23 science Jobs für dich gefunden.

For one of our clients, a global manufacturing company specialized in the life sciences sector, we are looking for a Manufacturing Scientist based in the canton of Fribourg.  Your Impact:Implement and optimize robust, compliant, and high-performing manufacturing processes aligned with quality strategyCapitalize on and share your expertise throughout the entire product lifecycleDraft, review, and approve key technical documents (batch records, procedures,

Hast Du Lust, mit Deinem Know-how in der Steuerungstechnik Anlagen zum Laufen zu bringen, welche höchste Standards in der Pharma- und Life-Science-Welt setzen?Unser Kunde ist genau das: Eiin international führender Anbieter von hochspezialisierten Anlagen für die Pharma-, Biopharma- und Life-Science-Industrie. Am Hauptsitz im Thurgau und an weiteren weltweiten Standorten entwickelt er innovative Lösungen für Labor- und Produktionsanwendungen.

Unseren Kundin wurde 1987 gegründet und beschäftigt heute rund 30 Mitarbeitende. Die Firma vertreibt Ware im Bereich Diagnostik/Life-Science für den Schweizer Markt. Zu den Kunden zählen Spitäler, Labore, Hochschulen und Forschungsinstitute.Wir suchen eine/n Einkaufsexperten als Stv. Head of Supply Chain 80-100%Operative stellvertretende Verantwortung für die Bereiche Beschaffung und AuftragsabwicklungProaktive Unterstützung des Abteilungsleiters bei

Dans le cadre d'un mandat pour un grand groupe de l'industrie horlogère, nous recherchons un(e) ingénieur(e) expérimenté(e) en science des matériaux. Votre mission principale sera de développer et d'optimiser la mise en œuvre d'alliages de métaux précieux. Vous piloterez l'industrialisation de nouveaux alliages et procédés, tout en apportant votre expertise technique aux équipes. VOS MISSIONSPilotage de projets d'industrialisation : Diriger des projets de

You should bring following skills:proven track record in embedded SW development and SW projects, specifically in a C/C++/RTOS and TCP/IP environment (NOT embedded Linux!)ability to create high quality UML designs and write corresponding  C++ code ability to guide Embedded SW domain resources in terms of quality, estimations, work results. Strong in execution, results driven.proven track record in Requirements Engineering (System Requirements -->

Du bist ein erfahrener Data Engineer mit Leidenschaft für den Microsoft Stack (Fabric, Power BI) und hast ein Händchen für KI? Dann suchen wir dich, um unsere Fabric-Lakehouse-Architektur zu entwerfen und mit uns den Grundstein für datenbasierte Entscheidungen zu legen! Beschreibung der AufgabenEntwerfen, implementieren und optimieren der Fabric-Lakehouse-Architektur inkl. ELT-Pipelines und Capacity-ManagementEntwickeln, betreuen und performance-tunen

Bist Du gelernte/r Sanitär- oder Heizungsmonteur/in und bereit für eine neue Herausforderung im anspruchsvollen Anlagenbau? Möchtest Du Dein handwerkliches Geschick in der Verarbeitung von Edelstahlrohrleitungen für Hightech-Anlagen einsetzen, die mit "heissem Dampf und reinstem Wasser" für höchste Reinheit in der Pharmaindustrie sorgen?Unser Kunde ist ein weltweit führender Hersteller von Reinigungs- und Sterilisationsanlagen für die anspruchsvolle

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

Operational Integration LeadThe Operational Integration Lead, also known as Technical Package Lead (TPL) is a key role in the successful operational integration of mechanical changes to an existing commercial production line. Key Responsibilities:• Act as the primary point of contact for the operational integration assigned engineering scope items, ensuring seamless coordination between technical execution (external engineering partner) and GMP

For our client based in Aubonne, we are currently looking for a Regulatory Compliance Specialist for a 12-month contract.Your role:As a Regulatory Compliance Specialist, you will ensure that local manufacturing activities and GMP documentation remain fully aligned with regulatory filings.You will assess and manage change controls, ensuring timely and accurate reporting to Health Authorities.You will review and approve GMP documents, ensuring compliance

