[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-clinical-compliance-specialist-mwd-medical-devices":3,"similar-clinical-compliance-specialist-mwd-medical-devices":33},{"id":4,"slug":5,"title":6,"skills":7,"budget":18,"duration":18,"location":19,"onsitePercent":20,"contractType":21,"foundAt":22,"category":23,"description":27,"rawText":28,"webTitle":6,"webText":29,"language":30,"projectId":31,"sourceUrl":32},6439,"clinical-compliance-specialist-mwd-medical-devices","Clinical Compliance Specialist (m\u002Fw\u002Fd) Medical Devices",[8,9,10,11,12,13,14,15,16,17],"Clinical Evaluation","Medical Writing","MDR","ISO 14155","Post-Market Clinical Follow-up","Systematische Literaturrecherche","Medizinprodukte","Statistik","Zahnmedizin","Regulatorische Anforderungen",null,"Bensheim",100,"contracting","2026-05-28T07:25:35+00:00",{"id":24,"slug":25,"label":26},14,"medical_tech","Medizintechnik","Durchführung und Pflege klinischer Bewertungen für Medizinprodukte über den gesamten Produktlebenszyklus. Erstellung von Clinical Evaluation Plans und Reports, systematische Literaturrecherchen und Post-Market Clinical Follow-up. Unterstützung bei Audits und Zusammenarbeit mit internen und externen Stakeholdern.","Clinical Compliance Specialist (m\u002Fw\u002Fd) Medical Devices\nProjektnummer: FE46-75222-MA\nStandort: Bensheim, Hessen\nArbeitsweise: Vor Ort\nLaufzeit: Keine Angabe\nStartdatum: Keine Angabe\n\nDiese Herausforderungen übernimmst du:\n- Durchführung und Pflege klinischer Bewertungen für Medizinprodukte über den gesamten Produktlebenszyklus\n\n- Erstellung von Clinical Evaluation Plans (CEP) und Clinical Evaluation Reports (CER)\n\n- Planung, Durchführung und Dokumentation systematischer Literaturrecherchen\n\n- Planung und Umsetzung von Post-Market Clinical Follow-up (PMCF) Maßnahmen inklusive Reporting\n\n- Abstimmung von Inhalten, Timelines und Dokumentation mit internen Stakeholdern\n\n- Mitwirkung bei Post-Market Surveillance (PMS) und anderen regulatorischen Prozessen (z. B. SSCP)\n\n- Unterstützung bei Audits im Bereich Clinical Compliance\n\n- Zusammenarbeit mit internen Schnittstellen sowie externen Beratern und Lieferanten\n\nDas bringst du mit:\n- Abgeschlossenes Masterstudium in Naturwissenschaften, Bioingenieurwesen, Zahnmedizin oder vergleichbarer Studiengang, bevorzugt mit Promotion\n\n- Erste Erfahrung in Clinical Evaluation, Medical Writing oder klinischer Forschung, idealerweise im Bereich dentaler Medizinprodukte\n\n- Kenntnisse in systematischen Literaturrecherchen, klinischer Forschung (klinische Prüfungen), Medical Writing und\u002Foder Zahnmedizin\n\n- Kenntnisse regulatorischer Anforderungen für Medizinprodukte (z. B. MDR), relevanter Normen (z. B. ISO 14155) und Leitlinien (z. B. MDCG, MEDDEV 2.7\u002F1)\n\n- Grundkenntnisse in Statistik sowie klinischer Forschung\n\n- Selbstständige und verantwortungsbewusste Arbeitsweise\n\n- Kommunikationsstärke sowie teamorientierte und serviceorientierte Arbeitsweise\n\n- Verhandlungssichere Deutsch- und sehr gute Englischkenntnisse in Wort und Schrift\n\nSkills: Arbeitsweise, Audits, Dokumentation, ISO, MDR, Medical Devices, Medical Writing, Medizinprodukte, Planung, Reporting, Statistik, Umsetzung, Zahnmedizin\n\nAnsprechpartner:\nViktoria Eidenmüller\nTalent Acquisition Specialist\nFERCHAU GmbH, Niederlassung Mannheim\nLandteilstraße 33\n68163 Mannheim\n+49 621 40164-124\nmannheim@ferchau.com","Wir suchen einen Clinical Compliance Specialist (m\u002Fw\u002Fd) für den Bereich Medical Devices am Standort Bensheim, Hessen. In dieser Position übernehmen Sie die Durchführung und Pflege klinischer Bewertungen für Medizinprodukte über den gesamten Produktlebenszyklus.\n\nIhre Hauptaufgaben umfassen die Erstellung von Clinical Evaluation Plans (CEP) und Clinical Evaluation Reports (CER), die Planung und Durchführung systematischer Literaturrecherchen sowie die Dokumentation dieser Prozesse. Sie planen und setzen Post-Market Clinical Follow-up (PMCF) Maßnahmen inklusive Reporting um und stimmen Inhalte, Timelines und Dokumentation mit internen Stakeholdern ab.