[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-product-quality-review-writer":3,"similar-product-quality-review-writer":33},{"id":4,"slug":5,"title":6,"skills":7,"budget":18,"duration":19,"location":20,"onsitePercent":21,"contractType":22,"foundAt":23,"category":24,"description":28,"rawText":29,"language":30,"projectId":31,"sourceUrl":32},2643,"product-quality-review-writer","Product Quality Review Writer",[8,9,10,11,12,13,14,15,16,17],"GMP","Product Quality Review","PQR","EU-GMP-Leitfaden","Pharma","Qualitätskontrolle","MS Office","Veeva","Deutsch","Englisch",null,"01.06.2026 - 31.05.2027","Hamburg",0,"contracting","2026-05-13T16:08:05+00:00",{"id":25,"slug":26,"label":27},14,"medical_tech","Medizintechnik","Erstellung von Product Quality Reviews (PQR) gemäß EU-GMP-Leitfaden. Datensammlung und Auswertung aus Produktion, Qualitätskontrolle und Logistik. Analyse von Abweichungen und Reklamationen zur Bewertung der Produktqualität.","Product Quality Review Writer\n\nJob ID:\n3136\nJetzt loslegen\n\nOrt\n\nHamburg\n\nRahmendaten\n\n\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 16.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">\u003Cstrong>Product Quality Review Writer\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan>\u003Cbr> \u003Cbr> \u003Cbr> \u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">\u003Cstrong>Rahmenbedingung\u003C\u002Fstrong>\u003Cbr> \u003Cbr> Start: 01.06.2026\u003Cbr> Ende: 31.05.2027\u003Cbr> Auslastung: 5 Tage Woche \u003Cbr> Ort: 100 % Remote (Einarbeitung vor Ort)\u003Cbr> \u003Cbr> \u003Cbr> \u003Cstrong>Aufgabe\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cul> \u003Cli> \u003Cp>\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">\u003Cstrong>Erstellung von Product Quality Reviews (PQR):\u003C\u002Fstrong> Fachgerechte Ausarbeitung gemäß den Anforderungen des EU-GMP-Leitfadens.\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp> \u003Cli> \u003Cp>\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">\u003Cstrong>Datensammlung & Auswertung:\u003C\u002Fstrong> Systematische Erfassung und Zusammenführung aller produktbezogenen Daten aus den Fachbereichen Produktion, Qualitätskontrolle und Logistik.\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp> \u003Cli>\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">Analyse von Abweichungen, Reklamationen und Änderungsanträgen (Changes) zur Bewertung der Prozesskonstanz und Produktqualität.\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003C\u002Ful> \u003Cbr> \u003Cbr> \u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">\u003Cstrong>Anforderungen\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cul> \u003Cli> \u003Cp>\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">Fundierte Berufserfahrung im GMP-regulierten Umfeld.\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp> \u003Cli> \u003Cp>\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">\u003Cstrong>Spezialisierung:\u003C\u002Fstrong> 5 – 10 Jahre einschlägige Erfahrung spezifisch in der Erstellung von PQRs.\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp> \u003Cli> \u003Cp>\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">Professionelle \u003Cstrong>Hands-on-Mentalität\u003C\u002Fstrong> mit Fokus auf \u003Cstrong>Umsetzungsstärke.\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp> \u003Cli> \u003Cp>\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">\u003Cstrong>von Vorteil: \u003C\u002Fstrong>Sicherer Umgang mit MS Office und \u003Cstrong>Veeva\u003C\u002Fstrong>.