[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-qms-dms-system-owner":3,"similar-qms-dms-system-owner":37},{"id":4,"slug":5,"title":6,"skills":7,"budget":21,"duration":22,"location":23,"onsitePercent":24,"contractType":25,"foundAt":26,"category":27,"description":31,"rawText":32,"webTitle":6,"webText":33,"language":34,"projectId":35,"sourceUrl":36},10894,"qms-dms-system-owner","QMS & DMS System Owner",[8,9,10,11,12,13,14,15,16,17,18,19,20],"QMS","DMS","GMP","GxP","CAPA","Change Control","Document Control","Veeva Vault","TrackWise","MasterControl","SAP DMS","Regulatory Affairs","Quality Assurance","Negotiable",null,"India",0,"contracting","2026-06-03T14:35:27+00:00",{"id":28,"slug":29,"label":30},14,"medical_tech","Medizintechnik","Verwaltung und Wartung von kontrollierten Dokumenten, SOPs und Qualitätsunterlagen in regulierten Industrien. Unterstützung von Qualitätssystemen wie Document Management, Change Control und CAPA. Sicherstellung der Compliance mit GMP, GxP und FDA-Standards.","Lassen Sie Ihre Karriereträume wahr werden.\n\n \n Bei uns erhalten Sie die Beratungsleistungen, Ressourcen und Kontakte, um sich Ihren SAP- oder IT-Traumjob zu sichern.\n\n \n\n \n\n \n \n\n \n \n \n\n \n\n - Home\n- Jobs\n- QMS & DMS System Owner\n\n \n \n \n QMS & DMS System Owner\n\n \n\n Stellenausschreibung\n\n \n - \n India, Asia Ort\n \n\n - \n Negotiable Gehalt\n \n\n - \n Life Sciences Technologie\n \n\n - \n Freiberuflich Art\n \n\n - \n Remote Arbeitsplatz\n \n\n \n \n\n \n \n \n \n \n Jetzt bewerben\n \n \n\n \n\nKey Responsibilities:\n\n- Administer and maintain controlled documents including SOPs, work instructions, policies, forms, and quality records.\n * Coordinate document lifecycle activities including creation, review, approval, training, revision, archival, and retirement.\n * Support quality systems such as Document Management, Change Control, CAPA, Deviations, Training Management, Audit Management, and Supplier Quality.\n * Review document change requests and assess impact on existing quality processes.\n * Collaborate with Quality Assurance, Regulatory Affairs, Manufacturing, and business stakeholders to ensure timely document updates and approvals.\n * Maintain compliance with GMP, GxP, FDA, EU, and internal quality standards.\n * Support internal audits, external audits, and regulatory inspections by providing required documentation and evidence.\n * Monitor quality metrics, generate reports, and identify opportunities for continuous improvement.\n * Provide user support, training, and guidance on QMS and DMS processes and tools.\n * Ensure accurate record retention, document traceability, and inspection readiness at all times.\n\nRequirements:\n\n* Bachelor's degree or equivalent experience.\n * Experience supporting QMS and DMS environments in regulated industries.\n * Knowledge of GMP, GxP, CAPA, Change Control, and document control processes.\n * Experience with electronic quality systems such as Veeva Vault, TrackWise, MasterControl, SAP DMS, or similar platforms.