CDMO selection | Technological fit | CMC | Comparability & biosimilarity | Regulatory pathway| FDA & EMA quality readiness | Facilities design | Due Diligence | Business cases | Manufacturing and supply agreements

I am a executive with over twenty years of experience covering all aspects of biopharmaceutical business: development, manufacturing, clinical and commercial supply, facilities establishment and portfolio development. Main my clients are life sciences companies in Europe and the US.

Prior to establishing my consulting business, I spent sixteen years with Teva biologics business segment as executive and nearly three years with biologics CDMO. I managed a team of professionals involved into process development, manufacturing, projects management and business development. Under my management it was established three biologics facilities, launched few commercial biopharma products, business expanded geographically to US.

I earned a BSc/MSc in bionegineering/biotechnology in Vilnius Gediminas Technical University and EMBA in Baltics Management Institute. 

Email: giedrius.zunda@zbiotechconsulting.com

Phone: +37061630956