# MSAT DP Sterile Process Lead at UCB

UCB is hiring an MSAT DP Sterile Process Lead. Level rates it Little AI ●○○○; you can [apply on UCB](https://jobsbylevel.com/go/f1972064-9229-4c6c-b4aa-586e3852c796?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. Braine L'alleud, Walloon Brabant, Belgium.

## Details

- Company: [UCB](https://jobsbylevel.com/companies/ucb)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Braine L'alleud, Walloon Brabant, Belgium
- Posted: October 26, 2026
- Apply: https://jobsbylevel.com/go/f1972064-9229-4c6c-b4aa-586e3852c796?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=msat-dp-sterile-process-lead-at-ucb-902625

## Prepare for this job

The job page lists 5 likely interview questions for this offer, with a CV checklist: https://jobsbylevel.com/jobs/msat-dp-sterile-process-lead-at-ucb-902625

## Description

Make your mark for patients To join our Internal Manufacturing, Biologics Manufacturing Science and Technology team, based in our office in Braine-L'Alleud, Belgium or Bulle, Switzerland , we are seeking a highly experienced MSAT DP Sterile Process Lead to provide technical leadership for sterile drug product manufacturing operations and future expansion projects. About the role This role combines deep expertise in aseptic processing, technology transfer, facility start-up, contamination control and operational excellence. As a recognized Subject Matter Expert (SME), you will play a key role in supporting the design, qualification and operation of next-generation sterile manufacturing facilities, including isolator-based filling technologies. You will serve as a key technical partner to Manufacturing, Quality, Engineering, Validation and Regulatory teams while driving continuous improvement and fostering technical excellence across the organization. You will lead the operational delivery of sterile drug product technology transfers from process scale-up through commercial validation and the full product lifecycle. This position is ideal for an experienced professional passionate about sterile manufacturing, problem solving, knowledge sharing and technical leadership. Who you’ll work with You will be working in a multidisciplinary team that brings together manufacturing science and technology, quality, regulatory, analytical, supply and site colleagues. You will coordinate internal and external partners, build constructive team dynamics and provide clear progress, risk and decision updates to the Sterile Manufacturing Science and Technology leadership team. What you’ll do Participate in the design, start-up, qualification and operational readiness of new sterile manufacturing facilities, including isolator-based filling operations, contamination control strategies, aseptic process simulations and process validation activities. Lead cross-functional technology transfer and industrialization projects for sterile drug product manufacturing, ensuring alignment across Manufacturing, Quality, Regulatory Affairs, Validation, Engineering, Analytical Sciences and Supply Chain. As a subject matter expert (SME) for aseptic processing and sterile manufacturing technologies, provide technical oversight for sterile manufacturing processes, ensuring compliance with global regulatory expectations, cGMP requirements and industry best practices. Drive second-line technical troubleshooting for complex manufacturing issues, leading structured investigations, root-cause analyses, risk assessments and implementation of sustainable CAPAs. Author, review and approve technical protocols, validation documentation, internal standard, study plans, reports, investigations, trend analyses and scientific justifications supporting manufacturing operations and regulatory submissions. Serve as a technical authority during audits, inspections, regulatory interactions and due diligence activities related to sterile manufacturing operations. Lead a Sterile Manufacturing Community of Practice by sharing best practices, industry trends, lessons learned and emerging technologies, while developing organizational knowledge and technical capabilities to the organization. Contribute to due diligence for manufacturing site selection, technology assessments and strategic investments by evaluating technical capabilities, operational readiness and compliance risks. Manage project scope, timelines, resources, budgets, risks and mitigation plans to ensure successful execution of MSAT objectives and business priorities. Interested? For this role we’re looking for the following education, experience and skills: Master's degree in Engineering, Pharmaceutical Sciences, Biotechnology, Chemical Engineering or related discipline. 8+ years of experience in sterile pharmaceutical manufacturing, MSAT, Process Engineering, Technical Services or Manufacturing Support. Demonstrated

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/msat-dp-sterile-process-lead-at-ucb-902625

Source: https://jobsbylevel.com/jobs/msat-dp-sterile-process-lead-at-ucb-902625

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