Position: Associate

Job type: Full-time

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Job content

  • MNC in Pharmaceutical industry
  • Full education training
  • Good team atmosphere
Responsibilities
  • Review of cGMP and other GxP documents to ensure company processes comply
  • Train and provide assistance to less experienced members of the QA team on quality procedures, protocols, and documentation
  • Coordinate investigation of quality issues with customers and suppliers
  • Review, approve and communicate root cause and corrective action to stakeholders
  • Deviation reporting, assist complaint investigation, report writing and review.
Experience

3-5 years Quality Assurance experience in Pharmaceutical industry.

PIC/s GMP experience is plus

English ability is plus

Education
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Deadline: 20-12-2024

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