Elan Personal AG

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    "title": "Produktionsexperte",
    "description": "Roche Schweiz schlägt die Brücke zwischen Pharmazie und Diagnostik. Wichtige Forschungs- und Entwicklungsfunktionen sind hier angesiedelt. Für unsere langjährige Kundin, die F. Hoffmann - La Roche AG in\nKaiseraugst\n, suchen wir eine/n\nProduktionsexperte\nHintergrund:\nDie Abteilung “CoRE” (Compounding, Raw Material, Equipment) ist Teil der Manufacturing Unit “Sterile Filling” am Produktionszentrum Kaiseraugst. In der Abteilung CoRE werden verschiedene Lösungen für flüssige Arzneiformen hergestellt. Darüber hinaus finden in der Abteilung auch Freeze-and-Thaw-Aktivitäten sowie die Stopfen- und Equipmentbehandlung statt.\nAufgaben & Verantwortlichkeiten:\nFreeze & Thaw: Bedienung und Überwachung spezialisierter F/T-Anlagen zum kontrollierten Auftauen und Einfrieren von APIs.\nCompounding: Durchführung von Einwaage-, Vorbereitungs- und Mischprozessen zur Weiterverarbeitung der aufgetauten APIs und Hilfsstoffe zu fertigen pharmazeutischen Lösungen.\nEquipment- & Stopfenbehandlung: Vorbereitung, Reinigung, Sterilisation von Primärpackmitteln und Produktions-Equipment in den Reinraumklassen D und C.\nProzessdurchführung: Exakte Abarbeitung von Herstellanweisungen (MES) nach cGMP-Richtlinien.\nProzessüberwachung: Probenentnahmen, Monitoring von Prozessparametern und Dokumentation von Abweichungen.\nReinraum- & Anlagenhygiene: CIP/SIP-Prozesse, manuelle Reinigung und strikte Einhaltung der Hygienerichtlinien.\nMust Haves:\nAbgeschlossene Ausbildung als Chemie- und Pharmatechnologe:in, Pharmakant:in oder ähnlich\nHohes Qualitäts- und Regelbewusstsein; exakte Arbeitsweise nach SOPs\nErfahrung in pharmazeutischer Produktion, idealerweise Compounding\nRoutine in Reinraumklassen D und C\nSicherer Umgang mit elektronischen Herstelldokumentationssystemen (MES)\nBereitschaft zur Schichtarbeit\nSehr gute Deutschkenntnisse B2 in Wort und Schrift\nGMP\nWas Ihnen geboten wird:\nEine Chance, in einem der bedeutendsten Pharmaunternehmen der Welt mitzuwirken\nModerner Campus mit viel Grünflächen und Begegnungszonen\nAbwechslungsreiches Tätigkeitsprofil\nWeiterbildungsmöglichkeiten durch temptraining\nMitarbeit in einem dynamischen und motivierten Team\nGerne können Sie Ihre vollständigen Bewerbungsunterlagen an Frau Diana Afonso senden.\nBasel Basel-Land Aargau Chemie Produktion Pharma GMP MES Reinigung Sterilisation API",
    "datePosted": "2026-08-25",
    "validThrough": "2026-09-24",
    "employmentType": "FULL_TIME",
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    "@id": "https://ch-jobs.com/job/business-process-expert-for-master-data-of-cmo-1#jobposting",
    "title": "Business Process Expert for Master data of CMO",
    "description": "Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a\nBusiness Process Expert for Master data of CMO\nBackground:\nThe Business Process Expert (BPE) serves as a critical bridge between global process standards and local operational execution. This role is embedded within a specific function (e.g., Site, Manufacturing, or Supply Chain) while partnering closely with the Global Business Capability Owner (BCO) Center of Excellence. As a change agent, the BPE is empowered to drive process alignment and harmonization at the site level, ensuring that local requirements are integrated into global designs while maintaining an end-to-end (E2E) mindset.\nTasks & Responsibilities:\nProcess Design & Alignment\nAct as a change agent to drive global process changes and alignment at the site or local level, partnering closely with Data Content Owners (DCOs) and Master Data Specialists (MDSs) to ensure master data changes are deployed timely and accurately.\nProvide local and site-specific requirements from the user network into the global process design to ensure fit-for-purpose solutions.\nCoordinate with other BPEs, Subject Matter Experts (SMEs), and Super Users to discuss ideas across processes and systems.\nPlay a critical role in process harmonization by utilizing in-depth process knowledge to align local practices with global standards.\nCross-Functional Orchestration: Facilitate the resolution of operational bottlenecks and define process enhancements that deliver measurable business value.\nGovernance & Adoption: Champion the implementation and rigorous adherence to global process standards and governance frameworks.\nSystem & Operational Support\nAct as the site expert for both business processes and relevant systems (e.g., SAP S/4 HANA, OMP).\nSupport site-specific data analysis, analytics, reporting, and troubleshooting.\nEnsure the execution of processes is robust and remains aligned with the intended global design.\nDefine and manage change requests (I2Rs) during the sustainment phase, acting as the primary interface for users to submit improvement ideas via ServiceNow and presenting them to the BCO network for endorsement.\nTraining & Change Management\nLead the revision, alignment, and retirement of local Standard Operating Procedures (SOPs).\nContribute to the creation and revision of Global Standard Processes (GSPs) and network SOPs, WI & Playbooks\nLead the onboarding and training of new team members for site-specific processes and systems.\nSupport site-wide information sharing and deployment activities during project transitions.