QP

☞ Pauwels Consulting

Visualizza: 100

Giorno di aggiornamento: 21-11-2025

Località: Braine-l’Alleud Walloon Brabant

Categoria: Altra

Industria: Staffing Recruiting

Posizione: Entry level

Tipo di lavoro: Full-time

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Contenuto del lavoro

In coordination with the relevant management, the QP is responsible for the implementation and maintenance of an effective Quality Management System.

The QP:

  • Ensures that operations related to raw materials, imported or manufactured bulk pharmaceutical products, and packaged finished products comply with national and/or international regulations and guidelines (cGMP).
  • Ensures that products conform to their marketing authorization dossiers.
  • Makes decisions regarding batch release, rejection, or rework of products.
  • Proactively supports operations in identifying, developing, and implementing quality and operational excellence improvements in response to business needs, technical changes, and regulatory requirements.
Main responsibilities

  • Release and certification of the above-mentioned product batches, including the management of legal samples.
  • Management of quality deviations, investigations, CAPAs, market/client complaints, recalls, temporary and permanent change controls, and authorization of retests and reprocessing/rework.
  • Review and approval of Product Quality Reviews (PQR) and Line Quality Reviews.
  • Drafting, reviewing, and approving procedures related to the scope of activity.
  • QA monitoring and support for projects defined by QA management, specifically those related to release activities.
  • Conducting internal audits and participating in customer audits and regulatory inspections within the scope of responsibility
What are we looking for?

  • Degree in Industrial Pharmacy with a valid Qualified Person (QP) registration number.
  • Experience in a GMP pharmaceutical environment in a similar role and/or in Quality Assurance, Production, or Quality Control.
  • Strong knowledge of international GMP regulations relevant to the activities.
  • Strong sense of confidentiality and integrity.
  • Excellent team spirit and interpersonal skills, including effective written and verbal communication.
  • Ability to communicate effectively and interact easily with production teams on the shop floor and QC/QA laboratory staff.
  • Capacity to work under pressure.
  • Strong problem-solving skills and ability to propose constructive and innovative solutions.
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Scadenza: 05-01-2026

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