Our client, a world
leader in life sciences and biotechnology, is looking for an “Associate
Scientist - Downstream Bioprocess” based in Foster City, CA.
Job Duration: Long
Term Contract (Possibility of Extension)
Pay Rate : $54.50/hr on
W2
Company Benefits: Medical, Paid Sick
leave, 401K
The ideal candidate will have practical experience executing downstream purification processes in a pilot, manufacturing, or process development environment and be comfortable operating chromatography and filtration equipment while working within controlled documentation and schedule-driven workflows.
Key Responsibilities
- Plan and execute pilot-scale downstream purification runs, including clarification, chromatography, TFF, viral filtration, depth filtration, and centrifugation.
- Prepare buffers and reagents and perform equipment setup, operation, cleaning, and teardown.
- Operate ÄKTA chromatography systems and UNICORN software for process execution and data collection.
- Pack and unpack chromatography columns and support chromatography process activities.
- Operate single-use equipment and filtration systems in a pilot-scale environment.
- Monitor process performance, analyze run data, identify process issues, and troubleshoot deviations in real time.
- Accurately document activities in SOPs, batch records, run sheets, and technical summaries.
- Communicate observations, process results, and troubleshooting findings to cross-functional teams.
- Support process scale-up, comparability studies, technology transfer, and laboratory readiness activities.
- Follow applicable safety, quality, and controlled-documentation procedures.
- Support occasional weekend or extended-hour coverage based on process schedules.
Required Qualifications
Preferred Qualifications
- End-to-end downstream purification experience rather than experience limited to a single unit operation.
- Biologics pilot plant or manufacturing experience.
- Experience supporting process development, scale-up, technology transfer, or comparability activities.
- Experience with single-use technologies and equipment.
- GMP/cGMP or GMP-adjacent experience.
- Experience with controlled documentation, batch records, SOPs, and deviation reporting
If interested, please
send us your updated resume at
hr@dawarconsulting.com
/
kavitha@dawarconsulting.com
akansha@dawarconsulting.com