[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"project-global-project-manager":3,"similar-global-project-manager":39,"matching-freelancers-global-project-manager":216},{"id":4,"slug":5,"title":6,"description":7,"skills":8,"budget":23,"duration":24,"location":25,"onsitePercent":26,"contractType":27,"foundAt":28,"category":29,"rawText":33,"webTitle":34,"webText":35,"language":36,"projectId":37,"sourceUrl":38},15964,"global-project-manager","Global Project Manager","Principal Project Manager für medizinische Geräte und pharmazeutische Projekte mit Fokus auf 21CFR820.30 Design Control. Verantwortung für Projektmanagement über alle Entwicklungsphasen hinweg in globalem Umfeld. Erfordert 8-11 Jahre Erfahrung, davon mindestens 5 Jahre in Medizingeräte-, Pharma- oder Biopharmaindustrie.",[9,10,11,12,13,14,15,16,17,18,19,20,21,22],"Project Management","Medical Device Development","Pharmaceutical Development","21CFR820.30 Design Control","Microsoft Project","Smartsheet","Google Suite","PMP Certification","Risk Management","Budget Management","Team Leadership","Vendor Collaboration","English","German",null,"12+ Monate","Basel",100,"temp_work","2026-06-24T10:21:34+00:00",{"id":30,"slug":31,"label":32},14,"medical_tech","Medizintechnik","Global Project Manager\n\ntemporary\nGlobal Project Manager\nGlobal Project Manager: Project Manager \u002F Medical Device \u002F Pharmaceutical \u002F Biopharmaceutical \u002F 21CFR820.30 \u002F design control requirements \u002F PMP \u002F English  \u002F German\nBackground:\nWe are looking for a Principal  Project Manager (PM) to manage a range of projects, based on their stage and complexity. This role encompasses a variety of assignments including development pipeline, line extensions, post-approval, technology, and continuous improvement initiatives. The PM will work independently, effectively prioritizing and managing workload to meet team goals with limited direction. The role includes flexibility for global time zone interactions and occasional travel to external partners for collaboration and planning activities.\nThe Perfect Candidate  holds a Bachelor’s degree in Engineering or a related field, supported by 8 to 11 years of professional experience, including a minimum of 5 years within the medical device, pharmaceutical, or biopharmaceutical sectors. They should possess significant expertise in managing drug or medical device development and commercialization projects, with a focus on combination products and vendor collaboration. Proficiency in industry-standard project management tools, such as Microsoft Project, Smartsheet, and Google Suite, is required, alongside a thorough understanding of 21CFR820.30 design control requirements. A PMP certification is considered a valuable asset for this role. Furthermore, the candidate should demonstrate the ability to manage complex projects independently within a fast-paced environment and possess excellent communication and relationship-building skills. Fluency in English is required, while proficiency in German, Japanese, or Danish is advantageous\nTasks & Responsibilities:\nWhat You’ll Do:\nIn collaboration with the Technical Development Team Lead (TDTL) & Device Team Leader (DTL), the PM will translate device strategy into actionable plans, focusing on three key areas:\nPlanning: Define „inspection ready“ Design & Development Plans\nExecution: Drive team activities to meet project and design control deliverables\nTeam Dynamics: Ensure effective communication and facilitate team performance in a regulated environment using various processes and tools for planning, communication, budget, schedule, compliance, and risk management\nProject Management responsibilities:\nMaintains