notification on the HA portal, inform the departmant, keeps record.
Involves to regular weekly check of Health Authority Letters from portal with Regulatory Affairs Specialist and inform the department..
Sets monthly regulatory intelligence assessment meeting and joins the assessment meeting for tracking announcements, guidelines, or laws with regulatory affairs colleagues.
Prepares product notification dossier by collecting artworks, pictures, and required information.
Supports regulatory department activities like documentation, archiving etc.
Provides keeping cabinet indexes up to date.
Weekly uploads Health Authority Letters, Product Submission dossier and product notification dossier to the CEDMS system.
Requirements:
Currently enrolled in Pharmacy (5th year) or Chemical Engineering (3rd–4th year, based on course load)
Strong analytical mindset with a sense of ownership — able to take full responsibility for assigned projects from start to finish
Proactive and outgoing; comfortable reaching out to different stakeholders and following up independently
Eager to learn regulatory department processes, including variation applications and compliance tracking
Detail-oriented, with the ability to support risk assessment preparation and follow up on sample/lab-related processes
Interest in gaining hands-on exposure across both pharmaceutical and cosmetic product categories
Available to work 4 days/week, with 2–3 days at office.
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