Überblick über die Statistik des Gehaltsniveaus für "Technical Logistics Specialist in Deutschland"

Speculative application  Skills: Acne, Actinic Keratosis, Acute Myelogenous Leukemia (AML), AIDS, Allergic Rhinitis, Allergy, Alzheimer's, Anaesthetics, Antibiotics, Anti-infectives, Anxiety, arrhythmia, Asthma, Autoimmune diseases, Autoimmune Disorder, Bacterial Vaginosis, Breast Cancer, Cardiology, Cardiovascular, chemotherapy, Chronic Lymphocytic Leukaemia, Chronic Myeloid Leukemia, Chronic Obstructive Pulmonary Disease, Clinical Pathology, CLL, Congestive Heart Failure, COPD, Cosmetics, Cystic Fibrosis, Dementia, Dentistry, Depression, Dermatology, Diabetes, Diagnostics, Dietetics, Endocrine, Endocrinology, Epilepsy, Family Medicine, Fibromyalgia, Gastroenterology, gastrointestinal, Genetic Diseases, GI, Glioblastoma Multiforme (GBM), Gynaecologic, Gynaecology, Gynecology, Haematology, Haemophilia, Heart Disease, Hematology, Hemopure Anemia, Hepatitis, Hepatology, HIV, Hodgkin's disease, Hypertension, IBD, Immunogenicity, Immunopharmacology, Infections, Infectious Diseases, Influenza, Internal Medicine, Joint Replacement, Lymphoma, Mantle Cell Lymphoma, Melanoma, Menopause, Metabolic, Migraine, Multiple Sclerosis, Musculoskeletal, Myelodysplastic Syndrome, Neonatology, Nephrology, Neurodegenerative disorders, Neurology, Neuroscience, NEUROSURGERY, non small cell lung cancer, Non-Hodgkin Lymphoma, nutraceuticals, Nutrition, OA, Obstetrics, Oncology, Ophthalmology, Oral Health, Orphan Diseases, Orphan drug, Orthobiologic Bone graft, Orthopedic Surgery, Orthopedics, Osteoarthritis, Otitis Externa, Otolaryngology, Ovarian Cancer, Paediatric, Pain, Painful Diabetic Neuropathy, Parkinson’s Disease, Physiology, Podiatry, Post-Menopausal Osteoporosis, Primary Immune Deficiency, Primary Sjogren’s Syndrome, Prostate cancer, Prostatic hyperplasia, Psychiatry, Psychology, Pulmonary, Pulmonology, RA, Rare Disease, Respiratory, retinopathy, Rheumatoid Arthritis, Rheumatology, Rhinitis, Rosacea, Schizophrenia, Seasonal Allergic Rhinitis, Severe Hemophilia, Skin Melanoma, Sleep Disorder, Sleep Medicine, Small Lymphocytic Lymphoma, Small Molecule, Smoking Cessation, Solid Tumors, surgery, Systemic Lupus Erythematosus, Systemic Sclerosis, Tissue Ablation, Transplant, Trauma, Traumatology, Type 2 Diabetes Mellitus, Urology, Vaccine, Vaccines, Vascular Diseases, Weight Loss, Women’s Health, Administrative Assistant, Agile Project Manager, Artwork Coordinator, Associate Director Clinical Operations, Associate Project Manager, Auditor, Biomedical Engineer, Biometrics Manager, Biosample Operations Manager, Biostatistician, Biostatistics Associate Director, Brand Team Lead, Business Administration Associate, Business Administration Manager, Business Analyst, Business Development Associate, Business Development Director, Business Development Manager, CEO, Change Manager, Chemical Project Manager, Chemist, Chemistry, Manufacturing & Control Lead (CMC), Chief Financial Officer, Chief Operating Officer, Chief Technical Officer, Clinical Data Associate, Clinical Data Manager, Clinical Data Specialist, Clinical Development Manager, Clinical Engineer, Clinical Lead, Clinical Operations Director, Clinical Operations Manager, Clinical Pharmacologist, Clinical Programmer, Clinical Project Manager, Clinical Research Associate, Clinical Research Director, Clinical Research Manager, Clinical Research Physician, Clinical Research Specialist, Clinical Study Coordinator, Clinical Study Manager, Clinical Supply Coordinator, Clinical Supply Manager, Clinical Trial Assistant, Clinical Trial Educator, Clinical Trial Manager, Clinical Trial Specialist, CMC Manager, Commercial Manager, Communication Manager, Compliance Associate, Compliance Manager, Computer System Validation Specialist, Contract Associate, Contracts Manager, Country Manager, Customer Service Associate, Data Analyst, Data Analytics Assistant, Data Engineer, Data Management Associate Director, Data Management, Manager, Database Programmer_Designer, Demand Planner, Demand Manager, Developer, Diagnostic Specialist, Director of Contracts & Licensing, Dispensary Assistant, Document Specialist, Drug Safety Associate, Drug Safety Director, Drug Safety Manager, Early Access Project Manager, EHS associate, Electronic Data Capture Manager, Electrophysiologist, Employer Engagement Manager, Engineer (out of industry), Epidemiologist, Exploratory Project Manager, Feasibility Manager, Freelance, FSP Clinical Manager, Global Clinical Data Manager, Graduate, Head of Clinical Data Management, Head of Clinical Operations, Head of Risk Management, Health Economist, Health Information Associate, Healthcare Compliance Manager, HR Associate, HR Manager, Imaging Operations Lead, Inhouse Clinical Research Associate, Intern, Investigator, IT Project Manager, Junior Clinical Data Manager, Junior Clinical Research Associate, Junior Pharmacovigilance officer, Junior SAS Programmer, KOL, Laboratory Assistant, Laboratory Manager, Legal Advisor, Licensing Coordinator, Logistics Associate, Logistics Manager, Logistics Supervisor, Manufacturing Manager, Manuscript Editor, Market Access Manager, Market Access Specialist, Market Insights Specialist, Market Research Associate, Marketing Associate, Material Coordinator, Medical Advisor, Medical Assistant, Medical Devices Project Manager, Medical Director, Medical Information Assistant, Medical Information Associate, Medical Information Manager, Medical Manager, Medical Monitor, medical publisher, Medical Representative, Medical Research Associate, Medical Reviewer, Medical Science Liaison, Medical Technologist, Medical Writer, Medico-economic affairs, Meeting Coordinator, MHRA Pharmacovigilance Inspector, Microbiologist, Occupational Therapist, Office Manager, Ophthalmologist, Packaging Associate, Packaging Coordinator, Patient Recruitment Coordinator, Payroll Specialist, Pharmaceutical Physician, Pharmacist, Pharmacokineticist, Pharmacology Director, Pharmacovigilance Manager, Pharmacovigilance Officer, Physiotherapist, Planning analyst, Policy Officer, Post Doctoral Researcher, Preclinical Project Manager, Principal Biostatistician, Principal Scientist, Privacy Officer, Product manager, Production Manager, Production Specialist, Program Development Manager, Programmer Analyst, Programming Associate Director, Project Assistant, Project Manager (other industry), Proposal Developer, Psychiatrist, Psychologist, Publications Manager, QPPV, Qualified Person, Quality Assurance Assistant, Quality Assurance Complaint Specialist, Quality Assurance Director, Quality Assurance Manager, Quality Assurance Specialist, Quality Control Associate, Quality Control Manager, Quality Control Specialist, Quality Engineer, Quality Manager, Quality Specialist, R&D Manager, R&D Project Manager, Record Specialist, Recruitment & Screening Co-ordinator, Registration Specialist, Regulatory Affairs Administrator, Regulatory Affairs Associate, Regulatory Affairs Director, Regulatory Affairs Manager, Regulatory Affairs VP, Regulatory Documentation Scientist, Regulatory Information Specialist, Regulatory labelling specialist, Regulatory Program Manager, Regulatory Site Activation Manager, Remote Site Monitor, Senior, Research Coordinator, Research Funding Manager, Research Team Manager, Resources Manager, Respiratory Physiotherapist, Sales Manager, Sales Rep, Sample Manager, SAS Programmer, Scientific Advisor, Scientific Affairs Associate, Scientist, Senior Associate Supply Chain (GMP), Senior