[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-msat-engineer-process-management":3,"similar-msat-engineer-process-management":35},{"id":4,"slug":5,"title":6,"skills":7,"budget":19,"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},6167,"msat-engineer-process-management","MSAT Engineer Process Management",[8,9,10,11,12,13,14,15,16,17,18],"Process Development","Product Development","GxP","Compliance","Quality Management","Root Cause Analysis","SAP","Deviation Management","Process Optimization","German","English",null,"12+ months","Rotkreuz",100,"permanent","2026-05-27T07:21:17+00:00",{"id":26,"slug":27,"label":28},14,"medical_tech","Medizintechnik","MSAT Engineer für Prozess- und Produktentwicklung in regulierter Pharmaumgebung. Verantwortlich für Compliance, Qualitätsmanagement, Root Cause Analysis und Prozessoptimierung. Erfordert GxP-Erfahrung und Deutsch\u002FEnglisch-Kenntnisse.","MSAT Engineer Process Management\n\nPermanent\nMSAT Engineer Process Management\nMSAT Engineer Process Management: Process and Product Development \u002F Gxp \u002F Compliance & Quality \u002F Root Cause Analysis \u002F German\u002F English\nBackground:\nAs an MSAT Engineer, you will have a direct impact on and bring value to our patients and customers. Supported by your squad and chapter team, you will start with core compliance tasks-such as non- conformity, change, and document management and continuously grow in your role, taking on increased responsibility for products and processes.\nFor our team in Rotkreuz, we are looking for an experienced engineer to provide technical support for our existing production in daily business as well as for improvement projects within a matrix structure. If you have a background in a regulated environment, a knack for compliance, a big-picture mindset, and thrive in a fast-paced, agile environment where no two days are the same, you will fit right in!\nThe Perfect Candidate:\nThe perfect candidate is a proactive engineer or natural scientist with experience in a highly regulated, GxP-compliant environment and a strong command of both English and German (B2+). They possess a data-driven mindset capable of managing deviations, optimizing production processes, and utilizing SAP to handle non-conformities and quality lifecycles. Ultimately, they are a collaborative, hands-on problem solver who can independently manage stakeholder relationships, maintain technical supplier connections, and ensure complete audit readiness.\nTasks & Responsibilities:\nCompliance & Quality Lifecycle: Manage non-conformities, changes, and documentation in SAP (covering processes, methods, materials, and equipment)\nManage technical relationships with external suppliers and collaborate closely with internal departments-including Logistics, Development, and Quality-to ensure a seamless product supply\nRoot Cause Analysis: Enact structured problem-solving processes to ensure fact-based, data- driven root cause analysis and identify effective countermeasures\nDeviation Management: Support the investigation and processing of deviations within the S&C sensors and reagents production\nProcess Optimization: Adopt and optimize production processes to improve quality, increase yield, and lower costs for your respective products\nControl Loops: Establish, maintain, and continuously improve control loops\nStakeholder Management: Independently communicate with and gather crucial information from various cross-functional stakeholders\nRegulatory Compliance: Ensure strict adherence to existing frameworks, regulatory guidelines, and department-specific requirements.