HYDERABAD · FULLTIME
Medical Manager

Sandoz
Hyderabad · onsite · Posted 5d ago
Sourced from
Not disclosed2–4 yrsfulltimeHyderabad
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Section · 01
About this role
Your Key Responsibilities
Your responsibilities include, but not limited to:
What you'll bring to the role:
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, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported!
Join us!
Your responsibilities include, but not limited to:
- Timely renewal of the Marketing Authorizations as a part of the life cycle management activity of the products by providing documents viz.
- Clinical expert statements, non-clinical expert statements, addendum to clinical overviews.
- Providing support to the respond to the Deficiency letters received from the HA by preparing a literature-based robust scientific response document.
- Supporting the Global Labelling team in activities viz. harmonization of Product labels and Indication expansion activities.
- Providing quality documents with up-to-date scientific rigor supporting marketing authorisations; with minimal follow-up queries from stakeholders including HAs.
What you'll bring to the role:
- Candidate must have medical background and a good understanding of medical and pharmacological fundamentals
- Understanding of fundamentals of drug development and drug life-cycle management
- 2-3 years of medical writing/ regulatory medical writing experience; responding to HA queries/ deficiency letters; exposure to writing for peer reviewed journals is good to have
- Experience of working in a matrix set-up as an individual contributor,
- demonstratable learning agility and ability deliver in tight timelines
- Medical regulatory writing.
- Regulatory label updates.
- Critical-path thinking.
- Good working knowledge of MS-office suite
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, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported!
Join us!
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Section · 02
Skills
Medical Regulatory writingCritical-path thinkingRegulatory label updatesms office suite
Section · Company
About Sandoz

Sandoz
Pharma
1.8k+
employees
1886
140 years old
Basel, Basel-Stadt
CH
₹13L PA avg
Avg at Sandoz
About
Sandoz is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide.
Industries
Pharma
Employee ratings
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