Jobs · Quality Assurance · Wisconsin

Quality Engineer

American Orthodontics · Sheboygan, WI · 5 days ago
On-siteQuality AssuranceFull-time

About the role

Leads efforts to measure, analyze, and improve product and process quality. Uses data-driven decision-making, structured problem-solving, and cross-functional collaboration to resolve existing quality issues and drive continuous improvements.

Responsibilities

  • Lead investigations of quality issues, including internal nonconformities and customer complaints.
  • Manage Corrective and Preventative Action (CAPA) activities, including root cause analysis, solution identification, implementation, and effectiveness verification.
  • Own the CAPA process and identify opportunities to improve its effectiveness, efficiency, and cross-functional coordination.
  • Analyze quality data, communicate trends to cross-functional teams, and identify opportunities for product and process improvement.
  • Develop and implement effective measurement and inspection methods.
  • Establish systems for data collection, management, and monitoring to support data-driven decision-making and problem-solving.
  • Support new product development activities by defining inspection processes and providing training to ensure product quality, performance, and regulatory compliance requirements are met.
  • Collaborate with engineering and production teams to establish appropriate sampling plans for evaluating product and process quality.
  • Participate in internal and external audits; determine appropriate corrective and preventative actions to address audit findings.
  • Support process verification and validation activities, including the development and execution of IQ, OQ, and PQ protocols and reports.
  • Provide technical guidance to engineers, technicians, and cross-functional teams on quality principles, best practices, and problem-solving methodologies.
  • Perform additional responsibilities as requested to achieve business objectives.

Qualifications

  • BS degree in Engineering, Quality, or a related field, with 3–5 years of experience.
  • Experience with medical devices or other highly regulated industries/products desired.
  • Demonstrated ability to work and make decisions independently and lead others to the completion of assigned tasks.
  • Demonstrated ability to communicate effectively both verbally and in written form.

Physical requirements

  • Must be able to sit, stand, and/or walk for up to 8–10 hours per day.
  • Must be able to occasionally lift up to 25 pounds.
  • May require occasional early morning or late evening teleconferences.
  • May require occasional visits to suppliers.

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