full understanding of program milestones for the Core, Lifecycle, Technical Development and associated teams and links them to the Device Team plan\nEffectively applies PM best practices and utilizes tools for planning, communication, team building, collaboration, decision-making, issue & risk management, lessons learned, knowledge management and budget tracking\nDevelops & updates Design & Development Plan and establishes contingency plans as needed\nEnsures transparent communication of key team information and escalates issues as appropriate\nEstablishes positive team dynamics through team building\nPromotes collaborative environment across team members\nFacilitates efficient decision-making and issue resolution\nIdentifies team risks and mitigation plans\nProject Planning and Execution:\nManages project scope and facilitate necessary changes\nFacilitates project plan development and execution, and monitor the project schedule\nIntegrates deliverables with other teams linked to the product\nEnsures effective team dynamics and positive team environments\nRisk and Issue Management:\nAnticipates and manage risks with proactive contingency plans\nFacilitates risk management process and issue resolution\nCollaboration and Team Building:\nAssesses Team dynamics and leads team building activities to enable and sustain a high performing team environment\nEstablish relationships and network with other stakeholder Teams and PMs\nCommunication:\nDevelops and adapts project communication tools to drive awareness of project progress and risks across stakeholders including external collaborators (e.g. dashboard)\nActs as Device Team Leader back-up for Team communication as required\nLiaises with other Teams to manage cross-functional activities and issues and risks\nMeeting and Budget Management:\nFacilitate effective team meetings with clear outcomes and follow-up actions\nForecast and monitor team resources and project costs\nKnowledge Management:\nEstablishes centralized Team access to all relevant project information\nManages Team uncontrolled document repository (e.g. Project History File)\nConducts lessons learned exercises during project execution and share outcomes to a broader audience\nGovernance:\nEffectively navigates the Device Team through business process stage-gates\nSupports Team Leader with technical advisory and governance committee reviews at pre-defined check-in points and\u002For identifies appropriate check-in points\nContinuous Improvement Initiatives:\nLeads business process continuous improvement initiatives through applying project lessons: business process updates, PM tool optimization & implementation, best practice sharing and driving awareness across teams\nMust Haves:\nBachelor’s degree in Engineering or a related field.\n8 to 11 years of experience, with at least 5 years in a relevant industry, preferably within a global medical device, pharmaceutical, or biopharmaceutical company\nExperience in project management in drug and\u002For medical device development and commercialization, particularly with combination products\nProficiency in Project Management best practices and software (Microsoft Project, Smartsheet, Google suite)\nPMP certification is an asset.\nKnowledge of 21CFR820.30 design control requirements\nExperience with vendor \u002F partner collaboration.\nExcellent communication and relationship-building skills.\nAbility to manage complex projects independently in a fast-paced, team-based environment.