Our client is a leading medical device contract manufacturer with operations in Singapore, Malaysia, and China. They are looking for a
QMS Engineer
to support and enhance their Quality Management System across multiple sites.
Working Hours:
Monday – Friday, 8:30am – 6:00pm
Job Responsibilities
Maintain and improve the Quality Management System (QMS) to ensure compliance with ISO 13485 and regulatory requirements
Plan and conduct internal audits, and support external customer and certification audits
Manage document control, including SOPs, work instructions, and quality records
Support the implementation and validation of electronic QMS/document control systems
Drive continuous improvement initiatives and provide quality training across the organization
Requirements
Diploma or Degree in Engineering or a related discipline
Minimum 2–3 years of QMS experience in a manufacturing environment
Hands-on experience with ISO 13485 Quality Management System is required
Experience in internal auditing, document control, and quality documentation is an advantage
Strong communication, analytical, and organizational skills
Interested candidates who wish to apply for the advertised position are encouraged to click
"Apply Now"
to submit their application.
We regret that only shortlisted candidates will be notified.
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