Medical Affairs Job at Sandoz
A rare chance has emerged for medical professionals as Sandoz seeks a Medical Affairs Analyst & Writer in Telangana, India. This Medical Affairs Job in Telangana focuses on supporting the Early Program Biosimilar Pipeline. Sandoz is inviting applications from qualified candidates with relevant experience in the pharmaceutical or healthcare industry.
About Sandoz:
Sandoz is a global leader in biosimilar and generic medicines, operating within the healthcare sector. The organisation is dedicated to delivering affordable medications, impacting the lives of over 1 billion people across more than 100 countries. With a commitment to innovation and sustainability, Sandoz aims to enhance access to high-quality healthcare solutions worldwide.
Job Details:
- Job Title: Medical Affairs Analyst & Writer
- Job ID: REQ-10030919
- Location: Telangana, India
- Job Type: Full-time
- Employment Type: Regular
Job Description:
Responsible for supporting Early Program Biosimilar Pipeline Support within the Medical Affairs Operations organisation based out of GCC India. The role supports analytical, scientific, and medical writing activities and contributes to accurate, timely, and fit-for-purpose outputs aligned to project objectives and stakeholder needs.
Your Key Responsibilities:
- Support medical writing, analytical, desk research, and competitive intelligence activities in line with defined project objectives and quality expectations.
- Perform evidence gathering, information review, and analysis across relevant medical and scientific topics.
- Support synthesis of information into summaries, content pieces, slide-based materials, and other fit-for-purpose outputs.
- Contribute to development of molecule overviews, insight summaries, and other Early Program biosimilar support materials.
- Support timely and aligned delivery of outputs in collaboration with team members and relevant stakeholders.
- Use relevant databases, analytical platforms, and AI-enabled tools responsibly to support information gathering, analysis, and synthesis, as applicable.
- Maintain documentation quality and follow confidentiality requirements when handling proprietary or pipeline-related information.
- Contribute to knowledge sharing, process consistency, and continuous improvement across the Early Program support stream.
Essential Requirements for the Medical Affairs Job:
- Advanced degree or equivalent qualification in medicine, or related field preferred, with 5–8+ years of experience in the pharmaceutical/healthcare industry, ideally with 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, including high awareness of its limitations.
- Aware of specific confidentiality requirements of pipeline work.
- Experience working in a cross-functional and global environment.
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