Engineer, Process Development hybrid (JP13072)
Company: 3 Key Consulting
Location: Thousand Oaks
Posted on: April 2, 2026
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Job Description:
Job Title: Engineer, Process Development hybrid (JP13072)
Location: Thousand Oaks, CA. 91320 (hybrid) Business Unit: Drug
Substance Technology and Engineering Employment Type: Contract
Duration: 1 year(s) with likely extensions and/or conversion to
permanent. Rate : $38 - $42/hour W2 Posting Date: 8/6/2024. Notes:
Only qualified candidates need apply. Onsite 3-4 days a week at
Thousand Oaks, CA. campus. Standard business hours with some after
hour support. On site minimum 3 days per week. Must have biotech
background/experience, plus must have cell culture and/or
purification experience 3 Key Consulting is hiring! We are
recruiting a Engineer, Process Development for a consulting
engagement with our direct client, a leading global biotechnology
company. Job Description: Our ideal candidate will have 2-4 years
of relevant experience working in drug and animal cells; and strong
process knowledge. Experience purifying cells (biologics
purifications), drug substance GMP manufacturing. We are seeking a
Process Development Engineer to join the Drug Substance Technology
Engineering team at our client’s Thousand Oaks, CA. facility.
Providing process engineering support for human therapeutic
products in clinical development through commercial production, our
client’s mission is to translate developmental processes to
commercial reality for patients through scientific expertise and
engineering innovation. 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. Top
Must Have Skill Sets: Drug substance biologics process development,
pilot plant or manufacturing technical support Purification of
monoclonal antibodies Experience in GMP environment (preferably in
drug substance) 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 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 Must have biotech background/experience, plus must
have cell culture and/or purification experience Why is the
Position Open? Backfill. Red Flags: Short duration stints in prior
jobs Resume does not accurately reflect true experience Cultural
fit - manager described the team as easy going, growth motivated,
organized, and respectful. Too senior or experienced for the
position (not looking for more than 5 years of experience)
Interview Process: Phone interview Panel interview with 3-4
individuals in the team (with manager and director) We invite
qualified candidates to send your resume to
resumes@3keyconsulting.com . If you decide that you’re not
interested in pursuing this particular position, please feel free
to take a look at the other positions on our website
www.3keyconsulting.com/careers. You are also welcome to share this
opportunity with anyone you think might be interested in applying
for this role. Regards, 3KC Talent Acquisition Team
Keywords: 3 Key Consulting, Tustin , Engineer, Process Development hybrid (JP13072), Engineering , Thousand Oaks, California
