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- ...Manpower Für einen unserer Pharma-Kunden mit Sitz in Visp suchen wir einen Process Engineer . Description: Ihre Aufgaben: ? Planung und Realisierung von Teil- und Kleinprojekten, z. B. verfahrenstechnische Berechnungen und Optimierungen in der Anlage...ConsigliatoSostituzione
- ...Your mission We are looking for an Experienced Qualification Engineer to play a defining role in our ambitious expansion in Visp.... ...engineering pharmaceutical technology medical technology chemistry process engineering or similar or completed technical or scientific...ConsigliatoTempo pieno
- ...Ihre Aufgaben Planung und Durchführung von technischen Teilprojekten im Anlagenumfeld, inkl. Prozessoptimierung und Engineering-Berechnungen Erstellung von Machbarkeitsanalysen und Konzeptstudien für Neu- und Umbauten, inkl. Budget- und Zeitplanung Durchführung...ConsigliatoTempo pieno
- Senior SAP Basis Engineer (Remote) We are seeking an experienced and proactive Senior SAP Basis Engineer to join a global IT team supporting... ...Support backup, recovery, and disaster recovery processes across SAP landscapes Collaborate with development, functional...ConsigliatoRemote job
- Senior Bioprocess Engineer (Biologics) Location: Visp, Switzerland — 100% on-site Function: Operations / Manufacturing Science & Technology... ...logistics; support delivery of training as needed. Provide process support to Downstream Processing (e.g., capture, intermediate...ConsigliatoTempo pienoLavoro urgente
- About the role We’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP...Consigliato
- ...environment – ideally with strong knowledge of processes related to monoclonal antibodies.... ...investigations of deviations in the manufacturing process of monoclonal antibody-based products.... ...in Pharmacy, Biotechnology, Chemistry, Engineering, or a related field. At least 5 years...Consigliato
- ...supplier coordination, and ensuring compliance with procurement processes while working under the guidance of senior procurement... ...work packages within Capex projects, coordinating closely with Engineering, Project Management, Quality, and Finance. Tracking & Compliance...ConsigliatoLavoro urgente
- ...will ensure that every technology transfer is seamless every process is robust and our commitment to patient safety is never compromised... ...An MSc or PhD in Pharmaceutical Technology Chemical/Process Engineering or a relevant scientific discipline. A proven track record...Consigliato
- ...You’ll be the proud owner of the Quality Management System, ensuring it’s not just a collection of binders, but a living, breathing engine of excellence. System Ownership: Take the wheel on Deviations, Change Control, Document Management, and Training. Risk...Consigliato
- ...Effectiveness Checks, as solutions to correct deviations and prevent future recurrence. Ensure cGMP compliance through the investigation process, and to drive their quality records to completion and timely closure. Support the business through ongoing change and process...Consigliato
- ...ideal reviewer has great attention to detail, is able to work independently, and possesses a thorough knowledge of the manufacturing process they are reviewing. Location: On-Site in Visp (no home office) – Dealing with paper-based documentation. Key Responsibilities...ConsigliatoHome office
- ...this is your opportunity to grow in a dynamic GMP environment. As a Filling Operator you are a crucial pillar in our production process. Your area of responsibility includes: Operating our highly automated modern filling plant for liquid pharmaceuticals monitor the...ConsigliatoTempo pienoLavoro a turniTurno di giorno
- ...Prepare manage and track CAPA plans including coordination with internal stakeholders and customers Own and manage core quality processes including Audit and Inspection Management Deviations CAPAs Change Control Document Management and Training Lead and support...ConsigliatoTempo pieno
- ...Contract type: Full-time Language: German (mandatory); English a strong plus The role Join a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ...ConsigliatoTempo pieno
- ...Reviewers should have great attention to detail, be able to work independently, and have a thorough knowledge of the manufacturing process they are reviewing. Tasks Review paperbased executed batch records within the specified timeframe. Track, report and monitor batch...Home office
- ...practices during critical manufacturing steps (e.g. line clearance material dispensing equipment setup). Witness and verify critical process steps in-process controls (IPCs) and reconciliations. 2. Line Clearance and Batch Execution Monitoring Perform and document...Tempo pienoLavoro urgente
- ...is your opportunity to grow in a dynamic GMP environment. As a Compounding Operator you are a crucial pillar in our production process. Your area of responsibility includes: Control and execution of the manufacturing of product solutions on a pilot scale the core...Tempo pienoLavoro a turni
- ...seasoned quality leader who can not only manage complex quality processes but also drive cultural transformation build high-performing... ...apply sound risk management principles to QA decision-making and process optimization. Your profile We are looking for someone with...Tempo pieno
- ...libraries according to current Good Manufacturing Practices (GMP) including supporting the investigation of new defects. Contribute to process improvements including the critical task of improving and reviewing batch records. Learn how to effectively perform risk...Tempo pienoLavoro urgente