QA/ QC System Expert

Haleon; Gurgaon; On-site; INR 1,200,000 - 2,000,000; Full time

Job summary

Haleon is seeking a QA Digital Expert to drive digital transformation within Quality Assurance. You will implement and optimize systems like eQMS, LIMS, and MES to improve data integrity and compliance with GMP and regulatory expectations.

You will collaborate with IT and QA to define requirements and ensure smooth integration across manufacturing, QC and QA. The role emphasizes data governance, paperless processes, CSV validation, and analytics-driven continuous improvement, with

Qualifications

• Bsc/Msc Science graduate with 3+ years of experience in manufacturing, QA, or technical operations.

Responsibilities

• Lead digital QA systems implementation (eQMS, LIMS, QMS software) and ensure integration across manufacturing, QC and QA.
• Ensure ALCOA+ data integrity and regulatory compliance through governance and audits.
• Drive paperless initiatives (electronic batch records, digital workflows) and automate deviations, CAPA, change control, and training management.
• Ensure CSV compliance and review validation docs (URS, IQ/OQ/PQ) for GMP systems.
• Use data analytics to identify trends, risks, and opportunities; develop KPIs and dashboards for quality metrics.
• Oversee QA document management, instrument calibration planning, and SOP reviews.

Skills

Digital QA systems

Data integrity

Process digitalization

System validation

Analytics

Leadership

Education

BSc/MSc in Science

Tools

SAP QM

SAP QR Lane

Smart LIMS

Proficy

Veeva

Job description

## QA/ QC System ExpertApplylocations: India - Haryana - Gurgaontime type: Full timeposted on: Posted Todaytime left to apply: End Date: August 28, 2026 (29 days left to apply)job requisition id: 546539Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.**About the role**The QA Digital Expert is responsible for driving digital transformation initiatives within the Quality Assurance function. This role focuses on implementing, managing, and optimizing digital quality systems (eQMS, LIMS, MES) to enhance compliance, data integrity, and operational efficiency in alignment with GMP and regulatory requirements**Role Responsibilities****Project Start Up Phase:*** Timely input to the process/ equipment’s quality system requirements.* Ensures that appropriate systems are implemented and maintained* Ensures the right validation protocols are developed for the new site validation and documentation.* SAP QM Master data Set Up* SAP QR Lane Set Up* Smart LIMS Set Up for Lab Instruments* Proficy Set Up* VEEVA Set Up For Plant and regulatory Licenses**Once the site is operational: Commercial production****1. Digital Quality Systems Implementation*** Lead implementation and enhancement of digital QA systems (eQMS, LIMS, QMS software, TrackWise, Veeva, etc.).* Collaborate with IT and QA teams to define system requirements and workflows.* Ensure smooth system integration across manufacturing, QC, and QA functions.**2. Data Integrity & Compliance*** Ensure compliance with ALCOA+ data integrity principles and regulatory expectations (USFDA, MHRA, EU GMP).* Design and monitor data governance frameworks.* Conduct periodic data integrity audits and risk assessments.**3. Process Digitalization*** Drive paperless initiatives (electronic batch records, electronic logbooks, digital workflows).* Automate quality processes such as deviations, CAPA, change control, training management.* Improve data visibility through dashboards and reporting tools.**4. System Validation & Compliance*** Ensure CSV (Computer System Validation) compliance for all GxP systems.* Review and approve validation documentation (URS, IQ/OQ/PQ, validation reports).* Maintain audit readiness for computerized systems.**5. Analytics & Continuous Improvement*** Utilize data analytics to identify trends, risks, and improvement opportunities.* Develop KPIs and dashboards for quality metrics.* Support predictive quality and risk-based decision-making.* Should be able to handle team**6. QA Document management*** Lab Equipment PM and Calibration Planner* Reviews Operational, Quality etc SOP* Reviews QMS Document as and when needed* Issue and retrieval of control copies***Why you?*****Basic Qualifications:*** Bsc/Msc Science Graduate with 3+yrs of experience* Experience in the healthcare/FMCG industry in the area of manufacturing, quality or technical operations.* Experience with eQMS* Knowledge of LIMS, SAP, Proficy systems* Strong understanding of Computer System Validation (CSV / CSA)* Familiarity with data integrity principles (ALCOA+)* Basic understanding of analytics / BI tools**Preferred Qualifications:*** Detail-oriented with analytical mindset* Excellent documentation and compliance knowledge* Problem-solving and decision-making skills* Effective communication and stakeholder management**Job Posting End Date**2026-08-28