
1. Preparing and implementing the quality assurance policies and procedures.
2. Ensuring that standards and safety regulations are observed and met.
3. Addressing issues occurred during the processes and proposed solutions with the supervisor.
4. Recording and filing documents of quality assurance activities and completing an audit report.
5. Providing recommendations for an improvement of processes to achieve a quality standard.
6. Supporting all inspection activities on the production processes.
7. Conducting product testing and final inspections when needed or required.
8. Assisting Head of Quality Assurance and Regulatory Affairs as requested.
1. Bachelor's Degree in Science or related field.
2. At least 1 year of experience in the medical devices industry or related regulated products is required e.g. ISO13485, ISO15189, GMP for medical devices, etc.
3. Having knowledge and experience in internal audit is an advantage.
4. Self-oriented, good organizational skill, and communication skill are required.
5. Ability to read, write, and communicate in English.