[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-global-quality-manager-mfd":3,"similar-global-quality-manager-mfd":38},{"id":4,"slug":5,"title":6,"skills":7,"budget":21,"duration":22,"location":23,"onsitePercent":24,"contractType":25,"foundAt":26,"category":27,"description":31,"rawText":32,"webTitle":33,"webText":34,"language":35,"projectId":36,"sourceUrl":37},13205,"global-quality-manager-mfd","Global Quality Manager (m\u002Ff\u002Fd)",[8,9,10,11,12,13,14,15,16,17,18,19,20],"Quality Assurance","GMP\u002FGDP","Regulatory Compliance","Deviation Management","CAPA","Inspection Management","Clinical Trial Management","English fluency","German (asset)","Master Quality Agreements","Complaint Management","Good Documentation Practices","Veeva Vault QMS (nice to have)",null,"12+ Monate","Basel",100,"permanent","2026-06-16T13:06:18+00:00",{"id":28,"slug":29,"label":30},14,"medical_tech","Medizintechnik","Für ein großes Pharmaunternehmen in Basel wird ein hochqualifizierter Global Quality Manager gesucht, der als Delegate des Swiss Responsible Person fungiert und Global QA Oversight über das gesamte IMP Distribution Network wahrnimmt. Die Position erfordert umfangreiche Erfahrung in Quality Assurance, GMP\u002FGDP-Compliance und regulatorischer Dokumentation. Der Kandidat wird Deviation Management, Inspection Management und Quality Decision-Making für klinische Studien verantworten.","Global Quality Manager (m\u002Ff\u002Fd)\n\nPermanent\nGlobal Quality Manager (m\u002Ff\u002Fd)\nGlobal Quality Manager (m\u002Ff\u002Fd)  – Quality Assurance \u002F GMP \u002F GDP \u002F Pharma \u002F English\nProject:\nFor our customer a big pharmaceutical company in Basel we are looking for a highly qualified Global Quality Manager (m\u002Ff\u002Fd).\nBackground:\nAbout the Organization\nJoin IMP Quality Distribution, a critical function within Global Quality Assurance. We are responsible for maintaining the quality and\ncompliance of Investigational Medicinal Products (IMP) throughout the clinical supply chain. Our team acts as the appointed Delegate of\nthe Swiss Responsible Person (FvP) and holds Global QA oversight over the entire IMP Distribution Network (Depots) and our key\nbusiness counterparter, Global Clinical Supply Chain Management Distribution (PTDS-L). We drive continuous improvement and ensure\nadherence to international GMP\u002FGDP standards.\nThe Opportunity\nWe are seeking a highly motivated and experienced Global Quality Manager to step into a role of significant reach. This position is\ninstrumental in safeguarding product quality and regulatory compliance for global clinical trials. You will utilize your expertise in quality\nsystems and supply chain distribution knowledge to provide guidance and maintain oversight over complex GxP processes.\nThe perfect candidate:\nAn exceptional candidate holds a Bachelor’s degree in a relevant scientific or technical field and brings a minimum of three years of comprehensive Quality Assurance experience deeply rooted in a regulated GMP\u002FGDP environment. They are completely fluent in English (with German being a strong asset), allowing them to confidently author Master Quality Agreements, manage clinical trial complaint systems, and articulate compliance strategies during high-stakes Health Authority Inspections. Finally, this individual is a proactive problem-solver who will seamlessly support clinical studies by approving complex IMP Supply & Release Flowcharts while actively driving continuous improvement projects across the distribution network.\nTasks & Responsibilities:\nRegulatory Compliance: Act as the appointed Delegate of the Swiss Responsible Person (FvP), providing necessary final Quality decision-making\nGlobal Oversight: Maintain Global QA oversight for the entire Roche IMP Distribution Network and its business counterparter PTDS-L.\nLead the Deviation Management process by performing product quality impact assessments. Provide crucial Quality oversight by reviewing and assessing final evaluations and statements from third parties, ensuring consistency with regulatory standards, and checking if proposed Corrective and Preventive Actions (CAPA) are appropriate.