\n * Strong communication, organizatio\n\n Reference\nCR\u002F134762_1780497289\n\n Date\n03.06.2026\n\n \n Jetzt bewerben\n \n \n\n \n\n \n \n \n \n Ähnliche Jobs\n\n \n \n Zurück\n \n \n \n \n \n \n Solution Analyst - QMS, DMS, LMS Consultant - Quality Document Management\n\n \n - India, Asia\n\n - Negotiable\n\n \n \n\n \n\n \n \n\n \n \n\n \n \n\n \n\n \n \n\n \n\n \n\n \n\n \n\n \n\n \n \n \n Das könnte Ihnen auch gefallen…\n\n \n\n \n Ähnliche Jobs\n\n \n\n \n \n \n\n \n \n\n \n\n \n\n \n \n \n \n \n \n \n Solution Analyst - QMS, DMS, LMS Consultant - Quality Document Management\n\n \n - India, Asia\n\n - Negotiable\n\n \n \n\n Key Responsibilities: Administer and maintain controlled documents including SOPs, work...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n SAC Consultant\n\n \n - India, Asia\n\n - Negotiable\n\n \n \n\n Role: SAC Consultant Location: India 100% remote Duration: 12 months B2B freelance contract plus...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n SAP SD OTC Consultant\n\n \n - Brazil, South America\n\n - Negotiable\n\n \n \n\n Job Title: SAP OTC \u002F SD Contract Type: B2B Contract Start Date: ASAP Duration: 6 months + possible...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n R&D Finance Planning & Controlling Specialist \u002F Expert\n\n \n - 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CFIN Consultant\n\n \n - Czech Republic, Eastern Europe\n\n - Negotiable\n\n \n \n\n Senior SAP MDG - CFIN - ECC+S4HANA - REMOTE We are seeking an experienced SAP MDG Techno-Functional...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n SAP PS Consultant\n\n \n - Hungary, Eastern Europe\n\n - Negotiable\n\n \n \n\n **SAP PS Consultant | Contract role | Hungary** For one of our international clients, RED is...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n Enterprise Functional Architect\n\n \n - Gothenburg, Sweden, Western Europe\n\n - Negotiable\n\n \n \n\n Enterprise Architect - Gothenburg, Sweden - Hybrid RED is currently looking for an Enterprise...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n DevOps Engineer - ITSM Migration & Plattformbetrieb - Remote\n\n \n - Germany, Western Europe\n\n - Negotiable\n\n \n \n\n Für ein anspruchsvolles Transformationsprojekt im Umfeld moderner IT-Service-Management-Plattformen...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n SAP SD Solution Design Manager \n\n \n - India, Asia\n\n - Negotiable\n\n \n \n\n RED is looking for an experienced SAP S\u002F4HANA SD Functional Consultant to support large-scale...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n SAP PP\u002FPS Lead - bis Ende 2027 - 90% Remote - Start ASAP\n\n \n - Germany, Western Europe\n\n - Verhandelbar\n\n \n \n\n Für unseren Kunden aus dem Maschinenbausuchen wir aktuell einen erfahrenen SAP PP\u002FPS Lead...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n Softwaretester - 6 Monate+ - vor Ort Rhein-Main - Start Juli\n\n \n - Germany, Western Europe\n\n - Negotiable\n\n \n \n\n Für ein internationales Projekt im Bereich Air Traffic Management (ATM) wird ein erfahrener...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n SAP OTC Consultant\n\n \n - Hyderabad, India, Asia\n\n - Negotiable\n\n \n \n\n SAP OTC Consultant Contract Overview Start Date: ASAP Contract Length: Until March 2027 + likely...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n \n \n \n ServiceNow Implementer - 12+ Monate - Remote - ASAP\n\n \n - Germany, Western Europe\n\n - Negotiable\n\n \n \n\n Für unseren (langjährigen) Endkunden suchen wir einen erfahrenen ServiceNow Implementer mit...\n\n \n\n \n Mehr Informationen\n\n Jetzt bewerben\n \n\n \n\n \n\n \n\n \n \n \n \n\n Alle ansehen\n\n \n\n \n\n \n\n \n \n \n \n Registrieren Sie sich bei RED Global.