IMRIS

QA Engineer

• Analyze medical device products for compliance to standards
• Participate in the Design Change process
• Author new SOPs and other documentation
• Review and approve Change Orders (COs), Nonconformance Report (NCRs), Corrective and Preventive Action (CAPA) records
• Work within a cross-functional team to support product development
• Perform Design History File audits
• Provide compliance guidance concerning development, application, and maintenance of quality standards
• Prepare, support, and ensure readiness for audits and inspections

Senior Quality Engineer