70 jobs found in Basel-Stadt

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    • basel, basel-stadt
    • contract
    General Information:Start Date: ASAP/ 01.11.2021Latest Start Date: 01.12.2021End Date: 28.02.2022Your ResponsibilitiesAbility to work within an Agile Scrum Team to perform specific development and configuration tasks according to Jira based User Stories / Functional SpecificationsCollaborate with the Tech Lead and Business Analyst to define Functional Specification and implement (code or configure) solution based on Functional SpecificationsActively participate in all Agile Ceremonies (Sprint Planning, Story Estimations, Retrospectives, Daily Scrums, etc.)Translate an architecture design into a functional solutionDocument Technical & Design SpecificationsYour Profile:5 + years experience in Cloud (Platform) Data EngineeringCertified and proficient in Agile ways of working with cross-functional teamsAWS Developer Certification with extensive hands-on experience with core AWS services such as Glue/Glue Studio, S3, Lambda, SageMaker, DynamoDB, Athena, Redshift, RDS, Step Functions, CloudWatch, EC2, SNS, SQS, etc.Experience in building AWS based data ingestion, processing, and analytics pipelines Substantial knowledge of ‘infrastructure as code’ and in particular with Terraform and AWS CLICI/CD systems (preferably GitLab and Jenkins) experience, including configuration management and automation tools (preferably Ansible and Puppet)Hands-on experience with Python coding and Bash shell scriptingNice to Haves:Former experience in the life sciences/ pharma industryKnowledge of Service Orchestration using Kubernetes and/or EKSKnowledge of various databases, both SQL and NoSQLAWS CloudFormation knowledgeExperience with SnowflakeKnowledge of more specialized languages such as ‘R’Experience with troubleshooting performance bottlenecks, considering both Linux, as well as Cloud Native environmentsDoes this sound like your next challenge? I look forward to receiving your application today.
    General Information:Start Date: ASAP/ 01.11.2021Latest Start Date: 01.12.2021End Date: 28.02.2022Your ResponsibilitiesAbility to work within an Agile Scrum Team to perform specific development and configuration tasks according to Jira based User Stories / Functional SpecificationsCollaborate with the Tech Lead and Business Analyst to define Functional Specification and implement (code or configure) solution based on Functional SpecificationsActively participate in all Agile Ceremonies (Sprint Planning, Story Estimations, Retrospectives, Daily Scrums, etc.)Translate an architecture design into a functional solutionDocument Technical & Design SpecificationsYour Profile:5 + years experience in Cloud (Platform) Data EngineeringCertified and proficient in Agile ways of working with cross-functional teamsAWS Developer Certification with extensive hands-on experience with core AWS services such as Glue/Glue Studio, S3, Lambda, SageMaker, DynamoDB, Athena, Redshift, RDS, Step Functions, CloudWatch, EC2, SNS, SQS, etc.Experience in building AWS based data ingestion, processing, and analytics pipelines Substantial knowledge of ‘infrastructure as code’ and in particular with Terraform and AWS CLICI/CD systems (preferably GitLab and Jenkins) experience, including configuration management and automation tools (preferably Ansible and Puppet)Hands-on experience with Python coding and Bash shell scriptingNice to Haves:Former experience in the life sciences/ pharma industryKnowledge of Service Orchestration using Kubernetes and/or EKSKnowledge of various databases, both SQL and NoSQLAWS CloudFormation knowledgeExperience with SnowflakeKnowledge of more specialized languages such as ‘R’Experience with troubleshooting performance bottlenecks, considering both Linux, as well as Cloud Native environmentsDoes this sound like your next challenge? I look forward to receiving your application today.
    • basel, basel-stadt
    • temporary
    Für unseren Kunden in der Sicherheitsbranche, suchen wir ab sofort einen pflichtbewussten und zuverlässigen Mitarbeiter Alarmzentrale / Disponent (m/w/d) Deine täglichen Aufgaben sind: Abwicklung von Alarmierungen und NotrufenEinsatzeröffnung und Disposition sämtlicher Pikett- und NotfallorganisationenSofort- und Koordinationsmassnahmen einleiten Weiterleiten der relevanten Informationen an die richtigen StellenZeitgenaue Protokollierung aller Ereignisse
    Für unseren Kunden in der Sicherheitsbranche, suchen wir ab sofort einen pflichtbewussten und zuverlässigen Mitarbeiter Alarmzentrale / Disponent (m/w/d) Deine täglichen Aufgaben sind: Abwicklung von Alarmierungen und NotrufenEinsatzeröffnung und Disposition sämtlicher Pikett- und NotfallorganisationenSofort- und Koordinationsmassnahmen einleiten Weiterleiten der relevanten Informationen an die richtigen StellenZeitgenaue Protokollierung aller Ereignisse
    • basel, basel-stadt
    • permanent
    Bringst Du mehrjährige Berufserfahrung als operativer Einkäufer im Bereich Elektronik oder Mechanik mit? Bist du technisch affin und hast ein grosses Verhandlungsgeschick? Wenn ja, dann suche ich genau Dich in der Funktion als Operativer Einkäufer Elektronik (m/w/d)Dein spannendes Aufgabengebiet beinhaltet:Verantwortlich für eine eigene Materialgruppe Optimierung und Erarbeitung effizienter Beschaffungsprozesse Organisieren und kontrollieren der ganzen Bestellabwicklung von A-Z Verantwortlich für die korrekte Lieferung und Qualität der Produkte Zuständig für das ganze Lieferantenmanagement und PreisverhandlungenErstellung und Ausführung diverser ProjekteDurchführung von Marktanalysen und Massnahmen daraus ergreifen Enge Zusammenarbeit mit dem strategischen EinkaufOptimierung der Prozesse
