Teams at Lavipharm S.A.

The Officer Regulatory Affairs will ensure compliance of marketed products, prepare regulatory dossiers, manage submission timelines, and update packaging materials.

Plan and execute financial, operational, compliance, and risk-based audits; evaluate governance and internal controls; identify control gaps and recommend corrective actions; prepare audit reports; support fraud and regulatory reviews; and use data analytics and ERP tools to improve audit quality.

Prepare and maintain CMC regulatory dossiers (CTD Module 3 and Module 2.3), ensure compliance with relevant regulations, implement RA policies, maintain regulatory databases and filing systems, coordinate with R&D/Quality/Operations, and provide CMC regulatory support across departments.