402 English-speaking jobs in Canton of Valais

Coordinate and support downstream production activities across various departments to ensure timely and compliant execution. Lead workforce planning, training, and performance management for DSP production support. Manage recruitment and onboarding of production personnel.

Lead and shape a comprehensive contamination control strategy in a GMP-regulated bioconjugates environment. Drive cross-functional collaboration, leverage contamination control expertise, and influence continuous improvement initiatives.

Leads and shapes a comprehensive contamination control strategy within a GMP-regulated bioconjugates environment, ensuring end-to-end compliance across manufacturing facilities. Drives cross-functional collaboration, leveraging contamination control expertise to influence continuous improvement initiatives. Authors and approves GMP documentation, including SOPs, deviations, change controls, and risk assessments. Partners with cross-functional teams to identify risks, manage deviations, and strengthen contamination prevention control practices. Acts as a QA Microbial Contamination Control and cleaning SME in meetings, audits, and inspections.

Biotechnologist to support manufacturing operations in a clean room environment. Ensures safe, clean, and compliant production of liquid and freeze-dried drug forms. Collaborates with the manufacturing team to meet production needs while adhering to GMP standards.

Reviews, assesses, and coordinates Vendor Change Notifications (VCNs) from suppliers. Ensures impact assessments are completed and VCNs are managed according to GMP requirements and regulatory expectations. Collaborates with internal stakeholders to support compliant supplier management.

Provides site support as part of the QA supplier management team. Reviews, evaluates, and coordinates supplier change notifications, ensuring compliance and timely implementation.

QA Project Manager will establish Quality Agreements, act as QA representative in project teams, and support customer audits. Requires a university degree in a relevant field and long-term GMP experience in the pharmaceutical industry.

Intern will review executed Batch Records, support batch release, analyze documentation, and assist with deviations and investigations. Must have a degree in a relevant field and proficiency in English. German language skills are a plus.

Project Engineer needed for a 7-month contract with extension planned. The role oversees capital investment projects in a mammalian cell production line, ensuring alignment with GMP standards and operational goals. Requires 5+ years of experience in biopharmaceutical manufacturing, project management, and GMP-compliant project execution.

Project Engineer needed for freelance/temporary employment in Visp. Define technical requirements, manage project roadmaps, and ensure GMP compliance. Experience in biopharmaceutical manufacturing, project management, and CQV activities required.

The Chief Steward enforces cleanliness standards in kitchens and back-of-house facilities, recruits and trains the stewarding team, and manages daily shift assignments. The role also involves overseeing equipment and chemical inventory, and coordinating with the F&B team for large events.

Provide basic and delegated medico-technical care to adults with multiple disabilities. Collaborate on individualized projects and promote the quality of life of the people supported.

Scheduler needed for a 12-month position with potential extension. Responsibilities include owning end-to-end program schedules, updating resource workloads, and leading meetings with stakeholders. Requires 5+ years of experience in pharmaceutical manufacturing scheduling, proficiency in Primavera P6, and fluency in English. German is a plus.

Experienced SAP EWM Functional Consultant needed for pharmaceutical project in Switzerland. Lead and support implementations, rollouts, and enhancements. Configure and optimize SAP EWM processes for pharma operations. Collaborate with international teams and ensure compliance with industry standards.

Process Analytics & Operational Intelligence Expert will build analytics-ready datasets, analyze process trends, and develop dashboards to improve operational performance.

Lead MES projects across all lifecycle phases, from requirement analysis to deployment. Maintain and optimize MES standards, ensuring compliance and alignment with guidelines. Collaborate with Operations, QA, Automation, and IT/OT teams to ensure seamless system integration and high system availability.

The Batch Record Review Intern supports the Quality Assurance team by reviewing, verifying, and organizing electronic GMP manufacturing documentation. This role involves reviewing executed batch records, clarifying comments, and supporting deviation and investigation processes.

Laboratory Technician will conduct routine HPLC analysis of biopharmaceuticals, adhering to SOPs, GMP, and safety rules. Experience with HPLC and a GMP environment is preferred. Fluency in English or German is required.

The Mont Cervin Palace seeks a Chief Steward to lead and manage the stewarding team in a high-volume hotel. Responsibilities include ensuring cleanliness, training staff, managing inventory, and coordinating with F&B management. Requires 2-5 years of experience in stewarding or F&B operations, knowledge of food safety and sanitation standards, and strong communication and leadership skills. Fluency in English is required, German and/or French is a plus.

Senior Bioprocess Engineer to manage operational activities, including tech transfer, material planning, and training. Lead interdisciplinary teams and guide activities for clinical and commercial manufacturing. Requires a Bachelor's, Master's, or PhD in a Life Science subject and significant experience in biomanufacturing. Excellent communication skills in English and/or German are essential.