\nSystem Owner: Manage the full lifecycle of quality documentation and Change Records, including establishing, reviewing, and approving critical documents and changes for both internal procedures and external business documents (PTDS-L).\nInspection Management: Actively drive and support all GxP inspections and audits.\nQuality Decision-Making: Manage Temperature Excursion Management for clinical trials, including performing assessments and\nmanaging Expert Statements\u002FOpinions.\nAdditional Responsibilities & Competencies\nSupport clinical studies by reviewing and approving IMP Supply & Release Flowcharts, Transfer requests, and Expert Opinions.\nEstablish and approve Master Quality Agreements and Quality Agreements.\nManage Complaint Management for clinical trials within the Roche network.\nSupport quality-related and business-driven projects within the IMP Distribution network.\nDrive continuous improvement activities\nProfessional Discipline: Assure GMP\u002FGDP compliance, adhere to Good Documentation Practices (GDP), and ensure training\ncompliance with PQS documents\nMust Haves:\nA Bachelor’s degree in a relevant scientific or technical field (e.g., Pharmacy, Chemistry, Biology, Engineering)\nProven and comprehensive experience (min. 3 years) in Quality Assurance with a strong focus on compliance\nDeep knowledge of a regulated GxP environment (GMP\u002FGDP)\nFluent speaker and writer in English (German is a plus). Fluency is essential for managing critical regulatory documentation, providing authoritative guidance to European sites, and ensuring successful support during Health Authority Inspections\nNice to Haves:\nFamiliarity with Veeva vault QMS\nRoche experience\nPTQ experience\nExperience in supplier management especially depots\nReference Nr.: 925022\nRole:  Global Quality Manager (m\u002Ff\u002Fd)\nIndustrie:  Pharma\nWorkplace:  Basel\nPensum: 100%\nStart: 21.08.2026\nDuration: 12++\nDeadline: 22.06.2026\nIf you are interested in this position, please send us your complete dossier. If this position does not fit your profile and you wish to be considered for another position directly, you can also send us your dossier via this ad or to jobs[at]itcag[dot]com.\nContact us for more information about our company, our positions or our attractive Payroll-Only programme: +41 41 760 77 01.\nAbout us:\nITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering.\nWe offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.\nApply Now\n\nIndustry\nPharmaceuticals\nLocation\nBasel-Stadt\nType\nPermanent\nSkill\nGlobal Quality Manager (m\u002Ff\u002Fd) - Quality Assurance \u002F GMP \u002F GDP \u002F Pharma \u002F English\n\nE-Mail: service@itcag.com","Global Quality Manager (m\u002Fw\u002Fd) – Pharma & GMP\u002FGDP","Für ein führendes Pharmaunternehmen suchen wir einen erfahrenen Global Quality Manager (m\u002Fw\u002Fd) zur Verstärkung unseres Quality Assurance Teams.\n\nÜber die Rolle:\nSie werden eine Schlüsselposition in der globalen Qualitätssicherung übernehmen und sind verantwortlich für die Aufrechterhaltung von Qualität und Compliance von Prüfpräparaten in der klinischen Lieferkette. Als ernannte Delegierte der Verantwortlichen Person wirken Sie als Global QA Oversight über das gesamte Verteilnetzwerk und treiben kontinuierliche Verbesserungen voran. Ihre Expertise in Qualitätssystemen und Supply-Chain-Verteilung ist entscheidend für die Sicherung der Produktqualität und regulatorischen Compliance in globalen klinischen Studien.\n\nIhre Aufgaben:\n• Regulatorische Compliance sicherstellen und finale Qualitätsentscheidungen treffen\n• Globale QA-Überwachung des gesamten Verteilnetzwerks und Geschäftspartner\n• Abweichungsmanagement leiten und Produktqualitäts-Auswirkungen bewerten\n• Qualitätsdokumentation und Change Records über den gesamten Lebenszyklus verwalten\n• Inspektionen im GxP-Bereich aktiv unterstützen und durchführen\n• Master Quality Agreements verfassen und klinische Beschwerdensysteme verwalten\n\nIhr Profil:\n• Bachelor-Abschluss in naturwissenschaftlichem oder technischem Fachgebiet\n• Mindestens 3 Jahre umfassende Quality Assurance Erfahrung in GMP\u002FGDP-Umgebung\n• Fließend Englisch (Deutsch von