Qualification & Cleaning Validation Corporate Process Owner

UCB

Eigenbrakel

Hybrid

EUR 130,000 - 180,000

Full time

14 days+

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Job summary

UCB is seeking a strategic, collaborative, and influential Qualification & Cleaning Validation Corporate Process Owner to join the Belgium Support Services & Braine Campus, based at our campus in Braine-l'Alleud, Belgium.

The role will govern global Qualification and Cleaning Validation processes, drive harmonization across sites, and maintain ongoing inspection readiness within UCB's Internal Manufacturing network.

Qualifications

  • Master's degree or equivalent experience in a scientific, engineering, or pharmaceutical field.
  • Minimum 10 years of pharmaceutical industry experience in Qualification and Cleaning Validation.
  • Strong knowledge of GxP regulations, CFR 21, EudraLex, and regulated manufacturing environments.
  • Solid understanding of Quality Management Systems, deviations, CAPAs, and change control processes.
  • Proven project management, stakeholder management, and strategic leadership capabilities.
  • Fluent communication skills in both French and English.

Responsibilities

  • Own and govern global Qualification and Cleaning Validation processes within the Quality Management System.
  • Develop and maintain global standards, procedures, and training materials.
  • Monitor process performance through KPIs, risks, deviations, CAPAs, and inspection outcomes.
  • Lead strategic projects and change initiatives supporting process improvement and harmonization.
  • Build strong stakeholder partnerships and facilitate global governance and decision-making forums.
  • Ensure GMP compliance and maintain continuous inspection readiness across manufacturing sites.

Skills

Fluent French & English

Education

Master's degree or equivalent in scientific/engineering/pharmaceutical field

Job description

We are looking for a strategic, collaborative, and influential Qualification & Cleaning Validation Corporate Process Owner to join our team within Belgium Support Services & Braine Campus, based at our UCB campus in Braine-l'Alleud, Belgium.

About The Role

As Qualification & Cleaning Validation Corporate Process Owner, you will play a key role in ensuring excellence, compliance, and continuous improvement across UCB's Internal Manufacturing network. You will own the governance of global Qualification and Cleaning Validation processes, drive harmonization across sites, and help maintain a permanent state of inspection readiness. You will also lead strategic initiatives that support operational performance, regulatory compliance, and sustainable quality standards worldwide.

Who You Will Work With

You will work closely with a global network of Subject Matter Experts (SMEs), Local Process Owners, Quality representatives, manufacturing sites, and cross-functional stakeholders. You will act as a key connector between sites and global functions, fostering collaboration, alignment, and the sharing of best practices across UCB's Internal Manufacturing organization.

What You Will Do
  • You will own and govern global Qualification and Cleaning Validation processes within the Quality Management System.
  • You will develop and maintain global standards, procedures, and training materials.
  • You will monitor process performance through KPIs, risks, deviations, CAPAs, and inspection outcomes.
  • You will lead strategic projects and change initiatives supporting process improvement and harmonization.
  • You will build strong stakeholder partnerships and facilitate global governance and decision-making forums.
  • You will ensure GMP compliance and maintain continuous inspection readiness across manufacturing sites.
Interested?

For this role, we are looking for the following education, experience, and skills:

  • Master's degree or equivalent experience in a scientific, engineering, or pharmaceutical field.
  • Minimum 10 years of pharmaceutical industry experience in Qualification and Cleaning Validation.
  • Strong knowledge of GxP regulations, including CFR 21, EudraLex, and regulated manufacturing environments.
  • Solid understanding of Quality Management Systems, deviations, CAPAs, and change control processes.
  • Proven project management, stakeholder management, and strategic leadership capabilities.
  • Fluent communication skills in both French and English.

At UCB, we value diversity, inclusion, and the unique perspectives that every colleague brings. If you are passionate about quality, continuous improvement, and leading global process excellence.

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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