\nFluent English is required. German, Japanese or Danish is of advantage\nReference Nr.: 925039\nRolle: Global Project Manager\nIndustrie: Pharma\nLocation: Basel\nPensum: 100%\nStart: 24.08.2026(Latest Start date 01.11.2026)\nDuration: 12 + Months\nDeadline: 30\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\nBasel\nType\ntemporary\n\nE-Mail: service@itcag.com","Global Project Manager (Medical Device & Pharma)","Wir suchen einen erfahrenen Principal Project Manager zur Leitung einer Vielzahl von Projekten in verschiedenen Entwicklungsphasen und Komplexitätsstufen. Diese Position umfasst Aufgaben im Bereich Entwicklungs-Pipeline, Produkterweiterungen, Post-Approval-Aktivitäten, Technologie und kontinuierliche Verbesserungsinitiativen.\n\nDer ideale Kandidat verfügt über einen Bachelor-Abschluss in Ingenieurwesen oder einem verwandten Fachgebiet sowie 8–11 Jahre Berufserfahrung, davon mindestens 5 Jahre in der Medizingeräte-, Pharma- oder Biopharma-Industrie. Sie bringen umfangreiche Expertise in der Verwaltung von Entwicklungs- und Kommerzialisierungsprojekten mit, insbesondere bei Kombinationsprodukten und Herstellerzusammenarbeit. Erforderlich sind Kenntnisse in branchenüblichen Projektmanagement-Tools wie Microsoft Project, Smartsheet und Google Suite sowie ein tiefes Verständnis der 21CFR820.30 Design-Control-Anforderungen. Eine PMP-Zertifizierung ist von Vorteil.\n\nIn enger Zusammenarbeit mit den Technical Development und Device Team Leads übersetzen Sie die Gerätestrategie in umsetzbare Pläne. Ihre Aufgaben umfassen die Definition inspektionsbereiter Design- und Entwicklungspläne, die Steuerung von Teamaktivitäten zur Erfüllung von Projekt- und Design-Control-Vorgaben sowie die Gewährleistung effektiver Kommunikation in einem regulierten Umfeld. Sie verwalten Meilensteine, wenden Best Practices an und nutzen Tools für Planung, Kommunikation, Budget-Tracking, Compliance und Risikomanagement.\n\nDie Position erfordert Unabhängigkeit, Priorisierungsfähigkeit und Flexibilität für globale Zeitzonen sowie gelegentliche Reisen. Fließend Englisch ist erforderlich; Kenntnisse in Deutsch, Japanisch oder Dänisch sind von Vorteil.","en","925039","https:\u002F\u002Fwww.itcag.com\u002Fjobs\u002Fglobal-project-manager-8166\u002F",{"items":40},[41,62,79,91,102,115,125,135,144,154,164,174,184,196,206],{"id":42,"slug":43,"title":44,"description":45,"skills":46,"budget":23,"duration":23,"location":58,"onsitePercent":26,"contractType":59,"foundAt":60,"category":61},15910,"laborant-analytik-mwd","Laborant Analytik (m\u002Fw\u002Fd)","Durchführung analytischer Prüfungen und Probenvorbereitung in einem Labor mit modernen Analyseverfahren wie HPLC, GC und Spektroskopie. Berechnung und Auswertung von Messergebnissen mit SAP\u002FLIMS sowie Dokumentation aller Ergebnisse gemäß GMP-Standards.",[47,48,49,50,51,52,53,54,55,56,57],"Chemielaborant","HPLC","GC","Spektroskopie","SAP","LIMS","Probenvorbereitung","GMP","Dokumentation","MS Office","Deutsch B2","Schwarzheide, Brandenburg","contracting","2026-06-24T08:25:27+00:00",{"id":30,"slug":31,"label":32},{"id":63,"slug":64,"title":65,"description":66,"skills":67,"budget":23,"duration":74,"location":75,"onsitePercent":76,"contractType":59,"foundAt":77,"category":78},15758,"testingenieur-fuer-mechanische-pruefungen-an-kunststoffkathetern","Testingenieur für mechanische Prüfungen an Kunststoffkathetern","Testingenieur für mechanische Prüfungen an Kunststoffkathetern in der Medizintechnik. Aufgaben umfassen Testmethodenentwicklung, -validierung, Betreuung mechanischer Designprüfungen und Berichtserstellung. Hybrid-Position (75% vor Ort) in Mannheim für 3 Monate mit Verlängerungsoption.",[68,69,70,71,32,72,73],"Testingenieur","Qualitätsingenieur","Maschinenbauingenieur","Leichtbauerfahrung","Mechanisches Testing","Kunststoffprüfung","3 Monate mit Option auf