Teva Quality Analyst 

India, Karnataka, Bengaluru 

996006795

• Ensures that the review of CMC documentation is completed in timely & compliant manner as per Teva CORP standards and related Guidance’s.
• Review of Method Development/Validation Protocols & Reports, Stability Protocols & Reports received from various Teva contracting sites, R&D units, Method Development & Stability Testing Centres.
• Review of BMR.
• Review of Instrument, Equipment Qualification/Calibration/maintenance
• Review of CSV documents
• Release of Materials
• Liaising with R&D Quality personnel located globally for data collection and arranging responses.
• Recommend actions and professionally communicate to R&D sites/ Quality units for continuous improvement in quality of products
• Receives guidance from Manager, Head GBS Quality and R&D Quality
  

• 5 to 10 years of experience in QA / QC function in the pharmaceutical industry
• Master’s Degree in Pharmacy or other natural sciences or Bachelor Degree in Pharmacy or other natural sciences
• Basic knowledge on worldwide cGxP regulations
• Good English language skills, other language skills could be helpful
• Good communication skills
• Basic knowledge of Computerised Systems. Knowledge of Systems in TEVA´s IT landscape (TrackWise, SAP, LIMS, Global Insights, Glorya etc.) would be of advantage
• Basic understanding R&D processes
• Engagement to drive improvements and ability to manage complexity

Associate Director Global Quality Function

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