Kuldeep Singh Dangi

WORK HISTORY

EDUCATION

ABOUT KULDEEP SINGH DANGI

Quality Control professional with 7+ years of experience in a USFDA-approved pharmaceutical manufacturing facility, specializing in GLP (Non-Routine Quality Control), regulatory compliance, audit readiness, and quality systems implementation.Currently working with Piramal Pharma Limited, I have hands-on experience supporting multiple global regulatory inspections, including USFDA, EU (FIMEA – Finland), WHO, DIGEMID (Peru), and CDSCO. My expertise includes data integrity (ALCOA+), Change Control (Trackwise), Pharmacopoeial evaluation and compliance (USP, EP, BP, JP, IP), investigations, CAPA management and risk-based testing strategies.I have successfully implemented and managed LabWare LIMS, Learning Management Systems (LMS), TrackWise, and SAP, ensuring inspection readiness, training compliance (EU GMP Chapter 2), and efficient QC operations. I have also contributed to laboratory cost optimization through vendor qualification and SAP-based procurement while maintaining GMP compliance.Certified LabWare LIMS 8 Administrator with hands-on experience in sample lifecycle management, Instrument Management, Lot management, Inventory Management, Stability Management.I am actively seeking international Quality Control opportunities and am open to relocation across Germany, Ireland, Netherlands, USA, and Australia, including employer-sponsored visa or job seeker pathways.