Role & responsibilities

- Execute analytical method validation, method verification, and method transfer activities as per approved protocols.

- Perform stability studies and routine analytical evaluations for API and intermediate samples.

- Operate analytical instruments such as HPLC, UPLC, GC, GC-HS, and Dissolution Systems.

- Ensure accurate documentation and adherence to GMP, GLP, and Data Integrity requirements.

- Support laboratory investigations related to OOS, OOT, deviations, and atypical results.

- Prepare analytical reports, protocols, and supporting validation documentation.

- Participate in continuous improvement initiatives and maintain laboratory compliance.

Preferred candidate profile

- 3-5 years of experience in Analytical Method Validation within API/Pharmaceutical industries.

- Hands-on exposure to HPLC, UPLC, GC, GC-HS, Dissolution, and Stability Studies.

- Sound knowledge of GMP, GLP, Data Integrity, Method Validation, and Method Transfer.

- Robust analytical, troubleshooting, and documentation skills.

📌 Officer / Senior Officer - QC Analytical Method Validation (AMV) (Ahmedabad)
🏢 DISHMAN CARBOGEN AMCIS
📍 Ahmedabad