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Specialist, Ra

Baxter
2+ years
INR 8 LPA – 14 LPA
Ahmedabad, India
1 July 2, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Specialist, Regulatory Affairs (RA)

Company: Baxter
Location: Ahmedabad, Gujarat, India
Department: Regulatory Affairs / Pharmacovigilance
Job Type: Full-Time


JOB OVERVIEW

The Specialist, Regulatory Affairs (RA) is responsible for supporting global pharmacovigilance and regulatory affairs activities related to aggregate safety reporting, Risk Management Plans (RMPs), Company Core Data Sheet (CCDS), Company Core Safety Information (CCSI), Reference Safety Information (RSI), signal management, and regulatory submissions. The role ensures timely preparation, review, coordination, and submission of global safety documents while maintaining compliance with international pharmacovigilance regulations and regulatory requirements.


KEY RESPONSIBILITIES

Aggregate Safety Reporting

  • Prepare, review, and coordinate Periodic Safety Update Reports (PSURs).

  • Support Periodic Benefit-Risk Evaluation Reports (PBRERs).

  • Prepare Periodic Adverse Drug Experience Reports (PADERs).

  • Support Addendum to Clinical Overview (ACO) activities.

  • Coordinate aggregate report scheduling and submissions.

  • Provide authoring support for aggregate safety reports.

  • Evaluate Requests for Information (RFI) related to safety reports.

  • Ensure timely submission of aggregate safety documents.

  • Coordinate with Global Pharmacovigilance and Regulatory Affairs teams.

Regulatory Affairs

  • Provide regulatory support for new product submissions.

  • Support post-approval regulatory activities.

  • Coordinate with global and local regulatory teams.

  • Ensure compliance with global regulatory timelines.

  • Support regulatory documentation and submission activities.

Risk Management Plan (RMP)

  • Assist in the preparation and maintenance of Risk Management Plans (RMPs).

  • Coordinate RMP submissions with global teams.

  • Monitor RMP submission timelines.

  • Support updates to risk management documentation.

Company Core Documents

  • Assist in developing Company Core Data Sheets (CCDS).

  • Prepare and maintain Company Core Safety Information (CCSI).

  • Develop and update Reference Safety Information (RSI).

  • Support Company Core Labeling updates.

  • Manage Core/National Core (CO/NCO) documentation.

Signal Management

  • Monitor emerging safety signals.

  • Perform safety signal evaluations.

  • Update CCDS, CCSI, and RSI based on identified safety signals.

  • Conduct periodic reviews of core safety documents.

  • Support local product labeling updates.

Labeling & Safety Documentation

  • Support global and local label updates.

  • Maintain product safety information.

  • Coordinate safety labeling revisions.

  • Ensure regulatory compliance of product labeling.

XEVMPD Management

  • Maintain the Extended EudraVigilance Medicinal Product Dictionary (XEVMPD).

  • Coordinate product registration within XEVMPD.

  • Generate and maintain EV Codes.

  • Monitor XEVMPD updates.

  • Ensure product data accuracy in EudraVigilance systems.

Regulatory Database Management

  • Monitor FluxGuard activities.

  • Support global generic label monitoring.

  • Maintain regulatory databases.

  • Ensure regulatory data integrity.

Cross-Functional Collaboration

  • Coordinate with Global Pharmacovigilance teams.

  • Work closely with Regulatory Affairs.

  • Collaborate with Product Safety teams.

  • Support local affiliates and global stakeholders.

  • Communicate with cross-functional departments to ensure timely deliverables.

Compliance & Quality

  • Ensure compliance with global pharmacovigilance regulations.

  • Follow internal SOPs and regulatory guidelines.

  • Maintain accurate regulatory documentation.

  • Support inspection and audit readiness.

  • Ensure timely completion of assigned regulatory activities.


EDUCATIONAL QUALIFICATIONS

Required

  • Bachelor's or Master's Degree in:

    • Pharmacy (B.Pharm/M.Pharm)

    • Life Sciences

    • Biotechnology

    • Biochemistry

    • Pharmaceutical Sciences

    • Related Healthcare Discipline


EXPERIENCE REQUIREMENTS

Preferred

  • Experience in Regulatory Affairs.

  • Experience in Pharmacovigilance.

  • Experience preparing Aggregate Safety Reports.

  • Knowledge of global regulatory submission requirements.

  • Experience with safety labeling and risk management documentation.