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Production Supervisor

Paramit Malaysia Sdn Bhd

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3-5 Years
a month ago
186 Viewed
6 Applied

Job Description

Job Responsibility

  • Monitoring the inspection activities in at QA.
  • Generating COC for all medical device outgoing shipments without error.
  • Generate new Final Inspection Reports for new parts and setup the sampling plan for the based on the procedure.
  • Lead the team on the product technical testing requirements and acceptance criteria.
  • Coordination of critical and urgent inspection with Asset Management, lot received and inspection.
  • Educating and training QA inspectors and leaders on the inspection requirements and methods.
  • Work with the FQA technician to generate the FQA quality inspection plan.
  • Verification of the non-conformance and abnormality with engineering, quality & production. Making acceptance and rejection decision based on the customers acceptance criteria.
  • Raise the Non-Conformance form and drive closure of the non-conformance that occurred at FQA.
  • Raise the shipment on-hold to contain and constrain non-conforming product shipment.
  • Compile weekly inspection data into PPM data, daily output, MORV clearance, FQA KPI reports.
  • Plan the headcount and overtime support based on the production operation plan.
  • Review and approval of HR related documentation generated by FQA.
  • Developing and maintaining QA policies and procedures.
  • Others as per assigned by the Supervisor.

Job Requirements

  • Degree in Science / Engineering.
  • At least 3 years of experience in Engineering and or QA functions in manufacturing of medical devices.
  • Knowledge of using quality tools
  • Knowledge and hands on experience in leading Quality operations.
  • Problem solving tools.
  • Knowledge in manufacturing of medical devices organization.

Job Benifits

  • Handphone allowance
  • Performance bonus
  • Meal subsidy
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