[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-dokumentationsmanager-post-market-surveillance-mwd":3,"similar-dokumentationsmanager-post-market-surveillance-mwd":35},{"id":4,"slug":5,"title":6,"skills":7,"budget":20,"duration":20,"location":21,"onsitePercent":22,"contractType":23,"foundAt":24,"category":25,"description":29,"rawText":30,"webTitle":6,"webText":31,"language":32,"projectId":33,"sourceUrl":34},12375,"dokumentationsmanager-post-market-surveillance-mwd","Dokumentationsmanager Post-Market Surveillance (m\u002Fw\u002Fd)",[8,9,10,11,12,13,14,15,16,17,18,19],"Pharmakovigilanz","MDR","IMDRF-Codierung","TrackWise","Veeva Vault","MS Office","SharePoint","SAP","Datenbanken","Literaturrecherche","Risikomanagement","Dokumentation",null,"Wehrheim, Hessen",0,"contracting","2026-06-11T09:31:18+00:00",{"id":26,"slug":27,"label":28},14,"medical_tech","Medizintechnik","Bearbeitung und Dokumentation von Post-Market-Meldungen in elektronischen Systemen wie TrackWise oder Veeva Vault. Prüfung eingehender Beschwerden, Durchführung von Vigilanzbewertungen nach MDR-Richtlinien und Meldung von Fällen an Behörden. Erstellung und Pflege von PMS-Plänen sowie Sicherheitsberichten.","Dokumentationsmanager Post-Market Surveillance (m\u002Fw\u002Fd)\nProjektnummer: FE74-90498-WIPL\nStandort: Wehrheim, Hessen\nArbeitsweise: Remote\nLaufzeit: Keine Angabe\nStartdatum: Keine Angabe\n\nDas ist zukünftig dein Job:\n- Bearbeitung und Dokumentation von Post-Market-Meldungen in elektronischen Systemen wie TrackWise oder Veeva Vault \n\n- Prüfung eingehender Beschwerden auf Vollständigkeit und Nachverfolgung fehlender Angaben \n\n- Durchführung von Vigilanzbewertungen nach MDR-Richtlinien und IMDRF-Kodierung \n\n- Klassifizierung, Bewertung und fristgerechte Meldung von Fällen an Behörden gemäß länderspezifischer Vorgaben \n\n- Erstellung und Pflege von PMS-Plänen sowie regelmäßigen Sicherheitsberichten (z. B. PSUR) \n\n- Analyse von Trenddaten zur Identifikation meldepflichtiger Entwicklungen in Zusammenarbeit mit Risikomanagement \n\n- Auswertung interner\u002Fexterner Datenbanken zur Sicherstellung der Datenqualität für Management-Reviews \n\n- Erstellung fundierter Stellungnahmen zu Produktrisiken für Behördenanfragen und Auditvorbereitung\n\nDas bringst Du mit:\n- Abgeschlossenes Studium im Bereich Life Sciences, z. B. Biologie, Biotechnologie, Medizin oder vergleichbare Qualifikation; Promotion vorteilhaft \n\n- Mindestens zwei Jahre Erfahrung im Umfeld Vigilanz\u002FPharmakovigilanz (Industrie oder CRO) \n\n- Kenntnisse in wissenschaftlicher Dokumentation sowie Literatur- und Datenbankrecherche (z. B. PubMed, Embase) \n\n- Anwendung sicherer Methoden der Fallbewertung nach MDR sowie IMDRF-Codierungssystematik\n\n- Sicherer Umgang mit MS Office-Anwendungen sowie Erfahrung mit SharePoint-Tools\n\n- SAP-Kenntnisse wünschenswert\n\n- Kenntnisse der deutschen und englischen Sprache in Wort und Schrift\n\nSkills: Analyse, Anwendungen, Auswertung, Behörden, Bewertung, Biologie, Biotechnologie, Datenbanken, Dokumentation, MDR, MS, Management, PSUR, Pharmakovigilanz, Prüfung, Risikomanagement, SAP, SharePoint, Vault\n\nAnsprechpartner:\nMelina Braun\nJunior Talent Acquisition Spezialist\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 Dokumentationsmanager für die Post-Market Surveillance im Bereich Medizinprodukte und Pharmazie. In dieser Rolle sind Sie verantwortlich für die professionelle Bearbeitung und Dokumentation von Post-Market-Meldungen in etablierten elektronischen Systemen wie TrackWise oder Veeva Vault.