Conduct routine analysis of raw materials, intermediates, and finished products using techniques like HPLC, GC, UV, IR, and titration.
Ensure compliance with cGMP, ICH, and regulatory standards during testing and documentation.
Prepare and review Certificates of Analysis (CoA), standard operating procedures (SOPs), and test protocols.
Maintain laboratory instruments through regular calibration and validation.
Support vendor qualification by testing excipient samples and preparing evaluation reports.
Participate in investigations of out-of-specification (OOS) results and deviations.
Qualifications :
Bachelor’s or Master’s in Chemistry, Pharmaceutical Sciences, or related field.
1–5 years of experience in pharmaceutical QC, preferably in API or excipient testing.
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Quality Quality Control • Surat, Gujarat, India
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