Faraz Hussain
Cqv Engineer @Dechra
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WORK HISTORY
Cqv Engineer @Dechra
Spearhead end-to-end equipment lifecycle management—including procurement, transfers, qualification, and decommissioning—for CAPEX-funded initiatives within GMP-regulated environments.Ensure strict adherence to maintenance, calibration, and qualification schedules for QC instrumentation using systems such as BMRAM and CaliberLIMS, maintaining continuous inspection readiness.Manage third-party vendors for calibration, preventive maintenance, and qualification services, ensuring compliance with internal standards and regulatory expectations.Lead oversight of QC laboratory instrumentation; proactively monitor performance, troubleshoot technical issues, and support lab personnel to minimize downtime and ensure data integrity.Maintain alignment with site quality systems by authoring and reviewing deviations, initiating CAPAs, and partnering with QA for audits, inspections, and regulatory submissions.Drive implementation, execution, and continuous improvement of QC laboratory commissioning programs across chemistry and microbiology departments.Serve as CQV Subject Matter Expert (SME) for QC instrumentation, applying advanced knowledge of GMP system lifecycle from user requirement generation through validation and system retirement.Demonstrate extensive experience in GMP environments with a focus on QC Chemistry and Microbiology instrumentation, ensuring compliance with global quality standards.Lead investigations and resolution of QC instrumentation-related non-conformances, including OOS results, deviations, and quality events; contribute to robust root cause analysis and CAPA implementation.Act as a cross-functional liaison between QC labs, QA, manufacturing, and regulatory teams to ensure robust support of lab operations, audit readiness, and regulatory compliance.
ABOUT FARAZ HUSSAIN
Welcome to my LinkedIn profile! I\'m Faraz Hussain, a seasoned Validation Engineer with a…
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