148 English-speaking jobs in Visp

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world.

Join to apply for the HR Business Partner role at Vaxcyte Join to apply for the HR Business Partner role at Vaxcyte Get AI-powered advice on this job and more exclusive features. Join our Mission to Protect Humankind!

Direct message the job poster from Cpl Life Sciences Senior Consultant @ CPL Life Sciences - Contract Engineering UK/EU CPL Life Sciences is working with a global Biotechnology organization to recruit a QA Validation Specialist for a 12-month contract in Visp. Responsibilities include: Ensuring GMP compliance regarding equipment, facilities, and systems, aligned with regulatory guidelines.

If you are looking to advance your career in a dynamic and supportive setting, we invite you to explore this opportunity. Job Responsibilities: Project Controls Professional to support key CAPEX project for 1 year. Assigment can be at 50 to 80% per month. Remote work possible but strong site presence preferred. Focus on cost reporting, cash forecasting, cost rebookings.

Oxford Global Resources We are looking for Quality Assurance–oriented people to work at one of our clients in Visp, in the pharmaceutical industry. About the Client Our client is a global leading company in the pharmaceutical and biotechnology sector, specializing in the development and production of active ingredients, biopharmaceutical products, and innovative health solutions.

Join to apply for the QA Validation Specialist role at Actalent 2 days ago Be among the first 25 applicants Join to apply for the QA Validation Specialist role at Actalent Get AI-powered advice on this job and more exclusive features. We are seeking a QA Validation Specialist to join our client's team and support the validation of GMP-critical equipment, facilities, and systems.

Duration: ideally 04/08/2025 to 31/07/2026 with potential for extension Workload: 100% (can also be 50–80%) You will support a key CAPEX project in Visp, focusing on cost control and financial reporting.

We are seeking a QA Validation Specialist to join our client's team and support the validation of GMP-critical equipment, facilities, and systems. This role ensures compliance with user requirements, process parameters, and global regulatory standards.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world.

Today, Lonza is a global leader in life sciences operating across three continents. While Lonza works in science, there’s no magic formula to how they do it. Their greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, they let their people own their careers. Their ideas, big and small, genuinely improve the world.

The Process Engineer is responsible for all Process aspects including design, installation, operation and maintenance. The Process Engineer is assigned to develop, define and roll-out the process philosophies and standards in collaboration with QA, Operations and Engineering.

Direct message the job poster from CTC Resourcing Solutions Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a: QA Validation Specialist for a contract role of 12 months to be based in the Valais area , Switzerland.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world.

Join to apply for the Contract and Claim Manager role at Prime Life Sciences Continue with Google Continue with Google Join to apply for the Contract and Claim Manager role at Prime Life Sciences As a member of the global Capital Sourcing team, the Contract & Claim Manager is sought to be responsible for the Contracts & Claims management of a variety of projects during the project execution phase,

As part of The Adecco Group, Akkodis has extensive industrial experience and deep expertise in key technology areas.

Direct message the job poster from Gi Group Are you passionate about quality, scientific rigor, and innovation in the life sciences? Join a dynamic team where your expertise will directly contribute to ensuring the compliance and performance of critical GMP equipment, facilities, and systems.

In this role , you will support the validation and qualification of GMP-critical equipment, facilities, and systems to ensure compliance with regulatory standards. You will collaborate with cross-functional teams to maintain validated states, review validation documents, and assess change controls.

In this role , you'll support a major CAPEX project by managing cost reporting, cash flow forecasting, and change management. You will collaborate closely with project and finance teams to ensure project performance and financial accuracy. Start Date : 04/08/2025 Duration : approx.

Key Responsibilities Perform QA oversight of validation, qualification, and review activities to ensure GMP equipment, facilities, and systems are continuously maintained in a validated state. Schedule and prioritize personal tasks as well as tasks for junior team members under the guidance of the Validation Manager.