Job Description
Share Publication date 8 June 2026 Department Quality, Regulatory and Clinical Affairs Country Belgium Location Mechelen, Belgium (hybrid) or Europe based (remote) Work arrangement Hybrid 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 In-vitro diagnostics validation requirem...
Proven experience with:
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Submit ApplicationJob Details
- Location Belgium, Belgium
- Job Type Full-time
- Category Business Operations Specialists
- Posted Date July 06, 2026
- Application Deadline August 15, 2026