Überblick über die Statistik des Gehaltsniveaus für "Operations Research Scientist in Deutschland"

Ihre AufgabenZentrale Aufgaben der Position des Wissenschaftlers/der Wissenschaftlerin sind die Entwicklung und Optimierung von Diagnostika und Pharmazeutika auf Basis neuer und bestehender Methodiken zur Kontrolle von Rohstoffen, Produktionszwischenprodukten und EndproduktenInterdisziplinäre Zusammenarbeit mit unterschiedlichsten, am Entwicklungsprozess beteiligten AbteilungenEigenständige Selektion und Anwendung analytischer MethodenValidierung und Dokumentation der Testmethodik sowie kontinuierliche Analyse und Bewertung von Methodik, Material und Produkten in allen Phasen des EntwicklungsprozessesAuswertung, Zusammenfassung und Präsentation der VersuchsergebnisseDokumentation entsprechend der gültigen QVA’s und SOP’s und GMPEinhaltung von QM-Vorgaben und Vorgaben der Arbeitssicherheit und UmweltschutzIhre QualifikationenAbsolviertes naturwissenschaftliches Hochschulstudium oder Promotion in der Biologie, Chemie, Biochemie, oder in einem vergleichbaren StudiengangVorhandene Expertise in Forschung und Entwicklung; Kenntnisse gängiger, naturwissenschaftlicher MethodenErfahrung in diversen analytischen Methoden, ebenso Fähigkeit zur breitgefächerten, eigenständigen Anwendung dieser MethodikFreude an interdisziplinärer, enger TeamzusammenarbeitSehr gute Deutsch- und EnglischkenntnisseGute IT-Kenntnisse, hohe digitale AffinitätBegeisterung für den Bereich PharmaIhre VorteileDen Einstieg in ein global führendes GroßunternehmenEine umfangreiche und verantwortungsvolle HerausforderungÜbertarifliche Bezahlung und Branchenzuschläge ChemiePersönliche Betreuung und Beratung durch Ihre Trenkwalder GeschäftsstelleExklusive Mitarbeiterrabatte bei Reisen, Mode, Auto, Elektronik, etc.Gute Übernahmeperspektive durch unseren namhaften KundenUrlaubs- und Weihnachtsgeld ab 6 Monaten BetriebszugehörigkeitEinarbeitung bei unserem Kunden vor Ort im Rahmen eines PatensystemsZusätzlicher Freizeitausgleich durch flexibles Arbeitszeitkonto

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: LinkedIn Facebook Twitter Email

Location: Belgium - Hybrid  Schedule: 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….       TalentSource Life Sciences (the sponsor-dedicated division of CROMSOURCE), is searching for a Clinical Research MD to join one of our clients, one of the most innovative pharmaceutical companies in the world.     CROMSOURCE 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 while establishing a high-trust environment with their client counterparts.       The Clinical Research MD is a responsible member of a clinical team dedicated to the execution of medical strategies and the clinical and operational implementation of a clinical study. Provides active medical and scientific contributions to a cross-functional clinical team.The Physician provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and contributes to the content of clinical study reports and relevant documents for regulatory filings, and performs medical monitoring. Team matrix interactions include clinical team members, project management, quality assurance, quality monitoring and compliance, clinical supplies unit, TA strategy, regulatory affairs, data management, medical writing, biostatistics, global medical affairs, clinical pharmacology, clinical operations, health economics, epidemiology, and other scientific and business-related disciplines.Main Job Tasks and Responsibilities: Is responsible for medical monitoring/reporting and company safety officer activities.Works on clinical development plans, and trial protocols and contributes to clinical study reports.Evaluates adverse events (pre- and post-marketing) for relationship to treatment.Assists Regulatory Affairs in determining requirements for any corrective actions or health authority reporting.Interprets, reports, and prepares oral and written product research findings in conjunction with senior clinical staff in preparation for regulatory submissions.Liaises closely with clinical scientists and physicians across programs.Provides medical input to external activities such as liaison with external experts, steering committees, independent data, Monitoring Committees, and other committees related to studies or projects.Medical input related to trial-related questions.Provides medical training to the Clinical Trial Team members and other company stakeholders.Supervises Clinical leader.Assists Regulatory Affairs in the development of drug regulatory strategies.Supports general clinical activities involving product evaluation, labeling, and surveillance.Reviews medical literature and related new technologiesAssess medical publications emerging from the Team and its affiliates. Education and Experience:MD with four years' experience in clinical development in pharma or biotech, or equivalent in Academia, preferably including medical monitoring.Trained in GCP Good knowledge of regulatory requirements/ICH guidelines.Proficient in using Microsoft Office and in data visualization tools.Good organizational skills, able to work as part of a team and independently.Good communication skillsDetailed orientedEnglish oral and written communication skills Our Benefits in Belgium:Competitive SalaryGroup and hospitalization insuranceElectronic meal vouchersInternet reimbursementDedicated Line ManagerRegular face-to-face or phone meetings with the line managerFull annual performance review process 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 CROMSOURCE        CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                      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.     About TalentSource Life Sciences    TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role, and work autonomously.     CROMSOURCE is an equal opportunity employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.     Keywords: Clinical Research MD, Physician, CRO, Clinical Research Organisation, Contract Research Organisation, Clinical, Drugs, Medical Devices, Clinical TrialsSkills: Medical Practitioner, Clinical Research Organisation, clinical trials, CRO, Medical DevicesLocation: BelgiumShare: LinkedIn Facebook Twitter Email

