73 jobs found in Basel, Basel-Stadt

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    • basel, basel-stadt
    • temporary
    For Lonza Drug Product Services (DPS), a successful Contract Development and Manufacturing Organization (CDMO) branch, located in Basel, Switzerland Randstad (Switzerland) AG has exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join Lonza by applying for the position as Senior Technology Transfer Lead. This position is temporary until end of the year 2021. Key responsibilities:Ensure all activities are performed according to current quality, regulatory and health and safety standards. Manage technical activities for drug product transfers from clinical development to first commercial launch of assigned projectsDefine and monitor project scope, timing and progressLead setup, scale-up and implementation of the technical drug product manufacturing processes at GMP DP manufacturing site(s) and provide technical on-site supportResponsible for process implementation and technical transfer documentationDrive GMP change management strategy of assigned projects as well as initiate and manage GMP change control in systemSupport preparation of regulatory documentationLead and support critical GMP product / process deviations and corresponding implementation of corrective/preventive actions (CAPAs)Perform/support GMP and HA regulatory inspections and audits e.g. customer audits, PAI of assigned projectsEnsure all activities are performed according to current standards (Good Manufacturing Practice (cGMP), Health Safety Environment (HSE), Regulatory, etc.)Enable innovation and technical strategy projects, generate IP and contribute to scientific publications and conference talks, and evaluate and implement of new methods and technologies
    For Lonza Drug Product Services (DPS), a successful Contract Development and Manufacturing Organization (CDMO) branch, located in Basel, Switzerland Randstad (Switzerland) AG has exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join Lonza by applying for the position as Senior Technology Transfer Lead. This position is temporary until end of the year 2021. Key responsibilities:Ensure all activities are performed according to current quality, regulatory and health and safety standards. Manage technical activities for drug product transfers from clinical development to first commercial launch of assigned projectsDefine and monitor project scope, timing and progressLead setup, scale-up and implementation of the technical drug product manufacturing processes at GMP DP manufacturing site(s) and provide technical on-site supportResponsible for process implementation and technical transfer documentationDrive GMP change management strategy of assigned projects as well as initiate and manage GMP change control in systemSupport preparation of regulatory documentationLead and support critical GMP product / process deviations and corresponding implementation of corrective/preventive actions (CAPAs)Perform/support GMP and HA regulatory inspections and audits e.g. customer audits, PAI of assigned projectsEnsure all activities are performed according to current standards (Good Manufacturing Practice (cGMP), Health Safety Environment (HSE), Regulatory, etc.)Enable innovation and technical strategy projects, generate IP and contribute to scientific publications and conference talks, and evaluate and implement of new methods and technologies
    • basel, basel-stadt
    • temp to perm
    Bist du eine flexible, belastbare und engagierte Person? Verfügst du über ein Auge fürs Detail und kannst es dir vorstellen wieder in der Gastronomie zu arbeiten? Zur Ergänzung des gut eingespielten Teams unseres Kunden suchen wir per sofort:Servicemitarbeiter (m/w/d) in Basel 100%Deine Aufgaben:Gäste beraten und Bestellungen aufnehmenGetränke und Speisen fachgerecht servierenGäste-Rechnungen erstellen und einkassierenTägliches Mise en Place für das ganze Restaurant erstellenReinigungsarbeiten gemäss dem Hygienekonzept ausführen
    Bist du eine flexible, belastbare und engagierte Person? Verfügst du über ein Auge fürs Detail und kannst es dir vorstellen wieder in der Gastronomie zu arbeiten? Zur Ergänzung des gut eingespielten Teams unseres Kunden suchen wir per sofort:Servicemitarbeiter (m/w/d) in Basel 100%Deine Aufgaben:Gäste beraten und Bestellungen aufnehmenGetränke und Speisen fachgerecht servierenGäste-Rechnungen erstellen und einkassierenTägliches Mise en Place für das ganze Restaurant erstellenReinigungsarbeiten gemäss dem Hygienekonzept ausführen
    • basel, basel-stadt
    • temporary
    Wenn du dir neben deinem Studium etwas dazu verdienen willst oder nach einer Möglichkeit suchst dein Taschengeld etwas aufzustockenDann bist du genau richtig bei uns!Für unseren Kunden suchen wir flexible und motivierteServicemitarbeiter (m/w)Hauptaufgaben:bedienen und beraten der Gästeführen einer eigenen Stationmithilfe bei Banketten, Caterings, Events oder in Kantinenmise en place Aufgabenallgemeine Aufräum- und Reinigungsarbeiten
    Wenn du dir neben deinem Studium etwas dazu verdienen willst oder nach einer Möglichkeit suchst dein Taschengeld etwas aufzustockenDann bist du genau richtig bei uns!Für unseren Kunden suchen wir flexible und motivierteServicemitarbeiter (m/w)Hauptaufgaben:bedienen und beraten der Gästeführen einer eigenen Stationmithilfe bei Banketten, Caterings, Events oder in Kantinenmise en place Aufgabenallgemeine Aufräum- und Reinigungsarbeiten
    • basel, basel-stadt
    • temporary
    We are looking for a Demand Planning - Center of Excellence Specialist (m/f/d) for Lonza AG (100%). This is a temporary position for 24 months. The position is based in Basel, remote work is possible too. Today, Lonza is a global leader in life sciences operating across three continents. While Lonza works in science, there's no magic formula to how they do it. Their greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, they let their people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work Lonza wants to be part of. Key responsibilities:Accountable for ensuring Demand Planning, Management standard processes are followedSupport Global Lead Demand in IBP DP development Drive the implementation of approved Demand Planning blueprints (organizations, processes, activities, roles and responsibilities) Deploy Demand Planning processes, policies and tools through communication and training to enable continuous improvement of Division KPIsEnsure alignment with S&OP and Supply Planning Global Leads Expert knowledge in S&OP, support program deployment and ability to deliver training Deliver training to new team members, liaise with CoE team on training improvementCertify the IBP tool is being utilized fully and properly within LPB GroupOngoing responsibility for the development and maintenance of the Demand Planning community fostering knowledge and best practice sharingReview Business and Demand related KPIs, use as basis for planning improvement initiatives contributing to continuous improvements across the divisions
    We are looking for a Demand Planning - Center of Excellence Specialist (m/f/d) for Lonza AG (100%). This is a temporary position for 24 months. The position is based in Basel, remote work is possible too. Today, Lonza is a global leader in life sciences operating across three continents. While Lonza works in science, there's no magic formula to how they do it. Their greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, they let their people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work Lonza wants to be part of. Key responsibilities:Accountable for ensuring Demand Planning, Management standard processes are followedSupport Global Lead Demand in IBP DP development Drive the implementation of approved Demand Planning blueprints (organizations, processes, activities, roles and responsibilities) Deploy Demand Planning processes, policies and tools through communication and training to enable continuous improvement of Division KPIsEnsure alignment with S&OP and Supply Planning Global Leads Expert knowledge in S&OP, support program deployment and ability to deliver training Deliver training to new team members, liaise with CoE team on training improvementCertify the IBP tool is being utilized fully and properly within LPB GroupOngoing responsibility for the development and maintenance of the Demand Planning community fostering knowledge and best practice sharingReview Business and Demand related KPIs, use as basis for planning improvement initiatives contributing to continuous improvements across the divisions
    • basel, basel-stadt
    • temp to perm
    Für wiederkehrende und längere Einsätze und unserem Pool suchen wirKoch / KöchinAufgabenZubereitung und anrichten einzelner Gerichte sowie ganzer Menüs und à la carteVerantwortung auf allen PostenKontrolle und Verwaltung des WarenbestandsVerantwortung für die Einhaltung der strengen Hygienevorschriften gemäss HACCP
    Für wiederkehrende und längere Einsätze und unserem Pool suchen wirKoch / KöchinAufgabenZubereitung und anrichten einzelner Gerichte sowie ganzer Menüs und à la carteVerantwortung auf allen PostenKontrolle und Verwaltung des WarenbestandsVerantwortung für die Einhaltung der strengen Hygienevorschriften gemäss HACCP
    • basel, basel-stadt
    • permanent
    Für unseren Kunden im Raum Basel suchen wir genau dich ab sofort oder nach Vereinbarung einen:Kältetechniker (m/w/d)Deine Hauptaufgaben:Instandhaltung und Umbau von kältetechnischen Anlagen und SystemenStörungsbehebungen an kältetechnischen AnlagenDurchführung der periodischen WartungenPlanung, Kontrolle und Ausführung aller notwendigen Arbeiten in Zusammenarbeit mit den zuständigen internen und kundenseitigen StellenErstellen der notwendigen Dokumentationen, Rapporte etc.Leisten von Pikettdienst
