Als Partner von zahlreichen Unternehmen bieten wir attraktive Beschäftigungsmöglichkeiten und unterstützen unsere Mitarbeiter dabei, ihre beruflichen Ziele zu erreichen. Wir suchen ab sofort für unseren Kunden, ein international tätiges Logistik- und Supply-Chain-Unternehmen einen Inventory Administrator (m/w/d)!
Coordinates warehouse activities with activities of other functions such as production, parts sales, production control, and purchasing. Responsibilities also include establishing and maintaining efficiencies in the areas of Receiving, Shipping and Work Order Picking, leading to improvements in on-time performance of department pats flow and services.
Coordinates warehouse activities with activities of other functions such as production, parts sales, production control, and purchasing. Responsibilities also include establishing and maintaining efficiencies in the areas of Receiving, Shipping and Work Order Picking, leading to improvements in on-time performance of department pats flow and services.
Die 55.000 Mitarbeiter aus etwa 100 verschiedenen Ländern setzen sich jeden Tag mit Stolz und Leidenschaft für die beste Qualität der Produkte ein. Für den Standort in Hamburg-Fuhlsbüttel suchen wir Sie als Process and Performance Specialist (m/w/d) in Vollzeit. DIES SIND IHRE AUFGABEN: Analyse und Optimierung der Inbound- und Inventory-Prozesse gemeinsam mit dem Logistikdienstleister auf operativer und taktischer Ebene zur Sicherstellung hoher Sicherheits-, Qualitäts- und LeistungsstandardsDefinition, Implementierung und konsequente Nachverfolgung von Recovery- und Verbesserungsmaßnahmen auf Basis fundierter Performance-Analysen und ReportingsWeiterentwicklung von Layouts, Prozessen, Equipment und Tools im Bereich Inbound und Inventory im Rahmen der Logistiktransformation in Hamburg an beiden Standorten (Fuhlsbüttel und Wilhelmsburg)Aufbau und Pflege starker, partnerschaftlicher Beziehungen zu Logistikdienstleistern sowie zu internen Stakeholdern innerhalb von Satair und Airbus DAS BRINGEN SIE MIT: Abgeschlossenes Bachelorstudium im Bereich Supply Chain oder WirtschaftsingenieurwesenMindestens 5 Jahre Berufserfahrung in der Lagerlogistik, Prozessplanung,Prozessverbesserung und Supply Chain / LogisticsSehr gute Kenntnisse in SAP/R3Kenntnisse in PPS, Problemlösungsmethoden von VorteilGute Kenntnisse in KAIZEN, Change Management, Lean Management, Prozessmanagement und ProjektmanagementVerhandlungssichere Deutsch- und Englischkenntnisse WIR GARANTIEREN IHNEN: Wir zahlen ein tarifliches Gehalt sowie ggf.
Proficiency in Microsoft Office, ERP systems (preferably SAP), and CAD tools such as AutoCAD or SolidWorks. Familiarity with process optimization tools and methodologies (Lean, Six Sigma). Strong analytical and problem-solving skills.
Proficiency in Microsoft Office, ERP systems (preferably SAP), and CAD tools such as AutoCAD or SolidWorks. Familiarity with process optimization tools and methodologies (Lean, Six Sigma). Strong analytical and problem-solving skills.
Für einen unserer Großkunden suchen wir derzeit eine/n Mitarbeiter/ in zur Festanstellung, der die nachfolgenden Anforderungen erfüllt: Ihre Aufgaben: Annahme, Auspacken, Prüfung und Verbuchung von Waren im Wareneingang Erfassung aller Warenbewegungen im Warenwirtschafts- bzw.
Stellenbeschreibung Sie sind auf der Suche nach mehr als nur einem Job - Sie möchten einen Ort finden, an dem Ihre Fähigkeiten nicht nur gefragt, sondern auch wertgeschätzt werden?
Operativer Einkäufer Siemens (m/w/d) Sie suchen eine neue und abwechslungsreiche berufliche Herausforderung und möchten Ihr fachliches Know-how anwenden? Dann sind Sie bei uns richtig!
Techniker oder technischer Betriebswirt) oder ein technisch ausgerichtetes Studium – jeweils ergänzt durch mehrjährige Berufserfahrung in einem Produktionsunternehmen Nachweisliche Führungserfahrung im mehrschichtigen Produktionsumfeld Ausgeprägte mitarbeiterorientierte Führungskompetenz sowie eine klare und wertschätzende Kommunikationsstärke Fundierte Kenntnisse in der Anwendung von Lean-Management-Methoden (KVP, Lean-Mindset) und eine hohe Affinität zu technischen Prozessen kombiniert mit starken analytischen Fähigkeiten Strukturierte Problemlösungskompetenz, ausgeprägtes Planungs- und Organisationsgeschick sowie unternehmerisches Denken Sehr gute Deutschkenntnisse und gute Englischkenntnisse runden Ihr Profil idealerweise ab Klingt spannend? Dann freuen wir uns auf Ihre Bewerbung! Wir suchen übrigens auch für weitere Unternehmen in der Region Verstärkung – eine Bewerbung lohnt sich also in jedem Fall. Unsere Kundenunternehmen befinden sich in Allermöhe, Reinbek, Glinde, Lauenburg, Schwarzenbek und Geesthacht.