What we doWe are an exciting early-stage AI start-up creating the future of manufacturing! We believe that blue-collar workers are an essential part of this transformation. We are dedicated to empowering these workers by assisting them in their daily tasks and unlocking the full potential of manual labor through productivity and flexibility.We are utilizing cutting-edge technology, such as computer vision and artificial intelligence, to revolutionize manufacturing by providing workers with the tools they need to improve their productivity beyond current limitations. Our focus is initially on assembly processes, but we plan to expand to other areas, including material consignment and machine repair activities. By improving efficiency, we aim to make products more affordable and use resources more sustainably.Our team is led by experienced entrepreneurs Max and Silviu. Max has previously founded a company in manufacturing that digitized 40 factories, and Silviu holds a PhD in computer science and is a computer vision expert. He has previously led a team that developed a robot taxi service at Volkswagen and built a startup in the security industry. Our team includes members from top-tier universities such as ETH and MIT, as well as individuals with entrepreneurial experience in the fashion industry and at leading research institutions like Fraunhofer. At our company, we value hard work, creativity, and a willingness to learn and grow. We are committed to fostering a diverse and inclusive workforce and welcome candidates of all backgrounds. Additionally, we offer a comprehensive benefits package that includes medical insurance and a learning and development budget. Furthermore, we provide flexible scheduling options and the opportunity for employees to set their own schedule to support our employee's families and personal responsibilities.We are financially backed by Merantix, the world’s first AI Venture Studio. We are proud to be part of a team that includes some of the world’s most talented engineers, scientists, and entrepreneurs from prestigious universities such as Yale, Oxford, and Harvard. Our studio is based on the Berlin AI Campus, and we have already founded seven ventures to date, employing over 150 people between our studio and our ventures. This presents an opportunity for you to join our ecosystem and collaborate with AI and business experts from various industries, who will support you in your professional development and in balancing your personal and professional responsibilities.Your roleThis is an onsite role for our team in Berlin.We're on the lookout for a highly motivated hardware engineer intern to strengthen our team. You will be a key player, enhancing our engineering capacity and extending support to our customers to ensure seamless service delivery and innovative solutions.Your responsibilities will include:Assisting the setup, managing and monitoring of a fleet of Linux-based edge devices.Assisting with the setup and configuration of sensors: Set up, test, and optimize camera systems integral to our computer vision applications ensuring optimum performance and reliability.Deployment on Edge PC: Execute effective deployment strategies on edge PCs, contributing to the seamless operation of our computer vision technologies.Hardware Status Reports: Prepare and present detailed, accurate reports on the status of various hardware components, aiding in the swift identification and resolution of issues.Support Engineering Team: Play a pivotal role in supporting the engineering team with tasks like flashing cameras, acquiring hardware from suppliers, and installing Ubuntu on edge PCs.Your profileCurrently enrolled in or recently graduated from a bachelors or masters degree program in Computer Science, Electrical Engineering, or a related field.Tech-Savvy: Proficiency in programming languages like Python or C++, and familiarity with Linux operating systems.Strong problem-solving and analytical skills.Ability to work independently and as part of a team.Fluency in English (German not required).What we offerPaid internship positionA Brand new office situated on the AI Campus in Berlin where we closely cooperate with other exciting AI venturesNetworking and mentorship opportunities with leaders in the company and industry Supportive and inclusive culture that values diversity and promotes the advancement of underrepresented groups within the company.International Team: Within our current team, we have more than 10 nationalities and counting Engaging Topics and Excellence: Merantix offers unique insights into applied machine learning research and development, working with a group of highly talented engineers and entrepreneursEthics️: We are committed to developing ethical AI softwareDynamic working culture: We hold weekly and monthly events around AI Innovation and Implementation. We have a very flat hierarchy, open 360° feedback, and flexible working hours Learning and Development. Annual learning and development budget to attend conferences or purchase educational resources to develop additional skills further Standort Merantix, Berlin

The Opportunity: Under moderate supervision, perform warehouse operations such as loading/unloading trucks, stacking bags, handling product, palletizing, etc. Document all completed work and recording inventory data; utilizing scanners/computers as necessary. Interact regularly with peers and management to pursue continuous improvement of warehouse operations and promote teamwork. Operate forklifts and hand carts. Understand and adhere to all safety policies and procedures Wir – Ritter, part of Avantor- suchen einen Fachlagerist / Lagerlogistik (m/w/d), der für die fachgerechte Einlagerung und Warenbuchungen über ERP-System verantwortlich ist. Sie haben die Möglichkeit, in einem engagierten Team und mit flexiblen Arbeitszeiten ihre Fähigkeiten unter Beweis zu stellen. Wenn Sie eine Ausbildung zur Fachkraft für Lagerlogistik und eine Bereitschaft zur Schichtarbeit mitbringen– melden Sie sich jetzt! Ritter wurde von Avantor übernommen, um seine hochpräzisen Produkte und hochmodernen Fertigungskapazitäten mit dem Angebot von Avantor für kritische Laborautomatisierungsabläufe, seiner globalen Reichweite und seiner Leidenschaft für das Erreichen wissenschaftlicher Durchbrüche zu kombinieren. Wenn Sie sich unserem vereinten Team anschließen, haben Sie die einzigartige Möglichkeit, Ihre Karriere voranzutreiben und gleichzeitig Teil eines erfahrenen Teams zu sein, das sich in den letzten 60 Jahren einen bemerkenswerten Ruf als weltweiter Pionier in der Herstellung von Kunststoffprodukten erworben hat. Das sollten Sie mitbringen: Mehrjährige Berufserfahrung in der Logistik, vorzugsweise in einem Industrieunternehmen Ausbildung zur Fachkraft für Lagerlogistik bevorzugt oder zum Fachlageristen Staplerschein Erfahrung mit Ladungssicherung, Umlagerungen und Versand (Luft- Seefracht) Einlagern der Produktionsware (I-Punkte) Selbständige und strukturierte Arbeitsweise MS Office Kenntnisse (Outlook, Excel, Word, PowerPoint) Bereitschaft zur Schichtarbeit und Wochenendarbeit Deutsch in Wort und Schrift, Englische Grundkenntnisse wären von Vorteil Ihre Aufgaben: Fachgerechte Einlagerung von Waren und Warenbuchungen über ERP-System Identifizierung und Etikettierung der Waren beim Lagerzugang Versandvorbereitung für ausgehende Waren (Transport, kommissionieren, bereitstellen und Kennzeichnen der versandbereiten Waren) Präventive Bedienung und Wartung von Lagerfahrzeugen und -geräten Einhalten der Lagerordnung und Sauberkeit in allen internen Lagern und Hofbereichen Durchführen und Einhalten aller gesetzlichen Vorschriften im Wareneingang Wareneingangsprüfung und Dokumentation der Lieferung (systemseitige Warenvereinnahmung) Identifizieren und Verteilen von Paketdienstwaren Bestandskontrollen und Korrekturen im ERP System Durchführung der jährlichen und permanenten Inventur Über Ritter, ein Unternehmen von Avantor Ritter ist ein globaler Hersteller von Hochpräzisionsprodukten und gilt als der am schnellsten wachsende Hersteller von hochwertigen Robotern und Verbrauchsmaterialien für das Liquid Handling. Mit mehr als 400 talentierten Mitarbeitern an zwei Standorten in Deutschland ist unser Team für jeden Aspekt des Produktionsprozesses gerüstet, vom Design und Formenbau über das Spritzgießen mit einer Reihe von Maschinen (20 bis 660 Tonnen) bis hin zu Montage und Druck. Unser Produktportfolio besteht ausschließlich aus unseren eigenen Kreationen, die sich auf drei Kernbereiche konzentrieren: Kartuschen: Wir bieten ein weltweit führendes Sortiment an Kartuschensystemen für Verpackungsdichtstoffe, Klebstoffe, Druckfarben und mehr. Medizin: Wir bieten Verbrauchsmaterialien für den Labor-, Krankenhaus-, Medizin- und Veterinärbedarf, die alle in Reinraumumgebungen hergestellt werden. Baumaterialien: Zu unserem Angebot gehören Rasengitter, EquiTerr für die Errichtung von Reithallen und Pferdekoppeln sowie Lösungen für Parkplätze und Hangbefestigungen. Warum Avantor? Trauen Sie sich, Karriere zu machen. Schließen Sie sich unserem globalen Team von mehr als 14.000 Mitarbeitern an, die mit ihrer Leidenschaft für Entdeckungen und ihrer Entschlossenheit, Herausforderungen zu meistern, unermüdlich die lebensverändernde Wissenschaft voranbringen. Unsere Arbeit verändert das Leben der Menschen zum Besseren. Sie bringt neue Behandlungen und Therapien für Patienten auf den Markt und gibt einem Krebsüberlebenden die Chance, seine Tochter vor den Traualtar zu führen. Sie ermöglicht medizinische Geräte, die einem kleinen Jungen helfen, zum ersten Mal im Leben die Stimme seiner Mutter zu hören. Ergebnisse wie diese schaffen unbegrenzte Möglichkeiten für Sie, Ihre Talente einzubringen, neue Fähigkeiten zu erlernen und Ihre Karriere bei Avantor weiterzuverfolgen. Wir helfen Ihnen unbeirrt auf diesem Weg durch unsere vielfältige, gleichberechtigte und integrative Kultur, die personalisierte Lernerfahrungen beinhaltet, um Ihre berufliche Entwicklung und Ihren Erfolg zu fördern. Bei Avantor können Sie es wagen, über sich hinauszuwachsen und zu sehen, wie die Auswirkungen Ihrer Beiträge die Wissenschaft in Bewegung setzen, um eine bessere Welt zu schaffen. Bewerben Sie sich noch heute! #LI-EUR #LI-Onsite Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at ********** and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. Privacy Policy: We will use the personal information that you have submitted to us in order to consider your application for the relevant role. Your privacy is important to us. Please click here for our Privacy Policy which explains the purposes for which we will use your personal information and the ways in which we will handle and retain your information. It also explains the rights you have in relation to your information, and how to contact us with any queries or requests. 3rd Party Non-Solicitation Policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation. Avantor, a Fortune 500 company, is a leading global provider of mission-critical products and services to customers in the biopharma, healthcare, education & government, and advanced technologies & applied materials industries. Our portfolio is used in virtually every stage of the most important research, development and production activities in the industries we serve. One of our greatest strengths comes from having a global infrastructure that is strategically located to support the needs of our customers. Our global footprint enables us to serve more than 225,000 customer locations and gives us extensive access to research laboratories and scientists in more than 180 countries. We set science in motion to create a better world.Über das Unternehmen:Germany - Ritter GmbH

