Quality Management System Engineer (QMS)
Summary
A QMS Engineer maintains and improves the Quality Management System (QMS) to ensure compliance with ISO 13485 and regulatory standards, conducting audits, managing documentation, and driving quality improvements in a medical device manufacturing environment.
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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