94 jobs found in Basel, Basel-Stadt

filter2
clear all
    • basel, basel-stadt
    • temporary
    For Lonza Drug Product Services (DPS), a successful Contract Development and Manufacturing Organization (CDMO) branch, located in Basel, Switzerland Randstad (Switzerland) AG has exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join Lonza by applying for the position as Senior Technology Transfer Lead. This position is temporary until end of the year 2021. Key responsibilities:Ensure all activities are performed according to current quality, regulatory and health and safety standards. Manage technical activities for drug product transfers from clinical development to first commercial launch of assigned projectsDefine and monitor project scope, timing and progressLead setup, scale-up and implementation of the technical drug product manufacturing processes at GMP DP manufacturing site(s) and provide technical on-site supportResponsible for process implementation and technical transfer documentationDrive GMP change management strategy of assigned projects as well as initiate and manage GMP change control in systemSupport preparation of regulatory documentationLead and support critical GMP product / process deviations and corresponding implementation of corrective/preventive actions (CAPAs)Perform/support GMP and HA regulatory inspections and audits e.g. customer audits, PAI of assigned projectsEnsure all activities are performed according to current standards (Good Manufacturing Practice (cGMP), Health Safety Environment (HSE), Regulatory, etc.)Enable innovation and technical strategy projects, generate IP and contribute to scientific publications and conference talks, and evaluate and implement of new methods and technologies
    For Lonza Drug Product Services (DPS), a successful Contract Development and Manufacturing Organization (CDMO) branch, located in Basel, Switzerland Randstad (Switzerland) AG has exciting opportunities. Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join Lonza by applying for the position as Senior Technology Transfer Lead. This position is temporary until end of the year 2021. Key responsibilities:Ensure all activities are performed according to current quality, regulatory and health and safety standards. Manage technical activities for drug product transfers from clinical development to first commercial launch of assigned projectsDefine and monitor project scope, timing and progressLead setup, scale-up and implementation of the technical drug product manufacturing processes at GMP DP manufacturing site(s) and provide technical on-site supportResponsible for process implementation and technical transfer documentationDrive GMP change management strategy of assigned projects as well as initiate and manage GMP change control in systemSupport preparation of regulatory documentationLead and support critical GMP product / process deviations and corresponding implementation of corrective/preventive actions (CAPAs)Perform/support GMP and HA regulatory inspections and audits e.g. customer audits, PAI of assigned projectsEnsure all activities are performed according to current standards (Good Manufacturing Practice (cGMP), Health Safety Environment (HSE), Regulatory, etc.)Enable innovation and technical strategy projects, generate IP and contribute to scientific publications and conference talks, and evaluate and implement of new methods and technologies
    • basel, basel-stadt
    • temp to perm
    Für unseren Kunden aus der Region Basel, suchen wir per sofort oder nach Vereinbarung eine/nSchreiner für die Montage (m/w)Deine Perspektive:Unkomplizierter Einstieg nach VereinbarungZeitgemässe Entlohnung Attraktive ArbeitszeitenEin Unternehmen mit betireblichen fortbildungsprogramm oder vielseitigen Entwicklungsmöglichkeiten Deine Aufgaben:Du führst selbständige Arbeiten aus nach PlanDu bist zuständig für das Erstellen von Komponenten für Möbel- oder LadenbauDu übernimmst allg. Schreinerarbeiten wieDu unterstützt das Montageteam
    Für unseren Kunden aus der Region Basel, suchen wir per sofort oder nach Vereinbarung eine/nSchreiner für die Montage (m/w)Deine Perspektive:Unkomplizierter Einstieg nach VereinbarungZeitgemässe Entlohnung Attraktive ArbeitszeitenEin Unternehmen mit betireblichen fortbildungsprogramm oder vielseitigen Entwicklungsmöglichkeiten Deine Aufgaben:Du führst selbständige Arbeiten aus nach PlanDu bist zuständig für das Erstellen von Komponenten für Möbel- oder LadenbauDu übernimmst allg. Schreinerarbeiten wieDu unterstützt das Montageteam
    • basel, basel-stadt
    • temp to perm
    Bist du eine flexible, belastbare und engagierte Person? Verfügst du über ein Auge fürs Detail und kannst es dir vorstellen wieder in der Gastronomie zu arbeiten? Zur Ergänzung des gut eingespielten Teams unseres Kunden suchen wir per sofort:Servicemitarbeiter (m/w/d) in Basel 100%Deine Aufgaben:Gäste beraten und Bestellungen aufnehmenGetränke und Speisen fachgerecht servierenGäste-Rechnungen erstellen und einkassierenTägliches Mise en Place für das ganze Restaurant erstellenReinigungsarbeiten gemäss dem Hygienekonzept ausführen
    Bist du eine flexible, belastbare und engagierte Person? Verfügst du über ein Auge fürs Detail und kannst es dir vorstellen wieder in der Gastronomie zu arbeiten? Zur Ergänzung des gut eingespielten Teams unseres Kunden suchen wir per sofort:Servicemitarbeiter (m/w/d) in Basel 100%Deine Aufgaben:Gäste beraten und Bestellungen aufnehmenGetränke und Speisen fachgerecht servierenGäste-Rechnungen erstellen und einkassierenTägliches Mise en Place für das ganze Restaurant erstellenReinigungsarbeiten gemäss dem Hygienekonzept ausführen
    • basel, basel-stadt
    • temporary
