[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-mitarbeiter-mwd-quality-operations-pharma":3,"similar-mitarbeiter-mwd-quality-operations-pharma":33},{"id":4,"slug":5,"title":6,"skills":7,"budget":17,"duration":17,"location":18,"onsitePercent":19,"contractType":20,"foundAt":21,"category":22,"description":26,"rawText":27,"webTitle":28,"webText":29,"language":30,"projectId":31,"sourceUrl":32},11730,"mitarbeiter-mwd-quality-operations-pharma","Mitarbeiter (m\u002Fw\u002Fd) Quality Operations Pharma",[8,9,10,11,12,13,14,15,16],"HPLC","GC","Methodenvalidierung","Instrumentelle Analytik","GMP","Stabilitätsstudien","MS-Office","Englisch","SOP-Erstellung",null,"Frankfurt am Main",100,"contracting","2026-06-09T08:25:54+00:00",{"id":23,"slug":24,"label":25},14,"medical_tech","Medizintechnik","Durchführung und Koordination von Methodentransfer, Methodenvalidierung und Methodenverifizierung mit Schwerpunkt HPLC und GC in der Pharmabranche. Mitarbeit bei OOS\u002FOOT\u002FOOE-Bearbeitung, Prozessoptimierung und Stabilitätsstudien. Erstellung von Stabilitätsberichten, Trendbewertungen und SOPs.","Mitarbeiter (m\u002Fw\u002Fd) Quality Operations Pharma\nProjektnummer: FE27-56448-F\nStandort: Frankfurt am Main, Hessen\nArbeitsweise: Vor Ort\nLaufzeit: Keine Angabe\nStartdatum: Keine Angabe\n\nIhr Aufgabengebiet:\n- Durchführen und Koordinieren von Methodentransfer, Methodenvalidierung und Methodenverifizierung mit dem Schwerpunkt HPLC und GC\n\n- Mitarbeit bei der Bearbeitung von OOS, OOT, OOE und zeitnahe Meldung dieser Vorgänge\n\n- Mitarbeit bei Projekten zur Prozessoptimierung, Überwachung von Stabilitätsstudien, Erstellung und Pflegen von diversen Übersichten (Tabellen, Diagramme) etc.\n\n- Termingerechte Erstellung von Stabilitätsberichten und Trendbewertungen, sowie Überprüfung der Ergebnisse\n\n- Erstellung und Überarbeitung von SOP's\n\n- Mitarbeit bei der Vorbereitung von Stabilitätsstudien\n\nDas bringen Sie mit:\n- Erfolgreich abgeschlossene naturwissenschaftliche Ausbildung, einen naturwissenschaftlichen Bachelorabschluss oder eine vergleichbare Qualifikation\n\n- Erste praktische Erfahrung in der Methodenvalidierung und Transfer (HPLC, GC) und Kenntnisse in instrumenteller Analytik (insbesondere HPLC, GC, UV-Vis), Kenntnisse in TOC wünschenswert\n\n- Erste Erfahrungen in der Bearbeitung von OOS und Abweichungen\n\n- Kenntnisse in Stabilitätsstudien wünschenswert\n\n- Kenntnisse in GMP\n\n- Gute Englischkenntnisse und MS-Office-Kenntnisse\n\nSkills: GC, GMP, HPLC, MS, MS-Office, Methodenvalidierung, Pharma, Prozessoptimierung, SOP\n\nAnsprechpartner:\nSarina von Schwartzenberg\nTalent Acquisition Lead\nFERCHAU GmbH, Niederlassung Wiesbaden Pharma & Life Science\nAlte Schmelze 18-20\n65201 Wiesbaden\n+49 611 238775-25\nwiesbaden-pls@ferchau.com","Mitarbeiter Quality Operations Pharma (m\u002Fw\u002Fd)","Wir suchen einen engagierten Mitarbeiter (m\u002Fw\u002Fd) für unser Quality Operations Team im Bereich Pharma an unserem Standort in Frankfurt am Main. In dieser Rolle werden Sie ein vielseitiges und anspruchsvolles Aufgabengebiet in der pharmazeutischen Qualitätssicherung übernehmen.\n\nIhre Hauptaufgaben umfassen die Durchführung und Koordination von Methodentransfer, Methodenvalidierung und Methodenverifizierung mit Schwerpunkt auf HPLC und GC-Analytik. Sie werden bei der Bearbeitung von Out-of-Specification-, Out-of-Trend- und Out-of-Expectation-Vorgängen mitarbeiten und diese zeitnah melden. Darüber hinaus unterstützen Sie Projekte zur Prozessoptimierung, überwachen Stabilitätsstudien und erstellen sowie pflegen verschiedene Übersichten und Dokumentationen.\n\nWeitere Verantwortungen sind die termingerechte Erstellung von Stabilitätsberichten, Trendbewertungen und deren Überprüfung, die Erstellung und Überarbeitung von Standard Operating Procedures sowie die Vorbereitung von Stabilitätsstudien.