[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-analytical-instrument-qualification-aiq-qc-analytical-lifecycle":3,"similar-analytical-instrument-qualification-aiq-qc-analytical-lifecycle":30},{"id":4,"slug":5,"title":6,"skills":7,"budget":16,"duration":17,"location":18,"onsitePercent":18,"contractType":19,"foundAt":20,"category":21,"description":25,"rawText":26,"language":27,"projectId":28,"sourceUrl":29},2653,"analytical-instrument-qualification-aiq-qc-analytical-lifecycle","Analytical Instrument Qualification (AIQ) – QC Analytical Lifecycle",[8,9,10,11,12,13,14,15],"Analytical Instrument Qualification","IQ\u002FOQ\u002FPQ-Dokumentation","GMP","Annex 15","Data Integrity","21 CFR Part 11","QC-Umgebungen","Qualifizierungsdurchführung","Fixpreis bevorzugt","langfristige, wiederkehrende Projekte, Start ab ca. April",null,"contracting","2026-05-13T16:09:02+00:00",{"id":22,"slug":23,"label":24},14,"medical_tech","Medizintechnik","Planung, Erstellung und Durchführung von Analytical Instrument Qualifications gemäß internen SOPs im GMP-Umfeld. Erstellung von IQ\u002FOQ-Protokollen inkl. Risikoanalysen und Testplänen sowie deren Execution. Enge Zusammenarbeit mit internen QC-Teams, QA und Engineering.","Analytical Instrument Qualification (AIQ) – QC Analytical Lifecycle\n\nJob ID:\n3026\nJetzt loslegen\n\nOrt\n\nempty-city\n\nRahmendaten\n\n\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">\u003Cstrong>Einsatz:\u003C\u002Fstrong> Freelancer oder Ingenieurbüro (Fixpreis bevorzugt)\u003Cbr> \u003Cstrong>Start:\u003C\u002Fstrong> ab ca. April\u003Cbr> \u003Cstrong>Auslastung:\u003C\u002Fstrong> initial 1–2 FTE, skalierbar\u003Cbr> \u003Cstrong>Dauer:\u003C\u002Fstrong> langfristige, wiederkehrende Projekte\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cdiv style=\"margin-bottom: 0.0cm;margin-left: 0.0cm;margin-right: 0.0cm;margin-top: 0.0cm;text-align: center;\"> \u003C\u002Fdiv> \u003Cdiv style=\"margin-bottom: 0.0cm;margin-left: 0.0cm;margin-right: 0.0cm;margin-top: 0.0cm;text-align: center;\"> \u003Chr>\u003C\u002Fdiv> \u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cstrong>\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Aufgaben & Verantwortlichkeiten\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cul> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Planung, Erstellung und Durchführung von \u003Cstrong>Analytical Instrument Qualifications\u003C\u002Fstrong> gemäß internen SOPs\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Erstellung von \u003Cstrong>IQ\u002FOQ-Protokollen\u003C\u002Fstrong> inkl. Risikoanalysen und Testplänen\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cstrong>\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Execution von IQ\u002FOQ\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fstrong>\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\"> inkl. Dokumentation, Abweichungsmanagement und Abschlussberichten\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Enge Zusammenarbeit mit internen QC-Teams, QA und Engineering\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Mitarbeit in CapEx-Projekten von der Geräteinstallation bis zur Übergabe in die Routine\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Sicherstellung der \u003Cstrong>Data-Integrity- und Part-11-Compliance\u003C\u002Fstrong> im Qualifizierungskontext\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Arbeiten innerhalb eines etablierten globalen und lokalen Qualifizierungsframeworks\u003Cbr> (keine Neuentwicklung von Grundkonzepten erforderlich)\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003C\u002Ful> \u003Cdiv style=\"margin-bottom: 0.0cm;margin-left: 0.0cm;margin-right: 0.0cm;margin-top: 0.0cm;text-align: center;\"> \u003Chr>\u003C\u002Fdiv> \u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cstrong>\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Abgrenzung des Scopes\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan>\u003Cbr> \u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cstrong>\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Nicht im Fokus:\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cul> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Gerätekonfiguration \u002F Software-Setup (primär intern abgedeckt)\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Entwicklung neuer Qualifizierungsstrategien auf Greenfield-Niveau\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003C\u002Ful> \u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cstrong>\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Im Fokus:\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cul> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Strukturierte, effiziente \u003Cstrong>Qualifizierungsdurchführung\u003C\u002Fstrong> nach etablierten Prozessen\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Zuverlässige, auditfeste