\n\nIhre Aufgaben umfassen die Prüfung eingehender Beschwerden auf Vollständigkeit, die Durchführung von Vigilanzbewertungen nach MDR-Richtlinien und IMDRF-Kodierung sowie die Klassifizierung und fristgerechte Meldung von Fällen an Behörden gemäß länderspezifischer Vorgaben. Sie erstellen und pflegen PMS-Pläne, erarbeiten regelmäßige Sicherheitsberichte und analysieren Trenddaten zur Identifikation meldepflichtiger Entwicklungen in enger Zusammenarbeit mit dem Risikomanagement. Darüber hinaus werten Sie interne und externe Datenbanken aus und erstellen fundierte Stellungnahmen zu Produktrisiken für Behördenanfragen und Audits.\n\nFür diese Position benötigen Sie ein abgeschlossenes Studium in Life Sciences (Biologie, Biotechnologie, Medizin oder vergleichbar), wobei eine Promotion vorteilhaft ist. Mindestens zwei Jahre Erfahrung in Vigilanz oder Pharmakovigilanz sind erforderlich. Sie sollten sicher mit wissenschaftlicher Dokumentation, Literatur- und Datenbankrecherche umgehen können und fundierte Kenntnisse in MDR-Fallbewertung sowie IMDRF-Codierung mitbringen. Gute MS-Office- und SharePoint-Kenntnisse sind notwendig, SAP-Erfahrung ist wünschenswert. Fließende Deutsch- und Englischkenntnisse in Wort und Schrift sind erforderlich.\n\nDie Position ist remote ausgerichtet und bietet Ihnen die Möglichkeit, in einem regulatorisch anspruchsvollen Umfeld Ihre Expertise einzubringen.","de","FE74-90498-WIPL","https:\u002F\u002Ftouch.ferchau.com\u002Fde\u002Fde\u002Fprojekt\u002F508255",{"items":36},[37,52,66,82,98,115,130,152,172,187,210,225,238,257,271],{"id":38,"slug":39,"title":40,"skills":41,"budget":20,"duration":20,"location":48,"onsitePercent":49,"contractType":23,"foundAt":50,"category":51},12404,"mechatroniker-medizintechnik-mwd","Mechatroniker Medizintechnik (m\u002Fw\u002Fd)",[42,43,44,45,46,28,47],"Mechatronik","Montage","Systemintegration","Elektrische Prüfungen","Industriemechanik","Bestandsmanagement","Bayreuth",100,"2026-06-11T10:25:42+00:00",{"id":26,"slug":27,"label":28},{"id":53,"slug":54,"title":55,"skills":56,"budget":20,"duration":20,"location":62,"onsitePercent":49,"contractType":63,"foundAt":64,"category":65},12321,"produktionsmitarbeiter-logistik-pharma-mwd","Produktionsmitarbeiter Logistik Pharma (m\u002Fw\u002Fd)",[57,58,59,60,61,19],"Lagerlogistik","Logistik","Pharma","Produktion","Reinraum","Uetersen, Schleswig-Holstein","temp_work","2026-06-11T07:26:37+00:00",{"id":26,"slug":27,"label":28},{"id":67,"slug":68,"title":69,"skills":70,"budget":20,"duration":77,"location":78,"onsitePercent":79,"contractType":23,"foundAt":80,"category":81},12301,"projektmanagement-pharma-anlagen","Projektmanagement Pharma-Anlagen",[71,72,73,15,74,59,19,75,76],"Projektkoordination","Instandhaltung","GMP","Projektmanagement","Wartung","Planung","4 Monate, ab