Your responsibilities include, but not limited to:
Review and assess local country labels to identify deviations from the core labeling and propose topics for further cross-functional assessment during the periodic core labeling review process
Contribute to DRA activities regarding Sandoz safety risk communications/portfolio stewardship activities having labeling impact for their assigned projects/products.
Contribute to the creation of high quality documents supporting changes with internal and/or external experts including the preparation of responses to labeling related Health Authority queries
Ensure that key country label proposals which deviate from a proposed CDS or CDS amendment/update (e.g., US PI, EU SmPC) are brought to the attention -A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways.
Networks with senior internal and external personnel in own area of expertise.
Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt
Distribution of marketing samples (where applicable)
Essential Requirements
What you’ll bring to the role:
Cross Cultural Experience.
8+ years of relevant experience
People Challenges.
Functional Breadth.
Project Management.
Collaborating across boundaries.
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more
With investments in new development capabilities, production sites, current acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help m
📌 Global Labelling Manager (India)
🏢 Sandoz India
📍 India
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