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Medical Writer Job at Sandoz

Looking for a rewarding Medical Writer Job in the pharmaceutical industry? Sandoz is hiring a Medical Affairs Analyst & Writer for its Global Capability Centre in Telangana. This opportunity is ideal for experienced professionals passionate about scientific writing, evidence synthesis, and medical communications. If you’re exploring Sandoz Careers or seeking impactful Medical Affairs Jobs, this role offers the chance to contribute to global biosimilar programmes and innovative healthcare solutions.

Sandoz is a global leader in generic medicines and biosimilars, committed to making high-quality healthcare more accessible across the world. Operating in more than 100 countries, the company combines scientific innovation with affordability to improve patient outcomes. Through Sandoz Careers, professionals work on cutting-edge pharmaceutical projects in a collaborative environment that encourages continuous learning, innovation, and excellence across various Medical Affairs Jobs and scientific functions.

Company Sandoz Position Medical Affairs Analyst & Writer Job REQ
- Location Telangana, India Employment Type Regular Job Type Full-Time Shift Day Shift Department Medical Affairs Operations

The Medical Writer Job at Sandoz is an exciting opportunity for professionals with experience in medical writing, analytical research, and Medical Affairs. As a Medical Affairs Analyst & Writer, you will support the Early Program Biosimilar Pipeline by developing scientific content, conducting evidence reviews, and preparing analytical outputs for global stakeholders. This role is ideal for candidates interested in Medical Affairs Jobs within a leading multinational pharmaceutical company.

• Support medical writing, desk research, and analytical projects aligned with business objectives.
• Gather, review, and analyse scientific and medical literature.
• Develop evidence summaries, scientific reports, presentations, and content materials.
• Prepare molecule overviews and competitive intelligence reports for biosimilar programmes.
• Collaborate with global stakeholders to ensure timely project delivery.
• Utilise databases, analytical platforms, and AI-enabled tools responsibly.
• Maintain high-quality documentation while ensuring confidentiality of proprietary information.
• Contribute to process improvements and knowledge-sharing initiatives across Medical Affairs.

• Advanced degree or equivalent qualification in healthcare, medicine, or related field preferred, with 5–8+ years of experience in the pharmaceutical or healthcare industry.
• Experience in analytical writing, medical writing support, desk research, competitive intelligence support, and/or related Medical Affairs support models.
• Good understanding of information gathering, content synthesis, scientific/analytical writing, and structured output development.
• Exposure to diverse medical and scientific domains, ideally including biosimilars, oncology, immunology, or related therapeutic areas.
• Artificial Intelligence savvy, with a high awareness of its limitations and confidentiality requirements of pipeline work.
• Experience working in a cross-functional and global environment.

• Medical and scientific writing
• Literature review and evidence synthesis
• Analytical thinking
• Medical Affairs knowledge
• Competitive intelligence
• Scientific communication
• Research methodology
• AI-enabled information analysis
• Attention to detail
• Project management
• Cross-functional collaboration
• Excellent written and verbal communication skills