GSK Hiring Graduate Intern - CMC RA & Specialist QA Audit Intake
Are you seeking GSK Careers Bengaluru or a Regulatory Affairs Internship in India? Global biopharmaceutical leader GSK is recruiting life sciences and pharmacy professionals for two key positions at its Global Services center in Bengaluru.
These drug compliance and quality assurance vacancies are based at the Bengaluru Luxor North Tower office, operating under a hybrid schedule. The openings are suitable for freshers and experienced candidates holding degrees in Pharmacy, general Sciences, Biotechnology, Microbiology, or Chemistry (B.Pharm/M.Pharm/M.Sc/B.Sc). Selected candidates will author technical CMC documents, coordinate GxP audit schedules, and manage quality tracking databases. To write a resume detailing your dossier collation, CAPA tracking, or electronic QA formatting, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Role & Location | Job Details |
|---|---|
| Graduate Intern – CMC RA, Delivery, Small Molecules Mature Products 📍 Bengaluru (Hybrid) |
• Experience: 0–1 Years (Freshers / recent graduates) • Job ID: 444568 • Focus: Technical CMC writing, marketing authorization support, database tracking • Application Deadline: 11 July 2026 |
| Specialist – QAC Audit Intake Coordinator (Global Contract Operations) 📍 Bengaluru (Hybrid) |
• Experience: 3+ Years (Quality Assurance & GMP audit coordination) • Job ID: 440527 • Focus: Audit scheduling, CAPA tracking, supplier quality, eQMS compliance • Application Deadline: 9 July 2026 |
💼 Key Responsibilities
1. Graduate Intern – CMC Regulatory Affairs:
- Dossier Compilation: Draft and review technical Chemistry, Manufacturing, and Controls (CMC) regulatory files.
- Marketing Submissions: Support global marketing authorization submissions and product lifecycle records.
- Database Management: Input and organize compliance metadata within the Regulatory Information Management (RIM) database.
- Risk Escalation: Highlight quality issues and data inconsistencies in submissions to team leads.
- Global Collaboration: Coordinate with international regulatory hubs to streamline registration.
2. Specialist – QAC Audit Intake Coordinator:
- Audit Management: Coordinate, schedule, and log internal and external quality audits for global supplier networks.
- CAPA Surveillance: Manage Corrective and Preventive Action (CAPA) tracking, auditing records for resolution.
- QMS Maintenance: Update and archive audit findings, reports, and dashboards in the electronic QMS.
- Inspection Support: Prepare files and logs for national health authority regulatory inspections.
- Supplier Coordination: Interact with contract manufacturing organizations (CMOs) to align on compliance guidelines.
To learn how GSK regulatory affairs and quality assurance specialist salaries compare to conventional pharmacovigilance drug safety associate and clinical programming roles, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Intern Role: Bachelor's or Master's degree in Pharmacy, Life Sciences, Biotechnology, or Chemistry. Ideal for fresh graduates looking for a career start.
- Specialist Role: Bachelor's/Master's degree in Pharmacy, Chemistry, Microbiology, or related fields with a minimum of 3 years of active experience in pharmaceutical QA, GMP auditing, or quality operations.
- Documentation Capabilities: Strong attention to detail to check clinical parameters, formulation details, and guidelines.
- eQMS Knowledge: For the specialist role, experience using Quality Management Systems (e.g. Veeva, TrackWise) is preferred.
- Communication: Fluent English (written and verbal) to draft reports and interface with international site investigators.
For pharmacy and science graduates evaluating regulatory affairs compared to conventional laboratory quality control or chemical formulation careers, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join GSK?
- Work inside a global biopharmaceutical leader dedicated to getting ahead of disease together.
- Broad career exposure across respiratory, oncology, immunology, and infectious disease therapies.
- Modern offices in Bengaluru (Luxor North Tower) featuring a hybrid working model.
- Access to global corporate mentoring programs and international career networks.
To review your basic knowledge of clinical databases, safety protocols, and GCP guidelines before your screening assessments, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 RA & QA vs Healthcare IT
GSK RA and QA professionals author drug dossiers, track CAPA files, and audit GxP compliance metrics, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for GSK Candidates
- Highlight GMP Audit Exposure: For the coordinator role, name specific GMP/GxP audits you have coordinated or documented.
- Detail Academic RA Projects: For the intern role, highlight pharmacy project topics, referencing eCTD modules or dossiers.
- Specify QMS Systems: List databases (Trackwise, Veeva Vault, SAP, etc.) in which you hold data entry proficiency.
💬 GSK RA & QA Interview Questions
- Q1. What is the significance of the CMC section in a marketing authorization application?
Answer Guidance: The Chemistry, Manufacturing, and Controls (CMC) section details the drug substance and product composition, manufacturing method, analytical controls, and stability profiles, verifying product quality. - Q2. How do you track and verify a CAPA lifecycle?
Answer Guidance: I log the audit deviation, assign corrective actions with owners, track mitigation steps to completion, review objective evidence of completion, and log closure details inside the eQMS database. - Q3. Explain the term 'GxP' and its importance in pharmaceutical contract operations.
Answer Guidance: GxP represents general good practice quality guidelines (such as GMP, GCP, GDP). In contract operations, it ensures outsourced suppliers maintain safety, traceability, and product quality.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via GSK's official Workday careers board. Click the buttons below to apply:
Apply for Graduate Intern – CMC RA (Deadline: 11 July 2026) Apply for QA Audit Intake Coordinator (Deadline: 9 July 2026)❓ Frequently Asked Questions
Q. Is the GSK Graduate Intern role open to pharmacy freshers?
Yes, this is an internship position open to fresh B.Pharm/M.Pharm and MSc Life Science graduates.
Q. What is the application deadline for the Specialist QA Audit Coordinator?
The application deadline for the QAC Audit Intake Coordinator role is **9 July 2026**. Interested candidates must apply urgently.
Q. What is the work model for these positions?
Both roles feature a hybrid working arrangement at GSK's office in Luxor North Tower, Bengaluru.
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