[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-msat-process-specialist":3,"similar-msat-process-specialist":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},12415,"msat-process-specialist","MSAT Process Specialist",[8,9,10,11,12,13,14,15,16,17,18],"Process Engineering","Technical Process Development","Process Validation","Technology Transfer","Pharmaceutical Quality Systems","Regulatory Submission","CAPA Management","Risk Management","Communication Skills","English fluency","German (advantage)",null,"6+ months","Basel",90,"temp_work","2026-06-11T10:51:11+00:00",{"id":26,"slug":27,"label":28},14,"medical_tech","Medizintechnik","Gesucht wird ein hochqualifizierter MSAT Process Specialist für ein großes Pharmaunternehmen in Basel. Die Rolle umfasst Prozessentwicklung, Compliance, CAPA und Process Engineering mit Fokus auf Industrialisierung und technische Unterstützung im Produktionsnetzwerk. Mindestens 3 Jahre Erfahrung in Prozessengineering, technischer Prozessentwicklung oder Technologietransfer erforderlich.","MSAT Process Specialist\n\ntemporary\nMSAT Process Specialist\nMSAT Process Specialist: Process Development \u002FMSAT \u002F Compliance \u002F CAPA\u002F Process Engineering Process Scientists \u002F TPC \u002F DSTS, and DPTC) \u002F Manufacturing Site \u002F English\nProject:\nFor our customer a big pharmaceutical company in Basel, we are looking for a highly qualified\nMSAT Process Specialist\nBackground:\nDrug Product MSAT Process Specialist is the first-line connector between PTT global MSAT and our internal and external manufacturing sites. In this role you will be responsible for enabling successful process industrialization by supporting during TRs, ERs, PPQ and launch phase, driving systematic process improvements according to product and portfolio needs, owning second source transfers and providing hands-on second-level commercial product support in case of investigations, CAPAs and troubleshooting in close partnership with local MSAT functions and PTT`s Product Stewards and Product Technical Leads. This is a highly specialized and execution-obsessed process expert role that provides technical support across the site network on both product-specic and multi-product needs. In this role, you may be asked to represent the technological needs of the network in key technical\ngovernance forums and senior stakeholder interactions, including the Global MSAT Leadership Team, PTT capability teams (e.g., Process Scientists, TPC, DSTS, and DPTC), Manufacturing Site Leadership Teams, CDMO Organization Leadership Teams, TPM Enabling Teams, PT Strategy and PTD-LTs.\nThe Perfect Candidate possesses a degree in Chemical, Biochemical Engineering, or a related field, coupled with a minimum of three years of relevant industrial experience. This experience should be in platform-specific areas such as technical process development, process engineering, or manufacturing operations (e.g., DS Bio, DP SM). Essential Experience and Knowledge: Demonstrated experience (3+ years) in process engineering, technical process development, process validation, or technology transfer. Strong familiarity with pharmaceutical quality systems and industry-wide guidelines relevant to platform-specific process development and manufacturing. Proven knowledge of regulatory submission and health authority requirements. Expertise with platform-specific technology, processes, and equipment. Key Competency: Outstanding communicator, with advanced verbal and written communication skills, including the ability to effectively interact with senior leadership.\nTasks & Responsibilities:\n* Support Product Technical Leads and Product Stewards to ensure process industrialization (e.g. facility t and manufacturability, PPQ support as needed, etc…), coordinate and execute process gap assessments, integrating identified risks into the risk log and developing mitigation strategies.