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Job Summary Job Description (1) Collect and review Device Master Record (DMR) documents for Medline products subject to the regulatory requirements and project development plan; (2) Establish inspection criteria of new finished products, update and maintain inspection
Job Responsibilities IPQC/FQC/OQC/Technician training & management Process quality management Customer audit & complaint handling FAIR/MEWR/MEMO/TECN/ECR process review DMR/RNR/CAR process review WI/SIP/SOP/CP revision Quality & efficiency improvement Job Requirements Education: Bachelor’s degree or above in electronics, machinery or
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