The Analyst must:
• Proficient in operating HPLC
• Ensures that all work is carried out in compliance with company Safety policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs).
• Analyse API, Raw Materials and Finished products for Assay, Impurities & Dissolution study using HPLC instrument with minimum supervision.
• Review technical data, documents, and proposals as required.
• Troubleshoot technical issues/ difficulties with methods.
• Coordinate with team members to perform method transfers between R&D group to QC group.
• Promote and maintain a safe and healthy working laboratory environment in compliance with established health and safety procedures.
• Strong interpretation of routine analysis or tests.
• Be able to write lab reports.
• Ability to work directly from the USP or EP pharmacopeia to write protocols and execute methods.
• Be able to work under GMP guidelines and be proficient with USP and pharmaceutical testing.
• Competent research and study skills to learn about innovative methodologies and equipment used for problem-solving and troubleshooting.
• Design, preparation, and production of study materials including procedure manuals.
• Responsible for the testing of raw materials, finished products and stability samples by instrumental and wet chemistry methods and described in compendia references or in-house methods.
• Perform other duties as assigned by the Laboratory manager.
Note : The Analyst will have over minimum 3 to 5 years of laboratory testing experience
Education:
MSc in Analytical Chemistry, or diploma in related filed.
A solid background and understanding of Chemistry is mandatory
Experience working with Pharmaceuticals.
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1 - 5 Years
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