MSAT Bio DS Process Tech Transfer Expert

UCB; Eigenbrakel; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A global biopharmaceutical company is seeking an MSAT Bio DS Technology Transfer Expert in Braine-l’Alleud, Belgium. This role involves supporting technology transfers and ensuring compliance in manufacturing processes. Candidates should have a Master’s degree in life sciences and strong expertise in biotechnological manufacturing. Excellent English and French communication skills are essential. The company embraces a hybrid work model and provides a caring culture focused on collaboration and innovation.

Qualifications

• Strong understanding of biotechnological manufacturing processes and validation principles.
• Ability to manage complex projects and prioritize tasks.

Responsabilités

• Support technology transfer activities and implement process control strategies.
• Act as process expert post-transfer, owning documentation and supporting lifecycle management.
• Write risk assessments, protocols, and technical reports.

Connaissances

Excellent communication skills in English and French

Strong leadership skills

Problem-solving skills

Collaboration skills

Proficiency in MS Office tools

Formation

Master’s degree in biology, biotechnology, or related life sciences

Description du poste

Overview

Make your mark for patients. We are looking for a MSAT Bio DS Technology Transfer Expert based 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 manage transitions between commercial manufacturing facilities and between Clinical Manufacturing and internal or external facilities, providing documentation and ensuring compliance and optimal performance. You will drive continuous improvements and play a key 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 also be in contact with external partners and manufacturing sites, ensuring alignment and compliance across global operations.

What You Will Do

• Support technology transfer activities and implement process control strategies with stakeholders.
• Write risk assessments, protocols, and technical reports for Tech Transfer and validation runs.
• Coordinate sampling, analyses, and adherence to project timelines.
• Act as process expert post-transfer, owning documentation and supporting lifecycle management.
• Support Health Authority inspections and ensure compliance with cGMP requirements.
• 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:

• Master’s degree in biology, biotechnology, or related life sciences.
• Strong understanding of biotechnological manufacturing processes and validation principles.
• Excellent communication skills in English and French, both written and spoken.
• Ability to manage complex projects, prioritize tasks, and make decisions under pressure.
• Proficiency in MS Office tools and basic knowledge of statistics.
• 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, 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 [e-mail]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.