69 marketing English-speaking jobs in Visp

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.

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.

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.

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.

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.

Bioprocess Engineer needed for clinical and commercial manufacturing. Expertise in Upstream, Downstream processing, or Bio-conjugation technology required. Experience in bio-manufacturing and/or scaling up a biopharmaceutical facility is preferred. Master's degree or equivalent experience in a related Life Science field. Excellent English communication skills.

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.