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QA&QC Supervisor

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Onsite

QA&QC Supervisor

普业科技工程(北京)股份有限公司

QA&QC Supervisor

Skills

Testing & QACompliance

1 year ago

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Important information


Contract type:

Permanent

Location:

Shanghai, China

Work mode:

Onsite

Published on:

4 September 2026

What they need


该职位来源于猎聘 Job Description: PO Inspection: 1)Onsite and remote inspection for open orders and compile inspection report and upload the report into server on time. 2)Review inspection reports from QC team and work with the QC to determine whether any deviation/gaps from inspection protocol and minimum the errors in the report to improve the report quality. File the inspection reports to server. 3)Assist to file the inspection reports to server. 4)Assist to list upcoming shipment of open PO and make inspection plan bi-weekly. 5)Summary issues and protentional risk during team inspection and share with sourcing team monthly Compliant/Non conformity during shipment inspection Global sourcing 1)Follow up with suppliers to get CAPA about customer’s compliant 2)Follow up with suppliers of rework/CAPA from inspection issue.

Data Admin: 1)Assist to file the inspection reports to server. 2)Assist to list upcoming shipment of open PO and make inspection plan bi-weekly. QMS Audit(ISO13485)

  • Review suppliers’ documents and follow up 2)Pre-audit 3)Perform suppliers QMS audit when the supplier will be planned to qualified as approve supplier and evaluate whether their QMS is maintained effective or there is not any critical NC to impact the product safety and effectively. 4)Timely report your findings to management team. 5)CAPA follow up 6)Update QMS record list. CSR compliance audit: 1)Review suppliers’ documents and follow up 2)Pre-audit 3)CAPA Follow up 4)Timely report your findings to management team. 5)Update CSR record list Specification and Inspection procedure develop: 1)Work with Sourcing team to review the products related documents from supplier to develop internal specification and IP. 2)Issue the final document to supplier for their signature after the specification has been approved from management. Sampling: 1)Mass production sample saving.
  • Golden sample saving. Job Requirements: 1)Bachelor’s degree or above in Mechanical Engineering, or Material, or Industrial Engineer or medical device related engineering field required. 2)3+ years of working experience in quality-related positions is preferred. 3)Good understanding of quality system requirements (ISO 13485, ISO 9001 etc.) 4)Proficient in using Excel, Word and PowerPoint. 5)Excellent communication skills, meticulous and earnest in work, strong sense of responsibility and good team spirit. 6)CET-6 or above; candidates with strong English listening, speaking, reading and writing skills are preferred. 7)Those with medical industry working background will be given priority.

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