Life Sciences QA Validation Engineer – Permanent

ALTEN; Vlaanderen; Sur place; EUR 55 000 - 85 000; Plein temps

Avantages offerts par ce poste

A permanent contract

Company car

Meal vouchers

Résumé du poste

ALTEN Belgium is seeking a QA Validation Engineer to support the QA Engineering department across the complete lifecycle of qualification/validation projects. You will help ensure regulatory and procedural requirements are fulfilled for manufacturing, laboratory, building, utility, IT, and automation systems.

The role requires experience in chemical or pharmaceutical industries, strong knowledge of cGMP, and the ability to translate technical information for diverse audiences.

Qualifications

• Experience in chemical or pharmaceutical industries with qualification/validation.
• Knowledge of cGMP regulations and guidelines.
• Ability to translate technical information for all levels of the organization.
• Ability to estimate urgency, criticality and impact of decisions.
• Ability to multitask and work on multiple projects.

Responsabilités

• Review and approve qualification/validation documents and quality records (SOPs, URs, Impact/Risk analyses, test plans/scripts, change controls, CAPAs).
• Collaborate with engineering teams and other groups for new or upgraded systems and processes.
• Provide advice and support for qualification/validation activities and cGMP compliance.
• Address and follow up on deviations during qualification/validation activities.
• Communicate status to QA qualification/validation team members.

Connaissances

Quality assurance

Regulatory compliance

Cross-functional teamwork

Technical writing

Analytical thinking

English and Dutch fluency

Outils

TrackWise

Comet

TruVault

Kneat

Description du poste

ALTEN Belgium is seeking a QA Validation Engineer to support the QA Engineering department across the complete lifecycle of qualification/validation projects. You will help ensure regulatory and procedural requirements are fulfilled for manufacturing, laboratory, building, utility, IT, and automation systems.

The role requires experience in chemical or pharmaceutical industries, strong knowledge of cGMP, and the ability to translate technical information for diverse audiences.