Qualification & Validation Responsible
Location: Brussels, Belgium
Start date: ASAP
Overview
We are seeking an experienced Qualification, Validation & Metrology Manager to support GMP-regulated pharmaceutical manufacturing operations. The successful candidate will lead qualification and validation activities, oversee metrology programmes, and ensure compliance with regulatory and quality requirements across equipment, facilities, utilities, processes, and systems.
Responsibilities
- Coordinate and execute qualification activities for equipment, utilities, facilities, and computerised systems.
- Support process, packaging, and cleaning validation activities.
- Oversee calibration and metrology programmes to ensure GMP compliance.
- Manage deviations, CAPAs, change controls, and risk assessments related to validation activities.
- Prepare, review, and approve qualification and validation documentation.
- Support internal audits, client audits, and regulatory inspections.
- Collaborate with Quality, Engineering, Manufacturing, and external vendors to deliver compliant validation projects.
Requirements
- Significant experience in a GMP pharmaceutical manufacturing environment.
- Proven hands-on experience in qualification and validation activities (IQ/OQ/PQ).
- Demonstrated experience in metrology and calibration management.
- Strong knowledge of GMP, ICH guidelines, pharmaceutical quality systems, and risk management principles.
- Experience managing deviations, CAPAs, and change controls.
- Strong communication skills, attention to detail, and ability to work independently.
- Operational level of English.
Please note: This is a senior-level position. Demonstrable experience in both qualification/validation and metrology is essential.
FAQs
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