8 jobs found in Basel-Stadt

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    • basel, basel-stadt
    • contract
    For our customer, one of the world's leading pharmaceutical company in Basel, Switzerland, we are looking for a committed and reliable personality as a Biomedical Data Curation and Anonymization Specialist.As a skilled Biomedical Data Curation and Anonymization Specialist you will support research and development projects in digital pathology. You will curate pathology image datasets and associated metadata so that they are well organized and accurate, and will apply data anonymization tools to anonymize digital pathology images and associated image, clinical and genetic metadata. You will work with multiple stakeholders to locate, transfer, and prepare the data for use by pathologists and data scientists.Tasks and Responsibilities:You will be responsible for ensuring digital pathology (DP) images and multidimensional associated metadata ingested into the DP storage platform are well organized, anonymized and meet technical quality standards required for DP algorithm development. The role will not require visual assessment of image content; however, previous experience working with DP or other imaging modalities will help the successful candidate accomplish the listed tasks:Run data anonymization algorithms on digital pathology images, image metadata, clinical data, and genetic dataContribute to the maintenance and optimization of digital pathology image/data anonymization algorithmsUse and improve metadata storage and management toolsManage digital pathology project data, curate image, clinical, and genetic metadataSupport data transfers and ingestion from internal and external parties, carry out technical quality control on ingested dataCommunicate with external data providers about data transfer requirements, share technical issues with vendors, oversee and contribute to their resolutionWork closely with groups across the organization to locate and access data from diverse company internal systemsMust Haves:Min. Master’s degree in Computer Science, Data Science, or related field, or 3+ years working experience in a data curation, data anonymization or data management role Experience with general tools and techniques used in anonymization workflows and practical experience with R and PythonDemonstrated communication skills of technical information, both understanding and expressing requirements from stakeholders with a high level of bioinformatics expertise (i.e. an ability to both work with and communicate about large datasets containing imaging, clinical, demographic, genetic etc. data) Practical experience with cloud services (AWS, Azure, GCP) Experience in managing large datasetsBusiness fluency in English (written and spoken)Ability to work independently, follow up on verbal discussions with concrete action steps, and take initiativeStrong organizational skills with meticulous attention to detailOpen to embrace new ideas and ability to operate in a flexible mannerStrong interpersonal skills and a consultative mindset, with the ability to influence without direct authority, and to develop strong partnerships“Self-starter”; strong sense of responsibility with demonstrable comfort in an entrepreneurial environmentGood problem-solving ability, breaking down complex problems into distinct parts, managing uncertainty, understanding, anticipating interdependencies.Nice to Haves:Prior experience with digital pathology or imaging and clinical dataFamiliarity with Data modelingFamiliarity with database software and organizational systems such as LIMSIf 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. Please note that we are only considering applications from Swiss and EU-27/EFTA nationals or Swiss work permit holders for our open positions in Switzerland.
