Engineer, Drug Product Manufacturing/Processing - Hybrid; JP
Job in
Thousand Oaks, Ventura County, California, 91362, USA
Listed on 2025-10-18
Listing for:
3key Consulting, Inc.
Full Time
position Listed on 2025-10-18
Job specializations:
-
Engineering
Manufacturing Engineer, Process Engineer, Quality Engineering, Validation Engineer
Job Description & How to Apply Below
Job Title: Engineer, Drug Product Manufacturing / Processing - Hybrid (JP13084)
Location: Thousand Oaks, CA. 91320 (Hybrid)
Business Unit: Commercial Drug Product Processing Group
Employment Type: Contract
Duration: 1+ year with likely extensions and/or conversion to a permanent position.
Rate
: $38 - $42/hour W2
Posting Date: 8/14/2024.
Notes: Only qualified candidates need apply. MUST BE LOCAL to Thousand Oaks, CA. Consultant should be a Flexible Commuter. Consultant may be required to be onsite as needed based on business needs and can expect to be onsite on a weekly basis.
3 Key Consulting is hiring! We are recruiting an Engineer, Drug Product Manufacturing / Processing for a consulting engagement with our direct client, a leading global biotechnology company.
Job Description:
As a member of the process development team, the candidate will be focused on supporting senior staff to develop and characterize drug product technologies and manufacturing capabilities, as well as assist in the process validation and technology transfer of multiple products to the aseptic fill finish manufacturing plants at our client in Thousand Oaks, CA. and which includes various production lines.
- The candidate will support senior staff in the planning, execution and documentation of characterization, process validation and technology transfer projects.
- The candidate will be primarily responsible for executing characterization studies and other experiments at the lab scale and production scale to generate technical data packages using complex technology, while organizing data and analyzing results under supervision of senior staff.
- The candidate will be responsible for liaising with various drug product teams to ensure successful technology transfer, with associated documentation, of products.
- The candidate will assist in establishing the experimental design, develop and execute protocols, obtain reproducible and reliable results, analyze and document experimental results, and communicate results to cross functional groups.
- Familiarity with cGMP and experience in drug product / drug substance manufacturing or process development
- Knowledge of and hands-on experience with various drug product technologies
- Strong cross functional team player with good communication skills (oral and written)
- Apply fundamental engineering and scientific principles to resolve issues and evaluate effects of process improvements, equipment, scale, and raw materials
- Assist in the design and execution of experiments in order to characterize and enable implementation of new capabilities and process changes such as filling, lyophilization and analytical technologies
- Support technology transfer leads during the transfer of drug products into manufacturing sites (clinical and commercial), including make-a-batch exercises, process parameter risk assessments, process transfer documents, and change control assessments
- Support development and maintenance of technology transfer tools (clinical and commercial)
- Effectively communicate results of characterization studies, experimental execution and technology transfer initiatives
- Author/review/data verify technical documents, such as technical protocols, technical assessments, technical reports and draft standard operating procedures or guideline documents
- Conduct analysis of data generated, including statistical analysis using Minitab, JMP etc.
- Development of digital tools and models by leveraging data analytics and programming skills
- Support at scale characterization and/or process validation runs as person in plant
- 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.
- This is a drug product processing group any familiarity with this (unit operations in scope of drug product would be very helpful!)
- Strong interpersonal skills, must be motivated to learn, willing and comfortable with asking questions when they don't understand something and taking direction (rather than tasking based on assumption)
- Strong ability to think critically build…
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