Performing internal audits and inspections.Conducting risk assessments and developing risk assessment reports for the use of prohibited or restricted substances, ensuring adherence to safety protocols.Manage and maintain Corrective and Preventive Actions (CAPAs) to ensure quality control and regulatory compliance.Review and approve Deviations and Non-conformances.Coordinate and execute Change Controls (CCRs).Creating, review and maintenance of Standard Operating Procedures (SOPs) and Pharmaceutical Test Methods (PTMs) to uphold consistent processes and accuracy. Performing instrument or spreadsheet validation including writing Requirement Specification (RS), Installation Qualification and Operation Qualification Protocol (IQOQ).Conducting calibration and maintenance of instruments and writing and updating Instrument Performance Reviews (PERs) to assess instrument efficacy and accuracy.

Assisting QA manager with documentation, audits, record maintenance and records review.Writing, review and maintenance of Standard Operating Procedures (SOPs) and Pharmaceutical Test Methods (PTMs). Development, implementation and validation of analytical test procedures for the analysis of pharmaceutical raw material and finished products.Mentoring and training laboratory staff with testing procedures and analytical instrumentation.Performing chemical testing on raw materials and finished products and testing to evaluate product stability in accordance with BP, USP, EU and JP monograph as well as customer supplied and in-house methods.

Performing Chemical testing on raw materials and finished products using HPLC, UPLC, GC/GCMS, GF/AAS, TOC, UV-Vis, FT-IR and TLC in addition to a wide variety of wet chemical techniques.Development, implementation and validation of analytical test procedures for the analysis of pharmaceutical raw material and finished products.

Performing chemical testing on raw materials and finished products and testing to evaluate product stability in accordance with BP/USP monograph or approved methods. Sample analysis using instruments such as HPLC, GC/GCMS, GF-AAS, TOC, UV-Vis, FTIR and TLC in addition to a wide variety of wet chemical techniques.

Clinical research on stability study samples.Regular audits and inventory control of specimen collection.Standard operating procedure (SOP) writing.Processing samples according to specified procedures.