\nASPIRE Sustainment Accountabilities (enhancements & retrofit)\nSupporting Fit-Gap Assessments.\nSupporting Site Acceptance Testing (SAT) review and execution.\nParticipating in User Acceptance Testing (UAT).\nDriving Template Sustainment by utilizing the Idea-to-Request (I2R) process, including the prioritization of site-specific requirements within the global backlog.\nMust Haves:\nFunctional Expertise: Must be a functional expert within their team with above-average experience in relevant business processes (Supply Chain, Technical Operations, or Contract Manufacturing).\nInnovation Mindset: Demonstrates an E2E and innovative mentality with a positive, can-do attitude.\nChange Leadership: Possesses the influence skills necessary to act as an effective change agent and challenge the status quo.\nTechnical & System Proficiency: Hands-on understanding of how master data flows across core SAP S/4HANA modules (MM, PP, QM, SD) and PLM interfaces. Familiarity with the systems required to run the process, including underlying master and transactional data.\nBA/BS Degree, preferably in a technical, business or supply chain field. Masters Degree a plus\n8+ years in the pharma industry, supply chain management or in manufacturing.\nAPICS and/or SCOR certification, or equivalent relevant experience\nProficient knowledge and experience of SAP or ERP system\nLanguage Skills: English is a MUST\nWhat you will be offered:\nAn opportunity to work in one of the world's most important pharmaceutical companies\nModern campus with plenty of green spaces and meeting areas\nCentral location in Basel\nVaried job profile\nFurther training opportunities through temptraining\nWorking in a dynamic and motivated team\nIf you are interested please send your application documents addressed to Ms Diana Afonso.\nBasel-Stadt BPE Pharma Aargau Master Data SME SAP S/4HANA OMP BCO Process Operations Manufacturing Supply Chain",
    "datePosted": "2026-08-24",
    "validThrough": "2026-09-23",
    "employmentType": "FULL_TIME",
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    "@id": "https://ch-jobs.com/job/senior-quality-lead#jobposting",
    "title": "Senior Quality Lead",
    "description": "Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a\nSenior Quality Lead\nBackground:\nThe Senior Quality Lead is an experienced Quality Professional who supports the Roche/Genentech Organization through the development and delivery of Quality Assurance strategies, audits, and conclusions for various entities (e.g., molecules in development, post-approval products, affiliates, processes, programs). This role ensures effective implementation of Quality Assurance to stakeholders and Health Authorities by generating evidence and actionable data through complex audits and quality activities.\nTasks & Responsibilities:\nDesign and Implementation of Quality Strategies:\nEstablish relationships with business stakeholders and lead the development of molecule/product/process/affiliate-level approaches with appropriate measures (CtQ Factors)\nAnalyze quality data to identify trends and risks, providing insights to business partners\nDelivery of Activities to Assess Quality Status\nLead and perform complex audits and quality assessments.\nSynthesize individual audit issues into systematic conclusions and present findings and associated risks to senior stakeholders, ensuring quality data fulfills regulatory requirements and supports organizational goals\nDemonstration of Implementation to Health Authorities\nPlay a lead role in inspection preparation and management.\nProvide training to staff and ensure relevant materials are prepared for regulatory review\nExecution of PDQ Goals\nLead assigned goals and initiatives and drive the development or revision of PDQ processes\nNetworking:\nMaintain and influence partnerships with senior business stakeholders and PDQ domains\nFacilitate cross-functional collaboration to ensure quality standards are met globally\nCompliance:\nExpert knowledge in GxP regulations (FDA, EU, ICH guidance) and internal policies\nEnsure all activities are conducted in compliance with regulatory and company requirements\nMust Haves:\nBachelor’s degree or equivalent in a scientific or quality-related field. Advanced degree preferred\nSignificant experience in the pharmaceutical / biotech / medical device industry, including knowledge of the end to end development and operationalisation of products, and the associated GxP regulations and considerations (e.g., GCP,GVP, IVD/MD Regulations)\nMin. 5 years experience in leading GxP audits and managing complex quality projects\nIn-depth knowledge of drug development processes and global regulatory landscapes\nGood understanding of Information Systems, e.g., audit management and analysis reporting tools\nUnderstanding of business operations and strategies\nFluency in written and spoken English; bi or multi-lingual skills are desirable\nClinical Operations experience or quality function in system validations\nLeadership and Stakeholder Management: Demonstrates exceptional ability to influence, negotiate, and mentor while effectively managing relationships with diverse stakeholders in global settings.