Bruce Davis

Bruce Davis is a professional engineer and has many years of experience in the pharmaceutical industry. He has been involved in pharmaceutical engineering projects for API, secondary manufacturing and packaging for AstraZeneca. He led engineering teams in these areas, from early business thinking to concept development to project delivery and managed the global capital programme.

He has a wide international knowledge and has carried out business/engineering studies for new plants and new developments internationally.

He has led cross-functional Quality by Design (QbD)workshops.
For ISPE, he was the 2008 Chairman.

He a major contributor and leader of ISPE's Product Quality Lifecycle Implementation (PQLI) initiative, he also co-leads the Control Strategy team, which has brought new thinking into delivering Control Strategies to meet ICHQ8/Q9/Q10 requirements. He has also had involvement in many other ISPE matters, including chairing the Sterile Baseline® Guide task team.
He is secretary to ASTM E55.03 Committee on General Pharmaceutical Standards.
From beginning of 2009, he will running his own consultancy in Engineering for QbD.