BPharma & MPharma Job Vacancy in Bangalore at Teva Pharmaceuticals | Pharmacy Graduates Apply
Teva Pharmaceuticals, a global leader in generic medicines and healthcare solutions, is hiring a Quality Specialist II in Bangalore, India. This role offers the opportunity to ensure compliance with global quality standards, review critical pharmaceutical documentation, and collaborate with international teams. If you have substantial experience in QA/QC functions, method validation, and product quality reviews, this is your chance to advance your career with a trusted healthcare company.
- Job Position: Quality Specialist II
- Location: Bangalore, India – 560064
- Company: Teva Pharmaceuticals
- Job ID: 64031
About the Company
Teva Pharmaceuticals is the world’s leading manufacturer of generic medicines and a key producer of many products on the World Health Organization’s Essential Medicines List. Operating in nearly 60 countries, Teva ensures affordable healthcare for millions worldwide. Every day, over 200 million people benefit from Teva’s medicines, making a positive impact on global health and well-being.
Education:
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Master’s or Bachelor’s Degree in Pharmacy
Experience
- 2 to 8 years of experience in QA/QC functions within the pharmaceutical industry.
- Knowledge of worldwide cGxP regulations.
- Strong communication skills in English; proficiency in additional languages is a plus.
- Familiarity with computerized systems such as TrackWise, SAP, LIMS, and Global Insights.
- Hands-on experience in analytical method development, method validation, stability studies, equipment qualification, and product quality reviews.
- Ability to manage complexity and drive continuous improvements.
Quality Specialist Job Description
As a Quality Specialist II at Teva Pharmaceuticals, you will be responsible for reviewing pharmaceutical documentation to ensure compliance with corporate quality standards and compiling product quality reviews. The role requires collaboration with global QA/QC teams, contract manufacturers, and technical personnel to support Teva’s mission of delivering safe and high-quality medicines.
Quality Specialist Key Responsibilities
- Review CMC documentation, method development/validation protocols, stability protocols, and equipment qualification records.
- Ensure timely and compliant completion of Product Quality Reviews (PQRs) and Annual Product Reviews (APRs).
- Collaborate with Teva manufacturing sites, global quality units, and commercial affiliates for data collection and compliance.
- Liaise with third-party manufacturers and QA/QC teams worldwide to obtain documentation and address queries.
- Participate in change controls, deviations, SOP preparation, and self-inspections.
- Support training initiatives by preparing GMP training materials and conducting on-the-job training.
- Drive continuous process improvement and efficiency initiatives.
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