Director, Description Domain Owner

(2-Year Fixed Term Contract)

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 Description Domain Owner is accountable for defining and governing the Description data domain, ensuring product, material and related CMC description data is trusted, standardised and fit for future structured regulatory submissions. Working across Research & Development, Global Supply Chain, Regulatory and Quality organisations, the role will define the Description domain strategy, priorities, standards and business requirements required to support Structured Product Quality Submissions (SPQS), IDMP and future digital regulatory capabilities. The role will act as the primary business owner for Description domain decisions and will work closely with the SPQS Lead Data Steward, Technology teams and delivery partners to establish scalable, governed Description data products and future system-of-record capabilities.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Define and deliver the strategy, roadmap and governance model for the Description data domain.
• Act as the accountable business owner for Description domain standards, priorities, decisions and risks.
• Define business requirements for Description data products and future system-of-record capabilities.
• Drive harmonisation of product, material and related Description data across R&D, GSC, Regulatory and Quality organisations.
• Establish business rules, definitions and standards supporting structured regulatory data and future SPQS capabilities.
• Partner with Technology teams to support implementation of Description domain capabilities within SAP PLM and related platforms.
• Represent GSK in internal and external forums relating to Description data standards, regulatory data and digital transformation initiatives.

Responsibilities

• Own the Description domain roadmap, priorities and business outcomes.
• Define and approve business standards, definitions and rules governing Description data.
• Act as the decision owner for domain risks, issues, trade-offs and escalation activities.
• Define requirements for Description data products, federated ownership models and future system-of-record capabilities.
• Partner with the SPQS Lead Data Steward to embed stewardship requirements, governance processes and data quality controls.
• Drive alignment of Description data across business functions, systems and technology platforms.
• Translate evolving regulatory requirements into practical business capabilities and domain standards.
• Support delivery of Description pilot activities and future SPQS deployment initiatives.
• Monitor domain performance and drive continuous improvement activities.
  

Why You?
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• Bachelor's degree or equivalent experience in Life Sciences, Pharmaceutical Sciences, Data Management or a related discipline.
• Significant experience within pharmaceutical development, manufacturing, regulatory, quality or supply chain environments.
• Experience defining and implementing business standards, governance frameworks or data management capabilities.
• Experience leading cross-functional initiatives in large, matrix organisations.
• Strong stakeholder management, facilitation and influencing skills.
• Ability to make clear business decisions and drive alignment across multiple stakeholder groups.

Preferred Qualification
If you have the following characteristics, it would be a plus

• Experience with CMC product, material, substance or manufacturing data.
• Experience supporting IDMP, SPQS, ISO CMC or related regulatory data initiatives.
• Experience with SAP PLM or related product lifecycle management platforms.
• Experience defining system-of-record strategies, master data capabilities or enterprise data products.
• Participation in industry standards organisations or cross-company data initiatives.
• Experience leading business transformation or digital transformation programmes.

What you will gain

You will influence high-impact decisions and shape domain practice across GSK. You will work with experienced colleagues who share a clear purpose. You will grow your leadership skills and technical understanding while making work easier and safer for many teams. If you want to help GSK turn robust control design into faster, more reliable outcomes for patients, please apply.

How to apply

Please submit your CV and a short cover letter that explains why you are interested and how your experience maps to this role. We encourage applications from people with different backgrounds and experiences. We look forward to hearing from you.

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 115,500 to EUR 192,500The 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.

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. Click the Link where you will find answers to multiple questions we receive

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/