Jan is an expert in European regulations based on 20 years hands-on working in the field, as auditor, product reviewer, regulatory specialist and senior manager. He combines strong experience in quality, compliance, and regulations with a pragmatic, result driven approach at both operational and executive level.
Jan about Qserve:
"Our mission is to support all medical device manufacturers with a practical approach, translating existing regulations to understandable requirements."
Prior to Qserve, Jan was VP Medical Devices at BSI for 5 years, the largest Notified Body worldwide, where he was responsible for EMEA and AsiaPac and a member of the Executive Team.
Before joining BSI, he was Business Director at KEMA (now DEKRA), responsible for their Medical Device and System Certification businesses globally.
From his degree in biomedical materials, he has dealt as a technical reviewer with a large range of devices mostly in the non-active device area (disposables, implants, borderline products), in cardiovascular, orthopedic, ophthalmic and wound care fields.
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