Karius

life science

ReagentManufacturingAssociateI

Redwood City, California, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Reagent Manufacturing Associate I at Karius. Skills: reagent manufacturing, quality testing, documentation, process improvement. Support the production of critical reagents. manufacturing and qualifying reagents”

What You'll Achieve.

elevating patient care through microbial insights; advancing diagnostic science and technology to optimize the diagnosis and treatment of infectious diseases; improve the diagnostic landscape for infectious diseases; make rapid treatment decisions; support the production of critical reagents; conquer infectious diseases through innovations around genomic sequencing and machine learning; delivering unprecedented insights into the microbial landscape; providing clinicians with a comprehensive test capable of identifying more than a thousand pathogens directly from blood; helping industry accelerate the development of therapeutic solutions; deliver better care to many otherwise ineffectively treated patients; see how directly your work has a life-changing impact on people, and at scale

Industry & Context.

life science
Problems you'll solve

problem-solving skills

Eligibility Requirements

100% onsite, Subject to extended periods of sitting and/or standing, vision to monitor and moderate noise levels, Work is generally performed in an office, lab or clinical environment

What They're Looking For.

Must Have

0–2 years of relevant laboratory, reagent manufacturing, life sciences production, or regulated manufacturing experience, attention to detail, willingness to follow established procedures, commitment to accurate documentation and record-keeping

Nice to Have

Bachelor's degree in Biology, Molecular Biology, Genetics, Chemistry, Biochemistry, or a related field, Basic hands-on molecular biology experience, Exposure to NGS workflows, reagent manufacturing, or regulated environments such as ISO 13485, 21 CFR Part 820, cGMP, and/or GDP

What You'll Do.

Support the production of critical reagents

manufacturing and qualifying reagents

supporting RUO and IVD product workflows

performing quality testing

maintaining accurate documentation

support equipment readiness

validation activities

continuous process improvement

Support equipment qualification activities

preventive maintenance

basic troubleshooting

Assist with planning and execution of validation activities

reagent stability studies

shelf-life extension testing

Perform reagent manufacturing activities

and reconcile raw materials

verify material identity and quality

perform manual or semi-automated operations

Perform in-process and lot-release QC testing

support data analysis

review results for accuracy and completeness

Follow SOPs and work instructions

maintain organized manufacturing records

assist with drafting or revising SOPs

and material specifications

assist in identifying

and supporting resolution of nonconformance events

and related root cause investigations

How You'll Work.

Team & Collaboration

work closely with scientific and operational teams; Ability to work collaboratively with team members

Communication Scope

communication (verbal and written) skills

Process & Methodology

planning and execution of validation activities

Full Job Description

## Description About Karius Karius is a life science, venture-backed clinical metagenomics company, focused on elevating patient care through microbial insights. We are committed to advancing diagnostic science and technology to optimize the diagnosis and treatment of infectious diseases. Through the use of genomics and AI, we are driven to improve the diagnostic landscape for infectious diseases. Karius delivers unprecedented diagnostic insight detecting microbial cell-free DNA circulating in the body to assist physicians to make rapid treatment decisions. Position Summary: As a Reagent Manufacturing Associate I, you will support the production of critical reagents used in Karius’ NGS-based infectious disease diagnostic assays. This role is hands-on and process-focused, with responsibility for manufacturing and qualifying reagents, supporting RUO and IVD product workflows, performing quality testing, and maintaining accurate documentation in an ISO 13485-compliant environment. You will work closely with scientific and operational teams to support equipment readiness, material management, troubleshooting, validation activities, and continuous process improvement. The ideal candidate is detail-oriented, reliable, and comfortable working with chemical and biological materials in a fast-paced manufacturing setting where quality, consistency, and patient impact are central to the work. Why Should You Join Us? Karius aims to conquer infectious diseases through innovations around genomic sequencing and machine learning. The company’s platform is already delivering unprecedented insights into the microbial landscape, providing clinicians with a comprehensive test capable of identifying more than a thousand pathogens directly from blood, and helping industry accelerate the development of therapeutic solutions. The products Karius offers today are some of the most advanced solutions available to physicians who aim to deliver better care to many otherwise ineffectively treate

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