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Deepanshu Bhardwaj

@deepanshubhardwaj1

I drive GMP-compliant quality operations, batch release, and electronic quality systems for pharmaceutical manufacturing.

India

Message

What I'm looking for

I'm looking for a quality operations or quality assurance role where I can support GMP-compliant manufacturing, electronic quality systems, batch release, quality risk management, and inspection readiness.

I'm currently supporting Quality Operations at Novartis Healthcare, where I review GMP documentation and manage quality-system service requests in ESOPS, CONDOR, and Veeva Vault.

I create and review GxP documents, coordinate change controls through 1QEM, and support quality-operations transitions through training, stakeholder coordination, and process adoption.

Across Cipla, Baxter, and Alpa Laboratories, I've delivered batch release, deviation, CAPA, validation, audit readiness, and QA oversight for sterile manufacturing, filling, and packing operations.

Experience

Work history, roles, and key accomplishments

Current

Specialist - Quality Operations

Current

Novartis Healthcare Pvt. Ltd.

Mar 2022 - Present (4 years 6 months)

Hold accounts and perform service requests in quality systems like ESOPS, CONDOR and VEEVA VAULT, including format review of GMP/quality documentation. Create and review GxP documents, initiate and manage change control activities, and provide cross-functional quality support.

ESOPs Condor Veeva Vault 1QEM GMP Quality Operations Change Control Documentation Training

Senior Executive – Quality Assurance

Cipla Limited

Mar 2019 - Feb 2022 (2 years 11 months)

Performed end-to-end batch release activities, including review of batch manufacturing/packaging records, analytical results, deviations, OOS/OOT, CAPA and change controls. Coordinated batch disposition/release, managed data loggers, and handled nonconformance through TrackWise.

Trackwise Teamcenter CFS Batch Release Activities CAPA Deviations Change Control Data Integrity Process Validation Cleaning Validation Audit Readiness

Executive – In-Process Quality Assurance

Baxter Pharmaceuticals India Pvt. Ltd.

Oct 2015 - Feb 2019 (3 years 4 months)

Performed QA oversight activities across manufacturing, filling and packing operations, including line clearance and in-process parameter checks. Reviewed completed BMRs, BPRs, logbooks and operational printouts, and prepared trends for critical process variables.

GMP In Process Testing BMR BPR Review Line Clearance Process Monitoring Trend Analysis Audit Trail Review