In this role, you will lead MSAT-focused technology transfers for DSP processes, driving scalable biopharma manufacturing improvements. You’ll partner with cross-functional teams to ensure smooth design-to-scale transitions, and you’ll own execution, issue resolution, and documentation. Your work will emphasize GMP compliance, process optimization, and close collaboration with customers and operations. 

Start Date: 03/11/2025

Duration: 6 Months

Place of Work: Visp

Key Responsibilities

  • Support technology transfers from concept to scale, assisting design, qualification, and upscaling
  • Serve as the main interface between process donors and operations to ensure scalability and manufacturability
  • Manage campaign execution, communicate with customers, report batch performance, and close campaigns smoothly
  • Identify and resolve process issues with accuracy and regulatory alignment
  • Own documentation, including campaign reports, material change requests, and process deviations
  • Drive innovation by enabling new materials and optimizing existing ones

Job ID 41181208

Candidate Profile

  • Bachelor’s or Master’s degree (PhD preferred) in Biotechnology, Chemical Engineering, or related field
  • 5+ years in biopharma manufacturing or process development, ideally in Mammalian Manufacturing and MSAT
  • Experience in process validation, cleaning validation, material management, and deviation handling is a plus
  • Strong GMP and bioprocess technology knowledge
  • Languages: Fluent English; German is a plus
  • Demonstrated leadership, communication, and organizational skills
  • Team-focused, open-minded, and solution-driven
  • Agile, motivated, and proactive