81 English-speaking jobs in Visp

Manufacturing Specialist to support project setup and routine vaccine production. Responsibilities include process definition, qualification, execution of manufacturing activities, and documentation. Requires a chemical/biopharmaceutical education or equivalent experience and knowledge of biotechnological processes. Fluency in English is required.

CSV Engineer responsible for the validation of computerized systems on process engineering equipment and facilities. Prepares commissioning and validation documents, supervises deviations and changes, and coordinates CSV executions with internal and external groups. Requires a technical degree and significant experience in CSV within a regulated environment.

Senior QA Specialist will provide quality assurance oversight for site and facilities, focusing on shared utility systems and logistics areas. Responsibilities include providing QA support, leading deviation review boards, and reviewing change requests and CAPAs.

Biotechnologist needed for production in Visp, Switzerland. Requires chemical/biopharmaceutical education and experience in pharmaceutical production. Must be safety-conscious, knowledgeable in process engineering, and fluent in English. German language skills are advantageous. Willingness to work shifts is required.

Lead Expeditor needed to ensure timely delivery of materials and maintain efficient procurement processes. Coordinate with suppliers, manage reporting systems, and support internal stakeholders. Requires strong organizational, communication, and problem-solving skills. Proficiency in Microsoft Office, data analytics, and reporting is essential. Fluency in English is required. Relevant experience in a similar role, with CAPEX experience preferred. Must be able to work both on-site and remotely.

Lead and deliver customer programs from technology transfer to GMP manufacturing, ensuring quality, timeliness, and cost-effectiveness. Act as a trusted partner and main point of contact for customers, fostering transparent communication and long-term collaboration.

As a Vorsorge- und Finanzberatende, you will cultivate existing client relationships, acquire new clients, and provide comprehensive financial and retirement planning advice. You will develop and sell tailored solutions in retirement planning and asset building while representing the company in your sales area.

Manufacturing Specialist will execute production steps, interpret deviations, and support training within a cGMP environment. Requires a chemical/biopharmaceutical education, experience in pharmaceutical production, and fluency in English. German language skills are advantageous.

Biotechnologist with a background in chemical or biopharmaceutical sciences needed for production functions. Experience in pharmaceutical production and a safety-conscious work style are required. Fluent English, German is a plus.

DeltaV Automation Engineer needed for planning and realization of electrical MSR readiness within budget and timelines. Ensures seamless operation of high-automated Biologics facilities equipped with DeltaV and MES systems. Manages GMP-compliant activities, including testing, documentation, and change management. Collaborates with cross-functional teams to refine internal procedures and achieve optimized workflows.

Develop and maintain commissioning and qualification documents for new plants. Supervise deviations, manage changes, and implement CAPAs. Coordinate efforts between internal teams and external service providers.

Senior Operator/Biotechnologist supports production in a biopharmaceutical facility. Responsibilities include executing production steps, recognizing deviations, and training new team members. Requires a chemical/biopharmaceutical education, experience in pharmaceutical production, and fluency in English. German language skills are advantageous.

The EHS Manager drives the implementation and improvement of Environmental, Occupational Health, and Safety programs in collaboration with manufacturing facilities. This role serves as the primary EHS contact for Large Scale Plants in Visp, ensuring safe, compliant, and sustainable chemical manufacturing.

As a Process Expert MSAT, you will lead cross-functional teams in technology transfers, process design, and scale-up. You will act as the interface between process development and operations, ensuring process scalability and manufacturability.

Senior QA Specialist to join a multifunctional team in Bioconjugates Business unit. Will support the establishment and maintenance of quality management & compliance processes. Responsibilities include coordinating QA interests during project phases, reviewing and releasing records, and managing stakeholder needs. Requires a degree in Biotechnology/Biochemistry or related field, significant experience in biopharmaceutical manufacturing, and strong cGMP knowledge.

EHS Manager Process Safety will implement, supervise, and optimize EHS programs for the Visp site. Responsibilities include developing continuous improvement strategies, ensuring compliance with regulations, conducting risk analysis, and implementing EHS process safety standards.

Bioprocess Engineer needed for Upstream Processing, Downstream Processing, or BioConjugate Manufacturing. Master's Degree or equivalent experience in a Life Science field required. Knowledge of USP or DSP units and GMP experience necessary.

Manufacturing Specialist for Upstream or Downstream processing at Lonza's Visp site. Executes manufacturing activities according to cGMP guidelines, supports risk assessments, and assists with document preparation. Requires a chemical/biopharmaceutical education, knowledge of biotechnological processes, and fluency in English.

This GMP-compliant manufacturing role focuses on overseeing and optimizing cleaning operations within a mammalian asset in its startup phase. Responsibilities include managing cleaning processes, ensuring regulatory compliance, leading operational teams, and driving continuous improvements.

Execute end-to-end Drug Product manufacturing under GMP, including batch execution, documentation, and troubleshooting. Support process changes, CAPA activities, and ensure safe, timely, and quality-compliant production. Operate and maintain equipment for liquid and freeze-dried vial manufacturing. Train colleagues and support cross-functional teams.