Manufacturing Process Engineer I — Validation & Improvement

STAAR Surgical; Monrovia (CA); On-site; USD 80,000 - 90,000; Full time

Job summary

STAAR Surgical in Monrovia, CA is seeking a manufacturing-focused professional to support the manufacture of STAAR products. You will troubleshoot day-to-day issues, develop and execute validation protocols (IQ/OQ/PQ), and perform TMV on measurement equipment to ensure quality and compliance.

The role also involves root cause analysis, supporting non-conforming material reports and CAPAs, and collaborating with partners to drive continuous manufacturing improvements.

Qualifications

• Bachelor’s degree in technical discipline or equivalent.
• 1–2 years experience in a regulated industry.
• Lean/Six Sigma training is a plus.

Responsibilities

• Provide assistance in troubleshooting/resolving day to day manufacturing issues.
• Create and execute validation protocols (IQ, OQ, PQ) and summarize test results as required.
• Create and execute Test Method Validations (TMV) on measurement equipment.
• Conduct root cause analysis for issues found in production.
• Support open non-conforming material reports and CAPAs.
• Liaise with relevant partners in order to drive continuous improvements in manufacturing.

Skills

Team building

Prioritization

Education

Bachelor's degree in technical discipline

Lean/Six Sigma training

Tools

CAD software

Job description

STAAR Surgical in Monrovia, CA is seeking a manufacturing-focused professional to support the manufacture of STAAR products. You will troubleshoot day-to-day issues, develop and execute validation protocols (IQ/OQ/PQ), and perform TMV on measurement equipment to ensure quality and compliance.

The role also involves root cause analysis, supporting non-conforming material reports and CAPAs, and collaborating with partners to drive continuous manufacturing improvements.