[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-validierungsingenieur-mwd-in-direktvermittlung":3,"similar-validierungsingenieur-mwd-in-direktvermittlung":34},{"id":4,"slug":5,"title":6,"skills":7,"budget":18,"duration":18,"location":19,"onsitePercent":20,"contractType":21,"foundAt":22,"category":23,"description":27,"rawText":28,"webTitle":29,"webText":30,"language":31,"projectId":32,"sourceUrl":33},10958,"validierungsingenieur-mwd-in-direktvermittlung","Validierungsingenieur (m\u002Fw\u002Fd) in Direktvermittlung",[8,9,10,11,12,13,14,15,16,17],"GMP","Validierung","IQ\u002FOQ\u002FPQ","Qualitätsmanagement","Pharma","Medical Devices","Dokumentation","MS Office","Englisch","Softwarevalidierung",null,"Kleve, Nordrhein-Westfalen",100,"permanent","2026-06-04T02:26:08+00:00",{"id":24,"slug":25,"label":26},14,"medical_tech","Medizintechnik","Validierungsingenieur für GMP-regulierte Produktionsumgebung mit Fokus auf Batch-Freigaben, Qualifizierung neuer Produktionslinien (IQ\u002FOQ\u002FPQ) und Entwicklung von Produktionsprozessen. Verantwortung für Validierungsaktivitäten, Softwarevalidierung, Thermomapping und GMP-Dokumentation in den Bereichen Pharma, Food oder Medical Devices.","Validierungsingenieur (m\u002Fw\u002Fd) in Direktvermittlung\nProjektnummer: FE59-74765-DDDI\nStandort: Kleve, Nordrhein-Westfalen\nArbeitsweise: Vor Ort\nLaufzeit: Keine Angabe\nStartdatum: Keine Angabe\n\nIhr Gestaltungsbereich:\n- Durchführung der täglichen Batch-Freigaben für die laufende Produktion\n\n- Validierung und Qualifizierung neuer Produktionslinien (IQ\u002FOQ\u002FPQ)\n\n- Entwicklung und Implementierung neuer Produktionsprozesse für Kunden\n\n- Verantwortung für die termingerechte Planung und Durchführung aller Validierungsaktivitäten, einschließlich Softwarevalidierung, Thermomapping und Anlagenkalibrierung\n\n- Erstellung, Pflege und Prüfung von GMP-relevanter Dokumentation, insbesondere SOPs und Validierungsprotokollen\n\n- Durchführung praxisnaher Schulungen der Mitarbeiter:innen auf Basis der gültigen SOPs\n\nIhr Profil:\n- Erfolgreich abgeschlossenes Studium, z. B. im Bereich Bioengineering oder vergleichbare technische Ausbildung\n\n- Erfahrung im GMP-regulierten Umfeld, idealerweise in den Bereichen Qualitätsmanagement, Food, Pharma oder Medical Devices\n\n- Ausgeprägte Hands-on-Mentalität sowie eigenständige und strukturierte Arbeitsweise\n\n- Gute Englischkenntnisse in Wort und Schrift \n\n- Sicherer Umgang mit MS Office sowie Datenbankanwendungen\n\n- Kenntnisse im wissenschaftlichen Arbeiten und in der technischen Dokumentation\n\nSkills: Arbeitsweise, Dokumentation, Entwicklung, GMP, IQ, Implementierung, MS, Medical Devices, OQ, PQ, Pharma, Planung, Produktion, Prüfung, Qualifizierung, Qualitätsmanagement, Validierung\n\nAnsprechpartner:\nTom Otto\nConsultant DIRECT\nFERCHAU GmbH, Niederlassung Dresden DIRECT\nWiener Platz 6\n01069 Dresden\n+49 351 266283-14\ntom.otto@ferchau.com","Validierungsingenieur (m\u002Fw\u002Fd)","Wir suchen einen erfahrenen Validierungsingenieur (m\u002Fw\u002Fd) für eine Direktvermittlung an unserem Standort in Nordrhein-Westfalen. Sie arbeiten vor Ort und tragen wesentlich zur Qualitätssicherung und Prozessoptimierung bei.