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：
Senior Regulatory Affairs Manager位置：
Europe/Middle East/Africa, Turkey, Istanbul, Istanbul工作地点：
混合你会做什么
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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