\nAudit Readiness: Prepare for quality audits and successfully represent the Chapter during audit procedures\nMust Haves:\nEducation: A University degree in Natural Sciences or Engineering (e.g., Biotechnology, Biology, Chemistry, Material Science, Mechanical\u002FElectrical Engineering) and\u002For a completed apprenticeship with equivalent professional experience in a related field\nExperience & Mindset: First proven professional experience within a highly regulated environment, backed by a strong quality awareness (GxP mindset)\nEssential knowledge in process and product development\nCollaboration: High motivation for teamwork, excellent communication skills, and the ability to work independently within and across multi-disciplinary teams\nProactivity: Enthusiasm for taking on responsibility and proactively collaborating with a highly engaged team of engineers, operators, QA, and logistics\nHands-on Approach: A genuine interest in learning manufacturing technologies and continuously improving diverse BG&E processes to support our in-house production efficiently\nLanguages: Fluent communication skills in English and a good working knowledge of German (B2+)\nReference Nr.: 924970\nRolle: MSAT Engineer Process Management\nIndustrie:  Pharma\nLocation:  Rotkreuz\nPensum: 100%\nStart: 01.07.2026 (01.09.2026)\nDuration: 12+ months\nDeadline: 02\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\nPermanent\nSkill\nMSAT Engineer Process Management: Process and Product Development \u002F Gxp \u002F Compliance & Quality \u002F Root Cause Analysis \u002F German\u002F English\n\nE-Mail: service@itcag.com","Wir suchen einen erfahrenen MSAT Engineer für Process Management zur technischen Unterstützung unserer bestehenden Produktion sowie für Verbesserungsprojekte in einer Matrixstruktur. In dieser Position haben Sie direkten Einfluss auf Patientenversorgung und Kundenzufriedenheit.\n\nIhre Hauptaufgaben umfassen das Management von Compliance- und Qualitätslebenszyklen, einschließlich der Bearbeitung von Non-Konformitäten, Änderungen und Dokumentation in SAP-Systemen. Sie verwalten technische Beziehungen zu externen Lieferanten und arbeiten eng mit internen Abteilungen wie Logistik, Entwicklung und Qualität zusammen.\n\nEin wesentlicher Schwerpunkt liegt auf der strukturierten Root-Cause-Analyse zur Identifizierung effektiver Gegenmaßnahmen sowie dem Deviation Management bei der Untersuchung und Bearbeitung von Abweichungen in der Sensor- und Reagenzienproduktion. Sie optimieren Produktionsprozesse zur Qualitätsverbesserung, Ertragssteigerung und Kostensenkung.\n\nWir erwarten einen Universitätsabschluss in Naturwissenschaften oder Ingenieurwesen (Biotechnologie, Biologie, Chemie, Materialwissenschaften, Maschinenbau\u002FElektrotechnik) oder eine abgeschlossene Ausbildung mit entsprechender Erfahrung. Erfahrung in hochregulierten, GxP-konformen Umgebungen ist essentiell, ebenso wie sehr gute Deutsch- und Englischkenntnisse (B2+).