    Wenn du dir neben deinem Studium etwas dazu verdienen willst oder nach einer Möglichkeit suchst dein Taschengeld etwas aufzustockenDann bist du genau richtig bei uns!Für unseren Kunden suchen wir flexible und motivierteServicemitarbeiter (m/w)Hauptaufgaben:bedienen und beraten der Gästeführen einer eigenen Stationmithilfe bei Banketten, Caterings, Events oder in Kantinenmise en place Aufgabenallgemeine Aufräum- und Reinigungsarbeiten
    Wenn du dir neben deinem Studium etwas dazu verdienen willst oder nach einer Möglichkeit suchst dein Taschengeld etwas aufzustockenDann bist du genau richtig bei uns!Für unseren Kunden suchen wir flexible und motivierteServicemitarbeiter (m/w)Hauptaufgaben:bedienen und beraten der Gästeführen einer eigenen Stationmithilfe bei Banketten, Caterings, Events oder in Kantinenmise en place Aufgabenallgemeine Aufräum- und Reinigungsarbeiten
    • basel, basel-stadt
    • temporary
    We are looking for a Demand Planning - Center of Excellence Specialist (m/f/d) for Lonza AG (100%). This is a temporary position for 24 months. The position is based in Basel, remote work is possible too. Today, Lonza is a global leader in life sciences operating across three continents. While Lonza works in science, there's no magic formula to how they do it. Their greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, they let their people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work Lonza wants to be part of. Key responsibilities:Accountable for ensuring Demand Planning, Management standard processes are followedSupport Global Lead Demand in IBP DP development Drive the implementation of approved Demand Planning blueprints (organizations, processes, activities, roles and responsibilities) Deploy Demand Planning processes, policies and tools through communication and training to enable continuous improvement of Division KPIsEnsure alignment with S&OP and Supply Planning Global Leads Expert knowledge in S&OP, support program deployment and ability to deliver training Deliver training to new team members, liaise with CoE team on training improvementCertify the IBP tool is being utilized fully and properly within LPB GroupOngoing responsibility for the development and maintenance of the Demand Planning community fostering knowledge and best practice sharingReview Business and Demand related KPIs, use as basis for planning improvement initiatives contributing to continuous improvements across the divisions
    We are looking for a Demand Planning - Center of Excellence Specialist (m/f/d) for Lonza AG (100%). This is a temporary position for 24 months. The position is based in Basel, remote work is possible too. Today, Lonza is a global leader in life sciences operating across three continents. While Lonza works in science, there's no magic formula to how they do it. Their greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, they let their people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work Lonza wants to be part of. Key responsibilities:Accountable for ensuring Demand Planning, Management standard processes are followedSupport Global Lead Demand in IBP DP development Drive the implementation of approved Demand Planning blueprints (organizations, processes, activities, roles and responsibilities) Deploy Demand Planning processes, policies and tools through communication and training to enable continuous improvement of Division KPIsEnsure alignment with S&OP and Supply Planning Global Leads Expert knowledge in S&OP, support program deployment and ability to deliver training Deliver training to new team members, liaise with CoE team on training improvementCertify the IBP tool is being utilized fully and properly within LPB GroupOngoing responsibility for the development and maintenance of the Demand Planning community fostering knowledge and best practice sharingReview Business and Demand related KPIs, use as basis for planning improvement initiatives contributing to continuous improvements across the divisions
    • basel, basel-stadt
    • 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
    • permanent
    Bei Randstad zu arbeiten ist anders als nur in einer Organisation zu arbeiten. Denn bei Randstad setzen wir Menschen in den Mittelpunkt unseres Handelns. Das gilt für unsere Kunden, unsere Kandidaten, unsere Mitarbeiter und die Gesellschaft. Indem wir unsere Leidenschaft für Menschen mit der Kraft heutiger Technologien verbinden, unterstützen wir Menschen und Organisationen dabei, ihr wahres Potenzial zu verwirklichen. Wir nennen das Human Forward. Bist du unser neues Team Mitglied? Wir suchen nach einem/rConsultant mit kommerzieller DNA in Basel job beschreibungDies ist eine verkaufs-fokussierte Rolle, die die Gewinnung neuer und die Betreuung bestehender Kunden und deren Erwartungen, sowie umfangreiche Geschäftstätigkeiten beinhaltet. Um erfolgreich zu sein, musst du ergebnisorientiert und in der Lage sein, konkurrierende Anforderungen geschickt auszubalancieren.Du fragst dich, was genau das bedeutet? Wir erklären es dir näher:Du verwaltest die Markt-/Branchenzuordnung für Dein zugewiesenes Portfolio.Du bist verantwortlich für das Wachstum und die Entwicklung der Kundendatenbank durch den Aufbau von Kundenbeziehungen über Kaltakquise und Kunden-/Prospektbesuche in einem bestimmten lokalen Gebiet.Du führst Follow-up Gespräche mit Kunden und Interessenten zur Bestätigung der Personalpläne und des Kandidatenbedarfs.Du erarbeitest eine Strategie mit zukünftigen Kunden, um deren Rekrutierungspläne zu entwickeln um Dein Reichweite innerhalb ihrer Organisationen zu erweitern.Du unterstützt Unternehmen und Bewerbern aktiv durch die Vermittlung der richtigen Personen an die richtigen Stellen.Du übernimmst den gesamten Rekrutierungszyklus von der Ausschreibung der Stellen über die Prüfung von Lebensläufen bis hin zu persönlichen Gesprächen.
