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We Are Attending Meeting on the Mesa 2025

Meet with BIOVECTRA in Phoenix
October 6-8

BIOVECTRA’s state-of-the-art Biomanufacturing and Vaccine Center has the:

  • Capability to develop and manufacture plasmid DNA, mRNA, LNP formulations and fill finish
  • With scales ranging from mL to 30L, we have the ability to produce up to 160 million doses of mRNA vaccines per year
  • Capacity to prepare and package 70 million fill/finish doses per year for commercial distribution

BIOVECTRA is a North American CDMO specializing in the clinical-to-commercial scale production of high-quality regulated APIs and intermediates, including:

  • Fermentation & Biologics
  • Small Molecule Synthesis
  • Peptide & Small Molecule Purification
  • pDNA, mRNA & LNP 
  • Highly Potent APIs
  • Bioreagents
  • Fill/Finish

Our team – backed by 50+ years of experience – looks forward to the opportunity to put our flexible, innovative manufacturing solutions at your disposal.

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Meet With Us

Schedule a meeting with us and discover how we can support your projects and solve your most complex challenges.

SEO plus – Test

  • 20+ years at GSK, leading R&D activities on multiple vaccine programs
  • Recently held positions in industry include: Senior Director (Function Head), Protein Biochemistry; Director, Antigen Design & Prototype Production; and, Associate Director, Antigen Design and Protein Characterization.
  • Key areas of expertise are:
    • Process development of protein Biologics/Recombinant Antigens
    • Recombinant protein expression (mammalian, insect, yeast, bacterial)
    • Production/design of Viral Vectors, mRNA vaccines, Bacterial outer membrane vesicles
    • Protein Engineering and Structural Biology
    • Defining quality attributes, biophysical characterization of proteins, and analytical strategy
  • Post graduate degrees in Functional Genomics (Université Laval) and Bioinformatics (MIT); M. Sc. Microbiology and Immunology (Laval).
  • 25+ Patent & 5 Scientific Publications