57 English-speaking jobs in Visp

Electrical Design Engineer responsible for designing and developing electrical systems in industrial environments. Key duties include designing infrastructure, power distribution networks, and UPS systems while ensuring compliance with standards. Requires an engineering degree and 4-10 years of relevant experience.

Ensure compliance and data integrity by performing rigorous batch record reviews for life-saving medicines. Analyze electronic and paper records within MES, SAP, and LIMS environments, adhering to ALCOA and GDP principles.

Design and implement Emerson DeltaV automation solutions for biotech CAPEX projects. Configure control modules, graphics, and interfaces while developing GxP-compliant documentation. Requires engineering degree and DeltaV experience in regulated environments.

Design and implement DeltaV automation solutions for biotech CAPEX projects. Configure control modules, graphics, and interfaces while developing GxP-compliant documentation. Requires engineering degree and DeltaV experience in regulated environments.

EI&C PI Engineer needed for a project. Responsibilities include administering PI Data Archive, configuring PI AF, developing analytics, and integrating PI with manufacturing systems like DeltaV and PLCs. Requires experience with PI SDK, SQL, and GxP compliance.

Senior QA Specialist for a project role. Responsibilities include quality oversight for facility qualification, environmental monitoring, and leading investigations. Requires a degree in a life science and GMP experience.

Lead a multidisciplinary team in biologics manufacturing as Associate Director, Manufacturing DSP. Drive operational excellence, ensure production readiness, and manage complex manufacturing challenges within a GMP-regulated environment.

Process Validation Specialist develops validation strategies and executes protocols for commercial manufacturing. This role requires a PhD or Master's in a relevant science, GMP experience, and strong analytical skills.

Senior QA Specialist for QA Projects defines quality requirements for biopharmaceutical manufacturing processes and cGMP standards. This role owns quality responsibilities, reviews critical records, and ensures compliance in cross-functional teams.

DSP Bioprocess Engineer responsible for planning, executing, and monitoring commercial and clinical manufacturing campaigns in Downstream Processing. Acts as manufacturing subject matter expert ensuring cGMP compliance and leading process improvements.

QA Logistic Specialist ensures pharmaceutical quality and compliance across global supply chains. Responsibilities include verifying incoming materials, overseeing material qualification, and managing quality alerts under GMP standards. Requires a relevant degree and knowledge of quality systems like SAP and LIMS.

Leads technical transfer activities, including setup and implementation of sterile GMP DP manufacturing processes. Manages drug product transfers from clinical to commercial launch, ensuring cGMP compliance.

Design, build, and operate production-ready data infrastructure integrating operational data from MES, PI Historian, and other sources. Requires strong SQL, ETL/ELT experience, and knowledge of Azure data services in manufacturing environments.

Design, build, and operate production-ready data pipelines integrating operational data from sources like PI, MES, and ELN. Requires strong SQL, ETL/ELT experience, and knowledge of Azure data services in manufacturing environments.

Senior QA Specialist provides quality oversight for facility and cleanroom qualification. Responsibilities include environmental monitoring, investigating deviations, and supporting CAPAs within GMP environments. Requires a relevant degree and strong microbiological expertise.

QA Specialist supports contamination prevention and control for a global CMO. Responsibilities include facility and utility qualification, environmental monitoring, and ensuring compliance with regulatory standards. Requires a relevant scientific degree and GMP experience.

The Upstream Team Lead provides technical leadership and manufacturing support for USP operations, managing Bioprocess Engineers. This role oversees campaign execution, ensures cGMP compliance, and drives operational excellence.

MES System Engineer (EI&C) role maintaining and improving MES standards and system operations. Responsibilities include ensuring GMP compliance, supporting system enhancements, and integrating MES with automation and ERP platforms. Requires relevant technical degree and experience in regulated environments.

Automation Engineer to design, develop, and implement Emerson DeltaV solutions for pharmaceutical and biotech CAPEX projects. Requires experience with DeltaV, GMP, GAMP, and data integrity standards.

Design and specify instrumentation for process systems, selecting measurement technologies and maintaining documentation. Support DCS/PLC integration, commissioning, and GMP qualification activities. Requires relevant engineering degree and experience in regulated environments.