[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-sustaining-engineer-mwd":3,"similar-sustaining-engineer-mwd":35},{"id":4,"slug":5,"title":6,"skills":7,"budget":20,"duration":21,"location":20,"onsitePercent":22,"contractType":23,"foundAt":24,"category":25,"description":29,"rawText":30,"webTitle":6,"webText":31,"language":32,"projectId":33,"sourceUrl":34},11773,"sustaining-engineer-mwd","Sustaining Engineer (m\u002Fw\u002Fd)",[8,9,10,11,12,13,14,15,16,17,18,19],"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",null,"6 Monate, Start 01.07.2026",0,"contracting","2026-06-09T09:30:21+00:00",{"id":26,"slug":27,"label":28},14,"medical_tech","Medizintechnik","Gesucht wird ein Sustaining Engineer für die Unterstützung von Produkten nach dem Launch. Aufgaben umfassen die Koordination von Design- und Fertigungsänderungen, die Übernahme von Design Authority, die Bewertung von Non Conformance Reports sowie die Gewährleistung von Qualität und regulatorischer Compliance in der Medizintechnik.","Currently we are looking for a 'Sustaining Engineer (m\u002Fw\u002Fd)'.\n\nAuslastung: 70-80%\n\nEinsatzort: Remote\n\nZu Ihren Aufgaben gehören:\n\n+ Provide support to products post launch, coordinating design and manufacturing changes and improvements to meet defined specifications (esp. device and manufacturing requirements)\n\n+ Accept design authority following product launch and release into production. Ensure efficient ongoing transition into ongoing production by appropriate provision of a design authority service to operations and quality. \n\n+ Assessment of Non Conformance Reports (NCRs) and implementation of agreed corrective \u002F preventive actions to maintain regulatory compliance\n\n+ Maintain a strong and current understanding of relevant new product development and manufacturing technologies and their application to medical device design to meet or exceed customer, company and project needs\n\n+ Evaluation and documentation of the feasibility, reliability and risk of concepts and \u002F or prototypes through engineering testing and analysis in order to demonstrate that the product performance, manufacturability, safety and cost are consistent with the customer, regulatory and production requirements\n\n+ Develop timelines, cost and resource estimates for product changes and appraise management of performance against plan, communicating and reporting progress to project management to maintain and track compliance to project schedule\n\n+ Generate, modify and review design history file documentation in compliance with relevant regulatory requirements e.g. Quality System Regulations (QSR), Good Manufacturing Practice (GMP), International Standards Organisation (ISO) and in accordance with company development standards (e.g. PDD, TDP) throughout the product life cycle to ensure the design is fully documented\n\n+ To be responsible for contact to internal and external project sponsors with respect to company products to ensure maintenance of product line and communication and buy in of design change implementation where required\n\n+ Progress vendor activities in agreement with global sourcing relative to communication of specifications, development schedules and tracking in order to obtain components, supplies or equipment to support prototype or product procurement and assembly \n\n+ Deliver manufacturable designs acceptable to operations by applying design for manufacture