Riyaz Ahamed

Analytical Chemist with 4+ years of experience in pharmaceutical industry in Analytical Research and Development and Quality control in Various Therapeutic Segments like Active Pharmaceutical Ingredients, Oral Solid Dosage and Oral Liquids.

Senior Research Associate - KAWMAN PHARMA - Cuddalore, Tamil Nadu.

(2026-02)

Regulatory Audits: WHO

• Establish the Method Development and Method Validation Analysis as ICH guidelines and Monographs.
• Perform the Stability Studies Analysis and all aspects of analytical methodology, Method transfer and troubleshooting pertaining to the Development.
• Performed Degradation studies to demonstrate specificity of analytical methods and identify degradation pathways of API.
• Co-ordinate with synthesis team to perform the routine analysis for the ongoing products using various techniques and ensure which meets the quality standards align within the timeline.
• Prepare the validation documents, method monographs and protocol for analytical method validations and transfers.
• Led the Periodic Calibration for HPLC, UPLC, GC, UV-Vis Spectrophotometer,FT-IR Spectrophotometer, pH meter and Analytical Balance as per SOP.
• Evaluate the analysis of working standard against primary reference standards utilizing validated analytical methods to verify batch quality and suitability for regular analysis.
• Document the Procedure, accurate results and Records in LIMS according to GLP and GMP guidelines, supporting traceability for maintain the ALCOA++.
• To report any non-conformity / incident immediate to superior for further act.

Executive - STRIDES PHARMA SCIENCE Ltd - Pudhucherry.

(2022-04 - 2025-10)

Regulatory Audits: USFDA, WHO, MHRA

• Conducted the analysis of Dissolution, Assay, Related Substance and Physical parameters for Stability Samples.
• Carried Out periodic calibration for Dissolution apparatus, HPLC, UPLC, GC, IC,UV-Vis spectrophotometer, FT-IR spectrophotometer, pH meter, auto titrator, and analytical balance as Per SOP.
• Supported IQ and Executed OQ, PQ.
• Document the Qualification procedures, Results, and batch records in LIMS according to GLP and GMP guidelines, supporting traceability and audit readiness.
• Supported for OOS, OOT, deviation, and other QMS investigations.
• Assisted in quality system maintenance, periodic logbook review, and training to ensure the Instrument calibration and maintenance records as per GLP schedules to guarantee data integrity.
• Responsible for timely submission, review, approved and release of reports related to product testing.
• Collaborated on internal audits, regulatory inspections, and self-inspection processes for sustained compliance.

M.Sc. - Chemistry - St . Joseph's college of arts and science (Autonomous) (2021-04)