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Niche pharmacovigilance product expertise plus seniority reduces applicant pool despite metro location.
Role requires deep pharmacovigilance and medical affairs experience, so background fit is highly industry-specific.
Explicit 8–14 years plus regulated pharma and platform expertise creates high shortlisting strictness.
Own end-to-end management of Safety and Medical technology platforms, including backlog prioritization, agile delivery, and operational performance to support pharmacovigilance and regulatory compliance.
Develop and execute technology roadmap and strategy aligned with R&D and Consumer Health goals, including adoption of AI, automation, and advanced analytics.
Ensure compliance with GxP, data integrity, and regulatory requirements while leading continuous improvement, vendor management, and cross-functional stakeholder engagement.
8 to 14 years of relevant experience in Pharmacovigilance, Drug/Product Safety, Medical Affairs, or related domain.
Expertise with Safety and Medical technology platforms (e.g., Veeva Safety, ArisGlobal LifeSphere, Oracle Argus Safety) and understanding of Pharmacovigilance regulations and GxP compliance.
Experience managing SaaS and enterprise technology products within Agile methodologies.
Work Experience Required: 8-14 years. Notice period: Not explicitly mentioned in the JD.
Strong cross-functional collaboration skills working with Safety, Medical Affairs, Clinical, Regulatory, Quality, and Technology teams in a regulated environment.
Proven ability to balance compliance, innovation, and operational excellence in technology product management for safety and medical domains.
Experience implementing AI, automation, and advanced analytics in pharmacovigilance or medical affairs context, with global vendor and stakeholder management exposure.