    Bei Randstad zu arbeiten ist anders als nur in einer Organisation zu arbeiten. Denn bei Randstad setzen wir Menschen in den Mittelpunkt unseres Handelns. Das gilt für unsere Kunden, unsere Kandidaten, unsere Mitarbeiter und die Gesellschaft. Indem wir unsere Leidenschaft für Menschen mit der Kraft heutiger Technologien verbinden, unterstützen wir Menschen und Organisationen dabei, ihr wahres Potenzial zu verwirklichen. Wir nennen das Human Forward. Bist du unser neues Team Mitglied? Wir suchen nach einem/rConsultant mit kommerzieller DNA in Basel job beschreibungDies ist eine verkaufs-fokussierte Rolle, die die Gewinnung neuer und die Betreuung bestehender Kunden und deren Erwartungen, sowie umfangreiche Geschäftstätigkeiten beinhaltet. Um erfolgreich zu sein, musst du ergebnisorientiert und in der Lage sein, konkurrierende Anforderungen geschickt auszubalancieren.Du fragst dich, was genau das bedeutet? Wir erklären es dir näher:Du verwaltest die Markt-/Branchenzuordnung für Dein zugewiesenes Portfolio.Du bist verantwortlich für das Wachstum und die Entwicklung der Kundendatenbank durch den Aufbau von Kundenbeziehungen über Kaltakquise und Kunden-/Prospektbesuche in einem bestimmten lokalen Gebiet.Du führst Follow-up Gespräche mit Kunden und Interessenten zur Bestätigung der Personalpläne und des Kandidatenbedarfs.Du erarbeitest eine Strategie mit zukünftigen Kunden, um deren Rekrutierungspläne zu entwickeln um Dein Reichweite innerhalb ihrer Organisationen zu erweitern.Du unterstützt Unternehmen und Bewerbern aktiv durch die Vermittlung der richtigen Personen an die richtigen Stellen.Du übernimmst den gesamten Rekrutierungszyklus von der Ausschreibung der Stellen über die Prüfung von Lebensläufen bis hin zu persönlichen Gesprächen.
    • basel, basel-stadt
    • temporary
    For our client, a growing company in the pharmaceutical industry, we are looking for a :Planning Coordinator/Expert Location: BaselContract: Temporary for 6 months with possibility to extend or become permanentMain objective:This position is responsible to manage the operational planning incl. inbound flows (orders and shipments) and the associated tools/processes (incl. Artwork management). Acts as Super User in the management of the SAP setup (MM, IBP)Your Main Responsibilities:  Perform monthly supply planning operations in close cooperation with the Global Planning Manager (in Excel and SAP IBP)Supply PO placement with suppliers and follow upManagement of inbound flows incl. organization of inbound shipments from supplier to HUBSuper User SAP (MM,IBP) supporting the SAP implementations and ensuring correct setup of SAP in collaboration with the business and ITMaintain SAP Master Data accuracyManage/support projects in the Supply Chain areaEnsure operationally with external Artwork Supplier and internal functions management of Artwork changesYour profile:University Degree in Supply Chain or very Supply Chain related functionsMin 3 years on hand experience as Planning Coordinator/Expert with intense exposure to SAP and Artwork creation, preferably in the pharmaceutical/Consumer Health businessVery strong analytical thinkingSelf-starter, able to work independently and picking up responsibility in a newly created Supply chainContinuous Improvement mindset.Ability to work accurately under pressureAbility to work in remote teamsSAP (IBP, MM)MS Excel (very good knowledge incl. creation of own complex reports/spreadsheets)Very good English (must have),French & Italian (asset) Please note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position 
    For our client, a growing company in the pharmaceutical industry, we are looking for a :Planning Coordinator/Expert Location: BaselContract: Temporary for 6 months with possibility to extend or become permanentMain objective:This position is responsible to manage the operational planning incl. inbound flows (orders and shipments) and the associated tools/processes (incl. Artwork management). Acts as Super User in the management of the SAP setup (MM, IBP)Your Main Responsibilities:  Perform monthly supply planning operations in close cooperation with the Global Planning Manager (in Excel and SAP IBP)Supply PO placement with suppliers and follow upManagement of inbound flows incl. organization of inbound shipments from supplier to HUBSuper User SAP (MM,IBP) supporting the SAP implementations and ensuring correct setup of SAP in collaboration with the business and ITMaintain SAP Master Data accuracyManage/support projects in the Supply Chain areaEnsure operationally with external Artwork Supplier and internal functions management of Artwork changesYour profile:University Degree in Supply Chain or very Supply Chain related functionsMin 3 years on hand experience as Planning Coordinator/Expert with intense exposure to SAP and Artwork creation, preferably in the pharmaceutical/Consumer Health businessVery strong analytical thinkingSelf-starter, able to work independently and picking up responsibility in a newly created Supply chainContinuous Improvement mindset.Ability to work accurately under pressureAbility to work in remote teamsSAP (IBP, MM)MS Excel (very good knowledge incl. creation of own complex reports/spreadsheets)Very good English (must have),French & Italian (asset) Please note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position 
    • basel, basel-stadt
    • temp to perm
    Für wiederkehrende und längere Einsätze und unserem Pool suchen wirKoch / KöchinAufgabenZubereitung und anrichten einzelner Gerichte sowie ganzer Menüs und à la carteVerantwortung auf allen PostenKontrolle und Verwaltung des WarenbestandsVerantwortung für die Einhaltung der strengen Hygienevorschriften gemäss HACCP
    Für wiederkehrende und längere Einsätze und unserem Pool suchen wirKoch / KöchinAufgabenZubereitung und anrichten einzelner Gerichte sowie ganzer Menüs und à la carteVerantwortung auf allen PostenKontrolle und Verwaltung des WarenbestandsVerantwortung für die Einhaltung der strengen Hygienevorschriften gemäss HACCP
    • basel, basel-stadt
    • permanent
    Für unseren Kunden im Raum Basel suchen wir genau dich ab sofort oder nach Vereinbarung einen:Kältetechniker (m/w/d)Deine Hauptaufgaben:Instandhaltung und Umbau von kältetechnischen Anlagen und SystemenStörungsbehebungen an kältetechnischen AnlagenDurchführung der periodischen WartungenPlanung, Kontrolle und Ausführung aller notwendigen Arbeiten in Zusammenarbeit mit den zuständigen internen und kundenseitigen StellenErstellen der notwendigen Dokumentationen, Rapporte etc.Leisten von Pikettdienst
    Für unseren Kunden im Raum Basel suchen wir genau dich ab sofort oder nach Vereinbarung einen:Kältetechniker (m/w/d)Deine Hauptaufgaben:Instandhaltung und Umbau von kältetechnischen Anlagen und SystemenStörungsbehebungen an kältetechnischen AnlagenDurchführung der periodischen WartungenPlanung, Kontrolle und Ausführung aller notwendigen Arbeiten in Zusammenarbeit mit den zuständigen internen und kundenseitigen StellenErstellen der notwendigen Dokumentationen, Rapporte etc.Leisten von Pikettdienst
    • basel, basel-stadt
    • temp to perm
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen hoch motivierten Betriebselektriker oder Automatiker. (m/w)Deine Aufgaben:Störungsanalyse, Fehlerbehebung und Reparatur an Produktionsanlagen und InfrastrukturUmsetzung von technischen Optimierungen (Steuerung- , Regel und Antriebstechnik)Projektmitarbeit bei Umbauten, Neuinstallationen und Inbetriebnahmen von Maschinen und AnlagenNachführen von technischen Unterlagen und Schemas
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen hoch motivierten Betriebselektriker oder Automatiker. (m/w)Deine Aufgaben:Störungsanalyse, Fehlerbehebung und Reparatur an Produktionsanlagen und InfrastrukturUmsetzung von technischen Optimierungen (Steuerung- , Regel und Antriebstechnik)Projektmitarbeit bei Umbauten, Neuinstallationen und Inbetriebnahmen von Maschinen und AnlagenNachführen von technischen Unterlagen und Schemas
    • basel, basel-stadt
    • contract
    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
    • 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
    • permanent
    Bringst du eine hohe Kundenorientierung und Erfahrung im Küchenbereich mit? Suchst Du eine neue Herausforderung im Aussendienst? Wenn ja, dann suchen wir Dich ab sofort oder nach Vereinbarung alsFachverkäufer Aussendienst Küche (m/w/d)Deine Aufgaben sind folgende:Du bist verantwortlich für die Neukundengewinnung Du berätst die Kunden als Fachkraft Du betreust schon bestehende Kunden Du unterstützt bei der Offertenerstellung Du hilfst mit bei Ausstellungen
    Bringst du eine hohe Kundenorientierung und Erfahrung im Küchenbereich mit? Suchst Du eine neue Herausforderung im Aussendienst? Wenn ja, dann suchen wir Dich ab sofort oder nach Vereinbarung alsFachverkäufer Aussendienst Küche (m/w/d)Deine Aufgaben sind folgende:Du bist verantwortlich für die Neukundengewinnung Du berätst die Kunden als Fachkraft Du betreust schon bestehende Kunden Du unterstützt bei der Offertenerstellung Du hilfst mit bei Ausstellungen
    • basel, basel-stadt
    • temp to perm
    Für unseren Kunden im Raum Baselland suchen wir per sofort eine/n Lagermitarbeiter/in mit SUVA Staplerschein 100%Ihre Aufgaben:LagerwirtschaftungKommissionierung der WareEntgegennahme und Kontrolle der gelieferten WarenEinlagerung der WarenBereitstellung und Warenübergabe an unsere Kundschaft
    Für unseren Kunden im Raum Baselland suchen wir per sofort eine/n Lagermitarbeiter/in mit SUVA Staplerschein 100%Ihre Aufgaben:LagerwirtschaftungKommissionierung der WareEntgegennahme und Kontrolle der gelieferten WarenEinlagerung der WarenBereitstellung und Warenübergabe an unsere Kundschaft
    • basel, basel-stadt
    • 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
    • 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
    • permanent
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Rohschlosser (m/w/d) 100%Deine AufgabenEntwicklung und Fertigung von Rohrleitungen und Anlagen Verarbeiten von Stahl- & Edelstahlrohren Diverse Schweiß-Arbeiten
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Rohschlosser (m/w/d) 100%Deine AufgabenEntwicklung und Fertigung von Rohrleitungen und Anlagen Verarbeiten von Stahl- & Edelstahlrohren Diverse Schweiß-Arbeiten
    • basel, basel-stadt
