Process Development Engineer; Downstream and Drug Substance
Listed on 2026-09-03
-
Manufacturing / Production
Validation Engineer, Pharmaceutical Manufacturing -
Engineering
Validation Engineer
Location: Newbury Park
Biotechnology Process Engineer
Primary
Skills:
Cell Purification (advanced), Downstream (advanced), Drug Substance (advanced), Data Analysis (advanced), Technology Transfer (intermediate), Single-Use Technology (intermediate), Protocol Development (intermediate)
Contract Type: W2 Contract Duration: 6+ Months
Location:
Thousand Oaks CA (Onsite a minimum of 3-4 days a week) Pay Range: $40.00 - $43.00 Per Hour
Job Summary:
This role supports the advancement of human therapeutic products from development through commercial manufacturing. You will leverage your process engineering expertise to translate complex biological processes into viable commercial realities. Collaboration with cross-functional teams is essential to ensure the success of innovative manufacturing operations.
Key Responsibilities:
- Monitor and analyze manufacturing processes.
- Support technology transfer activities.
- Investigate and resolve process deviations.
- Draft and review technical documentation.
- Provide on-site manufacturing support.
Must-Have
Skills:
- Biotechnology industry background
- Downstream purification experience
- Excellent communication and collaboration
Domain / Industry
Experience:
Experience with in the biotechnology or pharmaceutical industry, specifically with therapeutic protein manufacturing, is preferred.
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