Teva Pharmaceuticals is Hiring: Medical Writer Job For Life Sciences – Apply Now!

Medical Writer Job at Teva Pharmaceuticals in Bangalore – Apply Now!

Join Teva Pharmaceuticals, the world’s leading generic medicines manufacturer, and contribute to making healthcare affordable and accessible. We are looking for a Medical Writer I to support global regulatory medical writing for clinical research documentation. If you have a background in life sciences, regulatory writing, and scientific communication, apply now!

About Teva Pharmaceuticals

Teva Pharmaceuticals is a global leader in the pharmaceutical industry, dedicated to making high-quality healthcare affordable and accessible. With operations in over 60 countries, Teva is the world’s leading generic medicines manufacturer and a key player in specialty pharmaceuticals. The company produces a wide range of medicines, including those on the World Health Organization’s Essential Medicines List, helping over 200 million people daily. With a strong focus on innovation, research, and patient well-being, Teva continues to develop advanced treatments in areas such as neurology, respiratory care, and oncology. Committed to excellence, diversity, and sustainability, Teva Pharmaceuticals is shaping the future of healthcare worldwide.

Job Details: 

Job Title: Medical Writer I – 1493

Location: Bangalore, India, 560064

Company: Teva Pharmaceuticals

Job Id: 61246

Job Summary:

A Manager, in Global Regulatory Medical Writing, writes and edits clinical regulatory documents, including submission summaries and other complex documents, provides basic-level oversight and guidance, as well as resource management for the direct 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 the project level
• May oversee contingent workers and/or vendors; may provide training to others as needed
• Offers leadership and basic accountability, provides strategic assistance, and planning support for clinical regulatory documents
• Writers and edits clinical regulatory documents, including submission summaries and other complex documents
• Ensures that these 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

Your experience and qualifications

• PhD or PharmD in life sciences (or other related field), or Master’s degree in life sciences (or other related field)
• PhD or PharmD with a minimum of 2 years of experience OR Master’s degree with a minimum of 4 years of experience

Why Join Teva Pharmaceuticals?

• Global Impact: Contribute to medicines that improve millions of lives worldwide.
• Career Growth: Work in an industry-leading pharmaceutical company.
• Diversity & Inclusion: Teva is an equal-opportunity employer, fostering an inclusive workplace.

APPLY ONLINE HERE

Keywords: Teva Pharmaceuticals, Medical Writer, Bangalore, India, Pharmaceutical Jobs