PHARMAFull-time
GPV Professional, Case Processing
BANGALORE (IN)ONSITEPOSTED: 9/30/2026
PHARMAFull-time
HIRING ORGANIZATIONTEVA PHARMACEUTICALSBiopharmaceuticals / Life Sciences
ROLE OVERVIEW
Support global pharmacovigilance case processing by accurately processing adverse events, maintaining high-quality safety data, performing medical coding and data verification, managing follow-ups, and meeting regulatory and operational timelines.
ROLE DEFINITION & RESPONSIBILITIES
- •Process serious and non-serious adverse events from various post-marketing sources
- •Perform accurate and consistent MedDRA medical coding for events in the safety database
- •Verify source documents against entered safety-database data, including suspect-drug coding, seriousness, causality, listedness, and narrative information
- •Evaluate the need for follow-up and raise queries with relevant stakeholders to obtain accurate information
- •Analyze case-processing quality and trends to support process stabilization and improvement
- •Coordinate with internal and external stakeholders and provide real-time status updates
- •Perform safety-database administrative and procedural activities in compliance with work instructions and GVP modules
- •Meet compliance metrics including case timelines, assigned training requirements, and turnaround times
- •Provide analytical support for investigations, audits, and inspections
- •Mentor and train new hires on case-processing activities and evaluate their progress
Reporting Hierarchy: Reports to the relevant pharmacovigilance/case-processing management structure; Exact reporting line and team size are not specified in the source posting
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- M.Pharm, Pharm.D, B.Pharm, or BDS
- Extensive knowledge of medical terminology, clinical pharmacology, patient treatment, diagnostic investigations, and pathology
- Sound knowledge of pharmacovigilance principles and international regulatory requirements related to drug and patient safety
- Excellent professional English communication skills
- Strong attention to detail
PREFERRED QUALIFICATIONS
- •Knowledge of Teva product portfolio and therapeutic areas
- •Understanding of mechanisms of action and product/patient safety profiles
- •Experience with pharmacovigilance safety databases
- •Experience supporting audits, inspections, investigations, trend analysis, or new-hire training
REQUIRED VERIFIED SKILLS
Pharmacovigilance
Case processing
MedDRA
Adverse event processing
Post-marketing surveillance
Safety database
Medical coding
Seriousness assessment
Causality assessment
Listedness assessment
Narrative writing
Follow-up management
GVP modules
Regulatory compliance
Quality management
TAT management
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Generous annual leave; reward plans; flexible working schedules depending on role; tailored health support; community and giving opportunities; career-development programs and internal growth opportunities through Twist
The source posting contains a Salary Range section but does not provide an actual salary figure. Salary amounts and bonus/equity have therefore been left undisclosed.
ORGANIZATION CONTEXT & CULTURE
Teva is a global biopharmaceutical company with a leading generics business and activities in innovative medicines, including neuroscience and immunology. The company focuses on improving health and delivering medicines to patients worldwide.
TEAM SIZE: 50,000+ employees
INDUSTRY: Biopharmaceuticals / Life Sciences
Culture: Teva describes its culture as high-performing, inclusive, collaborative, flexible, and focused on fresh thinking, employee development, wellbeing, and improving patient health.
EXPECTED CAREER ROADMAP
The role can provide progression within global pharmacovigilance from case-processing responsibilities into senior case-processing, quality review, safety operations, signal-management support, compliance, or pharmacovigilance leadership roles. Exposure to audits, inspections, trend analysis, mentoring, and international regulatory requirements can broaden future PV career opportunities.
APPLICATION ADVISORY
Emphasize your M.Pharm, Pharm.D, B.Pharm, or BDS qualification; highlight hands-on or academic knowledge of pharmacovigilance, MedDRA, adverse-event processing, medical terminology, and clinical pharmacology; demonstrate attention to detail and strong written English; mention safety-database experience if applicable; prepare examples of accurate data review, follow-up handling, compliance with timelines, and stakeholder communication.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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