\n\nIhre Aufgaben umfassen die Durchführung täglicher Batch-Freigaben für die laufende Produktion sowie die Validierung und Qualifizierung neuer Produktionslinien (IQ\u002FOQ\u002FPQ). Sie entwickeln und implementieren neue Produktionsprozesse für Kunden und sind verantwortlich für die termingerechte Planung und Durchführung aller Validierungsaktivitäten. Dazu gehören Softwarevalidierung, Thermomapping und Anlagenkalibrierung. Ein weiterer Schwerpunkt liegt in der Erstellung, Pflege und Prüfung von GMP-relevanter Dokumentation, insbesondere SOPs und Validierungsprotokollen. Zudem führen Sie praxisnahe Schulungen der Mitarbeiter auf Basis gültiger SOPs durch.\n\nWir erwarten ein erfolgreich abgeschlossenes Studium im Bereich Bioengineering oder eine vergleichbare technische Ausbildung. Idealerweise bringen Sie Erfahrung im GMP-regulierten Umfeld mit, vorzugsweise in den Bereichen Qualitätsmanagement, Food, Pharma oder Medical Devices. Eine ausgeprägte Hands-on-Mentalität, eigenständige und strukturierte Arbeitsweise sind essentiell. Gute Englischkenntnisse in Wort und Schrift sowie sicherer Umgang mit MS Office und Datenbankanwendungen werden vorausgesetzt. Kenntnisse im wissenschaftlichen Arbeiten und in der technischen Dokumentation runden Ihr Profil ab.\n\nDiese Position bietet Ihnen die Möglichkeit, in einem regulierten Umfeld Ihre Expertise einzubringen und Prozesse nachhaltig zu verbessern.","de","FE59-74765-DDDI","https:\u002F\u002Ftouch.ferchau.com\u002Fde\u002Fde\u002Fprojekt\u002F487726",{"items":35},[36,66,88,97,109,126,145,160,182,195,213,229,243,258,277],{"id":37,"slug":38,"title":39,"skills":40,"budget":18,"duration":18,"location":62,"onsitePercent":20,"contractType":63,"foundAt":64,"category":65},10930,"hardware-entwicklung","Hardware Entwicklung",[41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61],"Hardwareentwicklung","Elektronikentwicklung","Schaltungsentwicklung","Analog-\u002FDigitalelektronik","PCB-Design","Altium Designer","Eagle","KiCad","OrCAD","Zuken","Oszilloskop","Multimeter","Signalgenerator","Logikanalysator","Design Reviews","Verifikation","IEC 60601","ISO 13485","IEC 62304","ISO 14971","EMV-Anforderungen","Erlangen","contracting","2026-06-03T16:10:59+00:00",{"id":24,"slug":25,"label":26},{"id":67,"slug":68,"title":69,"skills":70,"budget":83,"duration":18,"location":84,"onsitePercent":85,"contractType":63,"foundAt":86,"category":87},10895,"solution-analyst-qms-dms-lms-consultant-quality-document-management","Solution Analyst - QMS, DMS, LMS Consultant - Quality Document Management",[71,72,8,73,74,75,76,77,78,79,80,81,82],"QMS","DMS","GxP","CAPA","Change Control","Document Control","Veeva Vault","TrackWise","MasterControl","SAP DMS","FDA Compliance","Quality Management","Negotiable","India",0,"2026-06-03T14:35:37+00:00",{"id":24,"slug":25,"label":26},{"id":89,"slug":90,"title":91,"skills":92,"budget":83,"duration":18,"location":84,"onsitePercent":85,"contractType":63,"foundAt":95,"category":96},10894,"qms-dms-system-owner","QMS & DMS System