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
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
#J-18808-Ljbffr