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Process Development Engineer

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: ACL Digital
Part Time position
Listed on 2026-01-11
Job specializations:
  • Engineering
    Process Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 40 - 42 USD Hourly USD 40.00 42.00 HOUR
Job Description & How to Apply Below

Process Development Engineer – Drug Substance Technology Engineering

Location:

Thousand Oaks, CA.

Base pay range: $40.00/hr - $42.00/hr.

We are seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at our Thousand Oaks facility. The engineer will provide process engineering support for human therapeutic products from clinical development through commercial production, translating developmental processes to commercial reality for patients through scientific expertise and engineering innovation. The role will apply purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing using single‑use technology, partnering with manufacturing, quality, analytical, and bench scientists in a highly dynamic manufacturing environment.

Onsite presence is required for a minimum of 3 days per week.

  • Provide process engineering support for human therapeutic products from clinical development through commercial production.
  • Apply purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing.
  • Partner with manufacturing, quality, analytical, and bench scientists in a dynamic manufacturing environment.
  • Maintain onsite presence minimum 3 days per week.

Ideal Candidate: 2‑4 years of relevant experience in drug and animal cell processes; strong process knowledge; experience purifying cells (biologics purifications) and drug substance GMP manufacturing. Previous client or biotech experience is a plus. Must have biotech background/experience plus purification experience.

  • 2-4 years of relevant experience in drug and animal cell processes.
  • Strong process knowledge and experience purifying cells (biologics purifications).
  • Experience with drug substance GMP manufacturing.
  • Biotech background/experience essential; purification experience also required.
  • Previous client or biotech experience is a plus.

All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, disability or any other protected status.

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