MQ Technician II

About the role

The MQ Technician II ensures that all products and processes meet established quality standards and regulatory requirements for medical devices. Working closely with manufacturing and operations teams, the role supports continuous improvement of production and quality control to deliver safe and effective products.

Key responsibilities

• Develop and implement quality processes in line with the Quality Management System, under immediate supervisor guidance.
• Participate in Tier 1 manufacturing reviews and report quality issues that impact product, system, or culture.
• Conduct in‑process and final product inspections, record results, and generate reports.
• Read and interpret drawings, specifications, and customer/provider requirements.
• Review procedures, work instructions, and visual standards to ensure efficiency and compliance.
• Collaborate with quality, engineering, and production representatives on quality matters.
• Maintain up‑to‑date knowledge of relevant standards and regulations.
• Support investigations of non‑conformities, CAPA, and complaints alongside quality engineers and core teams.
• Plan team activities to facilitate quality system changes and deliver on‑site training when needed.
• Perform line audits in manufacturing as part of the quality process.

Required profile

• Ability to work independently while receiving supervision from management.
• Strong understanding of quality system requirements and regulatory expectations.
• Proficiency in reading technical drawings and specifications.
• Commitment to company code of conduct, policies, and ethical practices.

Required skills

• Microsoft Word
• Microsoft Excel
• Microsoft PowerPoint
• Quality Management System implementation
• Line auditing
• CAPA investigation
• Product inspection
• Technical drawing interpretation