Quality System Specialist

Responsibilities:

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

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