Senior QA Validation Engineer – cGMP & Validation Lead

Prothya Biosolutions

Brussel Hoofdstad

Sur place

EUR 70 000 - 100 000

Plein temps

Il y a 12 jours

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Avantages offerts par ce poste

Health insurance
Meal vouchers
Eco-cheques
Flex Reward Plan
Homeworking after onboarding

Résumé du poste

Prothya Biosolutions seeks a Senior Engineer QA Validation to safeguard quality across cGMP systems. You will lead validation activities, review protocols and reports, and act as QA SPOC with project teams. The role requires a Master’s degree in a related field and 6–10 years’ experience in pharma or food sectors, with English proficiency and Dutch/French knowledge.

Brussels-based with on-site duties. You will contribute to ongoing quality improvements and support cross-functional teams in

Qualifications

  • As per the profile, a Master’s degree in a relevant field is preferred.
  • 6–10 years of experience in pharmaceutical or food sectors.
  • Familiarity with European and US GMP guidelines and SOPs is a plus.
  • Strong documentation and validation testing experience.

Responsabilités

  • Oversee qualification and validation protocols from a QA perspective.
  • Draft and review validation reports for equipment, utilities, IT validation, and processes.
  • Lead risk analyses and CAPA activities within QA validation.
  • Coordinate with project teams as QA SPOC and provide coaching to junior staff.

Connaissances

English fluency
Analytical thinking
Leadership
Problem solving

Formation

Master's degree (Chemistry/Industrial Pharmacy/Biotechnology)

Outils

SAP
MasterControl

Description du poste

Prothya Biosolutions seeks a Senior Engineer QA Validation to safeguard quality across cGMP systems. You will lead validation activities, review protocols and reports, and act as QA SPOC with project teams. The role requires a Master’s degree in a related field and 6–10 years’ experience in pharma or food sectors, with English proficiency and Dutch/French knowledge.

Brussels-based with on-site duties. You will contribute to ongoing quality improvements and support cross-functional teams in

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