Debiprasad Pani
Senior Executive at Micro Labs Limited
Anekal
7+ years of work experience
Sep 20251 y 1 moPresent
Bangalore
• Manage QMS activities including deviations, change controls, CAPA, investigations and associated quality documentation.
• Perform/support equipment qualification, process validation, cleaning validation and computerized/software qualification activities, as applicable to assigned projects.
• Support GMP-compliant quality processes, risk assessments, investigation workflows and cross-functional remediation.
• Electronic manufacturing / quality systems: eBMR, eLog, eQMS and eValidation exposure.
• Development / implementation exposure: Calibre eLog, Leucine eBMR and Leucine eLog.
• Transferable domain knowledge: GMP manufacturing processes, QMS workflows, validation requirements, electronic documentation and the interaction between manufacturing users, QA requirements and computerized systems.
• CSV / computerized systems: qualification and software-related exposure; experience level should be described according to the specific activities personally performed.
Feb 20257 mosAug 2025
Shamirpet, Telangana, India
Led QMS activities for manufacturing operations and supported compliance with quality and regulatory requirements.
• Handled equipment qualification, SOP preparation and validation-batch activities, connecting manufacturing requirements with quality
documentation.
• Provided training and cross-functional support on quality processes and procedures.
Computerised Systems Exposure : Nichelon • Calibre DMS • Calibre eBMR • Calibre eLog • Calibre QMS •
Apr 20231 yr 11 mosFeb 2025
Bengaluru, Karnataka, India
• Managed manufacturing operations across granulation, compression, coating and capsule filling, providing practical understanding of
end-to-end manufacturing workflows.
• Handled manufacturing QMS activities, equipment and software qualification, process validation and cleaning validation.
• Participated in audit readiness, compliance activities and internal/external audits.
• Contributed to development and implementation of e-BMR and e-Log systems, providing direct exposure to digitalization of manufacturing
documentation and workflows.
Computerised Systems Exposure : Compliancewire. eValidation (ValGenesis) • DocPro • TrackWise •
ComplianceWire • eConnect
Development / implementation exposure: Calibre eLog • Leucine eBMR • Leucine eLog
Transferable domain capability: Understanding of GMP manufacturing processes, QMS workflows, validation requirements, electronic
documentation and the interaction between manufacturing users, QA requirements and computerized systems.
Oct 20202 yrs 6 mosMar 2023
Bengaluru, Karnataka, India
• Managed compression and granulation operations with focus on GMP and quality compliance.
• Handled change controls, deviations, incidents and OOS investigations and performed RCA/corrective actions for OOT events.
• Developed practical understanding of production processes, documentation and quality-system requirements.
Systems: Nichelon • Calibre DMS • Calibre eBMR • Calibre eLog • Calibre QMS
Apr 20191 yr 7 mosOct 2020
Chennai, Tamil Nadu, India
Handled compression and granulation operations and supported shop-floor GMP compliance.
• Managed deviations, change controls, investigations and OOS/OOT events and executed SOP revisions.
• Built foundational experience in manufacturing processes, documentation and quality-system workflows.
Debiprasad’s AI Stack
Education
M.Pharm, Pharmaceutical Sciences
Institute of Pharmacy and Technology (IPT), Salipur
20172 yrs2019
Bachelor of Pharmacy - BPharm, Pharmaceutical Sciences
Institute of Pharmacy and Technology, Salepur
20134 yrs2017
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