[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-prozessingenieur-mwd-medizintechnik":3,"similar-prozessingenieur-mwd-medizintechnik":32},{"id":4,"slug":5,"title":6,"skills":7,"budget":18,"duration":18,"location":19,"onsitePercent":20,"contractType":21,"foundAt":22,"category":23,"description":26,"rawText":27,"webTitle":6,"webText":28,"language":29,"projectId":30,"sourceUrl":31},11706,"prozessingenieur-mwd-medizintechnik","Prozessingenieur (m\u002Fw\u002Fd) Medizintechnik",[8,9,10,11,12,13,14,15,16,17],"Anlagenqualifizierung","Automatisierungstechnik","Elektrotechnik","GMP","ISO 13485","Maschinenbau","Medizintechnik","Prozessvalidierung","Validierung","Verfahrenstechnik",null,"Frankfurt am Main",100,"contracting","2026-06-09T07:25:58+00:00",{"id":24,"slug":25,"label":14},14,"medical_tech","Prozessingenieur für Medizintechnik gesucht zur Implementierung und Optimierung von Produktions-, Oberflächenbehandlungs- und Reinigungsprozessen. Aufgaben umfassen Erstellung technischer Konzepte, Umsetzung von GMP-Anforderungen und Prozessvalidierung. Erforderlich: Studium in Maschinenbau\u002FMedizintechnik, Erfahrung in Anlagenqualifizierung und GMP-Kenntnisse.","Prozessingenieur (m\u002Fw\u002Fd) Medizintechnik\nProjektnummer: FE88-27596-F\nStandort: Frankfurt am Main, Hessen\nArbeitsweise: Vor Ort\nLaufzeit: Keine Angabe\nStartdatum: Keine Angabe\n\nIhr Aufgabengebiet:\n- Implementierung neuer bzw. Optimierung bestehender Produktions-, Oberflächenbehandlungs- und Reinigungsprozesse\n\n- Erstellung von technischen Konzepten, Spezifikationen und Lastenheften\n\n- Umsetzung von GMP-Anforderungen an Produktionsprozesse\n\n- Abstimmung, Planung und Durchführung der Qualifizierung \u002F Validierung von neuen oder bereits bestehenden Prozessen\n\n- Erstellung, Prüfung und Pflege von Validierungsdokumenten\n\n- Optimierung der Produktionsabläufe hinsichtlich Anlagenverfügbarkeit, Kosten und Qualität\n\nDas bringen Sie mit:\n- Abgeschlossenes Studium im Bereich Maschinenbau, Medizintechnik, Verfahrenstechnik, Elektrotechnik, Automatisierungstechnik\n\n- Erfahrung in der Anlagenqualifizierung \u002F Prozessvalidierung im Bereich Pharma oder Medizintechnik\n\n- Vertraut mit gängigen GMP-Anforderungen und Regelwerken an Medizinprodukte (ISO 13485\u002FQSR)\n\n- Sehr gute Deutsch- und Englischkenntnisse\n\nSkills: Anlagenqualifizierung, Automatisierungstechnik, Elektrotechnik, GMP, ISO, ISO 13485, Implementierung, Maschinenbau, Medizinprodukte, Medizintechnik, Optimierung, Pharma, Planung, Prozessvalidierung, Prüfung, Qualität, Qualifizierung, Umsetzung, Validierung, Verfahrenstechnik\n\nAnsprechpartner:\nSarina von Schwartzenberg\nTalent Acquisition Lead\nFERCHAU GmbH, Niederlassung Wiesbaden Pharma & Life Science\nAlte Schmelze 18-20\n65201 Wiesbaden\n+49 611 238 7750\nwiesbaden-pls@ferchau.com","Wir suchen einen erfahrenen Prozessingenieur (m\u002Fw\u002Fd) für die Optimierung und Implementierung von Produktionsprozessen in der Medizintechnik. Der Standort ist Frankfurt am Main.\n\nIhre Aufgaben umfassen die Implementierung neuer sowie die Optimierung bestehender Produktions-, Oberflächenbehandlungs- und Reinigungsprozesse. Sie erstellen technische Konzepte, Spezifikationen und Lastenheften und setzen GMP-Anforderungen an Produktionsprozesse um. Darüber hinaus koordinieren, planen und führen Sie die Qualifizierung und Validierung von neuen oder bestehenden Prozessen durch. Die Erstellung, Prüfung und Pflege von Validierungsdokumenten gehört ebenso zu Ihren Verantwortungen wie die Optimierung der Produktionsabläufe hinsichtlich Anlagenverfügbarkeit, Kosten und Qualität.