MPharm Job at Teva Pharmaceuticals | Apply Now for the Quality Analyst Role
Teva Pharmaceuticals is hiring a Quality Analyst for its facility in Verna, Goa. This MPharm Job focuses on Nitrosamine impurity analysis, a critical regulatory area in 2026 for both Drug Substances and Drug Products. Candidates with an M.Pharm or M.Sc. and 3–5 years of experience will lead analytical method development and validation using high-sensitivity techniques like LC-MS/MS to ensure global patient safety and cGMP compliance.
- Job Post: Quality Analyst
- Location: Goa, India, 403722
- Job Id: 65835
About The Company
Teva Pharmaceuticals is the world’s leading manufacturer of generic medicines, driven by a mission to make health more affordable and accessible to millions. With a global presence in nearly 60 countries and a diverse workforce of 37,000 employees, Teva provides essential treatments to approximately 200 million patients every single day. The company is a proud producer of numerous medicines on the World Health Organization’s Essential Medicines List (EML), bridging the gap between innovative biopharmaceuticals and affordable healthcare solutions.
Roles and Responsibilities
- Good Knowledge of Analytical Chemistry, especially in Analytical method Development & Validation for Nitrosamine Impurities in Drug Substance and Drug Product and a logical approach.
- Literature Search for the development of analytical methods.
- Familiarity with computerized systems such as TrackWise and Veeva Vault.
- Experience in cGMP/GLP environments and regulatory-compliant documentation.
- Strong attention to detail and ability to work effectively in a team setting.
- Good communication skills (oral and written).
- Sound knowledge of pharmaceutical Quality System, ICH guidelines, etc.
Experience and Qualifications
- 3-5 years of hands-on experience in analytical method development and validation.
- M.pharm
Benefits of This Role
Joining Teva Pharmaceuticals as a Quality Analyst offers the unique opportunity to become a specialist in Nitrosamine impurity analysis, one of the most critical and high-demand regulatory focus areas in modern pharmacy. Working for the world’s leading generic medicine manufacturer, you will master advanced high-sensitivity techniques like LC-MS/MS, positioning yourself as an expert in analytical method development and validation. Beyond the technical exposure, this role allows you to contribute directly to the safety of over 200 million patients daily while gaining invaluable experience with industry-standard digital systems like TrackWise and Veeva Vault.
