Kenvueは現在、以下求人を募集しております。
Regulatory and Medical Affairs Intern私たちがしていること
私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100年以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、ケアは私たちの才能です。
Who We Are
私たちのグローバルチームは、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活に影響を与える力を持つことを意味します。私たちは、人を第一に考え、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。
Role reports to:
Senior Regulatory Affairs Manager場所:
Europe/Middle East/Africa, Turkey, Istanbul, Istanbul勤務地:
ハイブリッドあなたがすること
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.
障害のある個人の方は、宿泊施設のリクエスト方法について障害支援ページを確認してください。