Owner",[71,72,8,73,74,75,76,77,78,79,80,93,94],"Regulatory Affairs","Quality Assurance","2026-06-03T14:35:27+00:00",{"id":24,"slug":25,"label":26},{"id":98,"slug":99,"title":100,"skills":101,"budget":18,"duration":18,"location":106,"onsitePercent":20,"contractType":63,"foundAt":107,"category":108},10855,"junior-specialist-clinical-supply-documentation-mwd","Junior Specialist Clinical Supply & Documentation (m\u002Fw\u002Fd)",[102,14,8,103,104,105,16],"Biotechnologie","Pharmazie","Medical Affairs","Deutsch","Biberach, Baden-Württemberg","2026-06-03T13:26:55+00:00",{"id":24,"slug":25,"label":26},{"id":110,"slug":111,"title":112,"skills":113,"budget":18,"duration":18,"location":122,"onsitePercent":123,"contractType":63,"foundAt":124,"category":125},10852,"pharma-und-life-science-ingenieur-medizintechnik-mwd","Pharma- und Life Science Ingenieur Medizintechnik (m\u002Fw\u002Fd)",[26,13,114,115,8,116,12,117,118,119,120,93,121,16],"Design Control","Verifizierung und Validierung","ISO","Life Science","Testmethoden","Risikomanagement","Qualifizierung","Polarion ALM","Kufstein, Tirol",50,"2026-06-03T13:26:35+00:00",{"id":24,"slug":25,"label":26},{"id":127,"slug":128,"title":129,"skills":130,"budget":18,"duration":141,"location":142,"onsitePercent":85,"contractType":63,"foundAt":143,"category":144},10804,"kis-systementwicklung-und-integration","KIS-Systementwicklung und Integration",[131,132,133,134,135,136,137,138,139,140],"KIS-Systeme","Medico","SAP IS-H","HL7","FHIR","Mirth","Administration","Customizing","Integration","Schnittstellenmanagement","6 Monate, Start 22.06.2026","Bochum","2026-06-03T11:26:25+00:00",{"id":24,"slug":25,"label":26},{"id":146,"slug":147,"title":148,"skills":149,"budget":18,"duration":18,"location":106,"onsitePercent":20,"contractType":157,"foundAt":158,"category":159},10801,"hauswirtschafter-teilzeit-50-pharmabranche-mwd","Hauswirtschafter Teilzeit 50% Pharmabranche (m\u002Fw\u002Fd)",[150,151,152,153,154,155,156,14],"Hauswirtschaft","Reinigung","Wäschepflege","HACCP","Hygienemanagement","GCP","Infektionsschutz","temp_work","2026-06-03T11:26:02+00:00",{"id":24,"slug":25,"label":26},{"id":161,"slug":162,"title":163,"skills":164,"budget":18,"duration":178,"location":179,"onsitePercent":85,"contractType":63,"foundAt":180,"category":181},10800,"administration-und-weiterentwicklung-von-klinischen-systemen","Administration und Weiterentwicklung von klinischen Systemen",[137,165,166,139,26,167,168,169,170,171,172,173,174,175,176,177],"Fehleranalyse","IT","PDMS","PDMS CHAA\u002FAI S","Ixserv","Hybase","POCcelerator","InstaCount","Demis","Epias","DRG Kodierung","MTS","BGA\u002FBZ","Keine Angabe","Berlin","2026-06-03T11:25:55+00:00",{"id":24,"slug":25,"label":26},{"id":183,"slug":184,"title":185,"skills":186,"budget":18,"duration":18,"location":106,"onsitePercent":20,"contractType":63,"foundAt":193,"category":194},10796,"technischer-servicemitarbeiter-humanpharmakologie-mwd","Technischer Servicemitarbeiter Humanpharmakologie (m\u002Fw\u002Fd)",[26,120,9,73,187,15,188,189,190,166,191,192],"MS Windows","MS