QC Supervisor: Bac Ninh, Yen Phong expansion industrial park
AP Technologies
Location: Gmap link
Roles & 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.
About AP-TECHNOLOGIES
- AP Technologies is a multinational medical device contract manufacturer (Head office in Singapore) that specializes in tight tolerance, precision medical components using the latest extrusion and molding processes. We utilize our comprehensive quality control system, state-of-the-art facility, and advanced statistical methodologies to maintain the highest quality standards in the industry.
- Vietnamese Company size: 100 – 200 staffs
