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KBI Biopharma

CDMO delivering cell line development

Engineer 1/2

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeBoulder, CO, USAIn-person

About the Job

Requirements

  • Engineer I requires a Bachelor of Science in Engineering or a related field.
  • Engineer II requires a Master of Science in Engineering or a related field, or a Bachelor of Science with 3+ years of relevant experience.
  • Knowledge of biotech unit operations and the ability to apply engineering skills to solve problems of moderate scope.
  • Strong technical writing and communication skills.
  • Ability to determine when additional technical resources are required.

Responsibilities

  • Provide engineering support during process development and technology transfer by evaluating and influencing process implementation strategies.
  • Monitor process performance in manufacturing and lead process troubleshooting efforts.
  • Author technical documents, including product impact assessments, product campaign summaries, and/or continued process verification reports.
  • Work under general guidance from a supervisor to resolve technical problems of moderate scope and complexity; plan and conduct own work; seek technical guidance for unusual or complex problems; and submit proposed project plans for supervisor approval.
  • Set priorities and lead initiatives and/or projects within the function.
  • Represent process development in providing technical solutions for specific projects.
  • Apply engineering skills to process engineering projects supporting process development, process transfer, and clinical/commercial manufacturing.

About the Company

KBI Biopharma

CDMO delivering cell line development

KBI Biopharma is a CDMO that accelerates the development of biological medicines by providing rapid cell line generation and process development for preclinical programs. It uses established mammalian and microbial expression systems (such as CHO K1, CHO S, CHO DG44, HEK293, and DXB11 E. coli) to create production cell lines and develop integrated manufacturing processes. Compared with competitors, it wins on speed, end-to-end capability, and flexibility across multiple platforms to move projects quickly from discovery to preclinical milestones for a diverse client base. Its goal is to reduce risk, shorten development timelines, and expand global access to life-saving biologic therapies.

Company size
1,001-5,000
Company stage
Late Stage VC
Total funding
$109.5M
Headquarters
Durham, NC
Founded
1996

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