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 focused on innovation and patient care.
- 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.
- SPQS Data Steward
- (2-Year Fixed Term Contract)
Locations - GSK HQ (UK), Barnard Castle (UK), Rixensart (Belgium), and Upper Providence (US)
- Reporting to - Executive 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.
- Act as the lead steward for SPQS data, standards and ownership practices, working in partnership with Domain Owners and accountable business functions.
- Coordinate federated ownership of critical CMC data assets across R&D, Global Supply Chain, Regulatory and Quality organisations.
- Translate Domain Owner decisions into operational standards, stewardship processes, controls and governance practices.
- Establish and maintain metadata standards, controlled vocabularies, business definitions and reference data structures supporting SPQS and future structured submissions.
- Drive data quality management processes, metrics, issue resolution and continuous improvement activities, ensuring consistency and traceability across the Description and Control domain data lifecycle.
- Partner with Technology teams and external delivery partners to embed stewardship and governance requirements into business processes, data products and digital solutions.
- Build awareness, adoption and data literacy through training, guidance, stakeholder engagement and stewardship community development.
- Basic Qualification
- 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
- Experience in pharmaceutical CMC, manufacturing, quality, regulatory or supply chain data management.
- Experience supporting IDMP, ISO, ICH 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.
- 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.
Closing date for applications: 8th 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.
This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown.
Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role.
If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process.
Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role.
Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.
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 where you can also request a call.
#J-18808-Ljbffr
SPQS Data Steward in London employer: Biopharma Careers
Boehringer Ingelheim UK is an exceptional employer that fosters a collaborative and innovative work culture, providing employees with the opportunity to grow professionally within the dynamic pharmaceutical industry. With a strong emphasis on employee development and well-being, the company offers comprehensive benefits and a supportive environment that encourages meaningful contributions to healthcare advancements.
StudySmarter Expert Advice🤫
We think this is how you could land SPQS Data Steward in London
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Biopharma Careers. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
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 Biopharma Careers.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Biopharma Careers. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Biopharma Careers is looking for. A tailored application can really make you stand out!
We think you need these skills to ace SPQS Data Steward 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 Biopharma Careers!
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 Biopharma Careers 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 Biopharma Careers!
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 Biopharma Careers, 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 Biopharma Careers
✨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 Biopharma Careers 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 Biopharma Careers’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.