    For our customer, one of the world's leading pharmaceutical company in Basel, Switzerland, we are looking for a committed and reliable personality as a Biomedical Data Curation and Anonymization Specialist.As a skilled Biomedical Data Curation and Anonymization Specialist you will support research and development projects in digital pathology. You will curate pathology image datasets and associated metadata so that they are well organized and accurate, and will apply data anonymization tools to anonymize digital pathology images and associated image, clinical and genetic metadata. You will work with multiple stakeholders to locate, transfer, and prepare the data for use by pathologists and data scientists.Tasks and Responsibilities:You will be responsible for ensuring digital pathology (DP) images and multidimensional associated metadata ingested into the DP storage platform are well organized, anonymized and meet technical quality standards required for DP algorithm development. The role will not require visual assessment of image content; however, previous experience working with DP or other imaging modalities will help the successful candidate accomplish the listed tasks:Run data anonymization algorithms on digital pathology images, image metadata, clinical data, and genetic dataContribute to the maintenance and optimization of digital pathology image/data anonymization algorithmsUse and improve metadata storage and management toolsManage digital pathology project data, curate image, clinical, and genetic metadataSupport data transfers and ingestion from internal and external parties, carry out technical quality control on ingested dataCommunicate with external data providers about data transfer requirements, share technical issues with vendors, oversee and contribute to their resolutionWork closely with groups across the organization to locate and access data from diverse company internal systemsMust Haves:Min. Master’s degree in Computer Science, Data Science, or related field, or 3+ years working experience in a data curation, data anonymization or data management role Experience with general tools and techniques used in anonymization workflows and practical experience with R and PythonDemonstrated communication skills of technical information, both understanding and expressing requirements from stakeholders with a high level of bioinformatics expertise (i.e. an ability to both work with and communicate about large datasets containing imaging, clinical, demographic, genetic etc. data) Practical experience with cloud services (AWS, Azure, GCP) Experience in managing large datasetsBusiness fluency in English (written and spoken)Ability to work independently, follow up on verbal discussions with concrete action steps, and take initiativeStrong organizational skills with meticulous attention to detailOpen to embrace new ideas and ability to operate in a flexible mannerStrong interpersonal skills and a consultative mindset, with the ability to influence without direct authority, and to develop strong partnerships“Self-starter”; strong sense of responsibility with demonstrable comfort in an entrepreneurial environmentGood problem-solving ability, breaking down complex problems into distinct parts, managing uncertainty, understanding, anticipating interdependencies.Nice to Haves:Prior experience with digital pathology or imaging and clinical dataFamiliarity with Data modelingFamiliarity with database software and organizational systems such as LIMSIf 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. Please note that we are only considering applications from Swiss and EU-27/EFTA nationals or Swiss work permit holders for our open positions in Switzerland.
    • 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
    • temporary
    Do you have good communication skills and strong experience in the bio-pharmaceutical industry?Are you experienced working with partner organizations (CMOs)?In this case you should have a look at this opportunity!To work for our client, a pioneering biotechnology company, we are looking for a: Senior Specialist, International Fill FinishLocation: BaselContract duration: to start asap for 12 monthsHere’s What You’ll Do: Support the (Associate) Director, International Fill Finish in various tasks related to the buildup of GMP production at Fill Finish Contract Manufacturing Organizations (FF CMOs). Act as a counterpart for FF CMOs team members to ensure on-time and in-full deliveries. Partner with Quality, Technical Development, Manufacturing Science and Technology, and Regulatory colleagues on specific aspects of the relationships with the FF CMOs.Ensure operational related activities at the FF CMOs are conducted to meet Company’s requirements (Compliance, Meeting Orders, Dispute resolution, Production Planning, Materials Management, Technology Issues, OpEx). Ensure externally manufactured drug products are produced and stored according to the appropriate documentation in order to obtain the required quality. Ensure that instructions relating to external production operations are strictly implemented by the  CMOs.Ensure in collaboration with quality that the appropriate qualification, maintenance, training and validations are performed to meet the appropriate Company requirements. Support and perform the reviews for process performance at FF CMOs. Monitor Key Performance Indicators of FF CMOs. Support preparation of periodic business and operations review meetings.  