Biostatistician, Senior Clinical Lead, Senior Clinical Research Associate, Senior Clinical Supply Chain Associate, Senior Clinical Team Manager, Senior Clinical Trial Manager, Senior Epidemiologist, Senior Medical Affairs Officer, Senior Nutrition Scientist, Senior Regulatory Affairs Manager, Senior Scientist, Site Engagement Manager, Site Visit Report Reviewer, SOFTWARE DEVELOPER, Software Engineer, Start Up Director, Start-up Manager, Start-Up Specialist, Strategy Lead, Study Authorisation Associate, Study Delivery Operational Specialist, Submissions Manager, Supply Chain Coordinator, Supply Chain Manager, Supply Chain Planner, Surgical Technician, Systems Administrator, Technical Project Leader, Technical Services Specialist, Training Associate, Training Manager, Translator, Validation Engineer, Vendor Manager, Veterinary Nurse, Warehouse Associate, Warehousing & Distribution Leader, BSc, CQA, GMC, MBA, MBChB, MD, MPhil, MRCPsych, MSc, No CRA Certificate, PGDip, Ph.D Statistics, Pharm D, PhD, PRINCE2, Registered Nurse, SAP, Six Sigma, SolTRAQs, Veterinary, 3PL, ADaM, Administration, Adverse Event management, Advocacy plans, Agile, AKTA, Analytical SEC, Animal Health, APICS, Applicant Tracking System Management, APS, ARISg, auditing, Batch release, Batch Review, BHV, Bioequivalence, Bioinformatics, Biologic, Biomarkers, biometrics, Biosamples, Biosimilars, Biostatistics, Biotech, Black Belt, Business Development, C++, Candidate Attraction, CAPA, CDISC, Cell Biology, Cell stem-based therapy, CER, Chemstations, Client communication, Clinical, Clinical Affairs, Clinical Data Management, Clinical Programming, Clinical Research Organisation, Clinical Trial Applications, clinical trials, close out visits, CMC, CMO, Commercialisation, Compassionate Use, Competent Authorities, Computer Systems Validation, Contract, CPIM, CRF Design, CRO, CSR, Data Analysis, data entry, Data Science, Data Warehouse, database design, Datalabs, DHPC, Distribution, Distribution Planning, DMC, Document Management, Downstream, Drug destruction, Drug Development, Drug Safety, DSUR, E2E, Early Access, Early Phase, EC Submissions, ECG, eCRF, EDC, electronic data capture, ELISA, Epidemiology, ePRO, ERP, eTMF, e-TMF, EU Legislation, Eudravigilance, European Federation of Pharmaceutical Industries, Export Management, FDA Audits, Feasibility, Finance, Forecast, FPLC, GCP, GDP, Gene Therapy, Global, Global Regulatory Affairs, GLP, GMP, Government Affairs, GS1 standards, Health Economics, Healthcare, Healthcare Compliance, Healthy Volunteers, Home-based, HPLC, IATA, ICF, ICH-GCP, Imaging, Immunology, IMP, IMPACT, IMPD, Import Management, IND, InForm, Informatics, International, Interviewing, Inventory Management, Investigator Payments, in-vitro, in-vivo, IRB Submissions, IRT, ISO 13485, ISO 13485:2003, ISO 14971, ISO 9001, ISO13485, IVRS, Java, Lab, Labelling, Laboratory, LEAN, Line Management, Logistics, MA-CC, Manufacturing, MAPP, Market Access, Market Insights, Market Intelligence, Market Research, Marketing, Marketing authorizations, Materiovigilance, MedDRA, Medical Affairs, Medical Communication, Medical Devices, Medical Information, Medical Writing, Medidata Rave, Monitoring, Monitoring Visit, MS Office, MS Project, My Trials, NMR, Office-based, Oracle, Outcomes Research, Outsourcing, Packaging, Paediatrics, Patient Outcomes, Permanent, PET scans, Pharma, Pharmaceutical, Pharmacodynamics, Pharmacoeconomics, Pharmacoepidemiology, Pharmacokinetic, Pharmacokinetics, Pharmacology, Pharmacovigilance, Pharmacy, Phase I, pipetting, PMP, Policy, Post Marketing, Postdoctoral research, Post-marketing, Preclinical, Pricing & Reimbursement, Pricing and Reimbursement, PROC, Process Excellence, Procurement, Product Management, Project Leadership, Project Management, PromoMats, Protein Characterisation, protocol development, Protocol writing, PSURs, Public Affairs, publishing, Purchasing, QP, Qualification Visit, Quality Assurance, Quality Control, Quality Management, Quality Management System, Radiology, Randomisation, Randomization, Rave, Reactovigilance, Real World Evidence, Recruitment, Regional Monitoring, Regulatory, Regulatory Operations, Regulatory submissions, Regulatory Systems Management, remote monitoring, RFI, Risk Management, risk-based monitoring, RMA, RMP, SAE, SAE reporting, Sales Inventory, Sample size estimation, Samples, SAS, Scrum, SDS-PAGE, SDTM, Serialisation, Shipments, shipping, Simoa, Site contracts, Site Engagement, site payments, SOX, SPC- CCDS, Spectroscopy, S-Plus, SPSS, SQL, Start-up activities, statistical analysis, Statistics, Study Management, Study Medication Labelling, Sunshine Act, Supplier Qualification, Supply Chain Distribution, Supply Chain Management, Supply Chain Planning, Supply Planning, SUSAR, SUSARs, TMF, Toxicogenomics, Toxicology, Trackwise, Training, Transport Management, Unicorn Purification System, UPLC, Upstream, UV-Vis Spectroscopy, validation, Veeva, Vendor Management, Venipuncture, VISIO, Western Blot, ZINC, Bratislava, Slovakia, Afrikaans, Argentinian, Armenian, Belgian, Bosnian, Bulgarian, Cambodia, Cantonese, Catalonian, Chinese, Croatian, Czech, Danish, Dutch, English, Flemish, French, Greek, Gujarati, Hebrew, Hungarian, Italian, Japanese, Korean, Latvian, Lithuanian, Luxembourgish, Macedonian, Malayalam, Mandarin, Montenegrin, Norwegian, Persian, Punjabi, Romanian, Russian, Serbian, Slovak, Slovene, Slovenian, Spanish, Swedish, Thai, Turkish, UkrainianLocation: GloballyShare: 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GEBHARDT Intralogistics GroupDie GEBHARDT Intralogistics Group ist einer der führenden Anbieter von Materialfluss- und innerbetrieblichen Logistiksystemen. Seit 70 Jahren entwickelt GEBHARDT maßgeschneiderte Komplettlösungen – von der Idee bis zur vollständigen Realisierung – im Bereich Transport, Materialfluss, Sortiertechnik, Montage- und Lagertechnik, einschließlich Steuerung & Automatisierung, Lagerverwaltungssysteme und IT-Integration.GEBHARDT Intralogistics GroupDie GEBHARDT Intralogistics Group ist einer der führenden Anbieter von Materialfluss- und innerbetrieblichen Logistiksystemen. Seit 70 Jahren entwickelt GEBHARDT maßgeschneiderte Komplettlösungen – von der Idee bis zur vollständigen Realisierung – im Bereich Transport, Materialfluss, Sortiertechnik, Montage- und Lagertechnik, einschließlich Steuerung & Automatisierung, Lagerverwaltungssysteme und IT-Integration.FÄHIGKEITEN, DIE BENÖTIGT WERDEN/YOUR CAPABILITIES:English version below:Abgeschlossene Ausbildung im technischen und industriellen Bereich sowie entsprechende Weiterbildung zum Techniker/Meister oder vergleichbare QualifikationenMehrjährige Erfahrung in Installation und Inbetriebnahme im Automationssektor (bevorzugt Förder- und Lagersysteme)Erfahrung im Umgang mit Kunden und der Pflege von KundenbeziehungenInitiative, Flexibilität, eigenständiges und lösungsorientiertes Arbeiten sowie ausgeprägte, nachgewiesene organisatorische und FührungsfähigkeitenGute Beherrschung von Englisch und Französisch in Wort und Schrift, weitere Sprachkenntnisse, wie Deutsch, sind von Vorteil__________________________________________________________________________Completed technical and industrial apprenticeship and further training as a technician/master craftsman or comparable qualificationsMany years of experience in installation and commissioning in the automation sector (preferably conveyor and warehouse systems)Initiative, flexible, independent, and solution-orientedProven organizational and leadership