Celerion Switzerland AG

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    "title": "On-Site IT Support Specialist",
    "description": "Depuis plus de 40 ans,\nCelerion\nest à la pointe de la recherche contractuelle bioanalytique mondiale, collaborant avec des innovateurs pharmaceutiques et biotechnologiques pour apporter plus rapidement de nouvelles thérapies aux patients. Notre site en pleine croissance à Fehraltorf/Zurich est au cœur de cette mission.\nL'OPPORTUNITÉ\nNous recherchons un\nSpécialiste Support Informatique Sur Site\ntechniquement polyvalent et orienté vers les personnes pour rejoindre notre équipe informatique mondiale à Zurich. En tant que l'un des principaux représentants informatiques sur site, vous serez le visage de confiance de l'informatique pour nos collègues suisses — combinant des compétences techniques approfondies avec un véritable engagement de service. Si vous aimez résoudre des problèmes complexes et souhaitez que votre expertise compte, ce poste est fait pour vous.\nResponsabilités clés :\nCe que vous apporterez :",
    "datePosted": "2026-09-21",
    "validThrough": "2026-10-21",
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    "title": "Bioanalytische/r Laborant/in (80–100%)",
    "description": "Façonnez avec nous les médicaments de demain.\nCelerion Switzerland AG\nfait partie de la société mondiale\nCelerion Inc\n. En tant que laboratoire bioanalytique certifié BPL, nous soutenons sur le site de Fehraltorf des entreprises pharmaceutiques et biotechnologiques internationales dans le développement de médicaments innovants. Avec nos services bioanalytiques de haute qualité, nous apportons une contribution importante au développement préclinique et clinique des médicaments.\nPour renforcer notre équipe en pleine croissance, nous recherchons une personne engagée en tant que\nTechnicien/ne de laboratoire bioanalytique\n.\nVos tâches\nEn tant que membre de notre laboratoire bioanalytique, vous contribuez directement au succès du développement des médicaments par des analyses précises et un travail soigné.\nSelon votre expérience et votre domaine de compétence, vous assumerez les tâches suivantes :\n• Réalisation de mesures bioanalytiques de principes actifs pharmaceutiques dans des échantillons biologiques par des méthodes immunologiques (LBS) ou LC-MS/MS\n• Préparation d’échantillons biologiques ainsi que manipulation de systèmes LC-MS/MS modernes (accent sur LC-MS)\n• Planification, réalisation et documentation d’analyses bioanalytiques conformément aux directives BPL\n• Réalisation et évaluation de validations de méthodes ainsi que l’analyse d’échantillons issus d’études précliniques et cliniques\n• Évaluation des résultats analytiques ainsi que garantie de la qualité et de l’intégrité des données\n• Participation aux tâches organisationnelles du laboratoire, à la maintenance des équipements ainsi qu’aux activités liées à la qualité\n• Contribution active à l’optimisation continue de nos processus de laboratoire\nCe que vous apportez\n• Formation achevée en tant que technicien/ne de laboratoire en chimie, biologie ou médecine (CTA, BTA, MTA ou qualification équivalente)\n• Expérience dans la manipulation d’échantillons biologiques\n• Connaissances approfondies en biochimie, chimie analytique et/ou chromatographie ainsi qu’en spectrométrie de masse\n• Travail autonome, structuré et conscient de la qualité\n• Documentation soignée et grande compréhension de la qualité\n• Bonnes connaissances orales et écrites en allemand et en anglais\n• Une expérience dans un environnement réglementé (BPL, BPC, BPF ou ISO) est un avantage\nCe qui vous attend\nChez Celerion, vous trouverez une activité responsable dans une entreprise internationale dont le travail contribue directement au développement de nouvelles thérapies. Nous favorisons une collaboration ouverte, l’excellence scientifique et le développement continu.\nNous vous offrons :\n• Une activité variée avec une contribution directe au développement de nouveaux médicaments\n• Une équipe collégiale, expérimentée et solidaire\n• Une intégration structurée ainsi qu’un développement professionnel ciblé\n• Une infrastructure de laboratoire moderne et parfaitement équipéeProjets passionnants et variés dans un environnement international\n• Horaires de travail flexibles pour une bonne conciliation entre vie professionnelle et vie privée\n• Conditions d’emploi attractives dans une entreprise prospère et en croissance\nAvons-nous suscité votre intérêt ?\nNous nous réjouissons de recevoir votre candidature !",
    "datePosted": "2026-09-15",
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    "title": "Mitarbeiter/in Quality Control 80-100%",
