Teva Pharmaceuticals, a global leader in the pharmaceutical industry and the world’s largest producer of generic medicines, is currently hiring for the position of Medical Writer I in Bangalore, India. This is an excellent opportunity for professionals with a Ph.D or Pharm.D in life sciences or related fields to join a company dedicated to improving global health and providing access to quality healthcare solutions.
About Teva Pharmaceuticals
Teva is a renowned name in the pharmaceutical sector, known for its commitment to innovation, research, and development. With a strong presence in over 60 countries, Teva focuses on delivering high-quality generic and specialty medicines to patients worldwide. The company’s mission is to make healthcare more accessible and affordable, ensuring better health outcomes for millions.
Job Details
- Post: Medical Writer I
- Experience: 2-4 years
- Qualification: Ph.D or Pharm.D in life sciences or related fields (Master’s degree with 4+ years of experience may also apply)
- Location: Bangalore, India
- Industry Type: Pharma/Healthcare/Clinical Research
- Functional Area: Medical Writing
- Application End Date: 30th April 2025
Job Description
As a Medical Writer I at Teva, you will play a crucial role in the development of clinical regulatory documents. Your responsibilities will include:
- Writing and editing clinical regulatory documents, including submission summaries and other complex documents.
- Ensuring documents are accurate, complete, and adhere to regulatory guidelines and editorial standards.
- Providing strategic assistance and planning support for clinical regulatory documentation.
- Overseeing contingent workers and vendors, and offering training as needed.
- Participating in the preparation and revision of document templates.
Candidate Profile
Teva is looking for candidates with:
- A Ph.D or Pharm.D in life sciences or related fields (Master’s degree candidates with 4+ years of experience are also eligible).
- A minimum of 2 years of experience for Ph.D/Pharm.D holders or 4 years of experience for Master’s degree holders.
- Strong writing, editing, and communication skills.
- Knowledge of regulatory guidelines and clinical documentation processes.
- Leadership skills and the ability to work collaboratively in a team environment.