skillsGood command of written and spoken English and Frensh, further language skills are an advantage. German language skills are advantageousAUFGABEN, DIE AUF SIE WARTEN/YOUR TASKS:English version below:Verantwortlich für die Ausführung und Überwachung der Baustelle eines Automatisierungsprojekts in Frankreich (Region Lille)Eröffnung der Baustelle (Büro, IT-Ausstattung, Arbeitsgenehmigungen, Eintrittsgenehmigungen usw.) unter Berücksichtigung des Vertrags, der Spezifikationen und der Kunden-/ProjektstandardsVerantwortlich für die Leitung eines Abschnitts der Baustelle und Anweisung und Anleitung der Mitarbeiter (intern und extern) hinsichtlich Arbeitssicherheitsbestimmungen, Kontrolle der Arbeitsergebnisse usw.Zusammen mit dem Sicherheitsspezialisten verantwortlich für die Arbeitssicherheit auf der Baustelle und Erstellung und Pflege aktueller RisikobewertungenVerantwortlich für die Durchführung und Überwachung der Implementierungsarbeiten: Dies umfasst die Ausführung der mechanischen und elektrischen Installation sowie die Inbetriebnahme in Bezug auf Inhalt und PersonalDefinition und Überwachung der Implementierungssequenz und -zeitplanung vor Ort unter Berücksichtigung des Einführungszeitplans des KundenZentraler Ansprechpartner für den Kunden und Projektleiter für den BaustellenabschnittErfassung und Bewertung von Über- und Untererfüllungen und Kommunikation dieser an das ProjektmanagementVerantwortlich für alle logistischen Belange auf der Baustelle__________________________________________________________________________Responsible for the execution and supervision of the installation of an Automation project in France (Lille area)Planning and preparing the construction site (office, IT supplies, work passes, entry permits, etc.) considering the contract, specifications and the customer/project standardsResponsible for the management of the installation on site. Monitoring the onsite installation sequence and schedule, taking into account the customer’s launch dateInstructing and guiding employees (internal & external) with regards to safety regulations. Together with the safety specialist, responsible for occupational safety on the construction site and create and maintain current risk assessmentsMonitoring the installation: This includes the execution of the mechanical & electrical installation and commissioning, in terms of content and personnelMain contact person to the customer and project manager on the construction siteRegularly report to the Turnkey project managementResponsible for all logistics related to the siteLEISTUNGEN, DIE WIR BIETEN:Wir bieten Ihnen einen modernen Arbeitsplatz in einem stark expandierenden Unternehmen mit einer abwechslungsreichen interessanten Aufgabenstellung. Wir suchen eine selbstständige, verantwortungsbewusste Verstärkung, die sich gut in unser Team einfügt und den weiteren Ausbau unseres Unternehmens kreativ mitgestaltet.Verantwortlichkeiten:English version below:Verantwortlich für die Ausführung und Überwachung der Baustelle eines Automatisierungsprojekts in Frankreich (Region Lille)Eröffnung der Baustelle (Büro, IT-Ausstattung, Arbeitsgenehmigungen, Eintrittsgenehmigungen usw.) unter Berücksichtigung des Vertrags, der Spezifikationen und der Kunden-/ProjektstandardsVerantwortlich für die Leitung eines Abschnitts der Baustelle und Anweisung und Anleitung der Mitarbeiter (intern und extern) hinsichtlich Arbeitssicherheitsbestimmungen, Kontrolle der Arbeitsergebnisse usw.Zusammen mit dem Sicherheitsspezialisten verantwortlich für die Arbeitssicherheit auf der Baustelle und Erstellung und Pflege aktueller RisikobewertungenVerantwortlich für die Durchführung und Überwachung der Implementierungsarbeiten: Dies umfasst die Ausführung der mechanischen und elektrischen Installation sowie die Inbetriebnahme in Bezug auf Inhalt und PersonalDefinition und Überwachung der Implementierungssequenz und -zeitplanung vor Ort unter Berücksichtigung des Einführungszeitplans des KundenZentraler Ansprechpartner für den Kunden und Projektleiter für den BaustellenabschnittErfassung und Bewertung von Über- und Untererfüllungen und Kommunikation dieser an das ProjektmanagementVerantwortlich für alle logistischen Belange auf der Baustelle__________________________________________________________________________Responsible for the execution and supervision of the installation of an Automation project in France (Lille area)Planning and preparing the construction site (office, IT supplies, work passes, entry permits, etc.) considering the contract, specifications and the customer/project standardsResponsible for the management of the installation on site. Monitoring the onsite installation sequence and schedule, taking into account the customer’s launch dateInstructing and guiding employees (internal & external) with regards to safety regulations. Together with the safety specialist, responsible for occupational safety on the construction site and create and maintain current risk assessmentsMonitoring the installation: This includes the execution of the mechanical & electrical installation and commissioning, in terms of content and personnelMain contact person to the customer and project manager on the construction siteRegularly report to the Turnkey project managementResponsible for all logistics related to the siteQualifikationen:English version below:Abgeschlossene Ausbildung im technischen und industriellen Bereich sowie entsprechende Weiterbildung zum Techniker/Meister oder vergleichbare QualifikationenMehrjährige Erfahrung in Installation und Inbetriebnahme im Automationssektor (bevorzugt Förder- und Lagersysteme)Erfahrung im Umgang mit Kunden und der Pflege von KundenbeziehungenInitiative, Flexibilität, eigenständiges und lösungsorientiertes Arbeiten sowie ausgeprägte, nachgewiesene organisatorische und FührungsfähigkeitenGute Beherrschung von Englisch und Französisch in Wort und Schrift, weitere Sprachkenntnisse, wie Deutsch, sind von Vorteil__________________________________________________________________________Completed technical and industrial apprenticeship and further training as a technician/master craftsman or comparable qualificationsMany years of experience in installation and commissioning in the automation sector (preferably conveyor and warehouse systems)Initiative, flexible, independent, and solution-orientedProven organizational and leadership skillsGood command of written and spoken English and Frensh, further language skills are an advantage. German language skills are advantageousÜber das Unternehmen:GEBHARDT FördertechnikBranche:Project managementWebsite:https://www.linkedin.com/company/gebhardt-f-rdertechnik-gmbh/>>>>>https://www.facebook.com/GEBHARDT.intralogistics.group/>>>>>https://twitter.com/GebhardtGroup