principles, implement and communicate feedback from manufacturing engineers, external suppliers and other sources to the R&D engineer\n\n+ Ensure a high product and process quality in collaboration with the quality department and all other departments\n\n Anforderungen: \n + Bachelor’s or Master’s degree in Engineering or equivalent professional education \u002F long years of experience\n\n+ Some years of experience in a regulated and highly industrial or scientific engineering design environment\n\n+ Project experience\n\n+ Experience in change management and non conformity handling for medical devices\n\n+ Understanding of a wide range of engineering technologies used in design and manufacturing\n\n+ Strong problem solving skills \n\n+ Understanding interfaces between functions, understanding the needs of others\n\n+ English and German on a professional level needed\n\n+ Strong cross-functional coordination and stakeholder management skills\n\n Zusätzliche Informationen: \n Konnten wir Ihr Interesse wecken? Dann freuen wir uns auf die Zusendung Ihres aussagekräftigen Expertenprofils unter Angabe Ihrer Stundensatzvorstellung. \n\n Projekt-Nr.: \n106367\n\nStellentyp: \nfreiberuflich\n\nEinsatzort: \nRemote\n\nStart: \n01.07.2026\n\nDauer: \n6 Month","Wir suchen einen erfahrenen Sustaining Engineer (m\u002Fw\u002Fd) zur Unterstützung unserer Produktentwicklung im Bereich Medizintechnik. Die Position ist mit einer Auslastung von 70–80 % ausgeschrieben und kann vollständig remote ausgeübt werden.\n\nIn dieser Rolle sind Sie verantwortlich für die technische Betreuung von Produkten nach deren Markteinführung. Sie koordinieren Design- und Fertigungsänderungen, um definierte Spezifikationen zu erfüllen und übernehmen die Designverantwortung während der Produktionsüberleitung. Dabei arbeiten Sie eng mit den Bereichen Betrieb und Qualität zusammen.\n\nZu Ihren Hauptaufgaben gehören die Bewertung von Abweichungsberichten (NCRs) und die Implementierung von Korrektur- und Präventivmaßnahmen zur Gewährleistung der regulatorischen Compliance. Sie evaluieren Konzepte und Prototypen durch technische Tests und Analysen, um Produktleistung, Herstellbarkeit, Sicherheit und Kosteneffizienz nachzuweisen. Darüber hinaus erstellen und pflegen Sie die erforderliche Dokumentation gemäß Quality System Regulations (QSR), Good Manufacturing Practice (GMP) und internationalen Standards (ISO) über den gesamten Produktlebenszyklus.\n\nSie entwickeln Zeitpläne und Ressourcenschätzungen für Produktänderungen, kommunizieren mit internen und externen Stakeholdern und stellen sicher, dass Fertigungsanforderungen erfüllt werden. Die Zusammenarbeit mit Lieferanten, Qualitätssicherung und Fertigungsteams ist zentral für Ihren Erfolg.\n\nWir erwarten einen Bachelor- oder Master-Abschluss in Ingenieurwissenschaften oder gleichwertige berufliche Qualifikation mit mehrjähriger Erfahrung in regulierten, industriellen oder wissenschaftlichen Umgebungen. Projektmanagement-Erfahrung, Kenntnisse im Change Management und in der Abweichungsbehandlung für Medizinprodukte sind erforderlich.","de","106367","https:\u002F\u002Fwww.solcom.de\u002Fde\u002Fprojektportal\u002Fprojektangebote\u002Fsustaining-engineer-m-w-d-106367?utm_source=RSS&utm_medium=RSS&utm_campaign=RSS-Feed",{"items":36},[37,62,79,92,109,127,145,166,177,192,209,222,233,246,258],{"id":38,"slug":39,"title":40,"skills":41,"budget":20,"duration":20,"location":58,"onsitePercent":59,"contractType":23,"foundAt":60,"category":61},11902,"it-anwendungsbetreuer-mwd-2","IT-Anwendungsbetreuer (m\u002Fw\u002Fd)",[42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57],"Fachinformatiker","Medizinische IT-Systeme","AIS","LIS","Jira","ServiceNow","Netzwerktechnik","TCP\u002FIP","Firewalls","VPN","IT-Sicherheit","Microsoft Windows Server","RDP","Citrix","Anwenderschulungen","Dokumentation","Rosenheim",100,"2026-06-09T14:27:06+00:00",{"id":26,"slug":27,"label":28},{"id":63,"slug":64,"title":65,"skills":66,"budget":20,"duration":20,"location":76,"onsitePercent":59,"contractType":23,"foundAt":77,"category":78},11872,"chemielaborant-qualitaetskontrolle-mwd","Chemielaborant Qualitätskontrolle (m\u002Fw\u002Fd)",[67,68,69,70,71,72,73,74,75,57],"Chemielaborant","Qualitätskontrolle","GMP","HPLC","GC","Chromeleon","CTA","PTA","CAPA","Miesbach, Bayern","2026-06-09T13:25:36+00:00",{"id":26,"slug":27,"label":28},{"id":80,"slug":81,"title":82,"skills":83,"budget":20,"duration":20,"location":76,"onsitePercent":59,"contractType":89,"foundAt":90,"category":91},11871,"chemielaborant-lab-technician-mwd-analytical-development","Chemielaborant \u002F Lab Technician (m\u002Fw\u002Fd) Analytical Development",[84,70,71,85,86,72,69,57,87,88],"Analytik","Methodenentwicklung","Validierung analytischer Methoden","Chromatographie","Spektrometrie","permanent","2026-06-09T13:25:25+00:00",{"id":26,"slug":27,"label":28},{"id":93,"slug":94,"title":95,"skills":96,"budget":20,"duration":20,"location":105,"onsitePercent":106,"contractType":23,"foundAt":107,"category":108},11741,"junior-quality-engineer-medical-devices-mwd","Junior Quality Engineer Medical Devices (m\u002Fw\u002Fd)",[97,98,99,100,101,102,103,104],"Audits","Elektrotechnik","Fehleranalyse","Lösungskompetenz","Management","Medical Devices","Deutsch","Englisch","Aschaffenburg",50,"2026-06-09T08:27:29+00:00",{"id":26,"slug":27,"label":28},{"id":110,"slug":111,"title":112,"skills":113,"budget":20,"duration":20,"location":124,"onsitePercent":106,"contractType":23,"foundAt":125,"category":126},11740,"manager-gxp-compliance-mwd","Manager GxP Compliance (m\u002Fw\u002Fd)",[114,115,116,117,75,118,119,120,121,122,123,103,104],"GxP","SOP","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},{"id":128,"slug":129,"title":130,"skills":131,"budget":20,"duration":20,"location":142,"onsitePercent":106,"contractType":23,"foundAt":143,"category":144},11739,"device-engineer-mwd","Device Engineer (m\u002Fw\u002Fd)",[132,57,133,134,135,136,137,138,139,140,141],"Design","Entwicklung","Entwicklungsprozesse","Integration","Kombinationsprodukte","Koordinierung","Planung","Risikomanagement","Umsetzung","Usability","Ingelheim am Rhein","2026-06-09T08:27:13+00:00",{"id":26,"slug":27,"label":28},{"id":146,"slug":147,"title":148,"skills":149,"budget":20,"duration":20,"location":163,"onsitePercent":106,"contractType":23,"foundAt":164,"category":165},11738,"product-lifecycle-engineer-mwd-medizintechnik","Product Lifecycle Engineer (m\u002Fw\u002Fd) Medizintechnik",[150,151,98,133,152,153,154,155,156,28,157,158,159,160,161,162],"Anlagenbau","Einkauf","Feinwerktechnik","Hydraulik","Maschinenbau","Mechanik","Medizinprodukte","Pneumatik","Produktion","QM","Service","Steuerung","Teamfähigkeit","Frankfurt am Main","2026-06-09T08:27:03+00:00",{"id":26,"slug":27,"label":28},{"id":167,"slug":168,"title":169,"skills":170,"budget":20,"duration":20,"location":163,"onsitePercent":106,"contractType":89,"foundAt":175,"category":176},11737,"mitarbeiter-mwd-customer-service-pharma","Mitarbeiter (m\u002Fw\u002Fd) Customer Service Pharma",[171,172,173,174,97,103,104],"Customer Service","SAP","MS Office","Auftragsabwicklung","2026-06-09T08:26:54+00:00",{"id":26,"slug":27,"label":28},{"id":178,"slug":179,"title":180,"skills":181,"budget":20,"duration":20,"location":189,"onsitePercent":106,"contractType":89,"foundAt":190,"category":191},11735,"mitarbeiter-mwd-regulatory-affairs-2","Mitarbeiter (m\u002Fw\u002Fd) Regulatory Affairs",[182,183,184,185,28,186,187,188],"Regulatory Affairs","Technische Dokumentation","MDD","MDR","Qualitätsmanagement","Analyse","Bewertung","Aschaffenburg, Bayern","2026-06-09T08:26:38+00:00",{"id":26,"slug":27,"label":28},{"id":193,"slug":194,"title":195,"skills":196,"budget":20,"duration":20,"location":206,"onsitePercent":106,"contractType":23,"foundAt":207,"category":208},11734,"referent-mwd-substance-product-management","Referent (m\u002Fw\u002Fd) Substance & Product Management",[197,198,199,200,201,202,203,204,205],"Chemie","Biologie","CLP-Verordnung","GHS","SAP-EHS","Datenpflege","REACH","Gefahrstoffeinstufung","Sicherheitsdatenblätter","Hanau, Hessen","2026-06-09T08:26:31+00:00",{"id":26,"slug":27,"label":28},{"id":210,"slug":211,"title":212,"skills":213,"budget":20,"duration":20,"location":163,"onsitePercent":106,"contractType":89,"foundAt":220,"category":221},11733,"junior-projektmanager-mwd-klinische-studien","(Junior) Projektmanager (m\u002Fw\u002Fd) klinische Studien",[214,215,216,217,218,104,219],"Projektmanagement","Projektplanung","Budgetierung","Angebotserstellung","Klinische Studien","Analytisches Denken","2026-06-09T08:26:21+00:00",{"id":26,"slug":27,"label":28},{"id":223,"slug":224,"title":225,"skills":226,"budget":20,"duration":20,"location":206,"onsitePercent":59,"contractType":230,"foundAt":231,"category":232},11732,"chemikant-mwd-pharmazeutische-produktion","Chemikant (m\u002Fw\u002Fd) pharmazeutische Produktion",[227,228,69,229,158,115,104,103],"Chemikant:in Ausbildung","EDV","Kommunikationsfähigkeit","temp_work","2026-06-09T08:26:13+00:00",{"id":26,"slug":27,"label":28},{"id":234,"slug":235,"title":236,"skills":237,"budget":20,"duration":20,"location":163,"onsitePercent":106,"contractType":23,"foundAt":244,"category":245},11731,"junior-qa-manager-mwd-pharma","Junior QA Manager (m\u002Fw\u002Fd) Pharma",[116,238,239,240,241,197,198,117,242,104,243],"cGMP","ISO","JIRA","Pharmazie","LIMS","Koordination","2026-06-09T08:26:03+00:00",{"id":26,"slug":27,"label":28},{"id":247,"slug":248,"title":249,"skills":250,"budget":20,"duration":20,"location":163,"onsitePercent":59,"contractType":23,"foundAt":256,"category":257},11730,"mitarbeiter-mwd-quality-operations-pharma","Mitarbeiter (m\u002Fw\u002Fd) Quality Operations Pharma",[70,71,251,252,69,253,254,104,255],"Methodenvalidierung","Instrumentelle Analytik","Stabilitätsstudien","MS-Office","SOP-Erstellung","2026-06-09T08:25:54+00:00",{"id":26,"slug":27,"label":28},{"id":259,"slug":260,"title":261,"skills":262,"budget":20,"duration":20,"location":163,"onsitePercent":59,"contractType":23,"foundAt":268,"category":269},11729,"servicetechniker-mwd-medizintechnik","Servicetechniker (m\u002Fw\u002Fd) Medizintechnik",[28,263,156,173,264,265,104,266,267],"Technischer Service","Excel","Lotus Notes","Beratung","Kommunikation","2026-06-09T08:25:45+00:00",{"id":26,"slug":27,"label":28}]