

Versatile professional demonstrating strengths in project management and cross-functional collaboration for drugs development. Adapts to changing demands through analytical and problem-solving capabilities. Committed to delivering high-quality outcomes in diverse international environments, leveraging strong interpersonal skills and rigorous attention to detail.
Accomplished Regulatory Affairs in Pharmaceutical certification and eager to apply knowledge and gain practical experience. Reputation for hard work, organization and willingness to learn new tasks.
Quality Systems Site Lead User
Analytical methods validation on DS/DP and intermediates produced from biotechnological processes for clinical and commercial phases
Project leader in process development from laboratory to industrial scales of peptides APIs
Project leader in R&D
Synthesis of protein-like structures for therapeutic applications
Microsoft Pack Office, SciFinder, Pymol, Topspin, Coreldraw, Chemdraw, Chromoleon, Minitab, Qumas, Trackwise, Cara
Regulatory Affairs Certificate – Pharma Industry / Entry to Regulatory (2026)
CMC Essentials certificate – overview of CMC Development / Educo Life Sciences (2026)
Certificate of International Volunteering in a Company (VIE) / Brussels, Be (2020)
Certificate ESOL examinations - English B2 / University of Cambridge (2010)