Verlängerung","Mannheim",75,"2026-06-23T12:46:46+00:00",{"id":30,"slug":31,"label":32},{"id":80,"slug":81,"title":82,"description":83,"skills":84,"budget":23,"duration":74,"location":75,"onsitePercent":88,"contractType":59,"foundAt":89,"category":90},15757,"spezialist-zur-komponentenspezifikation-dokumentation","Spezialist zur Komponentenspezifikation & Dokumentation","Ingenieur zur Komponentenspezifikation & Dokumentation in der Medizintechnik. Aufgaben umfassen technische Abstimmung mit Lieferanten, Dokumentation von Einkaufsspezifikationen, Auswertung von Erstinspektionen und Zeichnungsabgleich. Hybrid-Position in Mannheim für 3 Monate mit Verlängerungsoption.",[85,69,70,71,86,87,32],"Kunststoffingenieur","Katherherstellung","Mechanische Konstruktion",50,"2026-06-23T12:46:36+00:00",{"id":30,"slug":31,"label":32},{"id":92,"slug":93,"title":94,"description":95,"skills":96,"budget":97,"duration":23,"location":98,"onsitePercent":88,"contractType":99,"foundAt":100,"category":101},15696,"regulatory-affairs-specialist-mwd","Regulatory Affairs Specialist (m\u002Fw\u002Fd)","Regulatory Affairs Specialist in Geisingen, Baden-Württemberg. Festanstellung in Vollzeit mit hybridem Arbeitsmodell im Healthcare-Bereich.",[],"80.000-95.000 EUR\u002FJahr","Geisingen, Baden-Württemberg","permanent","2026-06-23T12:10:27+00:00",{"id":30,"slug":31,"label":32},{"id":103,"slug":104,"title":105,"description":106,"skills":107,"budget":111,"duration":23,"location":112,"onsitePercent":88,"contractType":99,"foundAt":113,"category":114},15639,"apotheker-als-quality-manager-mwd","Apotheker als Quality Manager (m\u002Fw\u002Fd)","Festanstellung als Quality Manager in einer Apotheke in Weiterstadt, Hessen. Vollzeitposition mit hybridem Arbeitsmodell. Jahresgehalt zwischen 60.000 und 80.000 EUR.",[108,109,110],"Pharmazie","Quality Management","Apotheker","60.000-80.000 EUR\u002FJahr","Weiterstadt, Hessen","2026-06-23T12:09:27+00:00",{"id":30,"slug":31,"label":32},{"id":116,"slug":117,"title":118,"description":119,"skills":120,"budget":121,"duration":23,"location":122,"onsitePercent":88,"contractType":99,"foundAt":123,"category":124},15431,"manager-production-mwd-spritzguss","Manager Production (m\u002Fw\u002Fd) – Spritzguss","Produktionsmanager für Spritzguss im Healthcare-Bereich in Iserlohn gesucht. Festanstellung in Vollzeit mit hybridem Arbeitsmodell. Gehalt zwischen 75.000 und 90.000 EUR pro Jahr.",[],"75.000-90.000 EUR\u002FJahr","Iserlohn","2026-06-23T12:05:19+00:00",{"id":30,"slug":31,"label":32},{"id":126,"slug":127,"title":128,"description":129,"skills":130,"budget":131,"duration":23,"location":132,"onsitePercent":88,"contractType":99,"foundAt":133,"category":134},15425,"qualitaetskontrolle-mwd-healthcare","Qualitätskontrolle (m\u002Fw\u002Fd) – Healthcare","Qualitätskontrolle-Position im Healthcare-Bereich in Stade, Niedersachsen. Festanstellung in Vollzeit mit hybridem Arbeitsmodell. Jahresgehalt zwischen 40.000 und 55.500 EUR.",[],"40.000-55.500 EUR\u002FJahr","Stade","2026-06-23T12:05:12+00:00",{"id":30,"slug":31,"label":32},{"id":136,"slug":137,"title":138,"description":139,"skills":140,"budget":111,"duration":23,"location":141,"onsitePercent":26,"contractType":99,"foundAt":142,"category":143},15418,"deputy-head-of-production-mwd","Deputy Head of Production (m\u002Fw\u002Fd)","Festanstellung als Deputy Head of Production im Healthcare-Bereich in Münster. Vollzeitposition mit Office-based Arbeitsmodell. Gehalt zwischen 60.000 und 80.000 EUR pro Jahr.",[],"Münster","2026-06-23T12:05:03+00:00",{"id":30,"slug":31,"label":32},{"id":145,"slug":146,"title":147,"description":148,"skills":149,"budget":150,"duration":23,"location":151,"onsitePercent":88,"contractType":99,"foundAt":152,"category":153},15412,"product-manager-medical-devices-mwd","Product Manager Medical Devices (m\u002Fw\u002Fd)","Product