Maravai LifeSciences

Nucleic acid reagents, mRNA technology, safety testing and CDMO services for biotech and biopharma companies

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Highlights

  • New on EvolcAdded 2026-11-11

Recent signals

What changed at Maravai LifeSciences in the last 6 months, newest first. Each line links to its public source.

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About Maravai LifeSciences

Maravai LifeSciences is a Nasdaq-listed (MRVI) group of life science brands that supplies products and services for the development of vaccines, therapeutics and diagnostics. Its brands include TriLink BioTechnologies, Glen Research, Cygnus Technologies and Alphazyme. Offerings include CleanCap mRNA capping technology, oligonucleotide materials for DNA and RNA synthesis, impurity detection assays and biologics safety testing, and contract development and manufacturing (CDMO) services.

Customers are biotech, biopharma and life science companies, contract development and manufacturing organizations, and academic and commercial research professionals. The company sells products and services to these customers.

The group describes itself as having over 35 years of history in nucleotide research. It has offices in San Diego, California and Leland, North Carolina. TriLink opened a GMP enzyme manufacturing facility. Current open roles include manufacturing associates, process development, finance, legal and sales leadership.

Product: Nucleic acid products and mRNA capping technology (CleanCap), oligonucleotide materials, impurity detection assays, and CDMO manufacturing and testing services.

Jobs at Maravai LifeSciences

No open positions in Europe right now.

Open roles at Maravai LifeSciences in the Americas (2)

United States 2. From Maravai LifeSciences's careers page or applicant tracking system; each role links to the employer.

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Website technologies

Tools and platforms detected on this company’s website, grouped by purpose. Dates record when Evolc observed them.

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Frontend frameworks

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Recruiting

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Website detection does not establish a paid subscription or company-wide use. Tools loaded after consent or sign-in may be missed. “No longer observed” does not prove the company stopped using a tool.