Lonza
Silvia Barchielli is an experienced regulatory affairs professional currently serving as a Senior Regulatory Affairs CMC Specialist at Lonza since April 2023, focusing on global CMC regulatory strategies and interactions with health authorities. Silvia has a robust background in regulatory affairs, including previous roles as a Regulatory Affairs Specialist at Bachem and a Consultant at PQE Group, where responsibilities included global registration of APIs and management of regulatory documentation. With a Master's degree in Chemistry and a further qualification in Pharmaceutical Marketing and Regulatory Affairs, Silvia possesses a comprehensive understanding of regulatory requirements and processes related to drug substances.
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