Our strategic partner is a leading multinational manufacturer of medicals devices, renowned for producing tight-tolerance, precision medical components through cutting-edge extrusion and molding processes. Currently, our strategic partner is expanding its business operations in Vietnam and is seeking to fill key positions for its activities in this new market.
Location: Bac Ninh, Vietnam
Job Responsibilities
- Perform quality control inspections at various stages of production in accordance with quality inspection standards.
- Responsible for product quality control and Coordinate with production for quality improvement.
- Maintain all quality records and retain samples collection comply with good writing practice GDP requirements.
- Responsible for validation or verification measurement and report writing.
- Report abnormalities in a timely manner and raise Non-Conformance Report (NCR) as and when necessary, when quality problem arises.
- Work with cross- functional teams to implement continuous improvement, track status of non-conformities and CAPA effectiveness.
- Responsible for changing implementation, follow up and feedback.
- Responsible for the identification and traceability of product are available. Ensure product identification is correct and traceable.
- Perform daily process audit according to the procedure.
- Responsible as Calibration administrator to follow up equipment in calibration master list and ensure they are calibrated correctly, provide accurate measurements and have proper identification.
- Assist in customer complaint analysis, investigation of quality issues and corresponding improvement measures.
- Create, revise WI or SOP related to QC inspection procedures. Reviews WI or SOP created by technicians.
- Maintain proper 5S housekeeping in the assigned area daily. Ensure safety regulations are being observed at the workplace.
- Ensures all quality records and retain samples collection comply with good writing practice.
- Authorize the release (COA) of products, COC review.
- Ensures FAI validation and documentation are completed
- Ensures daily process audit are completed and reviews findings and follow up on action item completion.
- Ensures trainings of QC inspectors and technicians are assigned and completed
- Supervise QC team for all related QC matters, disciplines, work schedule, and OT arrangement.
- Conducts internal audits with QA to ensure QMS is effectively implemented.
- Review and approves DHR
- Assist the superior to complete other tasks as assigned.
Job Requirements
- Diploma or above
- Proficient in English, and Vietnamese
- Proficient in Microsoft Word, Excel, PowerPoint
- Good at using computer (need to be able to use SharePoint, Microsoft teams, etc.)
- Must be meticulous, with good attention to details
- Good to have experience in supervisor/leader role in a medical device company.
- Strong communication and interpersonal skills to work effectively with cross-functional teams.
If you possess the required skills and experience and are ready to significantly contribute to the dynamic team, we warmly welcome your application at vy.cao@peoplewise.vn or application@peoplewise.vn.
About PeopleWise Vietnam:
PeopleWise Vietnam was founded with the mission of positively impacting our community by improving the quality of the labor force, addressing workforce dynamics, and enhancing its effectiveness. During our initial phase, we provided solutions and human resources consulting services to our partners worldwide, including workforce advisory, organizational diagnosis, career transition, training services, talent management, and staffing solutions that align with each organization’s values and vision, driving business success.
Visit us at our website: https://peoplewise.vn/
To apply for this job email your details to vy.cao@peoplewise.vn