Matt Barrows, Mba Email and Phone Number
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20+ years of Senior Leadership in cell and gene therapy, upstream and downstream operations, automation engineering, process improvements, regulatory compliance audits, and consent decree remediation. Biotechnology senior leader for preclinical & cGMP Bioprocess Clinical and Commercial manufacturing sites and engineering plant operations. Contributes to QMS and achieves quality and production, while taking people performance to new heights in complex cross-functional transformations. As Operations lead, designs new site programs and teams from scratch. And as GM, enhances engagement from teams, retains and grows talent, reduces risk exposure—and ultimately achieves loyalty, quality production, and operational excellence. • 1-year Expat Assignment as Automation Lead - Startup of Genzyme’s facility in Belgium. • 6-month dedicated assignment to complete Organization Redesign at Genzyme’s 750-person Allston Landing Facility. • Directed 3-year Consent Decree Remediation for Biologics Drug Substance MFG Quality Systems.• Facility Startup Leadership in both Clinical and Commercial Manufacturing—in the US and abroad. • Lead for Personalized Cancer Vaccines startup at Moderna’s innovative site in Norwood, Mass., US. • Head of Operational Readiness for expansion into second manufacturing site by Alexion Pharmaceuticals.• Initiate Lean Value-stream mapping initiative – implementing material and information-flow mapping & new SOPs. • Oversee design and build phases; and run and maintain operations. • Diverse background in Quality System remediation.
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Senior Vice President Quality And Tech OpsAviceda TherapeuticsDuxbury, Ma, Us
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ConsultantBarrows Consulting Group Nov 2024 - PresentConsulting services for Biotech and Pharmaceutical companies. Specializing in CMC, Manufacturing, Tech Transfer, Operational Excellence -
Chief Quality & Technical Operations OfficerTome Biosciences Jul 2022 - Nov 2024
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Executive Director - Commercial ManufacturingModerna Jan 2022 - Jun 2022Cambridge, Massachusetts, Us -
Senior Director Manufacturing - Clinical And Personalized CancerModerna Apr 2020 - Feb 2022Cambridge, Massachusetts, UsResponsible for Large Scale Clinical and Personalized Cancer Vaccine manufacturing at Moderna's Norwood, MA facility. Including production of Moderna's coronavirus vaccine candidate
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Director - Personalized Cancer Vaccine ManufacturingModerna Jul 2017 - Apr 2020Cambridge, Massachusetts, UsLeading Manufacturing team for 1st COVID-19 (corona virus) Vaccine as of early February 2020. Led the design and rapid startup of Moderna’s PVC operation at its innovative drug manufacturing facility in Norwood. As OPEX Lead, designed and led rollout of Operational Excellence program. Hired and trained staff which delivered against the Clinical Demand Plan (CDP), and which achieved operational excellence for the site shortly after beating a tough disposition timeline. • Oversee design and build phases & run and maintain operations with a team of 30 quality and operations staff. Hired and trained all management and staff. • Established operational excellence team: hiring and onboarding talent, setting targets, and developing KPIs. • Built portfolio of Continuous Performance Improvement projects (CPI) & master Continuous Improvement Plan (CIP). • Initiate Lean Value-stream mapping initiative – implementing material and information-flow mapping & new SOPs. • Analyzed and revamped operational quality systems into alignment with cGMP guidelines and best-in-class ideals. • Liaise with Digital Group on automation initiatives, Agile software development, & platform design/changes.
