82 switzerland English-speaking jobs in Visp

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.

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

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.

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.

Intern to support QA documentation, ensuring cGMP compliance in manufacturing activities. Reviews Batch Records, analyzes data, and assists with deviations and investigations. Requires a degree in a relevant field and proficiency in English.

Intern QC Lab Associate will carry out routine analysis, contribute to method implementation and validation, and support laboratory maintenance. Requires experience in analytical lab work and fluency in German or English.

Drive growth for Lonza's Specialized Modalities platform across mainland Europe. Build customer relationships, develop new business opportunities, and deliver tailored solutions.

Bioprocess Engineer needed for Upstream or Downstream Processing. Master's degree or equivalent experience in a Life Science field required. Knowledge of bioreactors or chromatography units and GMP experience necessary.

Cleaning Validation Expert needed for Large-Scale Mammalian facility in Visp. Develop and coordinate cleaning validation strategies, prepare documentation, and act as Subject Matter Expert for cleaning related matters. Master's or PhD in biotechnology, life sciences, or related disciplines required. Experience in biopharma cleaning and/or validation in a cGMP environment is essential.

Process Expert leads multi-functional teams for technology transfers, process implementation, and optimization of mammalian processes at manufacturing scale.

This internship supports the global Master Data department in Visp. Assist with data analysis, SAP master data maintenance, and gathering feedback from Subject Matter Experts. Develop training materials and deliver training sessions.

Intern supports material management and process-related activities in microbial cGMP manufacturing. Assists with material quality issues, single-use assembly design, and process documentation. Collaborates with cross-functional teams to ensure robust and compliant processes.

The Head of OE & PMO leads the Operational Excellence and PMO agenda, driving business results aligned with the Dedicated to Excellence strategy. The role leads and develops a team of OE Business Partners and OE/PMO Managers, coaches the Mammalian Operations leadership team, and embeds Lean Six Sigma principles. Responsible for Hoshin planning, X‑Matrix deployment, Project Portfolio Management (PPM), and PMO governance, the role translates strategy into actionable operational excellence and innovation projects.

Lonza is seeking motivated individuals to support vaccine production at a new plant in Visp. Responsibilities include defining and setting up production processes, operating equipment, and ensuring compliance with SOPs and regulations. Candidates with experience in pharmaceutical production or relevant qualifications are encouraged to apply.

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.

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.

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.

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.

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.