

To obtain a challenging and growth-oriented position in a progressive pharmaceutical organization where I can utilize my knowledge, technical skills, and dedication to achieve professional excellence while contributing effectively toward organizational goals and quality standards
Review and evaluate analytical raw data generated using Gas Chromatography (GC), High-Performance Liquid Chromatography (HPLC), Atomic Absorption Spectroscopy (AAS), Inductively Coupled Plasma Mass Spectrometry (ICP-MS), and Ultraviolet Spectroscopy (UV).
Review specifications, Standard Testing Procedures (STPs), Analytical Method Validation/Verification (AMV) protocols and reports, Analytical Method Transfer (AMT) protocols and reports, suitability protocols, General Testing Procedures (GTPs), and Standard Operating Procedures (SOPs).
Perform handling, documentation, and investigation of laboratory incidents, deviations in compliance with quality systems and regulatory requirements.
Manage and support change control procedures related to analytical methods, laboratory systems, instruments, and documentation.