Job Title: Senior Bioprocess Engineer (Contract Position)Location: Visp, Switzerland (100% On-site)Duration: August 2025 – August 2026Industry: Biopharmaceutical / Biotech ManufacturingJob SummaryA leading Biologics manufacturing site in Visp is expanding its operations and is seeking experienced Senior Bioprocess Engineers with proven expertise in Microbial, Mammalian, or BioConjugate manufacturing. This position is ideal for professionals passionate about driving improvement initiatives, operational readiness, and the successful implementation of new systems and processes. Key ResponsibilitiesOversee operational activities in Upstream, Downstream, or BioConjugates manufacturing including:
Technology transfer supportMaterial planning and logistics coordinationBatch record and SOP preparationTraining, troubleshooting, and deviation managementServe as the functional lead for assigned roll-out initiatives (e. g.
, SAP functionalities), including Change Management and manufacturing documentation updatesLead cross-functional teams including production staff, supervisors, and technical specialists to ensure successful project executionDevelop and maintain training materials for manufacturing, logistics, and related departmentsSupport clinical and/or commercial manufacturing activities in areas such as capture, purification, drug substance filling (DSP), or BioConjugate processingEnsure compliant and efficient operation of both single-use and stainless-steel systems for protein purificationKey RequirementsBachelor’s, Master’s, or PhD in Biotechnology, Biochemical Engineering, Biochemistry, or related Life SciencesProven experience in Biologics Manufacturing (DSP or BioConjugates) in a GMP-regulated environmentStrong knowledge of chromatography, filtration (ultra-/dia- and dead-end), and other downstream operationsExperience using SAP in a manufacturing/logistics context (BOMs, materials)Strong user experience with MES systemsExcellent verbal and written communication skills in English and GermanStrong organizational and documentation skillsDemonstrated ability to lead initiatives and drive change across cross-functional teamsPreferred AttributesSolid understanding of GMP and regulatory requirementsOpen-minded, proactive, and solution-oriented attitudeAbility to effectively train and support team membersCollaborative, team-first mindset with the ability to engage stakeholders at all levelsMust-HavesDemonstrated project management capability to lead roll-outs and improvement projectsHands-on experience in Biologics Production (Microbial, Mammalian, or BioConjugates)SAP expertise, especially in materials and logistics workflowsAbility to create, review, and deliver comprehensive training documentationFluent communication in German and EnglishCollaborative mindset with strong cross-departmental teamwork skills
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