    Bringst Du mehrjährige Berufserfahrung als operativer Einkäufer im Bereich Elektronik oder Mechanik mit? Bist du technisch affin und hast ein grosses Verhandlungsgeschick? Wenn ja, dann suche ich genau Dich in der Funktion als Operativer Einkäufer Elektronik (m/w/d)Dein spannendes Aufgabengebiet beinhaltet:Verantwortlich für eine eigene Materialgruppe Optimierung und Erarbeitung effizienter Beschaffungsprozesse Organisieren und kontrollieren der ganzen Bestellabwicklung von A-Z Verantwortlich für die korrekte Lieferung und Qualität der Produkte Zuständig für das ganze Lieferantenmanagement und PreisverhandlungenErstellung und Ausführung diverser ProjekteDurchführung von Marktanalysen und Massnahmen daraus ergreifen Enge Zusammenarbeit mit dem strategischen EinkaufOptimierung der Prozesse
    • basel, basel-stadt
    • temporary
    Do you wish to be part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative ?For our client, this pioneering biotechnology company, we are looking for a: Senior Associate, International Manufacturing Operations Location:BaselContract: Temporary for one year. This role is an exciting opportunity to be part of a growing Supply Chain/Manufacturing group. Reporting to Director of International Manufacturing, the successful candidate will work closely with the CMO manufacturing function and Supply Chain function to ensure that the SAP operations are accurate, on track, and in line with GMP compliance and regulatory requirements.Your Responsibilities: Weekly open order book management in collaboration with Manufacturing/Supply Chain in the CMO. The objective is to ensure that the CMO is on track to deliver all released process orders, on-time and in-full. Risks, Opportunities and Issues should be raised and resolved daily.  Daily, or Weekly, Toll material reconciliation process to ensure: All usage of company-owned toll manufacturing materials, by the CMO, is reconciled and accounted for, and that investigations are performed when reconciliation results are outside pre-defined thresholds. That material usage, and inventory transactions, at the CMO are accurately reflected in the SAP system, in a timely way. This can be achieved either through company/CMO system interfaces, or through a manual toll-reconciliation process owned by the Planner.  Execute good receipt and inventory movement transactions required to ensure cross system inventory placement / inventory accuracy Execute the regular raw materials booking within the open process orders in line with CMOs information.Executed Process Orders TECO once that the process orders operations are completed  Ensure compliance with GMP and regulatory requirements (including records management) and spearheads continuous improvements for quality financial flow processes. Your profile:Bachelor level degree in Supply Chain, Business or related field  Between 2 and 3 years of experience in the manufacturing Site preferably as Batch Record Reviewer  Experience in Operation of a highly regulated industry, like Pharmaceutical or related field.  Experience executing SAP Process Orders Raw Materials consumption/Booking .  Ability to manage multiple topics in a fast-paced environment and deal with different stakeholders from different domains in the organization.  Demonstrated ability to critically think and identify solutions.  Well organized – a natural ability to be organized in how you think, communicate and conduct your work  A curious mindset that allows you to constantly learn and challenge the status quo You would like to contribute to a fast-thinking and innovative company, changing the industry ? Apply nowPlease note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position
    Do you wish to be part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative ?For our client, this pioneering biotechnology company, we are looking for a: Senior Associate, International Manufacturing Operations Location:BaselContract: Temporary for one year. This role is an exciting opportunity to be part of a growing Supply Chain/Manufacturing group. Reporting to Director of International Manufacturing, the successful candidate will work closely with the CMO manufacturing function and Supply Chain function to ensure that the SAP operations are accurate, on track, and in line with GMP compliance and regulatory requirements.Your Responsibilities: Weekly open order book management in collaboration with Manufacturing/Supply Chain in the CMO. The objective is to ensure that the CMO is on track to deliver all released process orders, on-time and in-full. Risks, Opportunities and Issues should be raised and resolved daily.  Daily, or Weekly, Toll material reconciliation process to ensure: All usage of company-owned toll manufacturing materials, by the CMO, is reconciled and accounted for, and that investigations are performed when reconciliation results are outside pre-defined thresholds. That material usage, and inventory transactions, at the CMO are accurately reflected in the SAP system, in a timely way. This can be achieved either through company/CMO system interfaces, or through a manual toll-reconciliation process owned by the Planner.  