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Quality System Specialist


  • Coordinate with suppliers and verify supplier quality standards are in accordance to the requirements

  • Track and qualify or disqualify suppliers according to standards

  • Liaise with suppliers or support the senior supplier qual specialist to support documentation compilation and GMP/GDP review per procedural requirements

  • Monitor supplier quality performance by tracking product defects, delivery failures and other recorded incidents involving the supplier's failure to meet requirements

  • Support document centre activities

  • Maintain accurate quality records, certifications and database records

  • Compiles Supplier Quality Reports for Management

  • Support regular and routine supplier quality audits to ensure compliance with regulatory standards, waste elimination and continuous improvement

  • Any other task as assigned by Supervisor/Manager

  • Based in Tuas

About You:

  • Bachelor Degree with at least 1-2 years' experiences in pharma or biotech facility preferably familiar with biopharma QA Operations.

  • Possess GMP systems knowledge with Supplier Quality Management concept

  • Knowledge of quality management system, supplier quality management, current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) in a pharma or biotech facility

  • Must be team player, meticulous, strong analytical and organizational skills

  • Enthusiastic, interested and committed to support Quality systems processes and potential participation in new product introduction activities

Submit your resume to
Only shortlisted candidates will be contacted. 
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