About Teva Pharmaceuticals
Teva Pharmaceuticals is the world's largest producer of generic medicines, playing a crucial role in improving healthcare worldwide. With a strong presence in over 60 countries, Teva is dedicated to providing high-quality health solutions to millions of people. The company’s Global Business Services (GBS) in Bangalore is expanding, and Teva is looking for talented professionals to support its growth and innovative endeavors.Job Overview
Here’s a quick summary of the essential details:Vacancies | Pharmacovigilance Associate - Literature Review Pharmacovigilance Associate I & II - Patient Safety Operations |
---|---|
Qualification | B. Pharm, M. Pharm, Pharm D, BDS |
Organization Name | Teva Pharmaceuticals |
Experience | 2-6 years in Pharmacovigilance |
Location | Bangalore |
Job Opportunities at Teva Pharmaceuticals
Teva is offering exciting roles for Pharmacovigilance professionals at different levels. The positions available include Pharmacovigilance Associate - Literature Review and Pharmacovigilance Associate I & II - Patient Safety Operations. Below are the key details of the roles:1. Pharmacovigilance Associate - Literature Review
Key Responsibilities:- Conduct thorough literature reviews in the context of Individual Case Safety Reports (ICSR).
- Provide support for various Pharmacovigilance teams, including case processing, training, quality assurance, audits, and inspections.
- Utilize databases such as Embase, Medline, PubMed, and Ovid for literature searches.
- Education: B. Pharm, M. Pharm, Pharm D, or BDS.
- Experience: 2-6 years in Pharmacovigilance with a focus on literature review processes.
- Skills: Solid knowledge of Pharmacovigilance concepts, regulations, and procedures.
2. Pharmacovigilance Associate I & II - Patient Safety Operations
Key Responsibilities:- Perform case processing and related activities in alignment with Patient Safety Operations.
- Apply extensive knowledge of medical terminology, clinical pharmacology, and patient treatment.
- Conduct medical coding through MedDRA for all events in the safety database.
- Education: B. Pharm, M. Pharm, Pharm D, or BDS.
- Experience: 2-6 years in Pharmacovigilance, particularly in patient safety and medical coding.
- Skills: Proficiency in clinical pharmacology, medical terminology, and the use of MedDRA for coding.