Baxter Hiring for R&D, Regulatory Affairs & Pharmacovigilance Specialist Roles

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Baxter Hiring for R&D, Regulatory Affairs & Pharmacovigilance Specialist Roles
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Hiring for R&D, Regulatory Affairs & Pharmacovigilance Specialist 

🏢 Baxter
📍 Ahmedabad, Gujarat
🧪 R&D & Characterization
📑 Regulatory Affairs
💊 Pharmacovigilance

Baxter has announced multiple pharmaceutical and healthcare job openings in Ahmedabad for experienced professionals in R&D, Regulatory Affairs, Pharmacovigilance, and Analytical Characterization.

The company is hiring for:

  • Associate Scientist – II, R&D – SPO
  • Specialist, Regulatory Affairs (RA)
  • Associate Scientist II, R&D Characterization

These opportunities are ideal for professionals from Pharmacy, Pharmaceutics, Chemistry, Regulatory Affairs, Pharmacovigilance, and Analytical Sciences backgrounds.

📘 Career Guide: Pharmacovigilance Salary Guide India vs USA

📋 Baxter Recruitment 2026 – Overview

  • Company: Baxter
  • Location: Ahmedabad, Gujarat
  • Department: R&D / Regulatory Affairs
  • Employment Type: Full-Time
  • Experience: 3–10 Years
  • Industry: Pharmaceutical / Healthcare

🧪 1. Associate Scientist – II, R&D – SPO

  • Experience: Minimum 7 Years
  • Qualification: M.Pharm / Pharmaceutics or Equivalent
  • Last Date: 14 May 2026
  • Estimated Salary: ₹10 – ₹18 LPA

📌 Key Responsibilities

  • Support product launch and lifecycle management
  • Execute laboratory batches and investigations
  • Prepare technical reports and documentation
  • Maintain Design History File (DHF)
  • Support product compliance activities
  • Handle agency and customer product queries
  • Coordinate laboratory material availability

💻 Required Skills

  • Formulation development expertise
  • Technical documentation handling
  • Quality Management Systems (QMS)
  • Analytical and problem-solving skills
  • Lifecycle management knowledge

📑 2. Specialist, Regulatory Affairs (RA)

  • Experience: Regulatory Affairs / PV Experience Preferred
  • Qualification: Pharmacy / Life Sciences / Regulatory Affairs
  • Last Date: 15 May 2026
  • Estimated Salary: ₹8 – ₹16 LPA

📌 Key Responsibilities

  • Prepare PSUR, PBRER, and PADER reports
  • Support post-approval regulatory activities
  • Coordinate Risk Management Plan (RMP) submissions
  • Handle CCDS, CCSI, and RSI revisions
  • Manage XEVMPD database and EV code generation
  • Coordinate with global PV and regulatory teams

💻 Required Skills

  • Pharmacovigilance reporting knowledge
  • Regulatory compliance expertise
  • Signal management understanding
  • Labeling and safety documentation
  • Aggregate safety reporting exposure

📚 Learn PV Basics: Top Pharmacovigilance Interview Questions

🔬 3. Associate Scientist II, R&D Characterization

  • Experience: 8–10 Years
  • Qualification: M.Pharm / MSc Chemistry / PhD
  • Last Date: 15 May 2026
  • Estimated Salary: ₹14 – ₹24 LPA

📌 Key Responsibilities

  • Conduct Extractables & Leachables studies
  • Perform analytical characterization activities
  • Interpret chromatographic and spectroscopic data
  • Author technical protocols and reports
  • Support laboratory setup and compliance
  • Collaborate with CROs and global teams

💻 Required Skills

  • LC-MS, GC-MS, ICP-MS, HRMS expertise
  • Structure elucidation
  • Analytical method development
  • Impurity characterization
  • GMP and analytical validation knowledge

🎁 Why Join Baxter?

  • Global exposure in pharmaceutical R&D
  • Collaborative scientific environment
  • Career growth opportunities
  • Advanced analytical technology exposure
  • Regulatory and quality excellence
  • International project collaboration

🎓 Eligible Qualifications

  • B.Pharm
  • M.Pharm
  • Pharm.D
  • BSc / MSc
  • Life Sciences
  • PhD
  • Regulatory Affairs Background
  • Chemistry & Analytical Sciences

💡 Interview Tips

  • Revise formulation and analytical concepts
  • Understand regulatory documentation workflows
  • Prepare questions on PV reporting and compliance
  • Revise LC-MS, GC-MS, and analytical techniques
  • Be confident explaining previous projects and investigations
  • Review GMP, QMS, and ICH-GCP guidelines

📊 Interview Preparation: Healthcare & Data Interview Guide

📄 Resume Tips

  • Highlight R&D, Regulatory, or PV experience clearly
  • Mention analytical instruments and software exposure
  • Add publications, projects, and certifications
  • Keep resume ATS-friendly and professional
  • Include compliance and documentation experience
  • Use clean formatting with no spelling mistakes

📚 Career Guidance: Healthcare Knowledge Hub

❓ Frequently Asked Questions

  • Who can apply? Pharmacy, Life Sciences, Chemistry, and Regulatory professionals.
  • Which roles require experience? All roles require relevant industry experience.
  • Which location is hiring? Ahmedabad, Gujarat.
  • What analytical tools are preferred? LC-MS, GC-MS, ICP-MS, and HRMS.
  • Is pharmacovigilance experience preferred? Yes, for the RA Specialist role.

🚀 Job Application Links

📌 Important Note Before You Apply:

Please make sure to read the complete job description carefully before submitting your application. Ensure your qualifications, technical skills, and experience align with the selected role requirements before proceeding.
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