SharePoint","Datenmanagementsysteme","EKG-Geräte","Informationsmanagement","Gesundheitswesen","2026-06-03T11:25:26+00:00",{"id":24,"slug":25,"label":26},{"id":196,"slug":197,"title":198,"skills":199,"budget":18,"duration":209,"location":210,"onsitePercent":20,"contractType":157,"foundAt":211,"category":212},10751,"global-clinical-order-manager","Global Clinical Order Manager",[200,201,8,202,203,74,204,205,206,207,208],"Clinical Supply Chain Management","SAP","Veeva","ERP systems","Master Data","German language","English language","Document management","Deviation management","12+ months, Start ASAP (01.08.2026)","Kaiseraugst","2026-06-03T08:41:26+00:00",{"id":24,"slug":25,"label":26},{"id":214,"slug":215,"title":216,"skills":217,"budget":18,"duration":18,"location":226,"onsitePercent":20,"contractType":63,"foundAt":227,"category":228},10743,"rd-quality-manager-senior-auditor-mwd","R&D Quality Manager \u002F Senior Auditor (m\u002Fw\u002Fd)",[218,155,73,74,219,220,221,222,223,224,225,14],"Audits","Qualitätssicherung","FDA","MDR","ICH","Inspektionsmanagement","Qualitätsmanagementsysteme","Lieferantenaudits","Frankfurt am Main","2026-06-03T08:26:45+00:00",{"id":24,"slug":25,"label":26},{"id":230,"slug":231,"title":232,"skills":233,"budget":18,"duration":18,"location":240,"onsitePercent":20,"contractType":21,"foundAt":241,"category":242},7592,"initiativbewerbung-in-der-medizintechnik-mwd","Initiativbewerbung in der Medizintechnik (m\u002Fw\u002Fd)",[26,11,234,235,236,237,238,239],"Technische Redaktion","Prozessmanagement","Projektmanagement","Englischkenntnisse","Flexibilität","Kommunikationsfähigkeiten","Kiel","2026-06-03T02:29:28+00:00",{"id":24,"slug":25,"label":26},{"id":244,"slug":245,"title":246,"skills":247,"budget":18,"duration":18,"location":255,"onsitePercent":85,"contractType":63,"foundAt":256,"category":257},7535,"biomarker-expert-clinical-biosample-operations-mwd","Biomarker Expert - Clinical Biosample Operations (m\u002Fw\u002Fd)",[155,248,249,250,251,252,253,254],"Kommunikationsfähigkeit","Koordination","Logistik","Optimierung","Organisationstalent","Probennahme","Prüfung","Biberach an der Riß","2026-06-02T15:25:31+00:00",{"id":24,"slug":25,"label":26},{"id":259,"slug":260,"title":261,"skills":262,"budget":18,"duration":273,"location":274,"onsitePercent":18,"contractType":157,"foundAt":275,"category":276},7490,"technical-rd-analytical-project-lead","Technical R&D – Analytical Project Lead",[263,264,265,266,267,268,269,270,271,272],"HPLC","UHPLC","Mass Spectrometry","UV detection","Fluorescence","Analytical Chemistry","Chromatography","Project Management","Regulatory Documentation","English","12+ months","Basel","2026-06-02T13:06:41+00:00",{"id":24,"slug":25,"label":26},{"id":278,"slug":279,"title":280,"skills":281,"budget":18,"duration":290,"location":291,"onsitePercent":20,"contractType":63,"foundAt":292,"category":293},7364,"stellv-leitung-der-herstellung","Stellv. Leitung der Herstellung",[282,102,8,283,284,285,74,286,287,288,289],"Pharmatechnik","Aseptische Abfüllung","Batch Record Review","Change Controls","OEE-Systeme","Shopfloor-Management","Lean","OPEX","24 Monate (01.07.2026 - 30.06.2028)","Sachsen","2026-06-01T20:11:17+00:00",{"id":24,"slug":25,"label":26}]