\n* Drive systematic process and continuous technical product health and supply improvements based on insights, including second supply and change source strategies\n* Execute validated state support activities, such as WCB shipment, sample coordination for additional studies, and non-routine sampling planning, and respond to evolving conditions to ensure compliance (e.g. VICs, RCAs, etc.)\n* Provide technical expertise to technical runs and engineering runs, internally and externally\n* Provide hands-on second-level support (commercial product support) in the case of investigations, CAPAs and troubleshoot in close partnership with the internal and external manufacturing network\n* lead non-product specific RCAs and investigations on behalf of the internal manufacturing network\n* Leverage the pilot plant team to enable real-life and scaled experimentation to support process related projects (including validation studies) as well as process transfer to manufacturing sites\n* Ensure the implementation of network initiatives aligned and prioritized with manufacturing site plans\n* Incorporate\u002Fexecute portfolio-wide impacting aspects (e.g. direct material changes; Health Authority requirements; etc.)\n* Perform defined technical Product Life Cycle activities to ensure product robustness from development through divestment\n* Execute process-related mitigation of complaints and deployment of CAPAs across multiple sites or products\n* Drive technical sustainability improvements for product, process, and technology, including digital advancements\n* Closely collaborates with global and site functions (sometimes external) and leadership, including other gMSAT and PTT teams, particularly close partnership with E2E Product Technical Leads and DS or DP Technical Leads\n* Serve as a digital enabler translating business needs to digital strategy and digital product development teams\nMust Haves:\n* B.S. or M.S. degree in Chemical, Biochemical Engineering, or related discipline with 3+ years of relevant industrial experience in platform specific technical process development, process engineering or manufacturing operations (e.g. DS Bio, DP SM, etc.), PhD can be of advantage\n* Technical Expertise: 3- years demonstrated experience in process engineering, technical process development, process validation or technology transfer, with pharmaceutical quality systems and industry-wide guidelines pertinent to platform specific process development and manufacturing, with regulatory submission and health authority requirements, and with platform specific technology, processes and equipment\n* Outstanding Communicator: Advanced level of verbal and written communication skills (e.g., ability to define and articulate team deliverables) incl. towards senior leadership, a fluency in English is required, German is of advantage\n* 10% travel required\nReference Nr.: 924882\nRole: MSAT Process Specialist\nIndustrie: Pharma\nWorkplace: Basel\nPensum: 80 – 100%\nStart: ASAP(Latest start date 01.10.2026)\nDuration: 6++ months\nDeadline :18.06.2026\nIf you are interested in this position, please send us your complete dossier. If this position does not fit your profile and you wish to be considered for another position directly, you can also send us your dossier 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 programme: +41 41 760 77 01.\nAbout us: ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering.\nWe offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.\nApply Now\n\nIndustry\nPharmaceuticals\nLocation\nBasel-Stadt\nType\ntemporary\n\nE-Mail: service@itcag.com","Für ein führendes Pharmaunternehmen suchen wir einen erfahrenen MSAT Process Specialist zur Unterstützung unserer Produktionsstätten.\n\nIn dieser Rolle fungieren Sie als zentrale Schnittstelle zwischen globalen Prozessentwicklungsteams und internen sowie externen Produktionsstandorten. Sie verantworten die erfolgreiche Industrialisierung von Arzneimittelprozessen und unterstützen aktiv bei Technologietransfers, Validierungen und Markteinführungsphasen.