Make your mark for patients

 

We are looking for an MSAT DP Sterile Process Engineer to join our Internal & External Manuf Large Molecules MSAT, based in our office in Braine-l’Alleud, Belgium.

 

About the Role: 

 

As an MSAT DP Sterile Process Engineer, you will be responsible for managing technology transfers and optimizing processes for sterile drug products. You will work closely with various teams to ensure regulatory compliance, improve product quality, and optimize production costs.

 

 Who you’ll work with :

 

You will work with different departments of UCB, such as the External Manufacturing, Quality Assurance (QA), Vendors, QA MSAT and the Development.

 

Responsibilities:

 

Apply the company's health and safety policy and ensure compliance with applicable legislation.Lead the technology transfer with strong governance, coordinating technical, QA, QC, RA, analytical methods transfer, supply, and affiliate management aspects.Manage projects by adhering to budget, timelines, and risk mitigation plans, and report progress to the Head of DP Sterile MSAT.Identify and implement process improvements to enhance quality, reduce cycle times, and lower production costs.Ensure manufacturing processes comply with regulatory requirements and industry standards.Collaborate with the quality assurance team to ensure product quality and consistency, and lead critical investigations into process deviations.

 

Qualifications:

 

Master’s degree in engineering, Pharmaceutical Sciences, or a related field.Minimum of 5 years of experience in pharmaceutical manufacturing processes.Technical and industrial expertise in sterile pharmaceutical products.Experience in managing technology transfers.Experience with regulatory submissions and compliance in a GMP environment.Experience in project management.Financial understanding of the impact of Opex, Capex, and COGS drivers.Fluent in English (written and spoken).

 

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 equitable 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 and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.
 
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.