Sr. Quality Assurance Engineer

Posted: 12/05/2026 Location: Maple Grove, Minnesota, United States Salary: $110000 - $120000 Job type: Permanent


Quality Assurance Engineer - Medical Device
Northwest Minneapolis Metro


Position Overview


We are seeking a Quality Assurance Engineer to provide operational quality input and deliverables across manufacturing programs throughout the product lifecycle. This role also supports development activities transitioning into commercial manufacturing, including manufacturing readiness, audits, and clinical builds, to ensure a smooth launch and continuously accurate and compliant Design History File. This is a 6-month contract to hire opportunity with the intent to bring the right candidate on permanently.


This position does not offer visa sponsorship. Candidates must be authorized to work in the United States now and in the future without sponsorship.


Duties and Responsibilities

• Document Control & Audit Readiness: Author and approve SOPs, work instructions, and forms. Support internal audits and maintain inspection readiness across the quality system
• Data & Continuous Improvement: Compile and trend quality metrics to identify systemic issues. Present actionable insights to leadership and drive implementation of corrective and preventive actions
• Incoming Inspection & Supplier Quality: Oversee incoming inspection per approved sampling plans. Disposition nonconforming materials and coordinate supplier corrective actions to address recurring quality issues
• Equipment & Process Oversight: Provide quality oversight for IQ/OQ/PQ qualification activities. Review and approve protocols, reports, and change orders. Evaluate regulatory impact of equipment changes prior to implementation
• NC & CAPA Leadership: Manage nonconformances and CAPAs from initiation through effectiveness verification. Lead root cause analysis using structured methods (5-Why, fishbone). Trend data and report findings at management review
• Operations Quality Support:
  • Serve as the quality point of contact for production
  • Review batch records and travelers for GMP compliance
  • Support line clearances, first-article inspections, and process change reviews
  • Draft, collaborate on, and approve product and engineering work orders
  • Create and maintain up-to-date product Design History Files (DHF)
  • Advise project teams on best practices for quality and regulatory compliance
  • Own, review, and approve changes ensuring impacts and resulting actions are properly documented and executed
  • Receive, investigate, and document product complaints, interacting with customers as applicable
  • Support audits as Subject Matter Expert (SME) for QMS processes and product DHFs
  • Drive Product Lifecycle Management (PLM) architecture and changes as needed

• Bachelor's degree in a life science discipline or equivalent combination of education and experience
• 5+ years of experience in medical device development, or 3+ years in a Design Assurance or Quality Engineering role
• Experience working within quality systems as defined in 21 CFR 820 and ISO 13485
• Background as a development project team member on complex medical device programs, including systems-level work
• Understanding of ISO 14971 and application of risk management to product development and processes
• Demonstrated technical expertise and leadership in quality
• Strong attention to detail, organization, and accuracy
• Creative problem-solving ability with a track record of proposing practical solutions
• Strong written and verbal communication skills across disciplines and organizational levels
• Demonstrated use of quality tools and methodologies including nonconformances, CAPAs, and root cause analysis
• Experience with PLM software such as Windchill, Agile, or Propel
• Intermediate to advanced proficiency in Microsoft Office Suite
• Familiarity with statistical software such as Minitab preferred