Apply Now! Quality Assurance Job at Teva for B.Pharm & M.Pharm Candidates
Looking for a Quality Assurance Job in the pharmaceutical industry? Teva Pharmaceuticals is hiring for the position of Quality Specialist II in Bangalore, India. This excellent opportunity is ideal for candidates searching for B Pharm Jobs with 2–8 years of QA/QC experience. Eligible candidates with B.Pharm, M.Pharm, or other natural science qualifications can apply to work with a global biopharmaceutical leader, contributing to CMC documentation, Product Quality Reviews (PQR/APR), analytical method validation, and pharmaceutical quality systems while advancing their careers in a world-class quality environment.
- Job Title: Quality Specialist II
- Location: Bangalore, India
- ID: 68468
About the Company
Teva Pharmaceuticals is a leading global biopharmaceutical company with a strong presence in innovative medicines and one of the world’s largest generics businesses. The company focuses on advancing healthcare through innovation in neuroscience, immunology, and high-quality medicines while fostering a collaborative and inclusive work culture that supports professional growth and employee wellbeing.
Job Description
Teva is looking for a Quality Specialist II to support Global Quality Services by reviewing pharmaceutical quality documentation and ensuring compliance with corporate quality standards. The role involves reviewing CMC documentation, analytical methods, stability data, Product Quality Reviews (PQR/APR), Batch Manufacturing Records (BMR), and equipment qualification records while collaborating with global manufacturing sites and quality teams.
This Quality Assurance Job offers an excellent opportunity to work in a global pharmaceutical environment focused on quality compliance, continuous improvement, and regulatory excellence.
Key Responsibilities
- Review CMC documentation in a timely and compliant manner according to Teva Corporate standards.
- Review Method Development and Validation Protocols & Reports.
- Review Stability Protocols and Stability Reports.
- Review Instrument and Equipment Qualification records.
- Review Batch Manufacturing Records (BMR).
- Ensure Product Quality Reviews (PQR) and Annual Product Reviews (APR) are completed on time.
- Compile high-quality Product Quality Reviews and Annual Product Reviews.
- Retrieve quality and regulatory data from internal databases and systems.
- Coordinate with contract manufacturing organizations and global QA/QC teams for data collection.
- Recommend quality improvements to manufacturing sites and quality units.
- Collaborate with supervisors, managers, global quality units, commercial affiliates, and manufacturing sites.
Qualifications
- Bachelor’s Degree in Pharmacy (B.Pharm) or other Natural Sciences.
- Master’s Degree in Pharmacy (M.Pharm) or other Natural Sciences.
- 2–8 years of experience in QA/QC within the pharmaceutical industry.
- Basic knowledge of worldwide cGxP regulations.
- Good English communication skills.
- Good computer skills.
- Knowledge of TrackWise, SAP, LIMS, Global Insights, Glorya, or similar systems is an advantage.
- Understanding of pharmaceutical manufacturing, quality control, and contract manufacturing processes.
- Ability to manage complex quality processes and drive continuous improvement.
Preferred Skills
- Hands-on experience in Analytical Method Development.
- Method Validation for API and Finished Products.
- Stability Studies.
- Review of Instrument/Equipment Qualification records.
- Review of Batch Manufacturing Records (BMR).
- Experience in Product Quality Reviews (PQR/APR).
- Strong communication and collaboration skills.
