CSV Validation Engineer for cGMP Systems

Pauwels Consulting; Geel; Sur place; EUR 60 000 - 90 000; Plein temps

Résumé du poste

Pauwels Consulting is seeking a CSV Engineer for a leading pharmaceutical client to support the validation of cGMP‑critical computerized systems. You will execute validation activities across URS, SIA, DQ, IQ, OQ, PQ, RV and TM, and develop validation protocols and reports to ensure ongoing compliance.

You bring 3+ years in CSV within pharmaceutical or GMP environments, with hands-on experience in validation documentation, software packages, and computerized systems.

Qualifications

• 3+ years of experience in CSV within pharmaceutical or GMP environments.
• Hands-on validation documentation experience and execution of URS, IQ, OQ, PQ.
• Experience with software packages and computerized systems.
• Proactive, professional, ownership attitude and independent work.
• Fluent in English and Dutch.

Responsabilités

• Execute CSV validation activities including URS, IQ, OQ, PQ, RV and TM.
• Develop and maintain validation documentation such as protocols and reports.
• Ensure validated status remains compliant with cGMP and regulatory standards.
• Validate software packages and interpret industry standards as required.
• Collaborate with project teams and QA to meet deliverables.

Connaissances

CSV Validation

Documentation

Communication

Independence

English fluency

Dutch fluency

Outils

Software packages

Computerized systems

Description du poste

Pauwels Consulting is seeking a CSV Engineer for a leading pharmaceutical client to support the validation of cGMP‑critical computerized systems. You will execute validation activities across URS, SIA, DQ, IQ, OQ, PQ, RV and TM, and develop validation protocols and reports to ensure ongoing compliance.

You bring 3+ years in CSV within pharmaceutical or GMP environments, with hands-on experience in validation documentation, software packages, and computerized systems.