Vorteil)\n• Proaktive Problemlösungsfähigkeit und Compliance-Verständnis\n• Erfahrung mit regulatorischen Anforderungen und Health Authority Inspektionen\n\nWir bieten eine anspruchsvolle Position mit großer Verantwortung in einem internationalen Umfeld.","en","925022","https:\u002F\u002Fwww.itcag.com\u002Fjobs\u002Fglobal-quality-manager-mfd-8148\u002F",{"items":39},[40,58,75,96,110,123,138,154,174,194,212,230,248,262,278],{"id":41,"slug":42,"title":43,"skills":44,"budget":21,"duration":21,"location":54,"onsitePercent":24,"contractType":55,"foundAt":56,"category":57},13001,"chemielaborant-rd-mwd","Chemielaborant R&D (m\u002Fw\u002Fd)",[45,46,47,48,49,50,51,52,53],"Chemielaborant","Laborversuche","Analyseverfahren","Instrumentelle Analytik","Dokumentation","Kalibrierung","Laborsoftware","Arbeitssicherheit","Englisch","Bielefeld","contracting","2026-06-15T15:27:41+00:00",{"id":28,"slug":29,"label":30},{"id":59,"slug":60,"title":61,"skills":62,"budget":21,"duration":21,"location":71,"onsitePercent":72,"contractType":55,"foundAt":73,"category":74},13000,"junior-systems-specialist-pharma-mwd","Junior Systems Specialist Pharma (m\u002Fw\u002Fd)",[63,64,65,66,67,68,69,70],"Python","R","Datenanalyse","GMP","IT-Projektmanagement","Fehleranalyse","KI-Tools","Statistik","Biberach, Baden-Württemberg",50,"2026-06-15T15:27:31+00:00",{"id":28,"slug":29,"label":30},{"id":76,"slug":77,"title":78,"skills":79,"budget":21,"duration":21,"location":93,"onsitePercent":24,"contractType":25,"foundAt":94,"category":95},12988,"global-product-manager-mwd-tracheostomie","Global Product Manager (m\u002Fw\u002Fd) Tracheostomie",[80,81,82,83,84,85,86,87,88,89,90,91,92],"Portfoliomanagement","Produktmanagement","Excel","Power BI","Projektmanagement","Scrum","Prince2","Lean","Stakeholder-Management","Regulatorische Anforderungen","MS Office","Wettbewerbsanalysen","Business Case Entwicklung","Mainz","2026-06-15T15:25:58+00:00",{"id":28,"slug":29,"label":30},{"id":97,"slug":98,"title":99,"skills":100,"budget":21,"duration":21,"location":71,"onsitePercent":72,"contractType":55,"foundAt":108,"category":109},12945,"product-lifecycle-expert-packaging-labelling-mwd","Product Lifecycle Expert (Packaging\u002F Labelling) (m\u002Fw\u002Fd)",[101,102,103,84,104,105,106,107,53],"Pharmaindustrie","Verpackung","Kennzeichnung","Supply Chain Management","MS-Office","Prozessoptimierung","Deutsch","2026-06-15T13:26:07+00:00",{"id":28,"slug":29,"label":30},{"id":111,"slug":112,"title":113,"skills":114,"budget":21,"duration":21,"location":71,"onsitePercent":72,"contractType":55,"foundAt":121,"category":122},12942,"technische-assistenz-chromatographie-mwd","Technische Assistenz Chromatographie (m\u002Fw\u002Fd)",[115,116,66,117,49,118,119,120],"Chromatographie","Qualitätskontrolle","Analytische Chemie","Statistische Analyse","Planung","Koordination","2026-06-15T13:25:38+00:00",{"id":28,"slug":29,"label":30},{"id":124,"slug":125,"title":126,"skills":127,"budget":21,"duration":21,"location":135,"onsitePercent":72,"contractType":55,"foundAt":136,"category":137},12895,"key-user-lims-qc-experte-gmp-digitalisierung-mwd","Key User LIMS \u002F QC Experte GMP Digitalisierung (m\u002Fw\u002Fd)",[128,129,66,130,131,132,90,133,84,65,134,49,106],"LIMS-Systeme","LabWare","GxP","QC-Labor","SAP","Excel VBA","CSV","Frankfurt, Hessen","2026-06-15T11:26:09+00:00",{"id":28,"slug":29,"label":30},{"id":139,"slug":140,"title":141,"skills":142,"budget":21,"duration":21,"location":151,"onsitePercent":24,"contractType":25,"foundAt":152,"category":153},12894,"account-manager-fuer-medizintechnik-mwd","Account Manager für Medizintechnik (m\u002Fw\u002Fd)",[143,144,145,146,147,148,149,30,150,53,107],"Akquise","Analyse","Angebotserstellung","Feinwerktechnik","Kommunikationsfähigkeit","Marktanalysen","Maschinenbau","Vertrieb","Würzburg, Bayern","2026-06-15T11:26:01+00:00",{"id":28,"slug":29,"label":30},{"id":155,"slug":156,"title":157,"skills":158,"budget":21,"duration":21,"location":171,"onsitePercent":72,"contractType":55,"foundAt":172,"category":173},12893,"clinical-data-manager-clinical-data-management-spezialist-mwd","Clinical Data Manager \u002F Clinical Data Management Spezialist (m\u002Fw\u002Fd)",[159,160,161,162,163,164,165,166,167,84,90,53,168,169,170],"Clinical Data Management","EDC-Systeme","SAS","CDISC","ICH","GCP","FDA","Data Validation","Datenbank","eCRF","MedDRA","WHO-DD","Frankfurt","2026-06-15T11:25:54+00:00",{"id":28,"slug":29,"label":30},{"id":175,"slug":176,"title":177,"skills":178,"budget":21,"duration":21,"location":191,"onsitePercent":24,"contractType":55,"foundAt":192,"category":193},12892,"qualifizierungsingenieur-reinraum-hvac-gmp-mwd","Qualifizierungsingenieur Reinraum \u002F HVAC GMP (m\u002Fw\u002Fd)",[179,180,181,182,183,184,185,186,187,90,188,189,190],"Qualifizierung Reinräume","ISO 14644","GMP-Richtlinien","HVAC","Lüftungs- und Klimaanlagen","DQ\u002FIQ\u002FOQ\u002FPQ","Technische Dokumentation","Median Software","CAQ-Systeme","Prüftechnik","Verfahrenstechnik","Gebäudetechnik","Ingelheim am Rhein, Rheinland-Pfalz","2026-06-15T11:25:46+00:00",{"id":28,"slug":29,"label":30},{"id":195,"slug":196,"title":197,"skills":198,"budget":21,"duration":208,"location":209,"onsitePercent":24,"contractType":55,"foundAt":210,"category":211},12876,"freelance-clinical-research-associate-cra-oncology","Freelance Clinical Research Associate (CRA) - Oncology",[199,200,201,202,203,204,205,206,207],"Clinical Research Associate (CRA)","Oncology experience","GCP knowledge","Monitoring discipline","Database management","Data review","German language","English language","Protocol compliance","16 months, 0.8 FTE, Start June\u002FJuly 2025","Germany","2026-06-15T10:55:53+00:00",{"id":28,"slug":29,"label":30},{"id":213,"slug":214,"title":215,"skills":216,"budget":21,"duration":225,"location":226,"onsitePercent":24,"contractType":227,"foundAt":228,"category":229},12860,"junior-system-support-engineer-mwd","Junior System Support Engineer (m\u002Fw\u002Fd)",[217,218,219,220,221,222,223,224],"Technische Ausbildung (Mechatronik, Elektronik, Maschinenbau)","Service-Techniker Erfahrung","Hardware- und Software-Troubleshooting","Systeminstallation und -wartung","Deutsch fließend","Englisch fließend","Logisches Denken","Systematische Fehlersuche","12 Monate, Start 01.08.-01.09.2026","Rotkreuz","temp_work","2026-06-15T10:16:09+00:00",{"id":28,"slug":29,"label":30},{"id":231,"slug":232,"title":233,"skills":234,"budget":21,"duration":243,"location":244,"onsitePercent":245,"contractType":55,"foundAt":246,"category":247},12830,"release-train-engineer","Release Train Engineer",[235,233,236,237,106,238,239,240,241,242,107,53],"SAFe","Agile Beratung","Lean-Agile","Organisationsentwicklung","Azure DevOps","Miro","Lucidchart","CodeBeamer","3 Monate initial, dann 12-monatige Verlängerung möglich","Mannheim, Baden-Württemberg",20,"2026-06-15T08:46:05+00:00",{"id":28,"slug":29,"label":30},{"id":249,"slug":250,"title":251,"skills":252,"budget":21,"duration":21,"location":259,"onsitePercent":24,"contractType":55,"foundAt":260,"category":261},12761,"it-umstellung-und-systemtest-in-arztpraxis","IT-Umstellung und Systemtest in Arztpraxis",[253,254,255,256,257,258],"medatixx","x.isynet","IT-Systeme im medizinischen Umfeld","Systemtests","Konfiguration","Windows 10","Duisburg","2026-06-13T02:05:44+00:00",{"id":28,"slug":29,"label":30},{"id":263,"slug":264,"title":265,"skills":266,"budget":273,"duration":274,"location":275,"onsitePercent":24,"contractType":227,"foundAt":276,"category":277},12548,"chemielaborant-mwd","Chemielaborant (m\u002Fw\u002Fd)",[45,267,268,269,270,271,272],"CTA","Routineanalysen","Probenvorbereitung","Strahlenschutz","Qualitätssicherung","Deutsch C1","ca. 24-25 EUR\u002Fh","24 Monate (03\u002F2026 - 02\u002F2028)","Erlangen","2026-06-12T02:06:14+00:00",{"id":28,"slug":29,"label":30},{"id":279,"slug":280,"title":281,"skills":282,"budget":21,"duration":21,"location":291,"onsitePercent":24,"contractType":25,"foundAt":292,"category":293},12507,"physiklaborantlabortechniker-mwd-siemens-energy-global-gmbh-co-kg","Physiklaborant\u002FLabortechniker (m\u002Fw\u002Fd) - Siemens Energy Global GmbH & Co. KG",[283,284,285,286,49,50,287,288,289,290,107,53],"Physiklaborant","Labortechniker","Laborarbeit","Messungen","Materialphysik","Rheologie","Thermoanalyse","EDV","Mülheim an der Ruhr","2026-06-11T15:26:20+00:00",{"id":28,"slug":29,"label":30}]