Quality Manager | Med Device

• Maintain and document quality systems to ensure alignment with ISO, FDA, MDSAP, and other applicable regulatory standards.
• Provide support for Design Control and Product Development, including:
  • Contributing as a cross‑functional team member to enhance product and process designs
  • Coordinating and supporting verification activities and test protocols for new product introductions and design modifications
  • Managing and updating Design History Files (DHF) and Device Master Records (DMR)
• Coordinate and/or support Supplier Quality Management, including:
  • Overseeing the review and release of contract‑manufactured products
  • Evaluating trends and data related to complaints, supplier performance, and nonconforming materials
  • Conducting complaint investigations
  • Monitoring corrective action implementation and verifying effectiveness
  • Performing supplier audits
• Coordinate and/or support Risk Management activities, including:
  • Leading risk assessments such as Failure Modes and Effects Analysis (FMEA) and implementing appropriate risk controls
  • Maintaining Risk Management Files for assigned device families

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.