What we doWe are an exciting new AI start-up creating the future of manufacturing! We believe that blue-collar workers are an essential part of this transformation. We are dedicated to empowering these workers by assisting them in their daily tasks and unlocking the full potential of manual labor through productivity and flexibility.We are utilizing cutting-edge technology, such as computer vision and artificial intelligence, to revolutionize manufacturing by providing workers with the tools they need to improve their productivity beyond current limitations. Our focus is initially on assembly processes, but we plan to expand to other areas, including material consignment and machine repair activities. By improving efficiency, we aim to make products more affordable and use resources more sustainably.Our team is led by experienced entrepreneurs Max and Silviu. Max has previously founded a company in manufacturing that digitized 40 factories, and Silviu holds a PhD in computer science and is a computer vision expert. He has previously led a team that developed a robot taxi service at Volkswagen and built a startup in the security industry. Our team includes members from top-tier universities such as ETH and MIT, as well as individuals with entrepreneurial experience in the fashion industry and at leading research institutions like Fraunhofer. At our company, we value hard work, creativity, and a willingness to learn and grow. We are committed to fostering a diverse and inclusive workforce and welcome candidates of all backgrounds. Our job is 100% remote, and we actively support a healthy work-life balance. Additionally, we offer a comprehensive benefits package that includes medical insurance and a learning and development budget. Furthermore, we provide flexible scheduling options and the opportunity for employees to set their own schedule to support our employee's families and personal responsibilities.We are financially backed by Merantix, the world’s first AI Venture Studio. We are proud to be part of a team that includes some of the world’s most talented engineers, scientists, and entrepreneurs from prestigious universities such as Yale, Oxford, and Harvard. Our studio is based on the Berlin AI Campus, and we have already founded seven ventures to date, employing over 150 people between our studio and our ventures. This presents an opportunity for you to join our ecosystem and collaborate with AI and business experts from various industries, who will support you in your professional development and in balancing your personal and professional responsibilities.Your roleThis is a remote role. Therefore, you’d be able to work anywhere you want within Europe.We are looking for a very ambitious individual who wants to help us shape the future of manufacturing. Being one of the first business team members, you will help us identify, evaluate, and act on business development opportunities. You will develop and set up operations to grow our business. This is a highly impactful role as you will work directly with the founders, shaping the product and helping us deliver value to our customers.In short:Sales Strategy & Outreach: Research and identify potential customers, carry out strategic outreach to generate leads, and manage interactions to drive conversions.Presentation & Proposal Creation: Create compelling sales presentations tailored to potential customers, draft proposals addressing their specific needs, and ensure follow-ups to close sales deals.Data Management & Analysis: Maintain and manage the customer database, track and analyze sales data to understand trends, and provide reports to the team on sales performance.Exploring New Channels: Proactively identify and explore new channels, platforms, or strategies to enhance and optimize sales efforts, ensuring our reach and impact continue to grow.Your profileWe define ourselves by a culture of ownership and cooperation. We are looking for driven, capable, visionary, and prudent talents with proven track records of personal, academic, and professional achievement. You have an undergraduate degree or are in your final year at a top-­tier university, MA/MSc is a plus.You have gained professional experience in an impactful entrepreneurial environment, at a leading technology company, or in management consultancy/ venture capital.Superb English communication skills, both verbal and written, and interpersonal skills and an ability to effectively communicate with both business and technical teams.You have a long-­held interest in technology, both personally and professionally.You have strong organizational and multitasking skills with the ability to prioritize appropriately and effectively.You are available to work with us for full-time for 6 months at a time.What we offerPaid internship position.A Brand new office situated on the AI Campus in Berlin where we closely cooperate with other exciting AI ventures - although we work remotely, you can still work from the campus if you wishHardware allowance. We give you support to have all the equipment you would need to thrive on your jobInternational Team: Within our current team we have more than 10 nationalities and counting Engaging Topics and Excellence: Merantix offers unique insights into applied machine learning research and development, working with a group of highly talented engineers and entrepreneursEthics: We are committed to developing ethical AI softwareDynamic working culture: We hold weekly and monthly events around AI Innovation and Implementation. We have a very flat hierarchy, open 360° feedback, and flexible working hoursLearning and Development. Annual learning and development budget to attend conferences or purchase educational resources to develop additional skills further Standort Merantix, Berlin

