Make your mark for patients
We are looking for a MSAT Bio DS Tech Transfer Expert who is detail-oriented, collaborative, and solution-driven to join our Bio Drug Substance Manufacturing Science and Technology team, based at our UCB campus located in Braine-l’Alleud, Belgium.
About the role
As a MSAT Bio DS Technology Transfer expert, you will support technology transfers and commercial-scale process validations for final mammalian biotechnological manufacturing processes. You will carry out a smooth and efficient transition between commercial manufacturing facilities as well as between Clinical Manufacturing and internal or external commercial manufacturing facilities, by providing the necessary documentation and ensuring compliance and optimal performance. You will also be responsible for driving continuous improvements and will play a key role as a technical expert throughout the product lifecycle.
Who you will work with
You will collaborate with cross-functional teams including Quality Assurance, CMC-Development, Industrial Leads, Analytical Transfer & QC Readiness teams. You will be also in contact with external partners and manufacturing sites, ensuring alignment and compliance across global operations.
What you will do
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You will support technology transfer activities and implement process control strategies with stakeholders.
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You will be responsible for writing risk assessments, protocols, and technical reports for Tech Transfer and validation runs.
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You will manage coordination of sampling, analyses, and adherence to project timelines.
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You will act as process expert post-transfer, owning documentation and supporting lifecycle management.
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You will support Health Authority inspections and ensure compliance with cGMP requirements.
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You will identify and implement process improvements and cost optimization initiatives within approved parameters.
Interested?
For this role, we are looking for the following education, experience, and skills:
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Master’s degree in biology, biotechnology, or related life sciences field.
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Strong understanding of biotechnological manufacturing processes and validation principles.
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Excellent communication skills in English and French, both written and spoken.
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Ability to manage complex projects, prioritize tasks, and make decisions under pressure.
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Proficiency in MS Office tools and basic knowledge of statistics.
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Strong leadership, problem-solving, and collaboration skills with a proactive mindset.
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 [email protected]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
