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Clinical Safety Lab Manager

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About the vacancy

Operations
Strategic planning
Engineering
General
Regulatory Affairs
Clinical R&D
Staff
Project Management
R&D
R&D Other
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Manager Bachelor’s Degree (HBO, WO) Temporary to Permanent Full time 4500 - 8500 Groningen, Netherlands

About Your Next Job

Help shape a growing laboratory. Lead a team that makes a difference.

At QPS Netherlands, part of a global clinical research organization, our work helps pharmaceutical and biotechnology companies develop new medicines. Our new Clinical Safety Laboratory in Groningen supports that mission through testing that protects clinical trial participants and delivers reliable study data.

As Laboratory Manager, you will combine your hands-on laboratory expertise and people management experience to lead daily operations, develop your team, and help build the laboratory’s capabilities. If you enjoy turning ideas into practical improvements and helping people succeed, this is an opportunity to make a visible contribution.


About Your Next Colleagues

Join a collaborative, science-driven team supporting clinical research for global pharmaceutical and biotechnology clients.


About Your Tasks and Responsibilities

What You Will Do

  • Lead daily clinical safety laboratory operations to deliver high-quality, compliant, and efficient services.

  • Develop laboratory processes, systems, and workflows to support continued growth.

  • Supervise and develop laboratory staff, including hiring, training, coaching, and performance management.

  • Maintain compliance with applicable regulatory, quality, and safety requirements.

  • Oversee instrumentation, maintenance, and the introduction of new methods and services.

  • Coordinate laboratory planning and consumables to meet study and business needs.

  • Review study protocols and work with study teams, project management, and site leadership to ensure laboratory readiness and successful study execution.

  • Resolve operational and technical issues, drive improvements, and support responsive client communication.


About Your Skills and Experience

What We’re Looking For

  • Bachelor’s or master’s degree in Life Sciences or a related field.

  • 3+ years of relevant, hands-on experience in a regulated laboratory, ideally in clinical safety testing, a CRO, or a pharmaceutical setting.

  • Proven people management experience with direct responsibility for laboratory staff, including work allocation, coaching, staff development, and performance management.

  • Knowledge of laboratory quality systems and familiarity with GCP, ISO 15189, and applicable Dutch regulations.

  • Strong organizational and problem-solving skills, with a clear, collaborative communication style.

  • A hands-on approach and an interest in developing people and improving laboratory operations.

  • Business-level English and at least B1-level Dutch.

Relevant experience includes hands-on work in a regulated laboratory plus direct staff management beyond an academic research setting. Experience helping establish a laboratory or improve existing operations is an advantage.


Where Molecules Meet Opportunities

QPS combines the reach of a global CRO with the close working relationships of a local team, giving you the opportunity to shape a growing laboratory with support from experienced colleagues and direct communication with leadership. If you enjoy supporting people, improving processes, and helping a laboratory grow, we would like to hear from you.


You are eligible to work in EU

We only accept applicants who are eligible to work in the EU


Contact person

Femke Heijnen-van den Hazel

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QPS Netherlands B.V., based in Groningen, is part of QPS Holdings LLC, a global, full-service contract research organization supporting pharmaceutical and biotechnology companies from early discovery through clinical development. At our Groningen site, laboratory teams operate in a highly collaborative, regulated environment, delivering high-quality data for international studie



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