About us GXO ServiceTech is a leading reverse logistics specialist for electronics retailers, manufacturers and insurance providers with multiple locations across the UK and Europe. We provide a comprehensive service portfolio for a wide range of consumer electronics, including laptops, televisions, screens, mobile and gaming devices and domestic appliances. With unrivalled expertise in consumer electronics, we specialise in B2B returns, B2C services and on-site services. We are currently looking to strengthen our team in Dormagen and are looking for several committed and technology-enthusiastic (Junior / Senior) Technician (m/w/d) who would like to contribute and expand their expertise in a diverse working environment. Flat hierarchies and a motivated and competent team ensure professional work in a positive and pleasant working atmosphere. As a (Junior / Senior) Technician (m/w/d) your focus will be on the efficient and independent repair of brown or white goods. Your responsibilities will include, but are not limited to, testing defective devices, initiate hardware repairs, firmware updates, parts replacement and digital reporting. If you have the required skills and experience and are looking for the challenge of carrying out high-quality TV repairs as part of a dynamic team, we look forward to receiving your detailed application. Become part of our dedicated team and actively contribute to the success of our company. Your tasks Carrying out qualified hardware repairs and diagnosis at module and component level for flat screen televisions, etc. Carrying out firmware and software updates Replacement of module parts Disassembling televisions and recycling parts for stock Using the internal IT control system to update order status and finalise orders Taking a keen interest in repair and product quality Guidance and training of less experienced colleagues Job requirements Very good written and spoken communication skills (English and German) Ability to make decisions and show initiative Problem solving skills (analytical) Very good computer and IT skills, as well as MS Office user skills, especially Excel Relevant work experience in the technical field, TV repair or testing Familiarity and understanding of ESD precautions and procedures Flexibility, resilience and adaptability Motivation and enthusiasm for the job We offer Exciting tasks in a growing, international company A comprehensive and practical training programme A long-term workplace Flat hierarchies Please note that we only accept applications submitted via our online form on our careers page Questions about your application? Magda Rejman provides answers: -------------------------------------------------------------------------------------------------- Standort GXO Logistics, Inc., Dormagen

ABOUT NUMAHey! We're numa. We're a dynamic, diverse hospitality brand that's offering uniquely designed apartments for the modern traveler. We specialize in the beauty of convenience and the delight of a design, with a totally digital guest experience and properties designed with intention. Numa properties are located in the most exciting and vibrant neighbourhoods across Europe. We're not just disrupting the hospitality industry for our guests—behind the curtain, we're shaking up the way hotels operate. We've built a proprietary technology and data platform that makes running a hospitality operation more efficient than ever. We offer consistent quality and an unmatched guest experience. ABOUT THE ROLE:We are seeking a highly skilled, motivated, and impact-driven Due Diligence Specialist to join our team. As a key player, you will be entrusted with the responsibility of conducting numerous property inspections, delivering comprehensive reports crucial for informed decision-making. Executing both desktop and on-site evaluation of potential new properties, your tasks will include: Document review: Conduct comprehensive reviews of all documentation associated with new hotels Develop and maintain a checklist for tracking required documentation completion.Verify completeness and accuracy of documentation, ensuring compliance with company standards.Technical assessment and brand compliance:Evaluate physical condition of potential new properties and their alignment with numa brand standards, guidelines and requirements: design, operational, ICT, etc Evaluate the condition of existing systems: HVAC, electrical, plumbing, fire safety.Identify areas requiring refurbishment or improvements to meet numa requirements Identify deficiencies, repairs, upgrades Identify gaps or discrepancies between the site and the documentation Budget and timeline estimation:Develop detailed cost estimates for necessary renovations and operational upgrades to align with Numa standards Independently develop realistic timelines based on due diligence outcomesReporting:Compile and analyse data for detailed due diligence reports with photo documentationSummarise findings related to building status, brand alignment, budget estimates, and documentation complianceDevelop clear and concise recommendations based on due diligence findingsIndependently address concerns and red flagsCommunicate due diligence results and your recommendations effectively to internal and external stakeholdersContinuous Improvement:Participate in refining due diligence processes for enhanced efficiency Maintain close relationships with project managers to track project execution and incorporate learnings into the due diligence processEstablish a network of external technical consultants, advisors, and contractorsStay informed about industry best practices and independently incorporate relevant improvements ABOUT YOUUniversity degree in engineering, architecture, construction, real estate, business management, or similar Experience in due diligence processes, or project & construction management within the hospitality or real estate industry.Strong understanding of MEP systems and technical aspects of hotel operations.Ability to build and maintain good relationships with external partiesExcellent stakeholder management and strong communication skillsWell-developed technical and creative skills, thinking outside conventional solutionsA good eye for detail Excellent negotiation, communication, and presentation skills.Ability to work collaboratively with cross-functional teamsFluent in English is a requirement. Fluent in other European languages is a plus Flexibility to travel across Europe ABOUT OUR OFFERJoin an agile work environment with flat hierarchies where your ideas make an impact from the very beginningBuild your own success story based on what you do well and how you want to growElevate your physical and mental wellness with our monthly benefit allowancesGet to know your internationally diverse team during our events and retreatsSpend a free night at your nearest numa stay upon starting and enjoy a 30% employee discount on personal stays in the coolest neighbourhoods in Europenuma values the diversity of the people it hires and serves. Diversity at our company means fostering a workplace in which individual differences are recognised, appreciated, respected and responded to in ways that fully develop and utilise each person's talents and strengths. We therefore welcome applications from people of all races, ethnicities, disability statuses, ages, religions, gender identities, and sexual orientations.For more information on the processing of your personal data, please see our Privacy Notice.Über das Unternehmen:numa

