Explore Baxter Careers & Apply Now for Spec, PV Position

Baxter Careers: Apply Now for Spec, PV Position

Baxter Careers: Baxter is currently hiring a Spec, PV (Pharmacovigilance Specialist) in Ahmedabad, Gujarat. This role is designed for healthcare professionals who want to contribute directly to patient safety, adverse event evaluation, and global pharmacovigilance operations. If you have a background in medical sciences and are seeking a purpose-driven career in a global healthcare leader, this position offers an outstanding opportunity to make a meaningful impact.

Baxter Careers Job Details:

• Position: Spec, PV
• Job ID: JR-190289
• Location: Ahmedabad, Gujarat, India
• Job Category: Patient Safety

Baxter Careers: About the Company

Baxter is a global healthcare leader committed to saving and sustaining lives since 1931. The organization brings innovative medical products, therapies, and digital health solutions to patients across more than 100 countries. Guided by a mission-driven culture rooted in courage, trust, and collaboration, Baxter empowers its workforce to deliver excellence while transforming healthcare delivery for the future. The company fosters a diverse and inclusive environment where every individual is encouraged to grow, lead, and contribute to life-changing outcomes.

Qualifications

• Strong medical and clinical knowledge.
• Excellent written and verbal communication skills.
• Ability to work both independently and as part of a team.
• Strong multitasking and time-management skills under strict deadlines.
• Knowledge of global and regional pharmacovigilance regulations.
• Proficiency in working with pharmacovigilance safety systems.

Role

The Pharmacovigilance Specialist (Spec, PV) is a key member of Baxter’s Global Patient Safety (GPS)–Safety Operations team. The role involves managing individual case safety reports (ICSRs), ensuring high-quality review, documentation, assessment, and timely reporting of adverse event data from various global sources.

Key Responsibilities

• Processing adverse event reports from all source types, including review, full data entry, seriousness assessment, expectedness, causality evaluation, and event resolution.
• Ensuring correct suspect drug selection within the Pharmacovigilance Safety System.
• Preparing clear, accurate narratives summarising all medically relevant case information.
• Coding medical terms using standardised dictionaries (e.g., MedDRA).
• Ensuring accuracy and consistency of all entered medical data.
• Requesting investigation details and coordinating follow-up with reporters and local affiliates.
• Performing case quality checks and data cleanup for aggregate reporting, as needed.
• Maintaining compliance with regional and global drug safety regulations.

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