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Andrew Finnerty

QA Technical Specialist at Avectas

Andrew Finnerty has a decade of experience in the pharmaceutical and biologics industry. Andrew began their career in 2012 as a Quality Engineer at Corin Medical Ltd. Andrew then moved to LEO Pharma A/S as a Quality Coordinator. In 2013, they joined DePuy Orthopaedics as a Technology Transfer Engineer, where they produced and maintained appropriate and comprehensive quality process specifications. In 2014, they began working at GSK as a GMP Specialist, developing and maintaining GMP training manuals. In 2016, they worked at Zenith Technologies, Ringaskiddy, Cork as a Quality Engineer, where they provided Quality review/approval of executed validation documentation. Andrew then moved to Phillips-Medisize as a Design Assurance Engineer. In 2017, they became a Senior Quality Engineer at MGS Mfg. Group. In 2020, they joined Avectas as a QA Technical Specialist. Most recently, in 2021, they began working at MSD Dunboyne Biologics as a Digital and Data Quality Specialist, providing independent quality review and approval of system lifecycle documentation.

Andrew Finnerty obtained a BA in Business Studies with Honours from the University of the West of England between 1997 and 2000. Andrew also obtained a Postgraduate Diploma in Manufacturing and Management Information Systems from the same university during the same time period.

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Avectas

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Avectas is a cell engineering business focused on improving the cost, manufacturing, and patient outcomes for the next generation of cellular therapies. Avectas is developing a unique delivery technology platform, Solupore®, to enable the ex-vivo manufacture of gene-modified cell therapy products, with partners.


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Headquarters

Kildare, Ireland

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11-50

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