[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-junior-qa-manager-mwd-pharma":3,"similar-junior-qa-manager-mwd-pharma":34},{"id":4,"slug":5,"title":6,"skills":7,"budget":19,"duration":19,"location":20,"onsitePercent":21,"contractType":22,"foundAt":23,"category":24,"description":28,"rawText":29,"webTitle":6,"webText":30,"language":31,"projectId":32,"sourceUrl":33},11731,"junior-qa-manager-mwd-pharma","Junior QA Manager (m\u002Fw\u002Fd) Pharma",[8,9,10,11,12,13,14,15,16,17,18],"Change Control","cGMP","ISO","JIRA","Pharmazie","Chemie","Biologie","Deviation","LIMS","Englisch","Koordination",null,"Frankfurt am Main",50,"contracting","2026-06-09T08:26:03+00:00",{"id":25,"slug":26,"label":27},14,"medical_tech","Medizintechnik","Eigenverantwortliche Organisation und Überwachung von Change Control- und Nicht-Konformitäten-Prozessen unter cGMP\u002FISO-Anforderungen. Bearbeitung in JIRA-Modulen, Koordination von Boards und Zusammenarbeit mit R&D und Tochtergesellschaften. Mitarbeit bei Erstellung und Pflege von SOPs.","Junior QA Manager (m\u002Fw\u002Fd) Pharma\nProjektnummer: FE64-26804-F\nStandort: Frankfurt am Main, Hessen\nArbeitsweise: Hybrid\nLaufzeit: Keine Angabe\nStartdatum: Keine Angabe\n\nIhr Aufgabengebiet:\n- Eigenverantwortliche Organisation, Durchführung und Überwachung des Change Control- Prozesses unter Berücksichtigung von cGMP\u002FISO-Anforderungen\n\n- Bearbeitung von Change Controls des Produktionsstandorts im JIRA-Modul \"ECC\"\n\n- Organisation, Teilnahme, Protokollierung und Nachverfolgung des Change Control Boards\n\n- Koordination der Zusammenarbeit aller am Change Control Verfahren Beteiligten (z.B. R&D, Tochtergesellschaften)\n\n- Organisation, Durchführung und Überwachung des Nicht Konformitäten Prozesses\n\n- Bearbeitung und Genehmigung von Nicht-Konformitäten im JIRA-Modul \"Nicht-Konformitäten\" unter Berücksichtigung von cGMP\u002FISO-Anforderungen\n\n- Organisation, Teilnahme, Protokollierung und Nachverfolgung des Deviation and Material Review Boards\n\n- Mitarbeit bei der Erstellung und Pflege von bereichsspezifischen SOPs\n\nDas bringen Sie mit:\n- Erfolgreich abgeschlossenes naturwissenschaftliches Studium (Pharmazie, Chemie, Biologie) oder eine vergleichbare Qualifikation\n\n- Kenntnisse im beschriebenen Aufgabengebiet, der pharmazeutischen Analytik und Industrieerfahrung wünschenswert\n\n- Gutes schriftliches wie mündliches Englisch\n\n- Kenntnisse in den gängigen EDV-Office-Anwendungen sowie LIMS\u002FWAY wünschenswert\n\nSkills: Anwendungen, Biologie, Change Control, Chemie, Deviation, EDV, ISO, Koordination, Pharma, Pharmazie, R&D\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","Wir suchen einen Junior QA Manager (m\u002Fw\u002Fd) für einen Pharmastandort in Frankfurt am Main. Diese Rolle bietet die Gelegenheit, Qualitätssicherungsprozesse in einem regulierten Umfeld eigenverantwortlich zu gestalten und weiterzuentwickeln.\n\nIhre Aufgaben umfassen die Organisation, Durchführung und Überwachung von Change Control-Prozessen unter Berücksichtigung von cGMP- und ISO-Anforderungen. Sie bearbeiten Change Controls im entsprechenden Projektmanagementsystem, organisieren und protokollieren Change Control Board-Meetings und koordinieren die Zusammenarbeit aller beteiligten Abteilungen wie Forschung & Entwicklung und Tochtergesellschaften.\n\nDarüber hinaus sind Sie verantwortlich für die Organisation und Überwachung des Nicht-Konformitäten-Prozesses, einschließlich der Bearbeitung und Genehmigung von Abweichungen unter Einhaltung regulatorischer Anforderungen. Sie nehmen an Deviation and Material Review Boards teil, protokollieren diese und verfolgen Maßnahmen nach. Zusätzlich unterstützen Sie die Erstellung und Pflege von bereichsspezifischen Standard Operating Procedures.