[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-senior-instrument-integration-engineer":3,"similar-senior-instrument-integration-engineer":33,"matching-freelancers-senior-instrument-integration-engineer":233},{"id":4,"slug":5,"title":6,"description":7,"skills":8,"budget":18,"duration":19,"location":20,"onsitePercent":21,"contractType":22,"foundAt":23,"category":24,"rawText":28,"webTitle":6,"webText":29,"language":30,"projectId":31,"sourceUrl":32},17311,"senior-instrument-integration-engineer","Senior Instrument Integration Engineer","Senior Instrument Integration Engineer für Medizingeräteentwicklung mit Fokus auf Hardware-Software-Integration, Datenanalyse und statistische Methoden. Führungsrolle über den gesamten Instrumentenlebenszyklus von Konzept bis Markteinführung. Mindestens 5 Jahre Erfahrung in der Medizingeräteentwicklung erforderlich.",[9,10,11,12,13,14,15,16,17],"Systems Engineering","Medical Device Development","Data Analysis","Statistical Methods","Design of Experiments (DoE)","Hardware-Software Integration","Technical Leadership","Problem Solving","English",null,"12+ months","Rotkreuz",100,"temp_work","2026-07-01T10:51:28+00:00",{"id":25,"slug":26,"label":27},14,"medical_tech","Medizintechnik","Senior Instrument Integration Engineer\n\ntemporary\nSenior Instrument Integration Engineer\nSenior Instrument Integration Engineer: Medical Device \u002F Data Analysis \u002F Evaluation \u002F Instrument Development \u002F statistical methods \u002F  English\nBackground:\nAs an Instrument Integration Engineer, you take on a key role in ensuring the harmonious integration of hardware and software components to guarantee optimal instrument functionality. You accompany the entire instrument lifecycle-from the concept phase through development and validation to market launch. In this position, you contribute significantly to ensuring that all system components work together smoothly and, through your expertise, ensure that the final product meets the highest quality and performance standards. Your work forms the basis for the successful realization of modern diagnostic and analysis instruments that are indispensable in a variety of applications and industries.\nThe perfect candidate possesses the ability to work independently as well as in a team, combined with a spirit of innovation and pronounced problem-solving skills.\nTasks & Responsibilities:\nIntegration Leadership: Lead the integration of hardware and software components, driving activities throughout the entire instrument lifecycle. Act as the primary technical point of contact, ensuring seamless functionality and alignment with project goals.\nMethodological Planning: Independently design, plan, execute, and document development activities. Utilize advanced methodologies (e.g., Design of Experiments\u002FDoE) to optimize experimental planning and coordination.\nTechnical Problem Solving: Lead interdisciplinary troubleshooting and root cause analysis. Provide expert technical input to resolve complex issues with high autonomy.\nConcept & Strategy: Contribute to product concepts, system requirements, and architecture design, ensuring alignment with project goals and diagnostic standards.\nData-Driven Decision Making: Perform in-depth analysis of test results using statistical methods. Interpret trends and correlations to generate reports that drive strategic decision-making.\nSME & Mentorship: Act as the Subject Matter Expert (SME) for integration. Provide supervision and guidance to team members, foster open communication, and represent the project in internal and external R&D meetings.