Execute good receipt and inventory movement transactions required to ensure cross system inventory placement / inventory accuracy Execute the regular raw materials booking within the open process orders in line with CMOs information.Executed Process Orders TECO once that the process orders operations are completed  Ensure compliance with GMP and regulatory requirements (including records management) and spearheads continuous improvements for quality financial flow processes. Your profile:Bachelor level degree in Supply Chain, Business or related field  Between 2 and 3 years of experience in the manufacturing Site preferably as Batch Record Reviewer  Experience in Operation of a highly regulated industry, like Pharmaceutical or related field.  Experience executing SAP Process Orders Raw Materials consumption/Booking .  Ability to manage multiple topics in a fast-paced environment and deal with different stakeholders from different domains in the organization.  Demonstrated ability to critically think and identify solutions.  Well organized – a natural ability to be organized in how you think, communicate and conduct your work  A curious mindset that allows you to constantly learn and challenge the status quo You would like to contribute to a fast-thinking and innovative company, changing the industry ? Apply nowPlease note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position
    • basel, basel-stadt
    • contract
    Randstad Professionals is looking for an Associate Director, Signal Management for a major client. This position will be based in Basel .Startdate: ASAP (up to 3 month notice period possible)Contract: 12 monthsThis position will have a high degree of visibility and impact across the organization and will collaborate closely cross-functionally and cross-regionally. Your responsibilities:Provide dynamic strategic contribution to the direction and senior leaders of key pharmacovigilance activities across portfolio and throughout the clinical development and post-marketing phases of the life cycle including: Lead all signal management activities for assigned product(s)  Support implantation of signal detection strategy approved by VP of Pharmacovigilance  Review adverse event data, literature and other safety-related data for the purpose of signal detection  Collaborate with Clinical Safety and Risk Management (CSRM) physicians, safety scientists, and medical colleagues to review safety data for signal validation, prioritization, assessment and proposed action plans Partner with the Director, Pharmacovigilance – Signal Management to oversee digital signal detection and management tool.  Serve as an administrator of the tool  Propose and implement signal detection methods in the tool  Train, mentor and assist CSRM staff in using the tool.  Oversee signal tracking and signal notifications to external stakeholders  Generate periodic signal management compliance metrics Provide safety contents for risk management plans and periodic aggregate safety reports, including but not limited to PBRER/PSUR, PADER, DSUR, and IND annual reports in collaboration with Clinical Safety and Risk Management (CSRM) physicians, safety scientists, and medical colleagues Assess document requirements, gauge document complexity, and identify information gaps or other potential issues. In collaboration with the relevant project team, the author proposes or contributes to strategies to resolve any identified issues  Reviews applicable regulatory intelligence on global regulations/guidance documents and be able to advise report project teams as a Subject Matter Expert (SME) for signal management.  Understand relationships and dependencies between signal management and documents/analyses produced for regulators across the development of RMPs, DSURs, PBRERs, and other annual reports and/or deliverables  Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission  Provide project teams with expertise and strategic guidance on analysis and presentation of safety data and on benefit-risk assessment in documents  Produce high quality, accurate, and fit-for-purpose evaluation documents with clear conclusions, in response to internal or regulatory authority request for safety reasons  Review the worldwide medical/scientific literature to identify signals and applicable information for inclusion in aggregate safety reports in collaboration with CSRM colleagues  Draft regulatory response documents such as PRAC assessment reports  Draft other medical writing deliverables as needed If you are interested to take on these responsibilities you should have the following requirements:Degree in Pharmacy, Nursing, Epidemiology, Biosciences or equivalent healthcare degree with pharmaceutical industry background  Minimum 8 years relevant medical, scientific/clinical, or pharmaceutical experience, including at least 5 years’ experience in Pharmacovigilance  Excellent written and verbal communication skills with the ability to interpret and present safety data  Knowledge of FDA and EMA regulations, ICH guidelines, Good Clinical Practices, and the drug development process  Knowledge of drug safety/pharmacovigilance practices and tools  Ability to coordinate and prioritize multiple projects in a fast-paced environment with limited to little supervision  Background in vaccines is a plus  Demonstrated ability to develop, execute and follow-through complex projects to completion  Skilled at working effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view  Independently motivated, detail oriented and strong problem-solving ability  Excellent organizational skills and demonstrated ability to multitask in a fast-paced environment with changing priorities  Excellent written and verbal communication skills with the ability to interact across multiple functions Did we spark your interest? We look forward to receiving your online application. Please note a Swiss Work permit is mandatory and your residence needs to be in Switzerland for this position. 
