Engineer, Drug Product Manufacturing Process Development (JP14993)
Company: 3 Key Consulting
Location: Thousand Oaks
Posted on: April 1, 2026
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Job Description:
Job Title: Engineer, Drug Product Manufacturing Process
Development (JP14993) Location: Thousand Oaks, CA. 91320 Employment
Type: Contract Business Unit: Commercial Drug Product Duration: 1
year(s) – (with likely extensions and/or conversion to permanent)
Posting Date: 02/02/25 Pay Rate: $36 - $41/hour W2 Notes: Only
qualified candidates need apply. 3 Key Consulting is hiring an
Engineer, Drug Product Manufacturing Process Development for a
consulting engagement with our direct client, a leading global
biopharmaceutical company. Job Description: We are seeking a
skilled Process Development Engineer who can work independently to
support technical projects. The ideal candidate will have expertise
in laboratory testing, drug product fill finish processing,
holistic drug product process knowledge, technical transfer, and
drug product manufacturing. Excellent communication skills and
proficiency in technical writing are essential for this role. The
Process Development Engineer will: Author, data verify, and review
guideline documents, technical protocols, reports, product impact
assessments. Execute laboratory analytical testing such as:
viscosity, protein concentration, pH, osmolality. Execute
laboratory experiments such as pipetting, formulation, filtration.
Provide technical support for drug product process development,
including formulation, filtration, and filling
(vials/syringes/devices) of parenteral products. Assist in the
development and characterization of drug product processes and the
transfer of new technologies to commercial sterile fill/finish
sites. Support process development for commercial drug product
processing in areas such as sterile processing, process
characterization, tech transfer, and validation. Collaborate with
manufacturing and support functions to provide coordinated support
for commercial drug product manufacturing operations and technology
transfer. Participate in global cross-functional teams, working
effectively in a highly matrixed team environment to drive
efficiency and foster strong relationships. Troubleshoot issues
with drug product processing technologies and equipment, utilizing
data-driven analyses and visualizations to determine true root
causes. Why is the Position Open? Backfill. Top Must Have Skills:
Post graduation experience required Laboratory experience using
analytical equipment Evidence of good communication e.g. writing
documents and sharing results College degree in engineering or
similar (chemical engineer, bio engineer, pharmaceutical science,
etc) Day to Day Responsibilities: On site laboratory work, for
example testing viscosity with a rheometer Maintaining good
documentation practices with a laboratory notebook Analyzing and
summarizing results to be communicated out Documentation and data
verification 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
Red Flags: No recent relevant experience with analytical equipment
Poor communication / organization in resume Must be based in the US
Interview process: MS Teams Interview 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, Bakersfield , Engineer, Drug Product Manufacturing Process Development (JP14993), Science, Research & Development , Thousand Oaks, California
