22 offerte di lavoro trovate per quality control .

Your Passion, Our Precision: Join the Formula 1 Team!Our client, is a long-standing name in Formula 1, synonymous with precision, engineering excellence, and the relentless pursuit of peak performance. At our factory in Hinwil, Switzerland, we develop, manufacture, and assemble the components for our Formula 1 cars. To ensure our uncompromising quality standards, we are looking for a dedicated and detail-oriented Quality Control Inspector (m d) who

On behalf of our client, we are looking for a QS Analyst (Training & Document Control). Contract: Temporary unlimitedLocation: Le LocleHome office: max 1 day per weekAvailability: ASAP or with maximum 1-month noticeLanguages: French and English fluency requiredResponsibilities:Manage and maintain the electronic training system (assignment, data entry)Support the maintenance of the document control systemManage circulation of documents for approvalReview

Pour le compte de notre client basé dans le canton de Vaud, nous recherchons un/une Spécialiste / Senior Spécialiste, Assurance Qualité Opérations.Poste temporaire jusqu'à fin 2026 Start ASAPLe poste consiste à assurer la supervision qualité des activités de fabrication de biomédicaments au sein d’un site de production. ResponsabilitésAssurer le suivi qualité quotidien des activités de production (USP, DSP, préparation des milieux et tampons, zones de

Pour le compte de notre client basé dans le canton de Vaud, nous recherchons un/une Expert QA/QC.Poste temporaire jusqu'à fin 2026 Start ASAPAssurer la supervision qualité des activités de contrôle qualité (QC) et de la libération des lots de substances actives/produits, en garantissant la conformité avec les politiques Qualité, les BPF (cGMP) et les exigences réglementaires suisses, européennes et FDAResponsabilitésLibération de lotsCollecter et examiner

For our client, a pharmaceutical company committed to excellence and operating in the Greater Lausanne area, we are looking for a:Quality Assurance Specialist - GMP AuditorStart date: ASAPYour tasksReview and approve quality documents and data to ensure they follow GMP rules.Manage quality processes like deviations, CAPAs, and change controls to support continuous improvement.Bring your quality expertise to company projects and report on your

Pour le compte de notre client basé dans le canton de Vaud, nous recherchons un/une Expert QA Réglementaire.Poste temporaire jusqu'à fin 2026 Start ASAP Pour ce poste, vous assurez les activités d’assurance qualité réglementaire et conformité d’un site de production biopharmaceutique, en garantissant le respect des exigences GMP/GDP et des réglementations internationales. Ce poste couvre la supervision QA des activités liées aux affaires réglementaires,

?Die Arbeit, die du heute machst, könnte morgen das Leben retten.'Möchtest auch du deine mechanischen Fähigkeiten im weltweit größten Unternehmen für Healthcare-Design und Herstellungsdienstleistungen einbringen? Dann haben wir genau die richtige Stelle für dich.Für den Standort in Grenchen suchen wir möglichst ab sofort einen Quality Inspector 1 (m/w/d) in einem 100% Pensum :Deine Hauptaufgaben:Durchführung von Routine- und Wiederholungsprüfungen zur

Helicopter Quality ManagerFür unsere Kunden in Luzern suchen wir aktuell einen engagierten Quality Manager für den Bereich Helikopter.Ihre Hauptaufgaben: Sie sind die zentrale Ansprechperson für alle Qualitäts- und Safetymanagement-Themen in Kundenaufträgen und Projekten und überwachen sowie optimieren kontinuierlich die relevanten Prozesse.Sie stellen die Qualitätssicherung in der Helikopter-Instandhaltung sicher und bearbeiten alle Tätigkeiten im

Für meinen Kunden in Thun suche ich aktuell einen Quality Manager SCM: Vertragsart: Festanstellung Region: Thun Pensum: 100%Das kannst du bewegenQualitätssicherung entlang des Beschaffungsprozesses: Überwachung und Sicherstellung der Qualitätsstandards von Lieferanten und internen Prozessen. Durchführung von Audits und Prüfungen, um sicherzustellen, dass alle Beschaffungsprozesse den vorgegebenen Qualitätsrichtlinien entsprechen.Lieferantenmanagement:

For a leading pharmaceutical wholesaler in Switzerland, we are seeking an FvP Associate for a permanent position, based in Bale Canton. This is a pivotal role at the intersection of quality and logistics, where you will assist the Responsible Person and ensure the pharmaceutical products are always available, correctly documented, and safely transported in compliance with Good Distribution Practice (GDP) requirements. You will act as the key interface