\n\n \n \n \n Registrieren\n\n \n \n \n Wenn Sie sich bei RED Global registrieren, erhalten Sie personalisierte Benachrichtigungen zu Jobangeboten, bekommen sofortigen Zugang zu Hunderten neuer SAP- und Tech-Vakanzen und können sich schnell und einfach bewerben. Registrieren Sie sich noch heute und nutzen Sie die Vorteile, die RED Global für seine Kandidaten bereithält. \n \n\n  \n\n \n\n \n \n\n \n\n \n \n \n\n \n\n \n\n \n \n \n Our Partners","Wir suchen einen erfahrenen QMS & DMS System Owner für eine Freiberufler-Position im Life Sciences Technologie-Sektor. Diese Remote-Rolle bietet die Gelegenheit, Qualitätsmanagementsysteme und Dokumentenverwaltung in einer regulierten Industrie zu gestalten und zu optimieren.\n\nIn dieser Position sind Sie verantwortlich für die Verwaltung und Instandhaltung kontrollierter Dokumente, einschließlich Standard Operating Procedures, Arbeitsanweisungen, Richtlinien, Formulare und Qualitätsunterlagen. Sie koordinieren den gesamten Dokumentenlebenszyklus von der Erstellung über Überprüfung, Genehmigung und Schulung bis zur Archivierung und Außerbetriebnahme.\n\nSie unterstützen kritische Qualitätssysteme wie Dokumentenverwaltung, Change Control, CAPA, Abweichungsmanagement, Schulungsverwaltung und Audit-Management. Ihre Aufgaben umfassen die Bewertung von Dokumentänderungsanfragen, die Zusammenarbeit mit Quality Assurance, Regulatory Affairs und Manufacturing sowie die Sicherstellung der Einhaltung von GMP, GxP, FDA und EU-Standards.\n\nDarüber hinaus unterstützen Sie interne und externe Audits sowie behördliche Inspektionen, überwachen Qualitätsmetriken, erstellen Berichte und identifizieren Verbesserungsmöglichkeiten. Sie bieten Benutzersupport und Schulungen zu QMS- und DMS-Prozessen.\n\nGefordert werden ein Bachelor-Abschluss oder gleichwertige Erfahrung, Kenntnisse in GMP, GxP, CAPA und Dokumentenkontrollprozessen sowie Erfahrung mit elektronischen Qualitätssystemen wie Veeva Vault, TrackWise, MasterControl oder SAP DMS. Starke Kommunikations- und Organisationsfähigkeiten sind essentiell.","en","CR\u002F134762_1780497289","https:\u002F\u002Fwww.redglobal.de\u002Fjobs\u002Fjob\u002Fqms-dms-system-owner\u002FdqdkCd7Y",{"items":38},[39,69,78,92,111,130,145,167,182,200,216,232,247,266,283],{"id":40,"slug":41,"title":42,"skills":43,"budget":22,"duration":22,"location":65,"onsitePercent":66,"contractType":25,"foundAt":67,"category":68},10930,"hardware-entwicklung","Hardware Entwicklung",[44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64],"Hardwareentwicklung","Elektronikentwicklung","Schaltungsentwicklung","Analog-\u002FDigitalelektronik","PCB-Design","Altium Designer","Eagle","KiCad","OrCAD","Zuken","Oszilloskop","Multimeter","Signalgenerator","Logikanalysator","Design Reviews","Verifikation","IEC 60601","ISO 13485","IEC 62304","ISO 14971","EMV-Anforderungen","Erlangen",100,"2026-06-03T16:10:59+00:00",{"id":28,"slug":29,"label":30},{"id":70,"slug":71,"title":72,"skills":73,"budget":21,"duration":22,"location":23,"onsitePercent":24,"contractType":25,"foundAt":76,"category":77},10895,"solution-analyst-qms-dms-lms-consultant-quality-document-management","Solution Analyst - QMS, DMS, LMS Consultant - Quality Document Management",[8,9,10,11,12,13,14,15,16,17,18,74,75],"FDA Compliance","Quality