MSAT Process Expert – Mammalian Cell Culture DSP
Contract: 1 December 2026 – 31 August 2028
Duration: 21 months
Work arrangement: 100% onsite
About the role
Lonza's biologics organisation in Visp is expanding, and we are looking for an experienced MSAT Process Expert in Mammalian Cell Culture – Downstream Processing (DSP) to support its Ibex® Solutions platform.
Ibex® is Lonza's integrated biological manufacturing and development concept, supporting large-scale mammalian manufacturing processes of up to 20,000L.
As a Process Expert, you will take ownership of process scale-up, technology transfer, implementation and continuous optimisation, working closely with customers, process development teams and manufacturing operations.
You will lead cross-functional activities to ensure that processes are successfully transferred, implemented and maintained at manufacturing scale.
Key responsibilities
Technology Transfer & Process Implementation
- Lead cross-functional teams through technology transfer activities, including process design, scale-up and implementation at manufacturing scale.
- Manage the full project lifecycle, from planning and coordination through implementation, control and completion.
- Act as the interface between process donors, customers, process development and manufacturing operations.
- Ensure process scalability and manufacturability.
- Manage process-related information transfer, risks and change controls.
MSAT & Capital Projects
- Act as the MSAT process expert in capital investment projects involving the construction and commissioning of manufacturing units.
- Provide process-related technical input, including block-flow diagrams, media and buffer lists, and critical parameter lists.
- Support implementation of manufacturing processes at the site.
Manufacturing & Customer Support
- Interact directly with customers during technology transfer, campaign preparation, execution and closure.
- Provide daily reporting on batch status and performance.
- Support the resolution of process issues arising during manufacturing.
- Ensure process-related deviations, change requests and campaign reports are completed on time.
Quality, Compliance & Continuous Improvement
- Compile CMC sections for filing documents and technical content for validation reports.
- Execute GMP risk analyses for manufacturing processes.
- Contribute to standardised MSAT procedures and processes.
- Drive continuous improvement of process performance.
- Support MSAT initiatives, troubleshooting teams and technical task forces.
Leadership & Knowledge Sharing
- Mentor scientific and production staff.
- Deliver process-specific training to production teams.
- Evaluate and drive innovative developments within the area of expertise.
Candidate requirements
- Bachelor's or Master's degree in Biotechnology, Chemical Engineering or a related discipline.
- PhD preferred.
- More than 5 years of experience in biopharmaceutical manufacturing and/or process development.
- Experience in mammalian manufacturing is highly preferred.
- Strong understanding of GMP and bioprocess technologies.
- Experience with technology transfer, process scale-up and manufacturing implementation.
- Strong leadership and communication skills.
- Ability to work with customers and multidisciplinary project teams.
- Strong team orientation.
- Structured, organised and focused working approach.
- Agile, motivated and solution-oriented mindset.
- Open to new ideas and continuous improvement.
- Duration: 21 months.
- End date: 31 August 2028.
- Work arrangement: 100% onsite.