At a Glance
- Tasks: Lead digital products for collaborative content generation in a global biopharma company.
- Company: GSK, a leading global biopharma company focused on innovative health solutions.
- Benefits: Hybrid working model, competitive salary, and opportunities for professional growth.
- Other info: Join a dynamic team with a focus on innovation and collaboration.
- Why this job: Make a real impact on health by transforming scientific content processes.
- Qualifications: Experience in digital product management and understanding of regulatory content lifecycle.
The predicted salary is between 63000 - 77000 £ per year.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease.
It aims to positively impact the health of 2.5 billion people by the end of the decade through innovation in specialty medicines and vaccines, focusing on respiratory, immunology and inflammation, oncology, HIV, and infectious diseases.
The role
This position sits within R&D Digital and Technology, working across Medical Writing, Regulatory, Safety, CMC, Clinical and Publications.
The team designs and delivers digital products that transform how scientific and regulatory content is authored, reviewed and submitted.
As Senior Product Owner for Content Generation and Collaboration, you would lead the digital products enabling structured, collaborative and increasingly automated authoring of evidence and regulatory content.
You would represent technology for the content generation and collaboration workstream in a major strategic programme and mentor other Product Owners.
- What you would do
- Co-create the product vision and roadmap with business stakeholders, owning objectives, key results and the value case, and continuously testing ideas before committing capacity.
- Bring strong domain understanding of the evidence and regulatory content lifecycle, framing problems through jobs-to-be-done and challenging requirements that do not map to real user needs.
- Drive structured content capabilities, including modular authoring, component management and reuse, to improve the speed, quality and consistency of evidence preparation and authoring journeys.
- Lead as a technology partner, shaping trade-offs with architects and engineers, owning key technical decisions, and managing technical dependencies, non-functional requirements and technology risks alongside functional delivery.
- Work AI-first by using AI to accelerate discovery, drafting and scenario analysis for backlog decisions, coaching the team on responsible prompting, and judging where AI-assisted authoring adds value versus risk.
- Own end-to-end delivery of your product, including milestones, budget, roadmap and quality, validating value early through proofs of value and pilots before scaling.
- Build quality and compliance into delivery, safeguarding data integrity (ALCOA+), embedding Gx P, privacy and AI-governance requirements throughout change, and running risk assessments before major releases.
- Partner with and mentor colleagues across Medical Writing, Regulatory, Safety, CMC, Clinical and Publications, negotiating scope constructively and coaching junior Product Owners.
- Manage strategic technology suppliers and delivery partners to ensure deliverables, technical quality, documentation and knowledge transfer support the roadmap and GSK standards.
- What they are looking for
- Bachelor's degree or equivalent experience in a scientific, technical or related discipline (life sciences, computer science, engineering or similar).
- Significant experience in digital product management or product ownership in progressively senior roles, with the ability to independently own vision, roadmap and prioritisation for a complex workstream.
- Hands-on backlog ownership, including writing clear, testable user stories and acceptance criteria, running refinement with engineering, and prioritising using structured methods (RICE, WSJF, Mo SCo W).
- Experience in pharmaceutical R&D, clinical development or regulatory affairs, with direct exposure to scientific, regulatory or medical content authoring.
- Proven track record of owning end-to-end delivery for digital products, including value validation through pilots or proofs of value before scale-up.
- Strong understanding of enterprise application architecture, integrations and APIs, MCP, cloud environments, identity and access, data flows and non-functional requirements.
- Working knowledge of Gx P and validated systems, with sound data-integrity, quality and compliance judgement.
- Experience partnering with architects and engineers on technical trade-offs, with sufficient technical fluency to own product-level decisions and sense-check estimates.
- Demonstrated ability to work in global, matrixed organisations and influence cross-functional teams.
- (Preferred) Hands-on experience with structured content and component management, modular document design, or publications-management systems such as Veeva Vault, Certara Co Author or Arbortext.
- (Preferred) Experience with AI-assisted authoring or NLP-based solutions in regulated or scientific content domains.
- (Preferred) Familiarity with AI and ML solutions in regulated environments and associated validation and governance requirements.
- (Preferred) Experience leading a technology workstream within a large transformation programme in a complex enterprise environment.
- (Preferred) Familiarity with e CTD, structured content standards or the wider submission data landscape (e. g. IDMP).
- Working arrangements
The role is based in London, UK, on a hybrid (remote and on-site) basis.
Sr. Product Owner - Content Generation in London employer: GSK
GSK is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the heart of Stevenage. With a strong commitment to employee growth, you will have access to extensive development opportunities while working on groundbreaking medicine projects. The hybrid work model and future relocation to Cambridge provide a unique advantage, ensuring a vibrant environment for both personal and professional advancement.
StudySmarter Expert Advice🤫
We think this is how you could land Sr. Product Owner - Content Generation in London
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like GSK.
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We think you need these skills to ace Sr. Product Owner - Content Generation in London
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 GSK!
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 GSK that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at GSK!
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 GSK, 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 GSK
✨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 GSK that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
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.
✨Know Their Products
Take some time to familiarise yourself with GSK’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
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.
