Teva Pharmaceuticals has announced an opportunity for the position of Quality Specialist II in Bangalore. This pharmaceutical quality job is suitable for candidates with 2 to 8 years of QA/QC experience and an educational background in Pharmacy or Natural Sciences.
The Teva Quality Specialist II job involves reviewing CMC documentation, analytical method validation records, stability documentation, equipment qualification records, Batch Manufacturing Records (BMRs), and Product Quality Reviews (PQRs/APRs).
Candidates with experience in pharmaceutical Quality Assurance, Quality Control, analytical method validation, stability studies, cGxP compliance, BMR review, and PQR/APR preparation can consider this opportunity.
Key Responsibilities
As a Quality Specialist II at Teva, the selected candidate will be responsible for:
- Reviewing CMC documentation in a timely and compliant manner according to Teva corporate standards and applicable guidance.
- Reviewing analytical Method Development and Method Validation protocols and reports.
- Reviewing Stability Protocols and Stability Reports received from manufacturing sites, R&D units, and testing centres.
- Reviewing Instrument and Equipment Qualification records.
- Performing review of Batch Manufacturing Records (BMRs).
- Supporting timely completion of Product Quality Reviews (PQRs) and Annual Product Reviews (APRs).
- Compiling high-quality PQR/APR documentation for products manufactured at different manufacturing sites.
- Retrieving relevant information from quality and regulatory databases and systems.
- Coordinating with third-party contract manufacturers and global QA, QC, and technical support teams for data collection.
- Communicating recommendations to manufacturing sites and Quality Units to support continuous quality improvement.
- Working with supervisors, Global Quality Services, Quality Strategy teams, manufacturing sites, and commercial quality affiliates.
Qualification and Eligibility
Candidates interested in the Teva Quality Specialist II vacancy should meet the following requirements:
Educational Qualification
Candidates with either of the following educational backgrounds can apply:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- Bachelor’s degree in other relevant Natural Sciences
- Master’s degree in other relevant Natural Sciences
The official job description does not specify individual natural science disciplines. Candidates from related scientific backgrounds should assess whether their education and QA/QC experience align with the role.
Experience Required
Applicants should have:
2 to 8 years of experience in a QA or QC function within the pharmaceutical industry.
This means the position is primarily intended for experienced pharmaceutical QA/QC professionals rather than fresh graduates.
Skills Required
Teva is looking for candidates with knowledge or hands-on experience in:
- Pharmaceutical QA/QC
- cGxP regulations
- CMC documentation
- Analytical Method Development
- Analytical Method Validation
- API and Finished Product analytical testing
- Assay and impurity testing
- Dissolution testing
- Stability Studies
- Instrument/Equipment Qualification
- BMR review
- Product Quality Reviews (PQR)
- Annual Product Reviews (APR)
- Pharmaceutical manufacturing processes
- Contract manufacturing processes
- Computerised systems
- Quality documentation and compliance
Knowledge of systems such as TrackWise, SAP, LIMS, Global Insights, and Glorya would be an added advantage.
Good English communication skills and the ability to coordinate effectively with global teams are also important for this position.
Salary for Teva Quality Specialist II
Teva has not disclosed the salary range in the official job description.
For editorial reference, professionals with approximately 2–8 years of relevant pharmaceutical QA/QC experience in Bangalore may potentially see compensation in the broad range of approximately ₹5 lakh to ₹12 lakh per annum, depending on experience, current compensation, specialization, and interview performance.
Important: This is an editorial market estimate and is not an official salary range provided by Teva Pharmaceuticals. Candidates should confirm compensation directly with Teva during the recruitment process.
Benefits
According to Teva’s job description, employees may receive benefits including:
- Generous annual leave
- Employee reward plans
- Flexible working schedules depending on the role
- Access to health and wellbeing support
- Career development opportunities
- Learning programs
- Short-term internal projects
- Opportunities for internal career growth
- Access to Teva’s career development platform, Twist
- Opportunities to participate in community initiatives
Actual benefits may vary depending on role, employment terms, and company policies.
Why This Role Is Relevant for QA/QC Professionals
The Quality Specialist II position at Teva provides exposure to several important pharmaceutical quality activities, including CMC documentation, analytical method validation, stability studies, equipment qualification, BMR review, PQR/APR preparation, and global quality systems.
The position can be particularly relevant for professionals currently working in:
- Quality Assurance
- Quality Control
- Analytical Quality
- Pharmaceutical Documentation
- Stability
- Method Validation
- Manufacturing Quality
- Contract Manufacturing Quality
- Product Quality Review
How to Apply
