Biopharma Process Expert
vor 1 Woche
Join Lonza AG, a global leader in life sciences, as a Biopharma Process Expert in our MSAT Team Ibex Visp. As a senior expert in process science and manufacturing aspects, you will significantly contribute to the development of the MSAT toolbox and share the manufacturing responsibility as a long-term process owner.
Key Responsibilities:- Lead cross-functional teams as a process expert tasked with technology transfers (process design and up-scaling) and timely process implementation at manufacturing scale.
- Act as the interface between the process donor (customer, process development) and operations, ensuring process scalability and manufacturability.
- Secure success during technology transfer by applying formal processes and tools to manage the transfer of information, process-related risks, and change control.
- Resolve process issues that may arise during manufacturing, considering all regulatory requirements.
- Execute GMP risk analysis for manufacturing processes.
- Work as an MSAT process expert in Capital investment projects for building and commissioning of manufacturing units.
- Implement manufacturing processes in the plant.
- Interact directly with customers during tech transfer, campaign preparation, execution, and closure, including daily reporting of batch status and performance.
- Ensure timely compilation of process-related deviations, change requests, and campaign reports.
- Compile CMC sections in filing documents and technical content of validation reports.
- Contribute to the development and implementation of standardized MSAT procedures and processes.
- Responsible for continuous improvement of process performance.
- Supervise tasks in the area of local and global MSAT initiatives or lead major task forces or troubleshooting teams.
- Evaluate and drive innovative trends within the respective area of expertise.
- Act as a mentor for scientific and production staff in different fields of expertise.
- Perform process-specific trainings for production staff.
- PhD (preferred), Master's/Master's degree in biotechnology, chemical engineering, or related disciplines.
- Working experience in biopharma manufacturing and/or process development, preferably in mammalian manufacturing.
- Deep understanding of GMP and bioprocess technology.
- Very good communication skills and interaction with all kinds of interfaces within customers and the project organization.
- Fluency in English and German.
At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world.
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