Mag. Anilkumar Dande

"CQV Consultant with extensive experience in commissioning, qualification, and validation of pharmaceutical equipment, utilities, and processes. Expert in developing, reviewing, and executing IQ/OQ/PQ protocols and reports, ensuring full compliance with cGMP, GxP, and regulatory standards."

"QA Validations Officer / CQV Engineer with hands-on experience in commissioning, qualification, and validation of pharmaceutical equipment, utilities, and processes. Skilled in IQ/OQ/PQ execution, protocol preparation, report documentation, and ensuring compliance with cGMP, GxP, and regulatory standards. Adept at supporting audits, maintaining validation lifecycle documentation, and collaborating with cross-functional teams to ensure quality and operational excellence."

"Experienced QA Sr. Officer with extensive expertise in validations and qualifications within the pharmaceutical industry. Skilled in IQ/OQ/PQ of equipment, utilities, and processes, ensuring full compliance with cGMP and GxP standards. Proficient in preparing, reviewing, and approving validation protocols and reports, supporting audits, and maintaining regulatory-ready documentation."

"QA Officer with hands-on experience in IQ/OQ/PQ validations, equipment and process qualification, and ensuring compliance with cGMP and GxP standards. Skilled in preparing and reviewing validation protocols and reports, supporting audits, and maintaining high-quality standards in pharmaceutical operations. Collaborative, detail-oriented, and committed to continuous process improvement."

"Detail-oriented and proactive Quality Assurance professional with hands-on experience in validations and qualifications in the pharmaceutical industry. Skilled in executing and documenting IQ/OQ/PQ protocols, ensuring GxP compliance, and supporting the release of high-quality pharmaceutical products. Adept at cross-functional collaboration, maintaining audit readiness, and implementing process improvements to meet regulatory standards."

Additional Details, Specialized in Pharmaceutical Chemistry and Biotechnology Strong knowledge of drug formulation, analytical techniques, and bioprocessing Hands-on experience with laboratory research, quality control, and documentation Familiar with GMP, GLP, and regulatory guidelines Skilled in spectroscopic and chromatographic techniques (HPLC, UV, IR) Strong analytical, problem-solving, and teamwork skills.