Pharma QA Specialist - GMP & Compliance

Nalys; Wallonië; Sur place; EUR 55 000 - 90 000; Plein temps

Résumé du poste

Nalys is seeking a QA Officer – Pharmaceutical Manufacturing to join the Quality Assurance department at a pharmaceutical production site in Belgium. You will help ensure GMP compliance and maintain the site's quality management system, coordinating with production, QC, and regulatory teams on day-to-day quality activities.

This hands-on role requires a rigorous, detail-oriented mindset, strong cross-functional communication, and fluency in French with a good working level of English.

Qualifications

• Bachelor's or Master's in pharmacy, biology, chemistry, or related life sciences.
• At least 4 years in QA within pharmaceutical or biotech manufacturing.
• Experience with GMP, quality systems, deviation/CAPA management, and eQMS familiarity.

Responsabilités

• Reviewing and approving batch documentation (batch records, logbooks, in-process controls).
• Managing deviations, OOS/OOT investigations, and corrective and preventive actions (CAPA).
• Assessing and coordinating change controls and their quality impact.
• Ensuring GMP compliance, internal SOPs, and regulatory requirements.
• Participating in internal audits and supporting inspections.
• Drafting, reviewing, and updating quality procedures and work instructions.
• Monitoring and reporting quality KPIs to the QA Manager.
• Providing GMP guidance and training to production teams.
• Contributing to continuous improvement within the quality system.

Connaissances

QA experience

GMP knowledge

CAPA management

Batch documentation

Cross-functional communication

French fluent

English working level

Formation

Bachelor's or Master's degree in pharmacy/biology/chemistry or related life sciences

Outils

eQMS

Description du poste

Nalys is seeking a QA Officer – Pharmaceutical Manufacturing to join the Quality Assurance department at a pharmaceutical production site in Belgium. You will help ensure GMP compliance and maintain the site's quality management system, coordinating with production, QC, and regulatory teams on day-to-day quality activities.

This hands-on role requires a rigorous, detail-oriented mindset, strong cross-functional communication, and fluency in French with a good working level of English.