Our unwavering commitment to quality ensures the delivery of safe and effective products to patients, upholding a quality culture that adapts and evolves to meet patient needs
Job Summary
Our unwavering commitment to quality ensures the delivery of safe and effective products to patients, upholding a quality culture that adapts and evolves to meet patient needs.
The MQ TS Downstream Associate is responsible for primary contact of quality on the floor, particularly in Terminal sterilization, Visual Inspection and Packing areas of production, monitoring processes for compliance to cGMP standards.
The role includes performing batch start-up and end activities, equipment breakdown assessments, and identifying gaps to improve efficiency and reduce downtime.
Matching Summary
Our unwavering commitment to quality ensures the delivery of safe and effective products to patients, upholding a quality culture that adapts and evolves to meet patient needs.
Skills & Requirements
Must-have
cGMP compliance monitoring
Batch record review and release
Terminal sterilization process oversight
Visual inspection and packaging quality
Equipment audit trail review
Process troubleshooting abilities
Nice-to-have
Team environment collaboration
Process and procedure simplification
Effective written and oral communication
Key Requirements
M. Pharma or MSc degree
More than 1 year experience in pharmaceutical manufacturing quality assurance
Knowledge of current Good Manufacturing Practices (cGMP)