Main Responsibilities
Supporting technology transfers: From process design to upscaling, you'll support projects from concept to completion.
Acting as the key interface between process donors (customers, development teams) and operations to ensure scalability and manufacturability.
Managing campaign execution: Communicate directly with customers, report batch performance, and ensure smooth campaign closure.
Resolving process issues with precision and compliance, keeping regulatory standards top of mind.
Owning documentation: Compile campaign reports and manage material change requests and process-related deviations.
Driving innovation: Facilitate the implementation of new materials and optimize existing ones.
Qualifications and Experience
Relevant working / residency permit or Swiss / EU-Citizenship required
Bachelor’s or Master’s degree (PhD preferred) in Biotechnology, Chemical Engineering, or related fields.
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.
Deep understanding of GMP and bioprocess technology.
Fluent English; German is a strong asset.
Strong leadership, communication, and organizational skills.
Team-oriented, open-minded, and solution-driven.
Agile, motivated, and ready to take initiative.
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