Teva Pharmaceuticals is hiring for the position of GPV Professional, Case Processing in Bangalore, India. This opportunity is suitable for pharmacy and healthcare professionals with knowledge of pharmacovigilance, medical terminology, clinical pharmacology and drug safety.
The role involves processing serious and non-serious adverse event cases received from post-marketing sources, maintaining accurate safety data, performing medical coding and supporting compliance with pharmacovigilance procedures and regulatory requirements.
Teva Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Teva Pharmaceuticals |
| Job Title | GPV Professional, Case Processing |
| Department | Global Pharmacovigilance |
| Job Location | Bangalore, India |
| Qualification | M.Pharm / Pharm D / B.Pharm / BDS |
| Experience | Not specified |
| Job Type | Full-time |
| Work Mode | Not specified |
| Function | Pharmacovigilance / Case Processing |
| Salary / CTC | Not specified |
| Application Mode | Online |
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global pharmaceutical company with operations spanning innovative medicines and generic pharmaceuticals. The company works across therapeutic areas including neuroscience and immunology while supplying medicines to patients worldwide.
Teva’s work environment emphasizes collaboration, professional development and opportunities for employees to build expertise across different areas of the pharmaceutical industry.
Job Description
The GPV Professional, Case Processing role is focused on pharmacovigilance case management and post-marketing safety information.
The selected professional will be responsible for processing adverse event cases, reviewing source information, maintaining safety database records, performing MedDRA coding and supporting the quality and compliance of case-processing activities.
GPV Professional – Case Processing
The position requires a strong understanding of drug safety principles and the ability to accurately evaluate safety information received from different sources.
Key areas of work include adverse event processing, medical coding, case data verification, follow-up activities, safety database administration, compliance monitoring and communication with relevant stakeholders.
Educational Qualification / Eligibility Criteria
Candidates should have one of the following qualifications:
- M.Pharm
- Pharm D
- B.Pharm
- BDS
The vacancy specifically requires knowledge relevant to pharmacovigilance and patient safety activities.
Experience Requirements
The job description does not specify a particular number of years of experience.
Candidates should have relevant knowledge of pharmacovigilance case processing, medical terminology, clinical pharmacology and drug safety requirements.
Required Skills and Knowledge
Candidates should possess:
- Good understanding of pharmacovigilance principles.
- Knowledge of international regulatory requirements related to drug and patient safety.
- Strong understanding of medical terminology.
- Knowledge of clinical pharmacology.
- Understanding of diagnostic investigations and pathology.
- Knowledge of adverse event case processing.
- Familiarity with MedDRA medical coding.
- Ability to review and verify safety information from source documents.
- Strong attention to detail and data accuracy.
- Professional English communication skills, both written and verbal.
- Ability to work effectively with internal and external stakeholders.
Knowledge of Teva’s products, therapeutic areas, mechanisms of action and product/patient safety profiles is also identified as relevant to the position.
Key Responsibilities
The selected candidate will be responsible for activities including:
- Processing serious and non-serious adverse event cases received through post-marketing sources.
- Performing accurate medical coding using MedDRA within the safety database.
- Comparing source documents with safety database information to verify case data.
- Reviewing suspect drug information, seriousness, causality and listedness.
- Preparing accurate case narratives as required.
- Assessing the requirement for follow-up information and raising queries with relevant stakeholders.
- Supporting the timely transfer and completion of required safety information.
- Reviewing case-processing quality and identifying trends that may support process improvements.
- Managing assigned administrative and operational case-processing activities.
- Coordinating with internal departments and external stakeholders to obtain required information.
- Supporting safety database-related administrative and procedural activities.
- Performing assigned activities in accordance with applicable work instructions and GVP requirements.
- Meeting defined case-processing timelines, training requirements and turnaround-time targets.
- Providing analytical support during investigations, audits and inspections.
- Supporting trend analysis related to case processing and process performance.
- Guiding and training new team members on case-processing activities when assigned.
Work Location and Work Environment
The position is based in Bangalore, India.
The available job description does not specify whether the position follows an office-based, hybrid or remote work arrangement. Candidates should confirm the applicable work arrangement with Teva during the recruitment process.
Salary / CTC
The salary range for the GPV Professional, Case Processing position has not been specified in the available job description.
Candidates should confirm the applicable compensation package directly through the official recruitment process.
Employee Benefits and Career Development
Teva states that employees may have access to benefits and development opportunities designed to support professional growth and wellbeing.
The company mentions benefits such as annual leave, reward programs, flexible working arrangements depending on the role, health-related support and opportunities to participate in community initiatives.
For career development, Teva’s Twist platform provides access to learning programs, short-term projects and opportunities for internal career growth.
Specific benefits and eligibility may vary according to the employee’s role and applicable company policies.
Selection Process
The detailed selection process for this position has not been provided in the available vacancy information.
Candidates should follow the recruitment instructions provided by Teva and remain available for any assessment, interview or verification stages communicated by the company.
How to Apply for Teva Recruitment 2026
Eligible candidates interested in the GPV Professional, Case Processing position should apply through Teva’s official careers recruitment process.
Applicants should ensure that their resume clearly highlights relevant qualifications and knowledge in pharmacovigilance, adverse event case processing, medical coding, drug safety and regulatory requirements.
Existing Teva employees are instructed to apply through the company’s internal Twist career platform.
Important Details Before Applying
- The position is based in Bangalore.
- Eligible educational backgrounds include M.Pharm, Pharm D, B.Pharm and BDS.
- The role focuses on Global Pharmacovigilance and case processing.
- Experience requirements have not been specified in the provided job description.
- Knowledge of pharmacovigilance and international drug-safety requirements is important.
- MedDRA coding and safety database activities are key components of the role.
- Salary/CTC has not been disclosed.
- Work mode has not been specified in the provided information.
- Candidates should have strong professional English communication skills.
- Existing Teva employees should use the internal Twist career platform when applying.
Frequently Asked Questions
1. What is the job title at Teva?
The position is GPV Professional, Case Processing.
2. Where is the Teva GPV Professional job located?
The position is based in Bangalore, India.
3. What qualifications are accepted?
Candidates with M.Pharm, Pharm D, B.Pharm or BDS qualifications can be considered based on the requirements of the position.
4. What type of work is involved in this role?
The position involves pharmacovigilance case processing, adverse event evaluation, medical coding, safety database activities, data verification, follow-up and compliance-related work.
5. Is MedDRA knowledge required?
The role specifically involves medical coding through MedDRA, making familiarity with MedDRA relevant to the position.
6. Is experience in pharmacovigilance required?
The job description does not state a specific number of years of experience. However, it requires knowledge of pharmacovigilance principles and drug-safety requirements.
7. What is the salary for the Teva GPV Professional position?
The salary range has not been specified in the available job description.
8. What are the main responsibilities?
Major responsibilities include adverse event case processing, medical coding, safety database data verification, case follow-up, documentation, quality review, stakeholder coordination and compliance with applicable procedures.
9. Does Teva provide career development opportunities?
Teva describes career development opportunities through its Twist platform, including learning programs, short-term projects and opportunities for internal growth.
10. Where can existing Teva employees apply?
Existing employees are instructed to apply through Teva’s internal Twist career platform.
Important Note
Job availability, eligibility requirements, work arrangements, compensation, recruitment stages and other employment conditions may change at the discretion of the employer. Candidates should verify the latest information through Teva’s official careers channel before submitting an application.