Manufacturing Engineer - Medical Device Process Optimization

Grove Technical Resources; California (MO); On-site; USD 90,000 - 130,000; Full time

Job summary

Grove Technical Resources in Irvine, CA seeks an experienced Manufacturing Engineer to lead process optimization and equipment validation across multiple product lines in a regulated medical device setting.

The role emphasizes cross-functional collaboration with Product Development, Quality, and Operations to ensure manufacturability, compliance, and continuous improvement in a high-quality environment.

Qualifications

• Bachelor's Degree in Engineering or related discipline.
• 4+ years of relevant engineering experience (or Master's degree with 2+ years).
• Medical Device Manufacturing experience.
• Strong experience with Equipment & Process Validation/Qualification.
• Proven Project Management experience leading cross-functional projects.
• Experience implementing process improvements in a regulated manufacturing environment.

Responsibilities

• Lead equipment and process qualification/validation activities.
• Drive manufacturing process improvements focused on cost, quality, safety, and operational efficiency.
• Manage engineering projects including scope, budget, timelines, and resource allocation.
• Design and optimize manufacturing processes, production layouts, tooling, fixtures, and equipment installations.
• Collaborate with Product Development, Quality, and Operations teams to ensure manufacturability and compliance.
• Analyze manufacturing performance and implement corrective and preventive actions.
• Ensure manufacturing processes comply with applicable regulatory and quality requirements.
• Support business continuity, service, and quality improvement initiatives.

Skills

Lean Six Sigma

Equipment Validation

Project Management

Regulatory Compliance

Process Improvement

Education

Bachelor's Degree in Engineering

Job description

Grove Technical Resources in Irvine, CA seeks an experienced Manufacturing Engineer to lead process optimization and equipment validation across multiple product lines in a regulated medical device setting.

The role emphasizes cross-functional collaboration with Product Development, Quality, and Operations to ensure manufacturability, compliance, and continuous improvement in a high-quality environment.