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Andrzej has over 25 years of experience in pharmaceutical quality and site management, with a strong focus on the manufacture of sterile medicinal products, as well as solid dosage forms and active pharmaceutical ingredients (APIs). He has held the role of Site Quality Director in international organizations including GlaxoSmithKline, Polpharma, and Mylan.

He has extensive experience in the transformation and implementation of Quality Management Systems, Quality Risk Management, validation, computerized system implementation, capital investment projects, technology transfers, and the implementation of FDA requirements, particularly in sterile product manufacturing.

Andrzej holds an MSc degree in Chemical Technology from the Gdańsk University of Technology and an MBA from the Poznań University of Economics in cooperation with Georgia State University (USA). He is a co-founder and board member of the Polish Affiliate of the International Society for Pharmaceutical Engineering (ISPE).