    Für unseren Kunden im Raum Basel suchen wir genau dich ab sofort oder nach Vereinbarung einen:Kältetechniker (m/w/d)Deine Hauptaufgaben:Instandhaltung und Umbau von kältetechnischen Anlagen und SystemenStörungsbehebungen an kältetechnischen AnlagenDurchführung der periodischen WartungenPlanung, Kontrolle und Ausführung aller notwendigen Arbeiten in Zusammenarbeit mit den zuständigen internen und kundenseitigen StellenErstellen der notwendigen Dokumentationen, Rapporte etc.Leisten von Pikettdienst
    • basel, basel-stadt
    • temp to perm
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen hoch motivierten Betriebselektriker oder Automatiker. (m/w)Deine Aufgaben:Störungsanalyse, Fehlerbehebung und Reparatur an Produktionsanlagen und InfrastrukturUmsetzung von technischen Optimierungen (Steuerung- , Regel und Antriebstechnik)Projektmitarbeit bei Umbauten, Neuinstallationen und Inbetriebnahmen von Maschinen und AnlagenNachführen von technischen Unterlagen und Schemas
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen hoch motivierten Betriebselektriker oder Automatiker. (m/w)Deine Aufgaben:Störungsanalyse, Fehlerbehebung und Reparatur an Produktionsanlagen und InfrastrukturUmsetzung von technischen Optimierungen (Steuerung- , Regel und Antriebstechnik)Projektmitarbeit bei Umbauten, Neuinstallationen und Inbetriebnahmen von Maschinen und AnlagenNachführen von technischen Unterlagen und Schemas
    • basel, basel-stadt
    • contract
    Are you an experienced Project Manager in IT and you are looking for a long-term contracting challenge in Basel? Then do not hesitate to apply!This Senior Project Support Management position will be responsible for co-managing the main activities on a global scale and supporting the integration of this project with other program initiatives. Together with this, the position will be very focused on the End-to-End integration of the overall solution across the different work streams and for that reason the appropriate candidate must have excellent communication and socialization skills to build a strong network in Aspire and outside Aspire.his position is also expected to provide timely status reports to all stakeholders and escalate issues to the appropriate management level. Additionally, this position must effectively manage the projects across global locations and time zones and be able to travel internationally as needed. Tasks and responsibilities:Execution of multiple initiatives across the Global Template project and beyond, including interaction with other multidisciplinary teamsCoordinate the project activities with 3rd party software vendor and/or System Integrator resources as needed to ensure project delivery and the different work streams when requiredManage relationships with various technology and business communities to achieve project objectivesFacilitate project management activities across the entire project management methodologyTrack progress of activities against baseline scheduleConduct risk management planning, identification, analysis and monitoring on projects, formulating risk mitigation strategies and recommend solutionsManage the processes required to ensure timely and appropriate generation, collection, distribution, storage, retrieval, and ultimate disposition of project information and documentation necessary for successful communications across all stakeholders and any required updates to living system documents for validated systemsActively seek opportunities to and mentor to other project managersPromote and hold multidisciplinary conversations/discussion between different work streams and teams outside ASPIRESupport the definition and implementation of Data Governance around Aspire and group wiseSupport the implementation of an integrated view of the business through E2E scenarios following the business guidelinesSuggest improvements where necessary / appropriate to improve operational efficienciesEngage with interested parties within the company, verify business use cases and provide expert consultancy. Guide new projects and help our internal customers to understand how they benefit the mostPartner actively with Business as well as IT Business Partners Must haves:Min. Bachelor's degree in Computer Sciences, Life Sciences, Business, Analytics and Reporting; or equivalent work experience or any other higher certification 10+ years of experience as a successful Information Technology Project Manager with a strong IT BackgroundExperience in using structured project management processes with deep understanding of various SDLCs (Waterfall, Agile, iterative, etc.), SAP A&R technology and solutions and new Analytics implementation challenges  Experience in Change Management is needed Proven leadership abilities, experience in leading multifunctional teams Excellent oral and written communication skills English fluent (C1), German is a plusAbility to manage relationships with various technology and business communities to achieve project objectivesVery experience communicator which is used to talk with different stakeholders on different levels and feels confident in project setupsProven ability to obtain results in a global, matrix environmentDemonstrated success communicating across a variety of audiences, including business people and technologists (both up and down the organization)Exceptional listening, problem solving, negotiation, and facilitation skillsDemonstrated success handling initiatives of significant complexity and risk Nice to have:Experience within the Pharmaceutical and BioTech industryExperience managing IT projects in GxP validated environmentsCertification as Project Manager or Scrum Master is a plus If this role excites you, and you feel you could take this next challenge in your career, then I look forward to receiving your application today.
    Are you an experienced Project Manager in IT and you are looking for a long-term contracting challenge in Basel? Then do not hesitate to apply!This Senior Project Support Management position will be responsible for co-managing the main activities on a global scale and supporting the integration of this project with other program initiatives. Together with this, the position will be very focused on the End-to-End integration of the overall solution across the different work streams and for that reason the appropriate candidate must have excellent communication and socialization skills to build a strong network in Aspire and outside Aspire.his position is also expected to provide timely status reports to all stakeholders and escalate issues to the appropriate management level. Additionally, this position must effectively manage the projects across global locations and time zones and be able to travel internationally as needed. Tasks and responsibilities:Execution of multiple initiatives across the Global Template project and beyond, including interaction with other multidisciplinary teamsCoordinate the project activities with 3rd party software vendor and/or System Integrator resources as needed to ensure project delivery and the different work streams when requiredManage relationships with various technology and business communities to achieve project objectivesFacilitate project management activities across the entire project management methodologyTrack progress of activities against baseline scheduleConduct risk management planning, identification, analysis and monitoring on projects, formulating risk mitigation strategies and recommend solutionsManage the processes required to ensure timely and appropriate generation, collection, distribution, storage, retrieval, and ultimate disposition of project information and documentation necessary for successful communications across all stakeholders and any required updates to living system documents for validated systemsActively seek opportunities to and mentor to other project managersPromote and hold multidisciplinary conversations/discussion between different work streams and teams outside ASPIRESupport the definition and implementation of Data Governance around Aspire and group wiseSupport the implementation of an integrated view of the business through E2E scenarios following the business guidelinesSuggest improvements where necessary / appropriate to improve operational efficienciesEngage with interested parties within the company, verify business use cases and provide expert consultancy. Guide new projects and help our internal customers to understand how they benefit the mostPartner actively with Business as well as IT Business Partners Must haves:Min. Bachelor's degree in Computer Sciences, Life Sciences, Business, Analytics and Reporting; or equivalent work experience or any other higher certification 10+ years of experience as a successful Information Technology Project Manager with a strong IT BackgroundExperience in using structured project management processes with deep understanding of various SDLCs (Waterfall, Agile, iterative, etc.), SAP A&R technology and solutions and new Analytics implementation challenges  Experience in Change Management is needed Proven leadership abilities, experience in leading multifunctional teams Excellent oral and written communication skills English fluent (C1), German is a plusAbility to manage relationships with various technology and business communities to achieve project objectivesVery experience communicator which is used to talk with different stakeholders on different levels and feels confident in project setupsProven ability to obtain results in a global, matrix environmentDemonstrated success communicating across a variety of audiences, including business people and technologists (both up and down the organization)Exceptional listening, problem solving, negotiation, and facilitation skillsDemonstrated success handling initiatives of significant complexity and risk Nice to have:Experience within the Pharmaceutical and BioTech industryExperience managing IT projects in GxP validated environmentsCertification as Project Manager or Scrum Master is a plus If this role excites you, and you feel you could take this next challenge in your career, then I look forward to receiving your application today.