Make new discoveries, drive projects forward, accept responsibility: at Hochschule Bonn-Rhein-Sieg University of Applied Science (H-BRS), we depend on staff who do just this. In cooperation with around 1,000 colleagues, we develop new solutions to help find appropriate responses to the many challenges of our times. We do this to further improve the H-BRS with the 9000 students from more than 100 countries who are currently enrolled in ist 40 courses. Do you accept the challenge? By concession of the right to award doctorates for the Promotionskolleg NRW (PK NRW), direct doctoral studies at the H-BRS in conjunction with PK NRW have become possible. The realization of a PhD as a scientific employee is desired and supported. As of the next possible date we require - subject to the final project grant decision - the following for our Department of Engineering and Communication at the Sankt Augustin campus: Research-Associate or/and PhD student (d/m/w) for Solutions of Power-Electronic-Converters and Power-Hardware-in-the-Loopwith focus on Hardware-Development As a research associate, you will be responsible for scientific collaboration in the field of design and development of power electronic converters. The responsibility will be fulfilled as a team in collaboration with researchers having various level of experience and type of expertise. You are not expected to have expertise in all fields; rather we offer to work with the team to become expert. Your tasks: You will be responsible for scientific collaboration in the field of design and development of power electronic converters. The responsibility will be fulfilled as a team in collaboration with researchers having various level of experience and type of expertise. model and simulate power electronic circuits. develop circuit diagrams and PCB layouts. optimize switching-cells and gate-drives for SiC- and GaN-Semiconductors for power electronic circuits. develop and optimize test-benches for characterization of wide-bandgap-semiconductors and magnetic components. determine processor technologies, design and implement control and operation management for fast-switching power electronic converters. perform testing of power-electronic-converters with Power-Hardware-in-the-Loop-Systems. carry out installation and commissioning of fast-switching power electronic converters. create scientific reports and publications. support the team in other research projects. Our expectations: You have a Master’s or Bachelor’s degree (FH, TU/TH) in electrical engineering, sustainable engineering or a comparable course of study. ideally have knowledge of control/operation of power electronic circuits using microcontrollers and/or DSP’s/FPGA’s. ideally have experience in the area of power and/or hardware-in-the-loop. like to work in a team, determined to work and contribute, self-initiated and „think outside the box“. are enthusiastic about issues of application-oriented research. have English and German skills on C1-level. have previous knowledge in the field of design and realization of power electronic converters and their peripherals. What we offer: We as employers offer exciting, varied work in an innovative environment, full-time remunerated according to your qualifications up to salary group 13 TVL and of fixed duration until 30th September 2026. are family focused and offer flexible working hours and childcare facilities facilitate advanced training and continuing education for professional and personal development provide a library and a cafeteria value the liveable Rhineland area as an optimum environment for higher education – distinguished by unique local advantages such as the cathedral city of Cologne, the cosmopolitan city of Bonn, and the unspoilt countryside in the Eifel, Siebengebirge and Rhine districts We want to have more female scientists at our university and are therefore especially pleased to receive applications from female applicants with children are warmly welcomed. H-BRS is certified family-friendly – and proud of it. People with severe disabilities are an integral part of our university. They are given preference in the application procedure provided they are equally well qualified. If you have any further questions, please contact Prof. Dr. Marco Jung at +49 2241 865 316. Become part of Bonn-Rhein-Sieg University of Applied Sciences (H-BRS) and use our online form to send us your application by March 03,2024 (reference number 75/23). Standort Hochschule Bonn-Rhein-Sieg, Sankt Augustin

Make new discoveries, drive projects forward, accept responsibility: at Hochschule Bonn-Rhein-Sieg University of Applied Science (H-BRS), we depend on staff who do just this. In cooperation with around 1,000 colleagues, we develop new solutions to help find appropriate responses to the many challenges of our times. We do this to further improve the H-BRS with the 9,000 students from more than 100 countries who are currently enrolled in ist 40 courses. Do you accept the challenge? By concession of the right to award doctorates for the Promotionskolleg NRW (PK NRW), direct doctoral studies at the H-BRS in conjunction with PK NRW have become possible. The realization of a PhD as a scientific employee is desired and supported. As of the 1st Oktober 2023, we require - subject to the final project grant decision - the following for our Department of Engineering and Communication at the Sankt Augustin campus: Research-Associate or/and PhD student (d/m/w) for Solutions of Power-Electronic-Converters and Power-Hardware-in-the-Loopwith focus on Control As a research associate, you will be responsible for scientific collaboration in the field of design and development of power electronic converters. The responsibility will be fulfilled as a team in collaboration with researchers having various level of experience and type of expertise. You are not expected to have expertise in all fields; rather we offer to work with the team to become expert. Your tasks: You model and simulate power electronic circuits. investigate innovative control concepts for power electronic converters in various fields of application. carry out theoretical analyses in terms of control concepts of power electronic converters. develop and optimize control of test benches for characterization of wide-bandgap-semiconductors and magnetic components. determine processor technologies, design and implement control and operation management for fast-switching power electronic converters. perform testing of power-electronic-converters with Power-Hardware-in-the-Loop-Systems. carry out installation and commissioning of fast-switching power electronic converters. create scientific reports, publications and work on trend-setting research projects with a team. Our expectations: You have a Master’s or Bachelor’s degree (FH, TU/TH) in electrical engineering, sustainable engineering or a comparable course of study. ideally have knowledge of control/operation of power electronic circuits using microcontrollers and/or DSP’s/FPGA’s. ideally have experience in the area of power and/or hardware-in-the-loop. like to work in a team, determined to work and contribute, self-initiated and „think outside the box“. are enthusiastic about issues of application-oriented research. have English and German skills on C1-level. have previous knowledge in the field of design and realization of power electronic converters and their peripherals. What we offer: We as employers offer exciting, varied work in an innovative environment, full-time remunerated according to your qualifications up to salary group 13 TVL and of fixed duration until 30th September 2026. are family focused and offer flexible working hours and childcare facilities facilitate advanced training and continuing education for professional and personal development provide a library and a cafeteria value the liveable Rhineland area as an optimum environment for higher education – distinguished by unique local advantages such as the cathedral city of Cologne, the cosmopolitan city of Bonn, and the unspoilt countryside in the Eifel, Siebengebirge and Rhine districts We want to have more female scientists at our university and are therefore especially pleased to receive applications from female applicants with children are warmly welcomed. H-BRS is certified family-friendly – and proud of it. People with severe disabilities are an integral part of our university. They are given preference in the application procedure provided they are equally well qualified. If you have any further questions, please contact Prof. Dr. Marco Jung at +49 2241 865 316. Become part of Bonn-Rhein-Sieg University of Applied Sciences (H-BRS) and use our online form to send us your application by March 03,2024 (reference number 76/23). Standort Hochschule Bonn-Rhein-Sieg, Sankt Augustin

Make new discoveries, drive projects forward, accept responsibility: at Hochschule Bonn-Rhein-Sieg University of Applied Science (H-BRS), we depend on staff who do just this. In cooperation with around 1,000 colleagues, we develop new solutions to help find appropriate responses to the many challenges of our times. We do this to further improve the H-BRS with the 9,000 students from more than 100 countries who are currently enrolled in ist 40 courses. Do you accept the challenge? By concession of the right to award doctorates for the Promotionskolleg NRW (PK NRW), direct doctoral studies at the H-BRS in conjunction with PK NRW have become possible. The realization of a PhD as a scientific employee is desired and supported. As of the next possible date we require the following for the research project "FHIL-Reloaded - Development of a test infrastructure for the normative validation of dynamic processes of grid-forming decentralized generation plants" for our Department of Engineering and Communication at the Sankt Augustin campus: Research Associate or/and PhD student (d/m/f) for Power-Electronic-Converter-Development and Power-Hardware-in-the-Loop with focus on Power-Hardware-in-the-Loop As a research associate, you will be responsible for scientific collaboration in the field of design and development of power electronic converters. The responsibility will be fulfilled as a team in collaboration with researchers having various level of experience and type of expertise. You are not expected to have expertise in all fields; rather we offer to work with the team to become expert. Your tasks: You model and simulate power electronic circuits. develop circuit diagrams and PCB layouts. optimize switching-cells and gate-drives for SiC- and GaN-Semiconductors for power electronic circuits. develop and optimize test-benches for characterization of wide-bandgap-semiconductors and magnetic components. determine processor technologies, design and implement control and operation management for fast-switching power electronic converters. perform testing of power-electronic-converters with Power-Hardware-in-the-Loop-Systems. carry out installation and commissioning of fast-switching power electronic converters. create scientific reports and publications. support the team in other research projects. Our expectations: You have a master’s or bachelor’s degree (FH, TU/TH) in electrical engineering, sustainable engineering or a comparable course of study. ideally have knowledge of control/operation of power electronic circuits using microcontrollers and/or DSP’s/FPGA’s. ideally have experience in the area of power and/or hardware-in-the-loop. like to work in a team, determined to work and contribute, self-initiated and „think outside the box“. are enthusiastic about issues of application-oriented research. have English and German skills on C1-level. have previous knowledge in the field of design and realization of power electronic converters and their peripherals. What we offer: We as employers offer exciting, varied work in an innovative environment, full-time remunerated according to your qualifications up to salary group E13 TV-L and of fixed duration until 30th September 2026. are family focused and offer flexible working hours and childcare facilities facilitate advanced training and continuing education for professional and personal development provide a library and a cafeteria value the liveable Rhineland area as an optimum environment for higher education – distinguished by unique local advantages such as the cathedral city of Cologne, the cosmopolitan city of Bonn, and the unspoilt countryside in the Eifel, Siebengebirge and Rhine districts We want to have more female scientists at our university and are therefore especially pleased to receive applications from female applicants with children are warmly welcomed. H-BRS is certified family-friendly – and proud of it. People with severe disabilities are an integral part of our university. They are given preference in the application procedure provided they are equally well qualified. If you have any further questions, please contact Prof. Dr. Marco Jung at +49 2241 865 316. Become part of Bonn-Rhein-Sieg University of Applied Sciences (H-BRS) and use our online form to send us your application by March 03,2024 (reference number 10/23). Standort Hochschule Bonn-Rhein-Sieg, Sankt Augustin

