At a Glance
- Tasks: Lead the development of AI-enabled digital products for regulatory intelligence and health authority engagement.
- Company: Join GSK, a global biopharma company with a mission to impact 2.5 billion lives by 2030.
- Benefits: Flexible working culture, career growth opportunities, and a commitment to innovation in healthcare.
- Other info: Be part of a diverse team that values ambition, accountability, and doing the right thing.
- Why this job: Make a real difference in global health while working with cutting-edge technology and talented teams.
- Qualifications: Master’s degree and significant experience in digital product management within life sciences.
The predicted salary is between 80000 - 100000 £ per year.
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.
As Product Director, you are accountable for the digital products and platforms that power GSK’s regulatory intelligence and its engagement with global health authorities. Sitting within R&D Digital & Technology, you translate the needs of Regulatory Affairs, Clinical and wider R&D into a coherent, AI-enabled product vision — giving regulatory teams timely intelligence, structured insight and seamless tools to manage interactions with agencies such as the FDA, EMA, MHRA and PMDA.
You set the strategy and roadmap, lead and develop your product portfolio, and act as technical SME for the programmes that deliver these capabilities. You influence at VP/SVP level and role-model GSK’s values — Ambitious for patients, Accountable for impact, Do the right thing.
Responsibilities
- Own the product vision and roadmap for Regulatory Intelligence & Health Authority engagement, aligned to the Evidence Presentation & Regulatory strategy and translated into clear value hypotheses, OKRs and prioritised backlogs.
- Lead discovery with Regulatory Affairs, Global Labelling and Transparency teams to map end-to-end processes for regulatory intelligence, health authority questions and requests, and submissions.
- Drive the design and delivery of AI-enabled platforms that monitor, ingest and synthesise global regulatory developments, guidance, precedent and competitor activity into actionable, traceable, audit-ready insight.
- Own the digital tools supporting the planning, tracking and analysis of interactions and submissions with global agencies (FDA, EMA, MHRA, PMDA, NMPA), capturing history, commitments and outcomes to raise engagement quality.
- Champion an AI-first approach — making AI, NLP and analytics default tools for intelligence capture, signal detection and decision support, with robust validation of AI outputs.
- Lead agile delivery across product, engineering, data and design teams; own the backlog and release plan, manage budgets and vendors, and hold teams to account for quality, pace and measurable value.
- Embed quality, risk and compliance — GxP, privacy and AI governance — from the outset, ensuring platforms support transparent, auditable HA interactions and public disclosure commitments.
- Build trusted partnerships and influence at VP/SVP level across R&D, Quality, Legal and IT; coach and grow a high-performing, multi-disciplinary team, role-modelling GSK’s values and an inclusive, psychologically safe culture.
Basic Qualifications
- Master’s degree or equivalent experience in a scientific, technical or quantitative discipline (e.g. life sciences, computer science, engineering, mathematics).
- ~10+ years leading technology-focused transformation and ~5+ years of progressive experience in digital product management and leadership.
- Significant life-sciences experience with direct exposure to regulatory, clinical development or related functions.
- Track record of owning and scaling enterprise digital products, operating with sizeable budgets and vendor portfolios.
- Proven people-leadership experience, including line-managing and building high-performing product teams.
- Experience delivering AI, data and analytics-enabled products on modern data platforms and cloud technologies.
- Experience operating in a GxP / validated-systems context, with strong data integrity, quality and compliance judgement.
Preferred Qualifications
- Deep knowledge of the regulations, processes and technologies supporting the final mile of the clinical pipeline, including global health authority interactions and public transparency.
- Hands-on experience with AI-assisted authoring or NLP-based solutions in regulated or scientific-intelligence domains.
- Familiarity with GxP and validation expectations for systems used in regulatory submissions and evidence generation.
- Demonstrated executive influence with VP/SVP-level stakeholders to drive complex technology decisions and adoption.
- Experience scaling Agile ways of working across global, multi-disciplinary teams and managing strategic technology vendor partnerships.
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.
Product Director, Regulatory Intelligence and Engagement employer: GlaxoSmithKline
At GSK, we are committed to fostering a dynamic and inclusive work environment where innovation thrives. As a Product Director in Regulatory Intelligence and Engagement, you will have the opportunity to lead transformative projects that directly impact global health, while benefiting from our strong focus on employee development and a culture that values accountability and ambition for patients. With access to cutting-edge technology and a collaborative team, you will be empowered to grow your career and make a meaningful difference in the lives of billions.
StudySmarter Expert Advice🤫
We think this is how you could land Product Director, Regulatory Intelligence and Engagement
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We think you need these skills to ace Product Director, Regulatory Intelligence and Engagement
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at GlaxoSmithKline!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show GlaxoSmithKline that you're not just a fit for the job but also a safety-conscious candidate!
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Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At GlaxoSmithKline, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at GlaxoSmithKline
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at GlaxoSmithKline that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
