Quality Analyst
Goa, India, 403722
Who we are
How you’ll spend your day
- Good Knowledge of Analytical Chemistry especially in Analytical method Development & Validation for Nitrosamine Impurities in Drug Substance and Drug Product and logical approach.
- Literature Search for development of analytical methods.
- Familiarity with computerized systems such as TrackWise, 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
Teva’s Equal Employment Opportunity Commitment