Senior Medical Device Manufacturing Engineer — Validation

Grove Technical Resources, Inc.

Irvine (CA)

On-site

USD 110,000 - 150,000

Full time

2 days ago

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Job summary

Grove Technical Resources, Inc. seeks a Sr. Manufacturing Engineer for a 12+ month on-site role in Irvine, CA.

You will lead equipment qualification, validate processes, and drive Lean Six Sigma initiatives in medical device manufacturing. Responsibilities include cross-functional collaboration with R&D, QA, and Operations to ensure compliant, efficient production, optimize processes, reduce costs, and install/validate new equipment.

Qualifications

4+ years of manufacturing engineering experience, with medical devices preferred.
Strong background in validation activities (IQ/OQ/PQ) for equipment and processes.
Experience leading cross-functional projects with R&D, QA, and Operations.
Proven ability to apply Lean Six Sigma to reduce cost and improve quality.

Responsibilities

Lead manufacturing process and equipment qualification projects.
Drive process improvements, productivity, quality, and cost-reduction initiatives.
Support equipment installation, validation, and manufacturing optimization.
Collaborate with R&D, Quality, and Operations to ensure compliant, efficient production.
Apply Lean Six Sigma methodologies to improve manufacturing performance.