Nanogami is a highly innovative and rapidly growing startup in the field of DNA Origami-based nanotechnology (check out our DLD Talk or this article to learn more). Our international team is driven by a shared vision: to pioneer a novel generation of biochips set to unlock applications in research and diagnostics and thereby pushing the boundaries of personalised medicine to new heights. We recently secured significant funding by SPRIND - Germany’s Federal Agency for Disruptive Innovation to realize our ambitious growth trajectory and now aim to significantly expand our current team to support the at-scale commercialisation of our nanotechnology.Role Overview We are seeking a dedicated Laboratory Technician (f/m/d) to join our innovative biotechnology team. This role is pivotal in our lab operations, focusing on microbial culture management and bioreactor operations. Ideal for those passionate about biotechnology, it offers numerous opportunities for professional growth in a supportive, cutting-edge environment.What you will do Operate lab scale bioreactors.Maintain our microbial culture collection.Perform laboratory experiments, assays, and analyses under senior guidance and contribute to large-scale process improvements.Perform molecular cloning procedures, transformation of E. coli, cultivation of E. coli, downstream processingKeep comprehensive and well-organized laboratory records.Collaborate with researchers to troubleshoot experiments and optimize or develop new laboratory techniques and protocols, and participate in team meetings, provide feedback and contribute ideas for protocol optimization and experimental design.Perform routine laboratory maintenance tasks such as cleaning, organizing equipment and workspacesRequirementsTraining as a technical assistant (e.g. BTA or comparable) or Bachelor’s degree in biotechnology, molecular biology or in a related field1-2 years of experience working in a laboratory setting, preferably in the biotech industryComprehensive knowledge of biotechnological techniques and standard laboratory procedures - Experience with lab scale bioreactors, cultivating E. coli, molecular cloningFocused and reliable in executing laboratory tasks and standardized protocolsExcellent organisational and time management skills, with a positive and open attitude combined with the willingness to learn new thingsFlexible and responsive to dynamic work requirements.Effective in interdisciplinary team collaboration with a self-motivated and independent work ethic.Fluent in EnglishPreferred:Good understanding of German.Experience with M13 phages / Filamentous bacteriophagesExperience with Lambda phage handling/ cultivationExperience with pilot scale bioreactors (up to 200 L)BenefitsOpportunity to be part of a cutting-edge nanotechnology startup, and to make a lasting impact on the company and societyCompetitive compensation and benefits structure.An international, collaborative, and supportive work culture.Flexible working models.Über das Unternehmen:Nanogami

Join the Food Revolution to Combat Climate Change!Are you fueled by a passion for tackling some of the world’s most pressing challenges?Do you believe that technology and innovation can pave the way for a sustainable future?Do you want your job to directly impact sustainable food and a healthier planet?If your answer to these questions is a resounding "YES," then it's time to take a closer look at!TasksAs a Founders Associate at ProteinDistillery, you'll be the accelerator for change. You will assist our leadership team in navigating the multifaceted challenges, including strategizing for business development, conducting market research, handling data analysis, assist in preparing investor and partnership meetings and executing organizational tasks, while reporting directly to the C-level.If you're someone who thrives on intellectual agility and quick comprehension, eager to co-create and propel strategic initiatives, this role is for you.Requirements You're the Ideal Candidate If … You're eager to learn the ins and outs of launching a business in a rapidly evolving landscape. You excel at distilling complex subjects into concise, easily digestible information. You thrive on solving problems proactively and enjoy generating innovative yet practical solutions. Your knack for juggling multiple tasks and managing your time effectively sets you apart.Benefits Why Join ProteinDistillery Today?We're in the exciting start-up phase, offering a blank canvas to innovate without restrictions!Backed by top VCs and stellar angel investors, we have industry leaders already on board!Seize the moment! Food tech is at a pivotal crossroads, and sustainable options are on the rise. Help us make vegan food irresistibly delicious, compelling millions to make the quick switch from animal based mainstream! Workspace and Culture We're on the verge of building something huge — In the next three to four years, we envision a global team, hence the need for seamless remote operations. Initially, however, we feel that our culture and team spirit will thrive best by sharing physical space in our inviting offices based in Stuttgart & Berlin. A Note on Diversity & InclusionWe're committed to equal opportunities and value diversity. Our unifying factor is alignment with ProteinDistillery's mission and core values. We welcome applicants of any background, age, gender, or orientation.ProteinDistillery is a food-tech startup that develops a new generation of highly functional, vegan protein ingredients for food companies based on microorganisms - currently derived from brewer's yeast. We envision a more sustainable future through significant changes in the food system - a future where vegan alternatives match the original in every aspect and are free from additives. Our team consists of highly qualified entrepreneurs and scientists. In our own modern office with an adjacent small laboratory, we bring innovations to life every day. Standort ProteinDistillery, Berlin