    • basel, basel-stadt
    • permanent
    Für unseren Kunden suchen per sofort einen System Administrator in der Nähe von Basel.Deine Aufgaben:Administration, Installation, Erweiterungen, Betreuung und Überwachung der ICT InfrastrukturBearbeitung des Support und TroubleshootingErstellen und Nachführen der DokumentationMitgestaltung des PortfoliosDein Profil:Abgeschlossene Lehre oder Studium in der Systemtechnik (Quereinsteiger mit 3+ Jahren Erfahrung sind herzlich Willkommen)Fundierte Kenntnisse mit Office 365Erfahrung mit Cloud LösungenFliessende Deutschkenntnisse werden vorausgesetztFührerausweis Kat. BSehen Sie sich zu mindestens 70% in dieser Position? Warten Sie nicht und senden Sie uns Ihre Bewerbung oder rufen Sie uns für weitere Informationen an.
    Für unseren Kunden suchen per sofort einen System Administrator in der Nähe von Basel.Deine Aufgaben:Administration, Installation, Erweiterungen, Betreuung und Überwachung der ICT InfrastrukturBearbeitung des Support und TroubleshootingErstellen und Nachführen der DokumentationMitgestaltung des PortfoliosDein Profil:Abgeschlossene Lehre oder Studium in der Systemtechnik (Quereinsteiger mit 3+ Jahren Erfahrung sind herzlich Willkommen)Fundierte Kenntnisse mit Office 365Erfahrung mit Cloud LösungenFliessende Deutschkenntnisse werden vorausgesetztFührerausweis Kat. BSehen Sie sich zu mindestens 70% in dieser Position? Warten Sie nicht und senden Sie uns Ihre Bewerbung oder rufen Sie uns für weitere Informationen an.
    • basel, basel-stadt
    • temporary
    For our client, a growing company in the pharmaceutical industry, we are looking for a :Planning Coordinator/Expert Location: BaselContract: Temporary for 6 months with possibility to extend or become permanentMain objective:This position is responsible to manage the operational planning incl. inbound flows (orders and shipments) and the associated tools/processes (incl. Artwork management). Acts as Super User in the management of the SAP setup (MM, IBP)Your Main Responsibilities:  Perform monthly supply planning operations in close cooperation with the Global Planning Manager (in Excel and SAP IBP)Supply PO placement with suppliers and follow upManagement of inbound flows incl. organization of inbound shipments from supplier to HUBSuper User SAP (MM,IBP) supporting the SAP implementations and ensuring correct setup of SAP in collaboration with the business and ITMaintain SAP Master Data accuracyManage/support projects in the Supply Chain areaEnsure operationally with external Artwork Supplier and internal functions management of Artwork changesYour profile:University Degree in Supply Chain or very Supply Chain related functionsMin 3 years on hand experience as Planning Coordinator/Expert with intense exposure to SAP and Artwork creation, preferably in the pharmaceutical/Consumer Health businessVery strong analytical thinkingSelf-starter, able to work independently and picking up responsibility in a newly created Supply chainContinuous Improvement mindset.Ability to work accurately under pressureAbility to work in remote teamsSAP (IBP, MM)MS Excel (very good knowledge incl. creation of own complex reports/spreadsheets)Very good English (must have),French & Italian (asset) Please note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position 
    For our client, a growing company in the pharmaceutical industry, we are looking for a :Planning Coordinator/Expert Location: BaselContract: Temporary for 6 months with possibility to extend or become permanentMain objective:This position is responsible to manage the operational planning incl. inbound flows (orders and shipments) and the associated tools/processes (incl. Artwork management). Acts as Super User in the management of the SAP setup (MM, IBP)Your Main Responsibilities:  Perform monthly supply planning operations in close cooperation with the Global Planning Manager (in Excel and SAP IBP)Supply PO placement with suppliers and follow upManagement of inbound flows incl. organization of inbound shipments from supplier to HUBSuper User SAP (MM,IBP) supporting the SAP implementations and ensuring correct setup of SAP in collaboration with the business and ITMaintain SAP Master Data accuracyManage/support projects in the Supply Chain areaEnsure operationally with external Artwork Supplier and internal functions management of Artwork changesYour profile:University Degree in Supply Chain or very Supply Chain related functionsMin 3 years on hand experience as Planning Coordinator/Expert with intense exposure to SAP and Artwork creation, preferably in the pharmaceutical/Consumer Health businessVery strong analytical thinkingSelf-starter, able to work independently and picking up responsibility in a newly created Supply chainContinuous Improvement mindset.Ability to work accurately under pressureAbility to work in remote teamsSAP (IBP, MM)MS Excel (very good knowledge incl. creation of own complex reports/spreadsheets)Very good English (must have),French & Italian (asset) Please note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position 
    • basel, basel-stadt
    • temp to perm
    Für unseren Kunden im Raum Baselland suchen wir per sofort eine/n Lagermitarbeiter/in mit SUVA Staplerschein 100%Ihre Aufgaben:LagerwirtschaftungKommissionierung der WareEntgegennahme und Kontrolle der gelieferten WarenEinlagerung der WarenBereitstellung und Warenübergabe an unsere Kundschaft
    Für unseren Kunden im Raum Baselland suchen wir per sofort eine/n Lagermitarbeiter/in mit SUVA Staplerschein 100%Ihre Aufgaben:LagerwirtschaftungKommissionierung der WareEntgegennahme und Kontrolle der gelieferten WarenEinlagerung der WarenBereitstellung und Warenübergabe an unsere Kundschaft
    • basel, basel-stadt
    • permanent
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Rohschlosser (m/w/d) 100%Deine AufgabenEntwicklung und Fertigung von Rohrleitungen und Anlagen Verarbeiten von Stahl- & Edelstahlrohren Diverse Schweiß-Arbeiten
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Rohschlosser (m/w/d) 100%Deine AufgabenEntwicklung und Fertigung von Rohrleitungen und Anlagen Verarbeiten von Stahl- & Edelstahlrohren Diverse Schweiß-Arbeiten
    • basel, basel-stadt
    • permanent
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen motivierten Automobil-MechatronikerDeine Aufgaben:Service-,Reparatur-Diagnose-Arbeiten führst du nach Hersteller-Richtlinien gewissenhaft durch.Selbständige Überprüfung des Unterhaltes im Tram. Dabei erkennst du mögliche Störungen und behebst diese Sorgfältig.Du leistest einen hohen Beitrag zur Kundenzufriedenheit
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen motivierten Automobil-MechatronikerDeine Aufgaben:Service-,Reparatur-Diagnose-Arbeiten führst du nach Hersteller-Richtlinien gewissenhaft durch.Selbständige Überprüfung des Unterhaltes im Tram. Dabei erkennst du mögliche Störungen und behebst diese Sorgfältig.Du leistest einen hohen Beitrag zur Kundenzufriedenheit
    • basel, basel-stadt
    • permanent
    Für unseren Kunden suchen wir per sofort einen Network EngineerDeine Aufgaben:Konzept Erstellung und Umsetzung von Netzwerk und Security ProjektenPflege und Instandhaltung der KundennetzwerkeÜbernahme des Troubleshooting und Support Weiterentwicklung des PortfoliosDeine Kenntnisse:Abgeschlossene Lehre oder Studium im Bereich der Systemtechnik3+ Jahre BerufserfahrungErfahrung im Bereich Routing und SwitchingFundierte Kenntnisse mit WLAN und Firewall (Fortinet), CISCO und/oder ArubaFliessende Deutschkenntnisse werden vorausgesetztFührerausweis BSehen Sie sich zu mindestens 70% in dieser Position? Warten Sie nicht und senden Sie uns Ihre Bewerbung oder rufen Sie uns für weitere Informationen an.
