Jobs / United Kingdom / Glaxosmithkline LLC
Product Manager - Regulatory Vault
Glaxosmithkline LLC · 🇬🇧 UK – London – New Oxford Street
Sponsorship verdict
No sponsorship evidence yet
No government record and no wording either way. Not a refusal — ask the recruiter.
- No government sponsor record hereNo government sponsor record covers this employer in this country.
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- Can’t check pay against the visa rulesNo salary stated. UK Skilled Worker visa needs at least £41,700 a year (new-entrant (under 26, recent Student/Graduate visa) or STEM PhD: £33,400). Source: https://www.gov.uk/skilled-worker-visa/when-you-can-be-paid-less, rules effective 2025-07-22.
- Confirmed live todayWhen a source last listed this job as open.
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
Or apply yourself on the official page →
Why not apply?
No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.
SponsorApply flags time-wasters so your applications go where they can land. These come from the posting's own wording — read the original listing to confirm. See better-fit alternatives →
Sponsor Radar — Glaxosmithkline LLC
No government sponsor record covers this employer in this country.
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Glaxosmithkline LLC →
About the role
Are you passionate about making impactful contributions to the world of medicines and vaccines? GlaxoSmithKline (GSK) invites you to join our dynamic R&D Digital and Tech Team as a Product Manager - Regulatory Vault. In this pivotal role, you will drive the vision and roadmap for the evolution of GSK's Regulatory Vault (Veeva RIM), ensuring our regulatory processes are streamlined and efficient. As Product Manager - Regulatory Vault you will partner with business owners across R&D and other functions to shape product vision, prioritize work, and coordinate delivery with our Managed Service Provider. You will map user journeys, define requirements, and ensure features are configured and delivered to meet regulatory and business needs. Practical experience with regulatory processes and Veeva RIM (or similar RIM systems) is important; you will develop your product leadership skills while influencing configurable SaaS solutions. At GSK R&D, we are driven by an ambitious goal to expedite submission cycle times and enhance submission quality across over 160 markets. Our investment in a cutting-edge Veeva RIM-based Regulatory Vault is a testament to our commitment to excellence. This platform is an integral part of a comprehensive Veeva ecosystem, supporting the entire development process. GSK stays dedicated to influencing Veeva’s roadmap and extracting maximum value from our investments. Key Responsibilities: • Define and maintain the product backlog and roadmap for Regulatory Vault features aligned to stakeholder needs. • Elicit, document and prioritise requirements, user stories, and acceptance criteria. • Coordinate with the Managed Service Provider, internal IT, and business stakeholders to deliver features iteratively. • Support testing, release readiness, and change management to adoption. • Build domain knowledge of GSK R&D medicines and vaccines regulatory processes and contribute to product strategy. • Ensure delivered solutions comply with internal security, risk, and external regulatory expectations. • Provide input to vendor relationships and configuration choices; escalate and unblock issues as needed. Basic Qualifications: • Bachelor’s degree or comparable experience in computer science, life sciences, regulatory affairs, or related discipline. • Experience delivering IT-enabled solutions in a life sciences or regulated environment, including involvement in product ownership, business analysis, or project delivery. • Practical experience or familiarity with regulatory processes and systems; experience with Veeva RIM is highly desirable. • Strong collaboration, communication, and stakeholder management skills. Preferred Qualifications: • Veeva white belt or other relevant Veeva training (desirable). • Experience with submission publishing (eCTD/non-eCTD), Regulatory Intelligence tools, or RIM integrations. • Experience working with SaaS/configurable-off-the-shelf products and managed service partners. • Experience in GxP contexts or familiarity partnering with Risk, QA or Audit teams is advantageous. • Data-driven mindset and focus on delivering business value and simplification. Closing date for applications: 11th October 2026 Skills Agile Methodology, Backlogs, Cross-Functional Teamwork, Design Thinking, DevOps, Process Diagrams, Product Strategies, Project Management, Requirements Gathering, Services Management, Software Development, User Experience (UX), User Research, User Story Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, gro