At a Glance
- Tasks: Lead data stewardship for innovative pharmaceutical projects and ensure data quality across multiple domains.
- Company: Join GSK, a global biopharma leader dedicated to improving health worldwide.
- Benefits: Enjoy competitive salary, hybrid work model, and opportunities for professional growth.
- Other info: Be part of a dynamic team with a culture that values innovation and collaboration.
- Why this job: Make a real impact on healthcare by managing critical data for medicines and vaccines.
- Qualifications: Degree in Life Sciences or related field; experience in data management preferred.
The predicted salary is between 83250 - 138750 £ per year.
Locations - GSK HQ (UK), Barnard Castle (UK), Rixensart (Belgium), and Upper Providence (US)
Reporting to - Senior Director, CMC Data Strategy (SPQS)
Business Introduction
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
Position Summary
ICH M16 Structured Product Quality Submissions (SPQS) will fundamentally change how product quality information is created, governed and exchanged. The SPQS Lead Data Steward will lead implementation of the stewardship, ownership and data quality capabilities required to support future structured regulatory submissions. Working across Description, Control and future SPQS domains, the role will translate Domain Owner decisions into practical standards, stewardship processes, metadata requirements, controlled vocabularies and data quality controls. The role will work across R&D, Global Supply Chain, Regulatory and Quality organisations to establish sustainable data management practices that support SPQS deployment, digital transformation initiatives and long-term operational readiness.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Lead implementation of the SPQS data stewardship framework across Description, Control and future SPQS domains.
- Coordinate federated ownership of critical CMC data assets across R&D, GSC, Regulatory and Quality.
- Establish and maintain metadata standards, controlled vocabularies, business definitions and reference data structures supporting SPQS.
- Drive data quality management processes, issue resolution and continuous improvement activities.
- Support delivery of governed Description and Control data products and future structured submission capabilities.
- Partner with Domain Owners, Technology teams and external delivery partners to embed stewardship and governance requirements into business processes and digital solutions.
- Build awareness, adoption and data literacy through training, guidance and stakeholder engagement.
Responsibilities
- Act as the lead steward for SPQS data, standards and ownership practices.
- Coordinate stewardship activities across multiple business functions and data domains.
- Translate Domain Owner decisions into operational standards, controls and stewardship processes.
- Lead cross-system vocabulary alignment and harmonisation activities supporting SPQS.
- Define and monitor data quality controls, metrics and remediation activities.
- Support implementation of governance frameworks, ownership models and stewardship operating procedures.
- Ensure consistency and traceability across the Description to Control data lifecycle.
- Provide oversight of supplier-delivered data management, data quality and stewardship deliverables.
- Support audits, inspections and compliance activities relating to SPQS data assets.
Why You?
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Degree in Life Sciences, Pharmaceutical Sciences, Data Management, Engineering or a related discipline.
- Experience in data stewardship, data governance, master data management or related disciplines.
- Experience developing data standards, business rules, controlled vocabularies or metadata frameworks.
- Experience working across multiple business functions and stakeholder groups.
- Strong communication, facilitation and influencing skills.
- Experience operating within regulated environments.
Preferred Qualification
If you have the following characteristics, it would be a plus:
- Experience in pharmaceutical CMC, manufacturing, quality, regulatory or supply chain data management.
- Experience supporting IDMP, structured data, SPQS or related regulatory data initiatives.
- Experience implementing data ownership and stewardship frameworks.
- Experience with SAP PLM, enterprise data platforms or master data management solutions.
- Experience implementing data quality management processes and controls.
- Participation in industry standards or data governance initiatives.
Working Model
This role is hybrid. You will work from a UK office regularly and may work remotely part of the week. Attendance for team and stakeholder sessions is expected.
How to apply
If this role matches your skills and ambition, please apply. Share a brief note describing how your experience maps to the responsibilities and qualifications. We welcome applicants from all backgrounds and encourage people who meet most requirements to apply. Closing date for applications: 7th September 2026 (EOD)
Skills
- Data Governance
- Data Quality
- Data Quality Improvement
- Data Security
- Data Standards
- Incident Management
- Master Data
- Metadata Standards
Belgium Salary Range / Fourchette salariale – Belgique: EUR 83,250 to EUR 138,750
The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process.
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.
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.
SPQS Data Steward employer: GlaxoSmithKline
GSK is an exceptional employer that prioritises innovation and sustainability in its operations, making it a great place for professionals looking to make a meaningful impact in global logistics. With a strong emphasis on employee development and a collaborative work culture, you will have ample opportunities to grow your skills while working alongside talented teams in a hybrid UK-based environment. Join us to be part of a forward-thinking organisation that values your contributions and supports your career journey.
StudySmarter Expert Advice🤫
We think this is how you could land SPQS Data Steward
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like GlaxoSmithKline.
We think you need these skills to ace SPQS Data Steward
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at GlaxoSmithKline.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at GlaxoSmithKline. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at GlaxoSmithKline
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with GlaxoSmithKline.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help GlaxoSmithKline achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
