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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Director, Control Domain Owner - **Company:** GSK LLP - **Location:** Upper Providence Township, PA, United States - **Salary:** $115,500.0 - $192,500.0 - **Contract:** Temporary contract - **Skills:** Bioinformatics, Data Governance, Data Security, Laboratory Information Management Systems, Metadata Standards, Data Management - **Published:** August 25, 2026 - **Apply:** https://jobs.localjobnetwork.com/apply/add/88126951/1 ## About the Role * Bachelor's degree or equivalent experience in Life Sciences, Pharmaceutical Sciences, Analytical Sciences, Quality, Engineering or a related discipline. * Significant experience within pharmaceutical development, analytical sciences, quality, manufacturing or regulatory 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 specifications, analytical procedures, acceptance criteria, control strategy or quality data. * Experience supporting ICH, IDMP, or related regulatory data initiatives. * Experience working with LIMS, LES, Digital Specifications and Methods or related quality systems. * 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., Data Governance, Data Quality, Data Quality Improvement, Data Security, Data Standards, Incident Management, Master Data, Metadata Standards ## Description ICH M16 Structured Product Quality Submissions (SPQS) will fundamentally change how product quality information is created, governed and exchanged. The Control Domain Owner is accountable for defining and governing the Control data domain, ensuring specifications, analytical procedures, acceptance criteria and related control strategy data are trusted, standardised and fit for future structured regulatory submissions. Working across Research & Development, Global Supply Chain, Quality and Regulatory organisations, the role will define the Control domain strategy, priorities, standards and business requirements required to support Structured Product Quality Submissions (SPQS), Digital Specifications and future regulatory data capabilities. The role will act as the primary business owner for Control domain decisions and will work closely with the SPQS Lead Data Steward, Technology teams and delivery partners to establish scalable, governed Control data products and future digital specifications 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 Control data domain. * Act as the accountable business owner for Control domain standards, priorities, decisions and risks. * Define business requirements for Digital Specifications and Methods and future Control data products. * Drive harmonisation of specification, analytical method and control strategy data across R&D, Quality, Regulatory and Manufacturing organisations. * Establish business rules, definitions and standards supporting structured regulatory data and future SPQS capabilities. * Partner with Technology teams to support implementation of Digital Specifications, Methods and related Control domain capabilities. * Represent GSK in internal and external forums relating to analytical, specification and structured regulatory data initiatives. Responsibilities * Own the Control domain roadmap, priorities and business outcomes. * Define and approve business standards, definitions and rules governing specifications, analytical procedures, acceptance criteria and related Control data. * Act as the decision owner for domain risks, issues, trade-offs and escalation activities. * Define requirements for Digital Specifications, Control data products 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 Control data across R&D, Quality, Manufacturing, Regulatory and technology platforms. * Ensure consistency and traceability between Description data, Control data and future structured submission requirements. * Translate evolving regulatory requirements into practical business capabilities and domain standards. * Support delivery of Digital Specifications, Control pilot activities and future SPQS deployment initiatives. * Monitor domain performance and drive continuous improvement activities., 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., 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. 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/ GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. ## Related Videos - [Data Governance in the Era of AI](https://www.wearedevelopers.com/videos/1622-data-governance-in-the-era-of-ai) - [Blueprints for Success: Steering a Global Data & AI Architecture](https://www.wearedevelopers.com/videos/1577-blueprints-for-success-steering-a-global-data-ai-architecture) - [Crypto-secure Data Management with In-Database Blockchain](https://www.wearedevelopers.com/videos/632-crypto-secure-data-management-with-in-database-blockchain) - [Unlocking Value from Data: The Key to Smarter Business Decisions-](https://www.wearedevelopers.com/videos/1367-unlocking-value-from-data-the-key-to-smarter-business-decisions) - [How to govern Vibe Coding for the Enterprise](https://www.wearedevelopers.com/videos/100290-how-to-govern-vibe-coding-for-the-enterprise) - [AI beyond the code: Master your organisational AI implementation.](https://www.wearedevelopers.com/videos/1248-ai-beyond-the-code-master-your-organisational-ai-implementation) ## Related Articles - [Data Analyst Salary in the UK](https://www.wearedevelopers.com/magazine/278-data-analyst-salary-in-the-uk) - [Data Engineer Salary UK](https://www.wearedevelopers.com/magazine/253-data-engineer-salary-uk) - [UK Business Culture and Etiquette](https://www.wearedevelopers.com/magazine/326-uk-business-culture-and-etiquette) - [The Most Popular IT Jobs on the Market](https://www.wearedevelopers.com/magazine/376-the-most-popular-it-jobs-on-the-market) - [How We Built a Worry-Free System That Runs for 10+ Years – And What We’d Do Again](https://www.wearedevelopers.com/magazine/751-how-we-built-a-worry-free-system-that-runs-for-10-years-and-what-we-d-do-again) - [Software Engineer Salary London](https://www.wearedevelopers.com/magazine/252-software-engineer-salary-london)