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# QA Qualification & Validation Enginner

- **Company:** Amaris
- **Location:** Geel, Belgium (Remote available)
- **Contract:** Permanent contract
- **Skills:** Test Scripts, Trackwise
- **Published:** October 26, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=b7851f1b9f2e130a

## About the Role

* Experience in QA qualification and validation within a pharmaceutical or other regulated industry.
 * Strong knowledge of cGMP requirements and relevant pharmaceutical guidelines.
 * Experience reviewing qualification and validation protocols, reports and associated quality documentation.
 * Understanding of risk assessments, deviation management, change controls and CAPAs.
 * Ability to assess quality risks, prioritise activities and communicate decisions clearly.
 * Able to manage multiple priorities and work effectively with cross-functional teams.
 * Familiarity with quality management or validation platforms such as TrackWise, Kneat or similar systems is an advantage.
 * Fluency in Dutch and English is required.

## Description

As a QA Qualification & Validation Engineer, you will support quality assurance activities throughout the qualification and validation lifecycle, ensuring compliance with cGMP requirements, applicable regulations and internal quality standards., * Review and approve qualification and validation documentation, including User Requirements Specifications (URS), risk assessments, protocols, test plans, test scripts and final reports.

 * Provide QA oversight and guidance for the qualification and validation of pharmaceutical equipment, facilities, utilities and processes.
 * Ensure that qualification and validation activities comply with cGMP requirements, applicable regulations and internal quality standards.
 * Review and follow up on deviations, change controls and CAPAs related to qualification and validation activities.
 * Assess quality risks and ensure that appropriate actions are implemented and documented.
 * Support project teams throughout the equipment and system lifecycle, from project design and implementation to routine operations.
 * Collaborate with QA, engineering, operations, IT and other cross-functional teams to maintain a compliant GMP environment.