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Tier-1 brand plus metro location but niche regulatory AI specialization limits applicant density.
Strong pharmaceutical GxP and CSV experience required makes cross-industry transfers difficult.
Multiple mandatory years, regulated-pharma experience, and specialized AI and validation skills enforce strict shortlisting.
Own the end-to-end requirements lifecycle for Applied AI initiatives within a regulated pharmaceutical environment, ensuring scalable, compliant, and high-performing AI solution delivery.
Manage AI project lifecycles including backlog prioritization, sprint goal setting, and acting as a Proxy Product Owner when required to align with strategic objectives.
Lead AI prompt engineering, agentic workflow prototyping, GxP compliance, risk management, and audit readiness activities to ensure data integrity and regulatory adherence.
8+ years of IT Business Analysis experience supporting enterprise software and system integrations.
5+ years experience working in highly regulated environments, preferably pharmaceutical, biotech, medical devices, or clinical healthcare sectors.
3+ years Agile/Scrum product delivery experience, including backlog management and user story writing.
Location requirement: Hyderabad, India; English communication at C1+ level.
Experienced in bridging complex AI technologies with life sciences regulatory frameworks in high-velocity agile teams using agentic SDLC practices.
Proven skills in product ownership, stakeholder facilitation, and translating between business and technical perspectives, with capability to act decisively as a Proxy PO.
Advanced knowledge of AI systems, LLM prompt engineering, GxP compliance, validation standards, and dynamic requirements management in regulated healthcare settings.