Analyst Clinical Bioprocess Analytics

UCB S.A.; Eigenbrakel; Hybride; EUR 65 000 - 90 000; Plein temps

Résumé du poste

UCB S.A. in Belgium is seeking an Analyst in Clinical Bioprocess Analytics to support biologics manufacturing with analytical expertise, data generation, and documentation governance.

You will collaborate with manufacturing, quality, development and lab teams, contribute to change controls, ensure regulatory compliance, and help deliver reliable in-process monitoring while advancing innovative analytical technologies.

Qualifications

• Bachelor's or Master's degree in a scientific discipline.
• Experience managing controlled documentation within regulated environments.
• Expertise supporting procedure creation, revision, and document lifecycle activities.
• Experience coordinating change controls with cross-functional project teams.
• Strong practical experience with chromatography, electrophoresis, immunoassays, molecular techniques, or spectroscopy.
• Collaborative communication skills with curiosity for continuous improvement.

Responsabilités

• Provide analytical support during biologics manufacturing campaigns.
• Deliver timely in-process monitoring and control results.
• Manage sample coordination, equipment support, and troubleshooting activities.
• Foster implementation of innovative analytical technologies and processes.
• Support document creation, updates, and change controls collaboratively.
• Support inspections, audits, and quality compliance requirements.

Connaissances

Chromatography

Electrophoresis

Immunoassays

Molecular techniques

Spectroscopy

Formation

Bachelor's or Master’s degree in a scientific discipline

Description du poste

Make your mark for patients

We are looking for an Analyst in Clinical Bioprocess Analytics who is Collaborative, Curious, and Care-focused to join our Biological Method Development Sciences team, based at our UCB offices in Braine-l'Alleud, Belgium.

About the role

You will help ensure reliable analytical support for biologics manufacturing activities that ultimately contribute to patient solutions.
Working at the intersection of science and operations, you will provide analytical expertise during manufacturing campaigns, support innovative technologies and foster high-quality data generation.
You will also contribute to documentation governance, supporting procedures, process documentation and change management activities in partnership with project teams.
You will help transform scientific excellence into meaningful patient impact.

Who you will work with

You will join a collaborative community within Biological Method Development Sciences and work closely with manufacturing, quality, development, and laboratory teams. Together, you will foster reliable analytical operations, knowledge sharing, and continuous improvement.
You will also collaborate with external partners when supporting technology transfers and validation activities.
The team values curiosity, mutual support and scientific excellence to help deliver high-quality outcomes for patients.

What you will do

• You will provide analytical support during biologics manufacturing campaigns.
• You will deliver timely in-process monitoring and control results.
• You will manage sample coordination, equipment support, and troubleshooting activities.
• You will foster implementation of innovative analytical technologies and processes.
• You will support document creation, updates, and change controls collaboratively.
• You will support inspections, audits, and quality compliance requirements.

Interested?

• Bachelor's or Master's degree in a scientific discipline.
• Experience managing controlled documentation within regulated environments.
• Expertise supporting procedure creation, revision, and document lifecycle activities.
• Experience coordinating change controls with cross-functional project teams.
• Strong practical experience with chromatography, electrophoresis, immunoassays, molecular techniques, or spectroscopy.
• Collaborative communication skills with curiosity for 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.

Equal opportunity

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 [e-mail]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.