Biopharma Process & Equipment Reliability Engineer

3key Consulting, Inc.; Thousand Oaks (CA); On-site; USD 85,000 - 96,000; Full time

Job summary

3 Key Consulting, Inc. is hiring a Process & Equipment Reliability Engineer for Biopharmaceutical Drug Substance Manufacturing in Thousand Oaks, CA. This contract role supports system reliability and optimization with a 14+ month engagement, onsite at the client site.

Responsibilities include analyzing systems, conducting root cause analysis, leading improvement projects, and coordinating with cross-functional teams in a regulated biotech environment to ensure compliant and safe operations.

Qualifications

• Degree in engineering field or hands-on experience with mechanical, chemical, electrical, or related engineering.
• Experience investigating equipment or system problems using data and maintenance history.
• Experience producing clear technical records in a regulated environment.

Responsibilities

• Support system reliability and optimization, identify risks, and implement reduction strategies.
• Assist with technical investigations, root cause analysis, and equipment troubleshooting.
• Analyze data and help develop engineering solutions using data techniques (e.g., SPC, Six Sigma).
• Support new technology introductions through engineering assessments and equipment mods.
• Collaborate with cross-functional teams to communicate findings and drive solutions.
• Provide onsite day-to-day technical support for equipment and process issues.

Skills

Facilities engineering fundamentals

Equipment troubleshooting & data分析

Education

Master's degree or Bachelor's degree with experience

Job description

3 Key Consulting, Inc. is hiring a Process & Equipment Reliability Engineer for Biopharmaceutical Drug Substance Manufacturing in Thousand Oaks, CA. This contract role supports system reliability and optimization with a 14+ month engagement, onsite at the client site.

Responsibilities include analyzing systems, conducting root cause analysis, leading improvement projects, and coordinating with cross-functional teams in a regulated biotech environment to ensure compliant and safe operations.