Quality Assurance Specialist

Quality Assurance || Manufacturing Systems / Facility & Utility

📍 Geel, Belgium – Onsite

Role Overview

Support the QA Engineering department in ensuring that all qualification-related regulatory and procedural requirements are met throughout the full lifecycle (concept to retirement) of manufacturing, facility, and utility systems within a pharmaceutical environment. The role ensures ongoing cGMP compliance and quality oversight during projects and operations.

Responsibilities

• Review and approve qualification documentation (SOPs, URS, risk assessments, test plans, change controls, deviations, CAPAs).
• Ensure compliance with cGMP regulations and internal quality standards.
• Provide QA support for new and upgraded systems.
• Participate in cross-functional engineering project teams.
• Follow up on deviations during qualification activities.
• Communicate quality and compliance status to QA stakeholders.

Key Requirements

• Experience in pharmaceutical or chemical industry qualification activities.
• Knowledge of cGMP regulations.
• Experience with manufacturing and/or facility & utility systems.
• Familiar with change management and document systems (e.g., Trackwise, TruVault, Kneat).
• Strong communication skills.
• Fluent in English and Dutch.

Practicalities

• Geel, Belgium
• Full-time
• Onsite

Interested? Apply now or send your CV to l.ormrod@panda-int.com