Life Sciences Jobs | Teva Pharma Hiring | Apply Now
Looking for rewarding Life Sciences Jobs in the pharmaceutical industry? Teva Careers has announced an opportunity for the position of Quality Specialist II in Bangalore. This role is ideal for professionals with experience in quality assurance and quality control who want to build their careers in global pharmaceutical quality systems. If you are seeking QA/QC Jobs with a leading biopharmaceutical company, this opportunity could be your next career move.
- Job Title: Quality Specialist II
- Location: Bangalore, India
- ID: 68467
About the Company
Teva Pharmaceutical Industries is one of the world’s largest generic medicine manufacturers and a leading biopharmaceutical company. The organization focuses on improving patient health through innovative medicines and high-quality pharmaceutical products. With operations across numerous countries, Teva combines scientific innovation, regulatory excellence, and quality-driven manufacturing to deliver healthcare solutions globally. The company offers employees a collaborative environment, strong career development programs, and opportunities to work on impactful healthcare initiatives.
Key Responsibilities
- Review CMC documentation and quality records.
- Review analytical method development and validation reports.
- Review stability protocols and stability study reports.
- Review equipment and instrument qualification records.
- Review Batch Manufacturing Records (BMR).
- Compile Product Quality Reviews (PQRs) and Annual Product Reviews (APRs).
- Collaborate with manufacturing sites and global quality teams.
- Support quality improvement initiatives.
- Ensure compliance with global quality management systems.
- Communicate quality-related findings and recommendations.
Qualification
- Bachelor Degree or Master’s Degree in Natural sciences
- 2 to 8 years of experience in QA / QC function in the pharmaceutical industry.
Skills Required
- 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 of manufacturing, QC and Contract manufacturing processes.
- Engagement to drive improvements and ability to manage complexity.
- Hands-on experience on Analytical Method development, Method Validation for API and FP of different analytical methods (e.g. Assay, impurities, dissolution etc.) & Stability Studies.
- Hands-on experience on Review of Instrument/Equipment qualification records.
- Basic knowledge / hands on experience of review of BMR.
- Basic knowledge / hands on experience on Product Quality Reviews.
For professionals seeking Life Sciences Jobs, this opening through Teva Careers offers an excellent opportunity to build expertise in pharmaceutical quality systems and compliance. The Quality Specialist II role combines quality assurance, regulatory documentation, and global collaboration, making it an attractive option for candidates interested in advancing their careers in QA/QC Jobs within the pharmaceutical industry.