Drive for and implement agreed continuous improvements at FF CMOs. Coordinate reviews and approvals of various documentations from FF CMOs. In collaboration with Quality coordinate investigations and troubleshooting efforts at FF CMOsWrite or revise the appropriate GMP documentations. Frequently visit and maintain presence at the external partners’ sites and build strong interdependent relationships with the CMO Counterparts in order to assess the as is state & risks for action-oriented improvement plans. Performs other administrative duties as required. Here’s What You’ll Bring to the Table:Bachelor's Degree with 5-8 years of experience in biopharmaceutical operations or a Master’s Degree with 2-5 years industry experience; Degree in Engineering or Life Sciences is preferred.Proficiency in English required. Spanish and German are a plus. Good communication skills (verbal and written) to collaborate with other CMC team members and managers in a dynamic, cross-functional matrix environment.Ability to work with members of partner organizations (CMOs).Well organized – a natural ability to be organized in how you think, communicate and conduct your work.You drive for results – you set a high bar for yourself and others.Good critical thinker that can anticipate the needed next step and therefore can work independently.A curious mindset that allows you to constantly learn and challenge the status quo.Ability to navigate through ambiguity and rapid growth and adapt to change.  You would like to contribute to a fast-thinking and innovative company, changing the industry ?Apply now! Please note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position
    Do you have good communication skills and strong experience in the bio-pharmaceutical industry?Are you experienced working with partner organizations (CMOs)?In this case you should have a look at this opportunity!To work for our client, a pioneering biotechnology company, we are looking for a: Senior Specialist, International Fill FinishLocation: BaselContract duration: to start asap for 12 monthsHere’s What You’ll Do: Support the (Associate) Director, International Fill Finish in various tasks related to the buildup of GMP production at Fill Finish Contract Manufacturing Organizations (FF CMOs). Act as a counterpart for FF CMOs team members to ensure on-time and in-full deliveries. Partner with Quality, Technical Development, Manufacturing Science and Technology, and Regulatory colleagues on specific aspects of the relationships with the FF CMOs.Ensure operational related activities at the FF CMOs are conducted to meet Company’s requirements (Compliance, Meeting Orders, Dispute resolution, Production Planning, Materials Management, Technology Issues, OpEx). Ensure externally manufactured drug products are produced and stored according to the appropriate documentation in order to obtain the required quality. Ensure that instructions relating to external production operations are strictly implemented by the  CMOs.Ensure in collaboration with quality that the appropriate qualification, maintenance, training and validations are performed to meet the appropriate Company requirements. Support and perform the reviews for process performance at FF CMOs. Monitor Key Performance Indicators of FF CMOs. Support preparation of periodic business and operations review meetings.  Drive for and implement agreed continuous improvements at FF CMOs. Coordinate reviews and approvals of various documentations from FF CMOs. In collaboration with Quality coordinate investigations and troubleshooting efforts at FF CMOsWrite or revise the appropriate GMP documentations. Frequently visit and maintain presence at the external partners’ sites and build strong interdependent relationships with the CMO Counterparts in order to assess the as is state & risks for action-oriented improvement plans. Performs other administrative duties as required. Here’s What You’ll Bring to the Table:Bachelor's Degree with 5-8 years of experience in biopharmaceutical operations or a Master’s Degree with 2-5 years industry experience; Degree in Engineering or Life Sciences is preferred.Proficiency in English required. Spanish and German are a plus. Good communication skills (verbal and written) to collaborate with other CMC team members and managers in a dynamic, cross-functional matrix environment.Ability to work with members of partner organizations (CMOs).Well organized – a natural ability to be organized in how you think, communicate and conduct your work.You drive for results – you set a high bar for yourself and others.Good critical thinker that can anticipate the needed next step and therefore can work independently.A curious mindset that allows you to constantly learn and challenge the status quo.Ability to navigate through ambiguity and rapid growth and adapt to change.  You would like to contribute to a fast-thinking and innovative company, changing the industry ?Apply now! Please note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position
