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    • selzach, solothurn
    • temporary
    Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und eint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.DePuy Synthes Companies of Johnson & Johnson ist das größte und umfassendste Orthopädieunternehmen der Welt. DePuy Synthes bietet eine beispiellose Breite und Tiefe unterschiedlicher Technologien, Produkte, Dienstleistungen und Programme in den Bereichen Orthopädie, Traumatologie, Wirbelsäule, Sportmedizin, Neurologie, Gesichts- und Schädelchirurgie, Power Tools und Biomaterialien an. Unsere breite Palette an innovativen und qualitativ hochwertigen Angeboten trägt dazu bei, die Gesundheit und das Wohlbefinden von Menschen auf der ganzen Welt nachhaltig zu verbessern. Zu den Haupttätigkeiten gehören unter anderem:EtikettierungsarbeitenDurchführung von Warenbewegungen mittels SAP und aller prozessrelevanten HilfsmittelBefolgen der Richtlinien bezüglich Verhaltenskodex, Ethik-, und Compliance-Programmen sowie anderer relevanter Regelungen
    Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und eint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.DePuy Synthes Companies of Johnson & Johnson ist das größte und umfassendste Orthopädieunternehmen der Welt. DePuy Synthes bietet eine beispiellose Breite und Tiefe unterschiedlicher Technologien, Produkte, Dienstleistungen und Programme in den Bereichen Orthopädie, Traumatologie, Wirbelsäule, Sportmedizin, Neurologie, Gesichts- und Schädelchirurgie, Power Tools und Biomaterialien an. Unsere breite Palette an innovativen und qualitativ hochwertigen Angeboten trägt dazu bei, die Gesundheit und das Wohlbefinden von Menschen auf der ganzen Welt nachhaltig zu verbessern. Zu den Haupttätigkeiten gehören unter anderem:EtikettierungsarbeitenDurchführung von Warenbewegungen mittels SAP und aller prozessrelevanten HilfsmittelBefolgen der Richtlinien bezüglich Verhaltenskodex, Ethik-, und Compliance-Programmen sowie anderer relevanter Regelungen
    • lausanne, vaud
    • temporary
    Pour le compte de mon client, je recherche nettoyeur spécifique ou nettoyeur de chantier : catégorie NLes tâches :nettoyage vitre - surfaceutilisation monobrosse- autolaveuse - shampooineusetraitement des sols - cristallisation - moquette -nettoyage chantier / façade / panneaux solaires / grafitisdésinfectionconciergerietonte de gazondéneigement
    Pour le compte de mon client, je recherche nettoyeur spécifique ou nettoyeur de chantier : catégorie NLes tâches :nettoyage vitre - surfaceutilisation monobrosse- autolaveuse - shampooineusetraitement des sols - cristallisation - moquette -nettoyage chantier / façade / panneaux solaires / grafitisdésinfectionconciergerietonte de gazondéneigement
    • winterthur, zürich
    • permanent
    Die Kistler Instrumente AG sucht für ihren Standort in Winterthur eine motivierte und aufgestellte Persönlichkeit als Teamleiter/in Server & Storage.In dieser Funktion betreust du die gesamte virtuelle Systemlandschaft der Kistler-Gruppe. Dabei bewirtschaftest du die bestehenden Tools und bist gleichermassen aktiv an der Umsetzung von Change-Projekten beteiligt. Wir setzen dabei auf deine Fachkenntnisse und deine Beraterkompetenz. Zu den Hauptaufgaben gehören:Führen des Server- und Storage-Teams mit drei Mitarbeitenden Aufsetzen und Administrieren der virtuellen Server Landschaft (Windows- und Linux-Server auf Basis von VMware) für die Kistler Gruppe sowie Unterstützen der Applikations-SetupsBetreuen hochverfügbarer Server- und Speicherumgebungen insbesondere NetApp-Storage, MS Sharepoint, MS Exchange, MS SQLWarten der Systeme inkl. Durchführen von Updates und UpgradeMonitoring der Systeme, Support und Dokumentieren von Server- und SpeicherumgebungenMitarbeiten in den Bereichen Operations und Helpdesk (2nd Level)Enge Zusammenarbeit mit internen Schnittstellen auf allen Ebenen in Change-Projekten
    Die Kistler Instrumente AG sucht für ihren Standort in Winterthur eine motivierte und aufgestellte Persönlichkeit als Teamleiter/in Server & Storage.In dieser Funktion betreust du die gesamte virtuelle Systemlandschaft der Kistler-Gruppe. Dabei bewirtschaftest du die bestehenden Tools und bist gleichermassen aktiv an der Umsetzung von Change-Projekten beteiligt. Wir setzen dabei auf deine Fachkenntnisse und deine Beraterkompetenz. Zu den Hauptaufgaben gehören:Führen des Server- und Storage-Teams mit drei Mitarbeitenden Aufsetzen und Administrieren der virtuellen Server Landschaft (Windows- und Linux-Server auf Basis von VMware) für die Kistler Gruppe sowie Unterstützen der Applikations-SetupsBetreuen hochverfügbarer Server- und Speicherumgebungen insbesondere NetApp-Storage, MS Sharepoint, MS Exchange, MS SQLWarten der Systeme inkl. Durchführen von Updates und UpgradeMonitoring der Systeme, Support und Dokumentieren von Server- und SpeicherumgebungenMitarbeiten in den Bereichen Operations und Helpdesk (2nd Level)Enge Zusammenarbeit mit internen Schnittstellen auf allen Ebenen in Change-Projekten
    • bern, bern
    • temporary
    Du hast erste Erfahrungen in der Qualitätsprüfung und möchtest dein Wissen in einem internationalen Unternehmen erweitern? Übernimmst du gerne Verantwortung und arbeitest gerne in einem jungen und dynamischen Team? Unser Kunde braucht deine Unterstützung als Mitarbeiter in der Endkontrolle (w/m) 100% Deine Aufgaben:Prüfen der Hergestellten Einzelteilen auf Qualität uns SicherheitSelbständiges beheben von keine Fehlern an den EinzelteilenAusfüllen von Lieferung und LagerpapiereErledigen der Aufträge gemäss Produktionsliste
    Du hast erste Erfahrungen in der Qualitätsprüfung und möchtest dein Wissen in einem internationalen Unternehmen erweitern? Übernimmst du gerne Verantwortung und arbeitest gerne in einem jungen und dynamischen Team? Unser Kunde braucht deine Unterstützung als Mitarbeiter in der Endkontrolle (w/m) 100% Deine Aufgaben:Prüfen der Hergestellten Einzelteilen auf Qualität uns SicherheitSelbständiges beheben von keine Fehlern an den EinzelteilenAusfüllen von Lieferung und LagerpapiereErledigen der Aufträge gemäss Produktionsliste
    • winterthur, zürich
    • permanent
    Bist du ein leidenschaftlicher Network Admin Spezialist und hast Freude am führen eines kleinen Teams? Dann suchen wir dich für die Verantwortungsvolle Aufgabe als Teamleader im ICT Team am modernen Kistler Standort in Winterthur. Zu den Hauptaufgaben gehören:Verantwortlich für die weltweite Administration der Netzwerke und deren Komponenten in ca. 60 Offices und mehreren Datacentern weltweitAdministrieren, Überwachen und Auswerten der globalen Netzwerk-Sicherheitslösungen Betreuung und Performance-Überwachung der InternetzugängeAuf- und Ausbau der Kistler IoT- und Cloud-Netzwerk-Komponenten Führen eines zweiköpfigen SpezialistenteamsLeiten und Umsetzen von Netzwerk- und Sicherheits-ProjektenErstellen von Design- und Betriebshandbüchern
    Bist du ein leidenschaftlicher Network Admin Spezialist und hast Freude am führen eines kleinen Teams? Dann suchen wir dich für die Verantwortungsvolle Aufgabe als Teamleader im ICT Team am modernen Kistler Standort in Winterthur. Zu den Hauptaufgaben gehören:Verantwortlich für die weltweite Administration der Netzwerke und deren Komponenten in ca. 60 Offices und mehreren Datacentern weltweitAdministrieren, Überwachen und Auswerten der globalen Netzwerk-Sicherheitslösungen Betreuung und Performance-Überwachung der InternetzugängeAuf- und Ausbau der Kistler IoT- und Cloud-Netzwerk-Komponenten Führen eines zweiköpfigen SpezialistenteamsLeiten und Umsetzen von Netzwerk- und Sicherheits-ProjektenErstellen von Design- und Betriebshandbüchern
    • st. margrethen sg, st. gallen
    • temporary
    Hast du Freude am Kommissionieren und an allg. Arbeiten im Lager und suchst eine neue Herausforderung? Dann bist du unser neuer Lagermitarbeiter (m/w/d) 100% Deine Aufgaben als Lagermitarbeiter:Entladen, UmladearbeitenVerpackung und VersandKommissionierenAllg. Lagertätigkeiten
    Hast du Freude am Kommissionieren und an allg. Arbeiten im Lager und suchst eine neue Herausforderung? Dann bist du unser neuer Lagermitarbeiter (m/w/d) 100% Deine Aufgaben als Lagermitarbeiter:Entladen, UmladearbeitenVerpackung und VersandKommissionierenAllg. Lagertätigkeiten
    • martigny, valais
    • permanent
    Vous êtes Chef de Projet Application Métier ?Toujours prêt à construire et délivrer les meilleures solutions ?Alors peut-être que nous pourrions discuter de cette opportunité !Mon client est une société évoluant dans le domaine industriel à Martigny (VS). Si vous intégrez leurs équipes, vous bénéficierez de nombreux avantages notamment de travailler dans un environnement à la pointe de la technologie!Que ferez-vous ?En tant que Chef de Projet Application Métier, votre role sera d'assurer le bon déroulement de la migration PLM du site de production (budget alloué, méthodologie d'organisation, planification, suivi des indicateurs de performance, accompagnement du changement).Que recherchent-ils ?- Expérience confirmée dans un poste similaire idéalement (PLM) sur 3Dexperience.- Expérience dans le milieu industriel très apprécié. - Capable de prendre des responsabilités.- De langue maternelle française, vous êtes capable de communiquer en anglaisVous pensez pouvoir vous épanouir au sein de ce type d'univers ?Alors prévoyons un échange téléphonique!
    Vous êtes Chef de Projet Application Métier ?Toujours prêt à construire et délivrer les meilleures solutions ?Alors peut-être que nous pourrions discuter de cette opportunité !Mon client est une société évoluant dans le domaine industriel à Martigny (VS). Si vous intégrez leurs équipes, vous bénéficierez de nombreux avantages notamment de travailler dans un environnement à la pointe de la technologie!Que ferez-vous ?En tant que Chef de Projet Application Métier, votre role sera d'assurer le bon déroulement de la migration PLM du site de production (budget alloué, méthodologie d'organisation, planification, suivi des indicateurs de performance, accompagnement du changement).Que recherchent-ils ?- Expérience confirmée dans un poste similaire idéalement (PLM) sur 3Dexperience.- Expérience dans le milieu industriel très apprécié. - Capable de prendre des responsabilités.- De langue maternelle française, vous êtes capable de communiquer en anglaisVous pensez pouvoir vous épanouir au sein de ce type d'univers ?Alors prévoyons un échange téléphonique!
