Job Summary
You will prepare and maintain quality control (QC) reports, perform manual inspections of medical device parts and plastics, update customer drawings, assist engineers with customer buy-off, support ISO document maintenance, and summarize monthly non-conformance material reports (NCMR) to ensure product quality and compliance.
Responsibilities
- Prepare and maintain detailed QC reports to track inspection outcomes and quality status
- Perform manual inspections of medical device parts and plastic components to verify compliance with specifications
- Update customer drawings and QC reports to reflect current product and quality information
- Assist engineers during customer buy-off processes to facilitate product approval
- Support the Management Representative in maintaining ISO documentation for quality management system compliance
- Summarize and report monthly non-conformance material reports (NCMR) and provide status updates
- Interpret technical drawings with a focus on tolerancing to ensure accurate inspections
- Use conventional measuring equipment, tools, and gauges to conduct precise measurements
- Apply computer skills to document and manage quality data efficiently
- Demonstrate a willingness to learn new tasks and maintain a proactive, can-do mindset
Job Requirements
- Relevant educational certificates as a minimum qualification.
- At least 1-2 years of related working experience.
- An engineering background is preferred to support technical understanding and quality assurance tasks.