    Für unseren Kunden suchen wir per sofort einen Network EngineerDeine Aufgaben:Konzept Erstellung und Umsetzung von Netzwerk und Security ProjektenPflege und Instandhaltung der KundennetzwerkeÜbernahme des Troubleshooting und Support Weiterentwicklung des PortfoliosDeine Kenntnisse:Abgeschlossene Lehre oder Studium im Bereich der Systemtechnik3+ Jahre BerufserfahrungErfahrung im Bereich Routing und SwitchingFundierte Kenntnisse mit WLAN und Firewall (Fortinet), CISCO und/oder ArubaFliessende Deutschkenntnisse werden vorausgesetztFührerausweis BSehen Sie sich zu mindestens 70% in dieser Position? Warten Sie nicht und senden Sie uns Ihre Bewerbung oder rufen Sie uns für weitere Informationen an.
    • basel, basel-stadt
    • contract
    For our pharmaceutical client in Basel, we are looking for a  Regulatory Affairs CMC ManagerStart: asapContract: until Dec 2021, with possibility of extensionJob Purpose:Under supervision, provide timely preparation of high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies.Major Activities:Author high-quality CMC documentation for HA submission, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle.Prepare CMC responses to health authority questions during development, registration and product lifecycle.Identify the required documentation for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelinesIdentify content, quality and/or timeliness issues with source documents, or any other potential authoring issues that may impact submission quality or timelines, as early as possible.5.Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends.6.Actively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learned.Establish and maintain sound working relationships with partners and customers.Assume activities in support of the general department such as DRAGON support, annual and product renewal writing, coordination/collection/storage of source documentation needed for direct submission to HAs, other database entry activities (specialized department functions).Ideal Background:Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent. Desirable: Advanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent.Languages: Fluent English required (oral and written).Experience/Professional requirement:Regulatory experience preferred, and/or experience in drug/biopharmaceuticalsWorking knowledge of chemistry/biotechnology, analytics or pharmaceutical technology. Knowledge of the drug development process desirable. Ability to critically evaluate data from a broad range of scientific disciplines.Knowledge/experience of regulations, guidelines for NCEs and product life cycle maintenance desirable.Ability to work successfully with extended, multinational project teams and coordinate activities simultaneously on multiple projects under pressure of time and workload.Effective planning, organizational and interpersonal skills.Reasonable approach to risk assessment.Excellent written/spoken communication and negotiation skills.
    For our pharmaceutical client in Basel, we are looking for a  Regulatory Affairs CMC ManagerStart: asapContract: until Dec 2021, with possibility of extensionJob Purpose:Under supervision, provide timely preparation of high quality CMC regulatory documentation and support to contribute to global regulatory submissions and strategies.Major Activities:Author high-quality CMC documentation for HA submission, with support and guidance, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements throughout project lifecycle.Prepare CMC responses to health authority questions during development, registration and product lifecycle.Identify the required documentation for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelinesIdentify content, quality and/or timeliness issues with source documents, or any other potential authoring issues that may impact submission quality or timelines, as early as possible.5.Keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends.6.Actively participate as a member of the global team by contributing to the regulatory strategy, identifying the critical issues and lessons learned.Establish and maintain sound working relationships with partners and customers.Assume activities in support of the general department such as DRAGON support, annual and product renewal writing, coordination/collection/storage of source documentation needed for direct submission to HAs, other database entry activities (specialized department functions).Ideal Background:Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent. Desirable: Advanced Degree in Science (Chemistry, Pharmacy, Biochemistry, Biotechnology) or equivalent.Languages: Fluent English required (oral and written).Experience/Professional requirement:Regulatory experience preferred, and/or experience in drug/biopharmaceuticalsWorking knowledge of chemistry/biotechnology, analytics or pharmaceutical technology. Knowledge of the drug development process desirable. Ability to critically evaluate data from a broad range of scientific disciplines.Knowledge/experience of regulations, guidelines for NCEs and product life cycle maintenance desirable.Ability to work successfully with extended, multinational project teams and coordinate activities simultaneously on multiple projects under pressure of time and workload.Effective planning, organizational and interpersonal skills.Reasonable approach to risk assessment.Excellent written/spoken communication and negotiation skills.
    • basel, basel-stadt
    • contract
    Do you want to work in a big pharmaceutical company? Do you have at least 3 years experience in the laboratory working on in-vitro immune cell assays? You should then read the following lines!Our client, based in Basel, is looking for a Laboratory Associate for a one year mission. Background:The Immunosafety team supports the whole portfolio with questions of unwanted immune activation, unwanted immunosuppression, risk of anti-drug antibodies and immuno PD in the pre-clinical space. As a research associate you will support us on this mission with a broad set of immunology assays. General information:• Start date: 01.10.2021• Latest start date: 01.11.2021• End date: 1 year after start• Extension: No• Location: Basel• Work load: 100%• Department: Immunosafety (PNBPD)• Team: 25 team members Tasks and responsibilities:• Address fundamental scientific questions, be responsible for the design and execution of experimental work, and conduct data analysis• Develop and run in vitro immune cell assays (cytokine release assays, purification and cultivation of PBMC, purification differentiation of immune cell subsets, differentiation and activation assays)• Will routinely independently set-up and perform multi-color flow cytometry experiments• Characterize compounds in different cellular assays• Share knowledge by active collaboration with other scientists and associates inside and outside the group• Attend and present at internal meetings• Keep accurate electronic records• Contribute to the organization of the laboratory as assigned Must haves:• Vocational training or Bachelor Degree in Cell Biology, Molecular Biology, Immunology, Pharmacology (*****)• Min. 3 years experience in a research lab with a focus on in-vitro immune cell assays, including whole blood and PBMC isolation, cultivation and differentiation (****)• Prior experience in cytokine analysis (ELISA or multiplex methods) (***)• Excellent experience in the design and troubleshooting of multi-color (8+ markers) flow cytometry panels on BD instruments (FACS / Durchflusszytometrie) (***)• In vivo experience with mice and LTK1 certificate (***)• Good skills in data analysis software (FlowJo, Prism) and in conduct and documentation original research in independent fashion (**)• Excellent oral and written communication skills in English; German or French is a plus Nice to haves:• Prior experience in the pharmaceutical industry• Experience in immunology, cancer biology and/or drug discovery• Motivated and reliable team player, but also able to work independentlyWorking hours:• Flexible within regular working hours after consultation with Line ManagerDo not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered. 
