Kenvueは現在、以下求人を募集しております。
STAŻ ZAWODOWY w dziale Regulatory Affairs w Warszawie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:
HEAD OF REGULATORY AFFAIRS CEE/R&D SITE LEAD WARSAW場所:
Europe/Middle East/Africa, Poland, Mazowieckie, Warsaw勤務地:
ハイブリッドあなたがすること
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.
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