\nAnalytical and Strategic Thinking: strong data and digital literacy, with the critical thinking ability to synthesize complex or ambiguous information into clear, actionable insights.\nExecution and Independence: Combines strong organizational and project management skills with the capacity to work effectively—both independently and collaboratively—within international, agile matrix organizations.\nCommunication: Utilizes advanced presentation and communication skills to drive decision-making and foster cross-functional collaboration\nWhat you will be offered:\nAn opportunity to work in one of the world's most important pharmaceutical companies\nModern campus with plenty of green spaces and meeting areas\nCentral location in Basel\nVaried job profile\nFurther training opportunities through temptraining\nWorking in a dynamic and motivated team\nIf you are interested please send your application documents addressed to Ms Diana Afonso.\nBasel-Stadt Quality Lead GxP GCP GVP IVD MD Audit Projects Drug Development Management Global Regulatory Reporting",
    "datePosted": "2026-08-24",
    "validThrough": "2026-09-23",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/senior-quality-lead",
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    "@id": "https://ch-jobs.com/job/fachmitarbeiter-in-zentrale-dienste-finanzen-hr-projekte-50#jobposting",
    "title": "Fachmitarbeiter/in Zentrale Dienste – Finanzen, HR & Projekte 50%",
    "description": "Unsere Kundin ist eine etablierte medizinische Institution in der Region Basel. Für den weiteren Ausbau ihrer zentralen Dienste suchen wir per sofort oder nach Vereinbarung eine engagierte, selbständige und vielseitige Persönlichkeit als\nFachmitarbeiter/in Zentrale Dienste – Finanzen, HR & Projekte 50%\nIn dieser abwechslungsreichen Funktion übernehmen Sie eine wichtige Querschnittsaufgabe und unterstützen die Organisation mit Ihrem Zahlenverständnis, Ihrer analytischen Denkweise und Ihrer Freude an Projekten und Prozessoptimierungen. Sie arbeiten weitgehend selbständig, sind eng mit verschiedenen internen Stellen vernetzt und tragen dazu bei, Strukturen, Abläufe und Instrumente kontinuierlich weiterzuentwickeln.\nIhre Aufgaben:\nFinanzen & Personal:\nErstellung und Aufbereitung von Auswertungen, Analysen und Berechnungen im Finanz- und Personalwesen\nBudget & Kennzahlen:\nAufbereitung von Budgetauswertungen, Datenanalysen und Entscheidungsgrundlagen\nProjektmanagement:\nSelbständige Mitarbeit und Übernahme von Teilprojekten, beispielsweise bei der Einführung eines neuen Lohnsystems oder der Weiterentwicklung eines MaG-Konzepts\nVertragsmanagement:\nKoordination, Pflege und strukturierte Verwaltung von Verträgen und relevanten Dokumenten\nProzessmanagement:\nAnalyse, Dokumentation und kontinuierliche Optimierung bestehender Prozesse und Abläufe\nDigitalisierung:\nUnterstützung bei der Weiterentwicklung und Digitalisierung von Arbeitsprozessen sowie bei der Einführung neuer digitaler Lösungen\nDaten- und Personenschutz:\nWeiterentwicklung und Optimierung der entsprechenden Prozesse\nÜbernahme weiterer vielseitiger Aufgaben im Bereich der Zentralen Dienste\nIhr Profil:\nSie verfügen über eine kaufmännische oder vergleichbare Ausbildung und bringen mehrjährige Berufserfahrung in den Bereichen Finanzen, Administration, HR oder zentrale Dienste mit. Idealerweise haben Sie bereits Erfahrung in der Projektarbeit sowie in der Optimierung und Entwicklung von Prozessen.\nZusätzlich punkten Sie mit:\nVernetztem, ganzheitlichem und analytischem Denken sowie ausgeprägtem Zahlenverständnis\nSehr guten MS-Office-Kenntnissen und hoher IT-Affinität\nSelbständiger, strukturierter und zuverlässiger Arbeitsweise\nEiner offenen, kommunikativen Persönlichkeit sowie einem verantwortungsvollen und diskreten Umgang mit vertraulichen Informationen\nWir bieten Ihnen:\nEine vielseitige und verantwortungsvolle Fachfunktion mit abwechslungsreichen Aufgaben\nEin familiäres, wertschätzendes und gleichzeitig professionelles Arbeitsumfeld\nDie Möglichkeit, Prozesse aktiv mitzugestalten und die Organisation weiterzuentwickeln\nEin hoher Home-Office-Anteil sowie grosse Flexibilität bei der Arbeitszeitgestaltung\nEin moderner Arbeitsplatz in attraktiver Umgebung mitten in der Natur und gleichzeitig zentral gelegen\nFortschrittliche und attraktive Anstellungsbedingungen\nEin Pensum von 50 % mit einer Tätigkeit, die sich ideal mit weiteren beruflichen oder persönlichen Verpflichtungen kombinieren lässt\nGerne können Sie Ihre Bewerbung an Nadine Rutz senden.\nGesundheitswesen Teilzeit Baselbiet Projekte Strategie Planung",
    "datePosted": "2026-08-24",
    "validThrough": "2026-09-23",
    "employmentType": "FULL_TIME",
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    "@id": "https://ch-jobs.com/job/teamleiter-in-lohnbuchhaltung-payroll-80-100#jobposting",
    "title": "Teamleiter/in Lohnbuchhaltung / Payroll 80-100%",