    Randstad Professionals is looking for an Associate Director, Signal Management for a major client. This position will be based in Basel .Startdate: ASAP (up to 3 month notice period possible)Contract: 12 monthsThis position will have a high degree of visibility and impact across the organization and will collaborate closely cross-functionally and cross-regionally. Your responsibilities:Provide dynamic strategic contribution to the direction and senior leaders of key pharmacovigilance activities across portfolio and throughout the clinical development and post-marketing phases of the life cycle including: Lead all signal management activities for assigned product(s)  Support implantation of signal detection strategy approved by VP of Pharmacovigilance  Review adverse event data, literature and other safety-related data for the purpose of signal detection  Collaborate with Clinical Safety and Risk Management (CSRM) physicians, safety scientists, and medical colleagues to review safety data for signal validation, prioritization, assessment and proposed action plans Partner with the Director, Pharmacovigilance – Signal Management to oversee digital signal detection and management tool.  Serve as an administrator of the tool  Propose and implement signal detection methods in the tool  Train, mentor and assist CSRM staff in using the tool.  Oversee signal tracking and signal notifications to external stakeholders  Generate periodic signal management compliance metrics Provide safety contents for risk management plans and periodic aggregate safety reports, including but not limited to PBRER/PSUR, PADER, DSUR, and IND annual reports in collaboration with Clinical Safety and Risk Management (CSRM) physicians, safety scientists, and medical colleagues Assess document requirements, gauge document complexity, and identify information gaps or other potential issues. In collaboration with the relevant project team, the author proposes or contributes to strategies to resolve any identified issues  Reviews applicable regulatory intelligence on global regulations/guidance documents and be able to advise report project teams as a Subject Matter Expert (SME) for signal management.  Understand relationships and dependencies between signal management and documents/analyses produced for regulators across the development of RMPs, DSURs, PBRERs, and other annual reports and/or deliverables  Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission  Provide project teams with expertise and strategic guidance on analysis and presentation of safety data and on benefit-risk assessment in documents  Produce high quality, accurate, and fit-for-purpose evaluation documents with clear conclusions, in response to internal or regulatory authority request for safety reasons  Review the worldwide medical/scientific literature to identify signals and applicable information for inclusion in aggregate safety reports in collaboration with CSRM colleagues  Draft regulatory response documents such as PRAC assessment reports  Draft other medical writing deliverables as needed If you are interested to take on these responsibilities you should have the following requirements:Degree in Pharmacy, Nursing, Epidemiology, Biosciences or equivalent healthcare degree with pharmaceutical industry background  Minimum 8 years relevant medical, scientific/clinical, or pharmaceutical experience, including at least 5 years’ experience in Pharmacovigilance  Excellent written and verbal communication skills with the ability to interpret and present safety data  Knowledge of FDA and EMA regulations, ICH guidelines, Good Clinical Practices, and the drug development process  Knowledge of drug safety/pharmacovigilance practices and tools  Ability to coordinate and prioritize multiple projects in a fast-paced environment with limited to little supervision  Background in vaccines is a plus  Demonstrated ability to develop, execute and follow-through complex projects to completion  Skilled at working effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view  Independently motivated, detail oriented and strong problem-solving ability  Excellent organizational skills and demonstrated ability to multitask in a fast-paced environment with changing priorities  Excellent written and verbal communication skills with the ability to interact across multiple functions Did we spark your interest? We look forward to receiving your online application. Please note a Swiss Work permit is mandatory and your residence needs to be in Switzerland for this position. 
    • basel, basel-stadt
    • contract
    Das Department Technische Compliance ist auf der Suche nach einem/r Compliance Experte (m/w/d) für die Betreuung & Implementierung von Qualitätssystemen innerhalb des Engineerings & Energiebetrieben/Werkstätten. Allgemeine Informationen: • Startdatum: asap• Spätestmögliches Startdatum: 01.11.2021• Enddatum: Jahresvertrag• Verlängerung: Wahrscheinlich• Workload: 80-100%• Home Office: nach Absprache zeitweise möglich  Aufgaben & Verantwortlichkeiten: • Unterstützung interner Kunden als anerkannter Berater in sämtlichen technischen GMP Fragestellungen, z.B. Umsetzung von Qualifizierungsanforderungen• Monitoring von Key Performance Indices und Fälligkeiten• Business Process Support für Risk-, Deviation-, Change- und CAPA-Management in enger Kollaboration mit den Qualitätsorganisationen am Standort• Inspektionssupport für den Bereich Technik, Kontakt zu den Subject Matter Experts• Unterstützung und aktive Mitarbeit in agilen Organisationsformen• Unterstützung im Records-Management Must Haves: • Abgeschlossenes technisches Studium oder vergleichbare Ausbildung mit langjähriger Berufserfahrung • Mind. 3 Jahre praktische Erfahrung im Bereich Compliance/Qualitätssicherung von pharmazeutischen, chemischen oder biotechnologischen Anlagen • Praktische Erfahrung in der Umsetzung von technischen GMP-Anforderungen der Zulassungsbehörden (RHI, FDA, EMA etc.) in Investitionsprojekten bzw. in der galenischen/chemischen Produktion• Gute EDV-Kenntnisse (GSuite), Erfahrung in TrackWise, Condor und Veeva von Vorteil• Sehr gute Deutsch- und Englisch- Kenntnisse in Wort und Schrift Persönliche Anforderungen: • Teamplayer mit exzellenten Kommunikationseigenschaften und Verhandlungsfähigkeiten, gepaart mit der Fähigkeit effektive und vertrauensvolle Beziehungen mit Kollegen und Mitarbeitern auf verschiedensten Ebenen aufzubauen• Eigenverantwortliche und selbständige Bearbeitung komplexer Aufgaben sowie zuverlässige Durchsetzung vereinbarter Prioritäten• offen für neue Ideen und hinterfragen konventionelle Denkmuster.
