Quality Assurance Jobs – Teva Quality Specialist Hiring
Teva Pharmaceuticals is hiring a Quality Specialist II in Bangalore, offering one of the most sought-after quality assurance jobs for life science graduates. This exciting opportunity gives you the chance to work with the world’s leading generic medicine manufacturer, making it an ideal pick for candidates seeking impactful life science jobs and high-growth Teva jobs in India.
- Job Title: Quality Specialist II
- Location: Bangalore, India, 560064
- Job ID: 64038
ABOUT THE COMPANY:
Teva Pharmaceuticals operates across nearly 60 countries, providing accessible and affordable healthcare solutions worldwide. As the world’s largest producer of generic medicines and a leading contributor to the WHO Essential Medicines List, Teva ensures over 200 million people receive quality medicines daily. The company values diversity, innovation, and global collaboration while continually working to improve health outcomes.
JOB OVERVIEW:
- Ensure timely and compliant completion of Product Quality Reviews (PQRs) and Annual Product Reviews (APRs) per Teva Corporate Quality Management Systems.
- Collaborate with Teva manufacturing sites, Global Quality Units, and Commercial Affiliates for PQR/APR compilation.
- Retrieve data from quality and regulatory databases and maintain high-quality review standards.
- Liaise with global QA/QC teams, third-party manufacturers, and technical support personnel for data collection.
- Provide recommendations for continuous product quality improvement.
- Maintain accurate and contemporaneous SharePoint updates and escalate issues when necessary.
EDUCATIONAL REQUIREMENTS:
- Master’s or bachelor’s degree in natural sciences.
- 2 to 8 years of QA/QC experience in the pharmaceutical industry.
- Basic understanding of worldwide cGxP regulations.
- Knowledge of computerized systems such as SAP, LIMS, TrackWise, and Global Insights is advantageous.
KEY RESPONSIBILITIES:
- Compile high-quality PQRs/APRs across multiple Teva manufacturing sites.
- Liaise with global QA teams and contract manufacturers for timely data collection.
- Initiate PR/PO processes and maintain PQR receipt records.
- Support change controls, deviations, SOP preparation, and self-inspection activities.
- Participate in process improvement initiatives and GMP training programs.
- Provide training on procedures and prepare training materials.
- Review analytical method development, method validation, equipment qualifications, stability studies, and BMRs.
- Assist in contract manufacturing quality processes and documentation.
- Ensure adherence to timelines, data accuracy, and Teva’s global quality standards.
This Quality Specialist II role at Teva offers an exceptional platform for professionals passionate about quality assurance and pharma excellence. If you want to grow globally, strengthen your expertise, and contribute to essential healthcare solutions, this Teva opportunity is the perfect match for your quality assurance jobs career path.
