Quality Control and Validation Specialist

☞ Oxford Global Resources

Visualizza: 115

Giorno di aggiornamento: 06-12-2025

Località: Heist-op-den-Berg Antwerp

Categoria: Garanzia di qualità / Controllo di qualità

Industria: Pharmaceutical Manufacturing

Posizione: Entry level

Tipo di lavoro: Full-time

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Contenuto del lavoro

Be at the forefront of ensuring the safety, quality, and compliance of pharmaceutical processes, contributing to the advancement of innovative healthcare solutions.

Job Description
As a Process Validation Specialist, you will play a crucial role in ensuring the safety, quality, and compliance of manufacturing processes. Your responsibilities include participating in functional meetings, performing periodic reviews of cleaning processes, coordinating re-qualification studies, and providing support to cleaning projects. This role involves collaboration with various departments, including validation, production, and laboratories, to maintain validated states and address deviations.

Responsibilities

  • Attend and actively contribute to functional meetings essential for the execution of assigned activities.
  • Perform periodic reviews of cleaning processes a production departments to control the validated state.
  • Coordinate and execute yearly re-qualification studies at IPTs, with a focus on one primary IPT and serving as a backup for another.
  • Provide assistance to cleaning projects’ development and validation, covering partswashers, Clean In Place (CIP), and manual cleaning methods.
  • Coordinate activities with validation, production, and laboratories.
  • Schedule appointments with production and laboratories.
  • Create Laboratory Information Management System (LIMS) requests.
  • Execute studies and evaluate data results.
  • Support the monitoring program for potential cross-contamination by sampling non-product contact surfaces.
  • Administer and conduct root cause analysis for deviations.

Profile

  • Master’s or bachelor’s degree in chemistry/sciences/pharmaceutics or equivalent.
  • Relevant experience in Pharmaceutical Processes, Validation, and Project Management.
  • Proficient technical writing skills.
  • Knowledge of English (speaking, writing, reading).
  • Fluent, communicative, diplomatic.
  • Team player, collaborative.
  • Motivated to work in a challenging environment.
  • Interest in working on the shop floor.
  • Quality and scientific mindset.
  • Action-oriented, analytical thinking.
  • Flexible and committed.
  • Autonomous.

Benefits

  • Directly employed by Oxford, initial project till the end of 2025, realistic long-term perspective
  • Mobile phone provided & monthly phone contribution
  • Monthly allowance for meal vouchers
  • Travel allowance
  • Hospital & Group insurance
  • Opportunities for education and training
  • Fulltime position, daytime work


Required: Current valid permit to work and live in Belgium.

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Scadenza: 20-01-2026

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