Birendra Das

verified-iconBirendra Das

Senior Executive in Quality Assurance

Birendra Das is a Senior Executive in Quality Assurance with over 8 years of experience in the pharmaceutical and biotechnology sectors, specializing in GxP compliance, microbiology, and quality systems implementation. He brings strong expertise in deviation and CAPA management, regulatory audit readiness, validation documentation, and data integrity in FDA, EMA, WHO, and MHRA-regulated environments. Skilled in QMS operations, change control, microbial testing, and validation of cleanroom and cell bank processes, Birendra ensures robust compliance and process sustainability. With hands-on experience using LIMS, TrackWise, and eVALGENESIS, he delivers consistent quality oversight across manufacturing and microbiology operations.

FORMERLY AT

Onesource Specialty Pharma Ltd

LOCATION

Banglore,India

AVAILABILITY

Full Time

Skills

Audit Management Systems

EM Documentation Tools

eVALGENESIS

GMP Documentation Systems

LIMS

Microbiology Testing Instruments

QMS Tools

Work Experience

Senior Executive – Quality Assurance

Onesource Specialty Pharma Ltd

Dec 2023 – Present

  • Ensures compliance with FDA, EMA, and other regulatory agencies across microbiology and manufacturing operations.

  • Conducts internal audits, quality risk assessments, and QRM reviews.

  • Drafts and approves validation documents using eVALGENESIS.

  • Performs root cause analysis for deviations, OOS, and OOL cases.

  • Manages CAPA effectiveness, microbiology data review, and audit readiness.

TECHNOLOGIES

eVALGENESIS, QMS Tools, Audit Management Systems, GMP Documentation Systems

eVALGENESIS, QMS Tools, Audit Management Systems, GMP Documentation Systems

Biocon Biologics

Sep 2020 – Dec 2023

  • Led QMS activities including deviations, CAPA, change control, and failure investigations.

  • Conducted OOS, OOT, and deviation investigations using TrackWise.

  • Authored SOPs, specifications, and EMPQ protocols for cleanrooms.

  • Performed validation for cell banks (Human Insulin, Insulin Glargine, PEG-GCSF).

  • Ensured regulatory compliance (cGMP, cGLP, cGDP) and audit readiness.

  • Implemented and optimized LIMS (LABWARE, NOVA, TrackWise) for QC workflows.

TECHNOLOGIES

LABWARE LIMS, NOVA LIMS, TrackWise, EMPQ Tools, Validation Protocol Systems

Quality Control Officer

Emcure Pharmaceuticals Ltd.

Oct 2017 – Sep 2020

  • Conducted microbiological testing (microbial limits, water analysis, GPT).

  • Managed environmental monitoring and documentation for classified areas.

TECHNOLOGIES

Microbiology Testing Instruments, LIMS, EM Documentation Tools

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