Sr. Manufacturing Engineer - Medical Device

Grove Technical Resources, Inc.; Irvine (CA); On-site; USD 110,000 - 150,000; Full time

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.

Skills

Equipment & Process Validation / IQ/OQ

Medical Device Manufacturing

Project Management & Cross-Functional

Lean Manufacturing & Six Sigma

Process Improvement & Cost Reduction

Education

Bachelor's degree in Engineering or related field

Job description

Hiring: Sr. Manufacturing Engineer - Medical Device

Location: Irvine, CA (100% Onsite)

Contract: 12+ Months

Type: W2 contract

Key Skills Required:

Equipment & Process Validation / Qualification (IQ/OQ/PQ)

Medical Device Manufacturing Experience

Project Management & Cross-Functional Leadership

Lean Manufacturing & Six Sigma

Process Improvement, Cost Reduction & Manufacturing Optimization

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 processes.

Apply Lean Six Sigma methodologies to improve manufacturing performance.

Requirements:

Bachelor's degree in Engineering or a related field.

4+ years of manufacturing engineering experience (2+ years with an advanced degree).

Strong background in medical device manufacturing and validation activities.