\nInnovation: Actively contribute to innovation efforts, including intellectual property creation and the continuous improvement of quality management and integration processes.\nMust Haves:\nA Bachelor’s or Master’s degree, or a Swiss Federal Diploma from a University of Applied Sciences (FH) or College of Higher Education (HF) in a scientific or technical field (e.g., Biotechnology, Biomedical Engineering), or equivalent experience\nMinimum of 5 years of professional experience in medical device development\nStrong understanding of Systems Engineering principles and their application in instrument development\nProven proficiency in data analysis, evaluation, and the application of statistical methods\nFluent in English (written and spoken); German is a plus\nHigh level of autonomy, proactive problem-solving, strong leadership\u002Fmentorship capabilities, and a commitment to collaborative, cross-functional teamwork\nNice to haves:\nTools \u002F IT knowledge is an advantage but not a must: Python, Jira, Retina\nReference Nr.: 925054\nRolle: Senior Instrument Integration Engineer\nIndustrie: Pharma\nLocation: Rotkreuz\nPensum: 100%\nStart: ASAP (01.09.2026)\nDuration: 12+ months\nDeadline: 07\u002F06\u002F2026\nIf this position has piqued your interest, please send us your complete resume. If this position does not quite match your profile and you would like to receive other positions directly, you can also send us your resume via this ad or to jobs[at]itcag[dot]com.\nContact us for more information about our company, our positions, or our attractive payroll-only program: +41 41 760 77 01.\nAbout us:\nITech Consult is an ISO 9001:2015-certified Swiss company with offices in Germany and Ireland. ITech Consult specializes in placing highly qualified candidates for temporary staffing in the fields of IT, life sciences, and engineering. We offer temporary staffing and payroll services. This is free of charge for our candidates, and we do not charge any additional fees for payroll services.\nApply Now\n\nIndustry\nPharmaceuticals\nLocation\nZug\nType\ntemporary\n\nE-Mail: service@itcag.com","Wir suchen einen erfahrenen Senior Instrument Integration Engineer zur Unterstützung unseres Entwicklungsteams. In dieser Schlüsselrolle verantworten Sie die nahtlose Integration von Hardware- und Softwarekomponenten über den gesamten Instrumentenlebenszyklus – von der Konzeptphase über Entwicklung und Validierung bis zur Markteinführung.\n\nAls technischer Ansprechpartner führen Sie die Integrationsprozesse an und stellen sicher, dass alle Systemkomponenten optimal zusammenwirken. Sie planen und dokumentieren Entwicklungsaktivitäten eigenverantwortlich und nutzen fortgeschrittene Methoden wie Design of Experiments (DoE) zur Optimierung. Durch interdisziplinäre Problemlösung und Ursachenanalyse tragen Sie zur Behebung komplexer technischer Herausforderungen bei.\n\nIhre Aufgaben umfassen die Mitwirkung an Produktkonzepten, Systemanforderungen und Architekturdesign sowie die datengestützte Analyse von Testergebnissen mittels statistischer Methoden. Als Subject Matter Expert für Integration unterstützen Sie Teamkollegen, fördern offene Kommunikation und vertreten das Projekt in internen und externen Meetings. Darüber hinaus tragen Sie aktiv zu Innovationsinitiativen und zur kontinuierlichen Verbesserung von Qualitätsmanagementsystemen bei.