    • permanent
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen motivierten Automobil-MechatronikerDeine Aufgaben:Service-,Reparatur-Diagnose-Arbeiten führst du nach Hersteller-Richtlinien gewissenhaft durch.Selbständige Überprüfung des Unterhaltes im Tram. Dabei erkennst du mögliche Störungen und behebst diese Sorgfältig.Du leistest einen hohen Beitrag zur Kundenzufriedenheit
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen motivierten Automobil-MechatronikerDeine Aufgaben:Service-,Reparatur-Diagnose-Arbeiten führst du nach Hersteller-Richtlinien gewissenhaft durch.Selbständige Überprüfung des Unterhaltes im Tram. Dabei erkennst du mögliche Störungen und behebst diese Sorgfältig.Du leistest einen hohen Beitrag zur Kundenzufriedenheit
    • basel, basel-stadt
    • contract
    Are you an experienced Project Manager in IT and you are looking for a long-term contracting challenge in Basel? Then do not hesitate to apply!This Senior Project Support Management position will be responsible for co-managing the main activities on a global scale and supporting the integration of this project with other program initiatives. Together with this, the position will be very focused on the End-to-End integration of the overall solution across the different work streams and for that reason the appropriate candidate must have excellent communication and socialization skills to build a strong network in Aspire and outside Aspire.his position is also expected to provide timely status reports to all stakeholders and escalate issues to the appropriate management level. Additionally, this position must effectively manage the projects across global locations and time zones and be able to travel internationally as needed. Tasks and responsibilities:Execution of multiple initiatives across the Global Template project and beyond, including interaction with other multidisciplinary teamsCoordinate the project activities with 3rd party software vendor and/or System Integrator resources as needed to ensure project delivery and the different work streams when requiredManage relationships with various technology and business communities to achieve project objectivesFacilitate project management activities across the entire project management methodologyTrack progress of activities against baseline scheduleConduct risk management planning, identification, analysis and monitoring on projects, formulating risk mitigation strategies and recommend solutionsManage the processes required to ensure timely and appropriate generation, collection, distribution, storage, retrieval, and ultimate disposition of project information and documentation necessary for successful communications across all stakeholders and any required updates to living system documents for validated systemsActively seek opportunities to and mentor to other project managersPromote and hold multidisciplinary conversations/discussion between different work streams and teams outside ASPIRESupport the definition and implementation of Data Governance around Aspire and group wiseSupport the implementation of an integrated view of the business through E2E scenarios following the business guidelinesSuggest improvements where necessary / appropriate to improve operational efficienciesEngage with interested parties within the company, verify business use cases and provide expert consultancy. Guide new projects and help our internal customers to understand how they benefit the mostPartner actively with Business as well as IT Business Partners Must haves:Min. Bachelor's degree in Computer Sciences, Life Sciences, Business, Analytics and Reporting; or equivalent work experience or any other higher certification 10+ years of experience as a successful Information Technology Project Manager with a strong IT BackgroundExperience in using structured project management processes with deep understanding of various SDLCs (Waterfall, Agile, iterative, etc.), SAP A&R technology and solutions and new Analytics implementation challenges  Experience in Change Management is needed Proven leadership abilities, experience in leading multifunctional teams Excellent oral and written communication skills English fluent (C1), German is a plusAbility to manage relationships with various technology and business communities to achieve project objectivesVery experience communicator which is used to talk with different stakeholders on different levels and feels confident in project setupsProven ability to obtain results in a global, matrix environmentDemonstrated success communicating across a variety of audiences, including business people and technologists (both up and down the organization)Exceptional listening, problem solving, negotiation, and facilitation skillsDemonstrated success handling initiatives of significant complexity and risk Nice to have:Experience within the Pharmaceutical and BioTech industryExperience managing IT projects in GxP validated environmentsCertification as Project Manager or Scrum Master is a plus If this role excites you, and you feel you could take this next challenge in your career, then I look forward to receiving your application today.