    • allschwil, basel-stadt
    • contract
    For our client, a pharmaceuticals and biotechnology company based in Allschwil, we are currently looking for a Clinical Data Standards Architect.  The Clinical Data Standards Architect (CDSA) - Data Delivery implements and maintains efficient standard content in the data delivery tools (SAS, LSAF Excel based libraries) that can be applied across all the diseases areas and therapeutic areas or that are specific to a specific therapeutic are or disease area.The CDSA defines and maintains the standard delivery metadata supporting the data flow from data collection to data delivery (DRM and SDTM). To that end, the CDSA is responsible for defining and maintaining the metadata supporting the Data transfer Agreements (DTA) with third parties, DRM and SDTM model and the data mapping of source data, eCRF data and third-party transfer data (eDT) to DRM and SDTM.The CDSA configures standards to the specific needs and requirements of a Therapeutic Area, compound, or Disease Area, generating the expected efficiencies through optimal adoption and reuse of standards. The CDSA also supports the functions adopting the standards in the clinical trials, in close collaboration with the CDSA responsible for the data collection standards.Deliverables:Implement the standard metadata in the data delivery tools with the goal of creating efficiencies within the trials, consistency across the trials and automating the data flow from source data to DRM and to SDTMExamples:o Study Data Tabulation Model (SDTM)o Annotated Case Report Forms (CRFs)o Support the data transfer agreement (DTA) standards with SDTMo Data Review Model (DRM)o Mapping metadata from data collection (CRF and DTA) to DRMo Mapping metadata from DRM to SDTMImplement standard content in the delivery tools compliant to the industry standards and health authority regulations, meeting best practices in computer system validation, where applicableResponsible for the correct testing and QC of the mapping metadata and therefore collaborates with the respective functions in Integrated Data Analysis and Reporting (IDAR)Annotate the eCRF or eCOA with SDTM metadata and collaborates with his/her team members on the correctness of the annotated case report form meeting submission, scientific and operational requirements, and guidelinesDefine and maintain the clinical data delivery standards in line with the needs in clinical trials to meet additional scientific or operational requirements. To that end you will guarantee that formal change management control and versioning of the standards is applied and adhered toGovern formally all the changes to standards and manages multiple versions in line with adoption needs of the clinical trials and drug development programsProvide the necessary support to the clinical programming teams to achieve consistent adoption of standards in the studies (internally or outsourced to a CRO). To that end, you pro-actively support identifying the standards supporting the trial objectives.• Tailor the global standards to the specific needs of Therapeutic Areas or Disease Ares, while maintaining the traceability and lineage of the metadata. Document and correctly manage the lineage between global standards and the pre-configured (tailored) standards.Provide the necessary support to the clinical programming teams to achieve consistent adoption of standards in the studies (internally or outsourced to a CRO). To that end, you pro-actively support identifying the standards supporting the trial objectives.Interfaces – Primary/Other:Primary interfaces: The clinical data standards team and the data acquisition experts and the data managers in the data management function and the clinical programmers.Other Interfaces: Clinical Analysis Standards, the clinical team (statistician, physician, …), CDISC working groups.Education and Experience Guidelines:Experience with coding and running SAS programs is requiredKnowledge of Rave eDC (Medidata Solutions) is a preferredExpertise with CDISC standards: SDTM, Controlled terminology and define .xml.Experience with SAS LSAF and Pinnacle 21 is a plusBS/BA degree in life sciences or computer science or equivalent by work experience3 years of relevant operational experience in clinical data management and standardsRelevant development experience in clinical data standards is strongly preferredExperience in prioritizing and managing multiple tasks simultaneouslyOutstanding written and verbal communication skills in EnglishIf 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. Please note that we are only considering applications from Swiss and EU-27/EFTA nationals or Swiss work permit holders for our open positions in Switzerland.
