Pharmacovigilance Specialist Job at Baxter in Gurgaon. PV safety operations role in Global Patient Safety. Apply online before February 13, 2026.
Company Overview
Baxter is a globally recognized healthcare organization with a legacy spanning over nine decades. The company is committed to improving patient outcomes by delivering innovative medical products and therapies that save and sustain lives. Operating across multiple countries, Baxter plays a critical role in patient safety, clinical care, and regulatory excellence. Its work culture is built on accountability, collaboration, and purpose-driven performance, offering professionals an opportunity to contribute meaningfully to global healthcare systems. Pharmacovigilance Specialist Job at Baxter
As part of its continued expansion in patient safety operations, Baxter is hiring for a Pharmacovigilance (PV) Specialist role at its Gurgaon location.
Job Location & Employment Type
- Job Location: Gurgaon, Haryana, India
- Employment Type: Full-Time
- Department: Global Patient Safety (GPS) – Safety Operations
- Work Mode: Onsite / Hybrid (as per company policy)
Open Positions / Department Details
- Job Title: Specialist – Pharmacovigilance (PV)
- Job Requisition ID: JR – 196467
- Business Function: Safety Operations
- Application Deadline: 13 February 2026
- Days Left to Apply: 4 Days
This position is part of Baxter’s Global Patient Safety (GPS) organization and focuses on individual case safety report (ICSR) processing and adverse event management. Pharmacovigilance Specialist Job at Baxter
Key Roles & Responsibilities
The Pharmacovigilance Specialist will function as a case owner within the Safety Operations team and will be responsible for end-to-end safety case management. Key responsibilities include: Pharmacovigilance Specialist Job at Baxter
- Processing adverse event reports from multiple sources, including spontaneous reports, literature, and clinical sources
- Performing comprehensive review and full data entry of ICSRs in the pharmacovigilance safety database
- Assessing seriousness, expectedness, reporter causality, and event outcome for reported cases
- Ensuring accurate selection of suspect drug(s) within the safety system
- Writing clear, medically sound case narratives summarizing relevant clinical information
- Coding adverse events, indications, and medical history using standard medical dictionaries (MedDRA)
- Ensuring data accuracy and completeness through medical review and validation
- Initiating and managing case follow-ups, including query generation and coordination with reporters and local affiliates
- Performing quality checks on safety cases when required
- Supporting case clean-up activities for aggregate reports and regulatory submissions
- Meeting global and regional regulatory timelines and quality expectations
This role requires strong medical judgment, attention to detail, and the ability to work under tight regulatory timelines. Pharmacovigilance Specialist Job at Baxter
Eligibility Criteria
Education
Candidates must possess one of the following:
- Degree in Pharmacy, Nursing, or Life Sciences
- Equivalent scientific or healthcare qualification
Experience
- Experience in the pharmaceutical industry, particularly in pharmacovigilance, regulatory affairs, or drug safety, is preferred
- 2–3 years of hospital, clinical, or patient care experience is an added advantage
- Prior exposure to global safety databases and case processing workflows is desirable
Skills Required
- Strong medical and clinical knowledge
- Excellent written and verbal communication skills
- Ability to prepare high-quality safety narratives and documentation
- Knowledge of global and regional pharmacovigilance regulations
- Ability to work effectively in a team-based environment
- Capability to work independently under strict deadlines and changing priorities
- Strong multitasking and organizational skills
- Willingness to learn and gain proficiency in pharmacovigilance safety systems
Pharmacovigilance Specialist Job at Baxter
Salary & Benefits
- Salary: As per company norms
- Competitive compensation aligned with industry standards
- Opportunity to work within a global patient safety organization
- Exposure to international pharmacovigilance regulations and processes
- Supportive, inclusive, and purpose-driven work culture
Selection Process
- Online application screening
- Technical and functional interview rounds
- HR discussion
The selection process may vary based on candidate experience and business needs. Pharmacovigilance Specialist Job at Baxter
How to Apply
- Application Mode: Online Application Only
- Interested candidates should apply through the official Baxter careers portal using the requisition ID JR – 196467.
Important Dates
- Last Date to Apply: 13 February 2026
Early application is strongly recommended due to the short application window.
Why Apply for This Pharma Job?
- Opportunity to work with a global healthcare leader
- Direct involvement in patient safety and adverse event management
- Exposure to international safety regulations and compliance standards
- Purpose-driven role contributing to safer medicines worldwide
- Strong professional growth in pharmacovigilance and regulatory science
- Inclusive and ethical workplace with zero tolerance for recruitment fraud
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent pharmaceutical job information platform and is not affiliated with Baxter or any hiring organization. Job details are shared based on publicly available information and official employer communications. Candidates are advised to verify all details directly from the official company website before applying. IndiaPharmaJobs.in does not charge any fees for job listings or applications. Pharmacovigilance Specialist Job at Baxter
Final Call-to-Action
If you have a background in pharmacy, nursing, or life sciences and are passionate about patient safety, apply now and become part of Baxter’s mission to save and sustain lives. Pharmacovigilance Specialist Job at Baxter
