Siddharth gupta

Hands-on experience in Quality Control Analytical Documentation, ensuring accuracy, compliance, and timely completion of all documentation activities. Skilled in sample receiving and handling, including verification, logging, and AR number generation as per departmental procedures. Knowledgeable in Stability Studies, including loading and unloading of stability samples, maintaining proper records, and ensuring conditions meet regulatory standards. Competent in preparing key QC documents such as data sheets, specifications, COAs, and other analytical documentation. Serving as Training Coordinator for the QC Analytical Department—managing training records, scheduling training sessions, and ensuring compliance with training SOPs. Responsible for maintaining and updating employee details and training documentation to support audits and regulatory inspections. Familiar with documentation practices aligned with GMP and GLP guidelines. Strong attention to detail, organizational skills, and ability to manage multiple tasks in a regulated environment.