    "description": "Unsere Kundin ist ein führender Anbieter von Lösungen für Personal- und Gebäudedienstleister in Europa. Mit innovativen digitalen Lösungen unterstützt sie Dienstleister dabei, ihre Prozesse effizient zu gestalten, schafft neue Job- und Karrieremöglichkeiten für Arbeitnehmende und verbindet Unternehmen mit passenden Arbeitskräften. Für den Standort Basel suchen wir eine erfahrene Persönlichkeit als\nTeamleiter/in Lohnbuchhaltung / Payroll 80–100 %\nFür das Payroll-/BPO-Team (Business Process Outsourcing) suchen wir im Auftrag eine erfahrene und engagierte Führungspersönlichkeit, die Verantwortung für die Lohnabrechnung mehrerer Kundenmandate mit Fokus auf das Personal-Temporärgeschäft übernimmt. Sie arbeiten eng mit den Kunden zusammen und stellen sicher, dass deren Mitarbeitende termingerecht und korrekt entlöhnt werden und sämtliche gesetzlichen Vorgaben eingehalten werden. Gleichzeitig gestalten Sie die Weiterentwicklung und Digitalisierung der Payroll-Prozesse sowie den gezielten Einsatz von KI aktiv mit.\nWas Sie bewegen:\nSie führen und entwickeln ein Team von Lohnabrechnungsspezialist – von der Rekrutierung bis zur Weiterentwicklung.\nSie verantworten die korrekte, termingerechte und GAV-konforme Lohnabrechnung verschiedener Kundenmandate.\nSie stellen die Einhaltung der gesetzlichen Vorgaben im Payroll sicher, insbesondere in den Bereichen Sozialversicherungen, Quellensteuer und MWST.\nSie bearbeiten anspruchsvolle Payroll-Sonderfälle und stehen Kund sowie internen Ansprechpartner beratend zur Seite.\nSie verantworten die Debitorenbuchhaltung und arbeiten eng mit der Finanzbuchhaltung zusammen.\nSie begleiten Audits und Kontrollen durch Behörden und Revisionsstellen.\nSie treiben die Digitalisierung und den Einsatz von KI zur Optimierung der Payroll-Prozesse aktiv voran.\nSie begleiten das Onboarding neuer Kunden und stellen auch bei wöchentlichen Lohnläufen reibungslose Abläufe sicher.\nWas Sie mitbringen:\nMehrjährige Berufserfahrung in der Lohnadministration und/oder Buchhaltung, idealerweise in der Personaldienstleistungsbranche\nEidg. Fachausweis im Personalwesen/Payroll oder eine vergleichbare Ausbildung (z. B. Studium in Betriebswirtschaft/HR)\nFundierte Kenntnisse im Sozialversicherungs-, Steuer- und Arbeitsrecht\nAusgeprägte Führungsstärke und Freude daran, ein Team zu motivieren und weiterzuentwickeln\nOrganisationstalent und die Fähigkeit, auch unter Zeitdruck den Überblick zu behalten\nSehr gute Kommunikations- und Sozialkompetenz in Deutsch und Englisch\nGutes IT-Verständnis sowie sichere MS-Office- und Payroll-Software-Kenntnisse\nFreude am Einsatz von KI-Tools wie ChatGPT oder Copilot zur effizienteren Gestaltung von Routineaufgaben\nVon Vorteil:\nErfahrung im BPO-Umfeld oder Personal-Temporärgeschäft\nGute Französischkenntnisse in Wort und Schrift\nWas die Position bietet:\nGestaltungsfreiheit:\nEine offene Unternehmenskultur bietet Ihnen Raum, Ihre Ideen einzubringen und Ihre Stärken zu entfalten.\nAttraktive Sozialleistungen:\nSie profitieren von sehr guten Leistungen im Bereich Gesundheit und Altersvorsorge.\nMehr Freizeit:\n25 Ferientage, 4 zusätzliche Brückentage sowie ein freier Tag an Ihrem Geburtstag.\nModernes Arbeitsumfeld:\nModerne Büros, Snacks und Getränke sowie ein gemeinsames Mittagessen einmal im Monat.\nWorkation:\nDie Möglichkeit, gelegentlich von Ihrem persönlichen Lieblingsort aus zu arbeiten.\nWeiterentwicklung:\nIndividuelle Weiterbildungs- und Entwicklungsmöglichkeiten werden aktiv unterstützt.\nHundefreundlich:\nAuch Ihr Vierbeiner ist nach einem kurzen Test am Arbeitsplatz willkommen.\nTeam & Events:\nSommerfeste, Weihnachtsfeiern und regelmässige Social Events sorgen für einen starken Teamzusammenhalt.\nGerne können Sie Ihre vollständigen Bewerbungsunterlagen an Frau Nadine Rutz senden.\nLead Teamlead Treuhand HR-Fachperson Mandate Dienstleister Vollzeit Remote International Basel City",
    "datePosted": "2026-08-21",
    "validThrough": "2026-09-20",
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    "@id": "https://ch-jobs.com/job/business-process-expert-for-master-data-of-cmo#jobposting",
    "title": "Business Process Expert for Master data of CMO",
    "description": "Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a\nBusiness Process Expert for Master data of CMO\nBackground:\nThe Business Process Expert (BPE) serves as a critical bridge between global process standards and local operational execution. This role is embedded within a specific function (e.g., Site, Manufacturing, or Supply Chain) while partnering closely with the Global Business Capability Owner (BCO) Center of Excellence. As a change agent, the BPE is empowered to drive process alignment and harmonization at the site level, ensuring that local requirements are integrated into global designs while maintaining an end-to-end (E2E) mindset.\nTasks & Responsibilities:\nProcess Design & Alignment\nAct as a change agent to drive global process changes and alignment at the site or local level, partnering closely with Data Content Owners (DCOs) and Master Data Specialists (MDSs) to ensure master data changes are deployed timely and accurately.\nProvide local and site-specific requirements from the user network into the global process design to ensure fit-for-purpose solutions.\nCoordinate with other BPEs, Subject Matter Experts (SMEs), and Super Users to discuss ideas across processes and systems.\nPlay a critical role in process harmonization by utilizing in-depth process knowledge to align local practices with global standards.\nCross-Functional Orchestration: Facilitate the resolution of operational bottlenecks and define process enhancements that deliver measurable business value.\nGovernance & Adoption: Champion the implementation and rigorous adherence to global process standards and governance frameworks.