Dr. Jie Jia

Give guidance, lead process, and support medical/clinical content-sensitive topics, questions, and projects for all medical device portfolios under the global framework. Cross-functioning, demonstrate working process between Medical and departments e.g. RA, QM, I&D, vigilance during Innovation, Development, Pre- and Post Market phase. Provide field-specific competitive landscape with medical and scientific know-how-based interpretation. Leverage, develop, and maintain a strong KOL and regulators network.

Service provider for Medical Device Manufacturer Consultant for strategic regulatory and technical support in medical device registration Compilation and update of Clinical Evaluation Report according to MEDDEV / MDR Consultant and conduction of Post-Market Surveillance (PMS) / Post-Market Clinical Follow-up (PMCF) / PMCF plan MEDDEV 2.7/1 rev. 4

Conducting multiple research projects i.a.: -Airway pathology of chronic bronchitis in new-borns -Chronic cigarette smoke induced immune disorder in lung, etc. -Gaining fully experimental and analytic experience with regards to in-vitro, ex-vivo and in-vivo animal treatment -Collaboration includes dark field imaging, conditional knockout mouse model, mouse lung transplantation, organ micro dissection, etc.

-Received medical training at the surgical, internal medicine, obstetrics & gynaecology and paediatrics unit -Participated in daily bed checks and operations -Prepared documents for patients, bed reporting under the supervision of senior doctor -Working through night shifts, and at the emergency unit including the independent realization of basic surgeries