Joost Steverlynck is Senior CMC Writer at Ardena Ghent. He supports pharmaceutical development and lifecycle management programs through the preparation of regulatory and technical documentation for both emerging biotech companies and established pharmaceutical organizations.
Joost brings more than five years of experience in the preparation of API-related documentation, including mutagenicity reports, synthesis criticality analyses, and nitrosamine risk assessments. His expertise focuses on supporting regulatory compliance and the development of high-quality CMC documentation across pharmaceutical development programs. At Ardena, he works closely with clients and multidisciplinary teams to support regulatory and technical documentation activities throughout the product lifecycle.
Joost obtained his Master of Science degree in Chemistry from KU Leuven in 2012 and earned his PhD with a specialization in the synthesis of conjugated polymers. He subsequently completed a postdoctoral fellowship at KAUST, where his research focused on organic electrosynthesis for pharmaceutical applications.