\nSystem & Operational Support\nAct as the site expert for both business processes and relevant systems (e.g., SAP S/4 HANA, OMP).\nSupport site-specific data analysis, analytics, reporting, and troubleshooting.\nEnsure the execution of processes is robust and remains aligned with the intended global design.\nDefine and manage change requests (I2Rs) during the sustainment phase, acting as the primary interface for users to submit improvement ideas via ServiceNow and presenting them to the BCO network for endorsement.\nTraining & Change Management\nLead the revision, alignment, and retirement of local Standard Operating Procedures (SOPs).\nContribute to the creation and revision of Global Standard Processes (GSPs) and network SOPs, WI & Playbooks\nLead the onboarding and training of new team members for site-specific processes and systems.\nSupport site-wide information sharing and deployment activities during project transitions.\nASPIRE Sustainment Accountabilities (enhancements & retrofit)\nSupporting Fit-Gap Assessments.\nSupporting Site Acceptance Testing (SAT) review and execution.\nParticipating in User Acceptance Testing (UAT).\nDriving Template Sustainment by utilizing the Idea-to-Request (I2R) process, including the prioritization of site-specific requirements within the global backlog.\nMust Haves:\nFunctional Expertise: Must be a functional expert within their team with above-average experience in relevant business processes (Supply Chain, Technical Operations, or Contract Manufacturing).\nInnovation Mindset: Demonstrates an E2E and innovative mentality with a positive, can-do attitude.\nChange Leadership: Possesses the influence skills necessary to act as an effective change agent and challenge the status quo.\nTechnical & System Proficiency: Hands-on understanding of how master data flows across core SAP S/4HANA modules (MM, PP, QM, SD) and PLM interfaces. Familiarity with the systems required to run the process, including underlying master and transactional data.\nBA/BS Degree, preferably in a technical, business or supply chain field. Masters Degree a plus\n8+ years in the pharma industry, supply chain management or in manufacturing.\nAPICS and/or SCOR certification, or equivalent relevant experience\nProficient knowledge and experience of SAP or ERP system\nLanguage Skills: English is a MUST\nWhat you will be offered:\nAn opportunity to work in one of the world's most important pharmaceutical companies\nModern campus with plenty of green spaces and meeting areas\nCentral location in Basel\nVaried job profile\nFurther training opportunities through temptraining\nWorking in a dynamic and motivated team\nIf you are interested please send your application documents addressed to Ms Diana Afonso.\nBasel-Stadt BPE Pharma Aargau Master Data SME SAP S/4HANA OMP BCO Process Operations Manufacturing Supply Chain",
    "datePosted": "2026-08-20",
    "validThrough": "2026-09-19",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/business-process-expert-for-master-data-of-cmo",
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    "@type": "JobPosting",
    "@id": "https://ch-jobs.com/job/produktionsexperten-f-r-die-abteilung-packaging-devices#jobposting",
    "title": "Produktionsexperten für die Abteilung Packaging Devices",
    "description": "Roche Schweiz schlägt die Brücke zwischen Pharmazie und Diagnostik. Wichtige Forschungs- und Entwicklungsfunktionen sind hier angesiedelt. Für unsere langjährige Kundin, die F. Hoffmann - La Roche AG in\nKaiseraugst\n, suchen wir eine/n\nProduktionsexperten für die Abteilung Packaging Devices\nHintergrund:\nDer Verpackungsbetrieb Kaiseraugst ist das Kompetenzzentrum für die Verpackung qualitativ hochwertiger Produkte nachgeltenden GMP Bestimmungen für den weltweiten Markt.\nDer Asset Assembly & Packaging Devices ist einer von vielen unterschiedlichen Technologiebereichen im Verpackungsbetrieb und zeichnet sich durch die Assemblierung und Verpackung von Fertigspritzen & Devices aus. Gestützt wird der Bereich durch ein innovatives Organisations- und Prozesskonzept mit engagierten Mitarbeitenden, welche neben dem Tagesgeschäft ihren eigenen Bereich aktiv mitgestalten.\nAufgaben & Verantwortlichkeiten:\nSelbstständige Durchführung der Verpackungstätigkeiten gemäss geltender GMP-Vorschriften inkl. Identifikation und Abrechnung von Materialien, Durchführen von In Prozess Kontrollen und Musterzüge, Warentransport und -entsorgung, Line Clearance\nSelbstständige Bedienung der Produktions- und Inspektionsanlagen und der dazugehörenden EDV-Systeme\nSelbstständige Dokumentation sämtlicher GMP-relevanter Arbeiten und Störungen (SAP, MES, OEE) und umgehende Meldung von festgestellten Abweichungen und fehlerhaften Zuständen\nSicherstellung der Verfügbarkeit von Formatteilen, Packmitteln und Verbrauchsmaterialien am Einsatzort.\nBewertung und Bearbeitung von Alarmen und Störungen inklusive Kommentierung dieser im OEE-Tool\nAusräumen und Reinigung der Produktions- und Inspektionsanlagen.\nEntsorgen des Abfalls an den Produktions- und Inspektionsanlagen.\nAbarbeiten der Produktionsaufträge in EDV-Systemen.