Location: Belgium - Office-basedSchedule: Full Time, Permanent Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for an international CRO can bring? Our team says it's the best of both worlds….   The sponsor-dedicated division of ClinChoice, is searching for a Regulatory Compliance Specialist to join one of our clients, one of the most innovative pharmaceutical companies in the world. ClinChoice is an international CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with their client counterparts.   The Regulatory Specialist assists and supports the Regulatory Affairs department in the execution of regulatory activities to ensure the timely global commercialization of products in compliance with applicable European regulations and international standards.Main Job Tasks and Responsibilities: Partner with the International execution team in the EMEA region.Coordinate, compile, and submit free distribution certificates.Support product registration internationally; Gather and collate information from the manufacturer as required.Provide support to the international team as requested in the development of relationships with RA affiliates, contribute to the development and implementation of the local registration strategy.Act as the EU regulatory Subject Matter Expert for the portfolio under his or her responsibility, supporting the day-to-day Regulatory Affairs activities.Develop strategic guidance and recommend regulatory requirements relevant to the Franchise.Review internal and external communications of the EMEA that refer to products and/or disease state information (Copy Review Process) and represents the department in relevant forums.Advise and provide regulatory impacts to Supply Chain initiatives for the department, be the Primary Point of Contact for the regulatory distribution controls of medical devices and support associated processes and system development.Write, review, and revise company SOPs, recommend efficiencies to processes, and drive Engineering Change Orders (including but not limited to SOPs, and EU labeling approval).Support announced and unannounced inspections by external and internal functions.Assist with organizational tasks: departmental meetings (logistics, formatting, minutes) and department POs, handling regulatory fees (Ariba).Work closely with internal partners across the organisation (including Legal manufacturers, importers, distributors, regional regulatory affairs, quality, supply chain, marketing, and medical affairs) to ensure that stakeholder voices are incorporated into strategies for product launches and product changes.Provide solutions to a variety of problems of moderate scope and complexity where data analysis requires the evaluation of intangible variables.Responsible for the communication of business-related issues or opportunities to the next level of management.Responsible for ensuring personal and Company compliance with all Federal, State, local, and Company regulations, policies, and procedures.Perform other duties assigned as needed.  Education and Experience: University/bachelor's Degree or Equivalent (Science, Engineering, Technical or Biomedical field or Law preferred).4-6 years of work experience in Regulatory Affairs or Quality Affairs preferredSkills:Good knowledge of medical device regulatory requirements in the EUAbility to work effectively in a matrixed organisation and to build partnerships with regional and franchise colleagues.Demonstrate project management skills.Proactive identification of new insights and solutionsExcellent communication, influencing, and presentation skills.Strong output orientation and sense of urgencyExcellent written and verbal communication skills in English (required) The Benefits of Working in Belgium:Competitive SalaryGroup and hospitalisation insuranceElectronic meal vouchersInternet reimbursementCompany Car with fuel card depending on the function.Dedicated Line Manager The Application Process Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.  If you would like to discuss the role before applying through the website @https://www.talentsourcelifesciences.com/jobs   please contact mailto:[email protected] for more information. Who will you be working for?   About ClinChoice      CROMSOURCE is now a ClinChoice Company. ClinChoice is a leading full-service CRO dedicated to offering high-quality one-stop service to the pharmaceutical, biotechnology, medical device and consumer products clients. Some of these services include Clinical Operations, Project Management, Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, and Pharmacovigilance. ClinCHoice has established major delivery centres across US, Canada, China, Europe, India, Japan and the Philippines. It has over 4,000 employees globally, with a strong and talented team, and a growing clinical operations presence across Asia, North America, and Europe.      Our Company Ethos Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates. Keywords: Regulatory Compliance Specialist, RA, Compliance Specialist, Regulatory Specialist, Medical Devices, Regulatory, Regulatory Affairs, Pharmaceutical, Pharma, CRO, Contract Research Organisation, Outsourced, Sponsor-dedicatedSkills: Regulatory Affairs Associate, CRO, Medical Devices, Outsourcing, Pharma, Pharmaceutical, Regulatory, Regulatory OperationsLocation: BelgiumShare: LinkedIn Facebook Twitter Email

Project assistant for GIS documentation (m/f/d) 1st solution consulting GmbH - that's us for 20 years - we are passionate about helping our clients to recruit, provide and manage IT consultants and engineers in the telecommunications sector and have developed into one of the leading specialists. With fast, agile and reliable processes, we support our clients from a wide range of industries, such as telecommunications, energy, logistics, finance and technology groups, with great commitment -- in the daily challenges of finding solutions. When can we meet you in person to talk about the position? To expand our existing service teams, we are looking for project staff for GIS documentation (m/f/d) throughout Germany. What we offer you A dynamic and committed team with a family spirit A systematic induction to fulfill the demanding and varied job combined with further education and training Personal development through professional training opportunities Flexible working hours and home office Independent and self-organized work An open-ended permanent position 30 days vacation per year What are your tasks You will be responsible for reviewing, editing and implementing network data to create map materials You will ensure that the GIS documentation is processed independently You communicate with other departments You design corresponding data models in accordance with legal requirements and guidelines for the complete provision of construction files You ensure that all deadlines and project goals are met on time and guarantee that the documentation is handed over on time What are our requirements You have a degree in a technical subject or university degree or have completed vocational training in a technical or commercial field. You should also have some experience in the use of GIS documentation tools (e.g. QGIS, ARCGIS, ITK, GEOSTRACT or similar) Ideally, you have experience in the documentation of passive telecommunications networks, backbone connections & route planning and desirably in project management. You are highly self-motivated, willing to learn and able to work under pressure, and you see yourself as a flexible, motivated team player You enjoy your work and make the most of your creative approach You have good MS Office skills If you are interested and feel called to work as a full member of a constantly growing company, then we look forward to receiving your application. If you have any questions, please call us on 0211 - 15 98 35 54 / 0172 1885 451 as well as by e-mail [email protected] at any time Additional information: Requirements for the applicant: Basic knowledge: CAD application AutoCAD, GIS (geo-info system), geo-information system (GIS) ArcInfo, geo-information system (GIS) GeoMedia, geo-information system (GIS) Smallworld, geo-information system ArcGIS, geo-information system QGIS, CAD application CADprocess/IsoDraw.

