- Location
- Telangana (Sandoz), India
- Type
- Full-time
- Department
- Healthcare
- Experience
- 5+ years
- Closing date
- Today
- Source
- Workday
Description
Job Description Summary
Responsible for supporting Early Program Biosimilar Pipeline Support within the Medical Affairs Operations organization 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.Job Description
Responsible for supporting Early Program Biosimilar Pipeline Support within the Medical Affairs Operations organization 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:
Your responsibilities include, but not limited to:
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.
What you’ll bring to the role:
Essential Requirements:
Early Program analytical and writing outputs are completed effectively and in line with defined quality, timeliness, and stakeholder expectations.
Outputs are accurate, well structured, and aligned to intended use.
Information gathering, content synthesis, and documentation activities are completed reliably and within agreed timelines.
Team delivery remains coordinated, process-driven, and supported by appropriate stakeholder alignment.
Identified issues / gaps are addressed in a timely manner, with appropriate follow-up and continuous improvement actions.Education: Advanced degree or equivalent qualification in life science, healthcare, pharmacy, medicine, or related field preferred with 5–8+ years 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 savy, including high awareness of its limitations. Aware of specific confidentiality requirements of pipeline work.
Experience working in a cross-functional and global environment.
You’ll receive:
Breakdown of benefits received in this role. Include flexible working, learning and development opportunities as well.
Why Sandoz?
Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have an ambition to do more so that everyone can achieve the basic human right of good health.
With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help even more people 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 careers, where diversity of thought is welcomed and where personal growth is supported!
Join us, help us make healthcare fairer and faster.
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Skills Desired
Clinical Research, Clinical Trials, Curiosity, Databases, Drug Development, Job Description, Lifesciences, Medical Communication, Medical Information, Medical Writing, Military Intelligence, Patient Care, Physics, Technical SupportSkills
Clinical TrialsPatient Care