Pour notre client, une entreprise internationale opérant dans le domaine pharmaceutique, nous recherchons un/e QC Analyst Senior Vous apportez une solide expérience de laboratoire, particulièrement en Chromatographie Liquide couplé à la spectrométrie de MS (LC-MS). Grâce à votre travail en tant que technicien de laboratoire, vous avez développé une bonne compréhension théorique et pratique des méthodes et de la technologie

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

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

For one of our clients, an international pharmaceutical company, we are seeking a Project Technical Lead (Automated Visual Inspection).General Information:Start date: ASAPDuration: until 28.02.2026Workplace: Opfikon, ZurichHome office: PossibleWorkload: 100%Working hours: StandardTasks & Responsibilities:Develop URS and TechSpecs for AVI in IV bag applicationsLead the end-to-end process of identifying, evaluating, and conceptualizing Automated Visual

Au sein de notre client à Aubonne, une nouvelle opportunité de rejoindre notre département de Contrôle de la Qualité est ouverte comme QC Microbiology Expert au sein de l’équipe QC Microbiology & Environmental Monitoring (QC M&EM) pour une durée de 5 mois. En collaboration avec une équipe polyvalente et dynamique, votre rôle sera de supporter l’ensemble des activités documentaires de l’équipe Environmental Monitoring du QC selon les procédures en place et

Location: Hybrid model possible (on-site work in Lisbon and remote) Workload: 100%  Contract Length: Until December 2025 with potential extension Team: Engineering ApplicationWe're seeking a skilled Siemens Teamcenter Developer to join our Engineering Application team. In this pivotal role, you will design, develop, and deploy robust Siemens Teamcenter solutions. You'll collaborate closely with cross-functional teams to ensure our PLM solutions align

For one of our clients, a biopharmaceutical company in canton Lucerne, we are looking for a motivated Supply Chain Specialist.General Information:Start date: ASAPDuration: 1 yearContract: temporary contract via RandstadExtension: possible, to be discussedWorkplace: canton LucerneHome office: possible up to 2 days/weekWorkload: 100%Tasks & Responsibilities: Create material specifications as part of the material qualification activities to support material

For our client, an international pharma company in Basel, we are looking for a Digital Biomarker Scientist to join an integrated team of scientists, technologists, data analysts and operationalization experts, that leverages mobile technologies like smartphones and wearables to collect objective and continuous sensor data from patients in clinical trials and clinical care.We co-create innovative digital biomarker concepts for sensitive and meaningful drug

Lieu : Orbe, SuisseEntité : Nestlé Product & Technology Center – CoffeeTaux d’activité : Temps plein 100%Type de contrat : TemporaireEntrée en fonction souhaitée : Octobre 2025Fin de mission : 31 mai 2026Durée : 8 moisRésuméPour notre client Nestlé Research and Development Orbe, nous recherchons un Technicien.ne de Laboratoire R&D pour œuvrer sur des produits et des technologies en lien avec différents types de produits (Café, céréales, produits liés à la

Are you a seasoned SAP Data Migration specialist with experience in local projects? Have you successfully contributed to end-to-end SAP data migration projects, possessing comprehensive knowledge of SAP modules and associated data migration tools? If you're seeking a new opportunity, we invite you to review the following job descriptions.Tasks & Responsibilities:Leads end-to-end data migration activities, ensuring the accuracy, completeness, and integrity

Are you a process-driven and solution-oriented Business Analyst with a passion for project management? We're looking for you to act as the primary interface between business stakeholders and the IT department, driving digital transformation!Key ResponsibilitiesBusiness Analysis & RequirementsCollect, analyze, and document business requirements from internal clients (lawyers and support functions such as Marketing, HR, Finance, BD).Translate business needs

No sponsorships for non-EU candidatesAs a Solution Architect with us, you will advise our European customers from the armed forces and defense industry on complex solutions and in meeting requirements, from assessing the current situation to finding solutions and implementing a wide range of technologies. Start date: immediately or by agreementType of employment: PermanentLocation: Bern + home office (max. 2 days). Working on site at the customer's

Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart date: 01.01.2026End date: 31.12.2026 As a QA Specialist, Quality Control Support, you will ensure QC activities comply with GMP, regulations, and UCB Quality Policies. You will proactively support operations, foster a strong quality culture, and drive continuous improvement in collaboration with QC, local teams, and other UCB sites. Your key responsibilities:Provide