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I am a Technical Project Manager with 10+ years of experience across pharmaceutical operations, quality systems, regulatory programs, drug launch support, analytics, and cross-functional project coordination. I thrive in healthcare environments and enjoy turning complex operational data into clear, strategic insights for leadership. I bring strong domain knowledge in healthcare and regulatory compliance, along with hands-on experience in KPI dashboards, data-driven reporting, and stakeholder communication. I excel at guiding end-to-end projects, mitigating risks, and aligning cross-functional teams to achieve launch readiness and sustainable performance.…I am a Technical Project Manager with 10+ years of experience across pharmaceutical operations, quality systems, regulatory programs, drug launch support, analytics, and cross-functional project coordination. I thrive in healthcare environments and enjoy turning complex operational data into clear, strategic insights for leadership. I bring strong domain knowledge in healthcare and regulatory compliance, along with hands-on experience in KPI dashboards, data-driven reporting, and stakeholder communication. I excel at guiding end-to-end projects, mitigating risks, and aligning cross-functional teams to achieve launch readiness and sustainable performance.

Pooja Dhamija

Project Manager, Data Analyst, Data Scientist, +3

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I am a Technical Project Manager with 10+ years of experience across pharmaceutical operations, quality systems, regulatory programs, drug launch support, analytics, and cross-functional project coordination. I thrive in healthcare environments and enjoy turning complex operational data into clear, strategic insights for leadership. I bring strong domain knowledge in healthcare and regulatory compliance, along with hands-on experience in KPI dashboards, data-driven reporting, and stakeholder communication. I excel at guiding end-to-end projects, mitigating risks, and aligning cross-functional teams to achieve launch readiness and sustainable performance.…I am a Technical Project Manager with 10+ years of experience across pharmaceutical operations, quality systems, regulatory programs, drug launch support, analytics, and cross-functional project coordination. I thrive in healthcare environments and enjoy turning complex operational data into clear, strategic insights for leadership. I bring strong domain knowledge in healthcare and regulatory compliance, along with hands-on experience in KPI dashboards, data-driven reporting, and stakeholder communication. I excel at guiding end-to-end projects, mitigating risks, and aligning cross-functional teams to achieve launch readiness and sustainable performance.

Available to hire

I am a Technical Project Manager with 10+ years of experience across pharmaceutical operations, quality systems, regulatory programs, drug launch support, analytics, and cross-functional project coordination. I thrive in healthcare environments and enjoy turning complex operational data into clear, strategic insights for leadership.

I bring strong domain knowledge in healthcare and regulatory compliance, along with hands-on experience in KPI dashboards, data-driven reporting, and stakeholder communication. I excel at guiding end-to-end projects, mitigating risks, and aligning cross-functional teams to achieve launch readiness and sustainable performance.

Skills

Experience Level

Expert

Expert

Expert

Expert

Expert

Expert

Expert

Intermediate

Language

English

Fluent

Hindi

Advanced

Work Experience

QA Head at Hind Pharma

January 1, 2024 - December 31, 2024

Led Quality Assurance operations while supporting regulatory documentation, compliance reporting, and manufacturing readiness initiatives. Managed regulatory documentation including DMF, SMF, validation protocols, and quality manuals. Developed Power BI dashboards to analyze quality trends, deviation patterns, and compliance performance metrics. Coordinated with production, engineering, supply chain, and regulatory teams to support product launch readiness and operational execution. Oversaw vendor qualification, supplier audits, and performance documentation. Prepared management reports and analytical summaries to support leadership reviews and audits.

Senior Executive – QA at Wyzon Biotics Pvt. Ltd.

February 1, 2023 - December 31, 2023

Supported regulatory documentation preparation and product dossier compilation activities. Coordinated with R&D and regulatory affairs teams to track product pipeline documentation and submission timelines. Prepared structured compliance reports and supported inspection readiness activities. Maintained documentation trackers and supported cross-functional coordination for audit preparation.

Executive – QA at Kaygee Labs Pvt. Ltd. (IPCA Group)

September 1, 2022 - January 31, 2023

Supported quality documentation and compliance tracking for manufacturing expansion projects. Monitored audit observations, CAPA progress, and regulatory readiness metrics. Prepared management reporting dashboards and documentation summaries. Coordinated cross-functional teams to ensure timely closure of compliance actions.

Executive – Corporate QA at Lupin Limited

November 1, 2021 - June 30, 2022

Provided project coordination support for corporate QA initiatives and system harmonization programs. Tracked CAPA closure timelines and compliance metrics across multiple manufacturing units. Supported audit preparation activities and regulatory inspection documentation reviews. Prepared performance summaries and management reports.

Senior Executive – QMS at Strides Pharma Science

February 1, 2020 - October 31, 2021

Managed validation documentation and compliance reporting projects. Supported data integrity initiatives and TrackWise system implementation. Coordinated CAPA investigations and audit compliance tracking. Prepared regulatory documentation summaries and performance reports.

Quality Control Analyst at Ind-Swift Limited

June 1, 2017 - February 29, 2020

Supported analytical validation projects and method transfer activities. Prepared regulatory documentation and technical reports for inspection readiness. Coordinated cross-functional review meetings and compliance documentation tracking. Maintained data accuracy and reporting standards.

Scientific Officer – QC at Panacea Biotech

October 1, 2015 - June 30, 2017

Supported new product introduction and technology transfer projects. Prepared SOPs, validation documentation, and calibration records. Coordinated testing activities with QA and R&D teams. Supported audit readiness and regulatory documentation preparation.