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Process Development Engineer; MAb​/Purification

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: Infotree Global Solutions
Full Time position
Listed on 2026-01-06
Job specializations:
  • Engineering
    Manufacturing Engineer, Process Engineer
  • Manufacturing / Production
    Manufacturing Engineer
Job Description & How to Apply Below
Position: Process Development Engineer (MAb/Purification)

Process Development Engineer (MAb/Purification)

Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our Thousand Oaks facility. The role provides process engineering support for human therapeutic products in clinical development through commercial production, translating developmental processes to commercial reality through scientific expertise and engineering innovation.

Location:

Thousand Oaks, CA – Onsite 3-4 days a week. The Engineer will apply purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in an innovative manufacturing suite using single-use technology. The role partners with manufacturing, quality, analytical, and bench scientists in a highly dynamic manufacturing facility. Standard business hours, with occasional after‑hour support.

Day to Day Responsibilities

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.

Basic Qualifications
  • Master’s degree or Bachelor’s degree with 2 years of relevant experience, or Associate’s degree with 6 years of experience, or High school diploma/GED with 8 years of experience.
  • 2-4 years of experience in drug and animal cells, with strong process knowledge.
Top 3 Must Have Skill Sets
  • Drug substance biologics process development, pilot plant or manufacturing technical support.
  • Purification of monoclonal antibodies.
  • Experience in a GMP environment, preferably in drug substance.
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