Key Responsibilities
Maintain, monitor, and improve the company’s Quality Management System (QMS) in compliance with ISO 9001 and other applicable standards.
Manage, review, and update-controlled documents such as procedures, work instructions, forms, and records to ensure accuracy, consistency, and version control.
Coordinate with cross-functional departments to ensure QMS implementation, audit readiness, and process compliance.
Assist in planning and conducting internal and external audits, including preparation, follow-up, and verification of corrective actions.
Support management review meetings by compiling audit results, performance data, and improvement recommendations.
Maintain document archives (digital and physical) and ensure traceability and accessibility.
Participate in continuous improvement initiatives and support integration with other management systems (ISO 14001, ISO 45001, etc.).
Qualifications
Bachelor’s degree in Quality Management, Industrial Engineering, or related fields.
Minimum 1 year of experience in QMS, ISO implementation, or document control (manufacturing experience preferred).
Good understanding of ISO 9001:2015 requirements and document control processes.
Proficient in Microsoft Office (Word, Excel, PowerPoint); experience with ERP or DMS systems is a plus.
Able to read and understand English quality standards and audit materials.