Tendering Stage /Pre-acquisition Reviews the Customer Specifications from the perspective of spares to identify requirements such as: reliability and availability criteria, delivery of the initial stock of spares etc. Prepares /reviews a Spare Parts Concept customized for different Reference Designs /Modules.
Dein nächster Karriereschritt läuft über uns! Gemeinsam mit unseren Partner in Reinbek suchen wir dich als Produktionsleiter im Rahmen der Direktvermittlung. Das wird dich überzeugen: Alles was du tun musst: Einfach job meets life kontaktieren und entspannt deinem neuen Job entgegenblicken!
What We Offer: Competitive compensation Full coverage of accommodation and transport during project assignments 50% employer contribution towards health insurance 30 vacation days per year for proper recovery and work-life balance 30% employer subsidy for company pension plan 80% of monthly public transport costs covered Additional employee benefits and perks beyond industry standards Your Responsibilities: Supervise and coordinate daily operations within the concrete tower production process Ensure compliance with safety regulations and budget targets across production phasesManage inventory and align production flow with other departments Work closely with engineering teams to continuously improve workflows and procedures Guide and support new team members during onboarding and integration into operations Your Profile: Solid experience in production or manufacturing environments Proven leadership skills in roles such as shift leader or team coordinator Willingness to travel for changing project assignments across locations Strong communication skills and fluency in English (written and spoken) Analytical thinking, structured working style, and a hands-on mindset Not sure if youre the right fit?
What We Offer: Competitive compensation Full coverage of accommodation and transport during project assignments 50% employer contribution towards health insurance 30 vacation days per year for proper recovery and work-life balance 30% employer subsidy for company pension plan 80% of monthly public transport costs covered Additional employee benefits and perks beyond industry standards Your Responsibilities: Supervise and coordinate daily operations within the concrete tower production process Ensure compliance with safety regulations and budget targets across production phasesManage inventory and align production flow with other departments Work closely with engineering teams to continuously improve workflows and procedures Guide and support new team members during onboarding and integration into operations Your Profile: Solid experience in production or manufacturing environments Proven leadership skills in roles such as shift leader or team coordinator Willingness to travel for changing project assignments across locations Strong communication skills and fluency in English (written and spoken) Analytical thinking, structured working style, and a hands-on mindset Not sure if you’re the right fit?
Design, conduct, and analyze in vivo studies involving intravenous injections, blood collection, and bleeding/thrombosis models Execute full end-to-end in vivo workflows, from study preparation to sample processing and documentation Characterize gene therapy candidates using molecular and biochemical assays such as ELISA, thrombin generation, and chromogenic assays Handle, prepare, and evaluate patient-derived blood and plasma samples for in vitro and ex vivo experiments Perform data analysis, interpret results, and present findings to the research team Maintain accurate, complete, and compliant documentation across all experimental steps Contribute to lab operations, including safety standards, inventory, equipment handling, and general organization Collaborate with cross-functional team members to ensure smooth coordination and progress on gene therapy studies Academic background in life sciences (MSc or BSc) or completed scientific apprenticeship with hands-on laboratory experience Active certification for animal experimentation (e.g., LTK1, FELASA, or equivalent) Proven hands-on experience with rodent work, including intravenous injections and blood sampling Ability to independently design, execute, and manage in vivo studies from start to finish Experience with molecular or biochemical assays relevant to hemostasis, thrombosis, or gene therapy Strong ability to plan experiments, analyze data, and interpret scientific results Fluency in English with clear communication skills Highly organized, proactive, and team-oriented mindset with strong reliability and attention to detail Opportunity to contribute directly to translational gene therapy research with high scientific impact Hands-on work with a combination of in vivo, ex vivo, and molecular biology techniques Collaborative environment with close teamwork and modern laboratory infrastructure Diverse and meaningful daily tasks involving both preclinical models and human biological samples Ihr Kontakt Referenznummer 865654/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Design, conduct, and analyze in vivo studies involving intravenous injections, blood collection, and bleeding/thrombosis modelsExecute full end-to-end in vivo workflows, from study preparation to sample processing and documentationCharacterize gene therapy candidates using molecular and biochemical assays such as ELISA, thrombin generation, and chromogenic assaysHandle, prepare, and evaluate patient-derived blood and plasma samples for in vitro and ex vivo experimentsPerform data analysis, interpret results, and present findings to the research teamMaintain