Test Method Validation

Job Summary

• We are seeking an Engineer to support product development and design verification activities for medical device programs.
• The ideal candidate will have strong experience in Design Controls, Design Verification & Validation (DV&V), Risk Management, and Quality Engineering within a regulated medical device environment.

Roles & Responsibilities:

• Review and support Design Verification deliverables, including protocols, reports, and summary reports.
• Review and support Test Method Validation activities and test fixture design qualification.
• Analyze regression impacts and ensure changes are properly assessed and justified.
• Support Installation Qualification (IQ) activities for non-product software and test equipment.
• Participate in risk management activities, including review and assessment of dFMEA for product subsystems.
• Collaborate with cross-functional teams on defect tracking, issue resolution, test execution, and quality improvement initiatives.
• Review build protocols, build reports, Device History Records (DHR), and configuration changes to assess impact on verification activities.
• Review engineering design changes, including mechanical and electrical drawings.
• Support the development and review of inspection plans for components and sub-assemblies.
• Ensure compliance with Design Control processes and applicable quality system requirements.
• Provide quality engineering support throughout the product development lifecycle.

Education & Experience:

• Bachelor's degree in Engineering or a related technical discipline.
• 5+ years of experience in Quality Engineering, Design Assurance, or Product Development Quality within the Medical Device industry.
• Strong knowledge of Design Controls, Design Verification & Validation (DV&V), and Risk Management processes.
• Experience reviewing Design Verification protocols, reports, and validation documentation.
• Hands-on experience with dFMEA, defect management, and root cause analysis.
• Familiarity with Device History Records (DHR), inspection plans, and configuration management.
• Experience reviewing mechanical and electrical engineering documentation.
• Knowledge of FDA Quality System Regulations, ISO 13485, and medical device development processes.
• Strong analytical, documentation, communication, and problem-solving skills.
• Experience with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Knowledge of CAPA, change control, and product lifecycle management processes.
• Experience supporting complex medical device product development programs.