DSP Process Expert MSAT

DSP Process Expert MSAT

Lonza

Visp, Switzerland

As a member of the MSAT (Manufacturing Science & Technology) Team Ibex Visp responsible for the successful transfer, scale up, supervision and optimization of biopharma processes. As a very experienced professional, you are regarded as an expert in process science and manufacturing aspects. In this role, you significantly contribute to the development of the MSAT toolbox and share the manufacturing responsibility as a long-term process owner.

Key responsibilities:

  • Leading cross-functional teams as a process expert tasked with technology transfers (process design and up-scaling) and timely process implementation at manufacturing scale. This includes the whole lifecycle of assigned projects from planning over coordination, implementation, control and project completion aligned with project management goals;
  • Act as the interface between the process donor (external customer, process development) and operations. Responsible to ensure process scalability and manufacturability;
  • Securing success during technology transfer by applying formal processes and tools to manage the transfer of information, process related risks and change control;
  • Responsible for the resolution of process issues that may arise during manufacturing, considering all regulatory requirements. This includes on call duty;
  • Responsible for execution of GMP risk analysis for the manufacturing processes;
  • Ensuring timely compilation of process related deviations, change requests and campaign reports as well as responsible for continuous improvement of process performance.

Key requirements:

  • PhD or equivalent experience (preferred), Master’s/Master’s degree in biotechnology, chemical engineering or related fields;
  • Working experience in biopharma manufacturing and/or process development preferable in of 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.

Apply Now

Don't forget to mention EuroPharmaJobs when applying.

Share this Job

More Job Searches

Switzerland      Biotechnology and Genetics      Manufacturing and Logistics      On-site      Pre-clinical Research and Development      Quality Assurance      Lonza     

EuroPharmaJobs Logo

© EuroJobsites 2025