\nKoordinieren und Durchführung der Umrüst Aktivitäten in Zusammenarbeit mit der Technik\nAktive Mitarbeit bei der Einführung, Optimierung und Anwendung von LPS Tools\nSicherstellung der Einhaltung aller Sicherheitsvorschriften\nMust Haves:\nErfahrung aus der pharmazeutischen Industrie, idealerweise in den Bereichen der Verpackung\nBereitschaft zur Normalarbeitszeit sowie Schichtarbeit im 2- bis 3-Schichtbetrieb\nGutes Prozess- und technisches Verständnis\nVersierter Umgang mit MS Office sowie Kenntnisse in SAP PM von Vorteil\nAbgeschlossene Berufslehre im mechanischen oder elektrischen Bereich\nDeutsch Kentnisse B2\nMehrjährige Berufserfahrung im GMP-Umfeld, sowie gute Kenntnisse in GMP\nWas Ihnen geboten wird:\nEine Chance, in einem der bedeutendsten Pharmaunternehmen der Welt mitzuwirken\nModerner Campus mit viel Grünflächen und Begegnungszonen\nAbwechslungsreiches Tätigkeitsprofil\nWeiterbildungsmöglichkeiten durch temptraining\nMitarbeit in einem dynamischen und motivierten Team\nGerne können Sie Ihre vollständigen Bewerbungsunterlagen an Frau Diana Afonso senden.\nBasel Basel-Land Aargau Chemie Produktion Pharma GMP Verpackung MES OEE",
    "datePosted": "2026-08-19",
    "validThrough": "2026-09-18",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/produktionsexperten-f-r-die-abteilung-packaging-devices",
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            "addressLocality": "BS",
            "addressCountry": "CH"
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    "@id": "https://ch-jobs.com/job/global-project-manager-1#jobposting",
    "title": "Global Project Manager",
    "description": "Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a\nGlobal Project Manager\nBackground:\nThe Principal Project Manager (PM) is responsible for managing a diverse range of projects, taking into account their respective stages and levels of complexity. The role encompasses various assignments, including development pipeline projects, line extensions, post-approval activities, technology initiatives, and continuous improvement programs. The Principal PM works independently, effectively prioritizing and managing workload to achieve team objectives with limited guidance. The position requires flexibility to collaborate across global time zones and includes occasional travel to external partners to support collaboration and strategic planning activities.\nTasks & Responsibilities:\nWhat You’ll Do:\nIn collaboration with the Technical Development Team Lead (TDTL) & Device Team Leader (DTL), the PM will translate device strategy into actionable plans, focusing on three key areas:\nPlanning:\nDefine “inspection ready” Design & Development Plans\nExecution:\nDrive team activities to meet project and design control deliverables\nTeam Dynamics:\nEnsure effective communication and facilitate team performance in a regulated environment using various processes and tools for planning, communication, budget, schedule, compliance, and risk management\nProject Management\nresponsibilities:\nMaintains full understanding of program milestones for the Core, Lifecycle, Technical Development and associated teams and links them to the Device Team plan\nEffectively applies PM best practices and utilizes tools for planning, communication, team building, collaboration, decision-making, issue & risk management, lessons learned, knowledge management and budget tracking\nDevelops & updates Design & Development Plan and establishes contingency plans as needed\nEnsures transparent communication of key team information and escalates issues as appropriate\nEstablishes positive team dynamics through team building\nPromotes collaborative environment across team members\nFacilitates efficient decision-making and issue resolution\nIdentifies team risks and mitigation plans\nProject Planning and Execution:\nManages project scope and facilitate necessary changes\nFacilitates project plan development and execution, and monitor the project schedule\nIntegrates deliverables with other teams linked to the product\nEnsures effective team dynamics and positive team environments\nRisk and Issue Management:\nAnticipates and manage risks with proactive contingency plans\nFacilitates risk management process and issue resolution\nCollaboration and Team Building:\nAssesses Team dynamics and leads team building activities to enable and sustain a high performing team environment\nEstablish relationships and network with other stakeholder Teams and PMs\nCommunication:\nDevelops and adapts project communication tools to drive awareness of project progress and risks across stakeholders including external collaborators (e.g. dashboard)\nActs as Device Team Leader back-up for Team communication as required\nLiaises with other Teams to manage cross-functional activities and issues and risks\nMeeting and Budget Management:\nFacilitate effective team meetings with clear outcomes and follow-up actions\nForecast and monitor team resources and project costs\nKnowledge Management:\nEstablishes centralized Team access to all relevant project information\nManages Team uncontrolled document repository (e.g. Project History File)\nConducts lessons learned exercises during project execution and share outcomes to a broader audience\nGovernance:\nEffectively navigates the Device Team through business process stage-gates\nSupports Team Leader with technical advisory and governance committee reviews at pre-defined check-in points and/or identifies appropriate check-in points\nContinuous Improvement Initiatives:\nLeads business process continuous improvement initiatives through applying project lessons: business process updates, PM tool optimization & implementation, best practice sharing and driving awareness across teams\nMust Haves:\nBachelor's degree in Engineering or a related field.