    "description": "Celerion ist eines der weltweit führenden Unternehmen der bioanalytischen Auftragsforschung und unterstützt seit mehr als 40 Jahren Pharma- und Biotechfirmen auf der ganzen Welt. Celerion bietet Dienstleistungen für die Zulassung von neuen Medikamenten - von frühen Entwicklungsarbeiten bis hin zu klinischen Studien mit dem Ziel, Patienten möglichst schnell zu helfen.\nAufgrund des stetigen Wachstums unseres Unternehmens und zur Verstärkung unserer Daten- und Berichtskontrolle innerhalb unserer Bioanalytik suchen wir eine engagierte Persönlichkeit als\nMitarbeiter/in Quality Control 80-100%\nIhr Aufgabengebiet\nÜberprüfung von Rohdaten, die während einer bioanalytischen Studie generiert werden\nKontrolle von weiterführenden Daten und Studienresultaten\nÜberprüfung von Berichten am Ende einer Studie\nAls Teil des QC Teams übernehmen Sie nach sorgfältiger Einarbeitung eigene Aufgaben.\nIhr Profil\nBachelor Biologie / (Bio-) Chemie oder Ausbildung als Chemie- oder Biologielaborant/in, CTA, BTA oder MTA\nTeam-player, verlässlich, genau, hochmotiviert, gute Selbstorganisation\nFachkenntnisse im Bereich LBA oder LC-MS/MS\ngute Deutsch- und Englischkenntnisse\nBerufserfahrung in einem regulierten Umfeld (GxP/ISO)\nFreude an einem Office-basierten Job\nWir bieten\nInteressante Tätigkeit in einem offenen, dynamischen Team\n„On the job“ Weiterbildung und Entwicklung\nModerne Infrastruktur\nWork-Life-Balance: flexible Arbeitszeiten (Mo bis Fr, keine Wochenenden, keine Schicht,), mind. 5 Wochen Ferien\nFinanzielles: Lohngleichheit zwischen den Geschlechtern, sehr gute Sozialleistungen, Bezug von REKA-Checks",
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    "title": "On-Site IT Support Specialist (100%)",
    "description": "For over 40 years,\nCelerion\nhas stood at the forefront of global bioanalytical contract research, partnering with pharmaceutical and biotech innovators to bring new therapies to patients faster. Our growing Fehraltorf/Zurich site is at the heart of that mission.\nTHE OPPORTUNITY\nWe are looking for a technically versatile and people-oriented\nOn- Site IT Specialist\nto join our global IT team in Zurich. As one of the primary on-site IT representatives, you will serve as the trusted face of IT for our Swiss colleagues — combining deep technical skills with genuine service commitment. If you thrive on solving complex problems and want your expertise to matter, this role is for you.\nKey Responsibilities:\nServe as a primary on-site IT point of contact and escalation lead for the Zurich site, coordinating with local and global IT teams as needed.\nDeliver comprehensive desktop and systems support across Microsoft operating systems, Microsoft 365, Adobe Acrobat/Creative Cloud, Oracle Client Tools, Citrix Virtual Apps and Desktop, and Microsoft Defender for Endpoint.\nExecute Install/Move/Add/Change (IMAC) activities and perform preventative maintenance to ensure optimal workstation performance.\nProvide hands-on support for Windows Server environments, Active Directory, and local network infrastructure — including switches, patch panels, and structured cabling — in coordination with centralized infrastructure teams.\nManage and resolve daily support activities via the ticket management system, maintaining accurate updates and clear user communication through to resolution.\nSupport local backup, restore, and archival processes; maintain working knowledge of ODBC connectivity and basic SQL client configuration.\nLead endpoint deployment and imaging activities using tools such as Microsoft Intune, SCCM/MECM, and Autopilot.\nEnsure all endpoint and infrastructure systems comply with GxP and data-integrity regulatory requirements, validated processes, and change control procedures.\nProvide IT onboarding training for new hires and ongoing end-user guidance to maximize productivity.\nAssist with on-site cabling, local switch installation, and network equipment troubleshooting.\nWhat You Will Bring:\nPost-secondary education in IT or a related field, or equivalent hands-on experience.\n3–5 years of proven technical support experience spanning desktops, servers, and networks.\nExcellent written and verbal communication skills in English are required; fluency in German is highly preferred.\nStrong proficiency with Microsoft operating systems and the broader Microsoft 365 ecosystem; experience with Adobe Acrobat, Microsoft Defender, Oracle clients, and Citrix environments.\nWorking knowledge of TCP/IP networking, DNS, DHCP, VLAN concepts, and basic switch configuration.\nFamiliarity with endpoint deployment tools such as Microsoft Intune, SCCM/MECM, and Autopilot.\nExcellent analytical and problem-solving skills, paired with a strong customer service orientation.\nMicrosoft certifications (Azure Administration, Windows Server Hybrid Administration, or Modern Desktop Administration Associate) are a distinct advantage.