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Teva Pharmacovigilance Associate I Jobs in Bengaluru 2026
Published on: September 29, 2026
Teva Pharmaceuticals has an opening for Pharmacovigilance Associate I – GPV Professional, Case Processing in Bengaluru, Karnataka. The role involves processing adverse event cases, medical coding, reviewing safety information and completing pharmacovigilance activities according to required procedures.
For B.Pharm, M.Pharm, Pharm.D and BDS graduates interested in drug safety and pharmacovigilance, this is a role worth exploring.
Job Status: Check the official Teva job listing for the latest vacancy status. You can also explore other openings on the Official Teva Careers Portal.
1. Teva Pharmacovigilance Associate I – Job Details
| Particular | Details |
|---|---|
| Company | Teva Pharmaceuticals |
| Position | Pharmacovigilance Associate I |
| Role | GPV Professional – Case Processing |
| Location | Bengaluru, Karnataka |
| Job Type | Full-time |
| Job ID | 563602813648787 |
| Qualification | B.Pharm, M.Pharm, Pharm.D, BDS |
| Experience | 0 to 2 Years (Freshers & Experienced Eligible) |
| Work Area | Global Pharmacovigilance |
2. What Does a Pharmacovigilance Associate Do?
The main focus of this position is case processing. The selected candidate will work with safety information received from post-marketing sources and help ensure that cases are accurately reviewed, coded and documented.
| Responsibility | What It Involves |
|---|---|
| Adverse Event Processing | Processing serious and non-serious adverse events |
| MedDRA Coding | Coding medical events using MedDRA |
| Data Verification | Comparing source documents with safety database information |
| Case Assessment | Reviewing seriousness, causality, listedness and suspect drug information |
| Narrative Writing | Preparing medical narratives for safety cases |
| Follow-Up | Identifying missing information and raising queries when required |
| Quality & Compliance | Following work instructions and GVP requirements |
| Stakeholder Coordination | Working with internal and external stakeholders |
| Trend Analysis | Supporting trend identification and process improvement |
The role can also involve supporting audits, inspections, investigations and training of new team members.
3. Key Terms Used in This Role
Some of the terms mentioned in the Teva job description may be unfamiliar to candidates who are new to pharmacovigilance.
| Term | Meaning |
|---|---|
| ICSR | Individual Case Safety Report containing information about a suspected safety event |
| MedDRA | Standardized terminology used to code medical information |
| Causality | Assessment of the possible relationship between a medicine and an event |
| Listedness | Whether the reported event is consistent with the known safety information for a product |
| GVP | Good Pharmacovigilance Practices — guidelines for maintaining and monitoring the safety of medicines |
4. Eligibility for Teva Pharmacovigilance Associate I
Teva’s job description lists the following educational qualifications:
| Qualification | Mentioned in Job Description |
|---|---|
| B.Pharm | Yes |
| M.Pharm | Yes |
| Pharm.D | Yes |
| BDS | Yes |
5. Skills Teva Is Looking For
The position requires a combination of pharmacy knowledge, pharmacovigilance understanding and attention to detail.
| Skill / Knowledge | Relevance to the Role |
|---|---|
| Medical Terminology | Helps in understanding reported safety information |
| Clinical Pharmacology | Useful when reviewing medicines and adverse events |
| Pharmacovigilance Principles | Important for safety case processing |
| MedDRA | Used for coding medical events |
| Regulatory Requirements | Helps ensure compliance with safety requirements |
| Communication Skills | Needed for documentation and stakeholder coordination |
| Attention to Detail | Important when reviewing and entering safety data |
Teva also mentions knowledge of its products, therapeutic areas and mechanisms of action.
6. What Should Freshers Know Before Applying?
If you are new to pharmacovigilance, it is useful to understand the basic concepts involved in adverse event reporting, case processing, MedDRA coding and safety databases.
You should also have a basic understanding of seriousness, causality, case narratives and pharmacovigilance reporting.
You don’t need to list skills or terminology on your resume unless you actually understand them. If you have relevant pharmacovigilance training, internship experience, academic projects or coursework, mention those clearly.
7. A Quick Look at MedDRA
MedDRA (Medical Dictionary for Regulatory Activities) is standardized medical terminology used in regulatory activities, including the classification and coding of medical information in safety reporting.
Since MedDRA coding is specifically mentioned in the Teva job description, having a basic understanding of it can be useful for candidates preparing for this type of role.
Official resource: MedDRA – Official Website
8. Pharmacovigilance Resources for Beginners
Candidates who want to understand the regulatory side of pharmacovigilance can refer to reliable resources such as:
These are useful reference materials for understanding pharmacovigilance and drug-safety requirements.
9. Why Pharmacovigilance Can Be a Career Option After B.Pharm
Pharmacovigilance is a career path for pharmacy graduates who are interested in drug safety, medical information, documentation and regulatory work.
Much of the work involves reviewing safety information, maintaining accurate records, coding medical events and following regulatory procedures.
10. How to Apply for the Teva Job
Candidates should apply through the official Teva careers website.
Official Job Listing:
Teva Pharmacovigilance Associate I – Bengaluru
Teva Careers:
Teva Careers
Before submitting your application, check the live listing for:
- Current vacancy status
- Experience requirement
- Qualification
- Job location
- Application instructions
11. Important Note for Applicants
This article is based on the Teva job description for Job ID 563602813648787 provided for this vacancy.
Job details can change, so the official Teva careers page should be treated as the final source for the current vacancy.
12. Frequently Asked Questions
What qualifications are required for this Teva job?
The job description lists B.Pharm, M.Pharm, Pharm.D and BDS.
Where is the position located?
The position is based in Bengaluru, Karnataka.
What is the main work of a Pharmacovigilance Associate?
The role involves adverse event case processing, MedDRA coding, safety data verification, narrative writing, follow-up and compliance activities.
Is this purely a medical coding job?
No. MedDRA coding is only one part of the position. The role also includes case review, data verification, narratives, follow-up and other pharmacovigilance activities.
Does Teva specify an experience requirement?
The job listing mentions 0–2 years of experience, making the position suitable for both freshers and candidates with some relevant experience.
What is the Job ID?
The Job ID is 563602813648787.
13. Related Career Guides
- Career Options After B.Pharm
- Career in Regulatory Affairs After B.Pharm
- Medical Coding After B.Pharm
14. Final Thought
The Teva Pharmacovigilance Associate I role is relevant for pharmacy graduates interested in drug safety and pharmacovigilance. The work involves case processing, medical coding, safety data review, follow-ups and compliance activities.
Before applying, check the official Teva job listing for the latest vacancy status and requirements.
