Andy Halsey Pe Email & Phone Number | Passionate leader, skilled at building and developing high performing teams to deliver sterile biologic medicines to patients. Subject matter expert in sterility assurance, aseptic processing, visual inspection, single use systems, root cause analysis, risk assessment, compliance, and validation of sterile facilities and operations. Licensed professional engineer with experience designing, building, validating, and operating sterile manufacturing facilities using both isolator and RABS technologies. Success in this business is built on proactive collaborations across organizations and stakeholders, especially between production, quality, and our supply partners. At the end of the supply chain there is a patient counting on us to get this critical part right the first time, every time. Delivery of sterile medicines is a complex endeavor; only with a relentless focus on continuous improvement, regulatory compliance, technology, and our people can we deliver the highest quality products while driving the business forward.

Andy Halsey Pe

Passionate leader, skilled at building and developing high performing teams to deliver sterile biolo...
Philadelphia, Pennsylvania, United States

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Andy Halsey Pe’s Location Philadelphia, Pennsylvania, United States

Andy Halsey Pe’s Current Industry Teva Pharmaceuticals

Andy Halsey Pe’s Prior Industry Gsk | Glaxosmithkline | Merck | Rpa Associates

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Senior Director, Biologics Manufacturing

2021-08-01 00:00:00 - Present

Manager, Pilot Plant Operations & Engineering

2013-11-01 00:00:00 - 2017-01-01 00:00:00

Sterile Manufacturing Supervisor

2011-10-01 00:00:00 - 2013-11-01 00:00:00

Facilities Engineer

2003-06-01 00:00:00 - 2006-10-01 00:00:00

Project Engineer/Manager

1999-06-01 00:00:00 - 2003-06-01 00:00:00

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Andy Halsey Pe is a Passionate leader, skilled at building and developing high performing teams to deliver sterile biologic medicines to patients. Subject matter expert in sterility assurance, aseptic processing, visual inspection, single use systems, root cause analysis, risk assessment, compliance, and validation of sterile facilities and operations. Licensed professional engineer with experience designing, building, validating, and operating sterile manufacturing facilities using both isolator and RABS technologies. Success in this business is built on proactive collaborations across organizations and stakeholders, especially between production, quality, and our supply partners. At the end of the supply chain there is a patient counting on us to get this critical part right the first time, every time. Delivery of sterile medicines is a complex endeavor; only with a relentless focus on continuous improvement, regulatory compliance, technology, and our people can we deliver the highest quality products while driving the business forward.