Medical Writer at Teva Pharmaceuticals, Bangalore – Apply Now!
Step into a purpose-driven career at Teva Pharmaceuticals, where innovation meets impact. We’re hiring a Medical Writer in Bangalore, India, to support the creation of essential clinical regulatory documents used in global drug development. If you’re passionate about scientific communication and want to contribute to public health, this is your opportunity to make a real difference.
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in the pharmaceutical industry, committed to improving health and increasing access to quality healthcare worldwide. With operations in nearly 60 countries and a diverse workforce representing a wide range of cultures and backgrounds, Teva is the world’s largest producer of generic medicines and a trusted provider of specialty pharmaceuticals. Every day, more than 200 million people rely on Teva’s medications, including many that appear on the World Health Organization’s list of essential medicines. At Teva, innovation is fueled by a mission to improve lives. The company integrates cutting-edge science with a deep understanding of patient needs, producing treatments that are both effective and accessible. With a robust pipeline of generic and branded drugs, as well as biosimilars, Teva continues to shape the future of medicine.
Joining Teva means being part of a purpose-driven organization that values integrity, collaboration, and excellence. Whether you’re working in research, manufacturing, regulatory affairs, or corporate strategy, your role at Teva has a direct impact on global health.
Job Details:
Job Role: Medical Writer
Location: Bangalore, India, 5600664
Company: Teva Pharmaceuticals
Job ID: 61562
The opportunity
- A Medical Writing Associate II, in Global Regulatory Medical Writing, writes and edits clinical regulatory documents. The individual provides basic-level guidance in the production of clinical research documentation used in drug development and product registrations.
How you’ll spend your day
- Primarily works at project level.
- Writes and edits clinical regulatory documents including study reports, protocols, briefing books, and other submission documents (e.g. aggregate reports, post authorization safety studies).
- Compiles, analyzes, and summarizes data from various sources.
- Conducts proofreading, editing, document formatting, and comment resolution.
- Ensures documents include the proper content and context (from a regulatory medical writing perspective) and clear and consistent medical/scientific messaging, are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards.
- May participate in the preparation/revision of document templates and SOPs.
- May train and support medical writers or external vendors/contractors on document planning, processes, and content development.
Your experience and qualifications
- Bachelor’s, Master’s, MD, PhD, PharmD in life sciences (or other related field)
- University degree with a minimum of 2+ years of relevant experience; advanced degree preferred.
- Experience with narratives, aggregate reports, and investigator brochures (IBs).
- 2+ years with an advanced degree preferred experience authoring protocols, clinical study reports, and submission documents.
