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Niche pharmacovigilance specialization reduces applicant pool despite a recognized global brand and Hyderabad location.
Pharmacovigilance and GxP compliance expertise makes candidates highly industry-specific and less transferable.
Explicit 8-14 years plus domain-specific safety, compliance, and platform experience required.
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Own end-to-end management of the Safety and Medical technology ecosystem, including backlog prioritization, delivery, enhancements, and operational performance for pharmacovigilance and medical affairs platforms.
Develop and maintain the technology roadmap aligned with R&D and Consumer Health strategy, ensuring compliance with regulatory and quality standards (GxP, CSV).
Lead continuous improvement, automation, and analytics initiatives to support scientific decision-making and operational efficiency within Safety and Medical functions.
8 - 14 years of relevant experience in Pharmacovigilance, Drug/Product Safety, Medical Affairs, or Medical Information technology.
Expertise with Safety and Medical platforms (e.g., Veeva Safety, ArisGlobal LifeSphere, Oracle Argus Safety) and strong understanding of Pharmacovigilance regulations, GxP compliance, and Computer System Validation (CSV).
Experience managing SaaS and enterprise technology products with Agile delivery methodologies.
Strong stakeholder management skills across Safety, Medical, Clinical, Regulatory, and Quality teams.
Experienced in managing complex, regulated Safety and Medical technology products with hands-on knowledge of compliance and validation processes.
Proven ability to partner cross-functionally with scientific, regulatory, and technical stakeholders to align technology solutions with strategic health and safety objectives.
Comfortable driving product strategy, Agile delivery, and digital innovation including AI-enabled solutions and advanced analytics within safety-critical environments.