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The site in Visp, Switzerland is growing and for the Biologics organization, experienced Process Experts and Senior Process Experts are sought for Ibex® Solutions, a recently launched unique biological manufacturing and development concept. Opportunities are available in both USP and DSP in Drug Substance for mammalian large-scale manufacturing (up to 20,000L). As a process owner, you are responsible for the successful scale up, supervision and optimization of mammalian processes.

Tasks

  • Lead cross-functional teams as a process expert tasked with technology transfers (process design and up-scaling) and timely process implementation at manufacturing scale.
  • Manage the whole lifecycle of assigned projects from planning, coordination, implementation, control, to project completion aligned with project management goals.
  • Act as the interface between the process donor (customer, process development) and operations.
  • Ensure 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.
  • Work as MSAT process expert in capital investment projects for building and commissioning of manufacturing units.
  • Deliver all input required for specific processes (block-flow diagrams, media and buffer lists, critical parameter lists).
  • Implement the manufacturing process 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.
  • Resolve process issues that may arise during manufacturing, considering all regulatory requirements.
  • Execute GMP risk analysis for the manufacturing processes.

Requirements

  • Bachelor or Master's degree, PhD preferred.
  • Preferred area of study: Biotechnology, chemical engineering or related disciplines.
  • More than 5 years of experience in biopharma manufacturing and/or process development, preferably in Mammalian Manufacturing.
  • GMP and deep understanding of bioprocess technology.
  • Fluency in English and German.
  • Strong leadership skills.
  • Very good communication skills and interaction with all kinds of interfaces within customers and the project organisation.
  • Strong team orientation.
  • Structured, focused and well-organized working attitude.
  • Open-minded for new ideas and suggestions.
  • Agile, highly motivated and dynamic drive.
  • Solution-oriented.
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Über uns
Lonza Group AG ist ein international tätiges Unternehmen für die Pharma-, Biotech- und Life-Science-Industrie. Das Unternehmen entwickelt und produziert Wirkstoffe, biopharmazeutische Produkte sowie spezialisierte Lösungen und unterstützt Kunden von der frühen Entwicklung bis zur industriellen Herstellung. Zudem stellt Lonza chemische und biotechnologische Komponenten für Anwendungen in Gesundheit, Ernährung und weiteren Industrien her.
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