    • basel, basel-stadt
    • permanent
    Do you already have a few years of experience as a global market researcher ? Do you have those years of experience in the pharmaceutical/biotech industry ? You should then have a look on the lines below!One of our clients, a global pharmaceutical company based in the Basel area, is looking for its next Associate Director, Global Market Research for a permanent contract.The functional scope of this position is anchored on primary market research, and includes secondary and primary competitive intelligence, as well as data analytics and scenario valuation modeling.Tasks:Design and lead the Global Insights program (primary MR & CI) for key asset(s) from RFP design, selection of the external partner(s), project management, delivery of the recommendations, to the activation of the recommendationsEnsure coordination & alignment of the Global Insights program across global, regional, and local teamsIdentifie & clearly articulate key business questions, determines the methodology best suited to meet those objectives and ensures optimal study design and execution.Serve as the “voice of the customer” to the Disease Area Strategy (DAS) team and then translate customer & market insights into actionable recommendations based on key insights.Facilitate and lead discussions with cross-functional teams regarding implications and relevant recommendations based on those insights generated from primary MR, CI and other analyses Profile:A Bachelor’s degree is required. An MBA or other advanced degree is preferred.A minimum of 8 years of relevant experience is required.Primary Market Research experience is required. Experience in business analytics or other analytical areas is preferred.Experience in the healthcare industry is needed, incl. understanding of science & marketing, ideally in the rare disease spaceA solid understanding of the product development process (NME declaration through launch) is preferred.Hands-on experience designing, implementing and presenting a range of primary market research and/or secondary & primary competitive intelligence and/or analytics/forecasting methodologies is preferred.Experience in developing novel approaches for insight generation is strongly preferred. Strong analytic and communication skills (written and oral) are required.Experience with secondary data sources and modeling is preferred.The ability to think analytically and apply good business judgment, as well as being capable of leading cross-functional teams of people is required.Strong project management skills, i.e., the ability to manage and prioritize multiple projects and requirements simultaneously, are required.  You feel like you are described within those lines ? Then do not waste a second and apply now!
    Do you already have a few years of experience as a global market researcher ? Do you have those years of experience in the pharmaceutical/biotech industry ? You should then have a look on the lines below!One of our clients, a global pharmaceutical company based in the Basel area, is looking for its next Associate Director, Global Market Research for a permanent contract.The functional scope of this position is anchored on primary market research, and includes secondary and primary competitive intelligence, as well as data analytics and scenario valuation modeling.Tasks:Design and lead the Global Insights program (primary MR & CI) for key asset(s) from RFP design, selection of the external partner(s), project management, delivery of the recommendations, to the activation of the recommendationsEnsure coordination & alignment of the Global Insights program across global, regional, and local teamsIdentifie & clearly articulate key business questions, determines the methodology best suited to meet those objectives and ensures optimal study design and execution.Serve as the “voice of the customer” to the Disease Area Strategy (DAS) team and then translate customer & market insights into actionable recommendations based on key insights.Facilitate and lead discussions with cross-functional teams regarding implications and relevant recommendations based on those insights generated from primary MR, CI and other analyses Profile:A Bachelor’s degree is required. An MBA or other advanced degree is preferred.A minimum of 8 years of relevant experience is required.Primary Market Research experience is required. Experience in business analytics or other analytical areas is preferred.Experience in the healthcare industry is needed, incl. understanding of science & marketing, ideally in the rare disease spaceA solid understanding of the product development process (NME declaration through launch) is preferred.Hands-on experience designing, implementing and presenting a range of primary market research and/or secondary & primary competitive intelligence and/or analytics/forecasting methodologies is preferred.Experience in developing novel approaches for insight generation is strongly preferred. Strong analytic and communication skills (written and oral) are required.Experience with secondary data sources and modeling is preferred.The ability to think analytically and apply good business judgment, as well as being capable of leading cross-functional teams of people is required.Strong project management skills, i.e., the ability to manage and prioritize multiple projects and requirements simultaneously, are required.  You feel like you are described within those lines ? Then do not waste a second and apply now!
    • basel, basel-stadt
    • contract
    Jeder Patient hat ein Anrecht auf Qualität und jeder Mitarbeiter ist für Qualität verantwortlich. Qualität verschafft Roche einen Wettbewerbsvorteil und liegt allem, was wir tun, zugrunde – vom Konzept bis zur kontinuierlichen Verbesserung. Da unsere Produkte Einfluss auf das Leben von Menschen haben, ist Qualität der wahre Massstab unseres Erfolgs.Der Qualifizierungsmanager ist verantwortlich für das CSV- und Qualifizierungs-Programm bei Basel DS Manufacturing sowie die Aktivitäten zur Erhaltung des qualifizierten Status in Zusammenarbeit mit dem Engineering und den Betreibern bei Basel Drug Substance Manufacturing (für biochemische und chemische Herstellungsverfahren)Hintergrund:• Startdatum: 01.07.2021• Spätestes Startdatum: 01.09.2021• Enddatum: 6 Monate nach Start• Verlängerung: möglich• Arbeitsort: Basel, Bau 1• Workload: 100%• Remote/Home Office: Zeitweise möglichAufgaben & Verantwortlichkeiten:• Management und Koordination von CSV- und Qualifizierungsprojekten Review und Genehmigung von Qualifizierungsplänen und Reports• Erstellen von Qualifizierungsstrategien, Risikoanalysen, Qualifizierungsplänen und-berichten sowie Beurteilung von Qualifizierungsreviews• Durchführen von Qualifizierungen in den Phasen DQ-IQ-OQ-PQ gem. Roche Q-System• Mitarbeit im KFQ Kernteam sowie Review und Genehmigung von KFQ-Listen• Koordination und Dokumentation von Globalen Change Anträgen• Abweichungsmanagement in Trackwise• Erstellen von GMP-Dokumenten: SOPs und Validierungsdokumenten.• Entwicklung und Anwendung von geeigneten Instrumenten zur Leitung und Überwachung der anvertrauten Projekte.• Entwicklung und Implementierung von Verbesserungsvorschlägen zu den Anlagen- und Gerätequalifizierungs- Konzepten• Management und Koordination von Risikoanalysen (QRM – Quality Risk Management)• Behörden- und Kunden-Audits: Unterstützung der Betriebe während der Audits. Hilfestellung bei der Umsetzung der Massnahmen• Selbstinspektionen: Begleitung von Audits. Hilfestellung bei der Umsetzung der Massnahmen• Problem Prävention: Bei der Durchführung der täglichen Arbeiten die Qualität stets im Fokus haben. Identifiziert Problembereiche und erarbeitet Lösungen zur Problemvermeidung• Sicherstellen der termingerechten Erreichung vorgegebenen Projektziele• Koordinieren der Zusammenarbeit mit den Produktions- und Supportabteilungen• Zusammenarbeit mit den Produktionsbetrieben, Engineering, Werkstatt, QC, QA, Labore und Technical Development• Mitarbeit und Leitung von spezifischen GMP-Projekten nach Bedarf oder gemäss Auftrag.• Mitarbeit bei der Implementierung von abteilungsübergreifenden und internen GMP-Konzepten unter Berücksichtigung der aktuellen GMP-Vorschriften.• Aufrechterhaltung des Quality-Systems beim Basel DS Manufacturing• Sicherstellung der Datenintegrität bei computerisierten SystemeMust haves:• Abgeschlossenes Studium im Bereich chemischer oder biochemischer Verfahrenstechnik oder vergleichbar *****• Mind. 3 Jahre Berufserfahrung in der Qualifzierung von Anlagen in einem GMP Umfeld *****• Mind. 3 Jahre Berufserfahrung in der chemischen oder pharmazeutischen Industrie im GMP Umfeld *****• Erste Berufserfahrung mit CSV von Laborgeräten ***• Gute EDV-Kenntnisse (MS Office, Google Mail & Kalender) **, COMOS von Vorteil• Sehr gute Deutsch und Englischkenntnisse werden vorausgesetzt
    Jeder Patient hat ein Anrecht auf Qualität und jeder Mitarbeiter ist für Qualität verantwortlich. Qualität verschafft Roche einen Wettbewerbsvorteil und liegt allem, was wir tun, zugrunde – vom Konzept bis zur kontinuierlichen Verbesserung. Da unsere Produkte Einfluss auf das Leben von Menschen haben, ist Qualität der wahre Massstab unseres Erfolgs.Der Qualifizierungsmanager ist verantwortlich für das CSV- und Qualifizierungs-Programm bei Basel DS Manufacturing sowie die Aktivitäten zur Erhaltung des qualifizierten Status in Zusammenarbeit mit dem Engineering und den Betreibern bei Basel Drug Substance Manufacturing (für biochemische und chemische Herstellungsverfahren)Hintergrund:• Startdatum: 01.07.2021• Spätestes Startdatum: 01.09.2021• Enddatum: 6 Monate nach Start• Verlängerung: möglich• Arbeitsort: Basel, Bau 1• Workload: 100%• Remote/Home Office: Zeitweise möglichAufgaben & Verantwortlichkeiten:• Management und Koordination von CSV- und Qualifizierungsprojekten Review und Genehmigung von Qualifizierungsplänen und Reports• Erstellen von Qualifizierungsstrategien, Risikoanalysen, Qualifizierungsplänen und-berichten sowie Beurteilung von Qualifizierungsreviews• Durchführen von Qualifizierungen in den Phasen DQ-IQ-OQ-PQ gem. Roche Q-System• Mitarbeit im KFQ Kernteam sowie Review und Genehmigung von KFQ-Listen• Koordination und Dokumentation von Globalen Change Anträgen• Abweichungsmanagement in Trackwise• Erstellen von GMP-Dokumenten: SOPs und Validierungsdokumenten.• Entwicklung und Anwendung von geeigneten Instrumenten zur Leitung und Überwachung der anvertrauten Projekte.• Entwicklung und Implementierung von Verbesserungsvorschlägen zu den Anlagen- und Gerätequalifizierungs- Konzepten• Management und Koordination von Risikoanalysen (QRM – Quality Risk Management)• Behörden- und Kunden-Audits: Unterstützung der Betriebe während der Audits. Hilfestellung bei der Umsetzung der Massnahmen• Selbstinspektionen: Begleitung von Audits. Hilfestellung bei der Umsetzung der Massnahmen• Problem Prävention: Bei der Durchführung der täglichen Arbeiten die Qualität stets im Fokus haben. Identifiziert Problembereiche und erarbeitet Lösungen zur Problemvermeidung• Sicherstellen der termingerechten Erreichung vorgegebenen Projektziele• Koordinieren der Zusammenarbeit mit den Produktions- und Supportabteilungen• Zusammenarbeit mit den Produktionsbetrieben, Engineering, Werkstatt, QC, QA, Labore und Technical Development• Mitarbeit und Leitung von spezifischen GMP-Projekten nach Bedarf oder gemäss Auftrag.• Mitarbeit bei der Implementierung von abteilungsübergreifenden und internen GMP-Konzepten unter Berücksichtigung der aktuellen GMP-Vorschriften.• Aufrechterhaltung des Quality-Systems beim Basel DS Manufacturing• Sicherstellung der Datenintegrität bei computerisierten SystemeMust haves:• Abgeschlossenes Studium im Bereich chemischer oder biochemischer Verfahrenstechnik oder vergleichbar *****• Mind. 3 Jahre Berufserfahrung in der Qualifzierung von Anlagen in einem GMP Umfeld *****• Mind. 3 Jahre Berufserfahrung in der chemischen oder pharmazeutischen Industrie im GMP Umfeld *****• Erste Berufserfahrung mit CSV von Laborgeräten ***• Gute EDV-Kenntnisse (MS Office, Google Mail & Kalender) **, COMOS von Vorteil• Sehr gute Deutsch und Englischkenntnisse werden vorausgesetzt
    • basel, basel-stadt
    • contract
    For one of our pharmaceutical company we are looking forPathologistStart: ASAPDuration: 6 monthsLocation: BaselWorkload: 100%Tasks:Member of a cross-functional Digital Pathology team to be at the forefront of tissue biomarker research for OncologyProvide expertise on analysis of tumor tissue and its application to Drug DevelopmentDrive key biomarker and pathology capabilities across the Discovery and Early Clinical Development Oncology pipelineDevelop a deep expertise through study analysis and thorough knowledge of literatureGuide and challenge the use of tissue biomarkersRequirements:Medical Doctor (*****)Board certification in pathology (*****)Experience in tissue biomarkers such as discovering/developing insights from the analysis of tumors and tissues into testable clinical hypotheses and image analysis (*****)Experience in imaging analysisExperience and interest in developing cutting-edge digital pathology approaches are required (***)Experience in supervising, exploring, developing and analyzing tissue analysis techniques such as immuno-histochemistry, multiplex immuno-fluorescence, image analysis and spatial-omics approach Nice to have:Background in cancer biology, cancer genetics and immunology (**)Previous R&D experience is a benefit, but not required
