Matthew R. McMenamin
GlaxoSmithKline
Validation Global Process Owner
Matthew McMenamin is currently Validation Global Process Owner in GlaxoSmithKline’s Pharma Supply Chain Quality and based in Upper Providence, Pennsylvania.
Previously at GSK, he was Head, Computer Compliance, Head, Process Validation & Product Lifecycle Management, Global Validation Director and Validation Manager in the biopharmaceuticals manufacturing facility in Upper Merion, PA.
He has over twenty years of experience in validation and production operations centered in biotechnology.
He is currently responsible for Central IT system in GSK’s Pharmaceutical Supply Chain. Matt holds a BS degree in Chemical Engineering from North Carolina State University.
Matt has been a member of ISPE since 2000 and is a Past President of the Delaware Valley Chapter of ISPE (International Society for Pharmaceutical Engineering).
He is also a member of several ISPE committees including the Guidance Document Committee, GAMP Americas, Process Validation Implementation Team, and several contributing Task Teams.
Previously at GSK, he was Head, Computer Compliance, Head, Process Validation & Product Lifecycle Management, Global Validation Director and Validation Manager in the biopharmaceuticals manufacturing facility in Upper Merion, PA.
He has over twenty years of experience in validation and production operations centered in biotechnology.
He is currently responsible for Central IT system in GSK’s Pharmaceutical Supply Chain. Matt holds a BS degree in Chemical Engineering from North Carolina State University.
Matt has been a member of ISPE since 2000 and is a Past President of the Delaware Valley Chapter of ISPE (International Society for Pharmaceutical Engineering).
He is also a member of several ISPE committees including the Guidance Document Committee, GAMP Americas, Process Validation Implementation Team, and several contributing Task Teams.