- 5 day work week, 8.30am to 5.30pm (OT when necessary)
- Full time, Permanent
Responsibilities:
- Perform inspections and tests on raw materials, in-process products, and finished goods to ensure adherence to quality standards
- Analyse and interpret test data, identify and resolve quality issues, and implement corrective and preventive actions
- Maintain detailed records and documentation related to quality control processes
- Assist in the development and improvement of quality control procedures and processes
- Collaborate with cross-functional teams to address quality concerns and support continuous improvement initiatives
- Comply with all relevant quality management systems, regulatory requirements, and standard operating procedures
Requirements:
- Higher Nitec & above in a relevant field such as Quality Assurance, Engineering, or a related technical discipline
- Minimum 2 years of experience in quality control or technical role, preferably in the medical device or pharmaceutical industry
- Possess some Calibration Experience with Documentation experience
- Basic understanding of metallic materials and precision engineering process
- Basic understanding of ISO 13485 and MSA
- Competent with Microsoft Office tools
- Knowledge in inspection, measurement system, and document control
.We regret to inform that only shortlisted candidates would be notified
EA License Number
Vivian Chen
R23116467
EA 24C2366
