● Sample and test raw materials and finished products using current pharmacopeias (USP, and BP).
● Prepare quality reports, including analytical reports, certificates of analysis (CoA), and stability reports.
● Participate in out-of-specification and failure investigations and recommend corrective actions.
● Assist in authoring and finalizing departmental SOPs.
● Assist in method development and method validation test protocols for finished products and generate the appropriate analytical methods.
Requirements
● Bachelor's or Master’s degree in Chemistry.
● Gender preference: Male.
● Ability to work night shifts.
● 1 year of experience in pharmaceutical or related industry.
● Working knowledge of laboratory equipment (including HPLC and GC) is a plus.
● Good command of English.
● Committed to learning and development.
● Ability to work accurately in a busy and demanding environment, adhering to strict deadlines.