\n\nFür diese Position bringen Sie einen erfolgreich abgeschlossenen naturwissenschaftlichen Abschluss (Ausbildung, Bachelor oder vergleichbare Qualifikation) mit. Praktische Erfahrung in Methodenvalidierung und -transfer (HPLC, GC) sowie Kenntnisse in instrumenteller Analytik sind erforderlich. Erste Erfahrungen in der Bearbeitung von Abweichungen und Kenntnisse in GMP sind notwendig. Wünschenswert sind Erfahrungen mit Stabilitätsstudien und TOC-Analytik.\n\nSie verfügen über gute Englischkenntnisse und sichere MS-Office-Anwendungen. Die Tätigkeit findet vor Ort statt und bietet die Möglichkeit, in einem dynamischen pharmazeutischen Umfeld zu arbeiten und Ihre analytischen Fähigkeiten weiterzuentwickeln.","de","FE27-56448-F","https:\u002F\u002Ftouch.ferchau.com\u002Fde\u002Fde\u002Fprojekt\u002F311893",{"items":34},[35,59,73,86,107,123,141,159,179,190,205,222,235,246,259],{"id":36,"slug":37,"title":38,"skills":39,"budget":17,"duration":17,"location":56,"onsitePercent":19,"contractType":20,"foundAt":57,"category":58},11902,"it-anwendungsbetreuer-mwd-2","IT-Anwendungsbetreuer (m\u002Fw\u002Fd)",[40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55],"Fachinformatiker","Medizinische IT-Systeme","AIS","LIS","Jira","ServiceNow","Netzwerktechnik","TCP\u002FIP","Firewalls","VPN","IT-Sicherheit","Microsoft Windows Server","RDP","Citrix","Anwenderschulungen","Dokumentation","Rosenheim","2026-06-09T14:27:06+00:00",{"id":23,"slug":24,"label":25},{"id":60,"slug":61,"title":62,"skills":63,"budget":17,"duration":17,"location":70,"onsitePercent":19,"contractType":20,"foundAt":71,"category":72},11872,"chemielaborant-qualitaetskontrolle-mwd","Chemielaborant Qualitätskontrolle (m\u002Fw\u002Fd)",[64,65,12,8,9,66,67,68,69,55],"Chemielaborant","Qualitätskontrolle","Chromeleon","CTA","PTA","CAPA","Miesbach, Bayern","2026-06-09T13:25:36+00:00",{"id":23,"slug":24,"label":25},{"id":74,"slug":75,"title":76,"skills":77,"budget":17,"duration":17,"location":70,"onsitePercent":19,"contractType":83,"foundAt":84,"category":85},11871,"chemielaborant-lab-technician-mwd-analytical-development","Chemielaborant \u002F Lab Technician (m\u002Fw\u002Fd) Analytical Development",[78,8,9,79,80,66,12,55,81,82],"Analytik","Methodenentwicklung","Validierung analytischer Methoden","Chromatographie","Spektrometrie","permanent","2026-06-09T13:25:25+00:00",{"id":23,"slug":24,"label":25},{"id":87,"slug":88,"title":89,"skills":90,"budget":17,"duration":103,"location":17,"onsitePercent":104,"contractType":20,"foundAt":105,"category":106},11773,"sustaining-engineer-mwd","Sustaining Engineer (m\u002Fw\u002Fd)",[91,92,93,94,95,96,97,98,99,100,101,102],"Medical Device Engineering","Design Authority","Non Conformance Report (NCR) Assessment","Design for Manufacturing","Regulatory Compliance (QSR, GMP, ISO)","Change Management","Project Management","Engineering Testing and Analysis","Vendor Management","Cross-functional Coordination","English","German","6 Monate, Start 01.07.2026",0,"2026-06-09T09:30:21+00:00",{"id":23,"slug":24,"label":25},{"id":108,"slug":109,"title":110,"skills":111,"budget":17,"duration":17,"location":119,"onsitePercent":120,"contractType":20,"foundAt":121,"category":122},11741,"junior-quality-engineer-medical-devices-mwd","Junior Quality Engineer Medical Devices (m\u002Fw\u002Fd)",[112,113,114,115,116,117,118,15],"Audits","Elektrotechnik","Fehleranalyse","Lösungskompetenz","Management","Medical Devices","Deutsch","Aschaffenburg",50,"2026-06-09T08:27:29+00:00",{"id":23,"slug":24,"label":25},{"id":124,"slug":125,"title":126,"skills":127,"budget":17,"duration":17,"location":138,"onsitePercent":120,"contractType":20,"foundAt":139,"category":140},11740,"manager-gxp-compliance-mwd","Manager GxP Compliance (m\u002Fw\u002Fd)",[128,129,130,131,69,132,133,134,135,136,137,118,15],"GxP","SOP","Change Control","Deviation","Risk Management","CSV","Qualifizierung","Validierung","Audit","Life Science","Mainz, Rheinland-Pfalz","2026-06-09T08:27:21+00:00",{"id":23,"slug":24,"label":25},{"id":142,"slug":143,"title":144,"skills":145,"budget":17,"duration":17,"location":156,"onsitePercent":120,"contractType":20,"foundAt":157,"category":158},11739,"device-engineer-mwd","Device