Digital Technology QC and Process Development Lead

UCB

Eigenbrakel

Hybride

EUR 70 000 - 90 000

Plein temps

14 jours+

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Avantages offerts par ce poste

Hybrid work model
Supportive company culture
Career development opportunities

Résumé du poste

A global biopharmaceutical company is seeking a Digital Technology QC and Process Development Lead to define the digital roadmap for QC Laboratories. The role involves implementing innovative solutions and ensuring GxP compliance while collaborating with various partners. The ideal candidate should have deep technical knowledge of QC lab systems, lead complex projects, and possess strong communication skills. This position promotes hybrid work with a focus on creating value for patients and fostering a collaborative environment.

Qualifications

  • Technical expertise in laboratory digital systems.
  • Proven experience in complex project management.
  • Knowledge of GxP regulations in the pharmaceutical industry.

Responsabilités

  • Develop digital roadmap aligned with QC/MSAT priorities.
  • Lead implementation of digital platforms and tools.
  • Ensure compliance with GxP and cybersecurity standards.

Connaissances

Deep technical understanding of QC/MSAT lab systems
Experience with data-provisioning platforms
Strong background in solution design and implementation
Knowledge of GxP-compliant operations
Ability to collaborate effectively in global teams
Fluent English

Outils

LIMS
Chromatography
Reporting tools

Description du poste

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
  • Develop and maintain a forward‑looking digital roadmap aligned with QC/MSAT business priorities and compliance needs.
  • Identify emerging technologies and propose innovative solutions that enhance laboratory efficiency and data integrity.
  • Lead implementation of digital platforms including LIMS, CDS, LES, data analytics tools, instrument connectivity, and workflow systems.
  • Manage cross‑functional project teams, resources, timelines, and vendor engagements to ensure end‑to‑end project success.
  • Ensure all digital initiatives adhere to GxP requirements, UCB standards, and cybersecurity expectations.
  • Serve as application owner for laboratory digital systems, ensuring reliable, compliant, high‑performing lifecycle management.
  • Coordinate incident management, system changes, release cycles, and continuous improvement activities across DT functions.
  • Oversee and optimize project and operational budgets while managing vendor quality and performance.
  • 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:
  • Deep technical understanding of QC/MSAT lab systems (e.g., LIMS, chromatography, reporting tools, ERP QA modules).
  • Experience with data‑provisioning platforms and advanced analytical capabilities.
  • Strong background in solution design, implementation, and complex project management within lab environments.
  • Knowledge of GxP‑compliant operations, ideally within the pharmaceutical industry.
  • Ability to translate complex technical concepts into clear, impactful communication.
  • 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!

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.

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