Matthew Maxwell Email & Phone Number | 21 years of experience in Biopharma manufacturing of large molecules and vaccines across Quality Control and Technical Services, supporting sterile fill finish operations and aseptic manufacturing. 7 years of experience building and leading effective technical teams to support new product introduction, validation activities, continuous process verification, MDCP regulations, continuous improvement, regulatory submissions and audit support I lead a team of scientists who provide technical and validation support to a high-volume, multi-product sterile fill finish manufacturing unit. My role is focused on leadership across aseptic vaccines formulation, syringe filling and automated visual inspection processes. I am responsible for ensuring that the aseptic adjuvant manufacturing process is performing as intended and that technical issues are resolved to support manufacture and timely batch disposition. Other responsibilities include process robustness, implementing cost reduction projects, supporting technology transfers, leading validation programs, and ensuring commercial supply through right first time initiatives.

Matthew Maxwell

21 years of experience in Biopharma manufacturing of large molecules and vaccines across Quality Con...
Greater Dublin, Greater Dublin, Ireland

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Matthew Maxwell’s Phone Numbers +353 45 447****

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Matthew Maxwell’s Location Greater Dublin, Greater Dublin, Ireland

Matthew Maxwell’s Current Industry Bristol Myers Squibb

Matthew Maxwell’s Prior Industry Pfizer | Baxter International

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Associate Director Of Manufacturing Science & Technology

2024-04-01 00:00:00 - Present

Technical Services Senior Manager

2016-03-01 00:00:00 - 2024-03-01 00:00:00

Biotechnology Scientist

2002-09-01 00:00:00 - 2004-04-01 00:00:00

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Matthew Maxwell is a 21 years of experience in Biopharma manufacturing of large molecules and vaccines across Quality Control and Technical Services, supporting sterile fill finish operations and aseptic manufacturing. 7 years of experience building and leading effective technical teams to support new product introduction, validation activities, continuous process verification, MDCP regulations, continuous improvement, regulatory submissions and audit support I lead a team of scientists who provide technical and validation support to a high-volume, multi-product sterile fill finish manufacturing unit. My role is focused on leadership across aseptic vaccines formulation, syringe filling and automated visual inspection processes. I am responsible for ensuring that the aseptic adjuvant manufacturing process is performing as intended and that technical issues are resolved to support manufacture and timely batch disposition. Other responsibilities include process robustness, implementing cost reduction projects, supporting technology transfers, leading validation programs, and ensuring commercial supply through right first time initiatives.