Teva GPV Case Processing Professional, Bangalore – B.Pharm/M.Pharm/BDS

Teva is hiring for a Teva GPV Job as GPV Professional, Case Processing, in Bangalore, India. Qualifications include M.Pharm, Pharm.D, B.Pharm, BDS.

Job Details

Company: Teva

Position: GPV Professional, Case Processing

Location: Bangalore, India

Job ID: 70380

Education: M.Pharm, Pharm.D, B.Pharm, BDS

Teva GPV Job: Key Responsibilities

  • Process serious and non-serious adverse events from various post-marketing sources.
  • Perform accurate and consistent medical coding using MedDRA (Medical Dictionary for Regulatory Activities).
  • Verify data between source documents and the Safety Database.
  • Evaluate events and suspect drug coding, seriousness, causality, listedness, and narrative writing.
  • Evaluate the need for follow-ups and queries with stakeholders to ensure accurate data transfer.
  • Analyze quality data for trending and process stabilization.
  • Take responsibility for assigned case-processing activities on a day-to-day basis.
  • Coordinate with internal and external stakeholders to obtain information required for operations.
  • Provide real-time status updates to the reporting manager.
  • Maintain effective communication with internal departments and external partners, authorities, and vendors.
  • Assist with Safety Database administrative and procedural activities.
  • Perform assigned tasks in compliance with work instructions and GVP modules.
  • Evaluate the quality of case processing and identify trends for process improvement.
  • Meet compliance metrics including case timelines, assigned training, and turnaround time (TAT).
  • Provide analytical support to peers and managers for investigations and trend analysis related to audits and inspections.
  • Mentor and train new hires on case-processing activities and evaluate their progress during the initial learning period.

This Teva GPV Job involves post-marketing adverse-event case processing, medical coding, safety-data review, and compliance with GVP modules.

Eligibility Criteria

Candidates should have any of the following educational qualifications: M.Pharm, Pharm.D, B.Pharm, BDS

Required Skills

  • Strong knowledge of pharmacovigilance principles
  • Understanding of international drug and patient safety regulations
  • Medical coding knowledge, particularly MedDRA
  • Knowledge of Safety Database activities
  • Analytical and trend-analysis skills
  • Excellent professional English communication skills
  • Strong writing and presentation skills
  • Attention to detail
  • Ability to coordinate with internal and external stakeholders
  • Ability to support investigations, audits, and inspections
  • Case-processing training and mentoring capabilities

How to Apply

Apply via the employer’s official career page: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE