Engineer, GMP Facilities & Equipment, Drug Substance Process Support (JP15973)

3 Key Consulting

  • Thousand Oaks, California
  • 10 days ago
  • $40–$46 Per Hour

Highlights

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 ExperienceNo Biotech/PharmaNo hands-on TroubleshootingNo GMP Interview process: Phone Screen and Panel (online), start immediately. 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.

Numbers & Facts

LocationThousand Oaks, California
Salary$40–$46 Per Hour

Description

Job Title: Engineer, GMP Facilities & Equipment, Drug Substance Process Support (JP15973)Location: Thousand Oaks, CA.Employment Type: ContractBusiness Unit: F&E Drug Substance Supply Duration: 1+ year with likely extensions and/or conversion to permanentPosting Date: 10/13/2026Pay Rate: $40 - $46/hour W2Notes:  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 teamTop Must Have Skills:GMP, Hands on troubleshooting, root cause analysis, Biotech/Pharma BackgroundDay to Day Responsibilities: Hands on troubleshooting, root cause analysis, continuous improvement, system ownership, lifecycle management, preventative maintenance and calibration coordinationBasic 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 experienceRed Flags:No Full-Time ExperienceNo Biotech/PharmaNo hands-on TroubleshootingNo GMPInterview 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.

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