sofort","Marburg",50,"2026-06-11T02:27:41+00:00",{"id":26,"slug":27,"label":28},{"id":83,"slug":84,"title":85,"skills":86,"budget":20,"duration":20,"location":95,"onsitePercent":49,"contractType":63,"foundAt":96,"category":97},12222,"mitarbeiter-qualitaetskontrolle-visuelle-pruefung-mwd","Mitarbeiter Qualitätskontrolle Visuelle Prüfung (m\u002Fw\u002Fd)",[87,73,88,89,90,91,60,92,93,94],"Arzneimittel","Inspektion","Labor","Lebensmittel","Pharmazie","Prüfung","Prüftechnik","SOP","Biberach an der Riß, Baden-Württemberg","2026-06-10T15:27:48+00:00",{"id":26,"slug":27,"label":28},{"id":99,"slug":100,"title":101,"skills":102,"budget":20,"duration":20,"location":112,"onsitePercent":49,"contractType":23,"foundAt":113,"category":114},12221,"technical-assistant-pharma-mwd","Technical Assistant Pharma (m\u002Fw\u002Fd)",[73,103,104,105,106,107,108,109,13,110,111],"Laboranalytik","Analyseverfahren","GelClot","UV-Scan","TOC-Analytik","Spektralphotometer","Methodenvalidierung","Deutsch","Englisch","Biberach an der Riß","2026-06-10T15:27:29+00:00",{"id":26,"slug":27,"label":28},{"id":116,"slug":117,"title":118,"skills":119,"budget":20,"duration":20,"location":127,"onsitePercent":49,"contractType":23,"foundAt":128,"category":129},12217,"produktkoordinator-pharma-mwd","Produktkoordinator Pharma (m\u002Fw\u002Fd)",[91,120,121,73,122,123,124,125,126,110,111],"Chemie","Biologie","MyLIMS","MS-Office","Qualitätsmanagement","Laborkoordination","Dokumentenerstellung","Biberach, Baden-Württemberg","2026-06-10T15:26:49+00:00",{"id":26,"slug":27,"label":28},{"id":131,"slug":132,"title":133,"skills":134,"budget":20,"duration":148,"location":149,"onsitePercent":49,"contractType":63,"foundAt":150,"category":151},12101,"hardware-product-owner-development-engineer","Hardware Product Owner & Development Engineer",[135,136,137,138,139,140,141,142,143,144,145,146,111,110,28,147],"Product Ownership","Scrum\u002FKanban","SAFe Framework","Elektronik-Design","Mechanik-Design","PCB-Schaltplan-Design","Technische Dokumentation","Integrationstests","Siemens Xpedition","Solidworks","CATIA","Azure DevOps","Motorsteuerung","01.10.2026 - 31.12.2029","Rotkreuz","2026-06-10T12:56:26+00:00",{"id":26,"slug":27,"label":28},{"id":153,"slug":154,"title":155,"skills":156,"budget":20,"duration":169,"location":149,"onsitePercent":49,"contractType":63,"foundAt":170,"category":171},12100,"production-engineer","Production Engineer",[157,158,159,160,161,162,163,164,165,166,167,168],"Technische Ausbildung (FH\u002Fstaatlich geprüfter Techniker)","Automatisierungstechnik","Projekttransfer in Produktion","Gestaltung von Produktionslinien","Materialverwaltung","GMP-Umfeld","Medizinprodukte","Change Management","Stakeholder Management","Deutsch (fließend)","Englisch (fließend)","SAP (nice to have)","12+ Monate, Start 01.06.2026 (spätestens 01.08.2026)","2026-06-10T12:56:17+00:00",{"id":26,"slug":27,"label":28},{"id":173,"slug":174,"title":175,"skills":176,"budget":20,"duration":20,"location":184,"onsitePercent":49,"contractType":23,"foundAt":185,"category":186},12072,"laborant-chemie-mwd","Laborant Chemie (m\u002Fw\u002Fd)",[177,120,178,179,89,180,19,76,181,182,183],"Chemielaborant","FTIR-Spektroskopie","Spektroskopie","ISO","Koordination","Qualität","Optimierung","Würzburg","2026-06-10T11:25:51+00:00",{"id":26,"slug":27,"label":28},{"id":188,"slug":189,"title":190,"skills":191,"budget":20,"duration":20,"location":207,"onsitePercent":49,"contractType":23,"foundAt":208,"category":209},11902,"it-anwendungsbetreuer-mwd-2","IT-Anwendungsbetreuer (m\u002Fw\u002Fd)",[192,193,194,195,196,197,198,199,200,201,202,203,204,205,206,19],"Fachinformatiker","Medizinische IT-Systeme","AIS","LIS","Jira","ServiceNow","Netzwerktechnik","TCP\u002FIP","Firewalls","VPN","IT-Sicherheit","Microsoft Windows Server","RDP","Citrix","Anwenderschulungen","Rosenheim","2026-06-09T14:27:06+00:00",{"id":26,"slug":27,"label":28},{"id":211,"slug":212,"title":213,"skills":214,"budget":20,"duration":20,"location":222,"onsitePercent":49,"contractType":23,"foundAt":223,"category":224},11872,"chemielaborant-qualitaetskontrolle-mwd","Chemielaborant Qualitätskontrolle (m\u002Fw\u002Fd)",[177,215,73,216,217,218,219,220,221,19],"Qualitätskontrolle","HPLC","GC","Chromeleon","CTA","PTA","CAPA","Miesbach, Bayern","2026-06-09T13:25:36+00:00",{"id":26,"slug":27,"label":28},{"id":226,"slug":227,"title":228,"skills":229,"budget":20,"duration":20,"location":222,"onsitePercent":49,"contractType":235,"foundAt":236,"category":237},11871,"chemielaborant-lab-technician-mwd-analytical-development","Chemielaborant \u002F Lab Technician (m\u002Fw\u002Fd) Analytical Development",[230,216,217,231,232,218,73,19,233,234],"Analytik","Methodenentwicklung","Validierung analytischer Methoden","Chromatographie","Spektrometrie","permanent","2026-06-09T13:25:25+00:00",{"id":26,"slug":27,"label":28},{"id":239,"slug":240,"title":241,"skills":242,"budget":20,"duration":254,"location":20,"onsitePercent":22,"contractType":23,"foundAt":255,"category":256},11773,"sustaining-engineer-mwd","Sustaining Engineer (m\u002Fw\u002Fd)",[243,244,245,246,247,164,248,249,250,251,252,253],"Medical Device Engineering","Design Authority","Non Conformance Report (NCR) Assessment","Design for Manufacturing","Regulatory Compliance (QSR, GMP, ISO)","Project Management","Engineering Testing and Analysis","Vendor Management","Cross-functional Coordination","English","German","6 Monate, Start 01.07.2026","2026-06-09T09:30:21+00:00",{"id":26,"slug":27,"label":28},{"id":258,"slug":259,"title":260,"skills":261,"budget":20,"duration":20,"location":268,"onsitePercent":79,"contractType":23,"foundAt":269,"category":270},11741,"junior-quality-engineer-medical-devices-mwd","Junior Quality Engineer Medical Devices (m\u002Fw\u002Fd)",[262,263,264,265,266,267,110,111],"Audits","Elektrotechnik","Fehleranalyse","Lösungskompetenz","Management","Medical Devices","Aschaffenburg","2026-06-09T08:27:29+00:00",{"id":26,"slug":27,"label":28},{"id":272,"slug":273,"title":274,"skills":275,"budget":20,"duration":20,"location":285,"onsitePercent":79,"contractType":23,"foundAt":286,"category":287},11740,"manager-gxp-compliance-mwd","Manager GxP Compliance (m\u002Fw\u002Fd)",[276,94,277,278,221,279,280,281,282,283,284,110,111],"GxP","Change Control","Deviation","Risk Management","CSV","Qualifizierung","Validierung","Audit","Life Science","Mainz, Rheinland-Pfalz","2026-06-09T08:27:21+00:00",{"id":26,"slug":27,"label":28}]