Downstream Bioprocess Associate
Job in
Foster City, San Mateo County, California, 94420, USA
Listed on 2026-10-12
Listing for:
The Planet Group
Per diem
position Listed on 2026-10-12
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Chemical Manufacturing, Validation Engineer
Job Description & How to Apply Below
- Work directly with pilot-scale chromatography, TFF, viral filtration, depth filtration, centrifugation, and single-use equipment.
- Build practical skills in scale-up, end-to-end run execution, controlled documentation, troubleshooting, and technology transfer.
- Contribute to multiple early- and late-stage biologics programs in a collaborative, fast-moving environment.
- Gain meaningful continuity through a 12-month contract that runs from your start date.
What You'll Do
- Plan and execute downstream purification runs, including clarification, chromatography, TFF, and viral filtration, in a schedule-driven pilot environment.
- Prepare buffers and reagents; set up, operate, clean, and tear down pilot-scale and single-use equipment.
- Pack and unpack chromatography columns, operate ÄKTA systems, and use UNICORN methods for run execution.
- Document work in SOPs, batch records, run sheets, and summaries; capture observations and deviations clearly.
- Monitor process performance, interpret data, troubleshoot during runs, and communicate findings to cross-functional partners.
- Support process scale-up, comparability activities, technology transfer, lab readiness, and occasional weekend or extended-hour coverage.
What You'll Bring
- Experience with downstream purification operations such as chromatography, TFF, viral filtration, depth filtration, centrifugation, and buffer preparation.
- Experience operating ÄKTA systems and working with UNICORN; chromatography column operation experience is strongly relevant.
- Clear technical communication, documentation, organization, and collaborative problem-solving skills.
- Your broader experience can come from bench, pilot, or manufacturing settings; hands-on pilot-scale work is the one must-have.
Nice to Have
- End-to-end purification process execution rather than experience with only one unit operation.
- Biologics pilot plant, manufacturing support, technology transfer, or GMP-adjacent experience.
- Experience with single-use facilities, controlled documentation, process scale-up, or comparability activities.
- Flexibility to support occasional weekend or extended-hour run coverage.
Education
- AA/AS degree with more than 4 years of relevant industry experience in downstream purification or bioprocessing; or
- BS/BE in chemical or biochemical engineering, biochemistry, biology, or a related discipline with more than 2 years of relevant experience.
Position Requirements
10+ Years
work experience
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