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Learn More About BIOVECTRA!

BIOVECTRA is a North American CDMO specializing in clinical-to-commercial scale production capabilities for biologics, synthetic small molecules, nucleic acids like pDNA and mRNA, highly potent APIs, bioreagents

Our teams, backed by 50+ years of experience and a proven track record of excellence, optimize, adapt, and perfect innovative technologies and drug substance development approaches to deliver world-class solutions for pharmaceutical manufacturing.

BIOVECTRA is a 2025 Biologics CDMO Leadership Award winner!

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Fermentation & Biologics

Leveraging decades of experience, we excel in microbial fermentation and biopharmaceutical manufacturing, developing new processes and optimizing existing ones to facilitate novel therapeutics.

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Small Molecule Synthesis

Our team offers robust solutions for synthetic small molecule projects, providing phase-appropriate support from IND applications through clinical trials to commercial supply.

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Peptide & Small Molecule Purification

We provide advanced purification techniques for peptides and small molecules, ensuring high-quality, scalable solutions tailored to your project's specifications.

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pDNA, mRNA,
& LNP

Leveraging our lipid and fermentation expertise, we offer integrated manufacturing services for nucleic acid-based therapeutics, including mRNA, plasmid DNA (pDNA), and lipid nanoparticle (LNP) formulations, supporting clients from biotech start-ups to blue-chip pharmaceutical companies.

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HPAPIs

With extensive experience in HPAPI process development and production for both small and large molecules, we are equipped to advance your project safely and efficiently, providing full support throughout the product life cycle.

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Bioreagents

BIOVECTRA offers a selection of high-quality bioprocessing reagents, available in various sizes from research quantities to multi-kilogram scale for manufacturing operations. Several of our bioprocessing reagents are available in cGMP grade, supporting your cGMP manufacturing operations.

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Fill/Finish

Our state-of-the-art sterile fill/finish facility caters to clients with high-value products, offering flexible approaches and fast turnaround times for a range of drug modalities, including recombinant proteins, peptides, nucleotides, gene therapies, and vaccines.

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How Can We Help?

We are committed to collaborating with you to advance your therapeutic projects. Please fill out the form below, and our team will reach out to discuss how we can support your specific needs.

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