Management","2026-06-03T14:35:37+00:00",{"id":28,"slug":29,"label":30},{"id":79,"slug":80,"title":81,"skills":82,"budget":22,"duration":22,"location":89,"onsitePercent":66,"contractType":25,"foundAt":90,"category":91},10855,"junior-specialist-clinical-supply-documentation-mwd","Junior Specialist Clinical Supply & Documentation (m\u002Fw\u002Fd)",[83,84,10,85,86,87,88],"Biotechnologie","Dokumentation","Pharmazie","Medical Affairs","Deutsch","Englisch","Biberach, Baden-Württemberg","2026-06-03T13:26:55+00:00",{"id":28,"slug":29,"label":30},{"id":93,"slug":94,"title":95,"skills":96,"budget":22,"duration":22,"location":107,"onsitePercent":108,"contractType":25,"foundAt":109,"category":110},10852,"pharma-und-life-science-ingenieur-medizintechnik-mwd","Pharma- und Life Science Ingenieur Medizintechnik (m\u002Fw\u002Fd)",[30,97,98,99,10,100,101,102,103,104,105,19,106,88],"Medical Devices","Design Control","Verifizierung und Validierung","ISO","Pharma","Life Science","Testmethoden","Risikomanagement","Qualifizierung","Polarion ALM","Kufstein, Tirol",50,"2026-06-03T13:26:35+00:00",{"id":28,"slug":29,"label":30},{"id":112,"slug":113,"title":114,"skills":115,"budget":22,"duration":126,"location":127,"onsitePercent":24,"contractType":25,"foundAt":128,"category":129},10804,"kis-systementwicklung-und-integration","KIS-Systementwicklung und Integration",[116,117,118,119,120,121,122,123,124,125],"KIS-Systeme","Medico","SAP IS-H","HL7","FHIR","Mirth","Administration","Customizing","Integration","Schnittstellenmanagement","6 Monate, Start 22.06.2026","Bochum","2026-06-03T11:26:25+00:00",{"id":28,"slug":29,"label":30},{"id":131,"slug":132,"title":133,"skills":134,"budget":22,"duration":22,"location":89,"onsitePercent":66,"contractType":142,"foundAt":143,"category":144},10801,"hauswirtschafter-teilzeit-50-pharmabranche-mwd","Hauswirtschafter Teilzeit 50% Pharmabranche (m\u002Fw\u002Fd)",[135,136,137,138,139,140,141,84],"Hauswirtschaft","Reinigung","Wäschepflege","HACCP","Hygienemanagement","GCP","Infektionsschutz","temp_work","2026-06-03T11:26:02+00:00",{"id":28,"slug":29,"label":30},{"id":146,"slug":147,"title":148,"skills":149,"budget":22,"duration":163,"location":164,"onsitePercent":24,"contractType":25,"foundAt":165,"category":166},10800,"administration-und-weiterentwicklung-von-klinischen-systemen","Administration und Weiterentwicklung von klinischen Systemen",[122,150,151,124,30,152,153,154,155,156,157,158,159,160,161,162],"Fehleranalyse","IT","PDMS","PDMS CHAA\u002FAI S","Ixserv","Hybase","POCcelerator","InstaCount","Demis","Epias","DRG Kodierung","MTS","BGA\u002FBZ","Keine Angabe","Berlin","2026-06-03T11:25:55+00:00",{"id":28,"slug":29,"label":30},{"id":168,"slug":169,"title":170,"skills":171,"budget":22,"duration":22,"location":89,"onsitePercent":66,"contractType":25,"foundAt":180,"category":181},10796,"technischer-servicemitarbeiter-humanpharmakologie-mwd","Technischer Servicemitarbeiter Humanpharmakologie (m\u002Fw\u002Fd)",[30,105,172,11,173,174,175,176,177,151,178,179],"Validierung","MS Windows","MS Office","MS SharePoint","Datenmanagementsysteme","EKG-Geräte","Informationsmanagement","Gesundheitswesen","2026-06-03T11:25:26+00:00",{"id":28,"slug":29,"label":30},{"id":183,"slug":184,"title":185,"skills":186,"budget":22,"duration":196,"location":197,"onsitePercent":66,"contractType":142,"foundAt":198,"category":199},10751,"global-clinical-order-manager","Global