Quality Specialist Job at Teva Pharmaceuticals in Bangalore | BSc Life Science Graduates Apply
Teva Pharmaceuticals is hiring a Quality Sr Specialist in Bangalore, India. This is an excellent opportunity for life science graduates with experience in pharmaceutical QA and GMP environments to join a global leader in generic medicines. The role offers responsibilities across quality assurance, compliance, audits, and regulatory support, ensuring the highest standards in pharmaceutical manufacturing.
- Job Position: Quality Sr Specialist
- Location: Bangalore, India – 560064
- Job ID: 63710
- Company: Teva Pharmaceuticals
About the Company
Teva Pharmaceuticals is the world’s leading manufacturer of generic medicines and a trusted producer of many products listed on the World Health Organization’s Essential Medicines List. With operations in nearly 60 countries, Teva’s mission is to make healthcare more affordable and accessible, helping over 200 million people worldwide every day.
Education:
Bachelor’s degree in Life Sciences or related field.
Experience:
- 3–5 years of experience in a Pharmaceutical QA GMP environment.
- Equivalent education and/or relevant work experience may be considered
Quality Specialist Job Description
The Quality Sr Specialist at Teva Pharmaceuticals will be responsible for reviewing and approving validation protocols, reports, change controls, SOPs, batch records, and other critical quality documents. The role also
involves supporting audits, inspection readiness programs, regulatory compliance, and vendor approval processes.Quality Specialist Job Key Responsibilities
- The Quality Specialist is responsible for reviewing and approving method validation, transfer, and development study protocols and reports.
- Approve calibration, maintenance, validation, and qualification documentation for instruments and software.
- Review and approve cleaning validation, verification, and environmental monitoring data.
- Approve SOPs, test methods, specifications, master batch, and packaging records.
- Conduct QA release of raw materials, components, and finished products.
- Support audits, inspection readiness, and vendor approval programs.
- Create, revise, and manage SOPs and controlled documents.
- Train and maintain proficiency in computerized quality systems.
- Support metrics, KPIs, and corporate standards gap assessments.
- Perform additional tasks as assigned by the manager.
