Computer System Validation Supervisor

☞ Panda International

Visualizza: 103

Giorno di aggiornamento: 17-11-2025

Località: Geel Antwerp

Categoria: Garanzia di qualità / Controllo di qualità

Industria: Pharmaceutical Manufacturing

Posizione: Mid-Senior level

Tipo di lavoro: Full-time

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Contenuto del lavoro

QA CSV Supervisor – Manufacturing Automation

Geel, Belgium | Contract

Join the QA Engineering team and play a key role in ensuring all Computer System Validation (CSV) activities for manufacturing automation systems meet the highest regulatory and quality standards. You’ll review and approve critical documentation, collaborate with engineering teams, and safeguard cGMP compliance throughout the entire system lifecycle.

About the Role

As a QA CSV Supervisor, you will:

  • Review and approve CSV documents & records (SOPs, user requirements, risk analyses, test plans/scripts, change controls, CAPAs, etc.).
  • Ensure compliance with cGMP regulations, guidelines, and company policies.
  • Provide QA guidance during the introduction of new or upgraded systems/processes.
  • Address and follow up on deviations during CSV activities.
  • Communicate quality, compliance, and planning updates to the QA Qualification team.
  • Collaborate with cross-functional engineering teams to integrate CSV requirements seamlessly.

Requirements

  • Proven experience in Computer System Validation within the pharmaceutical and/or chemical industry.
  • Strong knowledge of manufacturing automation systems (e.g., DeltaV).
  • Familiarity with problem report/change request systems (e.g., Comet) and document management tools (e.g., TruVault).
  • Knowledge of test tools (e.g., Kneat).
  • Solid understanding of cGMP regulations and industry guidelines.
  • Ability to translate technical concepts for different audiences.
  • Strong prioritization skills, with the ability to handle multiple projects simultaneously.
  • Excellent communication and teamwork skills.
  • Fluent in English & Dutch (spoken and written).

What We Offer

  • A challenging and impactful role within a world-class pharmaceutical environment.
  • Opportunity to work on cutting-edge manufacturing automation systems.
  • Competitive daily rate based on experience.
  • A dynamic, supportive, and cross-functional team environment.
  • Possibility to contribute to high-profile projects in a globally recognized company.
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Scadenza: 01-01-2026

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