who is analytical, collaborative, and proactive to join our
Characterisation and Material Sciences (CMS) department
, based out of our offices in
Slough, UK or Braine l'Alleud, Belgium.
About the Role
You will join a team of 60 experienced scientists responsible for the comprehensive characterisation of proteins using advanced techniques such as mass spectrometry, AUC, and higher-order methods. Your work will help elucidate protein structure, function, degradation pathways, and support critical quality attribute (CQA) assessment and control strategies. This role is not lab-based and focuses on supporting early-phase projects as they prepare for INDs, requiring both technical expertise and strong project management skills.
You will collaborate with colleagues in characterisation, formulation, analytical method development, upstream and downstream science, devices, quality control, stability, statistics, regulatory, and quality assurance. You'll also interact with teams across the UK, Belgium, Switzerland, the US, contract labs, and academic partners. The environment is dynamic, with multiple parallel activities and changing priorities, so adaptability and minimal supervision are essential.
Who You'll Work With
You will work closely with scientists across CMS, formulation, analytical, and regulatory teams, as well as with external contract labs and academic collaborators. You'll present data and insights to project teams and management, ensuring alignment and quality throughout the project lifecycle.
What You'll Do
Represent early-stage projects both technically and as a project manager
Input into the design of characterisation work packages
Contribute to critical quality attribute (CQA) assessments
Author and review analytical aspects of regulatory submissions, protocols, and reports
Liaise with scientists to obtain and interpret data
Communicate issues and findings to principal scientists and management
Manage documentation, including risk assessments and quality management system activities
Ensure quality processes are maintained and followed
Engage in self-learning by reviewing relevant scientific literature
Interested? For this role, you'll need:
Bachelor's degree required; Master's or PhD preferred
At least 5-10 years of industrial experience in biotechnology or pharmaceutical characterisation, with sustained project representation experience
Excellent knowledge of protein chemistry
Proficiency in electronic document management systems, quality management systems, and risk databases
Experience working with internal regulatory teams and responding to regulatory agency submissions
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 around 8,500 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.
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.
Beware of fraud agents! do not pay money to get a job
MNCJobs.co.uk will not be responsible for any payment made to a third-party. All Terms of Use are applicable.