As QA/RA Officer you maintain and further develop the electronic Quality Management System (eQMS) that is directed towards the design, development and manufacturing of in vitro diagnostic medical devices and diagnostic testing. You contribute to the expansion of the eQMS by developing and validating new modules, and as a writer to the creation of QA-related documentation. You act as a Document Controller and provide training to your colleagues regarding different aspects of the QMS. Outside the eQMS you will be performing internal and external (supplier) audits, assist in QA-related issues and perform QA-related duties when applicable.
Together we ensure the validation and implementation of clinically relevant scientific discoveries into reliable medical diagnostic assays for diagnosis, prognosis and drug effectiveness prediction that will ultimately contribute to improved patient care.
we live to make a difference. It is our mission to improve a patient's quality of life by enabling them to benefit from personal insights at the genomic level of their disease. That means we are continuously innovating the world of gene signature-based diagnostic testing. That also means we have a unique blend of characteristics. We have our soft side. Our culture is oftentimes described as familial, warm, loyal and highly engaged. We have our rational side where exact sciences are driving our mission. And when needed our passionate side surfaces to clear the way so we can serve society with science based solutions.
Send your resume and motivation letter to Deborah Wigmans (HR) via this link. If you have questions or want more information, don't hesitate to contact us. You'll find the contact details on our website. We will make sure it lands on the right desk!