The iPSC department at Evotec headquarters in Hamburg is seeking a highly motivated and dedicated Research Scientist (all genders) Stem Cell Full-time and permanent Your key responsibilities: Provide disease expertise to identify, develop, and validate new targets for the development of novel treatments in the area of neuroscience this can include but is not restricted to neurodegeneration, neuroinflammation, mental health and pain Lead drug discovery project(s) scientifically along the entire pre-clinical drug development process Provide proposals and scientific expertise to continuously advance and improve the iPSC drug discovery platform through new technologies and project ideas, both internally as well as in collaboration with our partners Maintain an awareness of cutting-edge technological advances and scientific knowledge to improve project performance Manage multidisciplinary teams and assign their work to meet project timelines and goals Deliver documents, technical reports and presentations in an accurate and timely manner Represent Evotec’s stem cell drug discovery capabilities internally and externally Your ideal qualifications: PhD in Biology or other relevant field with a strong focus iPSC biology and neuroscience research Experience in drug discovery from pharmaceutical or biotech industry is a plus High level of disease biology understanding relevant to neurodegeneration, neuroinflammation, mental health or pain In depth knowledge of human iPSC and other in vitro models in the relevant disease areas Profound knowledge and hands-on expertise of maintaining, manipulating and differentiating human iPSC Experience in assay development and adaptation for high throughput screening High level of motivation, initiative, flexibility and ability to work well in a cross-functional team Excellent communication & people skills as well as first experience in managing and professionally developing other scientists and technical staff Ability to work independently Full proficiency of English language – both written and spoken Our offer: A position within a vigorous and exciting professional environment promoted by an open culture and a spirit of community A diverse, international workforce with a dynamic working environment that fosters creativity, innovations and teamwork 30 days of annual holiday, monthly allowance for public transportation, and in-house canteen Capital forming benefits, flexible working hours, holiday pay, and annual bonus depending on performance To apply, please click on the “Apply” button and provide your application documents (CV and cover letter, including earliest possible start date and salary requirements). We are looking forward to getting to know you and to your application. FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap. ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities. Evotec is a life science company with a unique business model that delivers on its mission to discover and develop highly effective therapeutics and make them available to the patients. The Company’s multimodality platform comprises a unique combination of innovative technologies, data and science for the discovery, development, and production of first-in-class and best-in-class pharmaceutical products. Evotec leverages this “Data-driven R&D Autobahn to Cures” for proprietary projects and within a network of partners including all Top 20 Pharma and over 800 biotechnology companies, academic institutions, as well as other healthcare stakeholders. Evotec has strategic activities in a broad range of currently underserved therapeutic areas, including e.g. neurology, oncology, as well as metabolic and infectious diseases. Within these areas of expertise, Evotec aims to create the world-leading co-owned pipeline for innovative therapeutics and has to-date established a portfolio of more than 200 proprietary and co-owned R&D projects from early discovery to clinical development. Evotec operates globally with more than 5,000 highly qualified people. The Company’s 17 sites offer highly synergistic technologies and services and operate as complementary clusters of excellence. For additional information please go to www.evotec.com and follow us on X/Twitter @Evotec and LinkedIn. Please click on the link below to access and review our Privacy Information for Applicants: Privacy Information for ApplicantsÜber das Unternehmen:Evotec SE

The PositionA healthier future. That’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.With a department of more than 100 biostatisticians, data scientists and data managers at the Roche sites in Penzberg, Mannheim, Indianapolis and Sant Cugat des Vallès, we are supporting global projects to deliver new diagnostics to patients.As a Biostatistician / Data Scientist (f/m/d) in Personalized Healthcare, you and your future colleagues will focus on applying state-of-the-art statistical and data science methods to drive innovative projects in the field of personalized healthcare and companion diagnostics.Your key responsibilitiesYou will work as a project statistician and support the development of new biomarkers.You are responsible for planning and analyzing analytical and clinical studies.You will interact closely with the project team members (R&D, Clinical Operations, Clinical Development, Regulatory Affairs, external cooperation partners and customers) to capture data analysis requirements and to interpret and communicate the results in an understandable way.You will have the opportunity to apply multivariate machine learning methods for the development of new clinical algorithms.Your profileUniversity degree in (bio)statistics or related subjects (e.g. mathematics, epidemiology, physics), ideally with a PhD and extensive experience in statistics.You have experience in the life science/diagnostics/pharmaceutical industry or have successfully completed clinical data analysis projects in an academic environment.You are familiar with common diagnostic and statistical methods (e.g. logistic regression, ROC analysis, cut-off determination) and have experience in the design, analysis and evaluation of analytical and clinical studies.You have experience with statistical methods such as classification, survival and longitudinal analysis models and you are enthusiastic about the application and implementation of new statistical methods.You have excellent knowledge of R and LaTeX, ideally knitr or R markdown.You have excellent communication, organization and documentation skills as well as very good written and spoken English. German is an advantage.This position is a 2-year temporary contractYour applicationWe make things easier for you: Please upload only your current and informative CV and your certificate of your highest degree. However, we are happy to receive additional documents, such as a letter of motivation and certificates, which will help us to find out more about the reasons for your application.We look forward to receiving your application!Your contact to us! With people. For people.Do you need more support? Our Talent Acquisition Team welcomes your questions. Please send an email to**********Who we areAt Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.Roche at Penzberg, near Munich, employs more than 7,000 people. The site is one of the largest biotechnology centers in Europe and the only Roche site with research, development and production for both Pharmaceuticals and Diagnostics under one roof. From your beginning with Roche, our motivated team will welcome and support you. Numerous opportunities for personal development, flexible work hours, attractive compensation packages and special family assistance programs are available.Roche is an Equal Opportunity Employer.Über das Unternehmen:6164 Roche Diagnostics GmbH

Your missionAs a Health, Safety, and Environment (HSE) Specialist (m/w/d) & DGO at NVision, you occupy a pivotal role within our Business Operations Team. Your expertise and dedication not only reinforce our commitment to the safety and well-being of our workforce but also bolster the very foundation upon which our organization thrives. By ensuring the meticulous implementation and thorough execution of all HSE-related matters and overseeing our DG operations, you play a central part in promoting a proactive safety culture, thereby aiding NVision in maintaining an exemplary standard of operational excellence. Your role transcends mere compliance; you are instrumental in shaping a resilient and sustainable work environment that aligns with our corporate values, driving our mission forward, and contributing significantly to the broader success and growth of our organization.Tasks:Craft and enforce HSE & DG protocols, ensuring they align with existing legislation.Validate adherence to all legal, regulatory, and customer specific mandates.Preparation of all required documentation such as risk assessments, operating instructions and checklistsOversee and execute the proper shipment of dangerous goods internationally and, ensuring safe and compliant transportationManage the safe and compliant disposal of hazardous waste, aligning with all relevant regulationsFoster a culture that encourages safe behaviors, minimizing workplace hazardsEquip team members with the skills to assess risks, pinpoint hazards, and enact the necessary preventive measuresOversee our annual safety programs and spearhead the safety onboarding process for new hiresAid in devising regular checks, gauging our alignment with health, safety, and environmental standardsStay abreast of emerging legislations and maintain expertise in current HSE laws affecting our industryAssist local teams in dealings with regulatory bodies and produce necessary safety performance or incident reportsServe as the primary liaison with our occupational health provider, facilitating the creation and monitoring of the yearly planAdvise staff on the selection of appropriate safety gear, including personal protective equipmentLead investigations into workplace incidents, identifying root causes and recommending corrective actionsDevelop and establish emergency response plansExecution of DG Trainings for our EmployeesYour profileDegree in engineering or natural sciences or technical trainingOccupational safety specialist in accordance with § 6 ASiG and DGUV regulation 2Training as a hazardous goods officer (Gefahrgutbeauftragter) with a valid training certificate from the IHK (Chamber of Industry and Commerce) for road transport (ADR) and possibly other modes of transport (e.g. IATA)QHSE-specific advanced training or interest in further trainingSeveral years of professional experience in the HSE & DG environmentComprehensive knowledge of the legal framework, standards and regulationsVery good knowledge of German and EnglishWhy us?Competitive compensationOnsite working model with home-office opportuntiesAmple opportunity for personal initiatives, openness to new ideas and room for considerable personal impactImpactful product promoting better understanding and treatment of diseaseInternational team, from over 15 different nationalitiesEnjoyable work atmosphere with an open-door and open communications mentalityIndefinite employment contract30 vacation dayscontact informationAny questions? Please contact:Emilija StojanovskaTalent Acquisition Managermail: ********************About usNVision is a quantum biotech startup based in Ulm, Germany, with Tier 1 investors from Silicon Valley, Europe, and Israel. We are just leaving stealth mode, moving from local R&D to global commercialization and expansion. We are developing a technology that will enable MRI-based imaging of real-time metabolism in the body, with tremendous potential for research and applications in oncology, cardiology, neurology and more. What we are building is complex and fascinating and has vast potential for impactful applications. Our company brings together expertise in physics, chemistry, engineering, and medicine and we are collaborating with KOL scientists and clinicians from top medical and research centers such as Memorial Sloan Kettering in New York, MD Anderson in Texas, Technical University of Munich, Cambridge University in the UK and more.We offer a dynamic international working environment, with immense room for growth, that encourages personal initiative and open communication.Über das Unternehmen:NVision Imaging Technologies

