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Specialist Pv

0-2 years
upto 7 LPA
5 Dec. 2, 2025
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Specialist – Pharmacovigilance (PV) 

Baxter | Ahmedabad, Gujarat, India

Job ID: JR-190289
Category: Patient Safety
Location: Ahmedabad, Gujarat
Date Posted: 1 December 2025
Experience Required: Fresher
Employment Type: Full-Time


About Baxter

Baxter is a global healthcare leader committed to improving and sustaining patient lives. Since 1931, the organization has worked to deliver innovations that support hospitals, clinicians, and patients worldwide. With a culture built on courage, trust, and collaboration, Baxter empowers its teams to make meaningful contributions to global healthcare.
Joining Baxter means contributing to a mission-driven environment where every role plays a part in advancing patient safety and healthcare delivery.


Role Overview

The Pharmacovigilance Specialist will be part of the Safety Operations team within Global Patient Safety (GPS). This position supports end-to-end processing of Individual Case Safety Reports (ICSRs) and ensures accuracy, compliance, and timely reporting of adverse events.
This opportunity is suitable for freshers who want to begin a career in pharmacovigilance, case processing, and global drug safety operations.


Key Responsibilities

Case Processing & Data Entry

  • Review, process, and perform full data entry of adverse event reports from various sources.

  • Assess seriousness, expectedness, causality, and case outcomes.

  • Ensure correct identification of suspect drugs within the Pharmacovigilance Safety System.

  • Prepare high-quality case narratives summarizing all relevant clinical and medical details.

  • Code medical terms using MedDRA and other standardized safety dictionaries.

Quality, Compliance & Follow-Up

  • Ensure all case data is complete, accurate, and compliant with global and regional safety regulations.

  • Request additional information from reporters and track follow-ups in coordination with local affiliates.

  • Perform quality checks and case clean-up tasks where required, including preparation support for aggregate reports.

  • Maintain proficiency in Baxter’s PV safety system and adhere to internal SOPs and regulatory guidelines.


Required Skills & Competencies

  • Strong understanding of medical and clinical concepts.

  • Excellent verbal and written communication skills.

  • Ability to operate effectively in team environments while maintaining individual accountability.

  • Capability to work independently under strict timelines and shifting priorities.

  • Strong multitasking and organizational skills.

  • Basic knowledge of global pharmacovigilance regulations is an advantage.


Education

  • Degree in Pharmacy, Nursing, Life Sciences, or a related scientific field.

  • Freshers are eligible; prior exposure to regulatory or drug safety environments is an added advantage.


Equal Opportunity Commitment

Baxter is an equal opportunity employer committed to fostering an inclusive and diverse workplace. All qualified applicants are considered without discrimination based on race, gender, age, nationality, disability, or legally protected status.