Role & responsibilities :

Develop / Validate analytical methods for nitrosamines related activities using LCMS, GCMS, IC under guidance from senior team members.

Management of samples received from different sites for Nitrosamine project.

Testing of samples for nitrosamines related activities .

Trouble shooting of analytical instruments for difficulties faced during day-to-day operations.

Contribute in maintaining the prerequisites for Laboratory such as Column, Standards, Chemicals, Spares and Consumables etc.

Preparation of analytical protocols, reports, and technical documentation in compliance with regulatory standards.

Conduct routine instrument operation, calibration, and maintenance activities; escalate issues for troubleshooting.

Ensure accurate documentation of instrument usage, calibration records, and compliance.

Adhere to EHS guidelines and maintain secure laboratory practices.

Laboratory compliance and data integrity during day-to-day operations.





Participate in internal audits and contribute to readiness for external inspections.

Qualification:

M.Sc. In Chemistry or M.Pharm

Experience: 3-5 years of hands on experience in analytical method development and validation.

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.

📌 Quality Control Technician III (South Goa)
🏢 Teva Global Business Services
📍 South Goa