Teva Quality Specialist Job For Pharma – Apply Online
Quality Specialist III
Date: Sep 25, 2024
Location: Bangalore, India, 560052
Company: Teva Pharmaceuticals
Job Id: 58499
Who we are
Together, we’re on a mission to make good health more affordable and accessible, helping millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries with a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.
The opportunity
Ensures that the Product Quality Reviews (PQRs) / Annual Product Reviews (APRs) for Teva products are completed in a timely and compliant manner as per Teva’s CORP Quality Management systems. PQR/APR compilation and approval must be well-coordinated with the Teva Manufacturing Sites, Global Quality Units, and Commercial affiliates to meet the targets and ensure compliance.
- Compilation of high-quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieving data from the Quality and regulatory databases and systems.
- Liaising with third-party contract manufacturers and QA personnel located globally for data collection required for compilation of APRs/PQRs.
- Recommend actions and professionally communicate with sites/Quality units for continuous improvement in product quality.
- Receives guidance from Supervisor, Group Leader, Manager Global Quality Services, Associate Director Global Quality GBS, other Managers in Quality Strategy & Shared Services, EMSO Quality affiliates, Commercial Quality EU & IM, and TGO sites.
How you’ll spend your day
- Data Requesting and Compilation of PQRs
- Compilation of high-quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieving data from Quality and regulatory databases and systems.
- Liaising with third-party contract manufacturers and QA personnel globally for data collection required for APRs/PQRs.
- Follow up with CMOs for the receipt of data within time.
- Check quotations received from CMO and initiate PR/PO for QP’s approval.
- Once data is received, responsible for filling the PQR receipt checklist and scheduling the PQR in SharePoint.
- Escalate PQR issues to Supervisor, Group Leader, Manager PQR Centre.
- Contemporaneous update of SharePoint database.
- Quality Management Systems
- Initiate the process of change controls and deviations.
- Prepare local SOPs and related documents.
- Participate in the self-inspection process.
- Performance Management
- Participate in continuous process improvement projects to improve the unit’s efficiency.
- Training
- Prepare Training Materials for GMP training and on-the-job training.
- Provide training on procedures as needed.
- Miscellaneous Support
- Any other tasks assigned by management for the smooth functioning of the team.
Your experience and qualifications
- 1 to 3 years of experience in QA/QC functions in the pharmaceutical industry.
- Master’s Degree in Pharmacy or other natural sciences, or Bachelor’s Degree in Pharmacy or other natural sciences.
- Basic knowledge of worldwide cGxP regulations.
- Good English language skills; other language skills could be helpful.
- Good communication skills.
- Basic knowledge of computerized systems. Knowledge of systems in TEVA’s IT landscape (TrackWise, SAP, LIMS, Global Insights, Glorya, etc.) would be an advantage.
- Basic understanding of manufacturing, QC, and contract manufacturing processes.
- Engagement to drive improvements and ability to manage complexity.
- Hands-on experience in PQR compilation would be preferred.
Link to Original Notification to apply: Apply Here
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