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Tier-1 employer and Bengaluru location increase applicants, but niche GxP validation reduces competition.
Strong GxP and pharmaceutical validation requirements limit cross-industry transferability.
Mandatory GxP/regulatory experience and validation expertise make shortlisting highly selective.
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Own one or more GxP-regulated business systems through their entire lifecycle, ensuring compliance and measurable business value.
Lead system release readiness including change control, validation evidence packaging, and post-release quality tracking to minimise business disruption.
Drive user adoption and continuous improvement using user feedback, support data, and maintain system scorecards for reporting and governance.
Experience in pharmaceutical, life sciences, or equivalent regulated industry with demonstrated GxP system validation expertise (DTMS, GAMP 5, or equivalent).
Bachelor's degree in scientific, technical, or business discipline; Master's degree or equivalent experience preferred.
Ability to manage systems/projects/products full lifecycle and translate business requirements into technical/process solutions.
Work Experience Required: Not explicitly mentioned in the JD.
Experienced in regulated environments managing GxP-compliant systems with strong understanding of regulatory standards (21 CFR Part 11, EU GMP Annex 11).
Capable of balancing strategic system investment decisions with operational execution and stakeholder management across global cross-functional teams.
Skilled in applying KPI/OKR frameworks and leveraging support analytics and usability assessments to optimize system performance and user experience.