    For one of our pharmaceutical company we are looking forPathologistStart: ASAPDuration: 6 monthsLocation: BaselWorkload: 100%Tasks:Member of a cross-functional Digital Pathology team to be at the forefront of tissue biomarker research for OncologyProvide expertise on analysis of tumor tissue and its application to Drug DevelopmentDrive key biomarker and pathology capabilities across the Discovery and Early Clinical Development Oncology pipelineDevelop a deep expertise through study analysis and thorough knowledge of literatureGuide and challenge the use of tissue biomarkersRequirements:Medical Doctor (*****)Board certification in pathology (*****)Experience in tissue biomarkers such as discovering/developing insights from the analysis of tumors and tissues into testable clinical hypotheses and image analysis (*****)Experience in imaging analysisExperience and interest in developing cutting-edge digital pathology approaches are required (***)Experience in supervising, exploring, developing and analyzing tissue analysis techniques such as immuno-histochemistry, multiplex immuno-fluorescence, image analysis and spatial-omics approach Nice to have:Background in cancer biology, cancer genetics and immunology (**)Previous R&D experience is a benefit, but not required
    • genève, genève
    • permanent
    You are a Front end Dev UX  expert and you are looking for a new challenge ? we have your new opportunity. For one of our client based in Geneva we are looking for a Sharepoint Expert Your mission : UX analyses UI and design of the new applicationFront enD development ent testingParticipate to the Architecture designSupervise the providors involved in de developmentYour profile : Expert in UX And Design mockupProefficient  in Angular, AngularJS, Javascript, Typescript, HTML5, CSS3Knowledge of .NET : C#, VB, WPF, WCF, Winforms, PrismFrench and English mandatorySwiss residency
    You are a Front end Dev UX  expert and you are looking for a new challenge ? we have your new opportunity. For one of our client based in Geneva we are looking for a Sharepoint Expert Your mission : UX analyses UI and design of the new applicationFront enD development ent testingParticipate to the Architecture designSupervise the providors involved in de developmentYour profile : Expert in UX And Design mockupProefficient  in Angular, AngularJS, Javascript, Typescript, HTML5, CSS3Knowledge of .NET : C#, VB, WPF, WCF, Winforms, PrismFrench and English mandatorySwiss residency
    • zürich, zürich
    • permanent
    Für unseren Kunden ein schweizer IT Unternehmen in Zürich suchen wir einen Leiter System Engineering für die lernenden im 1. Lehrjahr. Aufgabengebiet:Du betreust zwischen 8-14 Lehrlinge während 3 Tagen aktiv und widmest dich den Vor- und Nachbereitungen während der anderen 2 Tage.Die eingesetzten Module werden Inhouse entwickelt und technologisch immer auf den neuesten Stand gebracht, was dir die Möglichkeit gibt neueste Entdeckungen mit einzubringenDu unterrichtest die kompletten System Engineering Module mit Windows Schwerpunkt so wie virtualisierte Umgebungen und Thematiken in der CloudAnforderungen:Deutsch auf Muttersprachenniveau5+ Jahre Hands-on! Erfahrung als System Engineer (kann bis zu 50/50 Windows/Linux sein)Studium oder Weiterbildung ist von Vorteil auf Höhe HF oder FH, wichtiger sind die notwendigen Hands-on BerufserfahrungenBreites IT-Engineering-Wissen, Client/Server-Engineering von lokalen bis hin zu hybriden Cloud-Umgebungen, Netzwerke und SecurityErfahrungen mit: Windows, Linux, Cloud Azure, VmWare, Hyper-V, PowershellWir richten uns an Kandidaten die......ihr Wissen gerne weitergeben...sachlich und fachlich gut kommunizieren können...lösungsorientiert und konstruktiv sind...sich in einer DU-Kultur wohl fühlen...direktes Feedback geben können und auch annehmen...einen gesunden Humor mitbringenWenn Du Dich in dieser Position wiedererkannt hast, schicke uns Dein komplettes Bewerbungsdossier oder rufe an. Gerne geben wir Dir alle weiteren Informationen die wir direkt von der Linie haben bekannt.
    Für unseren Kunden ein schweizer IT Unternehmen in Zürich suchen wir einen Leiter System Engineering für die lernenden im 1. Lehrjahr. Aufgabengebiet:Du betreust zwischen 8-14 Lehrlinge während 3 Tagen aktiv und widmest dich den Vor- und Nachbereitungen während der anderen 2 Tage.Die eingesetzten Module werden Inhouse entwickelt und technologisch immer auf den neuesten Stand gebracht, was dir die Möglichkeit gibt neueste Entdeckungen mit einzubringenDu unterrichtest die kompletten System Engineering Module mit Windows Schwerpunkt so wie virtualisierte Umgebungen und Thematiken in der CloudAnforderungen:Deutsch auf Muttersprachenniveau5+ Jahre Hands-on! Erfahrung als System Engineer (kann bis zu 50/50 Windows/Linux sein)Studium oder Weiterbildung ist von Vorteil auf Höhe HF oder FH, wichtiger sind die notwendigen Hands-on BerufserfahrungenBreites IT-Engineering-Wissen, Client/Server-Engineering von lokalen bis hin zu hybriden Cloud-Umgebungen, Netzwerke und SecurityErfahrungen mit: Windows, Linux, Cloud Azure, VmWare, Hyper-V, PowershellWir richten uns an Kandidaten die......ihr Wissen gerne weitergeben...sachlich und fachlich gut kommunizieren können...lösungsorientiert und konstruktiv sind...sich in einer DU-Kultur wohl fühlen...direktes Feedback geben können und auch annehmen...einen gesunden Humor mitbringenWenn Du Dich in dieser Position wiedererkannt hast, schicke uns Dein komplettes Bewerbungsdossier oder rufe an. Gerne geben wir Dir alle weiteren Informationen die wir direkt von der Linie haben bekannt.
    • basel, basel-stadt
    • contract
    For one of our clients in Basel we are looking for a Drug product lead in Biologics Pharmaceutical Development for a one year project. Job purpose To develop our growing pipeline of products we are looking for an experienced professional in the area of Late Phase Biologics Pharmaceutical Development. As a member of the team, you will play a key role in the development of formulation and processes for parenteral dosage forms for proteins for late phase clinical or commercial use. You will also be strongly involved in the generation of registration documents. Major accountabilities - Lead and co-ordinate the drug product team (functional experts) and represent Pharmaceutical Development on the CMC subteam. Fulfill all tasks and responsibilities related to own discipline.- Design, plan, perform and monitor all assigned drug product development activities applying state of the art technologies. Meet quality, quantity and timelines in all assigned projects.- Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s)- Interpret results, evaluate data, draw relevant conclusions, and write reports.- Generate scientific documents to hand over to internal partners (Manufacturing sites, Device Development, RegCMC, Clinics etc.).- Actively support generation of international registration documents for market authorization and interact with authorities where appropriate; act as technical expert in audits or inspections.- Contribute to overall development strategies and improvement of operational excellence of business processes.- Contribute to evaluation of new scientific technologies/equipment and proactively identify and realize opportunities for Invention Disclosures.- Represent pharmaceutical development in external collaborations.- Coach junior team members. Background • PhD or equivalent education in Pharmaceutical Technology, Biochemistry, Chemistry, Chemical Engineering or a related discipline with excellent theoretical and scientific knowledge.• Excellent English required (oral & written); good skills in German as site (local) language desired (oral)• Ideally 5-10 years relevant experience in pharmaceutical industry including thorough understanding of Pharmaceutical development activities for Biologics and/or process engineering of sterile dosage forms as well as a generally broad scientific and strategic background• Thorough track record of process transfer, validation and – importantly - regulatory submissions including health authority inspections.• In-depth background in commercial manufacturing and/or technical life cycle management of Biologics drug products is of advantage.• Demonstrated successful experience with working in interdisciplinary teams, track record of creativity, problem solving and productivity in projects 
    For one of our clients in Basel we are looking for a Drug product lead in Biologics Pharmaceutical Development for a one year project. Job purpose To develop our growing pipeline of products we are looking for an experienced professional in the area of Late Phase Biologics Pharmaceutical Development. As a member of the team, you will play a key role in the development of formulation and processes for parenteral dosage forms for proteins for late phase clinical or commercial use. You will also be strongly involved in the generation of registration documents. Major accountabilities - Lead and co-ordinate the drug product team (functional experts) and represent Pharmaceutical Development on the CMC subteam. Fulfill all tasks and responsibilities related to own discipline.- Design, plan, perform and monitor all assigned drug product development activities applying state of the art technologies. Meet quality, quantity and timelines in all assigned projects.- Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s)- Interpret results, evaluate data, draw relevant conclusions, and write reports.- Generate scientific documents to hand over to internal partners (Manufacturing sites, Device Development, RegCMC, Clinics etc.).- Actively support generation of international registration documents for market authorization and interact with authorities where appropriate; act as technical expert in audits or inspections.- Contribute to overall development strategies and improvement of operational excellence of business processes.- Contribute to evaluation of new scientific technologies/equipment and proactively identify and realize opportunities for Invention Disclosures.- Represent pharmaceutical development in external collaborations.- Coach junior team members. Background • PhD or equivalent education in Pharmaceutical Technology, Biochemistry, Chemistry, Chemical Engineering or a related discipline with excellent theoretical and scientific knowledge.• Excellent English required (oral & written); good skills in German as site (local) language desired (oral)• Ideally 5-10 years relevant experience in pharmaceutical industry including thorough understanding of Pharmaceutical development activities for Biologics and/or process engineering of sterile dosage forms as well as a generally broad scientific and strategic background• Thorough track record of process transfer, validation and – importantly - regulatory submissions including health authority inspections.• In-depth background in commercial manufacturing and/or technical life cycle management of Biologics drug products is of advantage.• Demonstrated successful experience with working in interdisciplinary teams, track record of creativity, problem solving and productivity in projects 
    • basel, basel-stadt
    • contract
    Computer System Validation SpecialistCSV-Spezialist/in im Bereich API-Anlagen (aktive pharmazeutische Wirkstoffe) - BS Das Department Technische Compliance ist auf der Suche nach einem/r CSV-Spezialist/in im Bereich API-Anlagen. Der Standort befindet sich in Basel.Das Arbeitsumfeld prozessnaher Computer-System-Validierungen umfasst übergeordnete datenverarbeitende Systeme wie z.B. MES (Manufacturing Execution System) undDatenbanken (z.B. PI-Server von OSISoft) im GMP-Umfeld (Good manufacturing practice) von API. Die gekoppelten Chemischen und Biotechnologischen Produktionsanlagen haben meist eine eigenständige Steuerung in Form von SPS/HMI, welche über eine Schnittstelle an das MES und/oder einen PI-Server zwecks Datenaustausch bzw. Datensicherung gekoppelt werden. Aufgaben & Verantwortlichkeiten:Durchführung von Computer-System-Validierungen (CSV) im Rahmen von Virtualisierung von Servern, z.B. Batch-ServerKoordination und Durchführung von Periodic Reviews von CSV-SystemeGMP-konforme Dokumentation der durchgeführten Arbeiten und Zusammenfassung deraufgetretenen DifferenzenErarbeitung von Lösungsvorschlägen zu den aufgetretenen Differenzen.Bewertung der Datenintegrität von IT-Systeme/Datenbanken anhand eines vorgegebenen Fragenkatalogs. Must haves:Abgeschlossene Ausbildung, Hochschule, FH, HTL oder Techniker in den Fachrichtungen: EMSR-Technik, Verfahrenstechnik, Automation oder vergleichbarMind. 3 Jahre Berufserfahrung im Bereich Computer-System-Validierung (CSV) Sehr gute GMP KenntnisseSehr gute Deutschkenntnisse in Wort und Schrift sowie gute EnglischkenntnisseGute EDV-Kenntnisse (MS Office, Google Mail & Kalender) Berufserfahrung im Qualifizierungsumfeld von VorteilBewirb Dich jetzt hier auf der Randstad Platform!
