At a Glance
- Tasks: Lead the Control data domain strategy and ensure high-quality standards for regulatory submissions.
- Company: Join GSK, a global biopharma leader committed to innovation and patient health.
- Benefits: Competitive salary, bonuses, and opportunities for professional growth in a dynamic environment.
- Other info: Inclusive workplace with a focus on diversity and career advancement.
- Why this job: Make a real impact on healthcare by shaping the future of medicine and vaccines.
- Qualifications: Bachelor's degree in relevant fields and experience in pharmaceutical development or quality assurance.
This job is with GSK, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.
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 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.
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.
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, 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.
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
Salary Range: EUR 115,500 to EUR 192,500. 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.
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.
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.
Director, Control Domain Owner in London 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.
StudySmarter Expert Advice🤫
We think this is how you could land Director, Control Domain Owner in London
✨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 Gsk.
We think you need these skills to ace Director, Control Domain Owner in London
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 Gsk.
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 Gsk. 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 Gsk
✨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 Gsk.
✨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 Gsk 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.