\n\nDarüber hinaus wirken Sie bei Post-Market Surveillance (PMS) und anderen regulatorischen Prozessen mit, unterstützen bei Audits im Bereich Clinical Compliance und arbeiten eng mit internen Schnittstellen sowie externen Beratern und Lieferanten zusammen.\n\nWir erwarten ein abgeschlossenes Masterstudium in Naturwissenschaften, Bioingenieurwesen, Zahnmedizin oder einem vergleichbaren Studiengang, bevorzugt mit Promotion. Erste Erfahrung in Clinical Evaluation, Medical Writing oder klinischer Forschung, idealerweise im Bereich dentaler Medizinprodukte, ist von Vorteil.\n\nSie sollten Kenntnisse in systematischen Literaturrecherchen, klinischer Forschung, Medical Writing und regulatorischen Anforderungen für Medizinprodukte (MDR) sowie relevanter Normen (ISO 14155) und Leitlinien mitbringen. Grundkenntnisse in Statistik, selbstständige Arbeitsweise, Kommunikationsstärke und verhandlungssichere Deutsch- sowie sehr gute Englischkenntnisse runden Ihr Profil ab.","de","FE46-75222-MA","https:\u002F\u002Ftouch.ferchau.com\u002Fde\u002Fde\u002Fprojekt\u002F506608",{"items":34},[35,52,65,82,97,113,136,147,168,189,197,213,225,240,254],{"id":36,"slug":37,"title":38,"skills":39,"budget":18,"duration":18,"location":48,"onsitePercent":49,"contractType":21,"foundAt":50,"category":51},6425,"quality-specialist-pharma-mwd","Quality Specialist Pharma (m\u002Fw\u002Fd)",[40,41,42,43,44,45,46,47],"GMP","Qualitätsmanagement","Pharmazie","Biotechnologie","Chemie","Risikomanagement","Audits","Teamfähigkeit","Biberach an der Riß",50,"2026-05-28T06:25:31+00:00",{"id":24,"slug":25,"label":26},{"id":53,"slug":54,"title":55,"skills":56,"budget":18,"duration":18,"location":62,"onsitePercent":49,"contractType":21,"foundAt":63,"category":64},6392,"qualitaetsmanager-mwd-medizintechnik","Qualitätsmanager (m\u002Fw\u002Fd) Medizintechnik",[41,26,57,46,58,59,60,61],"DIN 13485","MS Office","Reklamationsmanagement","Validierung","Qualifizierung","Schwerin","2026-05-28T02:26:01+00:00",{"id":24,"slug":25,"label":26},{"id":66,"slug":67,"title":68,"skills":69,"budget":18,"duration":18,"location":79,"onsitePercent":49,"contractType":21,"foundAt":80,"category":81},6391,"experte-bildverarbeitung-medizintechnik-mwd","Experte Bildverarbeitung Medizintechnik (m\u002Fw\u002Fd)",[70,71,72,26,73,74,75,76,77,78],"Bildverarbeitung","C++","Python","Algorithmusentwicklung","Physik","Informatik","Sensoren","Bildfilterung","Rekonstruktion","Mannheim","2026-05-28T02:25:47+00:00",{"id":24,"slug":25,"label":26},{"id":83,"slug":84,"title":85,"skills":86,"budget":18,"duration":18,"location":48,"onsitePercent":20,"contractType":21,"foundAt":95,"category":96},6390,"technischer-assistent-mwd-wasseranalytik","Technischer Assistent (m\u002Fw\u002Fd) Wasseranalytik",[87,88,89,90,91,40,92,93,94,61,60],"Biologielaborant","BTA","MTA","mikrobiologische Testmethoden","Environmental Monitoring","Dateneingabe","Dokumentation","Monitoring","2026-05-28T02:25:33+00:00",{"id":24,"slug":25,"label":26},{"id":98,"slug":99,"title":100,"skills":101,"budget":18,"duration":18,"location":110,"onsitePercent":49,"contractType":21,"foundAt":111,"category":112},6262,"softwareentwickler-c-medizintechnik-mwd","Softwareentwickler C++ Medizintechnik (m\u002Fw\u002Fd)",[71,102,103,104,105,106,107,26,108,109],"C#","C","CAN-Bus","Softwarearchitektur","Softwareentwicklung","Unit-Tests","Elektrotechnik","SCRUM","Jena","2026-05-27T11:28:50+00:00",{"id":24,"slug":25,"label":26},{"id":114,"slug":115,"title":116,"skills":117,"budget":18,"duration":131,"location":132,"onsitePercent":18,"contractType":133,"foundAt":134,"category":135},6245,"requirement-engineer","Requirement engineer",[118,119,120,121,122,123,124,125,126,127,128,129,130],"Requirements Engineering","ALM","CPRE\u002FIREB","CCBA\u002FIIBA","INCOSE","System Engineering","Software Engineering","Medical Engineering","IVD","V-model","EARS","German","English","12+ months","Rotkreuz","temp_work","2026-05-27T10:36:37+00:00",{"id":24,"slug":25,"label":26},{"id":137,"slug":138,"title":139,"skills":140,"budget":18,"duration":18,"location":144,"onsitePercent":18,"contractType":21,"foundAt":145,"category":146},6225,"requirement-engineer-hardwaresoftware-mfd","Requirement