    Computer System Validation SpecialistCSV-Spezialist/in im Bereich API-Anlagen (aktive pharmazeutische Wirkstoffe) - BS Das Department Technische Compliance ist auf der Suche nach einem/r CSV-Spezialist/in im Bereich API-Anlagen. Der Standort befindet sich in Basel.Das Arbeitsumfeld prozessnaher Computer-System-Validierungen umfasst übergeordnete datenverarbeitende Systeme wie z.B. MES (Manufacturing Execution System) undDatenbanken (z.B. PI-Server von OSISoft) im GMP-Umfeld (Good manufacturing practice) von API. Die gekoppelten Chemischen und Biotechnologischen Produktionsanlagen haben meist eine eigenständige Steuerung in Form von SPS/HMI, welche über eine Schnittstelle an das MES und/oder einen PI-Server zwecks Datenaustausch bzw. Datensicherung gekoppelt werden. Aufgaben & Verantwortlichkeiten:Durchführung von Computer-System-Validierungen (CSV) im Rahmen von Virtualisierung von Servern, z.B. Batch-ServerKoordination und Durchführung von Periodic Reviews von CSV-SystemeGMP-konforme Dokumentation der durchgeführten Arbeiten und Zusammenfassung deraufgetretenen DifferenzenErarbeitung von Lösungsvorschlägen zu den aufgetretenen Differenzen.Bewertung der Datenintegrität von IT-Systeme/Datenbanken anhand eines vorgegebenen Fragenkatalogs. Must haves:Abgeschlossene Ausbildung, Hochschule, FH, HTL oder Techniker in den Fachrichtungen: EMSR-Technik, Verfahrenstechnik, Automation oder vergleichbarMind. 3 Jahre Berufserfahrung im Bereich Computer-System-Validierung (CSV) Sehr gute GMP KenntnisseSehr gute Deutschkenntnisse in Wort und Schrift sowie gute EnglischkenntnisseGute EDV-Kenntnisse (MS Office, Google Mail & Kalender) Berufserfahrung im Qualifizierungsumfeld von VorteilBewirb Dich jetzt hier auf der Randstad Platform!
    • solothurn, solothurn
    • contract
    For one of our biotech client in Solothurn, we are looking for aExecution Systems - Project CoordinatorGeneral Information:Start date: Asap, latest August 2021 End date: 31.12.2021Location: Solothurn Job Overview:The Project Coordinator is an intermediate level resource providing department & project coordination support for the client. The Project Coordinator will also provide financial & budget support (CAPEX & OPEX) locally; and globally as needed. This role is responsible for coordination of project reporting, metrics, scheduling, resources, across the group. The Project Coordinator will work closely with the Head, project managers, and subject matter experts to ensure management of schedule, resources and budget between a matrix team of Process Automation, MES, data systems, CSV, Infrastructure, project workstream leads, technical leads, business process owners, and stakeholders (internal/external). This resource will work to coordinate activities across people in multiple geographies. Tasks and responsibilities:Support project managers (PMs) and subject matter experts (SMEs) in the development of project schedules & reports for group/systems to enable planning and predictability of group efficiency, project deliverables, operational activities and continuous improvement opportunities. This will provide visibility of activities & enable monitoring to inform escalation of risks and issues.Interact with various teams to coordinate activities, plan certain parts of projects/operational activities, and monitor progress as required.Support financial and budget tracking activities as required.Coordinate and organize meetings to ensure activities are on track for projects and operational activities, such as change coordination among department SMEs and with other functions on-site, and ensure visibility of risks/delays to PMs, SMEs, management and stakeholders.Support and coordinate communications between BES teams and other functions on site, and within the BES teams.Support PMs and SMEs in other related and relevant duties as required. Must-haves:3+ years experience supporting Pharma and/or IT projectsLife sciences project support experience, preferably BiotechProficient use of Microsoft Project, SharePoint and ExcelExcellent communication skills (written and verbal)BA or BS in Computer Science, Automation, Electrical, Chemical or Mechanical Engineering.
    For one of our biotech client in Solothurn, we are looking for aExecution Systems - Project CoordinatorGeneral Information:Start date: Asap, latest August 2021 End date: 31.12.2021Location: Solothurn Job Overview:The Project Coordinator is an intermediate level resource providing department & project coordination support for the client. The Project Coordinator will also provide financial & budget support (CAPEX & OPEX) locally; and globally as needed. This role is responsible for coordination of project reporting, metrics, scheduling, resources, across the group. The Project Coordinator will work closely with the Head, project managers, and subject matter experts to ensure management of schedule, resources and budget between a matrix team of Process Automation, MES, data systems, CSV, Infrastructure, project workstream leads, technical leads, business process owners, and stakeholders (internal/external). This resource will work to coordinate activities across people in multiple geographies. Tasks and responsibilities:Support project managers (PMs) and subject matter experts (SMEs) in the development of project schedules & reports for group/systems to enable planning and predictability of group efficiency, project deliverables, operational activities and continuous improvement opportunities. This will provide visibility of activities & enable monitoring to inform escalation of risks and issues.Interact with various teams to coordinate activities, plan certain parts of projects/operational activities, and monitor progress as required.Support financial and budget tracking activities as required.Coordinate and organize meetings to ensure activities are on track for projects and operational activities, such as change coordination among department SMEs and with other functions on-site, and ensure visibility of risks/delays to PMs, SMEs, management and stakeholders.Support and coordinate communications between BES teams and other functions on site, and within the BES teams.Support PMs and SMEs in other related and relevant duties as required. Must-haves:3+ years experience supporting Pharma and/or IT projectsLife sciences project support experience, preferably BiotechProficient use of Microsoft Project, SharePoint and ExcelExcellent communication skills (written and verbal)BA or BS in Computer Science, Automation, Electrical, Chemical or Mechanical Engineering.
    • basel, basel-stadt
    • contract
    For one of our client, a big pharmaceutical company in Basel, we are looking for a BTD Project Manager for a one year project.You will be working in the Biologics Technical Development (BTD) department.Job PurposeSupport BTD Technical Project Leader (TPL) in leading the technical (CMC) subteams for assigned projects and maintain cross-functional technical project plans & work packages in the Project Management system (Planview Horizon) for the Project Portfo-lio.Ensure operational excellence by proficient, accurate & harmonized project planning across BTD globally and warrant compliance of resource planning & tracking in line with the defined strategy/categorization. Provide downloads/reports of resources in respective IT-system and any other information to customers in BTD sub teams and line functions (BPAs).Major Activities• Organize meetings of the global technical subteam, facilitation of the agenda, follow-up of action items & providing minutes.• Assistant to Technical Project Leader (TPL) in leading the technical subteams for assigned projects.• Expert in the Project Management System Planview “Horizon” and other Portfolio Management relevant planning and tracking tools• Maintain the cross-functional BTD Project Plans for the assigned Portfolio in Horizon, Project Management System based on input from the TPL and Sub Team,• Liaise with Finance (BPA & Controller) for project cost tracking and phasing• Liaise with other GDD line functions (GDD GPM & Clinical Planner) to ensure timely update of BTD relevant work packages (WP), particularly prior to tollgate and other decision points• Generate regular Horizon & financial tool reports for portfolio & project reviews• Support development of processes, governance and best practices for data entry and maintenance in Horizon & other planning tools together with other resource planners & BTD PM• Ensures data entry & reporting are done in compliance to above defined processes and best practices together with other resource planners & BTD PMOKey Performance IndicatorsFree-Up resources of TPLProficient, Accurate & Harmonized BTD Project Planning in HorizonAligned approach across all BTD Projects for all BTD Line FunctionsImproved Data Accuracy & Quality for BTD Project Portfolio ForecastingImpact on the organization:Supports alignment & management of teams and optimized allocation of internal & external resources.Accurate and complete maintenance and communication of project/study information, timelines & resource forecasts.Ideal BackgroundEducation:Bachelor of Science in Pharma or Life Science. Business Administration Degree is an assetLanguages:Fluent English (oral and written).German desirableExperience/Professional requirement:1. At least 2-3 years’ experience in pharmaceutical industry in technical (CMC) development (potentially in other development functions, project management or finance as well), preferably with exposure to Biologics.Very good understanding and background of development and technical operations environments. Finance expertise is an asset.2. Very good knowledge of MS Excel & Sharepoint. Experience in Planview Horizon is an asset.3. Adaptable and flexible. Must demonstrate ability and willingness to learn new systems and processes quickly and readily. Willing and able to work hands-on with complex IT system4. Great attention to accuracy and detail. Demonstrated technical and database skills5. Strong customer focus; experience in working in service functions or providing customer support6. Experience in working within a global team environment and be a supportive team player.7. Solid organizational skills and ability to meet timelines.8. Must be able to work independently, and handle new assignment with minimal supervision
    For one of our client, a big pharmaceutical company in Basel, we are looking for a BTD Project Manager for a one year project.You will be working in the Biologics Technical Development (BTD) department.Job PurposeSupport BTD Technical Project Leader (TPL) in leading the technical (CMC) subteams for assigned projects and maintain cross-functional technical project plans & work packages in the Project Management system (Planview Horizon) for the Project Portfo-lio.Ensure operational excellence by proficient, accurate & harmonized project planning across BTD globally and warrant compliance of resource planning & tracking in line with the defined strategy/categorization. Provide downloads/reports of resources in respective IT-system and any other information to customers in BTD sub teams and line functions (BPAs).Major Activities• Organize meetings of the global technical subteam, facilitation of the agenda, follow-up of action items & providing minutes.• Assistant to Technical Project Leader (TPL) in leading the technical subteams for assigned projects.• Expert in the Project Management System Planview “Horizon” and other Portfolio Management relevant planning and tracking tools• Maintain the cross-functional BTD Project Plans for the assigned Portfolio in Horizon, Project Management System based on input from the TPL and Sub Team,• Liaise with Finance (BPA & Controller) for project cost tracking and phasing• Liaise with other GDD line functions (GDD GPM & Clinical Planner) to ensure timely update of BTD relevant work packages (WP), particularly prior to tollgate and other decision points• Generate regular Horizon & financial tool reports for portfolio & project reviews• Support development of processes, governance and best practices for data entry and maintenance in Horizon & other planning tools together with other resource planners & BTD PM• Ensures data entry & reporting are done in compliance to above defined processes and best practices together with other resource planners & BTD PMOKey Performance IndicatorsFree-Up resources of TPLProficient, Accurate & Harmonized BTD Project Planning in HorizonAligned approach across all BTD Projects for all BTD Line FunctionsImproved Data Accuracy & Quality for BTD Project Portfolio ForecastingImpact on the organization:Supports alignment & management of teams and optimized allocation of internal & external resources.Accurate and complete maintenance and communication of project/study information, timelines & resource forecasts.Ideal BackgroundEducation:Bachelor of Science in Pharma or Life Science. Business Administration Degree is an assetLanguages:Fluent English (oral and written).German desirableExperience/Professional requirement:1. At least 2-3 years’ experience in pharmaceutical industry in technical (CMC) development (potentially in other development functions, project management or finance as well), preferably with exposure to Biologics.Very good understanding and background of development and technical operations environments. Finance expertise is an asset.2. Very good knowledge of MS Excel & Sharepoint. Experience in Planview Horizon is an asset.3. Adaptable and flexible. Must demonstrate ability and willingness to learn new systems and processes quickly and readily. Willing and able to work hands-on with complex IT system4. Great attention to accuracy and detail. Demonstrated technical and database skills5. Strong customer focus; experience in working in service functions or providing customer support6. Experience in working within a global team environment and be a supportive team player.7. Solid organizational skills and ability to meet timelines.8. Must be able to work independently, and handle new assignment with minimal supervision