\nExperience in regulated environments, including lab instrumentation support, is advantageous.\nFull on-site availability in Fehraltorf/Zurich is required.\nWe look forward to your application. Kindly provide your resume in English.\nWhy Celerion?\nAt Celerion, your work as an IT Specialist is not just about keeping computers running — it is about enabling the scientists and clinicians who are accelerating the journey from laboratory to patient. You will be part of a global, collaborative IT team with the support and resources of an established international organization, while enjoying the close-knit atmosphere of our Swiss site.\nAre you interested in this position?\nThen we look forward to receiving your complete application documents via the link or via our homepage: https://www.celerion.com/careers\nCelerion Switzerland AG\nHuman Resources\nAllmendstrasse 32\n8320 Fehraltorf\nhttps://www.celerion.com",
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    "@id": "https://ch-jobs.com/job/infirmier-re-de-recherche-clinique-soir-es#jobposting",
    "title": "Infirmier(ère) de Recherche Clinique (Soirées)",
    "description": "Celerion s'engage à mener des recherches cliniques rapides et exceptionnelles grâce à la médecine translationnelle. Chaque jour, nous utilisons notre expérience, notre agilité et nos stratégies de recherche innovantes pour aider à commercialiser les médicaments plus rapidement.\nCelerion\nrecherche un(e)\ninfirmier(ère) de recherche à temps plein pour le poste de soirée\nafin d'assister nos essais cliniques. Il s'agit d'un rôle dynamique travaillant avec une population saine, offrant la possibilité d'apprendre sur la recherche clinique et de voir le processus de développement des médicaments en action.\nCherchez-vous une opportunité qui fera une différence dans l'avenir des soins de santé ? Si oui, nous avons hâte de vous rencontrer. Voulez-vous en savoir plus ?\n\\n\nResponsabilités\nVous serez responsable d'effectuer les événements programmés conformément au protocole de l'étude.\nVous travaillerez directement avec les gestionnaires d'étude pour assurer le succès de l'essai.\nVous travaillerez avec les participants dans le processus de recherche, sous notre supervision, en réalisant des contrôles des signes vitaux, des ECG, des prises de sang et la surveillance télémétrique.\nVous identifierez et signalerez également les événements indésirables pour aider dans le processus de recherche clinique.\nQualifications\nVous devez posséder une licence NE RN ou LPN en cours de validité et des compétences en évaluation clinique\nLa certification ACLS est un atout\nSolides compétences en informatique et en documentation\n\\n\nHoraires :\nVous devez être disponible pour travailler selon la planification suivante :\n*\nDu lundi au dimanche de 13h00 à 23h30 (l'enregistrement se fera entre 13h00 et 15h00)\n* Un week-end (samedi et dimanche) par mois.\n* Les horaires peuvent être 5x8 ou 4x10 selon la préférence de l'employé\nValeurs de Celerion : Intégrité Confiance Travail d'équipe Respect\nCelerion est un employeur garantissant l'égalité des chances. Tous les candidats qualifiés seront pris en considération pour un emploi sans distinction de race, couleur, religion, sexe, origine nationale, âge, orientation sexuelle, identité de genre, informations génétiques, état civil, statut de vétéran protégé qualifié ou handicap.\nNote :\nPour vous assurer de ne pas manquer d'importantes mises à jour de notre part, veuillez vérifier votre dossier Spam pour les e-mails provenant de @celerion.com, en particulier les invitations à des entretiens. Si vous en trouvez un, marquez-le comme \"Non indésirable\" afin que les futurs e-mails de Celerion arrivent dans votre boîte de réception. Veuillez noter que les comptes\nGmail\nont été particulièrement signalés comme étant dirigés vers le dossier Spam.",
    "datePosted": "2026-08-24",
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    "title": "(Senior) Bioanalytical Principal Investigator LBS / GLP Study Director (100%)",