    Das Department Technische Compliance ist auf der Suche nach einem/r Compliance Experte (m/w/d) für die Betreuung & Implementierung von Qualitätssystemen innerhalb des Engineerings & Energiebetrieben/Werkstätten. Allgemeine Informationen: • Startdatum: asap• Spätestmögliches Startdatum: 01.11.2021• Enddatum: Jahresvertrag• Verlängerung: Wahrscheinlich• Workload: 80-100%• Home Office: nach Absprache zeitweise möglich  Aufgaben & Verantwortlichkeiten: • Unterstützung interner Kunden als anerkannter Berater in sämtlichen technischen GMP Fragestellungen, z.B. Umsetzung von Qualifizierungsanforderungen• Monitoring von Key Performance Indices und Fälligkeiten• Business Process Support für Risk-, Deviation-, Change- und CAPA-Management in enger Kollaboration mit den Qualitätsorganisationen am Standort• Inspektionssupport für den Bereich Technik, Kontakt zu den Subject Matter Experts• Unterstützung und aktive Mitarbeit in agilen Organisationsformen• Unterstützung im Records-Management Must Haves: • Abgeschlossenes technisches Studium oder vergleichbare Ausbildung mit langjähriger Berufserfahrung • Mind. 3 Jahre praktische Erfahrung im Bereich Compliance/Qualitätssicherung von pharmazeutischen, chemischen oder biotechnologischen Anlagen • Praktische Erfahrung in der Umsetzung von technischen GMP-Anforderungen der Zulassungsbehörden (RHI, FDA, EMA etc.) in Investitionsprojekten bzw. in der galenischen/chemischen Produktion• Gute EDV-Kenntnisse (GSuite), Erfahrung in TrackWise, Condor und Veeva von Vorteil• Sehr gute Deutsch- und Englisch- Kenntnisse in Wort und Schrift Persönliche Anforderungen: • Teamplayer mit exzellenten Kommunikationseigenschaften und Verhandlungsfähigkeiten, gepaart mit der Fähigkeit effektive und vertrauensvolle Beziehungen mit Kollegen und Mitarbeitern auf verschiedensten Ebenen aufzubauen• Eigenverantwortliche und selbständige Bearbeitung komplexer Aufgaben sowie zuverlässige Durchsetzung vereinbarter Prioritäten• offen für neue Ideen und hinterfragen konventionelle Denkmuster.
    • 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
    • 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
    • contract
    For our client, a pharmaceutical company in the Basel area we are looking for anBioanalytical Manager Start date: middle May 2021, latest August 2021End date:18 monthsExtension: possibleWork location: BaselRemote/Home Office: home office at the momentBackground:This position will be focused on external CRO management. The successful candidate will look after studies done externally from a bioanalytical point of view (e.g measuring blood & tissue concentration in both humans & animals). This will be on both small and large molecules.Tasks & Responsibilities:Lead bioanalytical strategies to generate decision-enabling bioanalytical data with skilled data interpretation to meet and answer project needsResponsible for outsourcing activities in Bioanalytics (bioanalysis of non-clinical and clinical studies); resource and time planning, coordination and administrative management of studies with CROs.Manage the development, transfer and validation of specific and sensitive bioanalytical methods required for the development compound (drug), anti-drug antibodies (ADA), soluble targets and any concomitant/interaction compound in the given project.Manage and direct analysis of samples and timeline from preclinical and clinical studies for the project at CRO labs.Participate actively in PS subteams, act as primary contact person for DMPK project leader.Act as Bioanalytical Leader when required. Interact proactively with the assay development team.Ensure full compliance with the current global and local bioanalytical guidance and GxPs.Leadership in Bioanalysis: *remain current and continually develop expertise in bioanalytical science. Contribute to scientific consortia when required; *maintain current expertise in the validation and conduct of bioanalytical assays; *guide and manage the bioanalysis at CROs and ensure that most advanced and most efficient procedures are used.Provide technical leadership in issue resolution.Review protocols and other relevant documents and guide project teams in all aspects of bioanalytical work required for the project.Review and write reports for regulatory submissions; support filings and answer any questions about bioanalytics coming from the regulatory agencies.Maintain open links with other disciplines within the department and the organization.Advise Group Head concerning all needs relating to administrative processes, technologies and equipment. Inform him of all critical issuesMust haves:Minimum 3 years in a similar position focused on bioanalysis in pharma or CRO (pharma preferred) OR scientist focused on bioanalysisExcellent work experience on both large and small molecules bioanalysis (preferred and will receive 5 stars) IF not both, either large or smallStrong vendor management experience, looking after outsourced studies to external CROs (*****)Degree in biology/biochemistry (*****)
    For our client, a pharmaceutical company in the Basel area we are looking for anBioanalytical Manager Start date: middle May 2021, latest August 2021End date:18 monthsExtension: possibleWork location: BaselRemote/Home Office: home office at the momentBackground:This position will be focused on external CRO management. The successful candidate will look after studies done externally from a bioanalytical point of view (e.g measuring blood & tissue concentration in both humans & animals). This will be on both small and large molecules.Tasks & Responsibilities:Lead bioanalytical strategies to generate decision-enabling bioanalytical data with skilled data interpretation to meet and answer project needsResponsible for outsourcing activities in Bioanalytics (bioanalysis of non-clinical and clinical studies); resource and time planning, coordination and administrative management of studies with CROs.Manage the development, transfer and validation of specific and sensitive bioanalytical methods required for the development compound (drug), anti-drug antibodies (ADA), soluble targets and any concomitant/interaction compound in the given project.Manage and direct analysis of samples and timeline from preclinical and clinical studies for the project