Job Description
- Sampling and testing raw materials and finished products using current pharmacopeias (USP, 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 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 in 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.
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