    Are you an experienced Project Manager in IT and you are looking for a long-term contracting challenge in Basel? Then do not hesitate to apply!This Senior Project Support Management position will be responsible for co-managing the main activities on a global scale and supporting the integration of this project with other program initiatives. Together with this, the position will be very focused on the End-to-End integration of the overall solution across the different work streams and for that reason the appropriate candidate must have excellent communication and socialization skills to build a strong network in Aspire and outside Aspire.his position is also expected to provide timely status reports to all stakeholders and escalate issues to the appropriate management level. Additionally, this position must effectively manage the projects across global locations and time zones and be able to travel internationally as needed. Tasks and responsibilities:Execution of multiple initiatives across the Global Template project and beyond, including interaction with other multidisciplinary teamsCoordinate the project activities with 3rd party software vendor and/or System Integrator resources as needed to ensure project delivery and the different work streams when requiredManage relationships with various technology and business communities to achieve project objectivesFacilitate project management activities across the entire project management methodologyTrack progress of activities against baseline scheduleConduct risk management planning, identification, analysis and monitoring on projects, formulating risk mitigation strategies and recommend solutionsManage the processes required to ensure timely and appropriate generation, collection, distribution, storage, retrieval, and ultimate disposition of project information and documentation necessary for successful communications across all stakeholders and any required updates to living system documents for validated systemsActively seek opportunities to and mentor to other project managersPromote and hold multidisciplinary conversations/discussion between different work streams and teams outside ASPIRESupport the definition and implementation of Data Governance around Aspire and group wiseSupport the implementation of an integrated view of the business through E2E scenarios following the business guidelinesSuggest improvements where necessary / appropriate to improve operational efficienciesEngage with interested parties within the company, verify business use cases and provide expert consultancy. Guide new projects and help our internal customers to understand how they benefit the mostPartner actively with Business as well as IT Business Partners Must haves:Min. Bachelor's degree in Computer Sciences, Life Sciences, Business, Analytics and Reporting; or equivalent work experience or any other higher certification 10+ years of experience as a successful Information Technology Project Manager with a strong IT BackgroundExperience in using structured project management processes with deep understanding of various SDLCs (Waterfall, Agile, iterative, etc.), SAP A&R technology and solutions and new Analytics implementation challenges  Experience in Change Management is needed Proven leadership abilities, experience in leading multifunctional teams Excellent oral and written communication skills English fluent (C1), German is a plusAbility to manage relationships with various technology and business communities to achieve project objectivesVery experience communicator which is used to talk with different stakeholders on different levels and feels confident in project setupsProven ability to obtain results in a global, matrix environmentDemonstrated success communicating across a variety of audiences, including business people and technologists (both up and down the organization)Exceptional listening, problem solving, negotiation, and facilitation skillsDemonstrated success handling initiatives of significant complexity and risk Nice to have:Experience within the Pharmaceutical and BioTech industryExperience managing IT projects in GxP validated environmentsCertification as Project Manager or Scrum Master is a plus If this role excites you, and you feel you could take this next challenge in your career, then I look forward to receiving your application today.
    • basel, basel-stadt
    • temporary
    Bezeichnest Du Dich als eine/n Steuerfachspezielisten/in und bist interessiert, unseren Kunden für einen befristeten Zeitraum mit Deinen Kenntnissen und Erfahrungen zu unterstützen? Dann suche ich genau Dich alsFachspezialist Steuern 100% (m/w/d)Dein Aufgabenbereich:Erstellung von SteuerunterlagenKorrekte und fristgerechte Abgabe von EinkommenssteuererklärungenVorbereitung von Steuerzahlungen und Verlängerungen Berechnung, Validierung und Einreichung von Steuererklärungen Durchführen von Abstimmungen für die QuartalsendprüfungBeantwortung verschiedener Anfragen der staatlichen SteuerbehördenUnterstützung bei der Konzernsteuerplanung/-vorhersage, der Cashflow-Planung und der monatlichen SteuerberechnungVerfolgung der Steuerpositionen in der Bilanz und der Gewinn- und Verlustrechnung im Laufe des Jahres und Abgleich mit Cash-Flow-Prognosen/Planung
    Bezeichnest Du Dich als eine/n Steuerfachspezielisten/in und bist interessiert, unseren Kunden für einen befristeten Zeitraum mit Deinen Kenntnissen und Erfahrungen zu unterstützen? Dann suche ich genau Dich alsFachspezialist Steuern 100% (m/w/d)Dein Aufgabenbereich:Erstellung von SteuerunterlagenKorrekte und fristgerechte Abgabe von EinkommenssteuererklärungenVorbereitung von Steuerzahlungen und Verlängerungen Berechnung, Validierung und Einreichung von Steuererklärungen Durchführen von Abstimmungen für die QuartalsendprüfungBeantwortung verschiedener Anfragen der staatlichen SteuerbehördenUnterstützung bei der Konzernsteuerplanung/-vorhersage, der Cashflow-Planung und der monatlichen SteuerberechnungVerfolgung der Steuerpositionen in der Bilanz und der Gewinn- und Verlustrechnung im Laufe des Jahres und Abgleich mit Cash-Flow-Prognosen/Planung