\n\nSie bringen eine datengetriebene Denkweise mit, können eigenständig Stakeholder-Beziehungen managen und gewährleisten vollständige Audit-Bereitschaft. Als proaktiver, kollaborativer Problemlöser mit praktischer Herangehensweise passen Sie perfekt in unser agiles, schnelllebiges Arbeitsumfeld, in dem kein Tag dem anderen gleicht.","en","924970","https:\u002F\u002Fwww.itcag.com\u002Fjobs\u002Fmsat-engineer-process-management-8089\u002F",{"items":36},[37,59,75,92,108,127,141,154,169,183,196,208,219,233,244],{"id":38,"slug":39,"title":40,"skills":41,"budget":19,"duration":53,"location":54,"onsitePercent":55,"contractType":56,"foundAt":57,"category":58},6186,"senior-qa-compliance-expert-2","Senior QA Compliance Expert",[42,43,11,15,44,45,46,47,48,14,49,50,51,52],"GMP","Quality Assurance","CAPA","Change Control","EU-GMP-Leitfaden","ICH-Richtlinien","TrackWise Digital","S4 HANA","Pharmazie","Chemie","Biologie","11. Mai 2026 bis 31. März 2027","München",20,"contracting","2026-05-27T08:11:21+00:00",{"id":26,"slug":27,"label":28},{"id":60,"slug":61,"title":6,"skills":62,"budget":19,"duration":20,"location":21,"onsitePercent":19,"contractType":72,"foundAt":73,"category":74},6181,"msat-engineer-process-management-2",[63,9,10,11,12,13,14,15,16,64,65,66,67,68,69,70,71],"Process Management","Regulatory Compliance","Audit Readiness","Biotechnology","Biology","Chemistry","Material Science","Mechanical Engineering","Electrical Engineering","temp_work","2026-05-27T07:36:42+00:00",{"id":26,"slug":27,"label":28},{"id":76,"slug":77,"title":78,"skills":79,"budget":19,"duration":19,"location":89,"onsitePercent":22,"contractType":56,"foundAt":90,"category":91},5958,"product-manager-mwd","Product Manager (m\u002Fw\u002Fd)",[80,81,82,83,84,28,85,86,87,88],"Produktmanagement","Marketing","R&D","Vertrieb","Qualitätsmanagement","Wirtschaftswissenschaften","Gesundheitsmanagement","Wettbewerbsanalysen","Kommunikationsfähigkeit","Raubling","2026-05-26T10:27:10+00:00",{"id":26,"slug":27,"label":28},{"id":93,"slug":94,"title":95,"skills":96,"budget":19,"duration":19,"location":105,"onsitePercent":22,"contractType":56,"foundAt":106,"category":107},5511,"hardwareentwickler-produktbetreuung-medizintechnik-mwd","Hardwareentwickler Produktbetreuung Medizintechnik (m\u002Fw\u002Fd)",[97,98,99,100,101,14,102,28,103,104],"Elektrotechnik","Hardware-Design","Messtechnik","Linux","Python","MS Office","Validierung","Analyse","Erlangen","2026-05-22T14:25:48+00:00",{"id":26,"slug":27,"label":28},{"id":109,"slug":110,"title":111,"skills":112,"budget":19,"duration":19,"location":124,"onsitePercent":22,"contractType":56,"foundAt":125,"category":126},5471,"ingenieur-mwd-qualifizierung-und-validierung","Ingenieur (m\u002Fw\u002Fd) Qualifizierung und Validierung",[113,114,115,42,103,116,117,14,118,119,120,121,104,122,123],"Pharmatechnik","Biotechnologie","Bio-Verfahrenstechnik","Qualifizierung","Windchill","FMEA","IQ","OQ","Testspezifikation","Dokumentation","FAT","Mannheim","2026-05-22T13:27:31+00:00",{"id":26,"slug":27,"label":28},{"id":128,"slug":129,"title":130,"skills":131,"budget":19,"duration":136,"location":137,"onsitePercent":138,"contractType":56,"foundAt":139,"category":140},5295,"freiberuflicher-konstrukteur-3d-zeichnungen","Freiberuflicher Konstrukteur - 3D Zeichnungen",[132,133,134,135,28],"SolidWorks","3D-Konstruktion","Maschinenbau","Konstruktionstechnik","Dezember \u002F Januar 2025","Baden-Württemberg",2,"2026-05-21T16:39:19+00:00",{"id":26,"slug":27,"label":28},{"id":142,"slug":143,"title":144,"skills":145,"budget":19,"duration":19,"location":150,"onsitePercent":151,"contractType":23,"foundAt":152,"category":153},5293,"quality-spezialist-mwd-fuer-die-medizintechnik","Quality Spezialist (m\u002Fw\u002Fd) für die Medizintechnik",[146,147,28,148,84,149],"ISO 