Qserve Group is a global MedTech partner offering regulatory, clinical, and quality compliance services for medical devices and in‑vitro diagnostics. With a presence in Europe, China, and the United States, the company combines deep expertise in EU MDR, EU IVDR, and FDA requirements with hands‑on CRO capabilities to guide manufacturers through global market access. Its portfolio spans regulatory affairs, clinical trial design and execution, quality management system implementation, audits, and training, as well as acting as local agents for CE marking, US FDA, and NMPA registration. Qserve’s distinctive value lies in its integrated, end‑to‑end support that blends regulatory strategy, clinical insight, and compliance excellence, enabling clients to bring innovative MedTech solutions to market efficiently.
Open Positions
Open Application
No specific requirements mentioned
Junior HR Officer
The role requires some experience in HR administration or payroll support, an educational background in HR, and fluency in Dutch and English
Sales & Business Development Manager France
5+ years of experience in business development and/or technical sales, Bachelor's degree in business, sales, marketing, or a scientific discipline
Senior Consultant Medical Devices Quality & Regulatory Affairs
Technical degree in relevant field, 7+ years experience in medical device field, solid knowledge of quality assurance and regulatory affairs
Consultant Medical Devices Regulatory Affairs (AI & Machine Learning)
Technical degree in engineering or a related field, 4+ years of experience in the medical device sector, hands-on experience with AI/ML-based devices
Consultant Clinical Affairs
Technical degree, 4+ years of experience in clinical evaluation, and experience with systematic literature search