At a Glance
- Tasks: Lead the design and governance of structured component management across R&D.
- Company: Join GSK, a global biopharma company with a mission to improve health for billions.
- Benefits: Enjoy a hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Be part of an inclusive culture that values diversity and innovation.
- Why this job: Make a real impact in healthcare by shaping standards that accelerate scientific progress.
- Qualifications: Bachelor's degree in relevant fields and experience in content governance or regulatory operations.
The predicted salary is between 100000 - 120000 £ per year.
This job is with GSK, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.
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.
Position Summary
You will design, maintain, and drive the adoption of SCM standards-component definitions, metadata schemas, taxonomy, lifecycle governance, and content quality frameworks-across R&D. Ensures all SCM artefacts are audit-ready, compliant with regulatory requirements, and fit for automated downstream consumption, including AI-assisted and generative authoring workflows as these scale across R&D. This role offers growth, visible impact and the chance to shape how we unite science, technology and talent to get ahead of disease together.
Key Responsibilities
- Lead the SCM Horizontal governance operations, and provide a strong contribution to the vendor engagement and change management/adoption workstreams, in support of the Business Lead, SCM Horizontal.
- Define, document, and maintain SCM component standards: component taxonomy, metadata schemas, semantic conventions, versioning rules, and lifecycle governance (authoring through review, approval, reuse, and retirement) in collaboration with functional governance across R&D.
- Develop and maintain governance artefacts: standards documentation, decision frameworks, quality checklists, and templates for use across verticals.
- Operate the component registry: intake validation, provenance tracking, reuse permissions, change control, and audit trail management.
- Conduct standards compliance monitoring: assess adoption, identify deviations, produce compliance reports, and work with vertical teams to remediate gaps.
- Ensure alignment with external regulatory and clinical content standards (CDISC, SNOMED, MedDRA, HL7 FHIR, ICH eCTD, TransCelerate SDR) and internal GxP requirements.
- Contribute to audit and inspection readiness: ensure all governance artefacts, decision records, and component lifecycle evidence meet audit standards.
- Support evaluation of new use cases and tools-including AI-assisted and generative content authoring-against SCM governance criteria; produce structured assessment documentation.
- Advise on the governance implications of AI-enabled and generative authoring for SCM standards, ensuring components remain trustworthy, traceable, and audit-ready as automated content generation scales across R&D.
- Partner with Medical Writing, Regulatory, Quality, and Data Governance SMEs to validate and evolve standards in line with evolving programme and regulatory requirements.
- Build and deliver training and guidance materials for SCM standards across author, reviewer, and technical communities.
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Bachelor's degree in Information Science, Regulatory Affairs, Life Sciences, Medical Writing, or a related field. Advanced degree or relevant professional qualification preferred.
- Substantive experience in content governance, standards management, or regulatory operations in a regulated pharmaceutical or life sciences environment.
- Practical knowledge of structured content, component-based authoring, DITA, or equivalent content modelling approaches.
- Familiarity with GxP requirements and audit-ready documentation practices.
- Experience working with regulatory content standards (CDISC, ICH, MedDRA, SNOMED, or similar) is strongly preferred.
- Background in medical writing, regulatory submissions, or clinical operations is a strong advantage.
- Experience developing training materials and supporting adoption of new standards or processes.
- Experience leading enterprise-scale content transformation or digital authoring programmes-including structured/component content platforms, reuse strategies, and AI-enabled or generative authoring pilots-in a regulated life sciences environment is a strong advantage.
Other Job related skills
- Content modelling, taxonomy design, and metadata schema development.
- Standards documentation and governance framework design.
- Regulatory compliance and GxP content requirements.
- Data quality assessment and compliance monitoring.
- Stakeholder engagement and ability to achieve consensus across technical and non-technical audiences.
- Training design and knowledge transfer.
- Organisational change management, particularly for driving adoption of new standards and ways of working across large, cross-functional author and reviewer communities.
- Aware of AI/GenAI governance considerations for regulated content generation, including human-in-the-loop review and traceability.
Working Pattern
This role is a hybrid role and can be based at any of the following locations: UK, Stevenage, USA, Upper Providence, Belgium, Wavre, Canada, Mississauga.
What we look for in you
You bring a pragmatic, user-centred approach. You lead with curiosity and empathy. You make complex things simple and help teams move faster with confidence. If you want to make a meaningful impact by shaping how structured components are managed across a global science organisation, we'd like to hear from you.
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, color, 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.
Senior Director, Structured Component Management (SCM) Strategy, Operations & Governance employer: Gsk
GSK is an exceptional employer located in Greater London, offering a dynamic and inclusive work environment that fosters innovation and collaboration. As a Senior FinOps Product Manager, you will have the opportunity to drive impactful projects while benefiting from robust employee growth opportunities and a culture that values diverse perspectives. With a commitment to professional development and a focus on agile methodologies, GSK empowers its employees to thrive in their careers while contributing to meaningful advancements in cloud financial management.
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We think you need these skills to ace Senior Director, Structured Component Management (SCM) Strategy, Operations & Governance
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Expect some technical questions related to management theories and practices. Brush up on concepts like transformational leadership, servant leadership, or situational leadership. Be prepared to discuss how you would apply these theories to the role at Gsk, especially in the specific context of the challenges they’re currently facing.
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