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Salary
≈ $57k – $116k per year (Estimated)
Location
In office (Durham)
Seniority
Middle · 2+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 25, 2026. First seen by Alion on Sep 14, 2026. KBI Biopharma scores B on the Alion truth index.

Overview
Company
Impact
Profile match
KBI Biopharma is a contract development and manufacturing organization for biologics, providing mammalian and microbial cell line development, process, analytical and formulation development, and clinical and commercial manufacturing, headquartered in Durham, North Carolina. Founded in 1996, it is a subsidiary of the Japanese materials group JSR and runs sites in Durham, Boulder and Louisville in Colorado and Plan-les-Ouates near Geneva in Switzerland, with platforms such as SUREtechnology. It hires manufacturing and process development associates, scientists, QA and validation specialists, SAP and quality systems analysts, schedulers and facilities and EHS staff.

Position Summary

Responsible for supporting process development activities for downstream production processes, instruments and equipment.

Position Responsibilities

  • Support all downstream process development activities including execution of experiments, compilation and analysis of data and drafting of technical documents.
  • Assist in the evaluation, development and implementation of new downstream technologies leading to process improvements and efficiency of operation.
  • Assist with development of preliminary schedules along with material/personnel/equipment requirements to allow accurate and appropriate performance guarantees
  • Equipment troubleshooting and maintenance
  • General lab organization

Minimum Requirements

  • B.S. degree in biotechnology or related (or equivalent training) with 0-4 years experience or a M.S. degree with 0-2 years experience.
  • Research Associate II requires a B.S. degree and 2+ years experience or a M.S. degree.
  • Experience with downstream process development and chromatography equipment required. Excellent written and communication skills for customer service and ability to meet strict client deadlines. Flexibility of hours to support downstream processes. Knowledge of GMPs and biotechnology-derived product regulations preferred.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

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