    • basel, basel-stadt
    • temp to perm
    Exklusiv für unseren Kunden - suchen wir genau dich per sofort oder nach Vereinbarung - einen qualifizierten Sanitärinstallateur EFZ (m/w/d) Deine AufgabenDu bist für die Beratung und Bedienung der Kunden verantwortlichKontrolle des Wareneingangs Unterstützung bei Materialbeschaffung, Ausmass und KoordinationArbeiten nach Skizzen und BauplänenErfassen von Lieferscheine mittels EDV System ( SAP )
    Exklusiv für unseren Kunden - suchen wir genau dich per sofort oder nach Vereinbarung - einen qualifizierten Sanitärinstallateur EFZ (m/w/d) Deine AufgabenDu bist für die Beratung und Bedienung der Kunden verantwortlichKontrolle des Wareneingangs Unterstützung bei Materialbeschaffung, Ausmass und KoordinationArbeiten nach Skizzen und BauplänenErfassen von Lieferscheine mittels EDV System ( SAP )
    • basel, basel-stadt
    • 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
    • temporary
    Du bist eine neugierige, proaktive und teamfähige Person, die sich mit Gourmetkaffee von der Marke Nespresso identifiziert und bei Kunden als Botschafter die Philosophie vermittelst. Für den Standort in Basel suchen wir engagierte Verkäufer / Promoter für Nespresso (m/w) 40-60%Deine Aufgaben:Du begrüsst und informierst Kunden proaktiv als Erstkontakt über die Marke Nespresso und schaffst so ein unvergessliches KauferlebnisDu führst Kaffeedegustationen durch und gewährleistest eine fachkompetente Beratung und Verkauf von Nespresso Kaffee und Maschinen Durch deine offene Art kann der Assessoires, Maschinen und Kaffee Verkauf gesteigert werdenBei Fragen zu einfachen Störungen kannst du den Kunden kompetent beraten und eine Lösung anbietenDie monatliche Führung von Verkaufsrapporten, administrativen Aufgaben sowie die Sicherstellung der Sauberkeit des Verkaufspunkts gehören ebenfalls zu deinen Aufgaben
    Du bist eine neugierige, proaktive und teamfähige Person, die sich mit Gourmetkaffee von der Marke Nespresso identifiziert und bei Kunden als Botschafter die Philosophie vermittelst. Für den Standort in Basel suchen wir engagierte Verkäufer / Promoter für Nespresso (m/w) 40-60%Deine Aufgaben:Du begrüsst und informierst Kunden proaktiv als Erstkontakt über die Marke Nespresso und schaffst so ein unvergessliches KauferlebnisDu führst Kaffeedegustationen durch und gewährleistest eine fachkompetente Beratung und Verkauf von Nespresso Kaffee und Maschinen Durch deine offene Art kann der Assessoires, Maschinen und Kaffee Verkauf gesteigert werdenBei Fragen zu einfachen Störungen kannst du den Kunden kompetent beraten und eine Lösung anbietenDie monatliche Führung von Verkaufsrapporten, administrativen Aufgaben sowie die Sicherstellung der Sauberkeit des Verkaufspunkts gehören ebenfalls zu deinen Aufgaben
    • basel, basel-stadt
    • temp to perm
    Exklusiv für unseren Kunden im Raum Liestal, suchen wir per sofort oder nach Vereinbarung einen Elektroinstallateur (m/w) 100%Deine Aufgaben-Unterhalt und Reparatur von Elektroinstallationen-Installation von Elektroanlagen, Hausanschluss bis zur Steckdose-Materialmengenberechnungen-Arbeiten nach technischen Plänen und Schemata-Service- und Reparaturdienst
    Exklusiv für unseren Kunden im Raum Liestal, suchen wir per sofort oder nach Vereinbarung einen Elektroinstallateur (m/w) 100%Deine Aufgaben-Unterhalt und Reparatur von Elektroinstallationen-Installation von Elektroanlagen, Hausanschluss bis zur Steckdose-Materialmengenberechnungen-Arbeiten nach technischen Plänen und Schemata-Service- und Reparaturdienst
    • basel, basel-stadt
    • contract
    We are currently supporting a leading pharmaceutical company in the area of Basel, in their search for an experienced Senior Project Manager for Pharma Informatics (IT).Tasks and Responsibilities:As a Project Manager, you will assemble, guide, empower and serve the team through excellence in project delivery resulting in value creation for our business and eventually, our patients. You will be responsible for leading a team to deliver project outcomes, products and services in a complex IT environment by selecting the best project delivery method (i.e. Agile principles and practices or Waterfall) that best fit the business needs. Therefore, the Project Manager can take on one, or a combination, of the following roles in a squad, project or program: Program Manager, Project Manager, Squad Lead, Agile Coach or Scrum MasterAs part of one or more of those roles, you will be:Engage with Leadership, both business and IT, to collaborate on the delivery of value at a rate that is sustainable and digestible for the team and businessEnsure promised business value is being earned by leveraging the value creation or value maintenance frameworkOrchestrate the formation of a squad and once established, closely interact with the product owner, partners and the development teamSource of skills that are supplied by Pharma Informatics or other Technology partnersGuide the squad on self-organising to fill in the intentional gaps left in the Agile/Scrum frameworksCoach the team to learn and adopt agreed ways of working and reacting to potential challenges and questionsYour Profile:Has an agile mindset with ability to pivot between roles and approaches based on team needsChampions Agile principles and practices within the squad and leads by exampleHas a strong focus on delivering MVP’s, focused on incremental value rather than perfection.Has strong soft skills typically required in stakeholder engagement (empowering people, influencing, negotiation, conflict management)Exhibits servant leadership style towards the product owner, scrum master, development team and the wider organizationThis is a challenging and exciting job opportunity. Are you ready for it? Then don`t hesitate to send your application.
