Reg Submission Lead III, SDE - Pipeline
- Location Bengaluru, India
- Experience ~5-10 yrs
- Job type Full-time
- Posted 6 Oct 2026
- Qualification Master's / Bachelor's
You will be taken to GSK GCC Bangalore’s own careers page to apply. Job ID Job Code: J000578.
Job description
Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together. Find out more: Our approach to R&D
Position Summary
Submission Delivery Excellence (SDE) is a Regulatory Affairs function which brings together the planning, operation and execution aspects for key regulatory deliverables such as new chemical entities, product expansion dossiers, labeling outputs, license maintenance and lifecycle management dossiers and regulatory information management. This position will reside in the Pipeline group which is accountable for planning, production and submittal of Regulatory dossiers to GSK’s primary markets to support registration of new medicines in line with R&D objectives for marketed products and line extensions of regulatory licenses worldwide.
In this role, the position holder will be responsible for coordinating major and lifecycle regulatory submissions in our market expansion regions, managing and tracking project timelines, communicating with regulatory and operational staff across various functions, maintaining submission workplans and up-to-date knowledge of global regulations and guidelines to support internal stakeholders. The position holder will work closely with the GRL/Regional Rep (TG)/EU Agent/LOC (or equivalent) and functional teams to coordinate the appropriate content for specific submission packages within the Regulatory Vault system, maintain an accurate and current project plan and drive team members to deliver compliant submission dossiers to accelerated timelines.