Your Tasks From acquiring space and analysing projects to creating risk assessments - you always maintain an overview of projects and people. You manage approval processes and work closely with business partners and internal departments in a team-oriented manner. Then we should definitely get to know each other! Support in the development and planning of ground-mounted photovoltaic systems from securing land to construction readiness Support in the coordination and implementation of approval procedures as well as negotiations with authorities and municipalities Interdisciplinary dialogue with specialist departments regarding planning, design and profitability calculations Preparation of project documentation, risk assessments and decision papers Support in analysing and evaluating projects and carrying out due diligence processes with regard to approval processes, land securing, structural suitability and power grid connection, among other things Focus on independent project acquisition as well as in cooperation with partners and project developers Close cooperation with internal specialist departments, business partners, law firms and external consultants Your profile Completed studies in the field of renewable energies, landscape or environmental planning, architecture, construction or property management or industrial engineering Passion for renewable energies Nice to have: initial experience in project acquisition and project development Nice to have: experience in the field of photovoltaic or wind turbine construction Your skills: communicative team player (m/f/d) with a proactive, independent and responsible way of working, initiative and negotiating skills Willingness to travel nationally (approx. 30%) Class B driving licence Who we are We are a multicultural international company with a lot of team spirit. With employees in 5 different countries, we work to ensure a climate-friendly energy production for future generations. We build ground-mounted solar power plants throughout Europe and, as one of the world's largest O&M service providers, ensure our costumers’ plant operation for decades to come. Our aim is to protect the climate and ensure a cost-effective and secure energy supply. We foster acceptance of solar energy and thus contribute to the success of the energy transition. For future generations, we strive to make the world a little bit better. Whether Kolitzheim, Berlin, Nuremberg or Würzburg - in addition to our headquarters in Kolitzheim, we also offer jobs in our capital city office and at our co-working locations as well as remote work. What we offer Flat hierarchies with good development opportunities. Permanent contracts. A familial and collegial cooperation in an international environment. Flexible working hours and mobile working. Job-Bike-Leasing. VWL and bAV. Regular employee events. Curious? You can find all our benefits here: . Standort BELECTRIC GmbH, Berlin

Armacell provides numerous and diverse career opportunities. Add your talent to ours and make a difference around the world! Zur Verstärkung unserer Abteilung Logistik suchen wir für unseren europäischen Hauptsitz in Münster zum nächstmöglichen Termin mehrere engagierte Lageristen / Kommissionierer (m/w/d) zur unbefristeten Festanstellung. Ihre Aufgabe Sie sind verantwortlich für die Kontrolle der Lieferungen und das Verpacken, Versenden und Verladen von Fertigwaren Sie kontrollieren Wareneingänge und Warenausgänge und übernehmen die fachgerechte Lagerung der Güter Sie unterstützen bei der körperlichen Bestandsaufnahme unserer Vorräte Dazu arbeiten sie auch als Kommissionierer und stellen Waren und Güter nach Kundenbestellungen zusammen Ihr Profil Idealerweise haben Sie eine Ausbildung zum Fachlageristen oder eine vergleichbare handwerkliche Ausbildung abgeschlossen Sie sind höhensicher und besitzen einen Berechtigungsschein zum Führen und Bedienen von Flurförderzeugen, Staplern und/oder Kommissioniergeräten Sie verfügen über ein gutes Zahlenverständnis und eine gute Kommunikationsfähigkeit in Wort und Schrift Ihre Einsatzbereitschaft ist flexibel und Sie sind offen für den Schichtbetrieb Teamfähigkeit und Ihr Verantwortungsbewusstsein runden Ihr Profil ab Unser Angebot Neben einer abwechslungsreichen und herausfordernden Aufgabe in einem motivierten Team bieten wir Ihnen persönliche Entwicklungsmöglichkeiten, ein leistungsgerechtes Vergütungsmodell sowie weitere Sozialleistungen. Sie fühlen sich in einem lebhaften, internationalen Umfeld wohl und interessieren sich für einen zukunftsorientierten Arbeitsplatz? Wir freuen uns auf Ihre Online-Bewerbung! Kontakt Theresa Schinke, Recruiting Specialist T: 0251 7603-247 E: ********** Time Type: Full time As the inventors of flexible elastomeric foams for equipment insulation purposes, Armacell develops innovative and safe thermal, acoustic and mechanical solutions. By enabling energy efficiency for equipment we validate our global leadership in flexible technical foams. We drive substitution and innovation for our indirect customers and use world-class practices to strengthen our premium brand position. We grow by providing valuable solutions offering reliable, certified performance. Our high-caliber employees make all the difference in generating added value for customers. We empower our employees to positively impact our company and the communities we work with. We drive their performance thanks to aligned goals, while identifying and developing their talents. We create a culture of innovation in order to develop leading product and system solutions enabling our employees to Make a difference around the world. You have not found a suitable job opportunity for you today? You would like us to know you better? Do not hesitate to "introduce yourself" and share your resume.Über das Unternehmen:1400 Armacell Logistics GmbH

For our client, thyssenkrupp nucera in Dortmund , we are currently looking for a Buyer (m/f/d) . Do you have a completed apprenticeship, some work experience and a lot of motivation? Then use us as a springboard into an international and future-oriented group company! Here's what we offer Attractive salary and long-term job security through group affiliation Up to 30 days vacation per year Contribution to company pension scheme after end of probationary period Extensive social benefits, including Christmas and vacation bonuses Reimbursement of travel expenses As a rule, a permanent employment contract Good chances of being taken on by our business partners Tailored further training opportunities and free language courses A wide range of employee benefits Your tasks You carry out the inquiry and order call-off process and are also responsible for simple clarification of technical and commercial contractual queries. You monitor and track the production process at subcontractors. You coordinate the various interfaces internally and communicate with the supplier. You will send reminders to vendors and suppliers. You support the specialist purchasing department with activities and take on assigned tasks. Your profile You have completed vocational training in the commercial sector with appropriate further training as a specialist in purchasing, specialist in purchasing and logistics and have a strong affinity for technology, or a comparable qualification. You have initial professional experience in purchasing, expediting, supply chain management or similar. You have the ability to present complex issues in a simple and understandable way. You have an independent and results-oriented way of working, a strong analytical mindset as well as negotiating skills, persuasiveness and a high level of team orientation. Very good written and spoken German and English (both at least C1 level), another foreign language is an advantage. You have solid knowledge of the common MS Office applications, as well as initial experience in working with SAP-MM. Standort GULP – experts united, Dortmund