Clinical Order Manager",[187,188,10,189,190,12,191,192,193,194,195],"Clinical Supply Chain Management","SAP","Veeva","ERP systems","Master Data","German language","English language","Document management","Deviation management","12+ months, Start ASAP (01.08.2026)","Kaiseraugst","2026-06-03T08:41:26+00:00",{"id":28,"slug":29,"label":30},{"id":201,"slug":202,"title":203,"skills":204,"budget":22,"duration":22,"location":213,"onsitePercent":66,"contractType":25,"foundAt":214,"category":215},10743,"rd-quality-manager-senior-auditor-mwd","R&D Quality Manager \u002F Senior Auditor (m\u002Fw\u002Fd)",[205,140,11,12,206,207,208,209,210,211,212,84],"Audits","Qualitätssicherung","FDA","MDR","ICH","Inspektionsmanagement","Qualitätsmanagementsysteme","Lieferantenaudits","Frankfurt am Main","2026-06-03T08:26:45+00:00",{"id":28,"slug":29,"label":30},{"id":217,"slug":218,"title":219,"skills":220,"budget":22,"duration":22,"location":228,"onsitePercent":66,"contractType":229,"foundAt":230,"category":231},7592,"initiativbewerbung-in-der-medizintechnik-mwd","Initiativbewerbung in der Medizintechnik (m\u002Fw\u002Fd)",[30,221,222,223,224,225,226,227],"Qualitätsmanagement","Technische Redaktion","Prozessmanagement","Projektmanagement","Englischkenntnisse","Flexibilität","Kommunikationsfähigkeiten","Kiel","permanent","2026-06-03T02:29:28+00:00",{"id":28,"slug":29,"label":30},{"id":233,"slug":234,"title":235,"skills":236,"budget":22,"duration":22,"location":244,"onsitePercent":24,"contractType":25,"foundAt":245,"category":246},7535,"biomarker-expert-clinical-biosample-operations-mwd","Biomarker Expert - Clinical Biosample Operations (m\u002Fw\u002Fd)",[140,237,238,239,240,241,242,243],"Kommunikationsfähigkeit","Koordination","Logistik","Optimierung","Organisationstalent","Probennahme","Prüfung","Biberach an der Riß","2026-06-02T15:25:31+00:00",{"id":28,"slug":29,"label":30},{"id":248,"slug":249,"title":250,"skills":251,"budget":22,"duration":262,"location":263,"onsitePercent":22,"contractType":142,"foundAt":264,"category":265},7490,"technical-rd-analytical-project-lead","Technical R&D – Analytical Project Lead",[252,253,254,255,256,257,258,259,260,261],"HPLC","UHPLC","Mass Spectrometry","UV detection","Fluorescence","Analytical Chemistry","Chromatography","Project Management","Regulatory Documentation","English","12+ months","Basel","2026-06-02T13:06:41+00:00",{"id":28,"slug":29,"label":30},{"id":267,"slug":268,"title":269,"skills":270,"budget":22,"duration":279,"location":280,"onsitePercent":66,"contractType":25,"foundAt":281,"category":282},7364,"stellv-leitung-der-herstellung","Stellv. Leitung der Herstellung",[271,83,10,272,273,274,12,275,276,277,278],"Pharmatechnik","Aseptische Abfüllung","Batch Record Review","Change Controls","OEE-Systeme","Shopfloor-Management","Lean","OPEX","24 Monate (01.07.2026 - 30.06.2028)","Sachsen","2026-06-01T20:11:17+00:00",{"id":28,"slug":29,"label":30},{"id":284,"slug":285,"title":286,"skills":287,"budget":22,"duration":295,"location":263,"onsitePercent":22,"contractType":142,"foundAt":296,"category":297},7349,"rezept-und-methoden-spezialist","Rezept- und Methoden-Spezialist",[288,289,290,291,10,292,206,293,83,294,188],"Chemie- und Pharmatechnologie","PLS\u002FMES","PCS7","Unicorn Methodenrezeptierung","SOP","MSAT","Siemens","01.09.2026 bis 30.08.2027","2026-06-01T16:12:07+00:00",{"id":28,"slug":29,"label":30}]