    • rotkreuz, zug
    • contract
    For one of our client in Rotkreuz we are looking for a Biospecimen Management Scientist:Background:The Biospecimen Management team (BSM) at RDI leads the acquisition, management of biological materials and clinical samples and associated data designed to facilitate and advance RDI development activities. BSM collaborates with RMD's Life Cycle Teams, Projects, and Functional Areas to ensure that customer requirements for biological materials are agreed to, via formal established processes, communicated to on a periodic basis, and met per commitment in compliance with Good Laboratory Practices, Good Clinical Data Management Practices, Quality, and Business standards.General Information:• Start Date: ASAP / 16.07.2021• Latest Start Date: open• End Date: 6 months after start date• Extension: is an option• Work Location: Rotkreuz• Workload: 100%• Remote/Home Office: part-time possible, needs to be discussedTasks and Responsibilities:• Organization, coordination und communication with external Elpro people• Organization of sensor changings, eg. from -20°C to -80°C connection including defrosting, change of batteries, decontamination and decommissioning.• Supports daily operation associated with the BioRepository at RDI including; sample registration, shipment (import & export), and verification activities in a validated laboratory information management system.• Maintains an accurate inventory of biological materials in the biospecimen repository, conducts periodic checks for assessment, and resolves discrepancies as presented.• Conducts data management activities, such as, data file transfers from suppliers, tracking of source data files, data review, data transcription, data import, data quality and consistency checks, resolution of data discrepancies, and data export while working within a validated laboratory information management system.• Assumes accountability for data entry into validated database(s), ensures that information is entered accurately and consistently, and according to established formats.• Writing risk analysis by themselves.Must Haves:• At least a Bachelor's degree in a related biological environment or similar level of education (e.g. Microbiology, Biology, Molecularbiology or Life Sciences) (*****)• At least 2 years experience in the life sciences industry, preferred in a laboratory setting or clinical operations required. (*****)• Prior experience in research & diagnostics, pharmaceutical, clinical or medical device industry preferred. (***)• Working knowledge of laboratory inventory management systems (LIMs) and or/regulatory requirements a plus. (**)• Excellent data handling skills, meticulous and proficient with MS Excel is a MUST (*****)• Proficient in English is a must, German would be a plusNice to Haves:• Good organizational, written and verbal communication skills.• Team player, self-organized, motivated individual and solution driven individual who can maintain quality, accuracy and timeliness of deliverables. 
    For one of our client in Rotkreuz we are looking for a Biospecimen Management Scientist:Background:The Biospecimen Management team (BSM) at RDI leads the acquisition, management of biological materials and clinical samples and associated data designed to facilitate and advance RDI development activities. BSM collaborates with RMD's Life Cycle Teams, Projects, and Functional Areas to ensure that customer requirements for biological materials are agreed to, via formal established processes, communicated to on a periodic basis, and met per commitment in compliance with Good Laboratory Practices, Good Clinical Data Management Practices, Quality, and Business standards.General Information:• Start Date: ASAP / 16.07.2021• Latest Start Date: open• End Date: 6 months after start date• Extension: is an option• Work Location: Rotkreuz• Workload: 100%• Remote/Home Office: part-time possible, needs to be discussedTasks and Responsibilities:• Organization, coordination und communication with external Elpro people• Organization of sensor changings, eg. from -20°C to -80°C connection including defrosting, change of batteries, decontamination and decommissioning.• Supports daily operation associated with the BioRepository at RDI including; sample registration, shipment (import & export), and verification activities in a validated laboratory information management system.• Maintains an accurate inventory of biological materials in the biospecimen repository, conducts periodic checks for assessment, and resolves discrepancies as presented.• Conducts data management activities, such as, data file transfers from suppliers, tracking of source data files, data review, data transcription, data import, data quality and consistency checks, resolution of data discrepancies, and data export while working within a validated laboratory information management system.• Assumes accountability for data entry into validated database(s), ensures that information is entered accurately and consistently, and according to established formats.• Writing risk analysis by themselves.Must Haves:• At least a Bachelor's degree in a related biological environment or similar level of education (e.g. Microbiology, Biology, Molecularbiology or Life Sciences) (*****)• At least 2 years experience in the life sciences industry, preferred in a laboratory setting or clinical operations required. (*****)• Prior experience in research & diagnostics, pharmaceutical, clinical or medical device industry preferred. (***)• Working knowledge of laboratory inventory management systems (LIMs) and or/regulatory requirements a plus. (**)• Excellent data handling skills, meticulous and proficient with MS Excel is a MUST (*****)• Proficient in English is a must, German would be a plusNice to Haves:• Good organizational, written and verbal communication skills.• Team player, self-organized, motivated individual and solution driven individual who can maintain quality, accuracy and timeliness of deliverables. 
    • winterthur, zürich
    • permanent
    Für unseren international tätigen Kunden in Winterthur suchen wir einen IT Supporter im 1st und 2nd Level SupportDeine Aufgaben:Hardware/Software installieren, warten und konfigurieren1st und 2nd Level SupportIT-Systeme kontrollieren und überwachenAnsprechperson für IT-Problemen und FragenDokumentationDein Profil:Abgeschlossene Ausbildung oder ein abgeschlossenes Studium im IT-UmfeldOptimalerweise bringst du mehr als 4 Jahre Berufserfahrung mitErfahrung mit Microsoft Client- und ServerKenntnisse mit CheckpointFliessende Deutschkenntnisse werden vorausgesetztVon Vorteil: Führerausweis Kategorie B
    Für unseren international tätigen Kunden in Winterthur suchen wir einen IT Supporter im 1st und 2nd Level SupportDeine Aufgaben:Hardware/Software installieren, warten und konfigurieren1st und 2nd Level SupportIT-Systeme kontrollieren und überwachenAnsprechperson für IT-Problemen und FragenDokumentationDein Profil:Abgeschlossene Ausbildung oder ein abgeschlossenes Studium im IT-UmfeldOptimalerweise bringst du mehr als 4 Jahre Berufserfahrung mitErfahrung mit Microsoft Client- und ServerKenntnisse mit CheckpointFliessende Deutschkenntnisse werden vorausgesetztVon Vorteil: Führerausweis Kategorie B
    • genève, genève
    • contract
    You are in the Digital Marketing area ? You will be responsible for the good implementation and execution of projects based on a full growth hacking model. Your skills :Ability to exchange with the full digital project and a teamPropose the KPI’s for the digital products, and ongoing projectsDeep technical understanding (end to end)Manage the project’s launch scheduleCoordinate relationship with client and technical teams Analyse project results and identify the areas of improvementYour expertise :5 years experience in digital projects and growth hakingManaging multiple projects simultaneouslyBA experience 5 yearsAgile methodologies knowledgeStrong organization skillsYou have a great sense of service and communicationKPI’s good understanding
    You are in the Digital Marketing area ? You will be responsible for the good implementation and execution of projects based on a full growth hacking model. Your skills :Ability to exchange with the full digital project and a teamPropose the KPI’s for the digital products, and ongoing projectsDeep technical understanding (end to end)Manage the project’s launch scheduleCoordinate relationship with client and technical teams Analyse project results and identify the areas of improvementYour expertise :5 years experience in digital projects and growth hakingManaging multiple projects simultaneouslyBA experience 5 yearsAgile methodologies knowledgeStrong organization skillsYou have a great sense of service and communicationKPI’s good understanding
    • biel, bern
    • permanent
    Für unseren Kunden in Biel suchen wir eine erfahrene Person für die Position als IT & OT Projektleiter.Du bist der Dreh- und Angelpunkt zwischen dem Sitz in der Schweiz und Spanien und führst ein Projekt auf grüner Wiese für industrielle Produkte im Bereich der Hochspannung, Ultraschall, Röntgen, Laser, Hardware und Software.Das sind Deine Aufgaben:Leiten eines Greenfield Projektes im Bereich IT & OTEinführung von neuen Lösungen, best practices und IIOT AnsätzenSPOC für den ganzen Lifecycle, von der Vision bis zum Go lifeAufbauen der EntwicklungseinheitAufbau der modular aufgebauten Software, dazu gehören auch Architektur EntscheidungenTestprogramme schreiben und Software TestenSehr enge Zusammenarbeit mit internen Stakeholders in der Schweiz und SpanienDas erwarten wir von Dir mit einer 70% Kongruenz zu Deinem CV:Deutsch auf Level B2 und Englisch auf Level B2-C1Echtzeit Thematiken sind sehr wichtig, somit wird Wissen in diesem Bereich vorausgesetztVersierte Erfahrung in der Leitung und Entwicklung von individueller und kundenspezifischer Anwendungen im Bereich Software (modular)Sehr gute Kenntnisse im Bereich von IT UND OTSehr guter Kommunikator auf allen StufenErfahrung in der Eigenverantwortung für ein ProjektTechnisches Know-How sehr wünschenswert:Echtzeit-BetriebssystemeSteuerungenIndustrielle KommunikationAutomatisierungstechnologienFeldbusseHardwareDatenverwaltungsfunktionenAnbindungenC++ oder PythonDB wie SQL oder Cloud LösungenEtherCAD, EthernetBei den Softskills gibt es zwei wichtige Punkte: strukturiert und zielgerichtet!Wir suchen jemanden der nach wie vor auch Hands-on mitarbeitet. Gerne geben wir Dir noch weitere Informationen und freuen uns auf Deine Bewerbung.