\nMin. 8 to 11 years of experience, with at least 5 years in a relevant industry, preferably within a global medical device, pharmaceutical, or biopharmaceutical company\nExperience in project management in drug and/or medical device development and commercialization, particularly with combination products\nProficiency in Project Management best practices and software (Microsoft Project, Smartsheet, Google suite)\nPMP certification is an asset.\nKnowledge of 21CFR820.30 design control requirements\nExperience with vendor / partner collaboration.\nExcellent communication and relationship-building skills.\nAbility to manage complex projects independently in a fast-paced, team-based enviro",
    "datePosted": "2026-08-07",
    "validThrough": "2026-09-06",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/global-project-manager-1",
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    "@id": "https://ch-jobs.com/job/global-cmo-clinical-packaging-site-manager-1#jobposting",
    "title": "Global CMO Clinical Packaging Site Manager",
    "description": "Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a\nGlobal CMO Clinical Packaging Site Manager 80-100%\nBackground:\nThis role is responsible for the operational and strategic management of clinical drug labeling, packaging, and device assembly outsourced to a global network of Contract Manufacturing Organizations (CMOs). Operating within a strictly regulated GxP/GMP environment, the position serves as the central operational link between internal supply chain functions, procurement, and external manufacturing partners.\nThe core focus encompasses end-to-end CMO project execution—from initial onboarding, RFPs, and SOW contracting to budget ownership, SAP order processing, and active S&OP representation. The goal is to ensure reliable, high-quality, and cost-effective clinical supply delivery to meet global trial timelines.\nTasks & Responsibilities:\nCMO Site Management: Organize and oversee clinical drug labeling, packaging, and device assembly production outsourced to a global network of CMOs.\nProject & Delivery Oversight: Proactively manage CMO project onboarding, communications, timelines, and delivery performance for outsourced clinical packaging orders to meet supply chain needs while adhering to cost and quality standards.\nProcurement & Contracting: Partner with Procurement and key stakeholders to drive Request for Proposals (RFPs) and Statements of Work (SOWs), negotiate supply agreements, and select vendors.\nStrategy & Budgeting: Support leadership in defining supply strategies for non-standard supply chains. Own the budgeting process and submission for CMO project variable costs.\nProcess Ownership & Governance: Establish team scope and division of responsibilities with upstream functions (e.g., device CMO team). Define, track, and report CMO team KPIs.\nS&OP Representation: Actively drive network supply outcomes and represent the CMO function in the CD&OP process.\nManaging operational orders, and master data in SAP\nSupplier Relationship Management (SRM): Lead SRM activities and partner with CMOs to ensure long-term capability and capacity for predictable delivery.\nFinancial & Order Execution: Create and maintain Purchase Orders in the purchasing system, review/approve CMO invoices, and execute pre- and post-production order management in the ERP system.\nContinuous Improvement: Identify and champion process improvement opportunities, applying technical expertise to resolve complex supply chain issues. Serve as an SME/primary contact for key strategic initiatives.\nMust Haves:\nDegree: BA/BS degree, preferably in a technical, business, or supply chain discipline. Master’s degree is a plus\nWork Experience: 8+ years of experience in the pharmaceutical industry, supply chain management, or manufacturing.\nDomain Knowledge: Strong preference for experience in clinical drug manufacturing, clinical supply chain, or contract manufacturing management.\nGMP Experience: Required.\nIT / Tool Skills: Proficient knowledge and hands-on experience with SAP or equivalent ERP systems.\nLanguage Skills: Excellent written and spoken English (required); basic German skills are beneficial.\nShift Flexibility: Flexibility to adapt to global working hours (e.g., starting as early as 7:00 AM for SSF teams or working until 6:00 PM for Switzerland-based teams).\nSolid understanding of pharma supply chains, contract manufacturing, and clinical operations.\nProven project planning, project management, and resource management skills.\nStrong leadership experience in taking projects from initiation through final delivery.\nHigh cultural awareness and social competence for global stakeholder management.\nStrong analytical, problem-solving, and system-oriented skills with high attention to detail.\nHigh integrity and the ability to operate independently with minimal direction.\nExcellent cross-functional communication and presentation skills.\nNice to Have:\nProfessional certifications: APICS, SCOR, or equivalent relevant experience.\nProcess/Management training: PMP, Operational Excellence, Six Sigma, or Lean methodologies.\nWhat you will be offered:\nAn opportunity to work in one of the world's most important pharmaceutical companies\nModern campus with plenty of green spaces and meeting areas\nCentral location in Basel\nVaried job profile\nFurther training opportunities through temptraining\nWorking in a dynamic and motivated team\nIf you are interested please send your application documents addressed to Ms Marianne Buser.\nBasel-Stadt Supply Chain Management APICS SCOR PMP SAP ERP Pharmaceutical Supply Chain GMP Clinical Packaging Labeling CMO",
