Area of Responsibilities:
Contribute to esbtablish and maintain quality management system.
In charge of material/supplier/customer qualification, masterdata creation and updating timely.
Maintain the non-conformity control process, identify the oppprtunity of improvement and continuously push suppliers for effective counter measures.
Work with IT to drive SAP enhancement and other office automation better serving QA’s day-to-day work.
Manage the systems under authority’s supervision. Make sure the accuracy and completeness of data entry.
Quality documents & records control, maintain them in a current status.
Training or events to promote quality and compliance awareness.
Prepare for external audits readiness, i.e.NMPA inspection etc.
Other assignments by manager.
Person Specification
- Bachelor degree of engineering or above.
- Strong in logic thinking and problem solving.
- Good written and oral communication skills.
- Good command of English.
- Be knowledgeable of ERP system operation.- 3 years above hands-on experience in QA role of medical device / pharmaceutical industries.
- Experience in GxP / QMS implementation.
- Experience in prepararing for authority audit.- Highly responsible, self-driven.
- High efficiency.
- Assertive and scrupulous.