Senior Key Account Manger - North GermanyThe Senior Key Account Manager is responsible to drive sales growth in their respective territory by servicing existing Customers/Implanting Centers and initiating new Implanting Centers based on the strategic needs of the territory. The Sr. KAM will provide in-depth field support to customers during the market’s uptake phase by ensuring Implanting Center staff are fully trained and Implanting Centers are set up for success including all product logistics and approvals.In addition, the Sr. KAM will need to drive the referral network around each Implanting Center ensuring a continuous flow of new patients into the Implanting Centers. The patient funnel and reimbursement efforts will fundamental to the success of the territory. The Sr. KAM must have a hands-on approach, a strong customer-oriented personality, solid process management skills, possess strong communication skills as interactions will be with patients, patient groups, doctors, rehab specialists, and hospital staff. Key Responsibilities:Drive sales growth of the company Responsible for the in-depth site management of existing Implanting Centers (assure the numbers of implants according with the forecast)Initiate and develop new Implanting CentersProvide the initial training and Site Evaluation for all the centers Establish Referral Networks (Push & Pull strategies) that will funnel patients into Implanting CentersDevelop strategic partnerships with key opinion leaders and advocates to help in the promotion of the device through social mediaSupport and collaborate with the market access department for secure revenue in reimbursed centers.Assist and support the surgeon in the OR for the first implantations Ensure training is provided by Patient Pathway trainers to personnel of the Implanting Centers (e.g., visual rehab personnel, nurses, ODs, etc.)Help identify patients for testimonials to be used in various marketing initiativesPoint of contact for challenging clinical cases. Provide technical input into the management of these casesCollaborate with marketing department and support it in organizing and participate in mainly local trade shows, congresses, team meetingsRequired Education and Experience: University degree (fields of Business and/or Science preferred)At least 10+ years of experience in a medically related setting, preferably in ophthalmologyKnowledge of diagnostic tests in ophthalmologyRequired Knowledge, Skills, Abilities: Experience working successfully in a team and managing projectsExperience in surgical support within Operating room preferredStrong ethics and objectivityMust be able to work in a fast-paced, dynamic environment and foster constructive relationships with internal and external customersAbility to work well under pressure, action oriented, ability to quickly translate needs into action, proven ability to take initiative and follow-up independentlyMust possess superior interpersonal and organizational skillsMust be able to communicate effectively and efficiently with external/internal colleagues and patientsAbility to deal with an internationally diverse environmentCompetence in German and English (any other language is a plus)Good computer skills (MS Office applications).Experience in working with patients is a great plusMust be willing to travel up to 30 to 50%. Must be able to travel with short notice. No visa or other travel limitations.Interested?Apply Now! Standort CM Medical Recruitment, Düsseldorf

My client is one of the largest aftermarket supplier of nondiscretionary parts.They have their European HQ in Euskirchen and due to their recent growth they are looking to strengthen their team.These tasks are waiting for you:1. Ownership and Organization: Assume full ownership of supply chain planning activities and methodologies. Organize and streamline the supply chain planning process to ensure efficiency and accuracy. Drive continuous improvement initiatives to enhance planning capabilities. Support revolving SIOP (Sales Inventory and Operatiions Planning) process. 2. Process Optimization: Evaluate the existing complex Excel-based supply chain planning system. Identify inefficiencies and areas for improvement in disposition, demand planning, requirements analysis, stock policy, and safety stock management. Optimal sourcing identification to maximise service and cash, limiting the impact on margin.Develop and implement optimized processes to enhance overall supply chain efficiency. 3. Data Integration and Reporting: Extract information from various files and reports to create a consolidated and accurate view of supply chain data. Facilitate seamless communication and data sharing between different departments and interfaces. General master data management for supply chain related contents (like e.g. MOQs, Lead-times, Buy Prices) Implement robust reporting mechanisms to provide real-time insights into supply chain performance. Experience with Power BI (or similar) is an advantage. 4. Transition to Professional Planning Tool: Lead future transition from the current Excel-based tool to a professional supply planning tool (e.g., Add*One, Slimstock, or others). Collaborate with IT teams and external vendors to ensure a smooth implementation process. Develop and conduct training programs for team members to adapt to the new planning tool. 5. Collaboration: Foster collaboration with cross-functional teams, including procurement, production, and logistics, to align planning activities with overall business objectives. Work closely with stakeholders to understand their requirements and incorporate feedback into the planning process. Education and qualifications:1. Educational Background: Bachelor's degree in Supply Chain Management, Business, or a related field. Master's degree is a plus. 2. Experience: Minimum of 5 years of experience in supply chain planning, with a focus on demand forecasting, inventory management, and planning process optimization. Proven track record of successfully implementing and managing supply chain planning tools. 3. Technical Skills: Advanced proficiency in Excel and other data analysis tools. Experience with professional planning tools such as Add*One, Slimstock, or similar planning systems is an advantage. Familiarity with data integration and reporting tools. 4. Analytical Skills: Strong analytical and problem-solving skills with the ability to interpret complex data sets. Experience in statistical forecasting methods and demand planning. 5. Communication Skills: Excellent verbal and written communication skills. Ability to effectively communicate with diverse teams and stakeholders. 6. Project Management: Proven project management skills with the ability to lead and execute complex supply chain planning projects. PMP or other relevant certifications are a plus. 7. Adaptability: Demonstrated ability to adapt to changing business requirements and technologies. Openness to learning and adopting new planning methodologies. These are your advantages with us:You will receive a structured onboarding and a professional training periodOur corporate culture is characterized by openness and appreciation, with flat hierarchies and fast decision-making proceduresWe offer internal and external training programs for your personal developmentAlways an important factor: flexible working hours, home office, 30-day vacation entitlementAttractive staff discounts on our products, lunch allowances, as well as free drinksWe have very good traffic connections and free employee parking spaces Standort Syben Consulting, Euskirchen

