Baxter has announced multiple pharmaceutical and healthcare job openings in Ahmedabad, Gujarat for experienced candidates in Research & Development (R&D), Extractables & Leachables characterization, and Regulatory Affairs (RA). These Baxter careers are ideal for professionals from Pharmaceutics, Pharmacy, Chemistry, and Regulatory backgrounds looking to work in a globally recognized healthcare organization.

The latest Baxter job openings include:

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

Candidates with experience in formulation development, analytical characterization, pharmacovigilance documentation, and regulatory compliance are encouraged to apply.

Baxter Hiring 2026 – Job Overview

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

Key Responsibilities

• Support launch and lifecycle management of Baxter commercial products
• Execute laboratory batches and investigations
• Prepare technical reports and documentation
• Assist in Design History File (DHF) maintenance
• Support compendial product changes and compliance activities
• Handle agency and customer queries related to products
• Coordinate laboratory material and license availability

Qualifications

• Master’s in Pharmaceutics or equivalent
• Minimum 7 years of pharmaceutical industry experience
• Experience in formulation development and laboratory batch execution
• Strong analytical, communication, and problem-solving skills

Preferred Skills

• Product lifecycle management
• Pharmaceutical formulation development
• Technical documentation
• Quality Management Systems (QMS)

2. Specialist, Regulatory Affairs (RA)

Key Responsibilities

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

Qualifications

• Background in Pharmacy, Life Sciences, or Regulatory Affairs
• Experience in aggregate safety reporting and pharmacovigilance
• Knowledge of global regulatory submission processes
• Strong coordination and documentation skills

Preferred Skills

• Pharmacovigilance reporting
• Regulatory compliance
• Signal management
• Labeling and safety documentation

3. Associate Scientist II, R&D Characterization

Key Responsibilities

• Conduct Extractables & Leachables (E&L) studies
• Perform analytical characterization and structure elucidation
• Use advanced analytical instruments including LC-MS, GC-MS, ICP-MS, HRMS
• Interpret chromatographic and spectroscopic data
• Author technical protocols and reports
• Support laboratory setup and regulatory compliance
• Collaborate with CROs and global scientific teams

Qualifications

• M.Pharm, MSc Chemistry, or PhD in Chemistry-related field
• 8–10 years of analytical characterization experience
• Expertise in LC-MS, GC-MS, HRMS, or ICP-MS
• Knowledge of GMP and analytical validation

Preferred Skills

• Structure elucidation
• Impurity characterization
• Analytical method development
• Extractables & Leachables studies

Why Join Baxter?

Working at Baxter provides professionals an opportunity to contribute to global healthcare innovation. Baxter emphasizes:

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

How to Apply

Application Link For Associate Scientist II, R&D Characterization

Application Link For Associate Scientist – II, R&D – SPO

Application Link For Specialist, Regulatory Affairs