Life Sciences Job at Teva Pharma – For Medical Writing, Apply Now!
Join a global healthcare leader and shape the future of affordable medicine. Teva Pharmaceuticals is hiring a Manager – Medical Writing in Bengaluru, India, to support international regulatory documentation efforts. If you have a strong background in life sciences, exceptional writing skills, and a passion for regulatory science, this is your opportunity to contribute to a mission that impacts over 200 million lives daily.
- Job Title: Manager – Medical Writing
- Department: Global Regulatory Medical Writing
- Location: Bengaluru, Karnataka, India
- Employment Type: Full-Time
About The Company
At Teva Pharmaceuticals, we’re united by a mission: to improve access to high-quality medicines and enable healthier lives worldwide. As a leading global manufacturer of generics and specialty medicines, our products appear on the WHO Essential Medicines List and reach 200 million people daily. With operations in nearly 60 countries, we thrive on diversity, purpose, and innovation.
Life Sciences Job at Teva Pharma – Role Summary:
The Manager – Medical Writing is responsible for writing, editing, and managing regulatory medical documents, ensuring clarity, compliance, and consistency across global submissions. The role involves project-level leadership and strategic support in regulatory medical writing, and may also include vendor and team oversight.
Life Sciences Job at Teva Pharma – Key Responsibilities:
- Author and edit clinical regulatory documents, including submission summaries and complex regulatory dossiers.
- Ensure scientific accuracy, regulatory compliance, and clear medical messaging.
- Offer project-level leadership and planning for medical writing deliverables.
- Provide strategic guidance and editorial oversight to ensure consistency and high-quality output.
- Collaborate cross-functionally with regulatory, clinical, and scientific teams.
- Support document template development or revision initiatives.
- Oversee contingent workers and vendors when needed; may provide training.
Life Sciences Job at Teva Pharma – Required Qualifications:
- PhD or PharmD in Life Sciences or related field with a minimum of 2 years of medical writing experience
- Master’s degree in Life Sciences or related field with a minimum of 4 years of experience
- Demonstrated experience in writing regulatory and clinical documentation
- Familiarity with global regulatory standards and medical writing best practices
- Strong attention to detail and ability to manage timelines
What Teva Offers:
- Opportunity to contribute to global healthcare access
- Work in a mission-driven, diverse, and collaborative environment
- Potential to grow into broader strategic or leadership roles in regulatory affairs
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