\n\nFür diese Position bringen Sie ein abgeschlossenes Studium im Bereich Maschinenbau, Medizintechnik, Verfahrenstechnik, Elektrotechnik oder Automatisierungstechnik mit. Sie verfügen über nachgewiesene Erfahrung in der Anlagenqualifizierung und Prozessvalidierung im Pharma- oder Medizintechnikbereich. Kenntnisse gängiger GMP-Anforderungen und Regelwerke für Medizinprodukte (ISO 13485\u002FQSR) sind erforderlich. Sehr gute Deutsch- und Englischkenntnisse runden Ihr Profil ab.\n\nDiese Position bietet die Möglichkeit, in einem zukunftsweisenden Bereich tätig zu sein und Ihre Expertise in der Prozessoptimierung einzubringen.","de","FE88-27596-F","https:\u002F\u002Ftouch.ferchau.com\u002Fde\u002Fde\u002Fprojekt\u002F264961",{"items":33},[34,58,74,87,108,124,141,159,178,189,204,221,234,245,258],{"id":35,"slug":36,"title":37,"skills":38,"budget":18,"duration":18,"location":55,"onsitePercent":20,"contractType":21,"foundAt":56,"category":57},11902,"it-anwendungsbetreuer-mwd-2","IT-Anwendungsbetreuer (m\u002Fw\u002Fd)",[39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54],"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":24,"slug":25,"label":14},{"id":59,"slug":60,"title":61,"skills":62,"budget":18,"duration":18,"location":71,"onsitePercent":20,"contractType":21,"foundAt":72,"category":73},11872,"chemielaborant-qualitaetskontrolle-mwd","Chemielaborant Qualitätskontrolle (m\u002Fw\u002Fd)",[63,64,11,65,66,67,68,69,70,54],"Chemielaborant","Qualitätskontrolle","HPLC","GC","Chromeleon","CTA","PTA","CAPA","Miesbach, Bayern","2026-06-09T13:25:36+00:00",{"id":24,"slug":25,"label":14},{"id":75,"slug":76,"title":77,"skills":78,"budget":18,"duration":18,"location":71,"onsitePercent":20,"contractType":84,"foundAt":85,"category":86},11871,"chemielaborant-lab-technician-mwd-analytical-development","Chemielaborant \u002F Lab Technician (m\u002Fw\u002Fd) Analytical Development",[79,65,66,80,81,67,11,54,82,83],"Analytik","Methodenentwicklung","Validierung analytischer Methoden","Chromatographie","Spektrometrie","permanent","2026-06-09T13:25:25+00:00",{"id":24,"slug":25,"label":14},{"id":88,"slug":89,"title":90,"skills":91,"budget":18,"duration":104,"location":18,"onsitePercent":105,"contractType":21,"foundAt":106,"category":107},11773,"sustaining-engineer-mwd","Sustaining Engineer (m\u002Fw\u002Fd)",[92,93,94,95,96,97,98,99,100,101,102,103],"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":24,"slug":25,"label":14},{"id":109,"slug":110,"title":111,"skills":112,"budget":18,"duration":18,"location":120,"onsitePercent":121,"contractType":21,"foundAt":122,"category":123},11741,"junior-quality-engineer-medical-devices-mwd","Junior Quality Engineer Medical Devices (m\u002Fw\u002Fd)",[113,10,114,115,116,117,118,119],"Audits","Fehleranalyse","Lösungskompetenz","Management","Medical Devices","Deutsch","Englisch","Aschaffenburg",50,"2026-06-09T08:27:29+00:00",{"id":24,"slug":25,"label":14},{"id":125,"slug":126,"title":127,"skills":128,"budget":18,"duration":18,"location":138,"onsitePercent":121,"contractType":21,"foundAt":139,"category":140},11740,"manager-gxp-compliance-mwd","Manager GxP Compliance (m\u002Fw\u002Fd)",[129,130,131,132,70,133,134,135,16,136,137,118,119],"GxP","SOP","Change Control","Deviation","Risk Management","CSV","Qualifizierung","Audit","Life Science","Mainz, Rheinland-Pfalz","2026-06-09T08:27:21+00:00",{"id":24,"slug":25,"label":14},{"id":142,"slug":143,"title":144,"skills":145,"budget":18,"duration":18,"location":156,"onsitePercent":121,"contractType":21,"foundAt":157,"category":158},11739,"device-engineer-mwd","Device Engineer (m\u002Fw\u002Fd)",[146,54,147,148,149,150,151,152,153,154,155],"Design","Entwicklung","Entwicklungsprozesse","Integration","Kombinationsprodukte","Koordinierung","Planung","Risikomanagement","Umsetzung","Usability","Ingelheim am