\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp> \u003Cli> \u003Cp>\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">Analytisches Denken, Struktur und hohe Genauigkeit bei der Dokumentation.\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp> \u003Cli> \u003Cp>\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">Tiefes Interesse an den Abläufen im Arzneimittel-Lebenszyklus.\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp> \u003Cli> \u003Cp>\u003Cspan style=\"color: rgb(0,0,0);\">\u003Cspan style=\"font-size: 12.0px;\">\u003Cspan style=\"font-family: Arial , Helvetica , sans-serif;\">Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fp> \u003C\u002Ful>\n\nIhr persönlicher Ansprechpartner\n\nBei Fragen können Sie sich jederzeit melden!\n\nAdrian Rießenberger\n\nRecruitment Consultant Pharma\n\nMobil:\n\n+49 151 4636 8023\nE-Mail:\n\nE-Mail: a.riessenberger@neo-experts.com a.riessenberger@neo-experts.com\nGemeinsam zum perfekten Match.\n\nJetzt bewerben","de","3136","https:\u002F\u002Fwww.neo-experts.com\u002Fstellen-suche\u002Fproduct-quality-review-writer-28601-643b2",{"items":34},[35,54,70,90,113],{"id":36,"slug":37,"title":38,"skills":39,"budget":18,"duration":18,"location":50,"onsitePercent":51,"contractType":22,"foundAt":52,"category":53},4585,"laborant-zellkultur-mwd","Laborant Zellkultur (m\u002Fw\u002Fd)",[40,41,42,43,8,44,45,46,47,48,49],"Anlagen","Auswertung","Entwicklung","Fermentation","Herstellung","Optimierung","Planung","Teamfähigkeit","Zellkultur","Zelllinien","Biberach an der Riß",100,"2026-05-20T02:26:18+00:00",{"id":25,"slug":26,"label":27},{"id":55,"slug":56,"title":57,"skills":58,"budget":18,"duration":18,"location":50,"onsitePercent":51,"contractType":22,"foundAt":68,"category":69},4550,"technischer-assistent-hplc-analytik-mwd","Technischer Assistent HPLC-Analytik (m\u002Fw\u002Fd)",[59,8,60,61,62,63,64,65,66,67],"HPLC","Analytik","Methodenvalidierung","Dokumentation","Empower","LabWare-LIMS","MS-Office","Chemielaborant","Biologielaborant","2026-05-19T16:25:57+00:00",{"id":25,"slug":26,"label":27},{"id":71,"slug":72,"title":73,"skills":74,"budget":18,"duration":85,"location":86,"onsitePercent":87,"contractType":22,"foundAt":88,"category":89},4527,"project-engineer-mwd-pharma","Project Engineer (m\u002Fw\u002Fd) Pharma",[75,76,77,78,79,80,81,82,83,84],"Projektmanagement","GMP-Kenntnisse","Pharmazeutische Industrie","Verfahrenstechnik","Biotechnologie","Pharmatechnik","Chemieingenieurwesen","Maschinenbau","Englischkenntnisse","Kommunikationsfähigkeit","6 Monate","Ludwigshafen am Rhein",90,"2026-05-19T14:35:32+00:00",{"id":25,"slug":26,"label":27},{"id":91,"slug":92,"title":93,"skills":94,"budget":18,"duration":109,"location":110,"onsitePercent":51,"contractType":22,"foundAt":111,"category":112},4515,"testing-von-medizingeraeten","Testing von Medizingeräten",[95,96,97,98,99,100,101,102,103,104,105,106,107,108],"Testing","Testspezifikation","Jira","Python","C","C#","SQL","ISTQB","Elektronik","Informatik","Requirements Management","Polarion","Netzwerk","Datenbanken","13 Monate","Bensheim","2026-05-19T14:26:47+00:00",{"id":25,"slug":26,"label":27},{"id":114,"slug":115,"title":116,"skills":117,"budget":121,"duration":122,"location":123,"onsitePercent":124,"contractType":22,"foundAt":125,"category":126},4422,"mfc-und-c-entwickler-fuer-medizinischen-bereich","MFC und C++ Entwickler für medizinischen Bereich",[118,119,120],"C++","MFC","Reportstellung","auf Anfrage","3 Monate +","Ingolstadt",10,"2026-05-19T09:30:24+00:00",{"id":25,"slug":26,"label":27}]