| Location | Geel, Flemish Region, Belgium, Belgium |
|---|---|
| Business Sector | Pharmaceutical |
| Contact email | |
| Job ref | 26214 |
| Published | about 1 hour ago |
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.
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.
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.
Manufacturing automation systems (e.g., DeltaV)
Problem/change management systems (e.g., COMET)
Document management systems (e.g., TruVault)
Test tools (e.g., Kneat)
Location: Geel, Belgium (On-site)
Duration: Until 31 August 2026
Start Date: ASAP
Work Model: Full-time
Interested?
Send your CV to e.cabral@panda-int.com to apply or learn more.