[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-produktkoordinator-pharma-mwd":3,"similar-produktkoordinator-pharma-mwd":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},12217,"produktkoordinator-pharma-mwd","Produktkoordinator Pharma (m\u002Fw\u002Fd)",[8,9,10,11,12,13,14,15,16,17,18],"Pharmazie","Chemie","Biologie","GMP","MyLIMS","MS-Office","Qualitätsmanagement","Laborkoordination","Dokumentenerstellung","Deutsch","Englisch",null,"Biberach, Baden-Württemberg",100,"contracting","2026-06-10T15:26:49+00:00",{"id":25,"slug":26,"label":27},14,"medical_tech","Medizintechnik","Koordination und Steuerung von Laborprozessen im pharmazeutischen Umfeld mit Fokus auf GMP-konforme Dokumentation, Probenmanagement und regulatorische Compliance. Verantwortung für Abstimmung mit Schnittstellenpartnern und kontinuierliche Prozessoptimierung.","Produktkoordinator Pharma (m\u002Fw\u002Fd)\nProjektnummer: FE55-18414-UL\nStandort: Biberach, Baden-Württemberg\nArbeitsweise: Vor Ort\nLaufzeit: Keine Angabe\nStartdatum: Keine Angabe\n\nDas sind deine Aufgaben in unserem Team:\n- Erstellung und Pflege von Vorgabedokumenten in MyLIMS unter Berücksichtigung von GMP-Richtlinien\n\n- Steuerung und Priorisierung des Probenmanagements inklusive Versandorganisation\n\n- Planung, Koordination und Umsetzung komplexer Arbeitsabläufe im Laborumfeld\n\n- Abstimmung von Maßnahmen und Zeitplänen mit Schnittstellenpartner:innen wie Qualitätssicherung oder Produktion\n\n- Sicherstellung effizienter Prozessabläufe durch kontinuierliche Optimierung\n\n- Überwachung der Einhaltung regulatorischer Anforderungen bei Freigabeprozesse und Stabilitätsstudien\n\nWomit du uns überzeugst:\n- Abgeschlossene Ausbildung oder Studium im Bereich Pharmazie, Chemie, Biologie oder vergleichbare naturwissenschaftliche Qualifikation (z. B. CTA, BTA, PTA) \n\n- Erste Erfahrung im GMP-regulierten Umfeld sowie Kenntnisse zu regulatorischen Vorgaben \n\n- Gute MS-Office-Kenntnisse sowie Erfahrung mit Laborinformationsmanagementsystemen wie MyLIMS wünschenswert\n\n- Praktische Erfahrungen in der Dokumentenerstellung nach GMP-Vorgaben \n\n- Nachweisbare Berufserfahrung in der Koordination von Laborprozessen oder Qualitätsmanagement \n\n- Fließende Deutschkenntnisse sowie gute Englischkenntnisse für die Anwendung technischer Dokumente\n\nSkills: BTA, Biologie, CTA, Chemie, GMP, Koordination, MS, MS-Office, Optimierung, Pharma, Pharmazie, Planung, Produktion, Qualitätsmanagement, Qualitätssicherung, Steuerung, Umsetzung\n\nAnsprechpartner:\nMarlen Kopp\nTalent Acquisition Expert\nFERCHAU GmbH, Niederlassung Ulm\nLise-Meitner-Straße 8\u002F1\n89081 Ulm\n+49 731 96247-0\nulm@ferchau.com","Wir suchen einen engagierten Produktkoordinator (m\u002Fw\u002Fd) für unser Pharma-Team am Standort Biberach. In dieser Rolle tragen Sie wesentlich zur Koordination und Optimierung unserer Laborprozesse bei.\n\nIhre Aufgaben umfassen die Erstellung und Pflege von Vorgabedokumenten unter Berücksichtigung von GMP-Richtlinien, die Steuerung des Probenmanagements inklusive Versandorganisation sowie die Planung und Koordination komplexer Arbeitsabläufe im Laborumfeld. Sie arbeiten eng mit Schnittstellenpartnern wie der Qualitätssicherung und Produktion zusammen, um Maßnahmen und Zeitpläne abzustimmen. Darüber hinaus überwachen Sie die Einhaltung regulatorischer Anforderungen bei Freigabeprozessen und Stabilitätsstudien und tragen durch kontinuierliche Optimierung zu effizienten Prozessabläufen bei.