curriculum vitae
Selina Verardi, regulatory affairs consultant

education
Swiss Federal Diploma in Pharmacy, University of Basel, Switzerland,
2008
Master of Science in Pharmacy, University of Basel and Bern, Switzerland, 2008

summary of experience

Regulatory affairs professional with a decade of experience in the pharmaceutical and medical device sector. Strong technical background and comprehensive knowledge of European and Swiss Registration Procedures, specializing in MRP/DCP registrations and CE Marking. Demonstrates broad expertise in global registrations, CMC topics, and compliance with EU 2017/45 MDR requirements.

experience

SINCE 2023
Regulatory Affairs Consultant, REGULIX LTD, Switzerland

2019-2023
Regulatory Affairs Manager Medical Devices, Haag-Streit AG, Switzerland

2016-2018
Project Manager, Swiss Biobanking Platform (SBP), Switzerland

2010-2016
Regulatory Affairs Manager Medicinal Products, Bayer Consumer Care, Switzerland

languages
Mother tongue: German, Rhaeto-Romanic

Fluent in English, French
Italian, Spanish (basic skills)