Quality Assurance Trainee

hace 4 semanas

Madrid, Madrid, España Kenvue A tiempo completo

Position Overview

Kenvue is seeking a Quality Assurance Trainee to join our team.

About Us

At Kenvue, we harness the remarkable potential of everyday care. With a legacy spanning over a century and grounded in scientific expertise, we are home to renowned brands such as Neutrogena, Aveeno, Tylenol, Listerine, Johnson's, and BAND-AID Brand Adhesive Bandages. Our passion lies in science, while our talent is in care. Our diverse global workforce of approximately 22,000 dedicated individuals is driven by insights and innovation, committed to delivering exceptional products to our consumers. As a member of Kenvue, you have the opportunity to positively influence the lives of millions daily. We prioritize people, demonstrate unwavering care, build trust through science, and tackle challenges with courage. Exciting opportunities await you as we shape our future together.

Key Responsibilities

The Quality Assurance (QA) Trainee will play a vital role in upholding the necessary Quality Standards and Systems within the Spanish Consumer Health division. This position will also assist the Southern European & QA Cluster team in executing departmental strategies and services aimed at optimizing and harmonizing processes while identifying collaborative opportunities within the Cluster.

  • Consumer Quality Management System (QMS) & Continuous Improvement: Ensure the establishment and ongoing enhancement of all local or Cluster Standard Operating Procedures (SOPs) that govern GxP-related processes.
  • New Product Introduction (NPI) & Product Lifecycle: Oversee the quality approval process for all new products intended for the Iberian market, adhering to relevant procedures (Finished Product, FAI, Incoming Control, etc.), and manage product returns in coordination with the warehouse and distribution center.
  • Training: Conduct local monitoring and oversight of training in accordance with the Cluster Training Matrix.
  • Change Controls: Ensure that any modifications impacting distribution-related activities are effectively managed and supervised.
  • Document & Data Management: Implement a document and data management system that complies with Kenvue and local regulatory standards, ensuring proper handling, storage, and maintenance of quality records.
  • Non-Conformances (NC) & Corrective/Preventive Actions (CAPA): Process NCs and CAPAs through established systems, ensuring timely closure in accordance with Kenvue protocols.
  • Kenvue QA Community: Engage in workshops, projects, and task forces at the SE&F Cluster and EMEA Regional levels focused on quality-related initiatives.

Qualifications

Required Qualifications:

  • University degree in a scientific discipline, preferably in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field.
  • Proficiency in English.
  • Current knowledge of relevant pharmaceutical legislation and GDP regulations.

Desired Qualifications:

  • Intermediate proficiency in Portuguese.

What We Offer:

  • Competitive Total Rewards Package.
  • Opportunities for Learning & Development.
  • Access to Employee Resource Groups.

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