Job Description

● Sampling and testing of raw materials and finished products using current pharmacopoeias (USP, BP). ● Preparing 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 generating 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.

Employment Type

  • Full Time

Details

To see more jobs that fit your career