Associate Director Scientific Program Management (m/f/d) Are you a visionary scientific leader experienced in custom model generation of animal models, seeking a fulfilling career with a dynamic, growth-oriented company? If you excel in fostering sales collaboration, driving product expansion, and nurturing staff development, we invite you to join us in shaping the future of scientific program management. Taconic Biosciences is seeking an Associate Director Scientific Program Management to join our dedicated Scientific Services team in Leverkusen, Germany. This position works primarily remote (90%) with ad hoc needs to visit our sites. What we offer: Annual Bonus Program Subsidized private pension scheme Internet stipends Job bike leasing Work life balance Career advancement opportunities Commitment to training and providing you with the skills you need for success Coffee, water and tea are free Regular company events If you are looking for a rewarding career and the opportunity to grow, apply today! The Role: The Associate Director leads the Scientific Program Management (SPM) team focused on Taconic’s Custom Model Generation Services (CMGS). The CMGS-SPM is part of the larger global commercial organization responsible for establishing and managing customer relationships. Specifically, the CMGS-SPM leads in the articulation of the value proposition of Taconic CMGS to new and existing customers, acts as the sole “gate keeper” on project design and acceptance, and provides primary scientific expertise during project design, execution, and issue resolution. The Associate Director of the CMGS-SPM has influence through leadership and collaboration on product design and development, product quality initiatives, marketing efforts, and go-to-market strategies. This person is responsible for building this critical team of PhD scientists into a cohesive and influential group responsible for achieving annual growth targets for the portfolio. The CMGS-SPM Associate Director reports to the Director of Scientific Program Management. Core Responsibilities: Leadership and Management: Lead and manage the global Scientific Program Management organization. Determine staffing needs, recruit, hire, and assign Scientific Program Managers. Prioritize, resource, and guide initiatives while overseeing the organization's budget. Report to senior and executive leadership. Strategic Direction: Define and articulate the value proposition of Taconic’s GEMs Scientific Services. Guide the selection of single sales opportunities. Collaboration and Process Improvement: Collaborate with the Project Management Group (PMG) to design and implement global processes, workflows, and best practices. Assist in determining Project Manager assignments and priorities. Financial Accountability: Share accountability for the financial health of Taconic’s GEMs Scientific Services. Foster collaboration with Sales and Client Relations to acquire new customers and grow market share. Customer Satisfaction and Product Development: Improve overall customer satisfaction ratings. Spearhead the identification, development, and implementation of new products and services. Mentorship and Support: Act as the primary mentor and elevation level for Scientific Program Managers. Support career advancement and job satisfaction among team members. Technical Standards and Training: Support the development and implementation of global technical standards and methodologies. Participate in the evaluation and selection of necessary tools and training curricula. Cross-Functional Collaboration: Facilitate collaboration with ancillary support departments to promote and improve Taconic’s GEMs Scientific Services. Education and Experience: Master’s degree or equivalent in a scientific field (preferably biology or related life science). Ph.D. preferred. Minimum 5 years of relevant experience and/or training. Project Management Professional (PMP) or comparable certification a plus. Experience in a wide range of principles and methodology of a specialized professional field. Skill in designing, implementing, and coordinating assignments, operations, and/or programs. Experience in making decisions or recommendations significantly developing or changing organizational policies or procedures. Requires supervisory or middle management experience. Ability to listen empathetically and understand information presented by people with different communication styles and different points of view. Success in this position requires a decisive nature and ability to produce a record of outstanding judgment, a natural initiative to addressing issues and challenges of varied levels of complexity; a capacity to manage multiple issues and demands at any one time; and to lead in the resolution of issues and challenges for which there may be little historical precedent. Travel: Regular travel is required, generally no more than one trip per month. About Us: With a history of over 65 years of excellence, Taconic Biosciences is a global team of the best problem solvers in the industry. We partner with our clients to develop winning research strategies that accelerate the discoveries for prevention and treatment of disease. Taconic employees all over the world show up every day to deliver the best solutions for our clients while caring for ourselves, each other, and especially our animals. If you are a respectful, compassionate individual with a can-do attitude and a desire to do the right thing, we want you to join us! Better Together at Taconic Inclusion, Diversity, Awareness & Action. Taconic Biosciences is taking an active and intentional role in creating a company culture that encourages and appreciates the uniqueness in all people. Being you is what allows you to bring your best self to work. We are committed to ensuring that Taconic is a safe and fair workplace for everyone because it’s our differences that make us stronger. We are better together. Powered by JazzHR Standort Taconic Biosciences, Inc., Leverkusen

Abiomed is an innovative medical device business with an inspiring mission "Patients First" and a unique guiding company principle "Recovering hearts. Saving lives." With more than 2,000 employees, Abiomed is one of the fastest growing medical technology businesses in the world with corporate headquarters in Danvers, USA, and locations in Aachen and Berlin, Germany, Tokyo, Japan, and Singapore. Abiomed is part of Johnson & Johnson MedTech.Abiomed is an employer with attractive working conditions and an appreciative corporate culture that focuses on the needs of its employees. Abiomed inspires and retains exceptional talent through collaboration, passion and continuous development.Clinical Trial CoordinatorThe Clinical Trial Coordinator (CTC) supports Clinical Project and Program Managers in planning and coordinating activities in all aspects of clinical trial operations. This position requires appropriate interpretation of significant policies and procedures. It involves interaction with internal and external customers and partners, and must operate with a high degree of discretion, as the role involves handling information of a confidential and critical nature.Main tasks and responsibilities:Plan, coordinate, and arrange study communications and meetings on and off-site with both internal and external attendeesPrepare all necessary documents for the evaluation of new proposals and coordinate the decision process of new AR or ISS projectsManage the grant application platform which maintains all necessary documents and the communication with PIsSet up, update, maintain and close Trial Master Files. Assure currency and accuracy of required clinical trials documents Maintain project-specific regulatory document inventory systems which include a precise quality check (QC) process when documents are receivedCommunicate with investigator sites on collection of regulatory documentsCreate study materials, including newsletters, study updates, etc. under the direction of a Scientist or Clinical Program ManagerSource and distribute study suppliesInteract with Finance departments to support invoice processingInteract with the Sales and Customer service department to support and coordinate external needs and internal processes.Under guidance of Clinical Operations management, interact with internal stakeholders and external clients to coordinate the accomplishment of business needsRequirements:BS degree or BS degreeRelevant clinical or basic research experience working at an Investigator Site, Sponsor or Clinical Research OrganizationFamiliarity of clinical trial operations, ICH, GCP Guidelines Good working experience in a team environment across multi-functional areasHighly organized, self-motivated, detail-oriented, proactive, and accurateAbility to work with urgency and thrive in a high-energy, fast-paced environmentDemonstrate excellent communication, verbal and written, and interpersonal skillsFluent in written and spoken English and GermanDemonstrate proficiency in MS Office Suite: Word, PowerPoint, Excel, Project ABIOMED is an Equal Employment Opportunity employer. We are committed to the policy of providing equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, disability or national origin. Über das Unternehmen:Johnson and Johnson