    Do you want to work in a big pharmaceutical company? Do you have at least 3 years experience in the laboratory working on in-vitro immune cell assays? You should then read the following lines!Our client, based in Basel, is looking for a Laboratory Associate for a one year mission. Background:The Immunosafety team supports the whole portfolio with questions of unwanted immune activation, unwanted immunosuppression, risk of anti-drug antibodies and immuno PD in the pre-clinical space. As a research associate you will support us on this mission with a broad set of immunology assays. General information:• Start date: 01.10.2021• Latest start date: 01.11.2021• End date: 1 year after start• Extension: No• Location: Basel• Work load: 100%• Department: Immunosafety (PNBPD)• Team: 25 team members Tasks and responsibilities:• Address fundamental scientific questions, be responsible for the design and execution of experimental work, and conduct data analysis• Develop and run in vitro immune cell assays (cytokine release assays, purification and cultivation of PBMC, purification differentiation of immune cell subsets, differentiation and activation assays)• Will routinely independently set-up and perform multi-color flow cytometry experiments• Characterize compounds in different cellular assays• Share knowledge by active collaboration with other scientists and associates inside and outside the group• Attend and present at internal meetings• Keep accurate electronic records• Contribute to the organization of the laboratory as assigned Must haves:• Vocational training or Bachelor Degree in Cell Biology, Molecular Biology, Immunology, Pharmacology (*****)• Min. 3 years experience in a research lab with a focus on in-vitro immune cell assays, including whole blood and PBMC isolation, cultivation and differentiation (****)• Prior experience in cytokine analysis (ELISA or multiplex methods) (***)• Excellent experience in the design and troubleshooting of multi-color (8+ markers) flow cytometry panels on BD instruments (FACS / Durchflusszytometrie) (***)• In vivo experience with mice and LTK1 certificate (***)• Good skills in data analysis software (FlowJo, Prism) and in conduct and documentation original research in independent fashion (**)• Excellent oral and written communication skills in English; German or French is a plus Nice to haves:• Prior experience in the pharmaceutical industry• Experience in immunology, cancer biology and/or drug discovery• Motivated and reliable team player, but also able to work independentlyWorking hours:• Flexible within regular working hours after consultation with Line ManagerDo not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered. 
    • basel, basel-stadt
    • contract
    Do you want to work in a big pharmaceutical company? Do you have a first experience in Scientific Communications? You should then read the following lines! Our client, based in Basel, is looking for a Scientific Communications Leader for a one year mission. Background:This role will reside in the Haematological Malignancies Disease Area Team within PDMA. The focus will be to deliver publications and medical educational activities to support polatuzumab vedotin launch in DLBCL. You’re someone who wants to influence your own development. You’re looking for a role where you have the opportunity to pursue your interests across functions and geographies. Perfect Candidate:We are looking for a Scientific Communications Leader with a scientific education (PhD or PharmaD) and experience in publications. This person should have previous hands on in scientific communications already either in an agency or pharma. Finally, we are looking for someone with experience in vendor management, especially in budget management. General Information:• Start date: ASAP/ 01.10.2021• Latest start date: 01.11.2021• End date: 12 months• Extension: possible but not guaranteed• Work location: Basel• Workload: 100%• Home Office: currently yes, one day per week after Corona• Travelling: currently no, max. 5%• Team: 9 people, two other SCD’s in the Sub team• Used template: CH_Professional Scientific Communications Leader_LSW_CHF• Department: Lymphoma Lymphoid diseases (MDAJ) Tasks & Responsibilities:• Lead the development and delivery of polatuzumab vedotin publication plan in collaboration with cross-functional internal stakeholders and external authors• Collaborate with the medical team in planning and execution of various external and internal medical education activities, including, but not limited to, satellite symposia, and internal training materials and events• Be involved in planning and delivery of congress activities for polatuzumab vedotin as well as other molecules within the haematology therapy area• Drive excellence and innovation across the scientific communication activities in support of polatuzumab vedotin launch, including leading digital and social media initiatives• Provide strategic guidance to affiliates, where necessary, regarding scientific communication activities Must haves:• Strong scientific background with PhD or Pharmacy degree (****)• Min. 3-5 years of experience in hematological malignancies (****)• Experience in publication management and medical education is a must (****)• Hands on experience in scientific communications (either at a medical communications agency or working in a scientific/medical communications role in pharmaceutical industry) (****)• Experience in external agency management including handling budgets (****)• Fluent English is a must• Experience in gSuite is a plus, technical flair and open to learn new technologies• Proven ability to work closely and collaboratively with internal partners and external collaborators to deliver cross-functional initiatives• Cross-functional teamwork skills, including developing and maintaining trustful relationships, and productively resolving conflicts• Ability to operate successfully in a matrix environment with shared accountability and responsibilities• Very good communication and interpersonal skills, including inspiring and influencing as well as having a strong customer orientation and focus Do not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered. 
    Do you want to work in a big pharmaceutical company? Do you have a first experience in Scientific Communications? You should then read the following lines! Our client, based in Basel, is looking for a Scientific Communications Leader for a one year mission. Background:This role will reside in the Haematological Malignancies Disease Area Team within PDMA. The focus will be to deliver publications and medical educational activities to support polatuzumab vedotin launch in DLBCL. You’re someone who wants to influence your own development. You’re looking for a role where you have the opportunity to pursue your interests across functions and geographies. Perfect Candidate:We are looking for a Scientific Communications Leader with a scientific education (PhD or PharmaD) and experience in publications. This person should have previous hands on in scientific communications already either in an agency or pharma. Finally, we are looking for someone with experience in vendor management, especially in budget management. General Information:• Start date: ASAP/ 01.10.2021• Latest start date: 01.11.2021• End date: 12 months• Extension: possible but not guaranteed• Work location: Basel• Workload: 100%• Home Office: currently yes, one day per week after Corona• Travelling: currently no, max. 5%• Team: 9 people, two other SCD’s in the Sub team• Used template: CH_Professional Scientific Communications Leader_LSW_CHF• Department: Lymphoma Lymphoid diseases (MDAJ) Tasks & Responsibilities:• Lead the development and delivery of polatuzumab vedotin publication plan in collaboration with cross-functional internal stakeholders and external authors• Collaborate with the medical team in planning and execution of various external and internal medical education activities, including, but not limited to, satellite symposia, and internal training materials and events• Be involved in planning and delivery of congress activities for polatuzumab vedotin as well as other molecules within the haematology therapy area• Drive excellence and innovation across the scientific communication activities in support of polatuzumab vedotin launch, including leading digital and social media initiatives• Provide strategic guidance to affiliates, where necessary, regarding scientific communication activities Must haves:• Strong scientific background with PhD or Pharmacy degree (****)• Min. 3-5 years of experience in hematological malignancies (****)• Experience in publication management and medical education is a must (****)• Hands on experience in scientific communications (either at a medical communications agency or working in a scientific/medical communications role in pharmaceutical industry) (****)• Experience in external agency management including handling budgets (****)• Fluent English is a must• Experience in gSuite is a plus, technical flair and open to learn new technologies• Proven ability to work closely and collaboratively with internal partners and external collaborators to deliver cross-functional initiatives• Cross-functional teamwork skills, including developing and maintaining trustful relationships, and productively resolving conflicts• Ability to operate successfully in a matrix environment with shared accountability and responsibilities• Very good communication and interpersonal skills, including inspiring and influencing as well as having a strong customer orientation and focus Do not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered. 
