Job Description:
- Support new project/product development in validation activities, MSA, GR&R and establishing FMEA,
Quality Plan, Inspection criteria, WI, PWI, form.
- Promote and coordinate quality assurance efforts to ensure products conform to quality standards and meet
relevant regulatory requirements.
Maintain and ensure processes are aligned with procedures / work instructions and ISO standard.
Lead investigation, root cause analysis, resolution and closure of complaint, NCR and CAPA.
Participate in Internal audit and Continuous Improvement Project.
Responsible for coordinating and conducting supplier audits.
Coordinate with external party for environment control and monitoring.
Manage calibration program.
Perform any other duties as assigned from time to time.
Job Requirement:
- Diploma or bachelor's degree in quality or engineering.
- Min 2 years' experience in Quality Assurance role of Medical Device manufacturing, preferably in plastic injection molding and extrusion.
- Familiar with cGMP, ISO 9001 and ISO 13485 and regulatory requirement.
Internal Auditor certified preferred.
- 8D metholodgy and problem-solving skill.
- Good communication and presentation skill.
- People management.
- Good analytical skill and familiar with mini tab.
- Proficient in English and Chinese.
Good eyesight.