MSAT Lab Downstream Lead

Jobinhalt

Make your mark for patients.

We’re here because we want to build the future and transform patients’ lives for the better.

At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.

To strengthen our newly formed Global Biologics Manufacturing Sciences & Technology (MSAT) teamin Braine-l’Alleud (Belgium), we are looking for a talented individual to fill the position of: MSAT Lab Downstream Lead.

The MSAT Lab Downstream (DSP) Lead heads the Downstream lab activities and reports to the Head of Global Biologics MSAT.

The MSAT Lab DSP Lead is responsible for delivering on all lab-based Downstream MSAT activities by managing a team of bench-level scientists and technicians. The MSAT lab as a whole covers both the Upstream and Downstream aspects of the drug substance manufacturing process and focuses on:

• Acquiring and maintaining process expertise for late-stage and commercial products.
• Providing process expertise support.
• Transferring and maintaining small scale models from Development.
• Supporting Technology Transfers and Process Validations with lab-scale activities.
• Supporting Manufacturing campaigns with satellite runs.
• Providing deviation and investigation support through lab-scale experiments.
• Supporting Continuous Process Verification (CPV) activities.
• Supporting Lifecycle Management (LCM) activities.
• Improving the understanding, robustness and economics of commercial manufacturing processes.
• Evaluating new technologies.

The MSAT Lab DSP Lead is responsible and accountable for the timely delivery of the MSAT lab Downstream responsibilities.

The MSAT Lab DSP Lead will:

• Support the design and setup of the InfleXio MSAT lab.
• Manage the Downstream activities in the MSAT lab.
• Ensure accurate and complete documentation of any scientific experimental plan, data and report.
• Provide scientific leadership.
• Author and review technical protocols and reports.
• Lead, mentor and develop direct reports.
• Ensure that MSAT policies, Standard Operating Procedures and Work Instructions are developed and kept up to date.
• Ensure that the MSAT Lab DSP team members are appropriately trained in lab and HSE procedures.
• Ensure that the appropriate standards of quality, housekeeping and safety are being applied within the MSAT lab.
• Provide scientific leadership and ensure DSP lab support for Technology Transfers, Process Validations, Manufacturing operations and deviations/investigations as required, by design and execution of appropriate studies.
• Facilitate building of harmonized and standardized procedures for scale down models.
• Lead process optimization studies in support of LCM activities.
• Support Regulatory inspections and submissions.
• Build and maintain good working relationships with stakeholders.
• Establish and maintain familiarity with contemporary industrial standards, practices, technologies, literature and ways of performing lab studies.

Interested? For this position you’ll need the following education, experience and skills:

• PhD or master’s degree or equivalent experience in a relevant scientific discipline.
• At least 3 years of experience in the biopharmaceutical industry in downstream bioprocessing and 2 years of experience as a People Manager.
• Demonstrated Downstream subject matter expertise and hands-on Downstream laboratory experience is required.
• Experience in Technology Transfer and scale-up/scale-down of drug substance processes is a plus.
• Good understanding of biopharma operations and cGMP.
• Proven People and Project Management skills.
• Very good knowledge of English (both oral and written); knowledge of French is a plus.

Soft skills:

• Strong communication skills: ability to communicate effectively and connect with peers from different functions (matrix organization) to ensure projects are delivered.
• Very good technical writing skills.
• Excellent analytical thinking and problem-solving skills.
• Ability to manage multiple tasks and meet deadlines with a high tolerance for ambiguity.

Why you should apply?

At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.

If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.

About us

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.

At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.

Curious to know more? Please visit our website www.ucb.com.

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.