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Job Title: Engineer, GMP Facilities & Equipment, Drug Substance Process Support (JP15973)
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: F&E Drug Substance Supply
Duration: 1+ year with likely extensions and/or conversion to permanent
Posting Date: 10/13/2026
Pay Rate: $40 - $46/hour W2
Notes: Onsite day shift.
3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Position involves support of manufacturing and other engineering staff in the ongoing troubleshooting and improvements of the manufacturing process. Includes the initiation, execution, and completion of continuous improvement projects, particularly for equipment related scope. Perform hand-on field support, field evaluations, engineering design recommendations, third party vendor escort, cross functional collaboration with maintenance, instrumentation, manufacturing, quality, and process engineering within GMP / FDA regulated cleanroom. Skills: Hands-on equipment troubleshooting, drug substance manufacturing, continuous improvement, Maximo, Obsolete component analysis and functionally equivalence. Previous intern experience is a plus. Experience with automation (Delta V) is a plus, as well as experience with computer programming (SQL / VBA / PLC), drug substance systems, and/or chromatography, filtration, single-use and stainless-steel product trains, and various mixers.
Why is the Position Open?
Supplement additional workload on team
Top Must Have Skills:
GMP, Hands on troubleshooting, root cause analysis, Biotech/Pharma Background
Day to Day Responsibilities:
Hands on troubleshooting, root cause analysis, continuous improvement, system ownership, lifecycle management, preventative maintenance and calibration coordination
Basic Qualifications:
Master’s degree OR
Bachelor’s degree and 2 years of Engineering or Operations experience OR
Associate’s degree and 7 years of Engineering or Operations experience OR
High school diploma / GED and 8 years of Engineering or Operations experience
Red Flags:
No Full-Time Experience
No Biotech/Pharma
No hands-on Troubleshooting
No GMP
Interview process:
Phone Screen and Panel (online), start immediately.
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.
Location: Thousand Oaks, CA.
Employment Type: Contract
Business Unit: F&E Drug Substance Supply
Duration: 1+ year with likely extensions and/or conversion to permanent
Posting Date: 10/13/2026
Pay Rate: $40 - $46/hour W2
Notes: Onsite day shift.
3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Position involves support of manufacturing and other engineering staff in the ongoing troubleshooting and improvements of the manufacturing process. Includes the initiation, execution, and completion of continuous improvement projects, particularly for equipment related scope. Perform hand-on field support, field evaluations, engineering design recommendations, third party vendor escort, cross functional collaboration with maintenance, instrumentation, manufacturing, quality, and process engineering within GMP / FDA regulated cleanroom. Skills: Hands-on equipment troubleshooting, drug substance manufacturing, continuous improvement, Maximo, Obsolete component analysis and functionally equivalence. Previous intern experience is a plus. Experience with automation (Delta V) is a plus, as well as experience with computer programming (SQL / VBA / PLC), drug substance systems, and/or chromatography, filtration, single-use and stainless-steel product trains, and various mixers.
Why is the Position Open?
Supplement additional workload on team
Top Must Have Skills:
GMP, Hands on troubleshooting, root cause analysis, Biotech/Pharma Background
Day to Day Responsibilities:
Hands on troubleshooting, root cause analysis, continuous improvement, system ownership, lifecycle management, preventative maintenance and calibration coordination
Basic Qualifications:
Master’s degree OR
Bachelor’s degree and 2 years of Engineering or Operations experience OR
Associate’s degree and 7 years of Engineering or Operations experience OR
High school diploma / GED and 8 years of Engineering or Operations experience
Red Flags:
No Full-Time Experience
No Biotech/Pharma
No hands-on Troubleshooting
No GMP
Interview process:
Phone Screen and Panel (online), start immediately.
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.