98 marketing consultant jobs near me English-speaking jobs in Canton of Valais

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

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.

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, manages risk assessments, change requests, deviations, investigations, and CAPAs. Authors and approves GMP documentation, including SOPs, deviations, change controls, and risk assessments. Partners with cross-functional teams to identify risks, drive deviation management, and strengthen contamination prevention control practices. Acts as a QA Microbial Contamination Control and cleaning SME in meetings, audits, and inspections. Reviews and approves routine cleaning-relevant documents and finalizes records like SOPs, MBRs, Material Specifications, Deviations, Change Requests, Effectiveness Checks, Testing Protocols & Reports. Identifies emerging QA relevant topics and communicates with stakeholders, working on their development into new or existing Quality and Compliance strategies and/or standards. Supports continuous improvement programs to establish effective Quality Contamination Control.

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.

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.

MSAT Data Manager (f/m/d) will extract, structure, and curate manufacturing data to support data-driven decisions. Responsibilities include preparing process data for investigations, developing dashboards, and performing statistical analysis to evaluate process performance. The ideal candidate will have experience in biopharma manufacturing, data analytics, or a regulated environment and strong data handling and analysis skills.

MES Expert to author and adapt MES/PCS recipes for drug product manufacturing. Responsible for defining MES recipe concepts, building GMP documents, providing front line support, and training end users. Requires experience in MES recipe authoring, preferably in Emerson Syncade, and process knowledge in sterile drug product manufacturing.

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.

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.

Lead and deliver customer programs from technology transfer to GMP manufacturing, ensuring quality, timelines, and cost-effectiveness. Act as a trusted partner for customers, fostering transparent communication and collaboration.

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 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.

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.

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.

Own defined areas within the site Contamination Control Strategy, ensuring a sustained microbial state of control across facilities, equipment, processes, and supporting systems. Act as the technical lead for contamination control, hygiene, and microbiological QC topics. Provide visible shopfloor presence, hands-on technical support, and leadership on contamination control topics. Develop and improve hygiene concepts, gowning expectations, aseptic behavior, microbial hold times, and bioburden control strategies. Represent CCS and microbiological quality topics in projects, audits, regulatory inspections, and cross-functional governance forums. Drive continuous improvement, KPI delivery, training, and technical guidance.

Internship supporting the Global Master Data team in Visp. Assist with data analysis, SAP Master Data maintenance, and gathering feedback from Subject Matter Experts.

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.

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.