משרות תוצאות חיפוש מתאימות לבקשתך:

The opportunity
 

We are currently looking for a Quality Assurance Group Specialist for our manufacturing site in Vilnius who will ensure company’s GMP compliance with regulated activities.
How you’ll spend your day
 

Batch release documentation management;
Work with international Teva team related to DP testing and release;
Review batch manufacture protocols, analysis protocols, MS&T protocols;
Investigation and troubleshooting of laboratory, manufacturing deviations corrective and preventive actions, complaints and change control Management; 
KPIs management, collaboration with QC for products cycle time management;
Stability review and documentation management;
Quality shop floor;
QC AT review.