Job Description
Responsibilities:
● 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.