\n\nFür diese Position bringen Sie eine abgeschlossene Ausbildung oder ein Studium im Bereich Pharmazie, Chemie, Biologie oder eine vergleichbare naturwissenschaftliche Qualifikation (z. B. CTA, BTA, PTA) mit. Erste Erfahrungen im GMP-regulierten Umfeld sowie Kenntnisse zu regulatorischen Vorgaben sind erforderlich. Praktische Erfahrungen in der Dokumentenerstellung nach GMP-Vorgaben und nachweisbare Berufserfahrung in der Koordination von Laborprozessen oder im Qualitätsmanagement sind von Vorteil. Gute MS-Office-Kenntnisse sowie Erfahrung mit Laborinformationsmanagementsystemen sind wünschenswert. Fließende Deutschkenntnisse und gute Englischkenntnisse für die Anwendung technischer Dokumente runden Ihr Profil ab.\n\nWir bieten Ihnen die Möglichkeit, in einem regulierten Umfeld Verantwortung zu übernehmen und Ihre Fachkompetenz einzubringen.","de","FE55-18414-UL","https:\u002F\u002Ftouch.ferchau.com\u002Fde\u002Fde\u002Fprojekt\u002F507763",{"items":35},[36,53,69,91,111,128,151,166,179,199,214,231,248,267,277],{"id":37,"slug":38,"title":39,"skills":40,"budget":19,"duration":19,"location":49,"onsitePercent":21,"contractType":50,"foundAt":51,"category":52},12222,"mitarbeiter-qualitaetskontrolle-visuelle-pruefung-mwd","Mitarbeiter Qualitätskontrolle Visuelle Prüfung (m\u002Fw\u002Fd)",[41,11,42,43,44,8,45,46,47,48],"Arzneimittel","Inspektion","Labor","Lebensmittel","Produktion","Prüfung","Prüftechnik","SOP","Biberach an der Riß, Baden-Württemberg","temp_work","2026-06-10T15:27:48+00:00",{"id":25,"slug":26,"label":27},{"id":54,"slug":55,"title":56,"skills":57,"budget":19,"duration":19,"location":66,"onsitePercent":21,"contractType":22,"foundAt":67,"category":68},12221,"technical-assistant-pharma-mwd","Technical Assistant Pharma (m\u002Fw\u002Fd)",[11,58,59,60,61,62,63,64,65,17,18],"Laboranalytik","Analyseverfahren","GelClot","UV-Scan","TOC-Analytik","Spektralphotometer","Methodenvalidierung","MS Office","Biberach an der Riß","2026-06-10T15:27:29+00:00",{"id":25,"slug":26,"label":27},{"id":70,"slug":71,"title":72,"skills":73,"budget":19,"duration":87,"location":88,"onsitePercent":21,"contractType":50,"foundAt":89,"category":90},12101,"hardware-product-owner-development-engineer","Hardware Product Owner & Development Engineer",[74,75,76,77,78,79,80,81,82,83,84,85,18,17,27,86],"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":25,"slug":26,"label":27},{"id":92,"slug":93,"title":94,"skills":95,"budget":19,"duration":108,"location":88,"onsitePercent":21,"contractType":50,"foundAt":109,"category":110},12100,"production-engineer","Production Engineer",[96,97,98,99,100,101,102,103,104,105,106,107],"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":25,"slug":26,"label":27},{"id":112,"slug":113,"title":114,"skills":115,"budget":19,"duration":19,"location":125,"onsitePercent":21,"contractType":22,"foundAt":126,"category":127},12072,"laborant-chemie-mwd","Laborant Chemie (m\u002Fw\u002Fd)",[116,9,117,118,43,119,120,121,122,123,124],"Chemielaborant","FTIR-Spektroskopie","Spektroskopie","ISO","Dokumentation","Planung","Koordination","Qualität","Optimierung","Würzburg","2026-06-10T11:25:51+00:00",{"id":25,"slug":26,"label":27},{"id":129,"slug":130,"title":131,"skills":132,"budget":19,"duration":19,"location":148,"onsitePercent":21,"contractType":22,"foundAt":149,"category":150},11902,"it-anwendungsbetreuer-mwd-2","IT-Anwendungsbetreuer (m\u002Fw\u002Fd)",[133,134,135,136,137,138,139,140,141,142,143,144,145,146,147,120],"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":25,"slug":26,"label":27},{"id":152,"slug":153,"title":154,"skills":155,"budget":19,"duration":19,"location":163,"onsitePercent":21,"contractType":22,"foundAt":164,"category":165},11872,"chemielaborant-qualitaetskontrolle-mwd","Chemielaborant Qualitätskontrolle (m\u002Fw\u002Fd)",[116,156,11,157,158,159,160,161,162,120],"Qualitätskontrolle","HPLC","GC","Chromeleon","CTA","PTA","CAPA","Miesbach, Bayern","2026-06-09T13:25:36+00:00",{"id":25,"slug":26,"label":27},{"id":167,"slug":168,"title":169,"skills":170,"budget":19,"duration":19,"location":163,"onsitePercent":21,"contractType":176,"foundAt":177,"category":178},11871,"chemielaborant-lab-technician-mwd-analytical-development","Chemielaborant \u002F Lab Technician (m\u002Fw\u002Fd) Analytical Development",[171,157,158,172,173,159,11,120,174,175],"Analytik","Methodenentwicklung","Validierung analytischer Methoden","Chromatographie","Spektrometrie","permanent","2026-06-09T13:25:25+00:00",{"id":25,"slug":26,"label":27},{"id":180,"slug":181,"title":182,"skills":183,"budget":19,"duration":195,"location":19,"onsitePercent":196,"contractType":22,"foundAt":197,"category":198},11773,"sustaining-engineer-mwd","Sustaining Engineer (m\u002Fw\u002Fd)",[184,185,186,187,188,103,189,190,191,192,193,194],"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",0,"2026-06-09T09:30:21+00:00",{"id":25,"slug":26,"label":27},{"id":200,"slug":201,"title":202,"skills":203,"budget":19,"duration":19,"location":210,"onsitePercent":211,"contractType":22,"foundAt":212,"category":213},11741,"junior-quality-engineer-medical-devices-mwd","Junior Quality Engineer Medical Devices (m\u002Fw\u002Fd)",[204,205,206,207,208,209,17,18],"Audits","Elektrotechnik","Fehleranalyse","Lösungskompetenz","Management","Medical Devices","Aschaffenburg",50,"2026-06-09T08:27:29+00:00",{"id":25,"slug":26,"label":27},{"id":215,"slug":216,"title":217,"skills":218,"budget":19,"duration":19,"location":228,"onsitePercent":211,"contractType":22,"foundAt":229,"category":230},11740,"manager-gxp-compliance-mwd","Manager GxP Compliance (m\u002Fw\u002Fd)",[219,48,220,221,162,222,223,224,225,226,227,17,18],"GxP","Change Control","Deviation","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":232,"slug":233,"title":234,"skills":235,"budget":19,"duration":19,"location":245,"onsitePercent":211,"contractType":22,"foundAt":246,"category":247},11739,"device-engineer-mwd","Device Engineer (m\u002Fw\u002Fd)",[236,120,237,238,239,240,241,121,242,243,244],"Design","Entwicklung","Entwicklungsprozesse","Integration","Kombinationsprodukte","Koordinierung","Risikomanagement","Umsetzung","Usability","Ingelheim am Rhein","2026-06-09T08:27:13+00:00",{"id":25,"slug":26,"label":27},{"id":249,"slug":250,"title":251,"skills":252,"budget":19,"duration":19,"location":264,"onsitePercent":211,"contractType":22,"foundAt":265,"category":266},11738,"product-lifecycle-engineer-mwd-medizintechnik","Product Lifecycle Engineer (m\u002Fw\u002Fd) Medizintechnik",[253,254,205,237,255,256,257,258,102,27,259,45,260,261,262,263],"Anlagenbau","Einkauf","Feinwerktechnik","Hydraulik","Maschinenbau","Mechanik","Pneumatik","QM","Service","Steuerung","Teamfähigkeit","Frankfurt am Main","2026-06-09T08:27:03+00:00",{"id":25,"slug":26,"label":27},{"id":268,"slug":269,"title":270,"skills":271,"budget":19,"duration":19,"location":264,"onsitePercent":211,"contractType":176,"foundAt":275,"category":276},11737,"mitarbeiter-mwd-customer-service-pharma","Mitarbeiter (m\u002Fw\u002Fd) Customer Service Pharma",[272,273,65,274,204,17,18],"Customer Service","SAP","Auftragsabwicklung","2026-06-09T08:26:54+00:00",{"id":25,"slug":26,"label":27},{"id":278,"slug":279,"title":280,"skills":281,"budget":19,"duration":19,"location":287,"onsitePercent":211,"contractType":176,"foundAt":288,"category":289},11735,"mitarbeiter-mwd-regulatory-affairs-2","Mitarbeiter (m\u002Fw\u002Fd) Regulatory Affairs",[282,80,283,284,27,14,285,286],"Regulatory Affairs","MDD","MDR","Analyse","Bewertung","Aschaffenburg, Bayern","2026-06-09T08:26:38+00:00",{"id":25,"slug":26,"label":27}]