    Für unseren Kunden in Biel suchen wir eine erfahrene Person für die Position als IT & OT Projektleiter.Du bist der Dreh- und Angelpunkt zwischen dem Sitz in der Schweiz und Spanien und führst ein Projekt auf grüner Wiese für industrielle Produkte im Bereich der Hochspannung, Ultraschall, Röntgen, Laser, Hardware und Software.Das sind Deine Aufgaben:Leiten eines Greenfield Projektes im Bereich IT & OTEinführung von neuen Lösungen, best practices und IIOT AnsätzenSPOC für den ganzen Lifecycle, von der Vision bis zum Go lifeAufbauen der EntwicklungseinheitAufbau der modular aufgebauten Software, dazu gehören auch Architektur EntscheidungenTestprogramme schreiben und Software TestenSehr enge Zusammenarbeit mit internen Stakeholders in der Schweiz und SpanienDas erwarten wir von Dir mit einer 70% Kongruenz zu Deinem CV:Deutsch auf Level B2 und Englisch auf Level B2-C1Echtzeit Thematiken sind sehr wichtig, somit wird Wissen in diesem Bereich vorausgesetztVersierte Erfahrung in der Leitung und Entwicklung von individueller und kundenspezifischer Anwendungen im Bereich Software (modular)Sehr gute Kenntnisse im Bereich von IT UND OTSehr guter Kommunikator auf allen StufenErfahrung in der Eigenverantwortung für ein ProjektTechnisches Know-How sehr wünschenswert:Echtzeit-BetriebssystemeSteuerungenIndustrielle KommunikationAutomatisierungstechnologienFeldbusseHardwareDatenverwaltungsfunktionenAnbindungenC++ oder PythonDB wie SQL oder Cloud LösungenEtherCAD, EthernetBei den Softskills gibt es zwei wichtige Punkte: strukturiert und zielgerichtet!Wir suchen jemanden der nach wie vor auch Hands-on mitarbeitet. Gerne geben wir Dir noch weitere Informationen und freuen uns auf Deine Bewerbung.
    • lausanne, vaud
    • permanent
    Position of Medical Director (Permanent Contract) LausanneFor our client, a Swiss innovative medical device company base in Lausanne, developing and manufacturing a breakthrough imaging solution with the potential to improve patient care and cancer surgery outcome. Offering real-time ability to identify cancerous tissues and react immediately, this new visualisation modality holds the promise for a broad range of surgical and diagnostic applicationsResponsabilities :??????Reporting directly to the CEO, the Medical Director has the responsibility to support the Medical affairs needs. In this role, the Medical Director will partner closely with other teams to work with leadership to align and prioritize project work. - Design and develop clinical plans and protocol- Deliver and execute the clinical development plans- Develop a Medical Affairs Strategic Plan for Europe and US- Act as primary contact- Coordinate cross functional areas- Serve as Medical Expert- Document owner (or significant contributor) for Clinical Study Report- Presentation and Publication of Clinical Study Results- Provide clinical leadership and medical strategic input??????- Drive execution of the clinical program- Organisational Development and Compliance- Helps facilitate engagement with key subject matter experts- Develop a network of Key Opinion Leaders /investigators, interact with external stakeholders in alignment with customer needs and medical strategy.??????- Identify and engage international, national, and regional thought leaders- Participate in key external events??????- Keeps abreast of trends in health care??????Qualifications : - Medical Degree (M.D., D.O. or equivalent) with a strong background in clinical trial management, scientific investigation and proven ability to interpret scientific and study data required.- Professional experience - 10-15 years experience in the Medical device industry in a similar position. Global exposure and expertise in US & Europe.- Expertise in strategic aspects related to marketing needs (reimbursement, regulatory pathway)- Influencing Skills - Able to establish rapport, value and respect within a team, as well as with KOLs and other influential stakeholders, externally.- Interpersonal Skills - Strong personal credibility, written and oral communication skills.- Leadership Skills : Team orientated with the confidence, maturity and integrity to lead effectively.- Problem Solving Skills – Brings a high level of intellect and curiosity to work. Able to apply mature clinical and business judgement in making decisions.- Travel : This position may require some U.S. and european travel. Ability to travel domestically and internationally- Languages - Fluent in French and English; ability to speak, read, and write. Must be able to communicate clearly and accurately. Multiple languages is a plus- Regulations knowledge - Must be able to understand legally and technically written standards, regulations, procedures, test methods so as to communicate their intent.??????Prefered qualifications: Expertise in oncology; breast cancer and prostate in particular.Professional relationships with an established network of oncologists and surgeons.
    Position of Medical Director (Permanent Contract) LausanneFor our client, a Swiss innovative medical device company base in Lausanne, developing and manufacturing a breakthrough imaging solution with the potential to improve patient care and cancer surgery outcome. Offering real-time ability to identify cancerous tissues and react immediately, this new visualisation modality holds the promise for a broad range of surgical and diagnostic applicationsResponsabilities :??????Reporting directly to the CEO, the Medical Director has the responsibility to support the Medical affairs needs. In this role, the Medical Director will partner closely with other teams to work with leadership to align and prioritize project work. - Design and develop clinical plans and protocol- Deliver and execute the clinical development plans- Develop a Medical Affairs Strategic Plan for Europe and US- Act as primary contact- Coordinate cross functional areas- Serve as Medical Expert- Document owner (or significant contributor) for Clinical Study Report- Presentation and Publication of Clinical Study Results- Provide clinical leadership and medical strategic input??????- Drive execution of the clinical program- Organisational Development and Compliance- Helps facilitate engagement with key subject matter experts- Develop a network of Key Opinion Leaders /investigators, interact with external stakeholders in alignment with customer needs and medical strategy.??????- Identify and engage international, national, and regional thought leaders- Participate in key external events??????- Keeps abreast of trends in health care??????Qualifications : - Medical Degree (M.D., D.O. or equivalent) with a strong background in clinical trial management, scientific investigation and proven ability to interpret scientific and study data required.- Professional experience - 10-15 years experience in the Medical device industry in a similar position. Global exposure and expertise in US & Europe.- Expertise in strategic aspects related to marketing needs (reimbursement, regulatory pathway)- Influencing Skills - Able to establish rapport, value and respect within a team, as well as with KOLs and other influential stakeholders, externally.- Interpersonal Skills - Strong personal credibility, written and oral communication skills.- Leadership Skills : Team orientated with the confidence, maturity and integrity to lead effectively.- Problem Solving Skills – Brings a high level of intellect and curiosity to work. Able to apply mature clinical and business judgement in making decisions.- Travel : This position may require some U.S. and european travel. Ability to travel domestically and internationally- Languages - Fluent in French and English; ability to speak, read, and write. Must be able to communicate clearly and accurately. Multiple languages is a plus- Regulations knowledge - Must be able to understand legally and technically written standards, regulations, procedures, test methods so as to communicate their intent.??????Prefered qualifications: Expertise in oncology; breast cancer and prostate in particular.Professional relationships with an established network of oncologists and surgeons.
    • zürich, zürich
    • permanent
    Für unseren Kunden in der Stadt Zürich suchen wir eine erfahrene Person für die Position als Java Software Architect.Die Firma ist ein etabliertes, europaweit tätiges Unternehmen, welches seit rund 1.5 Jahren den Standort Schweiz aufbaut. Somit gibt es den Start-up Charakter innerhalb einer strukturierten Firma.Dein Fokus:Analyse, Konzeption und Umsetzung von anspruchsvollen SpezifikationenErstellen und Umsetzen von modernen ArchitekturkonzeptenImplementation von komplexen und skalierbaren MicroservicesEinbringung von Cloud LösungenEntwicklung von neuen und bestehenden Software FeaturesBeteiligung an der Auswahl von TechnologienAktive Teilnahme an Business Entscheidungen zum weiteren Ausbau der FirmaDeine Erfahrungen:Deutsch Niveau C1 unabdingbarVersierte Erfahrung in der Programmierung in Java - JEE - Jakarta EEGute Erfahrung in der Software Architektur / MicroservicesGute Kenntnisse im Bereich von Cloudlösungen wie Azure, AWS oder GoogleVertrauenswürdige Persönlichkeit mit Drive und UnternehmertumDer Wille etwas zu bewirken und die Firma im Wachstum langfristig zu begleitenNice to have:CI/CD KenntnisseSpring, SpringBootSonstige OO-ProgrammiersprachenDiese Stelle hat noch einiges mehr zu bieten und gerne gebe ich Dir diese Informationen. Ich freue mich auf Deine Bewerbung. 
    Für unseren Kunden in der Stadt Zürich suchen wir eine erfahrene Person für die Position als Java Software Architect.Die Firma ist ein etabliertes, europaweit tätiges Unternehmen, welches seit rund 1.5 Jahren den Standort Schweiz aufbaut. Somit gibt es den Start-up Charakter innerhalb einer strukturierten Firma.Dein Fokus:Analyse, Konzeption und Umsetzung von anspruchsvollen SpezifikationenErstellen und Umsetzen von modernen ArchitekturkonzeptenImplementation von komplexen und skalierbaren MicroservicesEinbringung von Cloud LösungenEntwicklung von neuen und bestehenden Software FeaturesBeteiligung an der Auswahl von TechnologienAktive Teilnahme an Business Entscheidungen zum weiteren Ausbau der FirmaDeine Erfahrungen:Deutsch Niveau C1 unabdingbarVersierte Erfahrung in der Programmierung in Java - JEE - Jakarta EEGute Erfahrung in der Software Architektur / MicroservicesGute Kenntnisse im Bereich von Cloudlösungen wie Azure, AWS oder GoogleVertrauenswürdige Persönlichkeit mit Drive und UnternehmertumDer Wille etwas zu bewirken und die Firma im Wachstum langfristig zu begleitenNice to have:CI/CD KenntnisseSpring, SpringBootSonstige OO-ProgrammiersprachenDiese Stelle hat noch einiges mehr zu bieten und gerne gebe ich Dir diese Informationen. Ich freue mich auf Deine Bewerbung. 
    • le locle, neuchâtel
    • temporary
    We are looking for a Senior Supplier Quality Specialist for one of our clients located near la Chaud-de-fonds. It is a mission of 1 year.Your Tasks: You will be responsible for validation of primarily injection molded components for their facility,You will qualify new suppliers to Supplier management processes.You will also provide Quality Engineering support to the team.You will develop and implement Inspection plans for Receiving Inspection activities at the site.You will perform special process validations and will do the audit of the suppliers. Your Profile: You have a bachelor degree in an Engineering discipline.You have minimum 5 years of experience in medical device or highly regulated industry as QA Supplier specialist.You have a strong understanding and experience with Injection Molding processes.Ability to communicate effectively in both French and English.Solid knowledge of the QSR and ISO9001 / EN46001 / ISO13485 quality requirements.Up to 50% travel, primarily in Switzerland and France.
    We are looking for a Senior Supplier Quality Specialist for one of our clients located near la Chaud-de-fonds. It is a mission of 1 year.Your Tasks: You will be responsible for validation of primarily injection molded components for their facility,You will qualify new suppliers to Supplier management processes.You will also provide Quality Engineering support to the team.You will develop and implement Inspection plans for Receiving Inspection activities at the site.You will perform special process validations and will do the audit of the suppliers. Your Profile: You have a bachelor degree in an Engineering discipline.You have minimum 5 years of experience in medical device or highly regulated industry as QA Supplier specialist.You have a strong understanding and experience with Injection Molding processes.Ability to communicate effectively in both French and English.Solid knowledge of the QSR and ISO9001 / EN46001 / ISO13485 quality requirements.Up to 50% travel, primarily in Switzerland and France.