\n\nSie verfügen über ein erfolgreich abgeschlossenes naturwissenschaftliches Studium (Pharmazie, Chemie oder Biologie) oder eine vergleichbare Qualifikation. Kenntnisse in Change Control, pharmazeutischer Analytik und Industrieerfahrung sind wünschenswert. Sie beherrschen Englisch in Wort und Schrift und sind sicher in gängigen Office-Anwendungen. Erfahrung mit LIMS-Systemen ist von Vorteil.\n\nDie Position ist hybrid ausgestaltet und bietet flexible Arbeitsweisen. Sie arbeiten in einem regulierten Umfeld, das hohe Standards und kontinuierliche Verbesserung erfordert.","de","FE64-26804-F","https:\u002F\u002Ftouch.ferchau.com\u002Fde\u002Fde\u002Fprojekt\u002F300922",{"items":35},[36,61,78,91,112,127,143,161,181,192,207,222,235,246,258],{"id":37,"slug":38,"title":39,"skills":40,"budget":19,"duration":19,"location":57,"onsitePercent":58,"contractType":22,"foundAt":59,"category":60},11902,"it-anwendungsbetreuer-mwd-2","IT-Anwendungsbetreuer (m\u002Fw\u002Fd)",[41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56],"Fachinformatiker","Medizinische IT-Systeme","AIS","LIS","Jira","ServiceNow","Netzwerktechnik","TCP\u002FIP","Firewalls","VPN","IT-Sicherheit","Microsoft Windows Server","RDP","Citrix","Anwenderschulungen","Dokumentation","Rosenheim",100,"2026-06-09T14:27:06+00:00",{"id":25,"slug":26,"label":27},{"id":62,"slug":63,"title":64,"skills":65,"budget":19,"duration":19,"location":75,"onsitePercent":58,"contractType":22,"foundAt":76,"category":77},11872,"chemielaborant-qualitaetskontrolle-mwd","Chemielaborant Qualitätskontrolle (m\u002Fw\u002Fd)",[66,67,68,69,70,71,72,73,74,56],"Chemielaborant","Qualitätskontrolle","GMP","HPLC","GC","Chromeleon","CTA","PTA","CAPA","Miesbach, Bayern","2026-06-09T13:25:36+00:00",{"id":25,"slug":26,"label":27},{"id":79,"slug":80,"title":81,"skills":82,"budget":19,"duration":19,"location":75,"onsitePercent":58,"contractType":88,"foundAt":89,"category":90},11871,"chemielaborant-lab-technician-mwd-analytical-development","Chemielaborant \u002F Lab Technician (m\u002Fw\u002Fd) Analytical Development",[83,69,70,84,85,71,68,56,86,87],"Analytik","Methodenentwicklung","Validierung analytischer Methoden","Chromatographie","Spektrometrie","permanent","2026-06-09T13:25:25+00:00",{"id":25,"slug":26,"label":27},{"id":92,"slug":93,"title":94,"skills":95,"budget":19,"duration":108,"location":19,"onsitePercent":109,"contractType":22,"foundAt":110,"category":111},11773,"sustaining-engineer-mwd","Sustaining Engineer (m\u002Fw\u002Fd)",[96,97,98,99,100,101,102,103,104,105,106,107],"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":25,"slug":26,"label":27},{"id":113,"slug":114,"title":115,"skills":116,"budget":19,"duration":19,"location":124,"onsitePercent":21,"contractType":22,"foundAt":125,"category":126},11741,"junior-quality-engineer-medical-devices-mwd","Junior Quality Engineer Medical Devices (m\u002Fw\u002Fd)",[117,118,119,120,121,122,123,17],"Audits","Elektrotechnik","Fehleranalyse","Lösungskompetenz","Management","Medical Devices","Deutsch","Aschaffenburg","2026-06-09T08:27:29+00:00",{"id":25,"slug":26,"label":27},{"id":128,"slug":129,"title":130,"skills":131,"budget":19,"duration":19,"location":140,"onsitePercent":21,"contractType":22,"foundAt":141,"category":142},11740,"manager-gxp-compliance-mwd","Manager GxP Compliance (m\u002Fw\u002Fd)",[132,133,8,15,74,134,135,136,137,138,139,123,17],"GxP","SOP","Risk Management","CSV","Qualifizierung","Validierung","Audit","Life Science","Mainz, Rheinland-Pfalz","2026-06-09T08:27:21+00:00",{"id":25,"slug":26,"label":27},{"id":144,"slug":145,"title":146,"skills":147,"budget":19,"duration":19,"location":158,"onsitePercent":21,"contractType":22,"foundAt":159,"category":160},11739,"device-engineer-mwd","Device Engineer (m\u002Fw\u002Fd)",[148,56,149,150,151,152,153,154,155,156,157],"Design","Entwicklung","Entwicklungsprozesse","Integration","Kombinationsprodukte","Koordinierung","Planung","Risikomanagement","Umsetzung","Usability","Ingelheim