Sandoz Benefits Overview

Owns the Veeva Clinical application lifecycle, including solution design, roadmap development, governance, integrations, data migrations, operational support, and continuous optimization. Provides technical leadership to stakeholders, vendors, engineers, and configurators while ensuring alignment with enterprise architecture, regulatory requirements, audit readiness, and business objectives. Leads global delivery and methodology improvements within Sandoz’s STEP transformation program.

Drive compliant healthcare and pharmaceutical sales by identifying high-potential healthcare professionals, building customer relationships, personalizing engagement, gathering insights, and developing value-added solutions. The role uses data to prioritize accounts, collaborates cross-functionally, supports customer and patient needs, and maintains ethical conduct aligned with the Sandoz Code of Ethics.

Manage regulatory life-cycle activities and marketing authorizations for a defined portfolio across five Nordic countries. Responsibilities include CMC documentation, safety updates, text management, health-authority responses, regulatory submissions, change controls, deviations, and compliance with Nordic and European legislation. The role partners closely with Global Regulatory Affairs, Supply Chain, QA/QC, and Commercial teams while providing regulatory guidance and ensuring timely implementation of approved product information.