    • basel, basel-stadt
    • contract
    Are you an experienced Project Manager/SCRUM Master and you are looking for an exciting opportunity in the pharmaceutical sector?Then you should read on! In this position you will have the opportunity to work as an Project Manager/SCRUM Master on a contracting project.Tasks and responsibilities:Responsible for managing all the day to day operational activities of the SLM teamFacilitate SLM Systems Lifecycle Management team meetings, and producing reports and meeting minutes that will be communicated to the other EpiCX teamsResponsible for managing expectations with all the sub-teams within the SLM Systems Lifecycle Management umbrellaWorking closely with the Systems Lifecycle Management SLM lead in managing finances and other resourcing related activities within the SLM areaWork closely with the SLM lead and other program leads to ‘connect the dots’Support JIRA management within the program - help the team responsible for performing health checks on tools used in the programFacilitate the flow of information within the SLM team to drive ownership and empowermentQualifications:Bachelor’s degree in Science, Information Systems, or related field5+ years of experience in a similar role or context (PM in a pharmaceutical IT/Systems Lifecycle Management environment)Expert knowledge in JIRA project management Business domain knowledge for one or more of the following areas: Commercial Excellence, CRM, Multichannel, analytical/dashboards, finance/procurementWorking knowledge experience of CRM release management activitiesDemonstrated experience in managing large teams and programsHave we sparked your interest? Do not hesitate to go ahead and apply!
    Are you an experienced Project Manager/SCRUM Master and you are looking for an exciting opportunity in the pharmaceutical sector?Then you should read on! In this position you will have the opportunity to work as an Project Manager/SCRUM Master on a contracting project.Tasks and responsibilities:Responsible for managing all the day to day operational activities of the SLM teamFacilitate SLM Systems Lifecycle Management team meetings, and producing reports and meeting minutes that will be communicated to the other EpiCX teamsResponsible for managing expectations with all the sub-teams within the SLM Systems Lifecycle Management umbrellaWorking closely with the Systems Lifecycle Management SLM lead in managing finances and other resourcing related activities within the SLM areaWork closely with the SLM lead and other program leads to ‘connect the dots’Support JIRA management within the program - help the team responsible for performing health checks on tools used in the programFacilitate the flow of information within the SLM team to drive ownership and empowermentQualifications:Bachelor’s degree in Science, Information Systems, or related field5+ years of experience in a similar role or context (PM in a pharmaceutical IT/Systems Lifecycle Management environment)Expert knowledge in JIRA project management Business domain knowledge for one or more of the following areas: Commercial Excellence, CRM, Multichannel, analytical/dashboards, finance/procurementWorking knowledge experience of CRM release management activitiesDemonstrated experience in managing large teams and programsHave we sparked your interest? Do not hesitate to go ahead and apply!
    • rotkreuz, zug
    • contract
    Are you an experienced Junior Technical Writer and you are looking for an exciting opportunity in the medical device sector?Then you should read on! In this position you will have the opportunity to work as a Junior Technical Writer on a contracting project.Tasks and responsibilities:Writes and updates end User, Service and Host Interface Documentation in English for the instruments and software while respecting project requirements and documentation standardsPlan, develops, organizes and edits operational procedures for user and service documentationIndependently collects information required to produce the documentsCooperates closely with service personnel, trainers, developers, and other subject matter expertsOrganizes documentation reviews by subject matter experts, and implements their input.Ensures that quality targets, timelines, and regulatory requirements are respectedQualifications:Degree in electronic or mechanical engineering, information technology, or natural sciences disciplineResilient and tenacious with a propensity to persevereProven experience in working in volatile, complex and ambiguous professional settings.Ability to quickly learn complex technical concepts and make them easily understandable in text, pictures and/or videosExcellent spoken and written command of English (native speaker or equivalent level)Have we sparked your interest? Do not hesitate to go ahead and apply!
    Are you an experienced Junior Technical Writer and you are looking for an exciting opportunity in the medical device sector?Then you should read on! In this position you will have the opportunity to work as a Junior Technical Writer on a contracting project.Tasks and responsibilities:Writes and updates end User, Service and Host Interface Documentation in English for the instruments and software while respecting project requirements and documentation standardsPlan, develops, organizes and edits operational procedures for user and service documentationIndependently collects information required to produce the documentsCooperates closely with service personnel, trainers, developers, and other subject matter expertsOrganizes documentation reviews by subject matter experts, and implements their input.Ensures that quality targets, timelines, and regulatory requirements are respectedQualifications:Degree in electronic or mechanical engineering, information technology, or natural sciences disciplineResilient and tenacious with a propensity to persevereProven experience in working in volatile, complex and ambiguous professional settings.Ability to quickly learn complex technical concepts and make them easily understandable in text, pictures and/or videosExcellent spoken and written command of English (native speaker or equivalent level)Have we sparked your interest? Do not hesitate to go ahead and apply!
    • geneva, genève
    • temporary
    Do you have a significant experience in project management defining strategy for different project development phase and therapeutic areas?Did you already lead cross functional teams in a global matrix environment?Are you known for your resilience and optimism, and looking for your next challenge?In this case, you should have a look at this opportunity!Our client, an international biotechnology industry based in the Geneva area, is looking for a:Director Global Project Lead (temporary contract - from September 2021 to March 2022) Functional Goal:Lead cross-functional development teams, define the program strategy in alignment with relevant governance bodies and supervise Project Managers in the execution of global development programs for the Biosimilar Unit. Lead the definition and implementation of the Target Product Profile with relevant functions and the overall product development strategy (integrated Development Plan, iDP). Lead the Global Program Leadership activities for several projects ensuring high standards of performance of the project teams and its individual members. By its central role for the programs, the person in charge is expected to make a critical contribution to the success of the Unit.Assume accountability for the delivery of either early or late stage projects from strategic perspective. Drive and lead the project teams from a strategic stand point. Provide critical cross-functional input into project strategy and ensure cohesion of the early or late stage project activities. Lead Project strategic initiatives.As member of the leadership team of the Program  Leadership and Managemnet  function, contribute to the strategy of the function.Act as deputy to Head of Program Leadership and Management when senior leadership input/attendance at meetings is required.Main Tasks:Key accountability:Define and get approved the strategy of either early or late stage portfolio in alignment with relevant government bodies. Active contribution in portfolio decisions.Accountable for driving the valuation of early or late stage projects, including external opportunities, leading the creation of assumptions and the alignment for project evaluation.Set priorities for either early or late stage project activities, escalate resource conflicts and contribute to resolution. Align resources needs and prioritization with government bodies. Drive definition of robust and focused Target Product Profiles (TPP) together with commercial function, generate comprehensive and consistent strategic development plans (iDP) with program team, drive definition of regulatory dossier strategy plans together with regulatory function. Contribute to the creation of storyline and key messages for the regulatory submissions (dossier and consultations); work with the regulatory lead to develop a global submission strategy; align the full development team to agreed strategy.Remain abreast of new developments in the biosimilar field, and contribute to building business insight and knowledge within the Biosimilars teamEnsure optimal steering of processes, and contribute to improvement of systems (processes, tools).Financial Dimension:Program budget accountability for several development projects.Prioritize program activities in line with the approved program strategy and plans; align resource needs with the biosimilar leadership members.Strategic Impact:Leading the development team, define the program strategy and driving the implementation of a global development program for the biosimilar unit with substantial impact on the success of the program and therefore the success of the whole unit.Preparation, creation:Drive development of a Target Product Profile (TPP).Based on the TPP, lead definition of development strategy, summarized in an iDP and ensure governance committee approval.Lead the development and the approval of a QTTP as quality target for the product.Execution:Lead Biosimilar Program Team (s) to ensure accountability and performance of the team and each function representative.Make necessary decisions for the product within the frame of the approved strategy or escalate to the governance committee if appropriate.Communicate transparently risk (changes in the risk profile), mitigations and options to ensure alignment of the Biosimilar unit behind the product strategy.Lead the creation of storyline and key messages for the regulatory dossier; work with the regulatory lead to develop a global submission strategy including submission plan.Support: Leading Portfolio Evaluation at project level.Support Business Development and Alliance Management in evaluation of opportunities and due diligence activities and in maintaining efficient working relationships with external partners.Cooperation with internal and external stakeholders:All members of the biosimilars governance committees and functions represented in the Project Team.Head of functions within biosimilar unit.R&D, Controlling, Finance, Portfolio, Manufacturing.Regulatory agencies; CROs, CMO and licensing partners. Qualification profile:Education:Advanced scientific/business degree with 10+ years’ experience in biopharma/biotech industry.Competencies and skills:Excellent organizational skills a must.Strategic orientation, leadership and management competencies (problem solving, influencing and decision making, driving teams to deliverables, …)Entrepreneurial spirit and action/results driven.Ability to critically evaluate scientific data obtained at different stages of development.Excellent communication skills, both oral and written.Strong interpersonal, networking and relationship skills required.Dynamic, energetic and positive mindset.Must be proficient with Microsoft Office programs and project management tools & concepts.Languages:Fluency in English essential, both oral and written; additional languages (German or French) are an asset.Work experience:Seniority in Program Leadership with minimum 5 years on complex projects having dealt with different project development phase and therapeutic areas.Demonstrated success operating in a global matrix organization with the full breadth of functions contributing to drug development.Experienced working in the field of biosimilars or biologics.Advanced knowledge of project management principles.if you recognize yourself in this ad, don't wait any longer and apply now! 
