Pharma Job Opportunity At Teva Careers | Quality Specialist Role | Apply Now
Looking for a pharma QA job with a global pharmaceutical company? Teva Careers is hiring a Quality Specialist II in Bangalore. This opportunity is ideal for B Pharm, M Pharm, and Life Sciences professionals with experience in pharmaceutical quality assurance, GMP compliance, CMC documentation review, and product quality management.
- Job Title: Quality Specialist II
- Job ID: 68467
- Location: Bangalore, India
About The Company
Teva Careers offers opportunities with one of the world’s leading biopharmaceutical companies, known for its innovative medicines and global generics business. Through this pharma QA job, professionals contribute to maintaining high-quality pharmaceutical products while working in a collaborative environment focused on quality, compliance, and continuous improvement.
Job Description
This pharma QA job at Teva Career focuses on reviewing pharmaceutical quality documentation, ensuring compliance with global cGxP standards, supporting Product Quality Reviews (PQR/APR), reviewing CMC documentation, and collaborating with manufacturing, quality, and regulatory teams across global sites. The role plays a key part in maintaining quality systems and ensuring regulatory compliance throughout the product lifecycle.
Key Responsibilities
- Review CMC documentation as per Teva quality standards.
- Review Method Development and Validation protocols and reports.
- Review Stability protocols and reports.
- Review Instrument and Equipment Qualification records.
- Review Batch Manufacturing Records (BMR).
- Prepare and compile Annual Product Reviews (APR) and Product Quality Reviews (PQR).
- Retrieve quality data from internal databases and quality systems.
- Coordinate with global manufacturing sites and contract manufacturers.
- Collaborate with QA, QC, Technical Support, and Commercial Quality teams.
- Recommend quality improvements and ensure regulatory compliance.
Eligibility Criteria
- Education: B Pharm, M Pharm, Bachelor’s or Master’s Degree in Natural Sciences
- Experience: 2–8 years in Quality Assurance or Quality Control within the pharmaceutical industry.
Required Skills
- Pharmaceutical Quality Assurance
- cGxP & GMP Compliance
- CMC Documentation Review
- Method Validation & Stability Studies
- PQR/APR & BMR Review
- Instrument Qualification
- Data Integrity & Quality Systems
- SAP, LIMS & TrackWise
- Analytical Documentation
- Communication & Collaboration
Why Join Teva?
Joining Teva Career through this pharma QA job allows you to work with one of the world’s leading pharmaceutical companies. You’ll gain exposure to global quality systems, collaborate with international teams, strengthen your expertise in GMP and regulatory compliance, and help deliver high-quality medicines that improve patients’ lives worldwide.
