Quality engineers

We are looking for multiple experienced QA Validation professionals, fluent in Dutch to support a high-impact Advanced Therapy Medicinal Products (ATMP) project.

You will play a key role in ensuring that all qualification and validation activities meet regulatory and procedural requirements throughout the full system lifecycle - from concept to retirement.

Open Profiles Across Specialisations

Depending on your background, you may be matched to one of the following focus areas:

• Manufacturing Systems Qualification
• Laboratory Systems Qualification
• Facility & Utility Systems Qualification
• IT/Automation Systems - Computer System Validation
• Specialised QA Validation Services

Key Responsibilities

• Review and approve validation documents and quality records (e.g. SOPs, URS, risk assessments, test plans, change controls, CAPAs).
• Provide QA support to engineering teams during the introduction of new or upgraded systems.
• Ensure compliance with cGMP, internal standards, and regulatory guidelines.
• Investigate and follow up on deviations during qualification/validation execution.
• Communicate progress and compliance status to QA stakeholders.

Your Profile

• 6-8 years of experience in QA/Validation within the pharmaceutical or chemical industry.
• Strong knowledge of cGMP regulations, validation principles, and system lifecycle management.
• Ability to translate technical content into clear, cross-functional communication.
• Skilled in prioritisation, decision-making, and working independently or in cross-functional teams.
• Excellent communication skills in English and Dutch (written and spoken).

Preferred System Knowledge

• Manufacturing, lab, building, utility, IT, and automation systems used in pharma/chemical environments.
• Familiarity with tools such as TrackWise, Comet, TruVault, and Kneat.

If you're ready to contribute to a cutting-edge ATMP project and bring your validation expertise to a collaborative, high-compliance environment - we'd love to hear from you.