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Head - Commercial Cell Culture OperationsAlexion Pharmaceuticals, Inc. Dec 2014 - Jun 2017Boston, Massachusetts, UsHead of Operational Readiness - Smithfield, RI March 2017 – July 2017Head of Alexion’s Operational Readiness Program for a major capital project with new capacity buildouts. Built and oversaw a cross-functional team that was responsible for the on-time delivery of Alexions’s $100MM expansion (into new Smithfield site). • Scope: Manufacturing, Clean Utilities, Warehouse & Distribution, Validation post-commissioning & qualification. • Collaborated with and provided executive leadership to Construction Project and Operational Project direct reports.Associate Director Commercial Upstream Operations Dec 2014 – March 2017Headed Alexion’s Commercial Cell Culture and Media Preparation Manufacturing teams in Smithfield, RI. Responsible for oversight of a 24X7 manufacturing process providing Soliris for patients with atypical hemolytic uremic syndrome and paroxysmal nocturnal hemoglobinuria—both ultra-rare diseases. Focusing on leadership coaching, team building, and continuous improvement—directed a Lean transformation with leadership, coaching, and team building cynosures.• Optimized and ran a portfolio of 30 process improvement projects. • Manufacturing Lead for capital expansion project.• Member of the Site Safety Leadership Team for new buildout. -
Associate DirectorGenzyme Mar 2007 - Dec 2014Paris, France, FrAssociate Director Bulk Manufacturing Consent Decree March 2011 – Dec 2014Head of Bulk Manufacturing Consent Decree remediation teams. Full accountability for implementing the consent decree (CD) workplan for the Allston Landing Bulk Manufacturing organization. Successful zero-issue remediation of: production controls, batch records and SOP remediation, contamination control, bioburden monitoring, hygiene & gowning, and sterilization and depyrogenation controls.Managed a team of Senior Managers, Manufacturing Specialists and Quality Engineers.Managed US FDA inter-facing & third-party consulting firm engaged onsite as the eyes-and-ears of the agency.6-month assignment as 1 of 3 leaders ‘taken off their day’ job to run a full organizational overhaul for Genzyme’s Allston Landing 500-person facility—guiding the site’s collaborative journey from one product to three, and back to one again; while realigning the business along its Value Streams. • Applied Lean principles & ‘Systems Thinking’ to achieve Upstream and Downstream operational excellence for a rare disease product. • Managed team of 4 Senior Managers, 10 Manufacturing Specialists, and 2 Quality Engineers. • Prepared and delivered mission-critical presentations to senior leadership and to Third-Party Quality oversight teams. • Successfully completed CD while re-establishing Production Controls Quality System -
Senior Manufacturing Manager - Downstream OperationsGenzyme 2007 - May 2011Paris, France, FrManage a team of supervisors, MFG specialists and 20+ operators across 2 shifts 7 days a week overseeing the protein purification of Myozyme, Cerezyme and Fabrazyme. Responsibilities include adherence to a demanding global production schedule, hiring and training manufacturing staff, deviation resolution and managing CAPA. Work directly with Materials and Scheduling groups to ensure on-time shipment of Cerezyme for filling and packaging. • Worked directly with the Global Operation Excellence Group implementing Lean concepts to the manufacturing floor.• Represented Protein Purification for multiple regulatory audits including FDA and European Medicines Agency (EMA). • Responded to inquiries from regulatory agencies; developed and implemented responses to audit observations.
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Manager - Automation EngineeringGenzyme 2005 - 2007Paris, France, FrSupervise Process Engineers in the Automation Engineering department at Allston Landing. Duties include, managing and scheduling process improvements project work while maintaining around the clock automation support for RS3, Delta V DCS and PLC systems for Cell Culture, Protein Purification and Support Services• Kept team cool and calm, and ran interference when undue pressures hit. • Maintained around-the-clock automation support for Delta V and PLC systems for Cell Culture, Protein Purification, and Support Services. • Functional role—Manager, Automation Engineering: Supervised 6 Process Engineers.
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Process Engineer Ii Belgium – Expat AssignmentGenzyme Oct 2004 - Oct 2005Paris, France, FrAutomation Engineering Manager—Managed the development of Automation Software for Genzyme Belgium plant • Coordinated transdisciplinary effort in Genzyme US; Genzyme Flanders; and Engineering firms in the U.S. and Ireland. • Developed functional requirements specifications; and process model diagrams; and mapping of the brand-new facility. • Engaged US & Flanders staff in achieving aggressive KPI metric targets. • Learned Automation at rapid-fire speed. | Obtained crash-course in PMP project management.
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Process Engineer - Automation EngineeringGenzyme 2001 - 2005Paris, France, FrExecuted validation protocols & managed Automation Specification documentation for Automation Engineering. Performed and led the validation effort, executing OQ protocols for newly developed automation software for Geel expansion. Partnered with Jacobs Engineering and Genzyme Belgium for Functional Requirements. Delta V and PLC software developmebt
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Manufacturing Associate - Protein PurificationGenzyme Jun 1999 - 2001Paris, France, FrPerformed multi-stage, large-scale column chromatography & microfiltration operations according to cGMP Guidelines.
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Manufacturing AssociateCollagenesis 1998 - 1999
Matt Barrows, Mba Skills
Matt Barrows, Mba Education Details
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D'Amore-Mckim School Of Business At Northeastern UniversityMaster Of Business Administration - Mba -
Worcester Polytechnic InstituteBiotechnology
Frequently Asked Questions about Matt Barrows, Mba
What company does Matt Barrows, Mba work for?
Matt Barrows, Mba works for Aviceda Therapeutics
What is Matt Barrows, Mba's role at the current company?
Matt Barrows, Mba's current role is Senior Vice President Quality and Tech Ops.
What is Matt Barrows, Mba's email address?
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What is Matt Barrows, Mba's direct phone number?
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What schools did Matt Barrows, Mba attend?
Matt Barrows, Mba attended D'amore-Mckim School Of Business At Northeastern University, Worcester Polytechnic Institute.
What skills is Matt Barrows, Mba known for?
Matt Barrows, Mba has skills like Capa, Gmp, Biotechnology, Purification, Protein Purification, Fda, Biopharmaceuticals, Manufacturing, Sop, Cell Culture, Quality System, 21 Cfr Part 11.
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