    • basel, basel-stadt
    • temporary
    Bezeichnest Du Dich als eine/n Steuerfachspezielisten/in und bist interessiert, unseren Kunden für einen befristeten Zeitraum mit Deinen Kenntnissen und Erfahrungen zu unterstützen? Dann suche ich genau Dich alsFachspezialist Steuern 100% (m/w/d)Dein Aufgabenbereich:Erstellung von SteuerunterlagenKorrekte und fristgerechte Abgabe von EinkommenssteuererklärungenVorbereitung von Steuerzahlungen und Verlängerungen Berechnung, Validierung und Einreichung von Steuererklärungen Durchführen von Abstimmungen für die QuartalsendprüfungBeantwortung verschiedener Anfragen der staatlichen SteuerbehördenUnterstützung bei der Konzernsteuerplanung/-vorhersage, der Cashflow-Planung und der monatlichen SteuerberechnungVerfolgung der Steuerpositionen in der Bilanz und der Gewinn- und Verlustrechnung im Laufe des Jahres und Abgleich mit Cash-Flow-Prognosen/Planung
    Bezeichnest Du Dich als eine/n Steuerfachspezielisten/in und bist interessiert, unseren Kunden für einen befristeten Zeitraum mit Deinen Kenntnissen und Erfahrungen zu unterstützen? Dann suche ich genau Dich alsFachspezialist Steuern 100% (m/w/d)Dein Aufgabenbereich:Erstellung von SteuerunterlagenKorrekte und fristgerechte Abgabe von EinkommenssteuererklärungenVorbereitung von Steuerzahlungen und Verlängerungen Berechnung, Validierung und Einreichung von Steuererklärungen Durchführen von Abstimmungen für die QuartalsendprüfungBeantwortung verschiedener Anfragen der staatlichen SteuerbehördenUnterstützung bei der Konzernsteuerplanung/-vorhersage, der Cashflow-Planung und der monatlichen SteuerberechnungVerfolgung der Steuerpositionen in der Bilanz und der Gewinn- und Verlustrechnung im Laufe des Jahres und Abgleich mit Cash-Flow-Prognosen/Planung
    • basel, basel-stadt
    • temp to perm
    Exklusiv für unseren Kunden - suchen wir genau dich per sofort oder nach Vereinbarung - einen qualifizierten Sanitärinstallateur EFZ (m/w/d) Deine AufgabenDu bist für die Beratung und Bedienung der Kunden verantwortlichKontrolle des Wareneingangs Unterstützung bei Materialbeschaffung, Ausmass und KoordinationArbeiten nach Skizzen und BauplänenErfassen von Lieferscheine mittels EDV System ( SAP )
    Exklusiv für unseren Kunden - suchen wir genau dich per sofort oder nach Vereinbarung - einen qualifizierten Sanitärinstallateur EFZ (m/w/d) Deine AufgabenDu bist für die Beratung und Bedienung der Kunden verantwortlichKontrolle des Wareneingangs Unterstützung bei Materialbeschaffung, Ausmass und KoordinationArbeiten nach Skizzen und BauplänenErfassen von Lieferscheine mittels EDV System ( SAP )
    • basel, basel-stadt
    • temporary
    Du bist eine neugierige, proaktive und teamfähige Person, die sich mit Gourmetkaffee von der Marke Nespresso identifiziert und bei Kunden als Botschafter die Philosophie vermittelst. Für den Standort in Basel suchen wir engagierte Verkäufer / Promoter für Nespresso (m/w) 40-60%Deine Aufgaben:Du begrüsst und informierst Kunden proaktiv als Erstkontakt über die Marke Nespresso und schaffst so ein unvergessliches KauferlebnisDu führst Kaffeedegustationen durch und gewährleistest eine fachkompetente Beratung und Verkauf von Nespresso Kaffee und Maschinen Durch deine offene Art kann der Assessoires, Maschinen und Kaffee Verkauf gesteigert werdenBei Fragen zu einfachen Störungen kannst du den Kunden kompetent beraten und eine Lösung anbietenDie monatliche Führung von Verkaufsrapporten, administrativen Aufgaben sowie die Sicherstellung der Sauberkeit des Verkaufspunkts gehören ebenfalls zu deinen Aufgaben
    Du bist eine neugierige, proaktive und teamfähige Person, die sich mit Gourmetkaffee von der Marke Nespresso identifiziert und bei Kunden als Botschafter die Philosophie vermittelst. Für den Standort in Basel suchen wir engagierte Verkäufer / Promoter für Nespresso (m/w) 40-60%Deine Aufgaben:Du begrüsst und informierst Kunden proaktiv als Erstkontakt über die Marke Nespresso und schaffst so ein unvergessliches KauferlebnisDu führst Kaffeedegustationen durch und gewährleistest eine fachkompetente Beratung und Verkauf von Nespresso Kaffee und Maschinen Durch deine offene Art kann der Assessoires, Maschinen und Kaffee Verkauf gesteigert werdenBei Fragen zu einfachen Störungen kannst du den Kunden kompetent beraten und eine Lösung anbietenDie monatliche Führung von Verkaufsrapporten, administrativen Aufgaben sowie die Sicherstellung der Sauberkeit des Verkaufspunkts gehören ebenfalls zu deinen Aufgaben
    • basel, basel-stadt
    • temp to perm
    Exklusiv für unseren Kunden im Raum Liestal, suchen wir per sofort oder nach Vereinbarung einen Elektroinstallateur (m/w) 100%Deine Aufgaben-Unterhalt und Reparatur von Elektroinstallationen-Installation von Elektroanlagen, Hausanschluss bis zur Steckdose-Materialmengenberechnungen-Arbeiten nach technischen Plänen und Schemata-Service- und Reparaturdienst
    Exklusiv für unseren Kunden im Raum Liestal, suchen wir per sofort oder nach Vereinbarung einen Elektroinstallateur (m/w) 100%Deine Aufgaben-Unterhalt und Reparatur von Elektroinstallationen-Installation von Elektroanlagen, Hausanschluss bis zur Steckdose-Materialmengenberechnungen-Arbeiten nach technischen Plänen und Schemata-Service- und Reparaturdienst
    • basel, basel-stadt
    • contract
    Do you want to work in a big pharmaceutical company? Do you have at least 3 years experience as a Packaging Engineer? You should then read the following lines! Our client, based in Basel, is looking for a Packaging Engineer for a 6 months contract. Technical support on manufacturing processes and technologies mainly for Contract Manufacturing Organizations (CMOs) with focus on packaging systems and packaging process, to ensure  maintenance of the qualified status of marketed products that are supplied by CMO’s through packaging lifecycle General Information: • Startdate: asap• Latest possible start date: 01.12.2021• End date: 6 month• Extension: possible• Workplace: Basel• Workload: 60-80 %• Home Office: possible• Team: 12  Tasks & Responsibilites • Provide technical expertise for packaging processes and technologies, with focus on technical transfer, shipping qualification, validation, technical issues, process improvements• Support quality and relevant team functions by provision of technical assessments to if impact on process changes, technical transfers, discrepancies, complaints associated to packaging systems and packaging processes• Upon request of the JMT (Joint Management Team), initiate, manage and assess changes (support change control, provide impact assessment, coordinate qualification activities) on the packaging systems E.g. change in materials, packaging configurations or process. (Can include evaluation and qualification of primary, secondary and tertiary packaging solutions incl. Setting up the related qualification documentation based on patient, product, regulatory, business or technical requirements)• Maintain the internal data-collection with information of validated status of products packed at CMOs• Support the CMO Artwork groups by verification and approval of technical drawings• Support packaging activities at specific CMOs by authoring packaging material specifications, preparation technical drawings and final approval of Artwork PDFs.• Work in close collaboration with all other packaging functions to ensure alignment, consistency and engagement with SME’s as needed• The activities include GMP tasks Must Haves: • Bachelor's degree in Engineering or equivalent work experience or any other higher certification• At least 5 years of direct experience in packaging engineering and technical Artworks related activities • Experience in document management • Knowledge of main systems as Autocad • Experience in a GMP regulated environment • Excellent communication skills in English, German is a plus• Ability to assess risks, make decisions and drive changes• Excellent at building and maintaining constructive relationships with internal and external stakeholders• Preferably understanding of cGMPs and health authority requirements. Do not waste any minutes, apply now!  We are looking forward to receiving your application. Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.   
