Process Development Engineer; Drug substance, Purification
Listed on 2026-01-06
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Engineering
Manufacturing Engineer, Validation Engineer
Process Development Engineer (Drug Substance, Purification)
Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our Thousand Oaks facility. Providing process engineering support for human therapeutic products in clinical development through commercial production, our mission is to translate developmental processes to commercial reality for patients through scientific expertise and engineering innovation.
Ideal Candidate: 2-4 years of relevant experience working in drug and animal cells. Strong process knowledge. Experience purifying cells (biologics purifications), drug substance GMP manufacturing.
Standard Business Hours - Some After Hour Support
Onsite a minimum of 3 days a week.
Must have biotech background/experience, plus must have purification experience.
Basic Qualifications- Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
- Drug substance biologics process development, pilot plant or manufacturing technical support
- Purification of monoclonal antibodies
- Experience in GMP environment (preferably in drug substance)
- The Engineer will apply cell culture and/or purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using single-use technology. Will partner with manufacturing, quality, analytical, and bench scientists to support a highly dynamic manufacturing facility.
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