Global biopharmaceutical leader GSK has announced exciting career opportunities for life sciences and pharmacy professionals in Bengaluru. The company is currently hiring for Graduate Intern โ CMC Regulatory Affairs (Delivery, Small Molecules Mature Products) and Specialist โ QAC Audit Intake Coordinator (Global Contract Operations).
These openings are ideal for B.Pharm, M.Pharm, MSc, Life Sciences, Pharmacy, Chemistry, Microbiology, and related graduates and experienced professionals looking to build careers in Regulatory Affairs, Quality Assurance, GMP, CMC Documentation, CAPA, and Pharmaceutical Compliance.
If you’re searching for GSK jobs in Bengaluru, Regulatory Affairs jobs 2026, Quality Assurance jobs in Pharma, or Life Sciences jobs in India, this recruitment offers an excellent opportunity to work with one of the world’s leading pharmaceutical companies.
About GSK
GSK is a global biopharmaceutical company committed to uniting science, technology, and talent to improve global healthcare. Operating in over 150 countries, GSK develops innovative medicines and vaccines across respiratory, oncology, immunology, infectious diseases, and HIV while maintaining world-class manufacturing and regulatory standards.
1. Graduate Intern โ CMC RA, Delivery, Small Molecules Mature Products
Location: Bengaluru (Hybrid)
Employment Type: Full-Time
Application Deadline: 11 July 2026
Job Overview
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 Skills
- Business Communication
- Digital Fluency
- Regulatory Compliance
- Scientific Documentation
- Matrix Collaboration
- Risk Identification
- Pharmaceutical Regulations
Educational Qualification
Suitable for candidates with:
- B.Pharm
- M.Pharm
- MSc Life Sciences
- Biotechnology
- Chemistry
- Pharmaceutical Sciences
- Related Life Science Degrees
Fresh graduates and recent postgraduates interested in Regulatory Affairs are encouraged to apply.
2. Specialist โ QAC Audit Intake Coordinator (Global Contract Operations)
Location: Bengaluru (Hybrid)
Employment Type: Full-Time
Application Deadline: 9 July 2026
Job Overview
The Quality Assurance Audit Intake Coordinator will manage audit workflows, CAPA tracking, quality documentation, supplier quality coordination, and regulatory inspection support across GSK’s Global Contract Operations network.
Key Responsibilities
- Coordinate internal and external audit requests.
- Schedule quality audits.
- Maintain audit records in Quality Management Systems.
- Track CAPA activities through completion.
- Prepare reports and quality dashboards.
- Support regulatory inspections.
- Coordinate with cross-functional global teams.
- Ensure compliance with GMP and GxP requirements.
Basic Qualifications
- Bachelor’s Degree in:
- Pharmacy
- Chemistry
- Microbiology
- Life Sciences
- Related disciplines
- Minimum 3 years experience in:
- Quality Assurance
- Audit Coordination
- GMP
- Quality Operations
Preferred Qualifications
- Supplier Quality Management
- CAPA Management
- Regulatory Inspection Support
- Electronic Quality Management Systems (eQMS)
- Risk Management
- Pharmaceutical Auditing
Why Join GSK?
Joining GSK provides opportunities to work in a globally recognized pharmaceutical organization focused on innovation and patient care.
Employees benefit from:
- Hybrid working model
- Global career opportunities
- Exposure to Regulatory Affairs and Quality Systems
- International project experience
- Inclusive workplace culture
- Learning and development programs
- Competitive compensation
- Career growth in pharmaceutical manufacturing and compliance
Who Should Apply?
These GSK openings are suitable for candidates with backgrounds in:
- B.Pharm
- M.Pharm
- Pharm.D
- MSc Life Sciences
- Biotechnology
- Microbiology
- Chemistry
- Pharmaceutical Sciences
- Regulatory Affairs
- Quality Assurance
- GMP Compliance
- Pharmaceutical Manufacturing
How to Apply
Application Link For Specialist – QAC Audit Intake Coordinator – GCC
Application Link For Graduate Intern โ CMC RA, Delivery, Small Molecules Mature Products
