Timothy Buckley

Timothy Buckley has extensive experience in the pharmaceutical industry, with their most recent role being Vice President of Global Quality at SK pharmteco since 2018. Prior to this, they held various positions at Bristol-Myers Squibb, including Head of Quality BMS Internal Pharma Manufacturing and Quality Director, starting in 2012. From 2003 to 2012, Timothy worked at Pfizer Ireland Newbridge as Director of Quality/Quality Operations Product Leader/QP. Earlier in their career, they served as QA/Validation Manager at Merck from 1996 to 2003 and as a Validation Specialist at Leo Pharmaceuticals from 1993 to 1996.

Timothy Buckley obtained a Bachelor of Applied Science (B.Sc., Applied Physics & Applied Chemistry) from Trinity College Dublin in the years 1985 to 1989. Timothy then pursued a Master of Science (M.Sc) in Analytical Chemistry from Dublin City University from 1990 to 1992. In 1995, they received ASME membership from Technological University Dublin. Lastly, in 2004 to 2005, they completed a Post grad Dip in Pharmaceutical Manufacture (QP) from Trinity College Dublin.