Product Manager - Regulatory Vault

Product Manager - Regulatory Vault

Full-Time 55000 - 65000 £ / year (est.) No working from home possible
Gsk

At a Glance

  • Tasks: Drive the vision for GSK's Regulatory Vault and streamline regulatory processes.
  • Company: Join GSK, a global biopharma leader committed to health innovation.
  • Benefits: Flexible working, competitive salary, and opportunities for personal growth.
  • Other info: Inclusive culture with a focus on collaboration and career advancement.
  • Why this job: Make a real impact in medicines and vaccines while developing your product management skills.
  • Qualifications: Bachelor's degree and experience in regulatory processes or IT solutions.

The predicted salary is between 55000 - 65000 £ per year.

This job is with GSK, an inclusive employer. 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, prioritise 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: Monday 29th June 2026

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, growing company where people can thrive.

We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at UKRecruitment.Adjustments@gsk.com where you can also request a call.

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide.

Important notice to Employment businesses/ Agencies: GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorisation before referring any candidates to GSK.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment.

Product Manager - Regulatory Vault employer: Gsk

GSK is an exceptional employer that fosters a culture of inclusivity and innovation, making it an ideal place for professionals passionate about advancing healthcare. With a commitment to employee growth, GSK offers robust development opportunities and a flexible working environment, allowing you to thrive while contributing to impactful projects in the biopharma sector. Join us in our mission to improve global health and be part of a team that values ambition, accountability, and doing the right thing.

Gsk

Contact Details:

Gsk Recruitment Team

We think you need these skills to ace Product Manager - Regulatory Vault

Product Management
Regulatory Processes
Veeva RIM
Stakeholder Management
Requirements Elicitation
User Story Documentation
Project Delivery