    "description": "Shape the future of bioanalysis for innovative medicines\nCelerion is a leading global contract research organization (CRO) specializing in early clinical research and bioanalytical services. For more than 40 years, we have partnered with pharmaceutical and biotechnology companies worldwide to accelerate the development of new therapies and bring life-changing medicines to patients faster.\nTo support the continued growth of our Bioanalytical Laboratory in Fehraltorf (Zurich area), Switzerland, we are looking for a motivated and scientifically driven professional to join our Ligand Binding Services (LBS) team as a:\n(Senior) Bioanalytical Principal Investigator LBS / GLP Study Director (100%)\nIn this role, you will take scientific and operational ownership of regulated bioanalytical studies and method validations. You will serve as the primary client contact, lead study execution from planning through reporting, and play a key role in delivering high-quality data to support drug development programs worldwide.\nYour Responsibilities\nStudy Leadership & Scientific Oversight\nLead and oversee GLP/GxP-compliant bioanalytical studies and method validations within the Ligand Binding Services (LBS) department.\nAct as Study Director and/or Principal Investigator with full responsibility for assigned studies or study phases.\nDevelop and approve study plans, validation protocols, analytical reports and associated study documentation.\nReview, evaluate and approve analytical data to ensure scientific integrity and regulatory compliance.\nEnsure all study activities are conducted in accordance with applicable SOPs, regulatory requirements and client expectations.\nClient Management\nServe as the primary scientific and operational contact for assigned clients.\nProvide regular project updates and maintain strong communication throughout the study lifecycle.\nSupport client meetings, scientific discussions and audits as required.\nOperational Excellence\nCoordinate laboratory activities and ensure efficient study execution.\nTrain, mentor and support assigned laboratory personnel.\nContribute to process improvements and continuous enhancement of laboratory operations and quality standards.\nSupport bioanalytical data management activities and documentation review processes.\nAdditional Responsibilities for Senior-Level Candidates\nLead complex or strategic client programs.\nProvide scientific mentoring and guidance to junior Principal Investigators and laboratory staff.\nAct as a subject matter expert for ligand-binding and cell-based assay technologies.\nContribute to business development activities, client presentations and scientific initiatives.\nYour Profile\nRequired Qualifications\nDegree in Biochemistry, Biology, Chemistry or a related scientific discipline; PhD is advantageous.\nMinimum 2 years of experience in bioanalysis or quantitative analytical sciences.\nHands-on experience with ligand-binding assays and/or cell-based assays.\nExperience working in a regulated environment (GLP, GCP, GMP and/or ISO standards).\nStrong analytical thinking and problem-solving skills.\nExcellent written and verbal communication skills in English.\nAbility to manage multiple projects while maintaining a high level of quality and attention to detail.\nPreferred Qualifications\nPrevious experience as a Study Director, Principal Investigator or equivalent scientific leadership role.\nKnowledge of biomarker, pharmacokinetic (PK), immunogenicity (ADA) or biologics bioanalysis.\nGood German language skills.\nExperience working directly with pharmaceutical or biotechnology clients.\nWhat We Offer\nThe opportunity to lead scientifically challenging projects for global pharmaceutical and biotech clients.\nExposure to innovative biologics, biomarkers and emerging therapeutic modalities.\nA collaborative, international and science-driven working environment.\nStructured onboarding and continuous professional development opportunities.\nModern laboratories and state-of-the-art infrastructure.\nFlexible working hours and attractive employment conditions.\nThe opportunity to grow your career within a globally recognized CRO.\nA workplace located near Zurich with easy access to excellent public transportation and recreational opportunities.\nWhy Join Celerion?\nAt Celerion, you will contribute directly to the development of new medicines while working alongside highly skilled scientists in a dynamic and supportive environment. We value scientific excellence, teamwork, integrity and innovation, and we are committed to helping our employees grow and succeed.\nCelerion is an equal opportunity employer. We welcome applications from candidates of all backgrounds and are committed to fostering an inclusive and diverse workplace.\nInterested?\nWe look forward to receiving your application.\nJoin us in advancing the development of tomorrow's medicines.",
    "datePosted": "2026-08-24",
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    "title": "Mitarbeiter/in Quality Control 80-100%",
