Laboratory Analyst in Mass Spectrometry

Make your mark for patients

We are seeking a Laboratory Analyst in Mass Spectrometry who is passionate about developing and validating methodologies under GMP (Good Manufacturing Practices) standards. As part of the PCMD team (Phys-Chem Method Development) within ADSB (Analytical Sciences for Biologicals), based at our Braine-l’Alleud campus in Belgium , you will immerse yourself in a dynamic environment where innovation drives progress.

About the Role

As a Laboratory Analyst in Mass Spectrometry, you will be tasked with developing and validating DDA and/or DIA methods for quantifying HCP (host cell proteins) in drug substance or in-process samples. Additionally, you will contribute to the development of multi-attribute methods.

Who you will work with

You will collaborate closely with the PCMD team, consisting of dedicated professionals focused on advancing analytical sciences for biologicals. Together, you will tackle challenges and drive breakthroughs in analytical development.

What You Will Do

• You will design experiments to optimize methodologies.
• You will autonomously manage and perform daily laboratory activities related to method development, validation, transfers, and support to process.
• You will prepare, review, and approve documentation, including procedures, protocols, and reports.
• You will analyze and verify data, presenting and discussing results in project team meetings.
• You will provide analytical expertise to projects and represent ADSB in cross-functional project teams.
• You will interact with regulatory teams for file preparation and submission, ensuring compliance with regulatory requirements.

Interested? For this role, we are looking for individuals with the following qualifications:

• Bachelor's degree in Chemistry, Biochemistry, or related field with demonstrated experience up to PhD with experience in quantitative proteomics.
• Experience in developing and validating analytical methodologies.
• Proficiency in mass spectrometry techniques.
• Experience in working in a regulated environment (eg, GxP, ISO) is a must.
• Excellent communication and collaboration skills.
• Fluent in English and good command in French.

If you are ready to embark on an exciting journey of scientific discovery and contribute to the advancement of biotherapeutics manufacturing processes, we encourage you to apply. Join us in our mission to make a meaningful impact on patients' lives through innovative science and collaborative teamwork.

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 on [email protected] . Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel. #J-18808-Ljbffr