- Method Development and Optimization using HPLC.
- Method Validation as per regulatory and ICH guidelines.
- Preparation, review, and technical input for Specifications and Methods of Analysis (MOA).
- Execution of GLP-related activities including instrument calibration, qualification, and standard management.
- Preparation and review of analytical documentation, protocols, and reports.
Preferred candidate profile
- M.Sc. (Analytical / Organic Chemistry) / M.Pharma.
- 0 to 8 years of experience in ADL within the API/Pharmaceutical industry.
- Hands-on experience with HPLC and analytical method development & validation.
- Sound knowledge of GLP, regulatory requirements, and laboratory documentation.
📌 Walk-in || Analytical Development Laboratory (Vadodara)
🏢 Ami Lifesciences
📍 Vadodara
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