Full-time Posted May 25, 2026
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Job Description

Responsibilities

  • Manage and ensure compliance with the Quality Management System under applicable standards such as ISO 9001, ISO 13485, and customer-specific requirements.
  • Ensure compliance with regulations applicable to medical and electronic products.
  • Lead internal, external, customer, and regulatory audits.
  • Develop and implement continuous improvement strategies focused on reducing defects, rework, and cost of poor quality.
  • Supervise Incoming Quality, IQC, IPQC, OQC, SQE, Document Control, and Supplier Quality areas.
  • Monitor and track quality key performance indicators (KPIs).
  • Coordinate root cause analysis and corrective/preventive actions using tools such as 8D, CAPA, Fishbone, 5 Why’s, and FMEA.
  • Ensure proper validation and control of electronic manufacturing and special processes.
  • Participate in New Product Introduction (NPI) transfers and engineering changes.
  • Ensure training an...

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