am Rhein","2026-06-09T08:27:13+00:00",{"id":25,"slug":26,"label":27},{"id":162,"slug":163,"title":164,"skills":165,"budget":19,"duration":19,"location":20,"onsitePercent":21,"contractType":22,"foundAt":179,"category":180},11738,"product-lifecycle-engineer-mwd-medizintechnik","Product Lifecycle Engineer (m\u002Fw\u002Fd) Medizintechnik",[166,167,118,149,168,169,170,171,172,27,173,174,175,176,177,178],"Anlagenbau","Einkauf","Feinwerktechnik","Hydraulik","Maschinenbau","Mechanik","Medizinprodukte","Pneumatik","Produktion","QM","Service","Steuerung","Teamfähigkeit","2026-06-09T08:27:03+00:00",{"id":25,"slug":26,"label":27},{"id":182,"slug":183,"title":184,"skills":185,"budget":19,"duration":19,"location":20,"onsitePercent":21,"contractType":88,"foundAt":190,"category":191},11737,"mitarbeiter-mwd-customer-service-pharma","Mitarbeiter (m\u002Fw\u002Fd) Customer Service Pharma",[186,187,188,189,117,123,17],"Customer Service","SAP","MS Office","Auftragsabwicklung","2026-06-09T08:26:54+00:00",{"id":25,"slug":26,"label":27},{"id":193,"slug":194,"title":195,"skills":196,"budget":19,"duration":19,"location":204,"onsitePercent":21,"contractType":88,"foundAt":205,"category":206},11735,"mitarbeiter-mwd-regulatory-affairs-2","Mitarbeiter (m\u002Fw\u002Fd) Regulatory Affairs",[197,198,199,200,27,201,202,203],"Regulatory Affairs","Technische Dokumentation","MDD","MDR","Qualitätsmanagement","Analyse","Bewertung","Aschaffenburg, Bayern","2026-06-09T08:26:38+00:00",{"id":25,"slug":26,"label":27},{"id":208,"slug":209,"title":210,"skills":211,"budget":19,"duration":19,"location":219,"onsitePercent":21,"contractType":22,"foundAt":220,"category":221},11734,"referent-mwd-substance-product-management","Referent (m\u002Fw\u002Fd) Substance & Product Management",[13,14,212,213,214,215,216,217,218],"CLP-Verordnung","GHS","SAP-EHS","Datenpflege","REACH","Gefahrstoffeinstufung","Sicherheitsdatenblätter","Hanau, Hessen","2026-06-09T08:26:31+00:00",{"id":25,"slug":26,"label":27},{"id":223,"slug":224,"title":225,"skills":226,"budget":19,"duration":19,"location":20,"onsitePercent":21,"contractType":88,"foundAt":233,"category":234},11733,"junior-projektmanager-mwd-klinische-studien","(Junior) Projektmanager (m\u002Fw\u002Fd) klinische Studien",[227,228,229,230,231,17,232],"Projektmanagement","Projektplanung","Budgetierung","Angebotserstellung","Klinische Studien","Analytisches Denken","2026-06-09T08:26:21+00:00",{"id":25,"slug":26,"label":27},{"id":236,"slug":237,"title":238,"skills":239,"budget":19,"duration":19,"location":219,"onsitePercent":58,"contractType":243,"foundAt":244,"category":245},11732,"chemikant-mwd-pharmazeutische-produktion","Chemikant (m\u002Fw\u002Fd) pharmazeutische Produktion",[240,241,68,242,174,133,17,123],"Chemikant:in Ausbildung","EDV","Kommunikationsfähigkeit","temp_work","2026-06-09T08:26:13+00:00",{"id":25,"slug":26,"label":27},{"id":247,"slug":248,"title":249,"skills":250,"budget":19,"duration":19,"location":20,"onsitePercent":58,"contractType":22,"foundAt":256,"category":257},11730,"mitarbeiter-mwd-quality-operations-pharma","Mitarbeiter (m\u002Fw\u002Fd) Quality Operations Pharma",[69,70,251,252,68,253,254,17,255],"Methodenvalidierung","Instrumentelle Analytik","Stabilitätsstudien","MS-Office","SOP-Erstellung","2026-06-09T08:25:54+00:00",{"id":25,"slug":26,"label":27},{"id":259,"slug":260,"title":261,"skills":262,"budget":19,"duration":19,"location":20,"onsitePercent":58,"contractType":22,"foundAt":268,"category":269},11729,"servicetechniker-mwd-medizintechnik","Servicetechniker (m\u002Fw\u002Fd) Medizintechnik",[27,263,172,188,264,265,17,266,267],"Technischer Service","Excel","Lotus Notes","Beratung","Kommunikation","2026-06-09T08:25:45+00:00",{"id":25,"slug":26,"label":27}]