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Pharmacovigilance Specialist (Global PV Agreements) at Bausch + Lomb

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If you’re looking to advance your career in pharmacovigilance (PV), this opportunity at Bausch + Lomb offers a strong platform in global drug safety and risk management. The company is hiring a Global Pharmacovigilance Agreements Specialist in Gurgaon, focusing on safety agreements and compliance within global PV operations.

This role is ideal for candidates with 2+ years of pharmacovigilance experience, particularly those familiar with Safety Data Exchange Agreements (SDEAs) and regulatory documentation.


About the Company

Bausch + Lomb is a globally recognized eye health company with over 170 years of legacy and a presence in 100+ countries. With a portfolio of over 400 products, the company plays a key role in advancing eye care and vision health worldwide.


Job Overview

  • Role: Pharmacovigilance Specialist (Global PV Agreements)
  • Location: Gurgaon, India
  • Department: R&D / Pharmacovigilance & Risk Management
  • Experience Required: 2+ years
  • Employment Type: Full-time

Key Responsibilities

As a Pharmacovigilance Specialist, your responsibilities will include:

  • Preparing, reviewing, and maintaining Safety Data Exchange Agreements (SDEAs)
  • Managing third-party and intercompany pharmacovigilance agreements
  • Performing quality control checks in agreement tracking systems
  • Acting as a liaison between internal teams, partners, and regulatory authorities
  • Supporting development of SOPs, WIs, templates, and trackers
  • Collaborating with departments such as:
    • Regulatory Affairs
    • Medical Affairs
    • Clinical Operations
    • Quality & Legal teams
  • Supporting global PV operations and agreement lifecycle management

Eligibility Criteria

Educational Qualification

  • Bachelorโ€™s degree in:
    • Pharmacy
    • Nursing
    • Life Sciences or related field

Experience

  • Minimum 2 years in pharmacovigilance
  • Experience in SDEA preparation or regulatory affairs preferred

Skills Required

  • Strong organizational and documentation skills
  • Knowledge of global pharmacovigilance regulations
  • Excellent communication and stakeholder management
  • Ability to work in a fast-paced, global environment

Salary & Benefits

  • Estimated Salary Range: โ‚น5.5 LPA โ€“ โ‚น9 LPA
  • Exposure to global pharmacovigilance operations
  • Opportunity to work with cross-functional international teams
  • Career growth in drug safety and regulatory affairs

Why This Role Matters

This pharmacovigilance job in Gurgaon offers hands-on experience in managing global safety agreementsโ€”an essential component of drug safety compliance. Professionals in this role contribute directly to ensuring patient safety and regulatory adherence worldwide.


How to Apply

Application Link

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