Engineer (m\u002Fw\u002Fd)",[146,55,147,148,149,150,151,152,153,154,155],"Design","Entwicklung","Entwicklungsprozesse","Integration","Kombinationsprodukte","Koordinierung","Planung","Risikomanagement","Umsetzung","Usability","Ingelheim am Rhein","2026-06-09T08:27:13+00:00",{"id":23,"slug":24,"label":25},{"id":160,"slug":161,"title":162,"skills":163,"budget":17,"duration":17,"location":18,"onsitePercent":120,"contractType":20,"foundAt":177,"category":178},11738,"product-lifecycle-engineer-mwd-medizintechnik","Product Lifecycle Engineer (m\u002Fw\u002Fd) Medizintechnik",[164,165,113,147,166,167,168,169,170,25,171,172,173,174,175,176],"Anlagenbau","Einkauf","Feinwerktechnik","Hydraulik","Maschinenbau","Mechanik","Medizinprodukte","Pneumatik","Produktion","QM","Service","Steuerung","Teamfähigkeit","2026-06-09T08:27:03+00:00",{"id":23,"slug":24,"label":25},{"id":180,"slug":181,"title":182,"skills":183,"budget":17,"duration":17,"location":18,"onsitePercent":120,"contractType":83,"foundAt":188,"category":189},11737,"mitarbeiter-mwd-customer-service-pharma","Mitarbeiter (m\u002Fw\u002Fd) Customer Service Pharma",[184,185,186,187,112,118,15],"Customer Service","SAP","MS Office","Auftragsabwicklung","2026-06-09T08:26:54+00:00",{"id":23,"slug":24,"label":25},{"id":191,"slug":192,"title":193,"skills":194,"budget":17,"duration":17,"location":202,"onsitePercent":120,"contractType":83,"foundAt":203,"category":204},11735,"mitarbeiter-mwd-regulatory-affairs-2","Mitarbeiter (m\u002Fw\u002Fd) Regulatory Affairs",[195,196,197,198,25,199,200,201],"Regulatory Affairs","Technische Dokumentation","MDD","MDR","Qualitätsmanagement","Analyse","Bewertung","Aschaffenburg, Bayern","2026-06-09T08:26:38+00:00",{"id":23,"slug":24,"label":25},{"id":206,"slug":207,"title":208,"skills":209,"budget":17,"duration":17,"location":219,"onsitePercent":120,"contractType":20,"foundAt":220,"category":221},11734,"referent-mwd-substance-product-management","Referent (m\u002Fw\u002Fd) Substance & Product Management",[210,211,212,213,214,215,216,217,218],"Chemie","Biologie","CLP-Verordnung","GHS","SAP-EHS","Datenpflege","REACH","Gefahrstoffeinstufung","Sicherheitsdatenblätter","Hanau, Hessen","2026-06-09T08:26:31+00:00",{"id":23,"slug":24,"label":25},{"id":223,"slug":224,"title":225,"skills":226,"budget":17,"duration":17,"location":18,"onsitePercent":120,"contractType":83,"foundAt":233,"category":234},11733,"junior-projektmanager-mwd-klinische-studien","(Junior) Projektmanager (m\u002Fw\u002Fd) klinische Studien",[227,228,229,230,231,15,232],"Projektmanagement","Projektplanung","Budgetierung","Angebotserstellung","Klinische Studien","Analytisches Denken","2026-06-09T08:26:21+00:00",{"id":23,"slug":24,"label":25},{"id":236,"slug":237,"title":238,"skills":239,"budget":17,"duration":17,"location":219,"onsitePercent":19,"contractType":243,"foundAt":244,"category":245},11732,"chemikant-mwd-pharmazeutische-produktion","Chemikant (m\u002Fw\u002Fd) pharmazeutische Produktion",[240,241,12,242,172,129,15,118],"Chemikant:in Ausbildung","EDV","Kommunikationsfähigkeit","temp_work","2026-06-09T08:26:13+00:00",{"id":23,"slug":24,"label":25},{"id":247,"slug":248,"title":249,"skills":250,"budget":17,"duration":17,"location":18,"onsitePercent":120,"contractType":20,"foundAt":257,"category":258},11731,"junior-qa-manager-mwd-pharma","Junior QA Manager (m\u002Fw\u002Fd) Pharma",[130,251,252,253,254,210,211,131,255,15,256],"cGMP","ISO","JIRA","Pharmazie","LIMS","Koordination","2026-06-09T08:26:03+00:00",{"id":23,"slug":24,"label":25},{"id":260,"slug":261,"title":262,"skills":263,"budget":17,"duration":17,"location":18,"onsitePercent":19,"contractType":20,"foundAt":269,"category":270},11729,"servicetechniker-mwd-medizintechnik","Servicetechniker (m\u002Fw\u002Fd) Medizintechnik",[25,264,170,186,265,266,15,267,268],"Technischer Service","Excel","Lotus Notes","Beratung","Kommunikation","2026-06-09T08:25:45+00:00",{"id":23,"slug":24,"label":25}]