106 English-speaking jobs in Canton of Valais

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.

DeltaV Automation Engineer will plan and execute electrical MSR readiness, ensuring seamless operation of Biologics facilities. Experience in pharmaceutical or biotech plant operation and maintenance is required. Proficiency in DeltaV, MES, SAP, and COMOS is highly desirable.

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.

Execute manufacturing activities in the Drug Product area following cGMP guidelines. Perform visual inspection of vials and provide technical support to the manufacturing team. Requires GMP experience and ability to work flexible shifts.

Senior CAPEX Planner Controller develops and manages integrated project schedules for large capital projects. Requires 5-10 years of experience, strong Primavera P6 skills, and essential experience in the pharmaceutical industry.

Assistant Housekeeping Manager assists in managing, training, and motivating the housekeeping team. Responsibilities include monitoring cleanliness standards, conducting inspections, handling guest complaints, and managing supplies and schedules.

The Commis de Cuisine assists in preparing meals, maintaining kitchen cleanliness, and managing supplies. They operate equipment, adhere to hygiene regulations, and contribute to order and cleanliness throughout the kitchen and storage areas.

The Sous Chef assists the Head Chef in menu planning, production, and preparation. They oversee daily kitchen operations, including mise en place, quality control, and staff supervision. The Sous Chef also shares responsibility for purchasing, equipment maintenance, and ensuring cleanliness and hygiene standards.

Manages all Food & Beverage operations including restaurants, bar, breakfast, room service, and events. Ensures luxury service standards and guest satisfaction. Oversees teams, monitors performance, and implements corrective actions. Develops and positions the hotel's F&B offering, drives revenue growth, and manages budgets. Ensures compliance with hygiene, safety, and quality standards. Leads, trains, and develops F&B teams.

Provides guest services, including information, reservations, and luggage handling. Manages mail, parcel post, and guest transfers. Coordinates emergency procedures and guest requests. Maintains inventory and ensures guest safety.

Lead Sterility Assurance and Microbial Control for Drug Product Module. Own the Contamination Control Strategy, providing technical leadership in aseptic processing and risk assessments. Requires scientific degree and extensive pharma experience.

Logistics Systems & SAP EWM Specialist drives SAP EWM/MM process optimization in a GMP-regulated environment. Responsibilities include managing end-to-end logistics, system integrations, testing, and ensuring compliance. Requires SAP EWM/MM experience.