    Do you want to work in a big pharmaceutical company? Do you have at least 3 years experience as a Packaging Engineer? You should then read the following lines! Our client, based in Basel, is looking for a Packaging Engineer for a 6 months contract. Technical support on manufacturing processes and technologies mainly for Contract Manufacturing Organizations (CMOs) with focus on packaging systems and packaging process, to ensure  maintenance of the qualified status of marketed products that are supplied by CMO’s through packaging lifecycle General Information: • Startdate: asap• Latest possible start date: 01.12.2021• End date: 6 month• Extension: possible• Workplace: Basel• Workload: 60-80 %• Home Office: possible• Team: 12  Tasks & Responsibilites • Provide technical expertise for packaging processes and technologies, with focus on technical transfer, shipping qualification, validation, technical issues, process improvements• Support quality and relevant team functions by provision of technical assessments to if impact on process changes, technical transfers, discrepancies, complaints associated to packaging systems and packaging processes• Upon request of the JMT (Joint Management Team), initiate, manage and assess changes (support change control, provide impact assessment, coordinate qualification activities) on the packaging systems E.g. change in materials, packaging configurations or process. (Can include evaluation and qualification of primary, secondary and tertiary packaging solutions incl. Setting up the related qualification documentation based on patient, product, regulatory, business or technical requirements)• Maintain the internal data-collection with information of validated status of products packed at CMOs• Support the CMO Artwork groups by verification and approval of technical drawings• Support packaging activities at specific CMOs by authoring packaging material specifications, preparation technical drawings and final approval of Artwork PDFs.• Work in close collaboration with all other packaging functions to ensure alignment, consistency and engagement with SME’s as needed• The activities include GMP tasks Must Haves: • Bachelor's degree in Engineering or equivalent work experience or any other higher certification• At least 5 years of direct experience in packaging engineering and technical Artworks related activities • Experience in document management • Knowledge of main systems as Autocad • Experience in a GMP regulated environment • Excellent communication skills in English, German is a plus• Ability to assess risks, make decisions and drive changes• Excellent at building and maintaining constructive relationships with internal and external stakeholders• Preferably understanding of cGMPs and health authority requirements. Do not waste any minutes, apply now!  We are looking forward to receiving your application. Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.   
    • basel, basel-stadt
    • contract
    Do you want to work in a big pharmaceutical company? Do you have experience in GCP and Pulmonary Hypertension Therapeutic Area or Cardiovascular/Cardiopulmonary? You should then read the following lines! Our client, based in Basel area, is looking for a Clinical Project Physician for a one year contract. The Project Physician is a responsible member of a clinical team dedicated to the development and execution of medical strategies and the clinical and operational implementation of a complex compound program. The Project Physician provides active medical and scientific contribution to a cross-functional clinical team. The Project Physician provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and takes ownership for the content of clinical study reports and relevant documents for regulatory filings. Team matrix interactions include project management, finance, legal, quality assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs, data management,medical writing, biostatistics, global medical affairs, clinical pharmacology, clinical operations, health economics, epidemiology and other scientific and business related disciplines. The Project Physician may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area Essential Functions: Responsible for medical monitoring/reporting and company safety officer activitiesWorks on clinical development plans, trial protocols and takes ownership of clinical study reportsEvaluates adverse events (pre and post-marketing) for relationship to treatmentAssists Regulatory Affairs in determining requirements for any corrective actions or health authority reportingMay act as a medical contact at the company for health authorities concerning clinical/medical issuesInterprets, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissionsClose interactions with Project Scientists and Physicians across programs Other Responsibilities : Assists Regulatory Affairs in the development of drug regulatory strategiesHelps explore and evaluate new product ideas to assist in identifying new market opportunitiesSupport general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillanceParticipate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc.Reviews medical literature and related new technologiesMay be asked to assess medical publications emerging from the Team and its affiliatesMay be responsible, with appropriate colleagues, for review of Company advertising and promotional materials Candidate Profile: MD (or equivalent) in relevant area with appropriate post-doctoral training and certificationExperience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filingsSpecific experience in phase II and III studies is a strong advantage.Submission experience a strong advantage.Experience in medical review.Ideally previous experience in the Pulmonary Hypertension Therapeutic Area, otherwise Cardiovascular/Cardiopulmonary experience is appreciated.English Fluent Do not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.
    Do you want to work in a big pharmaceutical company? Do you have experience in GCP and Pulmonary Hypertension Therapeutic Area or Cardiovascular/Cardiopulmonary? You should then read the following lines! Our client, based in Basel area, is looking for a Clinical Project Physician for a one year contract. The Project Physician is a responsible member of a clinical team dedicated to the development and execution of medical strategies and the clinical and operational implementation of a complex compound program. The Project Physician provides active medical and scientific contribution to a cross-functional clinical team. The Project Physician provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and takes ownership for the content of clinical study reports and relevant documents for regulatory filings. Team matrix interactions include project management, finance, legal, quality assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs, data management,medical writing, biostatistics, global medical affairs, clinical pharmacology, clinical operations, health economics, epidemiology and other scientific and business related disciplines. The Project Physician may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area Essential Functions: Responsible for medical monitoring/reporting and company safety officer activitiesWorks on clinical development plans, trial protocols and takes ownership of clinical study reportsEvaluates adverse events (pre and post-marketing) for relationship to treatmentAssists Regulatory Affairs in determining requirements for any corrective actions or health authority reportingMay act as a medical contact at the company for health authorities concerning clinical/medical issuesInterprets, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissionsClose interactions with Project Scientists and Physicians across programs Other Responsibilities : Assists Regulatory Affairs in the development of drug regulatory strategiesHelps explore and evaluate new product ideas to assist in identifying new market opportunitiesSupport general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillanceParticipate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc.Reviews medical literature and related new technologiesMay be asked to assess medical publications emerging from the Team and its affiliatesMay be responsible, with appropriate colleagues, for review of Company advertising and promotional materials Candidate Profile: MD (or equivalent) in relevant area with appropriate post-doctoral training and certificationExperience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filingsSpecific experience in phase II and III studies is a strong advantage.Submission experience a strong advantage.Experience in medical review.Ideally previous experience in the Pulmonary Hypertension Therapeutic Area, otherwise Cardiovascular/Cardiopulmonary experience is appreciated.English Fluent Do not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.