\n\nIhre Aufgaben umfassen:\n- Unterstützung bei der Prozessindustrialisierung und Machbarkeitsbewertungen\n- Durchführung von Prozesslückenanalysen und Entwicklung von Risikominderungsstrategien\n- Systematische Prozessverbesserungen basierend auf Produktanforderungen\n- Technische Unterstützung bei Untersuchungen, Abweichungsbearbeitungen und Troubleshooting\n- Koordination von Technologietransfers und Sekundärquellen-Strategien\n- Vertretung technischer Anforderungen in Governance-Foren und bei Stakeholder-Interaktionen\n\nIhr Profil:\n- Abschluss in Chemie-, Biochemie-Ingenieurwesen oder verwandtem Fachgebiet\n- Mindestens 3 Jahre Erfahrung in Prozessingenieurwesen, technischer Prozessentwicklung oder Produktionsbetrieb\n- Fundierte Kenntnisse pharmazeutischer Qualitätssysteme und Branchenrichtlinien\n- Nachgewiesene Expertise in Prozessvalidierung und Technologietransfer\n- Vertrautheit mit regulatorischen Anforderungen und Behördenvorgaben\n- Ausgezeichnete Kommunikationsfähigkeiten in Wort und Schrift\n- Fähigkeit zur Zusammenarbeit mit Führungskräften auf allen Ebenen\n\nDies ist eine spezialisierte Position für einen prozessorientierten Experten mit hohem Anspruch an Umsetzungsqualität. Die Stelle bietet die Möglichkeit, technische Innovationen in einem globalen Netzwerk voranzutreiben.","en","924882","https:\u002F\u002Fwww.itcag.com\u002Fjobs\u002Fmsat-process-specialist-8137\u002F",{"items":36},[37,53,74,87,103,119,136,151,173,193,208,231,246,259,278],{"id":38,"slug":39,"title":40,"skills":41,"budget":19,"duration":19,"location":48,"onsitePercent":49,"contractType":50,"foundAt":51,"category":52},12404,"mechatroniker-medizintechnik-mwd","Mechatroniker Medizintechnik (m\u002Fw\u002Fd)",[42,43,44,45,46,28,47],"Mechatronik","Montage","Systemintegration","Elektrische Prüfungen","Industriemechanik","Bestandsmanagement","Bayreuth",100,"contracting","2026-06-11T10:25:42+00:00",{"id":26,"slug":27,"label":28},{"id":54,"slug":55,"title":56,"skills":57,"budget":19,"duration":19,"location":70,"onsitePercent":71,"contractType":50,"foundAt":72,"category":73},12375,"dokumentationsmanager-post-market-surveillance-mwd","Dokumentationsmanager Post-Market Surveillance (m\u002Fw\u002Fd)",[58,59,60,61,62,63,64,65,66,67,68,69],"Pharmakovigilanz","MDR","IMDRF-Codierung","TrackWise","Veeva Vault","MS Office","SharePoint","SAP","Datenbanken","Literaturrecherche","Risikomanagement","Dokumentation","Wehrheim, Hessen",0,"2026-06-11T09:31:18+00:00",{"id":26,"slug":27,"label":28},{"id":75,"slug":76,"title":77,"skills":78,"budget":19,"duration":19,"location":84,"onsitePercent":49,"contractType":23,"foundAt":85,"category":86},12321,"produktionsmitarbeiter-logistik-pharma-mwd","Produktionsmitarbeiter Logistik Pharma (m\u002Fw\u002Fd)",[79,80,81,82,83,69],"Lagerlogistik","Logistik","Pharma","Produktion","Reinraum","Uetersen, Schleswig-Holstein","2026-06-11T07:26:37+00:00",{"id":26,"slug":27,"label":28},{"id":88,"slug":89,"title":90,"skills":91,"budget":19,"duration":98,"location":99,"onsitePercent":100,"contractType":50,"foundAt":101,"category":102},12301,"projektmanagement-pharma-anlagen","Projektmanagement Pharma-Anlagen",[92,93,94,65,95,81,69,96,97],"Projektkoordination","Instandhaltung","GMP","Projektmanagement","Wartung","Planung","4 Monate, ab sofort","Marburg",50,"2026-06-11T02:27:41+00:00",{"id":26,"slug":27,"label":28},{"id":104,"slug":105,"title":106,"skills":107,"budget":19,"duration":19,"location":116,"onsitePercent":49,"contractType":23,"foundAt":117,"category":118},12222,"mitarbeiter-qualitaetskontrolle-visuelle-pruefung-mwd","Mitarbeiter Qualitätskontrolle Visuelle Prüfung (m\u002Fw\u002Fd)",[108,94,109,110,111,112,82,113,114,115],"Arzneimittel","Inspektion","Labor","Lebensmittel","Pharmazie","Prüfung","Prüftechnik","SOP","Biberach an der Riß, Baden-Württemberg","2026-06-10T15:27:48+00:00",{"id":26,"slug":27,"label":28},{"id":120,"slug":121,"title":122,"skills":123,"budget":19,"duration":19,"location":133,"onsitePercent":49,"contractType":50,"foundAt":134,"category":135},12221,"technical-assistant-pharma-mwd","Technical Assistant Pharma (m\u002Fw\u002Fd)",[94,124,125,126,127,128,129,130,63,131,132],"Laboranalytik","Analyseverfahren","GelClot","UV-Scan","TOC-Analytik","Spektralphotometer","Methodenvalidierung","Deutsch","Englisch","Biberach an der Riß","2026-06-10T15:27:29+00:00",{"id":26,"slug":27,"label":28},{"id":137,"slug":138,"title":139,"skills":140,"budget":19,"duration":19,"location":148,"onsitePercent":49,"contractType":50,"foundAt":149,"category":150},12217,"produktkoordinator-pharma-mwd","Produktkoordinator Pharma (m\u002Fw\u002Fd)",[112,141,142,94,143,144,145,146,147,131,132],"Chemie","Biologie","MyLIMS","MS-Office","Qualitätsmanagement","Laborkoordination","Dokumentenerstellung","Biberach, Baden-Württemberg","2026-06-10T15:26:49+00:00",{"id":26,"slug":27,"label":28},{"id":152,"slug":153,"title":154,"skills":155,"budget":19,"duration":169,"location":170,"onsitePercent":49,"contractType":23,"foundAt":171,"category":172},12101,"hardware-product-owner-development-engineer","Hardware Product Owner & Development Engineer",[156,157,158,159,160,161,162,163,164,165,166,167,132,131,28,168],"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":26,"slug":27,"label":28},{"id":174,"slug":175,"title":176,"skills":177,"budget":19,"duration":190,"location":170,"onsitePercent":49,"contractType":23,"foundAt":191,"category":192},12100,"production-engineer","Production Engineer",[178,179,180,181,182,183,184,185,186,187,188,189],"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":26,"slug":27,"label":28},{"id":194,"slug":195,"title":196,"skills":197,"budget":19,"duration":19,"location":205,"onsitePercent":49,"contractType":50,"foundAt":206,"category":207},12072,"laborant-chemie-mwd","Laborant Chemie (m\u002Fw\u002Fd)",[198,141,199,200,110,201,69,97,202,203,204],"Chemielaborant","FTIR-Spektroskopie","Spektroskopie","ISO","Koordination","Qualität","Optimierung","Würzburg","2026-06-10T11:25:51+00:00",{"id":26,"slug":27,"label":28},{"id":209,"slug":210,"title":211,"skills":212,"budget":19,"duration":19,"location":228,"onsitePercent":49,"contractType":50,"foundAt":229,"category":230},11902,"it-anwendungsbetreuer-mwd-2","IT-Anwendungsbetreuer (m\u002Fw\u002Fd)",[213,214,215,216,217,218,219,220,221,222,223,224,225,226,227,69],"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":26,"slug":27,"label":28},{"id":232,"slug":233,"title":234,"skills":235,"budget":19,"duration":19,"location":243,"onsitePercent":49,"contractType":50,"foundAt":244,"category":245},11872,"chemielaborant-qualitaetskontrolle-mwd","Chemielaborant Qualitätskontrolle (m\u002Fw\u002Fd)",[198,236,94,237,238,239,240,241,242,69],"Qualitätskontrolle","HPLC","GC","Chromeleon","CTA","PTA","CAPA","Miesbach, Bayern","2026-06-09T13:25:36+00:00",{"id":26,"slug":27,"label":28},{"id":247,"slug":248,"title":249,"skills":250,"budget":19,"duration":19,"location":243,"onsitePercent":49,"contractType":256,"foundAt":257,"category":258},11871,"chemielaborant-lab-technician-mwd-analytical-development","Chemielaborant \u002F Lab Technician (m\u002Fw\u002Fd) Analytical Development",[251,237,238,252,253,239,94,69,254,255],"Analytik","Methodenentwicklung","Validierung analytischer Methoden","Chromatographie","Spektrometrie","permanent","2026-06-09T13:25:25+00:00",{"id":26,"slug":27,"label":28},{"id":260,"slug":261,"title":262,"skills":263,"budget":19,"duration":275,"location":19,"onsitePercent":71,"contractType":50,"foundAt":276,"category":277},11773,"sustaining-engineer-mwd","Sustaining Engineer (m\u002Fw\u002Fd)",[264,265,266,267,268,185,269,270,271,272,273,274],"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","2026-06-09T09:30:21+00:00",{"id":26,"slug":27,"label":28},{"id":279,"slug":280,"title":281,"skills":282,"budget":19,"duration":19,"location":289,"onsitePercent":100,"contractType":50,"foundAt":290,"category":291},11741,"junior-quality-engineer-medical-devices-mwd","Junior Quality Engineer Medical Devices (m\u002Fw\u002Fd)",[283,284,285,286,287,288,131,132],"Audits","Elektrotechnik","Fehleranalyse","Lösungskompetenz","Management","Medical Devices","Aschaffenburg","2026-06-09T08:27:29+00:00",{"id":26,"slug":27,"label":28}]