at CRO labs.Participate actively in PS subteams, act as primary contact person for DMPK project leader.Act as Bioanalytical Leader when required. Interact proactively with the assay development team.Ensure full compliance with the current global and local bioanalytical guidance and GxPs.Leadership in Bioanalysis: *remain current and continually develop expertise in bioanalytical science. Contribute to scientific consortia when required; *maintain current expertise in the validation and conduct of bioanalytical assays; *guide and manage the bioanalysis at CROs and ensure that most advanced and most efficient procedures are used.Provide technical leadership in issue resolution.Review protocols and other relevant documents and guide project teams in all aspects of bioanalytical work required for the project.Review and write reports for regulatory submissions; support filings and answer any questions about bioanalytics coming from the regulatory agencies.Maintain open links with other disciplines within the department and the organization.Advise Group Head concerning all needs relating to administrative processes, technologies and equipment. Inform him of all critical issuesMust haves:Minimum 3 years in a similar position focused on bioanalysis in pharma or CRO (pharma preferred) OR scientist focused on bioanalysisExcellent work experience on both large and small molecules bioanalysis (preferred and will receive 5 stars) IF not both, either large or smallStrong vendor management experience, looking after outsourced studies to external CROs (*****)Degree in biology/biochemistry (*****)
    • basel, basel-stadt
    • contract
    For our client, a pharmaceutical company in Basel we are looking for aClinical Trial LeaderStart date: asapEnd date: 31.12.2022Extension: possibleWork location: BaselWorkload: 100%Responsible for the management and clinical execution of assigned clinical trials within Translational Medicine (TM). Functions as the CTL on the planning and implementation of all operational aspects of assigned TM clinical trials from study concept to reporting according to timelines, budget, operational and quality standards (ICH/GCP/Novartis SOPs and procedures).Tasks & Responsibilities:Function as Clinical Trial Leader for assigned studies (scientific and/or operational complexity) including multi-country / multi-center trials. The main focus will be de- pendent on department workload and need).Responsible for leading and matrix managing the multidisciplinary CTT and support functions to ensure all trial deliverables are met according to timelines, budget, quality standards and operational best practicesAuthor of the clinical study protocol and other study essential documents.Responsible for ordering and management of clinical trial materials, including drug supplies and CRFs.In collaboration with outsourcing/planning/feasibility personnel, CTT, Local CPO representatives and CRAs, identify sites and manage study set-up, including responsibility for organizing and chairing the Investigator meeting(s) (as appropriate), and/or Site Initiation meeting(s).Train and support the CRA(s)/CRO(s) on study protocol and related questions and serve as point of contact for managing/answering questions relating to trial procedures and subjects’ eligibility.Ensure the set up and maintenance of the Trial Master File for assigned studies, ensuring all relevant study documents are filed and archived at the end of the study according to the appropriate guidelines.Interact with Investigator sites and CRAs/CROs/vendors to ensure smooth study set up and excellence of study conduct, reviewing site performance, protocol deviations, and maintaining awareness of issues raised.Assist in data review and interactions with the Data Manager, Statistician, and third parties (e.g. outsourced data management or data vendors) to ensure high-quality data are transferred/available in a timely manner.Responsible for report writing of assigned studies either directly contributing to and managing the report writing or liaising with the medical writing/narrative group to ensure the report is completed according to current requirement. Responsible for report publication.In collaboration with the Medical Expert and CTT, coordinate the ongoing medical/scientific review of the clinical trial data (as needed), and coordinate the data analysis and interpretation including the development of first interpretable results, the clinical study report, publications and internal/external presentations. May support the Medical Expert on project documentation e.g. Briefing books, IBs, Annual Safety Reports, responses to Health Authority questions, etc.Ensure a complete review is conducted of all study documentation within the assigned studies/project at the end of each study, with all essential documents appropriately archived and paper Trial Master Files physically transferred to the central archive.Responsible for the coordination of pre-audit activities for nominated projects ensuring a satisfactory outcome is achieved, and address corrective actions.Oversee the work of assigned support CTL(s), ensuring clear delegation/assignment of duties are documented.Contribute to the identification and evaluation of new clinical sites as appropriate for assigned studies.Provide CS&I expert advice to other departments and line functions (e.g. CQA, Drug Metabolism and Pharmacokinetics (DMPK), Drug Supply Management (DSM) as applicable to assigned studies.Must-haves:BSc or MSc in life sciences or nursing; a Ph.D. level scientist with life sciences background; PharmD or equivalent qualification or work experience.Relevant experience (5+ years) in clinical trial management (e.g. study management in a multi-national environment using different models for trial execution).Demonstrated leadership and problem-solving skills.Track record of managing multiple, complex clinical trials.Capable of clear written and verbal expression of ideas, an active/proactive communicator.Ability to interact with a wide range of people and build strong positive relationships.Potential for customer orientation awareness and focus.Excellent organizational skills and interpersonal skills.Ability to work independently and in a team environment managing multiple priorities.
