Marta Carnielli was born and grew up in Italy. After completing her studies in Pharmaceutical Chemistry, she moved to The Netherlands where she began her career in research at the Pharmacological chemistry Department of the University of Leiden.

In 1995 she joined the European Support Center of Ortho Clinical Diagnostics in Strasbourg (France).
After gaining experience in the area of Customer Technical Support and Training, she joined Ortho Quality Regulatory and Compliance Department where she held various roles of increasing responsibility within the Complaint Handling Unit and the Supply Chain Quality.

In 2011, she was appointed Safety Risk Management & Surveillance Senior Manager, responsible for global medical device vigilance reporting activities for Ortho for Transfusion Medicine products and for the Quality Management System at the Strasbourg site.

Since March 2017, she is Senior Manager, EMEA QRC; in this role she is responsible for quality, regulatory and compliance activities related to the commercial business in France, Italy, Iberia and the distributor markets in Eastern Europe, Poland, Africa and Middle East.

Marta Carnielli has a Master degree in Pharmacy and a Master in Pharmaceutical Chemistry from the University of Trieste, Italy and is a qualified Lead Auditor. She is the Chair of the MedTech Europe IVD Vigilance Working Group.

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