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Digital technology qc and process development lead

Braine-l'Alleud
Ucb Pharma
Publiée le 11 mars
Description de l'offre

Make your mark for patients


We are looking for a Digital Technology QC and Process Development Lead who is technically strong, collaborative, and passionate about driving digital transformation within laboratory environments to join our Quality Control (QC) and MSAT team at UCB, based in Braine-l’Alleud, Belgium.

About the Role

As the DT QC Lead, you will define and execute the digital technology roadmap for QC Laboratories and Process Development Laboratories. You will introduce innovative solutions that enhance efficiency, compliance, and scientific excellence—ensuring seamless delivery and resilience of critical digital systems. You will work closely with scientists, stakeholders, cross‑functional partners, and external vendors to elevate digital capabilities while maintaining strict GxP and cybersecurity compliance.


Who You’ll Work With

You will collaborate with QC and MSAT scientific users, Digital Technology (DT) partners, project managers, quality experts, and external technology vendors. You will also coordinate with cybersecurity teams, global DT functions, and internal business partners to ensure compliant, high‑performing digital operations across the lab ecosystem.


What You’ll Do

1. Develop and maintain a forward‑looking digital roadmap aligned with QC/MSAT business priorities and compliance needs.
2. Identify emerging technologies and propose innovative solutions that enhance laboratory efficiency and data integrity.
3. Lead implementation of digital platforms including LIMS, CDS, LES, data analytics tools, instrument connectivity, and workflow systems.
4. Manage cross‑functional project teams, resources, timelines, and vendor engagements to ensure end‑to‑end project success.
5. Ensure all digital initiatives adhere to GxP requirements, UCB standards, and cybersecurity expectations.
6. Serve as application owner for laboratory digital systems, ensuring reliable, compliant, high‑performing lifecycle management.
7. Coordinate incident management, system changes, release cycles, and continuous improvement activities across DT functions.
8. Oversee and optimize project and operational budgets while managing vendor quality and performance.
9. Act as the primary DT partner for QC and MSAT stakeholders, ensuring transparency, alignment, and strong value realization.


Interested? For this role we’re looking for:

10. Deep technical understanding of QC/MSAT lab systems (e.g., LIMS, chromatography, reporting tools, ERP QA modules).
11. Experience with data‑provisioning platforms and advanced analytical capabilities.
12. Strong background in solution design, implementation, and complex project management within lab environments.
13. Knowledge of GxP‑compliant operations, ideally within the pharmaceutical industry.
14. Ability to translate complex technical concepts into clear, impactful communication.
15. Ability to collaborate effectively in global, cross‑functional teams; fluent English required.


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!

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