    Do you have a significant experience in project management defining strategy for different project development phase and therapeutic areas?Did you already lead cross functional teams in a global matrix environment?Are you known for your resilience and optimism, and looking for your next challenge?In this case, you should have a look at this opportunity!Our client, an international biotechnology industry based in the Geneva area, is looking for a:Director Global Project Lead (temporary contract - from September 2021 to March 2022) Functional Goal:Lead cross-functional development teams, define the program strategy in alignment with relevant governance bodies and supervise Project Managers in the execution of global development programs for the Biosimilar Unit. Lead the definition and implementation of the Target Product Profile with relevant functions and the overall product development strategy (integrated Development Plan, iDP). Lead the Global Program Leadership activities for several projects ensuring high standards of performance of the project teams and its individual members. By its central role for the programs, the person in charge is expected to make a critical contribution to the success of the Unit.Assume accountability for the delivery of either early or late stage projects from strategic perspective. Drive and lead the project teams from a strategic stand point. Provide critical cross-functional input into project strategy and ensure cohesion of the early or late stage project activities. Lead Project strategic initiatives.As member of the leadership team of the Program  Leadership and Managemnet  function, contribute to the strategy of the function.Act as deputy to Head of Program Leadership and Management when senior leadership input/attendance at meetings is required.Main Tasks:Key accountability:Define and get approved the strategy of either early or late stage portfolio in alignment with relevant government bodies. Active contribution in portfolio decisions.Accountable for driving the valuation of early or late stage projects, including external opportunities, leading the creation of assumptions and the alignment for project evaluation.Set priorities for either early or late stage project activities, escalate resource conflicts and contribute to resolution. Align resources needs and prioritization with government bodies. Drive definition of robust and focused Target Product Profiles (TPP) together with commercial function, generate comprehensive and consistent strategic development plans (iDP) with program team, drive definition of regulatory dossier strategy plans together with regulatory function. Contribute to the creation of storyline and key messages for the regulatory submissions (dossier and consultations); work with the regulatory lead to develop a global submission strategy; align the full development team to agreed strategy.Remain abreast of new developments in the biosimilar field, and contribute to building business insight and knowledge within the Biosimilars teamEnsure optimal steering of processes, and contribute to improvement of systems (processes, tools).Financial Dimension:Program budget accountability for several development projects.Prioritize program activities in line with the approved program strategy and plans; align resource needs with the biosimilar leadership members.Strategic Impact:Leading the development team, define the program strategy and driving the implementation of a global development program for the biosimilar unit with substantial impact on the success of the program and therefore the success of the whole unit.Preparation, creation:Drive development of a Target Product Profile (TPP).Based on the TPP, lead definition of development strategy, summarized in an iDP and ensure governance committee approval.Lead the development and the approval of a QTTP as quality target for the product.Execution:Lead Biosimilar Program Team (s) to ensure accountability and performance of the team and each function representative.Make necessary decisions for the product within the frame of the approved strategy or escalate to the governance committee if appropriate.Communicate transparently risk (changes in the risk profile), mitigations and options to ensure alignment of the Biosimilar unit behind the product strategy.Lead the creation of storyline and key messages for the regulatory dossier; work with the regulatory lead to develop a global submission strategy including submission plan.Support: Leading Portfolio Evaluation at project level.Support Business Development and Alliance Management in evaluation of opportunities and due diligence activities and in maintaining efficient working relationships with external partners.Cooperation with internal and external stakeholders:All members of the biosimilars governance committees and functions represented in the Project Team.Head of functions within biosimilar unit.R&D, Controlling, Finance, Portfolio, Manufacturing.Regulatory agencies; CROs, CMO and licensing partners. Qualification profile:Education:Advanced scientific/business degree with 10+ years’ experience in biopharma/biotech industry.Competencies and skills:Excellent organizational skills a must.Strategic orientation, leadership and management competencies (problem solving, influencing and decision making, driving teams to deliverables, …)Entrepreneurial spirit and action/results driven.Ability to critically evaluate scientific data obtained at different stages of development.Excellent communication skills, both oral and written.Strong interpersonal, networking and relationship skills required.Dynamic, energetic and positive mindset.Must be proficient with Microsoft Office programs and project management tools & concepts.Languages:Fluency in English essential, both oral and written; additional languages (German or French) are an asset.Work experience:Seniority in Program Leadership with minimum 5 years on complex projects having dealt with different project development phase and therapeutic areas.Demonstrated success operating in a global matrix organization with the full breadth of functions contributing to drug development.Experienced working in the field of biosimilars or biologics.Advanced knowledge of project management principles.if you recognize yourself in this ad, don't wait any longer and apply now! 
    • yverdon-les-bains, vaud
    • permanent
    Nous recherchons pour notre client, actif dans le medical device, un Quality Engineer. Il s'agit d'une société suisse située pas loin de Orbe.Vos responsabilités: Vous allez définir, tester et implémenter des méthodes de mesure et de contrôle.Vous exécutez la calibration des instruments de mesure en interne et gérez les calibrations faites en externe.Vous programmez des machines de mesure tridimensionnel (MMT- 3D).Vous définissez et déployez des stratégies de contrôle pour les nouveaux produits.Vous analysez et évaluez les non-conformités produit-process. Vous assistez le département product engineering en mettant à sa disposition des solutions de mesure/ analyse.Vous participez à l’amélioration continue  pour les méthodes de mesure. Vous analysez des données et la performance opérationnelle des instruments de contrôle.Votre profil: Vous êtes ingénieur mécanique ou ingénieur sciences des matériaux.Vous avez au moins 3 ans d’expériences sur un site de production industriel de préférence en medical device.Vous avez de l’expérience en programmation MMT.Vous êtes autonome, avez le sens des responsabilités et avez une force de proposition.Vous avez un esprit analytique et une capacité rédactionnelle. Vous avez une bonne connaissance de microsoft office, minitab et CAO.Vous êtes familier avec les outils de qualité amélioration continue PDCA, CAPA, DMAIC.Vous parlez très bien le français et l’anglais.Offre: Nous vous offrons un CDI dans une société dynamique et familiale. 
    Nous recherchons pour notre client, actif dans le medical device, un Quality Engineer. Il s'agit d'une société suisse située pas loin de Orbe.Vos responsabilités: Vous allez définir, tester et implémenter des méthodes de mesure et de contrôle.Vous exécutez la calibration des instruments de mesure en interne et gérez les calibrations faites en externe.Vous programmez des machines de mesure tridimensionnel (MMT- 3D).Vous définissez et déployez des stratégies de contrôle pour les nouveaux produits.Vous analysez et évaluez les non-conformités produit-process. Vous assistez le département product engineering en mettant à sa disposition des solutions de mesure/ analyse.Vous participez à l’amélioration continue  pour les méthodes de mesure. Vous analysez des données et la performance opérationnelle des instruments de contrôle.Votre profil: Vous êtes ingénieur mécanique ou ingénieur sciences des matériaux.Vous avez au moins 3 ans d’expériences sur un site de production industriel de préférence en medical device.Vous avez de l’expérience en programmation MMT.Vous êtes autonome, avez le sens des responsabilités et avez une force de proposition.Vous avez un esprit analytique et une capacité rédactionnelle. Vous avez une bonne connaissance de microsoft office, minitab et CAO.Vous êtes familier avec les outils de qualité amélioration continue PDCA, CAPA, DMAIC.Vous parlez très bien le français et l’anglais.Offre: Nous vous offrons un CDI dans une société dynamique et familiale. 
    • luterbach, solothurn
    • contract
    Description:Responsible for Quality oversight to review and approval of validation and engineering life cycle documents (URS, FS, RTM, RA, DS, configuration spec, drawings etc), test protocols, CAPAs, deviations, change controls, work orders and any technical documentation in the scope of Facilities, utilities, equipment and Execution System (global and local computerized systems) to enable start up, commissioning and qualification of new Large Scale Manufacturing facility. Furthermore advice the project groups as appropriate and be an active member of the groups where the quality input is needed.Additional Info:This position requires co-operation with people at every level of the organization and from multiple functions, including engineering, automation, validation, Manufacturing personnel, SME’s on equipment and knowledge of biotechnology API production.Good communication skills in English, verbally and written. Technically orientated role including experience of the validation of laboratory, production equipment and knowledge of production methodology involved in biopharmaceutical drug substance production.Self-driven and take ownership and responsibility for own assignments. Value teamwork at all levels, performs work with an open-mind and ability to value input from colleagues and peers. Able to drive discussion to solve problems with cross functional teams.Be confident in making technical decisions. In addition must be able to prioritize tasks, be flexible and able to keep many activities running at a time.
    Description:Responsible for Quality oversight to review and approval of validation and engineering life cycle documents (URS, FS, RTM, RA, DS, configuration spec, drawings etc), test protocols, CAPAs, deviations, change controls, work orders and any technical documentation in the scope of Facilities, utilities, equipment and Execution System (global and local computerized systems) to enable start up, commissioning and qualification of new Large Scale Manufacturing facility. Furthermore advice the project groups as appropriate and be an active member of the groups where the quality input is needed.Additional Info:This position requires co-operation with people at every level of the organization and from multiple functions, including engineering, automation, validation, Manufacturing personnel, SME’s on equipment and knowledge of biotechnology API production.Good communication skills in English, verbally and written. Technically orientated role including experience of the validation of laboratory, production equipment and knowledge of production methodology involved in biopharmaceutical drug substance production.Self-driven and take ownership and responsibility for own assignments. Value teamwork at all levels, performs work with an open-mind and ability to value input from colleagues and peers. Able to drive discussion to solve problems with cross functional teams.Be confident in making technical decisions. In addition must be able to prioritize tasks, be flexible and able to keep many activities running at a time.
    • martigny, valais
    • permanent
    Vous êtes un Automaticien et vous parlez Français et  Allemand ?Toujours prêt à construire et délivrer les meilleures solutions ? Alors peut-être que nous pourrions discuter de cette opportunité ! Que ferez-vous?Participer à la mise en service des équipements et autres installations techniques en lien avec l’automation en assurant le bon fonctionnement des équipements automation (maintenances, mise à jour des programmes…).Assurer les dépannages et les investigations correspondantes et contribuer à la diminution des pannes dues à l'automation (analyses de causes, étude des récurrences, proposition de plan d’action et mise en œuvre). Que recherchent-ils ?Vous êtes AutomaticienVous maîtrisez totalement la programmation Siemens S7, TIA Portal et WinccParlez Français et Allemand  Vous pensez pouvoir vous épanouir au sein de ce type d'univers ? N’hésitez surtout pas à postuler!
    Vous êtes un Automaticien et vous parlez Français et  Allemand ?Toujours prêt à construire et délivrer les meilleures solutions ? Alors peut-être que nous pourrions discuter de cette opportunité ! Que ferez-vous?Participer à la mise en service des équipements et autres installations techniques en lien avec l’automation en assurant le bon fonctionnement des équipements automation (maintenances, mise à jour des programmes…).Assurer les dépannages et les investigations correspondantes et contribuer à la diminution des pannes dues à l'automation (analyses de causes, étude des récurrences, proposition de plan d’action et mise en œuvre). Que recherchent-ils ?Vous êtes AutomaticienVous maîtrisez totalement la programmation Siemens S7, TIA Portal et WinccParlez Français et Allemand  Vous pensez pouvoir vous épanouir au sein de ce type d'univers ? N’hésitez surtout pas à postuler!
    • fribourg, fribourg
    • permanent
    Vous êtes Team Leader Conceptions d'outils Mécaniques - Bilingue Français/Allemand ? La conception et la fabrication des outils n'ont aucun secret pour vous ? Alors peut-être que nous pourrions discuter de cette opportunité ? Mon client est une société évoluant dans le domaine de l'industrie qui est localisée à Fribourg. Si vous intégrez leurs équipes, vous bénéficierez de nombreux avantages notamment le droit de profiter du restaurant d'entreprise, une place de parking, un 13ème salaire, 5 semaines de congés.... Que ferez-vous ?Votre rôle sera principalement d'assurer le développement et la fabrication d'outils mécaniques (moules...) afin d’assurer la production de nouveaux produits.Vous aurez aussi en charge la gestion de l'équipe de 3 personnes. Que recherchent-ils ?- Idéalement, vous avez 3/5 ans d'expérience sur un poste similaire- Vous avez de bonnes connaissances dans les processus d'industrialisation.- Vous parlez Français et Allemand.- Vous maîtrisez SAP Vous pensez pouvoir vous épanouir au sein de ce type d'univers ? N’hésitez surtout pas à postuler !
    Vous êtes Team Leader Conceptions d'outils Mécaniques - Bilingue Français/Allemand ? La conception et la fabrication des outils n'ont aucun secret pour vous ? Alors peut-être que nous pourrions discuter de cette opportunité ? Mon client est une société évoluant dans le domaine de l'industrie qui est localisée à Fribourg. Si vous intégrez leurs équipes, vous bénéficierez de nombreux avantages notamment le droit de profiter du restaurant d'entreprise, une place de parking, un 13ème salaire, 5 semaines de congés.... Que ferez-vous ?Votre rôle sera principalement d'assurer le développement et la fabrication d'outils mécaniques (moules...) afin d’assurer la production de nouveaux produits.Vous aurez aussi en charge la gestion de l'équipe de 3 personnes. Que recherchent-ils ?- Idéalement, vous avez 3/5 ans d'expérience sur un poste similaire- Vous avez de bonnes connaissances dans les processus d'industrialisation.- Vous parlez Français et Allemand.- Vous maîtrisez SAP Vous pensez pouvoir vous épanouir au sein de ce type d'univers ? N’hésitez surtout pas à postuler !
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