Quality Analyst Jobs at Teva | Chemistry Graduates Apply Now
Are you looking for Quality Analyst jobs in the pharmaceutical industry? Teva Pharmaceuticals is hiring a skilled Quality Analyst in Goa, India. This role is ideal for professionals with strong analytical chemistry knowledge who want to grow their careers with a global pharmaceutical leader.
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic medicines and specialty pharmaceuticals. With operations in nearly 60 countries, Teva plays a critical role in improving access to affordable healthcare worldwide. Teva Careers offers professionals the opportunity to work on essential medicines, follow strong quality systems, and grow within a regulated, innovation-driven pharmaceutical environment.
Quality Analyst
- Location: Goa, India, 403722
- Company: Teva Pharmaceuticals
- Job Id: 65835
Who we are
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a wide range of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million
people worldwide take one of our medicines every day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.How you’ll spend your day
- Good Knowledge of Analytical Chemistry, especially in Analytical method development and 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.
Your experience and qualifications
- 3-5 years of hands-on experience in analytical method development and validation.
- M.Pharm/ M.Sc Chemistry.
