Job Title:
QA Computer System Validation (CSV)
About the Role:
We are looking for a QA Computer System Validation (CSV) Contractor to support the QA Engineering team in Geel, Belgium. This role ensures that all CSV-related regulatory and procedural requirements are met throughout the full system lifecycle — from concept and project phases to operational use and retirement — for manufacturing automation systems. You will work with engineering teams and other stakeholders to maintain compliance and support system introductions, upgrades, and process improvements.
Key Responsibilities:
- Review and approve CSV documents and records (SOPs, user requirements, risk assessments, test plans, test scripts, change controls, CAPAs).
- Support engineering teams in introducing new or upgraded systems.
- Provide guidance on CSV activities while ensuring compliance with cGMP standards.
- Address and follow up on deviations during CSV activities.
- Communicate status, compliance, and planning updates to relevant teams.
- Contribute to continuous improvement of CSV processes.
Requirements:
- 6–8 years of experience in CSV for manufacturing automation systems in the chemical or pharmaceutical industry.
- Strong knowledge of cGMP regulations and guidelines.
- Ability to translate technical information for different levels of the organization.
- Skilled in assessing urgency, criticality, and impact of decisions.
- Ability to manage multiple projects simultaneously.
- Self-motivated and effective in cross-functional teams.
- Fluent in English and Dutch (written and spoken).
- Bachelor's degree or equivalent in a relevant field.
Technical Skills (Preferred):
- Manufacturing automation systems (e.g., DeltaV)
- Problem/change management systems (e.g., COMET)
- Document management systems (e.g., TruVault)
- Test tools (e.g., Kneat)
Practical's:
- Location:
Geel, Belgium (On-site) - Duration:
Until 31 August 2026 - Start Date:
ASAP Work Model:
Full-time
Interested?
Send your CV to
e.-
to apply or learn more.
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