    "description": "Celerion ist eines der weltweit führenden Unternehmen der bioanalytischen Auftragsforschung und unterstützt seit mehr als 40 Jahren Pharma- und Biotechfirmen auf der ganzen Welt. Celerion bietet Dienstleistungen für die Zulassung von neuen Medikamenten - von frühen Entwicklungsarbeiten bis hin zu klinischen Studien mit dem Ziel, Patienten möglichst schnell zu helfen.\nAufgrund des stetigen Wachstums unseres Unternehmens und zur Verstärkung unserer Daten- und Berichtskontrolle innerhalb unserer Bioanalytik suchen wir eine engagierte Persönlichkeit als\nMitarbeiter/in Quality Control 80-100%\nIhr Aufgabengebiet\nÜberprüfung von Rohdaten, die während einer bioanalytischen Studie generiert werden\nKontrolle von weiterführenden Daten und Studienresultaten\nÜberprüfung von Berichten am Ende einer Studie\nAls Teil des QC Teams übernehmen Sie nach sorgfältiger Einarbeitung eigene Aufgaben.\nIhr Profil\nBachelor Biologie / (Bio-) Chemie oder Ausbildung als Chemie- oder Biologielaborant/in, CTA, BTA oder MTA\nTeam-player, verlässlich, genau, hochmotiviert, gute Selbstorganisation\nFachkenntnisse im Bereich LBA oder LC-MS/MS\ngute Deutsch- und Englischkenntnisse\nBerufserfahrung in einem regulierten Umfeld (GxP/ISO)\nFreude an einem Office-basierten Job\nWir bieten\nInteressante Tätigkeit in einem offenen, dynamischen Team\n„On the job“ Weiterbildung und Entwicklung\nModerne Infrastruktur\nWork-Life-Balance: flexible Arbeitszeiten (Mo bis Fr, keine Wochenenden, keine Schicht,), mind. 5 Wochen Ferien\nFinanzielles: Lohngleichheit zwischen den Geschlechtern, sehr gute Sozialleistungen, Bezug von REKA-Checks",
    "datePosted": "2026-08-18",
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    "title": "(Liquid Handling) Automation Specialist (80 – 100 %)",
    "description": "Celerion is one of the world's leading bioanalytical contract research organizations and has been supporting pharmaceutical and biotech drug development programs around the world for more than 40 years.\nDue to the steady growth of our company and to strengthen our bioanalytical laboratory in Fehraltorf / Zurich, we are looking for a\n(Liquid Handling) Automation Specialist (80 – 100 %)\nYou will convert bioanalytical assay workflows defined by R&D into robust, documented and supportable robotic routines.Your primary tasks would consist of programming using the VENUS and EVOware software, as well as regularly assessing our robots’ performance.As part of our team, you will become a key component to successfully use the liquid handling robots to improve the performance and throughput of our assays, and you will help Celerion maintain its competitive position in the market\nYour Profile\nBachelor’s or Master’s degree in a life-science discipline (e.g. Biology, Chemistry, Biotechnology).\n(Please note: this role targets a life-science background; engineering degrees are not the intended profile)\nSolid understanding of immunoassays and/or chromatographic methodsAt least 1 year demonstrated hands-on experience programming Hamilton liquid-handling robots using VENUS software to support automated workflows in a regulated laboratory environment Good written and spoken German is beneficialHighly collaborative and service-oriented mindsetStrong problem-solving skills with a hands-on approachStructured, detail-oriented, and quality-focusedAble to balance development work with operational support\nExperience with general-purpose programming languages such as Python, VB or SQL is beneficial but not required; proven Hamilton VENUS method-programming experience is essential.\nWe Offer You\nA technically specialized role in the interface of bioanalytical science, automation and regulated laboratory operations, with direct impact on throughput, standardization and reliability Structured onboarding and internal training programme.Opportunity to contribute and shape the continuous development of Celerion’s automation capabilities.Modern infrastructure and work environmentWork-life balance: flexible working hours (Monday to Friday, no weekends, no shift work), 5 weeks of vacationFinancial benefits: equal pay regardless of gender, excellent social benefits, and access to REKA vouchers\nDoes this sound like the right opportunity for you? We look forward to receiving your complete application, including your CV, references, diplomas, and other relevant documents.\nAdditional information can be found on our website:\nhttps://www.celerion.com/careers",
    "datePosted": "2026-08-12",
    "validThrough": "2026-09-11",
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    "@id": "https://ch-jobs.com/job/on-site-it-support-specialist-100#jobposting",
    "title": "On-Site IT Support Specialist (100%)",