Rhein","2026-06-09T08:27:13+00:00",{"id":24,"slug":25,"label":14},{"id":160,"slug":161,"title":162,"skills":163,"budget":18,"duration":18,"location":19,"onsitePercent":121,"contractType":21,"foundAt":176,"category":177},11738,"product-lifecycle-engineer-mwd-medizintechnik","Product Lifecycle Engineer (m\u002Fw\u002Fd) Medizintechnik",[164,165,10,147,166,167,13,168,169,14,170,171,172,173,174,175],"Anlagenbau","Einkauf","Feinwerktechnik","Hydraulik","Mechanik","Medizinprodukte","Pneumatik","Produktion","QM","Service","Steuerung","Teamfähigkeit","2026-06-09T08:27:03+00:00",{"id":24,"slug":25,"label":14},{"id":179,"slug":180,"title":181,"skills":182,"budget":18,"duration":18,"location":19,"onsitePercent":121,"contractType":84,"foundAt":187,"category":188},11737,"mitarbeiter-mwd-customer-service-pharma","Mitarbeiter (m\u002Fw\u002Fd) Customer Service Pharma",[183,184,185,186,113,118,119],"Customer Service","SAP","MS Office","Auftragsabwicklung","2026-06-09T08:26:54+00:00",{"id":24,"slug":25,"label":14},{"id":190,"slug":191,"title":192,"skills":193,"budget":18,"duration":18,"location":201,"onsitePercent":121,"contractType":84,"foundAt":202,"category":203},11735,"mitarbeiter-mwd-regulatory-affairs-2","Mitarbeiter (m\u002Fw\u002Fd) Regulatory Affairs",[194,195,196,197,14,198,199,200],"Regulatory Affairs","Technische Dokumentation","MDD","MDR","Qualitätsmanagement","Analyse","Bewertung","Aschaffenburg, Bayern","2026-06-09T08:26:38+00:00",{"id":24,"slug":25,"label":14},{"id":205,"slug":206,"title":207,"skills":208,"budget":18,"duration":18,"location":218,"onsitePercent":121,"contractType":21,"foundAt":219,"category":220},11734,"referent-mwd-substance-product-management","Referent (m\u002Fw\u002Fd) Substance & Product Management",[209,210,211,212,213,214,215,216,217],"Chemie","Biologie","CLP-Verordnung","GHS","SAP-EHS","Datenpflege","REACH","Gefahrstoffeinstufung","Sicherheitsdatenblätter","Hanau, Hessen","2026-06-09T08:26:31+00:00",{"id":24,"slug":25,"label":14},{"id":222,"slug":223,"title":224,"skills":225,"budget":18,"duration":18,"location":19,"onsitePercent":121,"contractType":84,"foundAt":232,"category":233},11733,"junior-projektmanager-mwd-klinische-studien","(Junior) Projektmanager (m\u002Fw\u002Fd) klinische Studien",[226,227,228,229,230,119,231],"Projektmanagement","Projektplanung","Budgetierung","Angebotserstellung","Klinische Studien","Analytisches Denken","2026-06-09T08:26:21+00:00",{"id":24,"slug":25,"label":14},{"id":235,"slug":236,"title":237,"skills":238,"budget":18,"duration":18,"location":218,"onsitePercent":20,"contractType":242,"foundAt":243,"category":244},11732,"chemikant-mwd-pharmazeutische-produktion","Chemikant (m\u002Fw\u002Fd) pharmazeutische Produktion",[239,240,11,241,171,130,119,118],"Chemikant:in Ausbildung","EDV","Kommunikationsfähigkeit","temp_work","2026-06-09T08:26:13+00:00",{"id":24,"slug":25,"label":14},{"id":246,"slug":247,"title":248,"skills":249,"budget":18,"duration":18,"location":19,"onsitePercent":121,"contractType":21,"foundAt":256,"category":257},11731,"junior-qa-manager-mwd-pharma","Junior QA Manager (m\u002Fw\u002Fd) Pharma",[131,250,251,252,253,209,210,132,254,119,255],"cGMP","ISO","JIRA","Pharmazie","LIMS","Koordination","2026-06-09T08:26:03+00:00",{"id":24,"slug":25,"label":14},{"id":259,"slug":260,"title":261,"skills":262,"budget":18,"duration":18,"location":19,"onsitePercent":20,"contractType":21,"foundAt":268,"category":269},11730,"mitarbeiter-mwd-quality-operations-pharma","Mitarbeiter (m\u002Fw\u002Fd) Quality Operations Pharma",[65,66,263,264,11,265,266,119,267],"Methodenvalidierung","Instrumentelle Analytik","Stabilitätsstudien","MS-Office","SOP-Erstellung","2026-06-09T08:25:54+00:00",{"id":24,"slug":25,"label":14}]