Für einen unserer Kunden, ein etabliertes und international tätiges Unternehmen im Pharmabereich mit Sitz in Winterthur, suchen wir zur Verstärkung des Teams per sofort oder nach Vereinbarung eine/nBatch Release Manager 100 %Ihre AufgabenKlassifizierung und Beurteilung von Abweichungen sowie Koordination der Aktivitäten im Rahmen der Bearbeitung von Abweichungen, inkl. Sicherstellung des rechtzeitigen Abschlusses von UntersuchungenUnterstützung bei der

Für unseren Kunden, ein internationales Unternehmen mit Sitz in Lenzburg, suchen wir eine*n Manufacturing Production Planning & Control Specialist (m/f/d).Zur Verstärkung unseres Teams in Lenzburg suchen wir eine/n technisch versierten und organisationsstarken Produktionsplaner/in für die BiMOS-Halbleiterproduktion. In dieser Position verantworten Sie souverän die termingerechte Fertigung und Lieferung unserer Produkte. Wenn Sie auch in arbeitsintensiven

Tasks:Drive the development of embedded software solutions in C/C++ and RTOS environments, ensuring code quality, performance, and compliance with project requirementsGuide and mentor embedded software engineers in day-to-day development tasks, quality control, effort estimation, and technical decision-makingSupport or lead the adoption of model-based development approaches (e.g. Simulink), including automated code generation for embedded targetsTranslate

For our client based in Corsier-sur-Vevey, we are currently looking for a Warehouse Specialist for an 8-month assignment.This role offers an exciting opportunity to contribute to a critical part of pharmaceutical operations while driving continuous improvement across the warehouse. Your role:  Goods Reception: Verify accuracy of incoming shipments, conduct inspections, and document discrepancies or damage.Sampling: Perform material sampling to meet

We are looking for a Senior Java Technical-Functional Expert to join our customdevelopment team. This role combines strong technical expertise in Java development with the ability to understand and support business processes in a complex environment.You will contribute to the design, development, and maintenance of applications, ensuring highstandards of quality, security, and performance. You will also play a key role in continuousimprovement

For our Client in Visp we are searching for a Technical Document Manager who is responsible for coordinating the creation, adaptation, version control, and approval workflows of key project documentation throughout all project phases.  Key Responsibilities: Responsible for performance qualification (PQ) from detailed design through execution. This includes both CapEx-driven mechanical adaptations managed by external engineering (EPCM) partner and OpEx

Are you a seasoned DevOps Engineer with a profound understanding of CI/CD, automation, source control systems, and packaging and deployments? Additionally, do you possess coding experience with C++? Are you seeking new professional challenges? If so, please find the job description below.Tasks & Responsibilities: Independent delivery of complex, broadly defined DevOps assignments Specification, planning, implementation, testing, and documentation of these

For our client, a leading company in the pharmaceutical sector, we are seeking an Analytical Scientist.In this role you will be joining a highly motivated and experienced team of analytical scientists. You will be responsible for leading analytical development activities for synthetic molecule projects, from early development to commercialization. This is an exciting opportunity to apply your expertise in a dynamic and challenging environment,

About the roleWe’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/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,

CQ EngineerFor our Client a biopharmaceutical company in the Aargau we are currently seeking a number of CQ engineers.The C & Q Execution Engineer is primarily responsible for the execution of the CQV activities corresponding to their project area’s equipment and processes. Key Responsibilities:System Boundary development + approvalDesign Qualification preparation, execution and approval. Includes release for IQ.Good Manufacturing Practice (GMP) Rapid

For our client, an international pharma company in Kaiseraugst, we are looking for a Qualification and CSV Expert to support qualification of embedded systems.General Information:Start date: ASAPPlanned duration: 2 yearsExtension: likelyContract: temporary contract via RandstadWorkplace: KaiseraugstWorkload: 100%Home Office: up to 20%Working hours: StandardTasks & Responsibilities: Implementation and documentation of qualification processes for our

For our client, an international company based in Elsau, we are looking for a dedicated Process/System Engineer (f/m/d). We represent a global leader in manufacturing exhaust aftertreatment systems for high-horsepower engines in both mobile and stationary operations. Their applications span a wide range, from marine engines with an output of 200kW up to massive power plant engines generating 20MW. In addition, our client is at the forefront of developing