\n\nGefordert werden ein Bachelor- oder Masterabschluss in einem naturwissenschaftlichen oder technischen Fachbereich (z. B. Biotechnologie, Biomedizintechnik) oder gleichwertige Erfahrung, mindestens 5 Jahre Berufserfahrung in der Medizinprodukte-Entwicklung, fundierte Kenntnisse in Systems Engineering sowie nachgewiesene Kompetenz in Datenanalyse und Evaluationsmethoden. Fließende Englischkenntnisse sind erforderlich. Idealerweise bringen Sie Unabhängigkeit, Teamfähigkeit, Innovationsgeist und ausgeprägte Problemlösungsfähigkeiten mit.","en","925054","https:\u002F\u002Fwww.itcag.com\u002Fjobs\u002Fsenior-instrument-integration-engineer-8184\u002F",{"items":34},[35,55,78,97,114,128,142,152,162,172,182,193,203,213,222],{"id":36,"slug":37,"title":38,"description":39,"skills":40,"budget":18,"duration":18,"location":52,"onsitePercent":21,"contractType":22,"foundAt":53,"category":54},17317,"qualitaetssicherungsmitarbeiter-produktion-mwd","Qualitätssicherungsmitarbeiter Produktion (m\u002Fw\u002Fd)","Qualitätssicherungsmitarbeiter für die Medizintechnik-Produktion in Hamburg. Aufgaben umfassen Qualitätsprüfungen, Einhaltung von Standards, Identifikation von Abweichungen und Dokumentation. Erforderlich: technische Ausbildung, 2+ Jahre Berufserfahrung, Kenntnisse in QS und SAP QM.",[41,27,42,43,44,45,46,47,48,49,50,51],"Qualitätssicherung","Fertigung","Produktion","SAP QM","ERP","Prüfmittel","Messtechnik","Technische Zeichnungen","Root Cause Analysis","Dokumentation","Prozessoptimierung","Hamburg","2026-07-01T11:25:36+00:00",{"id":25,"slug":26,"label":27},{"id":56,"slug":57,"title":58,"description":59,"skills":60,"budget":18,"duration":18,"location":73,"onsitePercent":74,"contractType":75,"foundAt":76,"category":77},17275,"complaint-management-officer-pharma-mwd","Complaint Management Officer Pharma (m\u002Fw\u002Fd)","Verantwortung für Reklamationsmanagement und Bearbeitung qualitätsrelevanter Kundenreklamationen in der Pharmabranche. Analyse von Reklamations- und Qualitätsdaten, Koordination von Produktrückrufen und Zusammenarbeit mit Behörden sowie internationalen Geschäftspartnern.",[61,41,62,63,64,65,66,67,68,69,70,71,72],"Reklamationsmanagement","GMP","GDP","GVP","Pharmazie","Chemie","Biologie","Analyse","Management","Koordination","Deutsch","Englisch","Frankfurt",50,"contracting","2026-07-01T09:26:22+00:00",{"id":25,"slug":26,"label":27},{"id":79,"slug":80,"title":81,"description":82,"skills":83,"budget":18,"duration":93,"location":94,"onsitePercent":21,"contractType":22,"foundAt":95,"category":96},17265,"qualifizierungsingenieur","Qualifizierungsingenieur","Qualifizierungsingenieur für temperatur-kontrollierte Anlagen\u002FRäume bei großem Pharmaunternehmen in Basel. Aufgaben umfassen Erstellung von Qualifizierungsdokumenten, GMP-konforme Dokumentation, Qualifizierungsreviews und Unterstützung bei Inspektionen\u002FAudits. Erforderlich: Abschluss in Automation\u002FMaschinenbau\u002FVerfahrenstechnik\u002FPharmatechnik\u002FBiotechnologie, 3+ Jahre Erfahrung in Anlagenqualifizierung, GMP-Kenntnisse, sehr gute Deutsch- und gute Englischkenntnisse.",[84,62,85,86,87,88,89,90,71,72,91,92],"Anlagenqualifizierung","CSV","Qualifizierungsdokumentation","Validierungssoftware","Verfahrenstechnik","Pharmatechnik","Biotechnologie","MS Office","Automation","12+ Monate","Basel, Kaiseraugst","2026-07-01T08:36:51+00:00",{"id":25,"slug":26,"label":27},{"id":98,"slug":99,"title":100,"description":101,"skills":102,"budget":18,"duration":110,"location":20,"onsitePercent":21,"contractType":111,"foundAt":112,"category":113},17252,"operator-reagents-operations-mwd","Operator Reagents Operations (m\u002Fw\u002Fd)","Für Roche Diagnostics International AG in Rotkreuz wird ein Operator Reagents Operations (m\u002Fw\u002Fd) für die Assemblierung und Testung von Fluid Packs an halbautomatischen Anlagen