Reliability Engineer

Grove Technical Resources, Inc.; Minnesota; On-site; USD 90,000 - 120,000; Full time

Job summary

Grove Technical Resources, Inc. seeks a Quality Systems professional to drive CAPA activities, change control, and validation within medical devices. You will collaborate with engineering, regulatory, and manufacturing teams to strengthen post-market quality and reliability.

The role emphasizes risk analysis, DOE, statistical evaluations, audits, and cross-site support across multiple sites, aligning with quality system requirements and regulatory expectations.

Qualifications

• Bachelor's degree with 4+ years of relevant experience in medical devices.
• OR Master's degree with 2+ years of relevant experience.
• Experience in medical devices, quality systems, reliability, CAPA, and regulatory environments preferred.

Responsibilities

• Support CAPA activities and quality improvement initiatives
• Provide manufacturing and project/program support
• Support multiple sites and cross-functional teams
• Understand and support quality and post-market quality deliverables
• Conduct reliability studies, risk analysis, DOE, and statistical evaluations
• Analyze product/process performance and identify opportunities to improve reliability
• Support audits, validations, and corrective actions
• Work with engineering, quality, regulatory, manufacturing, and other stakeholders

Skills

CAPA

Quality Systems

Regulatory requirements

Reliability engineering

Cross-functional support

Education

Bachelor's degree + 4+ years

Master's degree + 2+ years

Job description

• CAPA & Quality Systems – Experience with CAPA, Change Control, and Validation activities
• Medical Device Quality & Regulatory – Strong understanding of medical device regulatory requirements and post-market quality
• Reliability / Manufacturing & Cross-Functional Support – Reliability engineering, manufacturing support, project/program support, and collaboration across teams

Key Responsibilities

• Support CAPA activities and quality improvement initiatives
• Provide manufacturing and project/program support
• Support multiple sites and cross-functional teams
• Understand and support quality and post-market quality deliverables
• Conduct reliability studies, risk analysis, DOE, and statistical evaluations
• Analyze product/process performance and identify opportunities to improve reliability
• Support audits, validations, and corrective actions
• Work with engineering, quality, regulatory, manufacturing, and other stakeholders

Qualifications

• Bachelor's degree + 4+ years relevant experience
• OR
• Master's degree + 2+ years relevant experience
• Experience in medical devices, quality systems, reliability, CAPA, and regulatory environments preferred