Manager für Medical Devices in Neu Wulmstorf, Niedersachsen. Festanstellung in Vollzeit mit hybridem Arbeitsmodell. Gehalt zwischen 55.000 und 85.000 EUR pro Jahr.",[],"55.000-85.000 EUR\u002FJahr","Neu Wulmstorf","2026-06-23T12:04:56+00:00",{"id":30,"slug":31,"label":32},{"id":155,"slug":156,"title":157,"description":158,"skills":159,"budget":160,"duration":23,"location":161,"onsitePercent":88,"contractType":99,"foundAt":162,"category":163},15321,"senior-development-engineer-mwd","Senior Development Engineer (m\u002Fw\u002Fd)","Senior Development Engineer Position in Remchingen, Baden-Württemberg. Festanstellung im Hybrid-Arbeitsmodell mit Vollzeitbeschäftigung. Gehalt zwischen 80.000 und 100.000 EUR pro Jahr.",[],"80.000-100.000 EUR\u002FJahr","Remchingen, Baden-Württemberg","2026-06-23T12:02:47+00:00",{"id":30,"slug":31,"label":32},{"id":165,"slug":166,"title":167,"description":168,"skills":169,"budget":170,"duration":23,"location":171,"onsitePercent":88,"contractType":99,"foundAt":172,"category":173},15261,"design-elektroingenieur-mwd","Design Elektroingenieur (m\u002Fw\u002Fd)","Elektroingenieur für Design-Aufgaben in der Healthcare-Branche in Düren, Nordrhein-Westfalen. Festanstellung in Vollzeit mit hybridem Arbeitsmodell. Gehalt zwischen 58.000 und 72.000 EUR pro Jahr plus Life Science Benefits.",[],"58.000-72.000 EUR\u002FJahr","Düren","2026-06-23T12:01:30+00:00",{"id":30,"slug":31,"label":32},{"id":175,"slug":176,"title":177,"description":178,"skills":179,"budget":180,"duration":23,"location":181,"onsitePercent":88,"contractType":99,"foundAt":182,"category":183},15176,"regulatory-affairs-spezialist-mwd-35-std-woche","Regulatory Affairs Spezialist (m\u002Fw\u002Fd) – 35 Std Woche","Regulatory Affairs Spezialist in Vollzeit bei einer Healthcare-Organisation in Kiel. Hybrid-Arbeitsmodell mit 35 Stunden pro Woche. Festanstellung mit Jahresgehalt von 50.000–60.000 EUR.",[],"50.000–60.000 EUR\u002FJahr","Kiel","2026-06-23T11:59:28+00:00",{"id":30,"slug":31,"label":32},{"id":185,"slug":186,"title":187,"description":188,"skills":189,"budget":192,"duration":23,"location":193,"onsitePercent":88,"contractType":99,"foundAt":194,"category":195},15158,"experte-digitale-qualitaetssysteme-mwd-gmp","Experte Digitale Qualitätssysteme (m\u002Fw\u002Fd) GMP","Festanstellung als Experte für Digitale Qualitätssysteme im GMP-Bereich in Wiesbaden. Vollzeitposition im Hybrid-Arbeitsmodell. Gehalt zwischen 65.000 und 80.000 EUR pro Jahr.",[190,54,191],"Digitale Qualitätssysteme","Healthcare","65.000-80.000 EUR\u002FJahr","Wiesbaden","2026-06-23T11:58:58+00:00",{"id":30,"slug":31,"label":32},{"id":197,"slug":198,"title":199,"description":200,"skills":201,"budget":202,"duration":23,"location":203,"onsitePercent":88,"contractType":99,"foundAt":204,"category":205},15079,"ingenieur-sterilprozesse-mwd","Ingenieur Sterilprozesse (m\u002Fw\u002Fd)","Festanstellung als Ingenieur für Sterilprozesse in Kassel, Hessen. Vollzeitposition im Hybrid-Arbeitsmodell im Healthcare-Bereich. Gehalt zwischen 55.000 und 70.000 EUR pro Jahr.",[],"55.000-70.000 EUR\u002FJahr","Kassel","2026-06-23T11:57:19+00:00",{"id":30,"slug":31,"label":32},{"id":207,"slug":208,"title":209,"description":210,"skills":211,"budget":212,"duration":23,"location":213,"onsitePercent":26,"contractType":99,"foundAt":214,"category":215},15028,"technician-mwd-quality-control","Technician (m\u002Fw\u002Fd) Quality Control","Qualitätskontroll-Techniker (m\u002Fw\u002Fd) in Bad Homburg vor der Höhe gesucht. Vollzeitstelle mit Festanstellung im Healthcare-Bereich. Office-basierte Position.",[],"45.000-53.000 EUR\u002FJahr","Bad Homburg vor der Höhe","2026-06-23T11:56:01+00:00",{"id":30,"slug":31,"label":32},{"items":217},[]]