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

3key Consulting, Inc.; Thousand Oaks (CA); Vor Ort; USD 55.000 - 63.000; Teilzeit

Zusammenfassung

3key Consulting, Inc. is hiring an Engineer for a 1+ year contract in Thousand Oaks, CA, supporting GMP facilities and equipment for drug substance processes. Responsibilities include hands-on troubleshooting, continuous improvement, and cross-functional collaboration within GMP/FDA environments.

Onsite day shift with W2 pay of $40–$46 per hour. The role requires strong biotech/pharma background, experience with DeltaV automation, and proficiency in field support and data systems.

Qualifikationen

• Master’s degree OR Bachelor’s degree with 2+ years of engineering/operations experience.
• Associate’s degree with 7 years of engineering/operations experience.
• High school diploma / GED with 8 years of engineering or operations experience.

Aufgaben

• HAnds-on troubleshooting and root cause analysis.
• Drive continuous improvement and lifecycle management of equipment.
• Coordinate preventative maintenance and calibration.
• Own systems and collaborate across GMP/FDA regulated environments.

Kenntnisse

GMP

Hands-on troubleshooting

Root cause analysis

Biotech/Pharma background

DeltaV automation

SQL VBA PLC

Field support

Ausbildung

Master’s degree

Bachelor’s degree

Associate’s degree

High school diploma

Tools

Maximo

DeltaV

Jobbeschreibung

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

• Thousand Oaks, CA
• Biotech/Pharmaceutical

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
• 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.