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GenDx is seeking a Technician Operations (QC) to execute QC procedures and ensure molecular diagnostics kits meet high quality standards. You will analyze data, document results, and collaborate across Production and R&D in a regulated ISO 13485 environment.
The role involves hands-on lab work with PCR, gel electrophoresis, Sanger sequencing, NGS, and related techniques, contributing to patient safety and global transplant outcomes.
GenDx is a global leader in molecular diagnostic laboratory solutions for high resolution tissue typing of both donors and patients and monitoring transplant success. We combine our cutting-edge software solutions, reagents for DNA sequencing-based HLA typing and transplant surveillance strategies with our excellent customer support including a comprehensive education program. Our products are sold all over the world through direct sales and distributors. The GenDx office is based at Utrecht Science Park in The Netherlands. Since 2022, GenDx is part of the Eurobio Scientific Group, headquartered in Les Ulis, France.
With a highly educated and motivated team, we contribute to the quality of life of transplant patients. Do you want to be part of an innovative company that offers ample time for development? To strengthen our team, we offer a challenging position for amotivated and detail-oriented Technician Operations (QC).
As Technician in the Quality Control (QC) team at GenDx, you will play a key role in executing QC procedures for our pre- and post-transplant products. You will be responsible for ensuring that our molecular diagnostics kits and reagents meet the highest quality standards before they reach our customers.
As part of the dynamic Operations team, and the QC team specifically, no two days are the same in this role, but you can expect a combination of hands-on lab work, data analysis, and cross-team collaboration. Your work involves a range of molecular biology techniques, including (q)PCR, gel electrophoresis, Sanger sequencing, next-generation sequencing (NGS) and long-read sequencing technologies.
Since we produce high-quality diagnostic products under ISO 13485 standards, precise documentation is an essential part of the role. In addition to performing laboratory tests, your daily tasks will include analyzing results, documenting findings, and collaborating with colleagues from Production and R&D.
In this role, accuracy, attention to detail, and a strong commitment to patient safety are essential. The work you perform directly supports clinicians and laboratories around the world in making reliable transplant decisions, ultimately impacting patient outcomes.
You will join a motivated and knowledgeable team working in a dynamic, innovative, and internationally oriented environment focused on excellence in molecular diagnostics.
For more information you can contact Walinka van Tol, Associate Director Quality Control, at +31 (0)30 252 37 99.
To be considered for this position, you must be legally permitted to live and work in the Netherlands.