    • basel, basel-stadt
    • temp to perm
    Bist du eine flexible, belastbare und engagierte Person? Verfügst du über ein Auge fürs Detail und kannst es dir vorstellen in einem Hotel zu arbeiten? Dann bewirb dich jetzt bei uns als:Zimmerfrau in Basel 40 - 80%Deine Aufgaben:Reinigung von Hotelzimmer von 8:00 Uhr bis 15:00 UhrArbeitseinsatz auch am Wochenende
    Bist du eine flexible, belastbare und engagierte Person? Verfügst du über ein Auge fürs Detail und kannst es dir vorstellen in einem Hotel zu arbeiten? Dann bewirb dich jetzt bei uns als:Zimmerfrau in Basel 40 - 80%Deine Aufgaben:Reinigung von Hotelzimmer von 8:00 Uhr bis 15:00 UhrArbeitseinsatz auch am Wochenende
    • basel, basel-stadt
    • temp to perm
    Mehrjährige Berufserfahrung als HR-Fachperson; Vif, ausdauernd und organsiert - trifft das alles auf Dich zu? Dann suche ich genau Dich alsHR-Fachfrau 80-100% (m/w/d)In dieser spannenden Funktion bist du für die folgenden Aufgaben verantwortlich:Gesamte PersonaladministrationLohnbuchhaltungPersonalrekrutierungErste Ansprechperson bei PersonalfragenSozialversicherungswesen, Zeiterfassung, Ein- und AustritteDiverse HR-Projekte
    Mehrjährige Berufserfahrung als HR-Fachperson; Vif, ausdauernd und organsiert - trifft das alles auf Dich zu? Dann suche ich genau Dich alsHR-Fachfrau 80-100% (m/w/d)In dieser spannenden Funktion bist du für die folgenden Aufgaben verantwortlich:Gesamte PersonaladministrationLohnbuchhaltungPersonalrekrutierungErste Ansprechperson bei PersonalfragenSozialversicherungswesen, Zeiterfassung, Ein- und AustritteDiverse HR-Projekte
    • basel, basel-stadt
    • temporary
    Für unseren Kunden, ein bekanntes Catering-unternehmen in Basel, suchen wir, Bar- und Service-aushilfen & Allrounder für die ART Basel (m/w) 60-80% Ihre Aufgaben:Servieren von Speisen und GetränkenUnterstützung unseres Serviceteams & BackofficeteamsVorbereiten des täglichen Mise en placeInkasso sowie TagesabrechnungenEinhalten der Qualitäts- und Hygienestandards
    Für unseren Kunden, ein bekanntes Catering-unternehmen in Basel, suchen wir, Bar- und Service-aushilfen & Allrounder für die ART Basel (m/w) 60-80% Ihre Aufgaben:Servieren von Speisen und GetränkenUnterstützung unseres Serviceteams & BackofficeteamsVorbereiten des täglichen Mise en placeInkasso sowie TagesabrechnungenEinhalten der Qualitäts- und Hygienestandards
    • basel, basel-stadt
    • temporary
    Hilfsarbeiter (w/m/d)Wir suchen per sofort flexible Mitarbeiter, die für Kurzeinsätze einspringen können. Wir sprechen hier auch Bewerbern an, die nur an bestimmten Tagen verfügbar sind oder die Zeit neben dem Studium oder einem anderen Teilzeitstelle einteilen können.Folgende Einsätze erwarten Dich:Allgemeine Lagerarbeiten Umzüge aller ArtMontage und DemontageBesucherbetreuerLiftboys
    Hilfsarbeiter (w/m/d)Wir suchen per sofort flexible Mitarbeiter, die für Kurzeinsätze einspringen können. Wir sprechen hier auch Bewerbern an, die nur an bestimmten Tagen verfügbar sind oder die Zeit neben dem Studium oder einem anderen Teilzeitstelle einteilen können.Folgende Einsätze erwarten Dich:Allgemeine Lagerarbeiten Umzüge aller ArtMontage und DemontageBesucherbetreuerLiftboys
    • basel, basel-stadt
    • permanent
    Für unseren internationalen Kunden im Pharmabereich suchen wir per sofort, für einen temporären Einsatz, eine motivierte und engagierte Persönlichkeit in der Funktion als HR Coordinator 80-100% (m/w/d)In dieser spannenden Rolle bist Du für Folgendes verantwortlich:PersonaladministrationErste Ansprechperson bei internen PersonalfragenVorbereiten und Ändern von Dokumenten, einschließlich Korrespondenz, Berichte, Entwürfe, Memos und EmailsEventorganisation für interne MitarbeitendeEin- und AustritteUnterstützung bei der Einführung von HR-Systemen und / oder Änderungen
    Für unseren internationalen Kunden im Pharmabereich suchen wir per sofort, für einen temporären Einsatz, eine motivierte und engagierte Persönlichkeit in der Funktion als HR Coordinator 80-100% (m/w/d)In dieser spannenden Rolle bist Du für Folgendes verantwortlich:PersonaladministrationErste Ansprechperson bei internen PersonalfragenVorbereiten und Ändern von Dokumenten, einschließlich Korrespondenz, Berichte, Entwürfe, Memos und EmailsEventorganisation für interne MitarbeitendeEin- und AustritteUnterstützung bei der Einführung von HR-Systemen und / oder Änderungen
    • basel, basel-stadt
    • temporary
    Für unseren Kunden suchen wir top motivierte/n Maler/in mit EFZDeine AufgabenAbdecken/Abkleben Arbeitsflächen Grundierungsarbeiten und Spachtelarbeiten Einsatz im Neu-, Umbau- und Renovation Streichen von: Fassaden/ Fenster/ Türen/Holz/ Metall/ Kunststoff Tapezieren/ Kleistern/ Kleben/ Aufziehen
    Für unseren Kunden suchen wir top motivierte/n Maler/in mit EFZDeine AufgabenAbdecken/Abkleben Arbeitsflächen Grundierungsarbeiten und Spachtelarbeiten Einsatz im Neu-, Umbau- und Renovation Streichen von: Fassaden/ Fenster/ Türen/Holz/ Metall/ Kunststoff Tapezieren/ Kleistern/ Kleben/ Aufziehen
    • basel, basel-stadt
    • temp to perm
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen hoch motivierten Polymechaniker EFZ (m/w)Deine Aufgaben:Verantwortung für Service, Reparatur und Wartung Ansprechpartner bei technischen Problemen Organisation und Unterstützung externer Firmen Unterstützung bei Um-und Neubaumassnahmen Umsetzung von technischen Optimierungen Nachführen von technischen Unterlagen
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen hoch motivierten Polymechaniker EFZ (m/w)Deine Aufgaben:Verantwortung für Service, Reparatur und Wartung Ansprechpartner bei technischen Problemen Organisation und Unterstützung externer Firmen Unterstützung bei Um-und Neubaumassnahmen Umsetzung von technischen Optimierungen Nachführen von technischen Unterlagen
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