PHARMAFull-time
Graduate Intern – CMC Regulatory Affairs
BANGALORE (IN)HYBRIDPOSTED: 7/8/2026
PHARMAFull-time
HIRING ORGANIZATIONGSKPharmaceuticals / Healthcare / Life Sciences
ROLE DEFINITION & RESPONSIBILITIES
The Graduate Intern will support Chemistry, Manufacturing & Controls (CMC) Regulatory Affairs activities by preparing regulatory documentation, maintaining regulatory data, supporting product lifecycle management, and ensuring compliance with international regulatory standards.
Key Responsibilities
Prepare CMC technical regulatory documents.
Support global marketing authorization submissions.
Maintain regulatory information in RIM and structured data systems.
Ensure high-quality regulatory documentation.
Identify submission risks and escalate appropriately.
Collaborate with regulatory teams and stakeholders.
Learn global pharmaceutical regulatory requirements.
Support lifecycle management activities.
REQUIRED VERIFIED SKILLS
Business Communication
Digital Fluency
Regulatory Compliance
Scientific Documentation
Matrix Collaboration
Risk Identification
Pharmaceutical Regulations
COMPENSATION & REWARDS
₹0.3L - 0.5L per annum
The stipend/salary for interns or early-career profiles at this location is noted to range around ₹25,000 to ₹50,000 per month, which aligns with premier global biopharmaceutical standards in India.
ORGANIZATION CONTEXT & CULTURE
GSK (GlaxoSmithKline) is a global biopharma company with a purpose to unite science, technology, and talent to get ahead of disease together. The company focuses on the research, development, and manufacture of innovative vaccines and specialty medicines. GSK's products address a wide range of diseases, aiming to impact the health of millions worldwide.
TEAM SIZE: 70,000+ employees
INDUSTRY: Pharmaceuticals / Healthcare / Life Sciences
EXPECTED CAREER ROADMAP
GSK offers a globally recognized platform with extensive training in international regulatory guidelines, providing entry-level professionals an exceptional foundation for advancement into senior regulatory affairs and compliance roles.
APPLICATION ADVISORY
Highlight any academic projects involving regulatory dossier preparation, knowledge of CTD/eCTD structures, or digital data tools to differentiate your profile.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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