    We are currently supporting a leading pharmaceutical company in the area of Basel, in their search for an experienced Senior Project Manager for Pharma Informatics (IT).Tasks and Responsibilities:As a Project Manager, you will assemble, guide, empower and serve the team through excellence in project delivery resulting in value creation for our business and eventually, our patients. You will be responsible for leading a team to deliver project outcomes, products and services in a complex IT environment by selecting the best project delivery method (i.e. Agile principles and practices or Waterfall) that best fit the business needs. Therefore, the Project Manager can take on one, or a combination, of the following roles in a squad, project or program: Program Manager, Project Manager, Squad Lead, Agile Coach or Scrum MasterAs part of one or more of those roles, you will be:Engage with Leadership, both business and IT, to collaborate on the delivery of value at a rate that is sustainable and digestible for the team and businessEnsure promised business value is being earned by leveraging the value creation or value maintenance frameworkOrchestrate the formation of a squad and once established, closely interact with the product owner, partners and the development teamSource of skills that are supplied by Pharma Informatics or other Technology partnersGuide the squad on self-organising to fill in the intentional gaps left in the Agile/Scrum frameworksCoach the team to learn and adopt agreed ways of working and reacting to potential challenges and questionsYour Profile:Has an agile mindset with ability to pivot between roles and approaches based on team needsChampions Agile principles and practices within the squad and leads by exampleHas a strong focus on delivering MVP’s, focused on incremental value rather than perfection.Has strong soft skills typically required in stakeholder engagement (empowering people, influencing, negotiation, conflict management)Exhibits servant leadership style towards the product owner, scrum master, development team and the wider organizationThis is a challenging and exciting job opportunity. Are you ready for it? Then don`t hesitate to send your application.
    • basel, basel-stadt
    • temp to perm
    Bist du eine flexible, belastbare und engagierte Person? Verfügst du über ein Auge fürs Detail und kannst es dir vorstellen in einem Hotel zu arbeiten? Dann bewirb dich jetzt bei uns als:Zimmerfrau in Basel 40 - 80%Deine Aufgaben:Reinigung von Hotelzimmer von 8:00 Uhr bis 15:00 UhrArbeitseinsatz auch am Wochenende
    Bist du eine flexible, belastbare und engagierte Person? Verfügst du über ein Auge fürs Detail und kannst es dir vorstellen in einem Hotel zu arbeiten? Dann bewirb dich jetzt bei uns als:Zimmerfrau in Basel 40 - 80%Deine Aufgaben:Reinigung von Hotelzimmer von 8:00 Uhr bis 15:00 UhrArbeitseinsatz auch am Wochenende
    • basel, basel-stadt
    • temp to perm
    Mehrjährige Berufserfahrung als HR-Fachperson; Vif, ausdauernd und organsiert - trifft das alles auf Dich zu? Dann suche ich genau Dich alsHR-Fachfrau 80-100% (m/w/d)In dieser spannenden Funktion bist du für die folgenden Aufgaben verantwortlich:Gesamte PersonaladministrationLohnbuchhaltungPersonalrekrutierungErste Ansprechperson bei PersonalfragenSozialversicherungswesen, Zeiterfassung, Ein- und AustritteDiverse HR-Projekte
    Mehrjährige Berufserfahrung als HR-Fachperson; Vif, ausdauernd und organsiert - trifft das alles auf Dich zu? Dann suche ich genau Dich alsHR-Fachfrau 80-100% (m/w/d)In dieser spannenden Funktion bist du für die folgenden Aufgaben verantwortlich:Gesamte PersonaladministrationLohnbuchhaltungPersonalrekrutierungErste Ansprechperson bei PersonalfragenSozialversicherungswesen, Zeiterfassung, Ein- und AustritteDiverse HR-Projekte
    • basel, basel-stadt
    • temporary
    Für unseren Kunden, ein bekanntes Catering-unternehmen in Basel, suchen wir, Bar- und Service-aushilfen & Allrounder für die ART Basel (m/w) 60-80% Ihre Aufgaben:Servieren von Speisen und GetränkenUnterstützung unseres Serviceteams & BackofficeteamsVorbereiten des täglichen Mise en placeInkasso sowie TagesabrechnungenEinhalten der Qualitäts- und Hygienestandards
    Für unseren Kunden, ein bekanntes Catering-unternehmen in Basel, suchen wir, Bar- und Service-aushilfen & Allrounder für die ART Basel (m/w) 60-80% Ihre Aufgaben:Servieren von Speisen und GetränkenUnterstützung unseres Serviceteams & BackofficeteamsVorbereiten des täglichen Mise en placeInkasso sowie TagesabrechnungenEinhalten der Qualitäts- und Hygienestandards
    • basel, basel-stadt
    • temporary
    Hilfsarbeiter (w/m/d)Wir suchen per sofort flexible Mitarbeiter, die für Kurzeinsätze einspringen können. Wir sprechen hier auch Bewerbern an, die nur an bestimmten Tagen verfügbar sind oder die Zeit neben dem Studium oder einem anderen Teilzeitstelle einteilen können.Folgende Einsätze erwarten Dich:Allgemeine Lagerarbeiten Umzüge aller ArtMontage und DemontageBesucherbetreuerLiftboys
    Hilfsarbeiter (w/m/d)Wir suchen per sofort flexible Mitarbeiter, die für Kurzeinsätze einspringen können. Wir sprechen hier auch Bewerbern an, die nur an bestimmten Tagen verfügbar sind oder die Zeit neben dem Studium oder einem anderen Teilzeitstelle einteilen können.Folgende Einsätze erwarten Dich:Allgemeine Lagerarbeiten Umzüge aller ArtMontage und DemontageBesucherbetreuerLiftboys
30 of 94 jobs seen

It looks like you want to switch your language. This will reset your filters on your current job search.