engineer Hardware\u002FSoftware (m\u002Ff\u002Fd)",[118,128,127,141,142,143,126,129,130],"System Development","ALM tools","Medical Devices","Zug","2026-05-27T10:06:13+00:00",{"id":24,"slug":25,"label":26},{"id":148,"slug":149,"title":150,"skills":151,"budget":18,"duration":163,"location":164,"onsitePercent":165,"contractType":21,"foundAt":166,"category":167},6186,"senior-qa-compliance-expert-2","Senior QA Compliance Expert",[40,152,153,154,155,156,157,158,159,160,161,42,44,162],"Quality Assurance","Compliance","Deviation Management","CAPA","Change Control","EU-GMP-Leitfaden","ICH-Richtlinien","TrackWise Digital","SAP","S4 HANA","Biologie","11. Mai 2026 bis 31. März 2027","München",20,"2026-05-27T08:11:21+00:00",{"id":24,"slug":25,"label":26},{"id":169,"slug":170,"title":171,"skills":172,"budget":18,"duration":131,"location":132,"onsitePercent":18,"contractType":133,"foundAt":187,"category":188},6181,"msat-engineer-process-management-2","MSAT Engineer Process Management",[173,174,175,153,176,177,160,154,178,179,180,181,182,183,184,185,186],"Process Management","Product Development","GxP","Quality Management","Root Cause Analysis","Process Optimization","Regulatory Compliance","Audit Readiness","Biotechnology","Biology","Chemistry","Material Science","Mechanical Engineering","Electrical Engineering","2026-05-27T07:36:42+00:00",{"id":24,"slug":25,"label":26},{"id":190,"slug":191,"title":171,"skills":192,"budget":18,"duration":131,"location":132,"onsitePercent":20,"contractType":194,"foundAt":195,"category":196},6167,"msat-engineer-process-management",[193,174,175,153,176,177,160,154,178,129,130],"Process Development","permanent","2026-05-27T07:21:17+00:00",{"id":24,"slug":25,"label":26},{"id":198,"slug":199,"title":200,"skills":201,"budget":18,"duration":18,"location":210,"onsitePercent":20,"contractType":21,"foundAt":211,"category":212},5958,"product-manager-mwd","Product Manager (m\u002Fw\u002Fd)",[202,203,204,205,41,26,206,207,208,209],"Produktmanagement","Marketing","R&D","Vertrieb","Wirtschaftswissenschaften","Gesundheitsmanagement","Wettbewerbsanalysen","Kommunikationsfähigkeit","Raubling","2026-05-26T10:27:10+00:00",{"id":24,"slug":25,"label":26},{"id":214,"slug":215,"title":216,"skills":217,"budget":18,"duration":18,"location":222,"onsitePercent":20,"contractType":21,"foundAt":223,"category":224},5511,"hardwareentwickler-produktbetreuung-medizintechnik-mwd","Hardwareentwickler Produktbetreuung Medizintechnik (m\u002Fw\u002Fd)",[108,218,219,220,72,160,58,26,60,221],"Hardware-Design","Messtechnik","Linux","Analyse","Erlangen","2026-05-22T14:25:48+00:00",{"id":24,"slug":25,"label":26},{"id":226,"slug":227,"title":228,"skills":229,"budget":18,"duration":18,"location":79,"onsitePercent":20,"contractType":21,"foundAt":238,"category":239},5471,"ingenieur-mwd-qualifizierung-und-validierung","Ingenieur (m\u002Fw\u002Fd) Qualifizierung und Validierung",[230,43,231,40,60,61,232,160,233,234,235,236,221,93,237],"Pharmatechnik","Bio-Verfahrenstechnik","Windchill","FMEA","IQ","OQ","Testspezifikation","FAT","2026-05-22T13:27:31+00:00",{"id":24,"slug":25,"label":26},{"id":241,"slug":242,"title":243,"skills":244,"budget":18,"duration":249,"location":250,"onsitePercent":251,"contractType":21,"foundAt":252,"category":253},5295,"freiberuflicher-konstrukteur-3d-zeichnungen","Freiberuflicher Konstrukteur - 3D Zeichnungen",[245,246,247,248,26],"SolidWorks","3D-Konstruktion","Maschinenbau","Konstruktionstechnik","Dezember \u002F Januar 2025","Baden-Württemberg",2,"2026-05-21T16:39:19+00:00",{"id":24,"slug":25,"label":26},{"id":255,"slug":256,"title":257,"skills":258,"budget":18,"duration":18,"location":262,"onsitePercent":49,"contractType":194,"foundAt":263,"category":264},5293,"quality-spezialist-mwd-fuer-die-medizintechnik","Quality Spezialist (m\u002Fw\u002Fd) für die Medizintechnik",[259,260,26,261,41,46],"ISO 13485","Qualitätssicherung","CAPA-Maßnahmen","Karlsruhe","2026-05-21T16:39:08+00:00",{"id":24,"slug":25,"label":26}]