Johnson & Johnson Careers

QA Supervisor

Suzhou, China
Quality Assurance

Job Description

Requisition ID: 1805687237W

  • Designs and develops procedures and processes for recording, evaluating, and reporting quality and reliability. Ensures quality databases and files are regularly maintained, including quality system integration;
  • Support to ISO 13485, J&J standards and China GMP implementation:
  • Maintain quality records on quality testing, nonconformance, project outcomes, and stakeholder input filed in an accurate and timely manner;
  • Documents and maintains standard operating procedures for interactions with operations team. Responsible for DHR review and compliance;
  • Collects and organizes data and prepares reports for assigned quality processes. Documents quality improvement to quality systems.
  • Co-ordinates effectiveness reviews & develops action plans
  • Conducts root cause investigations related to training & identify / implement corrective actions
  • Participate the document review related to process, facilities and utilities validation and qualification;
  • Perform all job duties in accordance with:
  • J&J policies on information, assets protection, maintain password confidential, protect critical business information;
  • All J&J policies and local regulations;
  • The policy of healthcare and environmental programs;
  • The code of conduct policies.
  • the duties assigned by supervisor according to business requirement.

  • Good communication skills and team work spirit;
  • Continuous and versatile ability;
  • Experience on GMP and ISO 13485 quality system;
  • Basic office software skill;
  • Good verbal and English skill for communication;
  • University degree or above;
  • 3 years or above experiences related document management in MDD or GMP environment.

Primary Location
Johnson & Johnson Medical Suzhou Ltd. (7054)
Job Function
Quality Assurance
Requisition ID