Publication date 1 October 2025 Location Mechelen Country Belgium Workplace type Hybrid Travel percentage 0% Department R&D – Design Function type Full-time Contract type Employee Experience required Experience with IVD development, including in-depth knowledge of the regulatory context (IVDR and FDA), is mandatory; Experience with defining and optimizing IVD process infrastructure is mandatory; Profound research experience in molecular biology (focus on nucleic acids, (RT-)(q)PCR design and optimization); Scientifically sound way of working (hypothesis-driven testing and experimental set-up); Excellent scientific communication skills (presenting and writing, including abstracts, publications, grants, work instructions); Experience in the field of Oncological Pathology; Knowledge of relevant scientific databases, Bio-IT and statistical tools; Awareness of intellectual property and its implications. Education

PhD in science- or technology-related study domain with profound expertise in molecular biology (preferably in the field of oncology)

OR

Master in science- or technology-related study domain with at least 4 years of industrial research experience in molecular biology (preferably in the field of oncology).