    "description": "For over 40 years,\nCelerion\nhas stood at the forefront of global bioanalytical contract research, partnering with pharmaceutical and biotech innovators to bring new therapies to patients faster. Our growing Fehraltorf/Zurich site is at the heart of that mission.\nTHE OPPORTUNITY\nWe are looking for a technically versatile and people-oriented\nOn- Site IT Specialist\nto join our global IT team in Zurich. As one of the primary on-site IT representatives, you will serve as the trusted face of IT for our Swiss colleagues — combining deep technical skills with genuine service commitment. If you thrive on solving complex problems and want your expertise to matter, this role is for you.\nKey Responsibilities:\nServe as a primary on-site IT point of contact and escalation lead for the Zurich site, coordinating with local and global IT teams as needed.\nDeliver comprehensive desktop and systems support across Microsoft operating systems, Microsoft 365, Adobe Acrobat/Creative Cloud, Oracle Client Tools, Citrix Virtual Apps and Desktop, and Microsoft Defender for Endpoint.\nExecute Install/Move/Add/Change (IMAC) activities and perform preventative maintenance to ensure optimal workstation performance.\nProvide hands-on support for Windows Server environments, Active Directory, and local network infrastructure — including switches, patch panels, and structured cabling — in coordination with centralized infrastructure teams.\nManage and resolve daily support activities via the ticket management system, maintaining accurate updates and clear user communication through to resolution.\nSupport local backup, restore, and archival processes; maintain working knowledge of ODBC connectivity and basic SQL client configuration.\nLead endpoint deployment and imaging activities using tools such as Microsoft Intune, SCCM/MECM, and Autopilot.\nEnsure all endpoint and infrastructure systems comply with GxP and data-integrity regulatory requirements, validated processes, and change control procedures.\nProvide IT onboarding training for new hires and ongoing end-user guidance to maximize productivity.\nAssist with on-site cabling, local switch installation, and network equipment troubleshooting.\nWhat You Will Bring:\nPost-secondary education in IT or a related field, or equivalent hands-on experience.\n3–5 years of proven technical support experience spanning desktops, servers, and networks.\nExcellent written and verbal communication skills in English are required; fluency in German is highly preferred.\nStrong proficiency with Microsoft operating systems and the broader Microsoft 365 ecosystem; experience with Adobe Acrobat, Microsoft Defender, Oracle clients, and Citrix environments.\nWorking knowledge of TCP/IP networking, DNS, DHCP, VLAN concepts, and basic switch configuration.\nFamiliarity with endpoint deployment tools such as Microsoft Intune, SCCM/MECM, and Autopilot.\nExcellent analytical and problem-solving skills, paired with a strong customer service orientation.\nMicrosoft certifications (Azure Administration, Windows Server Hybrid Administration, or Modern Desktop Administration Associate) are a distinct advantage.\nExperience in regulated environments, including lab instrumentation support, is advantageous.\nFull on-site availability in Fehraltorf/Zurich is required.\nWe look forward to your application. Kindly provide your resume in English.\nWhy Celerion?\nAt Celerion, your work as an IT Specialist is not just about keeping computers running — it is about enabling the scientists and clinicians who are accelerating the journey from laboratory to patient. You will be part of a global, collaborative IT team with the support and resources of an established international organization, while enjoying the close-knit atmosphere of our Swiss site.\nAre you interested in this position?\nThen we look forward to receiving your complete application documents via the link or via our homepage: https://www.celerion.com/careers\nCelerion Switzerland AG\nHuman Resources\nAllmendstrasse 32\n8320 Fehraltorf\nhttps://www.celerion.com",
    "datePosted": "2026-08-11",
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    "@id": "https://ch-jobs.com/job/bioanalytische-r-laborant-in-80100-celerion-switzerland-ag-ch-sante-medical#jobposting",
    "title": "Bioanalytische/r Laborant/in (80–100%)",
    "description": "Celerion Switzerland AG sucht eine(n) Bioanalytische/r Laborant/in (80–100%) zur Verstärkung des Teams in .\n\n\nIhre Hauptaufgaben als Bioanalytische/r Laborant/in (80–100%):\n\n• Gestalten Sie mit uns die Arzneimittel von morgen.\n• Celerion Switzerland AG\n• ist Teil der weltweit tätigen\n• Celerion Inc\n• Zur Verstärkung unseres wachsenden Teams suchen wir eine engagierte Persönlichkeit als\n\n\nIhr Profil:\n\n• Formation et expérience en lien avec le poste\n\n• Capacité à travailler en autonomie et en équipe\n\n• Rigueur, ponctualité et sens des responsabilités\n\n\nBewerben Sie sich jetzt als Bioanalytische/r Laborant/in (80–100%) bei Celerion Switzerland AG in .",
    "datePosted": "2026-07-09",
    "validThrough": "2026-08-08",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/bioanalytische-r-laborant-in-80100-celerion-switzerland-ag-ch-sante-medical",
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