UCB Posted September 13, 2026

Digital Technology Solution Expert Regulatory Submissions

Anderlecht, Brussels, Belgium OTHER
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About this opportunity

Make your mark for patients

We are looking for a Digital Technology Solution Expert Regulatory Submissions who is collaborative, solution‑driven and curious to join us in our Digital Technology Regulatory team, based in our HQ office in Brussels, Belgium.

About The Role

This global role within UCB’s Digital Technology organization is accountable for the technical ownership and lifecycle management of Digital Technology systems and services supporting the regulatory submissions & registrations.

Acting as Digital Technology System Owner (DTSO) for supporting Veeva Vault RIM and adjacent technologies, the role is accountable for ensuring system availability, performance, security, maintainability, and scalability. It drives the sustained technical performance and evolution of the system, in alignment with the vendor product evolution, user and data requirements, and applicable regulatory obligations.

This global function supports applications subject to GxP regulatory requirements and is based in Belgium.

Who you’ll work with

You will act as the primary Digital Technology point of contact with a strong regulatory affairs acumen, working in close partnership with Functional System Owners, Data Owners, Process owners and Domain Lead, Veeva Integration Lead and Veeva COE.

Operating with a high level of autonomy and accountability, the DTSO oversees the system administration and ensures effective incident, change, and problem management. You will partner with colleagues across integration, security, compliance and enterprise platforms to ensure solutions work seamlessly and remain compliant. This role requires strong communication, partnership and the ability to navigate a diverse and international environment.

What You’ll Do

Manage projects and change requests to deliver high‑quality solutions on time and within agreed budgets ensuring effective use of allocated resources (including external service providers, contractors, and financial budgets) and adherence to agreed timelines.

Provide technical and architectural expertise to lead solution design, configuration development and implementation, and ensures that systems remain compliant with applicable GxP requirements, including validation (acting as DTSO), data integrity, and cybersecurity controls.

Ensure systems are operated and maintained in a compliant and validated state, in line with applicable regulatory requirements (e.g., GxP), including data integrity, cybersecurity, and audit/inspection readiness.

Collaborate closely with Functional System Owners (FSO), Data Owners, and Process Owners within regulatory stakeholders to understand business needs and translate them into effective, scalable, and cost‑efficient Digital Technology solutions, aligned with UCB governance, architecture principles, and strategic priorities.

Partners with both transversal and horizontal DT teams and subject matter experts to explore, prototype, and industrialize solutions (e.g., proof of concepts), leveraging internal capabilities or external strategic partners as appropriate.

Act as a key technical interface with strategic vendors to ensure Source (Veeva) capabilities evolve in line with UCB requirements, maximizing value delivery and alignment with business and regulatory expectations

Provide expert input into strategy, roadmap, and investment planning, ensuring alignment between technology capabilities and business priorities.

Maintain a strong understanding of industry trends, emerging technologies, and digital innovation to continuously enhance system capabilities and drive modernization of the technology landscape.

Interested? For this role we’re looking for the following education, experience and skills 

Bachelor’s or Master’s degree in a scientific, technical, digital or related field

Expertise in Veeva Vault ideally Vault RIM

At least 2 years of experience in managing projects within a DT/Digital environment.

Experience in life sciences industry is considered a plus.

Fluent in English, any other language is a plus

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

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Anderlecht, Brussels, Belgium
Employment type
OTHER

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 585 comparable Regulatory Affairs roles across 111 biopharma companies.

585Comparable roles tracked
536Currently active
111Companies hiring similar roles
52Countries represented

Salary context

157 of 585 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.

This roleSubject Not listed on this posting
Highest disclosed · Executive Director, Medical Writing · Regeneron Pharmaceuticals, Inc (USA) $285,600/yr – $475,900/yr
Peer group range $75,038 – $380,750 (median $187,050)

Where these roles are based

Top locations among the 585 comparable roles

United States238
India45
Japan34
United Kingdom34
Poland28
Ireland21

+ 46 more countries

Seniority mix

455 of 585 peers have a known seniority level

Manager185
Director74
Senior57
Associate Director56
Intern/Fellow/Postdoc24
Senior Director23
Principal16
Executive/VP10
Associate10

Therapeutic area mix

43 of 585 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology14
Immunology10
Dermatology & Aesthetics5
Rare Disease5
Vaccines & Infectious Disease3
Neuroscience3
Cardiovascular / CVRM2
Respiratory1

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.

40%similar
AbbVie Wavre, Wallonia Associate Director
Same function Same country
40%similar
GlaxoSmithKline Biologicals S.A. Belgium-Wavre, Belgium Manager
Same function Same country
40%similar
Johnson & Johnson Beerse, Belgium Manager
Same function Same country
40%similar
Johnson & Johnson Diegem, Belgium
Same function Same country
40%similar
Johnson & Johnson Beerse, Belgium Senior
Same function Same country
25%similar
Lilly Shanghai, Shanghai, China Associate Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

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 Regulatory Affairs 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.

40%
Associate Director, Regulatory Affairs, Europe Regulatory Policy & Intelligence
AbbVie · Wavre, Wallonia · Associate Director
Function Therapeutic area Seniority Country
40%
Manager, Global Labeling Product Leader
Johnson & Johnson · Beerse, Belgium · Manager
Function Therapeutic area Seniority Country
25%
Regulatory Affairs Associate Director
Lilly · Shanghai, Shanghai, China · Associate Director
Function Therapeutic area Seniority Country
25%
Associate Director, Regulatory Affairs Advertising & Promotion - Digital & Corporate Communications
AbbVie · Mettawa, IL · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 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.