Validation Engineer

QPS Netherlands is part of the global QPS organization, a leading full-service Contract Research Organization (CRO). Together with colleagues around the world, we support pharmaceutical and biotechnology companies in developing new medicines that improve lives.

We are looking for a practical and detail-oriented Validation Engineer to support our local laboratory operations across 2 Groningen locations: our main site and a new laboratory approximately 4 km away.

As Validation Engineer, you will help ensure that laboratory equipment, software, and facilities remain operational, reliable, and compliant. You will manage validation activities, coordinate maintenance and calibration, troubleshoot technical issues, and maintain accurate documentation.

Reporting to local leadership, you will work closely with laboratory teams, Quality, vendors, and technical specialists across our Groningen facilities.

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  Plan, coordinate, and perform Installation, Operational, and Performance Qualification (IQ/OQ/PQ), including requalification, for laboratory equipment and related software.

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  Maintain the operational and validated state of equipment, software, and facilities by coordinating maintenance, calibration, repairs, and software updates.

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  Prepare, review, and improve validation protocols, reports, equipment records, SOPs, and other controlled documentation.

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  Investigate technical issues using risk assessment and root-cause analysis, implement solutions, and identify opportunities to improve performance, efficiency, and quality.

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  Participate in the evaluation, selection, implementation, and validation of new equipment and software.

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  Train and advise laboratory personnel on the correct use of equipment, software, and facilities, as well as relevant technical developments.

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  Perform assigned activities within the QPS quality system and support broader maintenance engineering tasks when needed.

• A bachelor’s degree (HBO/BSc) in Engineering, Life Sciences, Laboratory Technology, or a related field, or a combination of education and relevant experience.

• Relevant experience with equipment validation, qualification, maintenance, calibration, or technical support, preferably within a regulated laboratory or industry.

• Experience with laboratory equipment and supporting software is preferred.

• Strong analytical and problem-solving skills, including risk assessment, troubleshooting, and root-cause analysis.

• Strong planning and project coordination skills, with the administrative precision needed to maintain clear and compliant documentation.

• A practical, flexible, and quality-focused approach, with a strong concern for standards and results.

• Effective communication skills and the ability to train and advise colleagues while working with laboratory teams, Quality, vendors, and other stakeholders.

• Proficiency with Microsoft Office; experience with LIMS or similar laboratory and business systems would be an advantage.

This job has a scheduled closing date of 28 September 2026; prescreen calls will occur the first week in October and onsite interviews during the following week.

At QPS, we are committed to maintaining a healthy and safe workplace. Our vaccination program, including Hepatitis B, supports that commitment. Participation may be required for some roles and voluntary or encouraged for others. By applying, you acknowledge your understanding of this policy.

If you enjoy combining hands-on technical work with validation, problem-solving, and continuous improvement, we would like to hear from you. Apply today by submitting your CV and motivation letter. To learn more about QPS, visit www.qps.com.