GlaxoSmithKline (GSK), a global biopharmaceutical leader, is hiring for the role of Apprentice – Submission Delivery Excellence, Lifecycle Management (LCM) at its Bengaluru Luxor North Tower location. This is a full-time apprenticeship opportunity ideal for candidates looking to build a strong foundation in Regulatory Affairs, dossier submissions, and global lifecycle management within a multinational pharma environment.
This opportunity is particularly relevant for pharmacy, life sciences, and regulatory affairs aspirants seeking hands-on exposure to global regulatory submissions, CMC variations, renewals, and health authority interactions.
📅 Application Deadline: January 11, 2026 (Apply Immediately)
📌 Key Responsibilities – Submission Delivery Excellence Role
As an Apprentice at GSK, you will work under managerial guidance and contribute to high-quality regulatory submissions across global markets.
Core Responsibilities Include:
- Deliver assigned regulatory submissions aligned with approved dossier strategies and timelines
- Coordinate with cross-functional teams (CMC, Clinical, Nonclinical, Manufacturing)
- Manage multiple regulatory activities including:
- CMC & Therapeutic Variations
- PBRER submissions
- Renewals and Site Registrations
- Tender-related documentation
- Support responses to health authority queries and regulatory agency requests
- Coordinate legalization, certification, and third-party documentation
- Ensure compliance with GSK regulatory processes and global standards
- Use regulatory intelligence tools to identify country-specific requirements
- Proactively identify and escalate regulatory risks impacting submissions
- Review peer deliverables and suggest process improvements
- Build regulatory knowledge across global guidelines and policies
This GSK regulatory apprenticeship provides real-world exposure to submission lifecycle management, making it a strong career entry point in pharma regulatory affairs.
🎓 Qualifications & Eligibility Criteria
Preferred Background:
- Degree in Pharmacy, Life Sciences, Biotechnology, or related discipline
- Strong interest in Regulatory Affairs and Global Submissions
- Basic understanding of:
- Dossier structures (CTD/eCTD)
- Pharmaceutical product registration processes
- Excellent communication, coordination, and documentation skills
- Ability to manage multiple deliverables and work cross-functionally
- Learning agility and attention to compliance and quality
Fresh graduates and early-career professionals with regulatory exposure or internships are encouraged to apply.
💼 Why Join GSK?
GSK is a purpose-driven global biopharma company focused on innovation in vaccines and specialty medicines.
Employee Benefits & Value Proposition:
- Exposure to global regulatory submissions
- Work with experienced regulatory professionals
- Strong learning culture and structured ways of working
- Inclusive, ethical, and growth-oriented organization
- Opportunity to build a long-term career in Regulatory Affairs & LCM
GSK’s culture emphasizes patient impact, accountability, and integrity, making it a trusted employer in the pharmaceutical industry.
📍 Job Location
📌 Bengaluru – Luxor North Tower, Karnataka
💰 Estimated Salary (India)
💵 ₹3.5 – ₹6.0 LPA (Estimated for Apprentice / Entry-Level Regulatory Roles)
Actual compensation may vary based on qualifications and company policy.
📨 How to Apply
