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.
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