Senior Key Account Manger - North GermanyThe Senior Key Account Manager is responsible to drive sales growth in their respective territory by servicing existing Customers/Implanting Centers and initiating new Implanting Centers based on the strategic needs of the territory. The Sr. KAM will provide in-depth field support to customers during the market’s uptake phase by ensuring Implanting Center staff are fully trained and Implanting Centers are set up for success including all product logistics and approvals.In addition, the Sr. KAM will need to drive the referral network around each Implanting Center ensuring a continuous flow of new patients into the Implanting Centers. The patient funnel and reimbursement efforts will fundamental to the success of the territory. The Sr. KAM must have a hands-on approach, a strong customer-oriented personality, solid process management skills, possess strong communication skills as interactions will be with patients, patient groups, doctors, rehab specialists, and hospital staff. Key Responsibilities:Drive sales growth of the company Responsible for the in-depth site management of existing Implanting Centers (assure the numbers of implants according with the forecast)Initiate and develop new Implanting CentersProvide the initial training and Site Evaluation for all the centers Establish Referral Networks (Push & Pull strategies) that will funnel patients into Implanting CentersDevelop strategic partnerships with key opinion leaders and advocates to help in the promotion of the device through social mediaSupport and collaborate with the market access department for secure revenue in reimbursed centers.Assist and support the surgeon in the OR for the first implantations Ensure training is provided by Patient Pathway trainers to personnel of the Implanting Centers (e.g., visual rehab personnel, nurses, ODs, etc.)Help identify patients for testimonials to be used in various marketing initiativesPoint of contact for challenging clinical cases. Provide technical input into the management of these casesCollaborate with marketing department and support it in organizing and participate in mainly local trade shows, congresses, team meetingsRequired Education and Experience: University degree (fields of Business and/or Science preferred)At least 10+ years of experience in a medically related setting, preferably in ophthalmologyKnowledge of diagnostic tests in ophthalmologyRequired Knowledge, Skills, Abilities: Experience working successfully in a team and managing projectsExperience in surgical support within Operating room preferredStrong ethics and objectivityMust be able to work in a fast-paced, dynamic environment and foster constructive relationships with internal and external customersAbility to work well under pressure, action oriented, ability to quickly translate needs into action, proven ability to take initiative and follow-up independentlyMust possess superior interpersonal and organizational skillsMust be able to communicate effectively and efficiently with external/internal colleagues and patientsAbility to deal with an internationally diverse environmentCompetence in German and English (any other language is a plus)Good computer skills (MS Office applications).Experience in working with patients is a great plusMust be willing to travel up to 30 to 50%. Must be able to travel with short notice. No visa or other travel limitations.Interested?Apply Now! Standort CM Medical Recruitment, Cologne

Orbem is an impact-driven deep tech startup from Munich, Germany. We develop fast, accurate, and accessible imaging solutions that provide access to otherwise unattainable sources of knowledge.We seek to make a difference – and develop solutions to sustainably feed the world, accelerate the transition to a green economy, and transform disease detection. Join us.Junior MRI Application SpecialistStarting date: As soon as possibleOur compensation package:€50,000 - €55,000 in yearly salary, and up to €5,000 in equity. Additionally up to €5,000 p.a. in company benefitsOffice location: Munich, GermanyThis position will require you to spend up to 40% of your time travellingYour roleYou contribute to establishing the foundations of our innovation efforts by assisting in pilot trials in the field. At the forefront of cutting-edge technology, you manage the trials and data acquisition. You collaborate with our interdisciplinary innovation team to organize logistics and support test runs operating our unique imaging systems. By leveraging your attention to detail and striving for improvements you help us unleash AI-powered imaging for everything and everyoneYour day to dayOn a typical day you will:take care of trial processes and work on their automationtrack ongoing lab studies by structuring scanned subjects into groups, labeling test material, and documenting the process with tools like Google Sheetsexamine and annotate MRI scans according to provided guidelines travel regularly to our customers' sitesYour teamAs an MRI Application Specialist you become part of our diverse and international Innovation team with teammates from six different countries. You’ll be collaborating with the Munich based Application Specialist, the Imaging team as well as with the AI team. Learn more about the team members, their work and challenges here: www.orbem.aiWhat we offerInternational environment: 5 different continents, 25+ nationalities driven by the same purpose: shedding light on the world’s toughest challengesAttractive package: You participate in Orbem’s success with stock options, which you receive on top of your salary. We also offer visa, relocation support and several benefits such as: yearly Learning & Development budget (€1,750), Fitness club membership (USC, Wellpass), Kita/Kindergarten fee reimbursement and more!Work-life balance:We commit to creating an environment where our employees can find the balance they need. This includes flexible working hours, 30 days per year of paid leave and sick child leaveMake a difference: You’ll work in a scale-up environment with the freedom to drive your own projects and make a visible impactYou join an ambitious team working on breakthrough technology: We offer you a plain playing field to explore and design. During your time with Orbem, we support you in discovering your strengths and defining a vision for your professional future. We hope to teach you some things, but more importantly we also want to learn from you. Apply now!Your experiences and skillsFit our valuesWe own every challenge: we enjoy complexity and thrive under uncertaintyWe strive for better: we seize any opportunity for growth and challenge the status quo. We are constantly learning and improvingWe imagine new frontiers: we think beyond ‘doable’ and ‘reasonable’. We design a sustainable and healthy future togetherScientific approachYou follow a data-based mindset, finding evidence through utilizing the highest standards of experimental researchYou are skilled at paying attention to detail, applying a good hand-eye coordination to the careful operation of test subjects in examinationWhat makes you stand out from other candidatesTechnical expertiseYou have experience in the poultry industryYou have solid knowledge of data management tools, e.g., Google Sheets, ExcelYou are fluent in English and FrenchYou own a driver’s licenseBehavioural competenciesYou embrace exploring new approaches to find the best solutionsYou are passionate about a patient, focused and detailed working styleYou iterate fast, ensuring up-to-date knowledge integrationYou enjoy traveling and changing your working environment Standort Orbem GmbH, Munich