    For our client, a pharmaceutical company in Basel we are looking for aClinical Trial LeaderStart date: asapEnd date: 31.12.2022Extension: possibleWork location: BaselWorkload: 100%Responsible for the management and clinical execution of assigned clinical trials within Translational Medicine (TM). Functions as the CTL on the planning and implementation of all operational aspects of assigned TM clinical trials from study concept to reporting according to timelines, budget, operational and quality standards (ICH/GCP/Novartis SOPs and procedures).Tasks & Responsibilities:Function as Clinical Trial Leader for assigned studies (scientific and/or operational complexity) including multi-country / multi-center trials. The main focus will be de- pendent on department workload and need).Responsible for leading and matrix managing the multidisciplinary CTT and support functions to ensure all trial deliverables are met according to timelines, budget, quality standards and operational best practicesAuthor of the clinical study protocol and other study essential documents.Responsible for ordering and management of clinical trial materials, including drug supplies and CRFs.In collaboration with outsourcing/planning/feasibility personnel, CTT, Local CPO representatives and CRAs, identify sites and manage study set-up, including responsibility for organizing and chairing the Investigator meeting(s) (as appropriate), and/or Site Initiation meeting(s).Train and support the CRA(s)/CRO(s) on study protocol and related questions and serve as point of contact for managing/answering questions relating to trial procedures and subjects’ eligibility.Ensure the set up and maintenance of the Trial Master File for assigned studies, ensuring all relevant study documents are filed and archived at the end of the study according to the appropriate guidelines.Interact with Investigator sites and CRAs/CROs/vendors to ensure smooth study set up and excellence of study conduct, reviewing site performance, protocol deviations, and maintaining awareness of issues raised.Assist in data review and interactions with the Data Manager, Statistician, and third parties (e.g. outsourced data management or data vendors) to ensure high-quality data are transferred/available in a timely manner.Responsible for report writing of assigned studies either directly contributing to and managing the report writing or liaising with the medical writing/narrative group to ensure the report is completed according to current requirement. Responsible for report publication.In collaboration with the Medical Expert and CTT, coordinate the ongoing medical/scientific review of the clinical trial data (as needed), and coordinate the data analysis and interpretation including the development of first interpretable results, the clinical study report, publications and internal/external presentations. May support the Medical Expert on project documentation e.g. Briefing books, IBs, Annual Safety Reports, responses to Health Authority questions, etc.Ensure a complete review is conducted of all study documentation within the assigned studies/project at the end of each study, with all essential documents appropriately archived and paper Trial Master Files physically transferred to the central archive.Responsible for the coordination of pre-audit activities for nominated projects ensuring a satisfactory outcome is achieved, and address corrective actions.Oversee the work of assigned support CTL(s), ensuring clear delegation/assignment of duties are documented.Contribute to the identification and evaluation of new clinical sites as appropriate for assigned studies.Provide CS&I expert advice to other departments and line functions (e.g. CQA, Drug Metabolism and Pharmacokinetics (DMPK), Drug Supply Management (DSM) as applicable to assigned studies.Must-haves:BSc or MSc in life sciences or nursing; a Ph.D. level scientist with life sciences background; PharmD or equivalent qualification or work experience.Relevant experience (5+ years) in clinical trial management (e.g. study management in a multi-national environment using different models for trial execution).Demonstrated leadership and problem-solving skills.Track record of managing multiple, complex clinical trials.Capable of clear written and verbal expression of ideas, an active/proactive communicator.Ability to interact with a wide range of people and build strong positive relationships.Potential for customer orientation awareness and focus.Excellent organizational skills and interpersonal skills.Ability to work independently and in a team environment managing multiple priorities.
    • 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
    • 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
    • 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
    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
    • 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
    • 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 Mitarbeiter-Pool 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 Mitarbeiter-Pool 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
    • 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
    • temp to perm
    Wir suchenLogistiker (m/w)Aufgaben· Be- und Entladen von LKW· Kommissionierung, Labeln und Verpackung der Ware· Eingangskontrolle und Einlagern von Waren· Kontrolle der ausgehenden Sendungen· Bearbeiten von Retouren· Mitarbeit bei der Inventurdurchführung· Disponieren der eingehenden und ausgehenden Sendungen· Diverse administrative Tätigkeiten
    Wir suchenLogistiker (m/w)Aufgaben· Be- und Entladen von LKW· Kommissionierung, Labeln und Verpackung der Ware· Eingangskontrolle und Einlagern von Waren· Kontrolle der ausgehenden Sendungen· Bearbeiten von Retouren· Mitarbeit bei der Inventurdurchführung· Disponieren der eingehenden und ausgehenden Sendungen· Diverse administrative Tätigkeiten
    • 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 Data 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 Data 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
    • temporary
    We are looking for a Capex Procurement Lead Buyer (m/f/d) for Lonza AG (100%). This is a temporary position for 12 months, with an option of extension. Remote work within Switzerland is possible, with regular days on site in Visp. 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: Supporting Procurement Category Manager to:Develop and execute a category strategy for Engineering Services that matches supply market capabilities with Lonza business needs.Lead supplier relationship management (SRM) and supplier development activities to ensure reliable supply and maximize the full value of supplier relationships.Drive supplier performance, compliance and accountability through supplier scorecards and performance metricsDevelop supply risk management strategies and drive development and implementation of appropriate risk mitigation plans.Manage relationships with suppliers acting as the primary point of contact for assigned suppliers.Work closely with Project Procurement colleagues to ensure category strategies are translated into project execution plans.Plan, lead and execute negotiations of commercial terms and contracting for framework, master and other major supply agreements.Ensure project sourcing objectives, actions and priorities are aligned both within Global Capex Procurement, Global Engineering and project stakeholders.Work closely with key stakeholders to develop cost reduction strategies and implementation plans that meet projects / business needs.Report savings monthly as well as maintain the project savings pipeline.Project procurement tasks, including:Procurement of services (consulting, engineering and planning) for the assigned investment projects.Development of project purchasing strategy, execution and coordination of procurement activities for assigned investment projects. Drive awareness of supply issues within the project, clarifying business impact and lead resolution plans.
