Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. APDC (TEVA Global Centre, Chennai) is high tech lab approved by USFDA & MHRA providing stability service for our global Teva network. Join TEVA Stability Team to learn and enrich your career in Quality.
Post : Quality Specialist, QC Analysts
Experience : 2 - 10 Years
Qualification : BSc / MSc / B.Pharmacy
Job Location : Hebbal, Bengaluru
Quality Specialist / Quality Sr. Specialist
• Compilation of high quality Annual Product Reviews (APRs), supporting quality system management with PQR Centre.
• Preparation & Review of SOPs and Its related documents, formulation plant experience.
• Liaising with third party contract manufacturers and QA personnel located globally for data collection required for compilation of APRs/PQRs PQRs.
• Review local SOPs and its related documents
• Recommend actions and professionally communicate to sites/Quality units.
QC Analysts
• Compilation and Review of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and system
• Ensure local Quality Management system is compliant with respective regulatory guidelines and Teva's Corp QMS (Gap Assessments).
• Performing self inspections of cross sectional departments as per timelines and verification of compliance report
• Prepare and Review the Training Materials for GMP training and on the job training.
Walk in Interview
Date : 18th June, 2023
Time : 09:00 am - 03:00 pm
Venue : Teva Pharmaceuticals, Brigade Senate 1, 2HWJ+V5V, Hebbal Kempapura, Bengaluru-560024
If unable to attend F2F interaction can share resumes to Apeksha.shinde@teva.co.in / snehal.mokashi@teva.co.in
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