Teva Careers: Apply Now for Medical Reviewer Position
Teva Careers: Teva Pharmaceuticals is seeking an experienced Lead GPV Professional, Medical Reviewer to join the Global ICSR Operations team in Bangalore. This role is ideal for an MBBS doctor with strong clinical knowledge and a passion for drug safety, regulatory science, and medical content evaluation. If you want to play a crucial role in ensuring patient safety worldwide, this opportunity offers significant impact and growth.
Teva Careers – Job details:
- Position: Lead GPV Professional, Medical Reviewer
- Location: Bangalore, India
About the Company:
Teva Pharmaceuticals is one of the world’s leading manufacturers of generic medicines and a trusted producer of many essential drugs used globally. Operating across nearly 60 countries, Teva’s mission is to make high-quality healthcare more affordable and accessible. With over 200 million people taking Teva medicines every day, the company continues to push boundaries in research, safety, and compliance. Working at Teva means joining a diverse, collaborative, and purpose-driven global team.
Teva Careers Qualifications
- MBBS or equivalent medical degree with a valid license to practice.
- 1–2 years of clinical experience (mandatory).
- Prior experience in pharmacovigilance or medical review (required).
- Strong understanding of clinical medicine, drug safety, and regulatory principles.
- Excellent written and spoken English.
Role Overview
The Lead GPV Professional, Medical Reviewer, supports the medical evaluation of Individual Case Safety Reports (ICSRs) from spontaneous sources and organized data collection. The role aims to maintain accuracy, medical consistency, and regulatory compliance in safety case documentation while collaborating closely with senior reviewers and cross-functional teams.
Key Responsibilities
- Assist in the medical review of trial-related AEs and post-marketing ADRs.
- Ensure narrative accuracy, medical consistency, seriousness, expectedness, and completeness of clinical data.
- Support MedDRA coding and contribute to causality and labeling assessments.
- Collaborate with senior reviewers for clarification of medical details and regulatory alignment.
- Participate in quality checks and support continuous improvement of case processing workflows.
- Contribute to internal training sessions, workshops, and team knowledge-sharing activities.
- Assist with audit and inspection readiness by maintaining compliant documentation.
- Stay updated on evolving pharmacovigilance regulations, best practices, and safety guidelines.
