Quality Engineer

Insight Global; Grand Rapids (MI); On-site; USD 65,000 - 105,000; Full time

Job summary

Insight Global is seeking a Quality Engineer for a medical device manufacturing client in Michigan. This role supports new product development, process validation, risk management, quality investigations, and continuous improvement to ensure product quality, regulatory compliance and risk mitigation throughout the lifecycle.

You will collaborate with Engineering, Operations, R&D and Manufacturing to drive quality improvements, CAPA and root-cause analyses, and support audits.

Qualifications

• 3+ years of quality engineering in regulated manufacturing.
• Experience with process validation, risk management, CAPA, and root cause analysis.
• Knowledge of FDA, ISO, GMP standards and regulations.
• Experience with statistical analysis tools.
• Lean, 5S, and Six Sigma familiarity.
• Strong communication and cross-functional collaboration.

Responsibilities

• Support new product development activities with risk assessments and design reviews.
• Develop and maintain risk management docs like DFMEA/PFMEA.
• Create and execute process validation protocols and reports.
• Lead root-cause investigations using 5 Whys and fishbone diagrams.
• Investigate nonconforming materials, complaints, and quality events.
• Support change control and quality system compliance.
• Use quality tools to analyze process and product performance.
• Collaborate with Engineering, Operations, R&D, and Manufacturing.
• Assist audits and regulatory compliance activities.
• Perform additional duties as assigned.

Skills

Quality engineering

Process validation

CAPA

Root cause analysis

Quality investigations

Cross-functional collaboration

Statistical analysis

Project management

Lean/Six Sigma

Tools

Minitab

Job description

Insight Global is seeking a Quality Engineer for one of our clients in the medical device/manufacturing industry. This individual will support new product development, process validation, risk management, quality investigations, and continuous improvement initiatives. The ideal candidate has experience in regulated environments and can effectively partner with cross-functional teams to ensure product quality, compliance, and risk mitigation throughout the product lifecycle.

Responsibilities

• Support new product development activities, including risk assessments, design controls, and specification reviews.
• Develop and maintain risk management documentation, including DFMEA and PFMEA analyses.
• Create and execute process validation protocols, reports, and associated quality documentation.
• Lead root cause investigations using tools such as 5 Whys, Fishbone Diagrams, and corrective action methodologies.
• Investigate nonconforming materials, customer complaints, and quality events to identify and implement corrective actions.
• Support change control processes and ensure compliance with quality management system requirements.
• Utilize statistical methods and quality engineering tools to analyze process and product performance.
• Partner with Engineering, Operations, R&D, and Manufacturing teams to drive quality improvements.
• Support internal and external audits, inspections, and regulatory compliance activities.
• Perform additional duties as assigned.

Qualifications

• 3+ years of quality engineering experience within a medical device, pharmaceutical, or other regulated manufacturing environment.
• Experience with process validation, risk management, CAPA, root cause analysis, and quality investigations.
• Knowledge of FDA, ISO, GMP, and other applicable quality standards and regulations.
• Experience with statistical analysis tools and methodologies.
• Familiarity with Lean Manufacturing, 5S, and/or Six Sigma principles.
• Strong project management, communication, and cross-functional collaboration skills.
• Proficiency with Microsoft Office and quality/statistical software such as Minitab.
• Ability to manage multiple priorities in a fast-paced environment.