    We are looking for a Capex Procurement Lead Buyer (m/f/d) for Lonza AG (100%). This is a temporary position for 12 months, with an option of extension. Remote work within Switzerland is possible, with regular days on site in Visp. 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: Supporting Procurement Category Manager to:Develop and execute a category strategy for Engineering Services that matches supply market capabilities with Lonza business needs.Lead supplier relationship management (SRM) and supplier development activities to ensure reliable supply and maximize the full value of supplier relationships.Drive supplier performance, compliance and accountability through supplier scorecards and performance metricsDevelop supply risk management strategies and drive development and implementation of appropriate risk mitigation plans.Manage relationships with suppliers acting as the primary point of contact for assigned suppliers.Work closely with Project Procurement colleagues to ensure category strategies are translated into project execution plans.Plan, lead and execute negotiations of commercial terms and contracting for framework, master and other major supply agreements.Ensure project sourcing objectives, actions and priorities are aligned both within Global Capex Procurement, Global Engineering and project stakeholders.Work closely with key stakeholders to develop cost reduction strategies and implementation plans that meet projects / business needs.Report savings monthly as well as maintain the project savings pipeline.Project procurement tasks, including:Procurement of services (consulting, engineering and planning) for the assigned investment projects.Development of project purchasing strategy, execution and coordination of procurement activities for assigned investment projects. Drive awareness of supply issues within the project, clarifying business impact and lead resolution plans.
    • 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 - 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
    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 im Raum Basel , suchen wir genau Dich ein Motivierten Laborant (m/w/d) 100%In dieser Position bist Du zuständig für die Durchführung praktischer Arbeiten im Labor zur Qualifizierung von Referenzstandards (HPLC, NMR, Titrationen, IR, MS, Restlösungsmittelbestimmungen etc.)Du dokumentierst GMP-konform die durchgeführten Arbeiten im LIMS sowie die Auswertung der resultierenden RohdatenDu hilfst mit bei der Erstellung von Protokollen, Berichten und AnalysenzertifikatenDu unterstützt bei der Verwaltung von Referenzstandards (Ausgabe der Standards, Überwachung von Ablaufdaten und Restmengen)Du hilfst mit bei Qualifizierungen, Kalibrierungen und Wartungen der analytischen LaborgeräteDein Tätigkeitsgebiet wird abgerundet durch Deine Unterstützung bei der Erstellung von Vorgabedokumenten (SOP's) und Analysenvorschriften
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Laborant (m/w/d) 100%In dieser Position bist Du zuständig für die Durchführung praktischer Arbeiten im Labor zur Qualifizierung von Referenzstandards (HPLC, NMR, Titrationen, IR, MS, Restlösungsmittelbestimmungen etc.)Du dokumentierst GMP-konform die durchgeführten Arbeiten im LIMS sowie die Auswertung der resultierenden RohdatenDu hilfst mit bei der Erstellung von Protokollen, Berichten und AnalysenzertifikatenDu unterstützt bei der Verwaltung von Referenzstandards (Ausgabe der Standards, Überwachung von Ablaufdaten und Restmengen)Du hilfst mit bei Qualifizierungen, Kalibrierungen und Wartungen der analytischen LaborgeräteDein Tätigkeitsgebiet wird abgerundet durch Deine Unterstützung bei der Erstellung von Vorgabedokumenten (SOP's) und Analysenvorschriften
    • basel, basel-stadt
    • temp to perm
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Chemielaborant (m/w/d) 100%Herstellung von sterilen und nicht sterilen halbfesten und flüssigen ArzneiformenVor- und Nachbereitung der Herstellung (wie Sterilisations- und Reinigungsprozesse)Bedienen der ProduktionsanlagenProtokollieren der durchgeführten Arbeiten in der ProduktionsdokumentationArbeiten unter GMP Bedingungen
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Chemielaborant (m/w/d) 100%Herstellung von sterilen und nicht sterilen halbfesten und flüssigen ArzneiformenVor- und Nachbereitung der Herstellung (wie Sterilisations- und Reinigungsprozesse)Bedienen der ProduktionsanlagenProtokollieren der durchgeführten Arbeiten in der ProduktionsdokumentationArbeiten unter GMP Bedingungen
    • basel, basel-stadt
    • temp to perm
    Für unseren Kunden im Baselbiet suchen wir genau dich Operator Utilities / Instandhaltungsfachmann (m/w/d)Deine Hauptaufgaben:Sicherstellung von Betrieb, Unterhalt und Störungsbehebung an VersorgungsanlagenAusführen von Unterhaltsarbeiten, Revisionsarbeiten Behebung von Störungen an wichtigen technischen Anlagen mit hoher Priorität Protokoll über die durchgeführten Kontroll- und UnterhaltsarbeitenUnterstützung bei Audit und InspektionsanforderungenUnterstützung bei der Erstellung und / oder Support von Notice of Events (NOE), CAPAs, Abweichungen sowie Charge ControlsSchichtdienst 24h Betrieb
    Für unseren Kunden im Baselbiet suchen wir genau dich Operator Utilities / Instandhaltungsfachmann (m/w/d)Deine Hauptaufgaben:Sicherstellung von Betrieb, Unterhalt und Störungsbehebung an VersorgungsanlagenAusführen von Unterhaltsarbeiten, Revisionsarbeiten Behebung von Störungen an wichtigen technischen Anlagen mit hoher Priorität Protokoll über die durchgeführten Kontroll- und UnterhaltsarbeitenUnterstützung bei Audit und InspektionsanforderungenUnterstützung bei der Erstellung und / oder Support von Notice of Events (NOE), CAPAs, Abweichungen sowie Charge ControlsSchichtdienst 24h Betrieb
    • 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
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