Roles & Responsibilities:
• Operate advanced analytical instruments such as HPLC, GC, ICP-MS for testing raw materials, finished products, and dosage forms.
• Perform method development, validation, and transfer for assays, related compounds, dissolution, and residual solvents.
• Prepare method development reports, study protocols, TT reports, and COA for development samples.
• Conduct stability analysis as per protocols and maintain accurate documentation in compliance with GLP and GDP.
• Participate in investigations, support continuous lab development through training, and adhere to SOPs.
• Manage laboratory inventory, raise procurement requests, and attend technical workshops to explore new techniques.
Qualification:
• Master’s degree in Science (MS/M.Sc) or M. Pharma preferred.
Experience:
• 5–7 years of experience in analytical method development, validation, and laboratory operations.
Skills:
• Good Laboratory Practices (GLP), Data Integrity, and Compliance – Advanced.
• Analytical Method Development & Validation – Intermediate.
• Documentation & Data Review, Interpretation, and Statistical Analysis – Intermediate.
• Stability Study Management – Advanced.
• Electronic Lab Notebook (ELN)/LIMS Management – Advanced.
• Adapts to organizational growth – Intermediate.
About the Organisation:
Amneal Pharmaceuticals is a global pharmaceutical company committed to innovation, quality, and compliance, delivering high-quality medicines while fostering a diverse and inclusive workplace.
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