Publication date 6 January 2025 Location Mechelen Country Belgium Workplace type Hybrid Travel percentage 0% Department Quality, Regulatory and Clinical Affairs Function type Full-time Contract type Employee Experience required Preferably at least 2 years of relevant experience in a quality function within the healthcare industry. Experience in an IVD – Medical Diagnostics manufacturing environment is a plus. Education Master’s degree in engineering or life sciences (biomedical, chemical, pharma…) or equivalent through experience/training.…).