Matthew Tyson

Matthew Tyson Email and Phone Number

Associate Director at Novartis Gene Therapies @ Novartis Gene Therapies
Basel, Baselstadt
Matthew Tyson's Location
Raleigh, North Carolina, United States, United States
Matthew Tyson's Contact Details

Matthew Tyson personal email

n/a
About Matthew Tyson

Biopharmaceutical professional with a strong background in downstream process development; with experience from pre-clinical, Phase I/II development and commercial process redevelopment.

Matthew Tyson's Current Company Details
Novartis Gene Therapies

Novartis Gene Therapies

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Associate Director at Novartis Gene Therapies
Basel, Baselstadt
Website:
novartis.com
Employees:
5
Company phone:
+41 61 324 11 11
Company email:
eric.althoff@novartis.com
Matthew Tyson Work Experience Details
  • Novartis Gene Therapies
    Associate Director, Drug Substance Product Leads
    Novartis Gene Therapies May 2022 - Present
    Basel, Baselstadt, Ch
  • Novartis Gene Therapies
    Senior Manager
    Novartis Gene Therapies Jan 2021 - May 2022
    Basel, Baselstadt, Ch
  • Novartis Gene Therapies
    Manager
    Novartis Gene Therapies May 2019 - Jan 2021
    Basel, Baselstadt, Ch
  • The Duke Human Vaccine Institute
    Downstream Lead
    The Duke Human Vaccine Institute Mar 2018 - May 2019
    Durham, North Carolina, Us
  • The Duke Human Vaccine Institute
    Scientist -Downstream
    The Duke Human Vaccine Institute Apr 2016 - Mar 2018
    Durham, North Carolina, Us
  • Gsk
    Scientific Associate Ii
    Gsk Mar 2015 - Apr 2016
    Brentford, Middlesex, Gb
    Downstream technical lead for recombinant subunit vaccine candidate produced in CHO. Responsible for planning and execution of experimentation to support downstream development activities, providing downstream support to stakeholders (upstream, analytical, formulation), aligning with other functional leads and project manager to ensure project timelines are met, and ensuring QbD principals were implemented in purification development activities. Acted as TD-DS viral clearance SME, this included authoring a strategic QbD Best Practice document that guides the process of ensuring viral safety of vaccine products, with a focus on viral clearance. Also acted in a support role for RNA vaccine candidate downstream development scale up and consistency runs.
  • Novartis Vaccines And Diagnostics
    Scientific Associate Ii
    Novartis Vaccines And Diagnostics May 2013 - Mar 2015
    Basel, Baselstadt, Ch
    As a member of the TD-Drug Substance team, developed and optimized purification processes for multiple vaccine candidates produced in CHO and MDCK cell culture, including recombinant secreted protein and split-subunit vaccine. This includes capture and intermediate chromatography resin screening (IEX, HIC, mix-mode, affinity) and development. Worked extensively with UNICORN™ software and ÄKTA purification systems. Performed and optimized tangential flow and normal flow unit operations. Performed process scale up and characterization activities, as well as tech transfer support. Acted as viral clearance SME for downstream group, including executing viral spiking studies at CRO’s, validating viral clearance scaled down models, evaluation of novel viral clearance technologies, and ensuring viral clearance claims align with regulatory considerations. Performed basic analytical techniques: SDS-PAGE, Western Blot, total protein assays, and spectrophotometry; and evaluated RP-HPLC, SEC-HPLC, qPCR, ELISA to support key downstream decisions. Performed all scientific operations/documentation in GDP compliant format and presented on scientific findings to forums of various sizes. Coordinated efforts between development units to ensure that individual efforts aligned with project timelines and goals.
  • Novartis Vaccines And Diagnostics
    Development Engineer I
    Novartis Vaccines And Diagnostics Aug 2012 - May 2013
    Basel, Baselstadt, Ch
    As a member of the TD-Drug Substance team, developed and optimized purification processes for a recombinant glycoprotein vaccine candidate produced in CHO cells. Screened and characterized multiple resins for both capture and polishing column chromatography steps; these resins include cation exchange, anion exchange, hydrophobic interaction, and mix-mode interaction resins. Led optimization efforts for the column chromatography polishing step; with the following key attributes driving optimization: purity, step yield, process efficiency, and product stability. Worked extensively with UNICORN™ software and ÄKTA purification systems. Performed and optimized ultrafiltration/diafiltration unit operations and performed basic analytical techniques: SDS-PAGE, Western Blot, and spectrophotometry to evaluate key process parameters. Performed all scientific operations/documentation in GMP compliant format and presented on scientific findings to forums of various sizes. Coordinated efforts between development units to ensure that individual efforts aligned with project timelines and goals.
  • Pfizer
    Manufacturing Science & Technology Intern
    Pfizer May 2011 - Aug 2011
    New York, New York, Us
    Worked with the purification team to develop purification processes for a recombinant carrier protein produced in bacteria. The main focus was on characterization of the ion exchange column chromatography step and the impurity profile of the column eluate. Worked extensively with UNICORN™ software and the Akta Pilot/Explorer purification systems. Also performed the following unit operations: centrifugation, depth filtration, ultrafiltration, diafiltration, and sterile filtration. Presented scientific findings to internal group meetings and larger departmental meetings.
  • Targacept, Inc.
    Molecular Design Intern
    Targacept, Inc. May 2010 - Aug 2010
    Winston-Salem, Nc, Us
    Worked with the Molecular Design team to create quantitative structure-activity relationship(QSAR) models to be used to screen small molecule libraries. These QSAR models have predictive power in determining possible biological indication a compound at the organism level, as well as that compound’s possible mechanism of action at the molecular level. Presented scientific findings to internal group meetings and larger departmental meetings.

Matthew Tyson Skills

Sds Page Protein Purification Molecular Biology Pcr Cell Culture Recombinant Dna Technology Biopharmaceuticals Column Chromatography Ultrafiltration Centrifugation Rna Isolation Rnai Western Blotting Gel Electrophoresis Diafiltration Vaccines Quality By Design Viral Clearance Membrane Separations Normal Flow Filtration Tangential Flow Filtration Ultracentrifugation Virus Purification

Matthew Tyson Education Details

  • North Carolina State University
    North Carolina State University
    Microbial Biotechnology
  • North Carolina State University
    North Carolina State University
    Zoology

Frequently Asked Questions about Matthew Tyson

What company does Matthew Tyson work for?

Matthew Tyson works for Novartis Gene Therapies

What is Matthew Tyson's role at the current company?

Matthew Tyson's current role is Associate Director at Novartis Gene Therapies.

What is Matthew Tyson's email address?

Matthew Tyson's email address is ma****@****csu.edu

What schools did Matthew Tyson attend?

Matthew Tyson attended North Carolina State University, North Carolina State University.

What skills is Matthew Tyson known for?

Matthew Tyson has skills like Sds Page, Protein Purification, Molecular Biology, Pcr, Cell Culture, Recombinant Dna Technology, Biopharmaceuticals, Column Chromatography, Ultrafiltration, Centrifugation, Rna Isolation, Rnai.

Who are Matthew Tyson's colleagues?

Matthew Tyson's colleagues are Ibneet Kaur, Jessica Massone, Mark Hopkins, María José Vargas Castro, David Ives, Gustavo Zagonel Silva, Aaron Xiong.

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