    "datePosted": "2026-08-04",
    "validThrough": "2026-09-03",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/global-cmo-clinical-packaging-site-manager-1",
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    "@id": "https://ch-jobs.com/job/solution-engineer-expert-80-100#jobposting",
    "title": "Solution Engineer/ Expert 80-100%",
    "description": "Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, Roche Diagnostics International AG in Rotkreuz, we are looking for a\nSolution Engineer/ Expert 80-100%\nBackground:\nThe Opportunity: Build the Foundation for Life-Saving Technology!\nAre you driven by a deep need to understand how systems work, from the kernel to the application layer? Do you see a working system not as an endpoint, but as a baseline for improvement, optimization, and hardening?\nWe are a specialized team of software and hardware experts at the heart of Roche's medical instrument development. We build and own \"Roche Linux\", a purpose-built, Debian-based platform that powers the next generation of medical devices. We are seeking a senior engineer to join our team, someone who combines deep technical mastery with a passion for craftsmanship and a relentless drive to make things better.\nIn this role, you will be a core contributor and consultant, ensuring the foundational operating system is robust, secure, and perfectly tailored to the demanding world of MedTech.\nTasks & Responsibilities:\nArchitect and Engineer our Core OS Platform: Take ownership of our custom Debian-based distribution. This includes everything from kernel customization and driver integration to the creation, maintenance, and optimization of Debian packages.\nMaster the Build and Release Pipeline: Evolve and improve the infrastructure and processes used to build, test, and release our Linux distribution, ensuring reliability and reproducibility.\nBe the Ultimate Escalation Point: Act as the go-to expert for complex, low-level system issues. Perform deep-dive troubleshooting, debugging, and root-cause analysis across both software and hardware.\nConsult and Empower Development Teams: Guide internal project teams on how to best leverage the Roche Linux platform.\nProactively Drive Improvement: Constantly seek out opportunities to enhance our distribution, tools, and processes. Whether it's improving system performance, strengthening security, or automating a complex workflow, you will be expected to identify needs and champion solutions.\nMust Haves:\nDeep, Hands-On Linux Mastery (10+ years): You are a seasoned professional who is comfortable across the entire Linux stack.\nCustom Distribution Engineering: Proven, extensive experience building, modifying, or maintaining a customized Linux distribution, with a strong preference for Debian (e.g.,using tools like debootstrap, molior, aptly).\nExpertise in Debian Packaging: You don't just apt-get install. You can create, patch, and maintain .deb packages from scratch, understanding policy, dependencies and best practices.\nStrong Scripting and Automation Skills: Fluency in Python and Shell scripting is essential for building tools and automating system tasks.\nFundamental Systems Knowledge: A solid grasp of operating system theory (process management, memory, filesystems), software build systems (make, CMake), and the full testing and packaging lifecycle.\nAdvanced English is mandatory; German is a welcome bonus.\nNice to Have:\nProficiency in a systems programming language like C or C++.\nExperience with embedded systems, the ARM platform, hardware drivers, and low-level hardware/software integration.\nKnowledge of modern infrastructure: Virtualization (KVM), Containers (Docker, Kubernetes), CI/CD pipelines, and Infrastructure as Code (Terraform).\nExperience with cloud platforms (e.g., AWS).\nWhat you will be offered:\nAn opportunity to work in one of the world's most important pharmaceutical companies\nModern campus with plenty of green spaces and meeting areas\nCentral location in Basel\nVaried job profile\nFurther training opportunities through temptraining\nWorking in a dynamic and motivated team\nIf you are interested please send your application documents addressed to Ms Marianne Buser.\nLinux Platform Engineering Debian Python Shell Scripting CMake Build Systems Docker Kubernetes KVM C++ AWS Automation",
    "datePosted": "2026-08-02",
    "validThrough": "2026-09-01",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/solution-engineer-expert-80-100",
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        "name": "Elan Personal AG",
        "value": "job-74126"
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