Dokumentation\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003C\u002Ful> \u003Cdiv style=\"margin-bottom: 0.0cm;margin-left: 0.0cm;margin-right: 0.0cm;margin-top: 0.0cm;text-align: center;\"> \u003Chr>\u003C\u002Fdiv> \u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cstrong>\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Fachliche Anforderungen (Must-have)\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cul> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Mehrjährige Erfahrung in \u003Cstrong>Analytical Instrument Qualification\u003C\u002Fstrong> im GMP-Umfeld\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Sicherer Umgang mit \u003Cstrong>IQ\u002FOQ\u002FPQ-Dokumentation\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Sehr gutes Verständnis von \u003Cstrong>GMP, Annex 15, Data Integrity, 21 CFR Part 11\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Erfahrung mit komplexen QC-Umgebungen\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cli style=\"margin: 0.0cm;\">\u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Fähigkeit, sich schnell in \u003Cstrong>firmeninterne SOPs und Prozesse\u003C\u002Fstrong> einzuarbeiten\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003C\u002Ful> \u003Cdiv style=\"margin-bottom: 0.0cm;margin-left: 0.0cm;margin-right: 0.0cm;margin-top: 0.0cm;text-align: center;\"> \u003Chr>\u003C\u002Fdiv> \u003Cdiv style=\"margin-bottom: 0.0cm;margin-left: 0.0cm;margin-right: 0.0cm;margin-top: 0.0cm;text-align: center;\"> \u003Chr>\u003C\u002Fdiv> \u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cstrong>\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Erwartetes Profil\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fstrong>\u003C\u002Fspan>\u003C\u002Fspan>\u003Cbr> \u003Cspan style=\"font-size: 12.0pt;\">\u003Cspan style=\"font-family: Aptos , sans-serif;\">\u003Cspan style=\"font-size: 11.0pt;\">\u003Cspan style=\"\">Gesucht wird \u003Cstrong>kein reiner Strategieberater\u003C\u002Fstrong>, sondern ein \u003Cstrong>sehr erfahrener, operativer Qualifizierungsexperte\u003C\u002Fstrong>, der innerhalb bestehender Strukturen effizient arbeitet und wiederkehrend einsetzbar ist.\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan>\u003C\u002Fspan> \u003Cdiv style=\"margin-bottom: 0.0cm;margin-left: 0.0cm;margin-right: 0.0cm;margin-top: 0.0cm;text-align: center;\"> \u003C\u002Fdiv>\n\nIhr persönlicher Ansprechpartner\n\nBei Fragen können Sie sich jederzeit melden!\n\nDavid Riepen\n\nConsultant Pharma\n\nMobil:\n\n+49 151 65743765\nE-Mail:\n\nE-Mail: d.riepen@neo-experts.com d.riepen@neo-experts.com\nGemeinsam zum perfekten Match.\n\nJetzt bewerben","de","3026","https:\u002F\u002Fwww.neo-experts.com\u002Fstellen-suche\u002Fanalytical-instrument-qualification-aiq---qc-analytical-lifecycle-ff537-1b35e",{"items":31},[32,51,67,87,110],{"id":33,"slug":34,"title":35,"skills":36,"budget":18,"duration":18,"location":47,"onsitePercent":48,"contractType":19,"foundAt":49,"category":50},4585,"laborant-zellkultur-mwd","Laborant Zellkultur (m\u002Fw\u002Fd)",[37,38,39,40,10,41,42,43,44,45,46],"Anlagen","Auswertung","Entwicklung","Fermentation","Herstellung","Optimierung","Planung","Teamfähigkeit","Zellkultur","Zelllinien","Biberach an der Riß",100,"2026-05-20T02:26:18+00:00",{"id":22,"slug":23,"label":24},{"id":52,"slug":53,"title":54,"skills":55,"budget":18,"duration":18,"location":47,"onsitePercent":48,"contractType":19,"foundAt":65,"category":66},4550,"technischer-assistent-hplc-analytik-mwd","Technischer Assistent HPLC-Analytik (m\u002Fw\u002Fd)",[56,10,57,58,59,60,61,62,63,64],"HPLC","Analytik","Methodenvalidierung","Dokumentation","Empower","LabWare-LIMS","MS-Office","Chemielaborant","Biologielaborant","2026-05-19T16:25:57+00:00",{"id":22,"slug":23,"label":24},{"id":68,"slug":69,"title":70,"skills":71,"budget":18,"duration":82,"location":83,"onsitePercent":84,"contractType":19,"foundAt":85,"category":86},4527,"project-engineer-mwd-pharma","Project Engineer (m\u002Fw\u002Fd) Pharma",[72,73,74,75,76,77,78,79,80,81],"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":22,"slug":23,"label":24},{"id":88,"slug":89,"title":90,"skills":91,"budget":18,"duration":106,"location":107,"onsitePercent":48,"contractType":19,"foundAt":108,"category":109},4515,"testing-von-medizingeraeten","Testing von Medizingeräten",[92,93,94,95,96,97,98,99,100,101,102,103,104,105],"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":22,"slug":23,"label":24},{"id":111,"slug":112,"title":113,"skills":114,"budget":118,"duration":119,"location":120,"onsitePercent":121,"contractType":19,"foundAt":122,"category":123},4422,"mfc-und-c-entwickler-fuer-medizinischen-bereich","MFC und C++ Entwickler für medizinischen Bereich",[115,116,117],"C++","MFC","Reportstellung","auf Anfrage","3 Monate +","Ingolstadt",10,"2026-05-19T09:30:24+00:00",{"id":22,"slug":23,"label":24}]