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Specialist, Ra

Baxter
3-8 years
₹7,00,000 – ₹16,00,000 per annum
Ahmedabad, India
15 June 24, 2026
Job Description
Job Type: Full Time, Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Job Title
Specialist – Regulatory Affairs (RA)

Company
Baxter

Location
Ahmedabad, Gujarat, India

Job Overview
The Specialist – Regulatory Affairs role focuses on pharmacovigilance and regulatory safety reporting activities, including aggregate safety reports, risk management plans, signal management, and global safety database maintenance. The role ensures compliance with global and local regulatory requirements across post-marketing surveillance and product lifecycle safety activities.


Key Responsibilities

1. Aggregate Safety Reporting (PSUR / PBRER / PADER)

  • Provide pharmacovigilance support for regulatory submissions and post-approval activities

  • Prepare, review, and coordinate PSUR, PBRER, and PADER reports

  • Manage authoring support and RFI responses

  • Coordinate scheduling and timely submission of safety reports

  • Liaise with regulatory affairs and PV teams to meet deadlines


2. Risk Management Plan (RMP) Activities

  • Assist in development and maintenance of Risk Management Plans

  • Coordinate with global and local regulatory teams for timely RMP submissions

  • Ensure alignment with regulatory submission timelines and requirements


3. CO/NCO Regulatory Activities

  • Support development and maintenance of CO/NCO documentation

  • Coordinate submissions with global and internal regulatory teams

  • Ensure compliance with submission timelines and regulatory expectations


4. Signal Management & Safety Labeling

  • Support designation and updates of Reference Safety Information (RSI)

  • Manage CCDS/CCSI generation, updates, and periodic reviews

  • Perform safety signal evaluation and implement label changes

  • Support local label updates based on global safety changes


5. Regulatory Safety Databases (XEVMPD)

  • Maintain Extended EudraVigilance Medicinal Product Dictionary (XEVMPD) database

  • Manage EV code updates and new product code creation

  • Ensure accuracy and compliance of safety product data across systems

  • Monitor global labeling updates through systems like Fluxguard


6. Cross-functional Collaboration

  • Work with global pharmacovigilance, regulatory, and safety teams

  • Ensure timely communication and coordination across stakeholders

  • Support alignment of global and local regulatory requirements


Required Skills & Experience

  • Experience in pharmacovigilance or regulatory affairs (safety reporting focus)

  • Knowledge of PSUR, PBRER, PADER processes

  • Understanding of RMP, signal management, and safety labeling

  • Familiarity with XEVMPD and regulatory safety databases

  • Strong knowledge of global PV regulations and guidelines

  • Good coordination and communication skills

  • Ability to manage multiple regulatory timelines


Preferred Skills

  • Experience in global pharmaceutical regulatory environment

  • Exposure to EU regulatory frameworks (EMA, EudraVigilance)

  • Knowledge of CCDS/CCSI processes

  • Strong documentation and reporting skills

  • Experience working with cross-functional global teams


Work Environment

  • Full-time office-based role (Ahmedabad)

  • Interaction with global regulatory and pharmacovigilance teams