Senior Regulatory Affairs Specialist (IVD experience required)

Share Publication date 8 June 2026 Department Quality, Regulatory and Clinical Affairs Country Austria France Germany Italy Spain United Kingdom Location Europe (remote based) Work arrangement Remote Travel percentage 10% Function type Full-time Contract type Employee Experience required

Min. 5 years of experience in Regulatory Affairs;

IVD/medical device experience preferred, especially PCR or software experience

Must have highly effective organizational and planning skills to apply daily in a multidisciplinary environment

Must be able to work effectively in a strongly matrixed team-oriented structure using excellent communication, interpersonal and relationship management skills to successfully interact with Clinical, Research and Development, Manufacturing, Quality, Marketing, Operations and corporate partner counterparts

Regulatory Affairs Certification is a plus

Proven experience with:

In-vitro diagnostics validat...