13485","Qualitätssicherung","CAPA-Maßnahmen","Audits","Karlsruhe",50,"2026-05-21T16:39:08+00:00",{"id":26,"slug":27,"label":28},{"id":155,"slug":156,"title":157,"skills":158,"budget":19,"duration":19,"location":165,"onsitePercent":166,"contractType":23,"foundAt":167,"category":168},5292,"senior-expert-validation-engineer-mwd","(Senior) Expert Validation Engineer (m\u002Fw\u002Fd)",[159,160,161,162,28,163,84,164],"Validation Engineering","Prozessentwicklung","ISO13485","Lean\u002FSix Sigma","Produktionsprozesse","Englisch","Nordrhein-Westfalen",80,"2026-05-21T16:39:01+00:00",{"id":26,"slug":27,"label":28},{"id":170,"slug":171,"title":172,"skills":173,"budget":179,"duration":19,"location":180,"onsitePercent":151,"contractType":23,"foundAt":181,"category":182},5291,"regulatory-affairs-manager-mwd","Regulatory Affairs Manager (m\u002Fw\u002Fd)",[174,175,146,176,28,177,178,11],"Regulatory Affairs","MDR","FDA","Risikomanagement","Change-Control","80.000 EUR p.a.","Bayern","2026-05-21T16:38:54+00:00",{"id":26,"slug":27,"label":28},{"id":184,"slug":185,"title":186,"skills":187,"budget":193,"duration":19,"location":180,"onsitePercent":151,"contractType":23,"foundAt":194,"category":195},5290,"senior-quality-manager-rd","Senior Quality Manager (R&D)",[12,43,188,189,190,191,146,192,177],"Quality Control","MedTech - MDR","MedTech - ISO13485","ISO 14971","EU MDR","100.000 EUR p.a.","2026-05-21T16:38:50+00:00",{"id":26,"slug":27,"label":28},{"id":197,"slug":198,"title":199,"skills":200,"budget":205,"duration":19,"location":180,"onsitePercent":151,"contractType":23,"foundAt":206,"category":207},5289,"quality-manager-mwd","Quality-Manager (m\u002Fw\u002Fd)",[12,43,188,189,190,201,202,203,204,149],"Six-Sigma","LEAN","8D","Qualitätsmanagementsystem","90.000 EUR p.a.","2026-05-21T16:38:43+00:00",{"id":26,"slug":27,"label":28},{"id":209,"slug":210,"title":211,"skills":212,"budget":216,"duration":19,"location":137,"onsitePercent":151,"contractType":23,"foundAt":217,"category":218},5288,"head-of-quality-assurance-mwd","Head of Quality Assurance (m\u002Fw\u002Fd)",[43,12,189,190,213,146,214,84,215],"ISO 9001","Führungserfahrung","Medizinprodukte","110.000 EUR p.a.","2026-05-21T16:38:34+00:00",{"id":26,"slug":27,"label":28},{"id":220,"slug":221,"title":222,"skills":223,"budget":19,"duration":230,"location":137,"onsitePercent":151,"contractType":56,"foundAt":231,"category":232},5287,"freiberuflicher-firmware-entwickler","Freiberuflicher Firmware-Entwickler",[224,225,226,227,228,229,146,28],"Firmware-Entwicklung","C\u002FC++","Embedded Systems","Microcontroller-Programmierung","IEC 60601","IEC 62304","Anfang Januar","2026-05-21T16:38:30+00:00",{"id":26,"slug":27,"label":28},{"id":234,"slug":235,"title":236,"skills":237,"budget":19,"duration":19,"location":241,"onsitePercent":151,"contractType":56,"foundAt":242,"category":243},5201,"technischer-redakteur-konstruktion-solidworks-mwd","Technischer Redakteur Konstruktion \u002F SolidWorks (m\u002Fw\u002Fd)",[132,238,239,28,175,240,102,134],"3D-CAD","Technische Dokumentation","Konstruktion","Lübeck","2026-05-21T15:25:53+00:00",{"id":26,"slug":27,"label":28},{"id":245,"slug":246,"title":247,"skills":248,"budget":19,"duration":258,"location":21,"onsitePercent":259,"contractType":72,"foundAt":260,"category":261},5099,"ivd-product-lead-external-manufacturing","IVD Product Lead External Manufacturing",[249,146,250,251,252,253,254,17,18,255,256,257],"IVD product management","IVDR","FDA 21 CFR","Product specification","Production process specification","Leadership","Engineering","Natural Science","OPEX\u002FCAPEX","12++ months",90,"2026-05-21T12:06:25+00:00",{"id":26,"slug":27,"label":28}]