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QC Inspector

Apply now Job no: 613366
Work type: Permanent
Location: Chengdu
Categories: Quality & Regulatory, Asia Pacific, Individual Contributor

Accountability 1:   Incoming inspection of medical device

  • The essential information appears on the product label, is decipherable, clear, readable and cross referenced with the delivery‚Äôs packing list and confirmed as matching and comply with<Provisions for Instructions and Labels of Medical Devices> (Decree No.6 of China Food and Drug Administration)
  • Check the accuracy of Labelling Content
  • Check the Certificate of Conformity (COC)
  • Release medical device in computerised system

Accountability 2:   Incoming inspection of non-medical device

  • The essential information appears on the product label and comply with <Quality Law of the people's Republic of China >.
  •       Check the Certificate of Conformity (COC)
  • Release non-medical device in computerised system

 

Accountability 3:   Review the cleaning record of warehouse.

  • Verification of the temperature and humidity ranges set for the warehouse  to make sue the warehouse temperature and humidity are consistent with the requirements indicated in the instructions for use or the labelling.

Accountability 4:   Other tasks

  • Support to maintain the quality management system for China local commercial organization to comply with China GSP regulations and Corporate Quality Management System.
  • Work closely with cross-functional team to create, maintain and continual optimize China local SOP documents to meet with GSP regulation and business needs.
  • Conduct and/or support the staff training and education on regulations and quality system.
  • Performs a broad variety of tasks as assigned

Qualifications: 

Minimum:

  • Good skills on cross communication with team-work oriented;
  • Experience on Excel and Word knowledge
  • Warehouse experience

 

Ideal:

  • At least 1 years professional experience in quality assurance in medical device industry.
  • Solid knowledge on China medical device regulations especially for GSP regulations, familiar with global medical device regulations is preferred.

Advertised: China Standard Time
Anticpated Application Closing: China Standard Time

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