im 2-Schicht-Betrieb gesucht. Die Rolle umfasst die selbstständige Bedienung und Überwachung von Produktionsanlagen unter Einhaltung von GMP- und Qualitätsvorschriften. Erforderlich sind eine abgeschlossene Berufsausbildung, sehr gute Deutschkenntnisse (B2) und Erfahrung in der Produktion.",[103,104,105,106,107,108,109],"Bedienung von Produktionsanlagen","Montage und Assemblierung","GMP-Kenntnisse","Qualitätskontrolle","Deutsch B2","Zuverlässige Arbeitsweise","Teamfähigkeit","12 Monate+","permanent","2026-07-01T07:51:16+00:00",{"id":25,"slug":26,"label":27},{"id":115,"slug":116,"title":117,"description":118,"skills":119,"budget":18,"duration":124,"location":18,"onsitePercent":125,"contractType":75,"foundAt":126,"category":127},17227,"senior-urs-engineer-mwd-containment-gmp","Senior URS Engineer (m\u002Fw\u002Fd) – Containment \u002F GMP","Erstellung von URS-Dokumenten für Containment-Anlagen im GMP-Umfeld mit Fokus auf Prozess- und Funktionsanforderungen unter Berücksichtigung regulatorischer Vorgaben. Abstimmung mit Engineering und Qualifizierung sowie Unterstützung bei technischer Angebotsbewertung.",[120,62,121,122,123,71,72],"URS-Dokumentation","Containment","Pharmaanlagen","FDA-Regulatorik","2 Monate mit Option auf Verlängerung, Start ab 24.07.2026",20,"2026-06-30T16:45:46+00:00",{"id":25,"slug":26,"label":27},{"id":129,"slug":130,"title":131,"description":132,"skills":133,"budget":18,"duration":18,"location":73,"onsitePercent":21,"contractType":22,"foundAt":140,"category":141},17193,"produktionshelfer-pharma-mwd","Produktionshelfer Pharma (m\u002Fw\u002Fd)","Montage und Verpackung von Autoinjektoren, Etikettierung pharmazeutischer Produkte und Materialzufuhr an Fertigungsanlagen im Schichtbetrieb. Durchführung von Produktionshelfertätigkeiten nach GMP-Richtlinien mit Fehlererkennung und Störungsbehebung an Maschinen.",[66,50,134,62,135,136,137,138,43,139],"Fertigungsanlagen","Hygiene","MES","Montage","Pharma","SAP","2026-06-30T15:25:46+00:00",{"id":25,"slug":26,"label":27},{"id":143,"slug":144,"title":145,"description":146,"skills":147,"budget":148,"duration":18,"location":149,"onsitePercent":74,"contractType":111,"foundAt":150,"category":151},17170,"specialist-vigilance-mwd","Specialist Vigilance (m\u002Fw\u002Fd)","Specialist Vigilance Position in Bad Homburg vor der Höhe, Hessen. Festanstellung in Vollzeit mit hybridem Arbeitsmodell. Jahresgehalt zwischen 60.000 und 82.000 EUR bei 37,5 Stunden pro Woche.",[],"60.000-82.000 EUR\u002FJahr","Bad Homburg vor der Höhe","2026-06-30T14:27:49+00:00",{"id":25,"slug":26,"label":27},{"id":153,"slug":154,"title":155,"description":156,"skills":157,"budget":158,"duration":18,"location":159,"onsitePercent":74,"contractType":111,"foundAt":160,"category":161},17163,"konstrukteur-mwd-healthcare","Konstrukteur (m\u002Fw\u002Fd) – Healthcare","Konstrukteur im Healthcare-Bereich in Schwelm, Nordrhein-Westfalen gesucht. Festanstellung in Vollzeit mit hybridem Arbeitsmodell. Gehalt 52.000–63.000 EUR pro Jahr plus Urlaub und Weihnachtsgeld.",[],"52.000–63.000 EUR\u002FJahr","Schwelm","2026-06-30T14:27:01+00:00",{"id":25,"slug":26,"label":27},{"id":163,"slug":164,"title":165,"description":166,"skills":167,"budget":169,"duration":18,"location":52,"onsitePercent":74,"contractType":111,"foundAt":170,"category":171},17142,"laborspezialist-mwd-gmp","Laborspezialist (m\u002Fw\u002Fd) GMP","Laborspezialist (m\u002Fw\u002Fd) mit GMP-Kenntnissen in Hamburg gesucht. Festanstellung in Vollzeit im Hybrid-Arbeitsmodell. Gehalt zwischen 40.000 und 55.000 EUR pro Jahr.",[62,168],"Laborarbeit","40.000-55.000 