accurate, complete, and compliant documentation across all experimental stepsContribute to lab operations, including safety standards, inventory, equipment handling, and general organizationCollaborate with cross-functional team members to ensure smooth coordination and progress on gene therapy studies Academic background in life sciences (MSc or BSc) or completed scientific apprenticeship with hands-on laboratory experienceActive certification for animal experimentation (e.g., LTK1, FELASA, or equivalent)Proven hands-on experience with rodent work, including intravenous injections and blood samplingAbility to independently design, execute, and manage in vivo studies from start to finishExperience with molecular or biochemical assays relevant to hemostasis, thrombosis, or gene therapyStrong ability to plan experiments, analyze data, and interpret scientific resultsFluency in English with clear communication skillsHighly organized, proactive, and team-oriented mindset with strong reliability and attention to detail Opportunity to contribute directly to translational gene therapy research with high scientific impactHands-on work with a combination of in vivo, ex vivo, and molecular biology techniquesCollaborative environment with close teamwork and modern laboratory infrastructureDiverse and meaningful daily tasks involving both preclinical models and human biological samples Ihr Kontakt Referenznummer 865654/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Einsatzort: Frankfurt am Main Start: 02.02.2026 | Laufzeit: bis 30.11.2026 Arbeitszeit: 37,5 Stunden/Woche | Arbeitszeitsouveränität, Homeoffice bis zu 2 Tage/Woche nach Einarbeitung Im Auftrag unseres Kunden, einem weltweit führenden Pharmaunternehmen, suchen wir Sie als: Supply Planner FBC (m/w/d) – Produktionsplanung Pharma Ihre Aufgaben Monatlich verantworten Sie die Capability Review für Ihren Produktionsschritt: Gemeinsam mit Operations, SMS, Scheduling und Maintenance validieren Sie zentrale Planungsannahmen und Kapazitätsengpässe , bereiten Szenarien (z.
YOUR TASKS Support the preparation, maintenance, and organization of technical training materials, presentations, and documentation Assist in managing and maintaining training equipment, tools, and workshop setups Create and edit documents, spreadsheets, and visual content using Microsoft Office Collaborate with trainers to digitize and optimize training content such as e‑learning modules Support SAP processes including purchase requests, order tracking and updating material availability Track inventory of tools, consumables and equipment used in trainings and initiate reorders when needed Use AI tools such as Copilot to draft, summarize or visually enhance technical training materials YOUR PROFILE Ongoing studies in Mechatronics, Industrial Engineering, Mechanical Engineering, Electrical Engineering or a similar field Strong organizational skills and a structured way of working Confident handling of Microsoft Office applications Interest in digital learning formats and technical content Reliable, proactive and able to work both independently and collaboratively YOUR BENEFITS Nordex offers a range of attractive benefits – here’s a selection of what you can look forward to.
Compensation In accordance with Massachusetts law, the expected salary for this full-time, benefited position is between $60,000 - $80,000. The actual compensation will be determined considering factors such as relevant skills and experience and other factors permitted by law. ------ What We Offer Competitive salary and benefits package.
Einsatzort: Frankfurt am Main Start: 02.02.2026 | Laufzeit: bis 30.11.2026 Arbeitszeit: 37,5 Stunden/Woche | Arbeitszeitsouveränität, Homeoffice bis zu 2 Tage/Woche nach Einarbeitung Im Auftrag unseres Kunden, einem weltweit führenden Pharmaunternehmen, suchen wir Sie als: Supply Planner FBC (m/w/d) – Produktionsplanung Pharma Ihre Aufgaben Monatlich verantworten Sie die Capability Review für Ihren Produktionsschritt: Gemeinsam mit Operations, SMS, Scheduling und Maintenance validieren Sie zentrale Planungsannahmen und Kapazitätsengpässe, bereiten Szenarien (z.
YOUR TASKS Support the preparation, maintenance, and organization of technical training materials, presentations, and documentation Assist in managing and maintaining training equipment, tools, and workshop setups Create and edit documents, spreadsheets, and visual content using Microsoft Office Collaborate with trainers to digitize and optimize training content such as e‑learning modules Support SAP processes including purchase requests, order tracking and updating material availability Track inventory of tools, consumables and equipment used in trainings and initiate reorders when needed Use AI tools such as Copilot to draft, summarize or visually enhance technical training materials YOUR PROFILE Ongoing studies in Mechatronics, Industrial Engineering, Mechanical Engineering, Electrical Engineering or a similar field Strong organizational skills and a structured way of working Confident handling of Microsoft Office applications Interest in digital learning formats and technical content Reliable, proactive and able to work both independently and collaboratively YOUR BENEFITS Nordex offers a range of attractive benefits – here’s a selection of what you can look forward to.
You advise IT teams on classification, protection requirements, and dependencies within the infrastructure and support them in implementing regulatory requirements such as NIS2 or DORA. What makes you stand out You hold a degree in (Business) Informatics or have completed a comparable education or training in the field of IT.