Các Phúc Lợi Dành Cho Bạn
Mô Tả Công Việc
1.1) In charge supplier quality management program.
1.2) Create/revise the supplier quality management documentations shall comply with ISO standards, Global documentations
1.3) Coordinate with stakeholder to create & executive the SQM audit plan.
1.4) Provide the quality reports related SQM subject
1.5) Be co supplier quality management trainer. Provide training on supplier quality management related subject matter.
1.6) Coordinate with Regional and Global SQM team to executive the SQM project, programs
2. Compliance programs for medical plants:
2.1) Be change control coordinator:
2.2) In charge compliance execution. Provide training on compliance related subject matters, include Change control, Trackwise system if needed
2.3) Compliance programs include: audit and internal audit, DIR, CAPA, Change control, calibration,...
2.4) Create/revise SOP regarding compliance shall comply with ISO standards, Global documentation
3. Involve improvement program and others:
3.1) Involve to improvement team if required
3.2) Initiative improvement idea
Yêu Cầu Công Việc
- Requires a full working knowledge of a technical or professional field. Exercises general application of technologies or
technical / professional concepts and concepts, and proposes a plan of action
- Have knowledge about quality management system such as ISO9001, ISO13485
- Good command in English