EUR\u002FJahr","2026-06-30T14:25:20+00:00",{"id":25,"slug":26,"label":27},{"id":173,"slug":174,"title":175,"description":176,"skills":177,"budget":178,"duration":18,"location":179,"onsitePercent":74,"contractType":111,"foundAt":180,"category":181},17141,"product-formulation-specialist-mwd-nutraceuticals","Product & Formulation Specialist (m\u002Fw\u002Fd) Nutraceuticals","Festanstellung als Product & Formulation Specialist im Bereich Nutraceuticals in Wunstorf, Niedersachsen. Hybrid-Arbeitsmodell mit Vollzeitposition. Gehalt zwischen 60.000 und 75.000 EUR pro Jahr.",[],"60.000-75.000 EUR\u002FJahr","Wunstorf, Niedersachsen","2026-06-30T14:25:12+00:00",{"id":25,"slug":26,"label":27},{"id":183,"slug":184,"title":185,"description":186,"skills":187,"budget":189,"duration":18,"location":190,"onsitePercent":21,"contractType":111,"foundAt":191,"category":192},17131,"cnc-mechaniker-medizintechnik-mwd-2","CNC-Mechaniker Medizintechnik (m\u002Fw\u002Fd)","CNC-Mechaniker für Medizintechnik in Vollzeitposition bei Neu Wulmstorf, Niedersachsen. Festanstellung mit Jahresgehalt von 37.000–55.000 EUR. Office-basierte Tätigkeit.",[188,27],"CNC-Bearbeitung","37.000–55.000 EUR\u002FJahr","Neu Wulmstorf","2026-06-30T14:23:52+00:00",{"id":25,"slug":26,"label":27},{"id":194,"slug":195,"title":196,"description":197,"skills":198,"budget":199,"duration":18,"location":200,"onsitePercent":74,"contractType":111,"foundAt":201,"category":202},17130,"qualitaetskontrolle-mwd-healthcare-2","Qualitätskontrolle (m\u002Fw\u002Fd) – Healthcare","Qualitätskontrolle-Position im Healthcare-Bereich in Neu Wulmstorf, Niedersachsen. Vollzeitstelle mit Hybrid-Arbeitsmodell. Jahresgehalt zwischen 40.000 und 55.500 EUR.",[],"40.000-55.500 EUR\u002FJahr","Neu Wulmstorf, Niedersachsen","2026-06-30T14:23:43+00:00",{"id":25,"slug":26,"label":27},{"id":204,"slug":205,"title":206,"description":207,"skills":208,"budget":209,"duration":18,"location":210,"onsitePercent":74,"contractType":111,"foundAt":211,"category":212},17129,"prozessingenieur-mwd-2","Prozessingenieur (m\u002Fw\u002Fd)","Prozessingenieur-Position in Dotternhausen, Baden-Württemberg. Festanstellung in Vollzeit mit hybridem Arbeitsmodell. Gehalt zwischen 70.000 und 95.000 EUR pro Jahr.",[],"70.000-95.000 EUR\u002FJahr","Dotternhausen","2026-06-30T14:23:35+00:00",{"id":25,"slug":26,"label":27},{"id":214,"slug":215,"title":216,"description":217,"skills":218,"budget":209,"duration":18,"location":219,"onsitePercent":74,"contractType":111,"foundAt":220,"category":221},17124,"product-development-lead-mwd-nutraceuticals","Product Development Lead (m\u002Fw\u002Fd) Nutraceuticals","Festanstellung als Product Development Lead im Bereich Nutraceuticals in Gehrden, Niedersachsen. Vollzeitposition mit hybridem Arbeitsmodell. Jahresgehalt zwischen 70.000 und 95.000 EUR.",[],"Gehrden, Niedersachsen","2026-06-30T14:22:52+00:00",{"id":25,"slug":26,"label":27},{"id":223,"slug":224,"title":225,"description":226,"skills":227,"budget":18,"duration":18,"location":73,"onsitePercent":21,"contractType":75,"foundAt":231,"category":232},17029,"qc-analytical-expert-mwd","QC Analytical Expert (m\u002Fw\u002Fd)","Durchführung und GMP-konforme Dokumentation chemisch-physikalischer Qualitätsprüfungen von Wirkstoffen und Fertigarzneimitteln. Betreuung und Weiterentwicklung von Qualitätssystemen sowie Planung und Auswertung von Methodenvalidierungen. Unterstützung bei Audits, Inspektionen und Einhaltung regulatorischer Vorgaben.",[62,106,228,66,65,90,229,50,230,91,72],"Methodenvalidierung","Change Control","Audits","2026-06-30T10:26:47+00:00",{"id":25,"slug":26,"label":27},{"items":234},[]]