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.