Digital Technology Lead Quality - Solution Architect
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Make your mark for patients
We are looking for a Digital Technology Lead Quality - Solution Architect who is collaborative, solution-oriented and accountable to join our Digital Technology team, based in Braine l’Alleud, Belgium.
About the role
As a DT Lead Quality - Solution Architect, you will take technical ownership of systems and services supporting our global Quality Assurance organization. You will manage digital solutions such as Veeva Vault Quality modules throughout their full lifecycle, ensuring they remain available, secure, scalable and compliant. You will help shape solution design, configuration, integrations and future platform developments while coordinating projects, system changes and operational activities. This is a hands-on role combining solution architecture, system ownership, project delivery and stakeholder partnership.
Who you’ll work with
You will be working in a global, cross-functional environment bringing together Quality Assurance, business process, data and Digital Technology expertise. You will collaborate closely with functional system owners, data owners, process owners, domain leads and integration specialists. You will also act as an important technical contact for Veeva and other external service providers. Together, you will ensure that solutions meet business needs, follow architectural standards and remain compliant with pharmaceutical quality, data integrity and cybersecurity requirements.
What you’ll do
Take technical ownership of Veeva Vault Quality systems throughout their lifecycle, including design, configuration, integration, maintenance, performance and sustainability
Translate Quality Assurance needs into scalable, effective and cost-efficient technology solutions aligned with business priorities, architectural principles and regulatory requirements
Lead the delivery of projects, platform enhancements and system changes, managing scope, timelines, risks, resources, external partners and allocated budgets
Ensure systems remain validated, secure, inspection-ready and compliant with pharmaceutical quality requirements, data integrity standards and cybersecurity controls
Coordinate system administration and oversee incident, change and problem management, proactively addressing risks that could affect service quality or delivery
Partner with Veeva and internal specialists to evaluate platform capabilities, develop solutions and support continuous improvement across different Vault Quality modules
Maintain clear delivery plans and progress updates, and contribute to communication, training materials and the onboarding of users and stakeholders
Interested? For this role we’re looking for the following education, experience and skills
A bachelor’s or master’s degree in technology, science, engineering or another relevant field, combined with a strong interest in evolving technologies
Professional experience and practical expertise working with Veeva Vault, ideally including solutions supporting Quality Assurance or other regulated business activities would be an advantage
Experience delivering projects within a digital or technology environment, with the ability to manage priorities, timelines, costs and risks would be an advantage
Experience with computerized system validation would be an advantage
Understanding of solution design, system configuration, integrations, validation, data integrity, cybersecurity and the operation of regulated technology systems
Strong stakeholder management and communication skills, with the ability to connect business requirements, technical possibilities and regulatory expectations
Fluency in English, together with an autonomous, adaptable and hands-on approach to problem-solving, collaboration and continuous improvement
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1523 comparable Quality roles across 149 biopharma companies.
Salary context
248 of 1523 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1523 comparable roles
+ 47 more countries
Seniority mix
690 of 1523 peers have a known seniority level
Therapeutic area mix
1 of 1523 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Notify me about similar jobs
Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
Or follow a whole field: get every new Quality job in Belgium, and choose locations and companies.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.