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Internship Commercial Quality

職務分類:
掲載日:
終了日:
ID:
2507039509W

この仕事を共有する:

Kenvueは現在、以下求人を募集しております。

Internship Commercial Quality

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:

Commercial Quality Specialist SP

場所:

Europe/Middle East/Africa, Spain, Community of Madrid, Madrid

勤務地:

フルオンサイト

あなたがすること

This is an exciting opportunity to join the Commercial Quality team of a world leading company in healthcare, in Spain!

The Commercial Quality (CQ) Intern is responsible for maintaining the appropriate Quality Standards and Systems for the operation of the Spanish Consumer Health organization. It will also support the Northen and Southern European & CQ Cluster team in implementing departmental strategies and services to optimize and harmonize processes and find opportunities to collaborate in the Cluster.

Key Responsibilities:

  • Consumer Quality Management System (QMS) & continuous improvement: Ensure that all local or Cluster Standard Operating Procedures (SOPs) that describe all GxP related processes are established ensuring adequacy and continuous improvement.

  • New Product Introduction (NPI) & Product Lifecycle: quality approval of all new products to be marketed in Iberia through the relevant procedures (Finished Product, FAI, Incoming Control, etc.), as well as managing product returns and interaction with warehouse and distribution center.

  • Training: Local monitoring and oversight of Training as per Cluster Training Matrix.

  • Change Controls: ensure that any changes affecting the distribution related activities are appropriately controlled and supervised.

  • Document & Data Management: ensure that a document and data management system is accurately implemented according to Kenvue and local regulatory requirements and that quality records are properly handled, stored and maintained.

  • Non-Conformances (NC) & Corrective/ Preventive Actions (CAPA): processing of NCs and CAPAs via the current systems and according to applicable Kenvue processes and on time closure.

  • Kenvue CQ Community: Participation in workshops and projects, task forces at NSE&F Cluster and EMEA Regional level on Quality related topics.

Qualifications

Experience and Skills required:

  • University Scientific degree preferably in Pharmaceutical Sciences, Chemistry, Chemical Engineering or similar.
  • Fluency in English
  • Up-to-date knowledge of relevant pharmaceutical legislation and GDP regulations.
  • Intermediate in Portuguese (valued)

What do we offer

  • Competitive package

  • Learning & Development Opportunities

  • Employee Resource Groups

  • Canteen on site

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