    For our client, a pharmaceuticals and biotechnology company based in Allschwil, we are currently looking for a Clinical Data Standards Architect.  The Clinical Data Standards Architect (CDSA) - Data Delivery implements and maintains efficient standard content in the data delivery tools (SAS, LSAF Excel based libraries) that can be applied across all the diseases areas and therapeutic areas or that are specific to a specific therapeutic are or disease area.The CDSA defines and maintains the standard delivery metadata supporting the data flow from data collection to data delivery (DRM and SDTM). To that end, the CDSA is responsible for defining and maintaining the metadata supporting the Data transfer Agreements (DTA) with third parties, DRM and SDTM model and the data mapping of source data, eCRF data and third-party transfer data (eDT) to DRM and SDTM.The CDSA configures standards to the specific needs and requirements of a Therapeutic Area, compound, or Disease Area, generating the expected efficiencies through optimal adoption and reuse of standards. The CDSA also supports the functions adopting the standards in the clinical trials, in close collaboration with the CDSA responsible for the data collection standards.Deliverables:Implement the standard metadata in the data delivery tools with the goal of creating efficiencies within the trials, consistency across the trials and automating the data flow from source data to DRM and to SDTMExamples:o Study Data Tabulation Model (SDTM)o Annotated Case Report Forms (CRFs)o Support the data transfer agreement (DTA) standards with SDTMo Data Review Model (DRM)o Mapping metadata from data collection (CRF and DTA) to DRMo Mapping metadata from DRM to SDTMImplement standard content in the delivery tools compliant to the industry standards and health authority regulations, meeting best practices in computer system validation, where applicableResponsible for the correct testing and QC of the mapping metadata and therefore collaborates with the respective functions in Integrated Data Analysis and Reporting (IDAR)Annotate the eCRF or eCOA with SDTM metadata and collaborates with his/her team members on the correctness of the annotated case report form meeting submission, scientific and operational requirements, and guidelinesDefine and maintain the clinical data delivery standards in line with the needs in clinical trials to meet additional scientific or operational requirements. To that end you will guarantee that formal change management control and versioning of the standards is applied and adhered toGovern formally all the changes to standards and manages multiple versions in line with adoption needs of the clinical trials and drug development programsProvide the necessary support to the clinical programming teams to achieve consistent adoption of standards in the studies (internally or outsourced to a CRO). To that end, you pro-actively support identifying the standards supporting the trial objectives.• Tailor the global standards to the specific needs of Therapeutic Areas or Disease Ares, while maintaining the traceability and lineage of the metadata. Document and correctly manage the lineage between global standards and the pre-configured (tailored) standards.Provide the necessary support to the clinical programming teams to achieve consistent adoption of standards in the studies (internally or outsourced to a CRO). To that end, you pro-actively support identifying the standards supporting the trial objectives.Interfaces – Primary/Other:Primary interfaces: The clinical data standards team and the data acquisition experts and the data managers in the data management function and the clinical programmers.Other Interfaces: Clinical Analysis Standards, the clinical team (statistician, physician, …), CDISC working groups.Education and Experience Guidelines:Experience with coding and running SAS programs is requiredKnowledge of Rave eDC (Medidata Solutions) is a preferredExpertise with CDISC standards: SDTM, Controlled terminology and define .xml.Experience with SAS LSAF and Pinnacle 21 is a plusBS/BA degree in life sciences or computer science or equivalent by work experience3 years of relevant operational experience in clinical data management and standardsRelevant development experience in clinical data standards is strongly preferredExperience in prioritizing and managing multiple tasks simultaneouslyOutstanding written and verbal communication skills in EnglishIf 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. Please note that we are only considering applications from Swiss and EU-27/EFTA nationals or Swiss work permit holders for our open positions in Switzerland.
