55 English-speaking jobs in Visp

Design, develop, and implement Emerson DeltaV automation solutions for pharmaceutical and biotech CAPEX projects. Configure control modules, graphics, and interfaces while ensuring GMP and GAMP compliance. Requires automation engineering degree and DeltaV experience.

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.

Automation Engineer MES/DeltaV implements and supports MES and Emerson DeltaV systems in biopharmaceutical manufacturing. Requires experience in regulated environments, knowledge of MES/DeltaV, and understanding of GMP.

Internship Global Master Data Analyst role involves data analysis, supporting SAP Master data maintenance and migration, and defining process requirements. Requires a degree in data/CS/IT/Math and English fluency.

EI&C DeltaV Engineer needed for freelance projects. Responsibilities include designing, developing, and implementing Emerson DeltaV solutions for pharma/biotech CAPEX. Requires experience with DeltaV, GxP documentation, and system integration.

EI&C Instrumentation Engineer to design and specify instrumentation for process systems, ensuring GMP compliance. Responsibilities include selecting measurement technologies, maintaining documentation, and supporting system integration and commissioning.

Develop, configure, and maintain automation and manufacturing software applications for pharmaceutical and biotechnology. Design integrations with DCS, MES, and databases using VBA, PowerShell, C, and SQL. Requires a relevant engineering degree and experience in GMP environments.

EI&C Instrumentation Engineer to design and specify instrumentation for process utility and infrastructure systems. Responsibilities include documentation, system integration (DCS, PLC, SIS), and GMP qualification in regulated manufacturing.

EI&C PI Engineer to manage and optimize PI systems for manufacturing. Responsibilities include maintaining PI Data Archive, AF, and developing PI Analytics. Requires experience with PI SDK, DeltaV, and GxP compliance.

Electrical Engineer – Low Voltage to design, develop, and implement electrical systems in automated industrial and pharmaceutical manufacturing. Requires 3+ years in low voltage systems, VFDs, and compliance with standards like NIN and ATEX.

Production Manager, Chromatography/DSP leads manufacturing operations for chromatography steps in the Drug Linker Asset. This role requires expertise in DSP, process development, and leading interdisciplinary teams while ensuring quality and cost control.

Support process validation across Upstream and Downstream operations. Assist in drafting, reviewing, and executing validation protocols and reports. Requires a university student in a relevant field with strong analytical and teamwork skills.

Lead Drug Linker Development and PD/MSAT/DSP Chemists, driving pipeline optimization and unit setup. Requires PhD in Chemistry/Engineering and 5-10 years in pharma process development.

DeltaV Automation Engineer role involves planning and realizing electrical MSR readiness and ensuring seamless operation of high-automated Biologics facilities using DeltaV and MES systems. Requires experience in Electrical/System Engineering and familiarity with GMP standards.

Lead MES DeltaV projects across the full lifecycle, strengthening system standards, and ensuring GMP-compliant performance. Requires a degree in a related field and experience in IT/OT or MES DeltaV within a regulated environment.

CSV Engineer for Biologics responsible for generating and executing computerized system validation on process engineering equipment. Duties include preparing validation documents, supervising projects, and ensuring adherence to protocols.

Drive new business and expand relationships for Drug Product Services across EMEA. Requires experience in aseptic filling and fill-finish services, biologics, or CDMO sales.

Own and execute the monthly Supply Planning cycle for Microbial operations, improving the Supply Plan, MPS, and capacity outlook. Requires experience in Supply Planning, S&OP, and SAP IBP/ECC.

Senior Scientist QC manages GMP reference standard qualification protocols and reports for biotechnological materials. This role requires a Master's in Life Sciences, cGMP experience, and expertise in analytical chemistry/biology.

Senior Category Manager and Buyer (Automation) leads procurement for automation systems (PLC, DCS, SCADA, MES) in large-scale pharmaceutical projects. Responsibilities include negotiating with OEMs, managing CAPEX, and implementing TCO strategies. Requires technical automation knowledge and pharma manufacturing experience.