GSK Hiring: CMC Regulatory Affairs Intern 2026 | Bengaluru – Apply Now!

About the Role

As a CMC Regulatory Affairs Intern, you will support the preparation of Chemistry, Manufacturing, and Controls (CMC) regulatory documents for global product registrations and lifecycle management.

Responsibilities

• Prepare CMC regulatory documents for global marketing authorizations
• Support lifecycle management and maintenance of registered products
• Execute regulatory activities using RIM and structured data tools
• Ensure high-quality and accurate regulatory data
• Identify risks in submission packages and communicate issues proactively
• Support preparation of regulatory information for global submissions
• Learn and apply global regulatory guidelines, policies, and procedures
• Collaborate with cross-functional teams to support regulatory compliance

What You'll Need

• B.Pharm, M.Pharm, B.Sc, M.Sc, Pharm.D, or Graduation in Pharmacy, Life Sciences, Biotechnology, Chemistry, or Related Discipline
• Strong Communication Skills, Analytical Thinking, Attention to Detail, Problem-Solving, Team Collaboration, Business Resilience, Time Management, and Learning Agility
• Technical skills in CMC Regulatory Affairs, Regulatory Documentation, Pharmaceutical Regulatory Compliance, Regulatory Information Management (RIM), Product Lifecycle Management, Regulatory Data Management, Scientific Documentation, Digital Regulatory Platforms, and Risk Assessment

Resume Tip

Highlight your experience in regulatory affairs, CMC documentation, and pharmaceutical regulatory compliance. Emphasize your analytical and problem-solving skills, as well as your ability to work collaboratively in a team environment.