    • münchenstein, basel-stadt
    • permanent
    Für unseren Kunden suchen per sofort einen Telematiker in der Nähe von Basel.Deine Aufgaben:Service/Provider Produkte installieren und programmierenBetreuung von ICT Projekten sowie das Produktportfolio weiterentwickelnTelefonie und IT-Netzwerke betreuen sowie Fehler behebenBetreuung von bestehenden SystemenOn-Premises ICT-Server-Infrastruktur sicherstellenDein Profil:Abgeschlossene Lehre als Telematiker oder Studium (Quereinsteiger mit 3+ Jahren Erfahrung sind herzlich Willkommen)Fundierte Kenntnisse mit Office 365Fliessende 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 Telematiker in der Nähe von Basel.Deine Aufgaben:Service/Provider Produkte installieren und programmierenBetreuung von ICT Projekten sowie das Produktportfolio weiterentwickelnTelefonie und IT-Netzwerke betreuen sowie Fehler behebenBetreuung von bestehenden SystemenOn-Premises ICT-Server-Infrastruktur sicherstellenDein Profil:Abgeschlossene Lehre als Telematiker oder Studium (Quereinsteiger mit 3+ Jahren Erfahrung sind herzlich Willkommen)Fundierte Kenntnisse mit Office 365Fliessende 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
    • 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
    • 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
    • permanent
    Für unseren Kunden, ein Schweizer Familienunternehmen, suchen wir per sofort oder nach Absprache eine erfahrene Person als Firmware Developer für den Standort Basel.Eckdaten:FestanstellungFirmensprache: DeutschTeamgröße: 4 MA plus TeamleiterFirma: AutomatisierungslösungenDeine Aufgaben:Kompletter Entwicklungs Lifecycle, von der Konzeption, über die Entwicklung bis hin zur ImplementierungSchwerpunkt sind Embedded Systems (IoT) mit starkem Fokus auf Cloud AzureFirmware Entwicklung in C/C++Entwicklung und Standardisierung neuer Produkte und AbläufeDokumentationenEnge Zusammenarbeit mit dem Produkt Entwicklungsteam um Lücken auf dem Markt zu erkennen und neue Lösungen zu erarbeitenDeine Erfahrungen:Deutsch auf Niveau C1 minimumAbgeschlossene Grundausbildung und Weiterbildung im Bereich Computer Science, Electrical Engineering3+ Jahre Hands-on Erfahrung als Embedded Engineer oder Firmware EntwicklerErfahrung in der Programmierung direkt auf dem Prozessor, backbone sowie auf OS (bis HW Treiber auf HAL Ebene)Erfahrungen mit Prozessoren wie ARM Cortex von M bis NXP und ST und/oder RTOS (Zephyr)C++11 gute ErfahrungErste Erfahrungen mit Azure oder AWS und GoogleControl Systems erste touchpoints (10-20% der Arbeit)Know how von GithubOO Entwicklung nur nach Notwendigkeit im Einsatz, keine Desktop ApplikationenSiehst du dich zu 70-80% in dieser Position wieder? Dann freuen wir uns über deine Bewerbung und geben dir gerne mehr Informationen zu der Stelle. 
    Für unseren Kunden, ein Schweizer Familienunternehmen, suchen wir per sofort oder nach Absprache eine erfahrene Person als Firmware Developer für den Standort Basel.Eckdaten:FestanstellungFirmensprache: DeutschTeamgröße: 4 MA plus TeamleiterFirma: AutomatisierungslösungenDeine Aufgaben:Kompletter Entwicklungs Lifecycle, von der Konzeption, über die Entwicklung bis hin zur ImplementierungSchwerpunkt sind Embedded Systems (IoT) mit starkem Fokus auf Cloud AzureFirmware Entwicklung in C/C++Entwicklung und Standardisierung neuer Produkte und AbläufeDokumentationenEnge Zusammenarbeit mit dem Produkt Entwicklungsteam um Lücken auf dem Markt zu erkennen und neue Lösungen zu erarbeitenDeine Erfahrungen:Deutsch auf Niveau C1 minimumAbgeschlossene Grundausbildung und Weiterbildung im Bereich Computer Science, Electrical Engineering3+ Jahre Hands-on Erfahrung als Embedded Engineer oder Firmware EntwicklerErfahrung in der Programmierung direkt auf dem Prozessor, backbone sowie auf OS (bis HW Treiber auf HAL Ebene)Erfahrungen mit Prozessoren wie ARM Cortex von M bis NXP und ST und/oder RTOS (Zephyr)C++11 gute ErfahrungErste Erfahrungen mit Azure oder AWS und GoogleControl Systems erste touchpoints (10-20% der Arbeit)Know how von GithubOO Entwicklung nur nach Notwendigkeit im Einsatz, keine Desktop ApplikationenSiehst du dich zu 70-80% in dieser Position wieder? Dann freuen wir uns über deine Bewerbung und geben dir gerne mehr Informationen zu der Stelle. 

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