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Elanco Hiring Analyst – GDPS (Pharmacovigilance) | 0 – 2 Years

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Elanco, a global leader in animal health, has announced a new opportunity for the position of Analyst – GDPS (Global Drug Product Safety) in Bangalore, India. This is an excellent opportunity for M.Pharm professionals with Pharmacovigilance experience and Veterinarians (DVM equivalent) looking to build or advance their careers in drug safety and adverse event case processing.

If you are passionate about pharmacovigilance, regulatory compliance, and ensuring patient and animal safety through accurate adverse event reporting, this role offers exposure to global safety operations within one of the world’s leading animal health companies.


Job Overview

  • Company: Elanco
  • Job Title: Analyst – GDPS
  • Department: Global Drug Product Safety (Pharmacovigilance)
  • Location: Bangalore, Karnataka, India
  • Job Type: Full-Time
  • Experience: 0–2 Years
  • Industry: Animal Health, Pharmacovigilance
  • Travel Requirement: 0%

About Elanco

Elanco (NYSE: ELAN) is one of the world’s leading animal health companies, dedicated to developing innovative products and services that prevent and treat diseases in farm animals and companion animals. With a strong focus on innovation, diversity, and scientific excellence, Elanco provides employees with opportunities to work on global healthcare challenges while making a positive impact on animal welfare.


Key Responsibilities

As an Analyst – GDPS, you will be responsible for global pharmacovigilance case processing activities, including:

  • Perform adverse event case processing in the Pharmacovigilance database.
  • Enter safety data accurately from source documents.
  • Conduct seriousness and causality assessments.
  • Assess reportability of adverse event cases.
  • Validate case information for accuracy and completeness.
  • Perform self-quality checks before submission.
  • Identify missing follow-up information when required.
  • Ensure cases are submission-ready within regulatory timelines.
  • Escalate processing issues that may delay submissions.
  • Participate in team meetings and continuous improvement initiatives.
  • Maintain compliance with global pharmacovigilance regulations and SOPs.
  • Meet productivity and quality KPIs.

Required Qualifications

Applicants should possess one of the following qualifications:

Eligible Candidates

  • Veterinarian (Equivalent to US DVM Degree) with or without Pharmacovigilance experience
  • M.Pharm with Pharmacovigilance Experience

Preferred Experience

  • 0–2 years of Pharmacovigilance experience
  • Experience in adverse event case processing is preferred.
  • Knowledge of pharmacovigilance regulations.
  • Understanding of medical terminology.
  • Familiarity with safety databases.
  • Strong communication and documentation skills.
  • Ability to manage multiple priorities.

Required Skills

Candidates should have:

  • Pharmacovigilance Case Processing
  • Adverse Event Reporting
  • Seriousness Assessment
  • Causality Assessment
  • Medical Terminology
  • Drug Safety
  • Regulatory Compliance
  • Quality Review
  • Safety Database Handling
  • Time Management
  • Communication Skills
  • Attention to Detail

Why Join Elanco?

Working at Elanco offers several advantages:

  • Global Animal Health Organization
  • International Pharmacovigilance Exposure
  • Career Growth Opportunities
  • Inclusive Work Culture
  • Competitive Compensation
  • Learning & Development Programs
  • Work with Global Safety Teams
  • Exposure to Worldwide Regulatory Standards

Who Should Apply?

This opportunity is ideal for:

  • M.Pharm professionals with Pharmacovigilance experience
  • Veterinary graduates interested in Drug Safety
  • Professionals seeking Pharmacovigilance Analyst jobs in Bangalore
  • Candidates looking for Global Drug Safety careers
  • Drug Safety Associates wanting to transition into multinational companies

How to Apply

Application Link

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