Senior Medical Writer Position at Teva Pharmaceuticals in Bangalore – Apply Now!
Looking to grow your career in the pharmaceutical industry? Join Teva Pharmaceuticals, the world’s leading manufacturer of generic medicines, as a Senior Medical Writer in Bangalore, India. This is your chance to work on global regulatory documentation that impacts millions of lives every day. With your expertise in medical writing and passion for science, you’ll contribute to making good health more affordable and accessible worldwide.
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in the pharmaceutical industry, committed to improving health and increas
ing 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: Senior Medical Writer
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job Id: 61563
The opportunity
- A Medical Writing Associate III, in Global Regulatory Medical Writing writes and edits clinical regulatory documents and provides solid medical writing support in the production of clinical research documentation used in drug development and product registrations.
How you’ll spend your day
- Primarily works at a 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 4+ years of relevant experience; advanced degree preferred.
- Proficient as lead author writing protocols, aggregate reports, and clinical study reports.
Keywords: Senior Medical Writer, Teva Pharmaceuticals, Bangalore, India, Medical Writing Associate, Pharma Industry, Senior Medical Writer Position
