Associate Scientist - Purification Process Development
$93,600–$93,600 year
On-siteOceanside, California, United States
Job Summary
Design and execute purification process development and characterization studies for biologics in pivotal and commercial stages. Perform laboratory-scale purification experiments, analyze data, and support scale-up and technology transfer at internal and external GMP facilities. Develop protocols, reports, and electronic records while providing technical support for manufacturing investigations. Mentor junior team members on strategies and process transfer, collaborating cross-functionally with Process Development, Manufacturing, Quality, and external partners to maintain compliance and data integrity standards.
Required Qualifications
- MS + 2 years or BS + 4 years of relevant experience in Chemical Engineering, Biochemistry, Bioengineering, or related discipline
- Strong hands-on experience with biologics purification process development
Desired Qualifications
- Chromatography and AKTA/UNICORN
- Tangential Flow Filtration (TFF)
- Normal Flow Filtration (NFF)
- Centrifugation
- High-throughput purification screening
- Virus inactivation/removal
- Process scale-up and GMP technology transfer
- Design of Experiments (DoE), statistics, and data analysis
- JMP and/or Spotfire
- Laboratory automation and data-management tools
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