OverviewArcfield is a leading provider of full lifecycle, mission-focused systems engineering and integration capabilities to the U.S. government and its allies. The company has more than 60 years of proven experience providing advanced engineering and analysis, IT and C5ISR capabilities to support our nation’s most critical national security missions. Headquartered in Chantilly, VA and with 16 offices around the world, Arcfield employs approximately 1,200 engineers, analysts, IT specialists, and other professionals who put our customers’ missions first, helping them solve their most complex challenges through innovations in modeling, simulation and analysis, digital transformation and C5ISR. Visit arcfield.com for more details.ResponsibilitiesAs a Computer Forensic Scientist, you will support US Army Europe/Africa G2 and other Intelligence related mission partners, as a key team member of a complex program that provides professional services in support of advisory and analysis efforts associated with Intelligence Warfighting Function (IWfF)mission areas. The USAREUR-AF Team will research, analyze, and produce near- and long-term all source assessments on terrorism / counterterrorism, and multi-discipline counter-intelligence issues in response to CG USAREUR-AF’s priority intelligence requirements and to enable U.S. and foreign partner counterintelligence operations. You will be a member of a team that supports the Intelligence Directorate of the Army Component Command of both the US European Command and US Africa Command.You will embed in either Wiesbaden Germany OR Vicenza Italy and may travel within the theaters as required.Analyze digital forensic Tactics, Techniques, and Procedures (TTPs) related to the exploitation of digital media captured or seized in support of CI activities. Configure, update, and maintain forensic equipment and software. Prepare specialized technical products, including comprehensive documentation of network topology and information flow processes. Demonstrate a comprehensive understanding of Microsoft (MS) Active Directory, Hypervisors, virtual machines, databases, and Domain management.Exhibit a thorough understanding of Routers, Switches, cable management, and the ability to configure devices to effectively manage traffic flow.Accurately prepare and complete tasks and milestones associated with DoD System Security Plans for the assigned managed domain.Prepare specialized technical products, including comprehensive documentation of network topology and information flow processes.Ensure the configuration, update, and maintenance of forensic equipment and software in compliance with established policies.QualificationsRequired: BS 8-10, MS 6-8, PhD 3-5Must POSSESS and be able to maintain aTS/SCI clearance​Equal Pay ActThis is the projected compensation range for this position. There are differentiating factors that can impact a final salary/hourly rate, including, but not limited to, Contract Wage Determination, relevant work experience, skills and competencies that align to the specified role, geographic location (For Remote Opportunities), education and certifications as well as Federal Government Contract Labor categories. In addition, Arcfield invests in its employees beyond just compensation. Arcfield ’s benefits offerings include, dependent upon position, Health Insurance, Life Insurance, Paid Time Off, Holiday Pay, Short Term and Long-Term Disability, Retirement and Savings, Learning and Development opportunities, wellness programs as well as other optional benefit elections. Min: $92,109.68 Max: $221,338.19EEO StatementEEOArcfield proactively fulfills its role as an equal opportunity employer. We do not discriminate against any employee or applicant for employment because of race, color, sex, religion, age, sexual orientation, gender identity and expression, national origin, marital status, physical or mental disability, status as a Disabled Veteran, Recently Separated Veteran, Active-Duty Wartime or Campaign Badge Veteran, Armed Forces Services Medal, or any other characteristic protected by law. Standort Arcfield, Wiesbaden

DESCRIPTION Have you ever wished to build high standard Operations Research and Machine Learning algorithms to optimize one of the most complex logistics network? Have you ever ordered a product on Amazon websites and wondered how it got delivered to you so fast, and what kinds of algorithms & processes are running behind the scenes to power the whole operation? If so, this role is for you. The team: Global transportation services, Research and applied science Operations is at the heart of the Amazon customer experience. Each action we undertake is on behalf of our customers, as surpassing their expectations is our passion. We improve customer experience through continuously optimizing the complex movements of goods from vendors to customers throughout Europe. Global transportation analytical teams are transversal centers of expertise, composed of engineers, analysts, scientists, technical program managers and developers. We are focused on Amazon most complex problems, processes and decisions. We work with fulfillment centers, transportation, software developers, finance and retail teams across the world, to improve our logistic infrastructure and algorithms. GTS RAS is one of those Global transportation scientific team. We are obsessed by delivering state of the art OR and ML tools to support the rethinking of our advanced end-to-end supply chain. Our overall mission is simple: we want to implement the best logistics network, so Amazon can be the place where our customers can be delivered the next-day. The role: Applied scientist, speed and long term network design The person in this role will have end-to-end ownership on augmenting RAS Operation Research and Machine Learning modeling tools. They will help understand where are the constraints in our transportation network, and how we can remove them to make faster deliveries at a lower cost. You will be responsible for designing and implementing state-of-the-art algorithmic in transportation planning and network design, to expand the scope of our Operations Research and Machine Learning tools, to reflect the constantly evolving constraints in our network. You will enable the creation of a product that drives ever-greater automation, scalability and optimization of every aspect of transportation, planning the best network and modeling the constraints that prevent us from offering more speed to our customer, to maximize the utilization of the associated resources. The impact of your work will be in the Amazon EU global network. The product you will build will span across multiple organizations that play a role in Amazon's operations and transportation and the shopping experience we deliver to customer. Those stakeholders include fulfilment operations and transportation teams; scientists and developers, and product managers. You will understand those teams constraints, to include them in your product; you will discuss with technical teams across the organization to understand the existing tools and assess the opportunity to integrate them in your product.You will engage with fellow scientists across the globe, to discuss the solutions they have implemented and share your peculiar expertise with them. This is a critical role and will require an aptitude for independent initiative and the ability to drive innovation in transportation planning and network design. Successful candidates should be able to design and implement high quality algorithm solutions, using state-of-the art Operations Research and Machine Learning techniques. Key job responsibilities Engage with stakeholders to understand what prevents them to build a better transportation network for Amazon Review literature to identify similar problems, or new solving techniques Build the mathematical model representing your problem Implement light version of the model, to gather early feed-back from your stakeholders and fellow scientists Implement the final product, leveraging the highest development standards Share your work in internal and external conferences Train on the newest techniques available in your field, to ensure the team stays at the highest bar About the team GTS Research and Applied Science is a team of scientists and engineers whom mission is to build the best decision support tools for strategic decisions. We model and optimize Amazon end-to-end operations. The team is composed of enthusiastic members, that love to discuss any scientific problem, foster new ideas and think out of the box. We are eager to support each others and share our unique knowledge to our colleagues. We are open to hiring candidates to work out of one of the following locations: Luxembourg, LUX BASIC QUALIFICATIONS Experience in building models for business application Experience in patents or publications at top-tier peer-reviewed conferences or journals Experience programming in Java, C++, Python or related language Experience in any of the following areas: algorithms and data structures, parsing, numerical optimization, data mining, parallel and distributed computing, high-performance computing PREFERRED QUALIFICATIONS Experience using Unix/Linux Experience in professional software development PhD, or a Master's degree and experience in Computer science, CE, machine learning or related technical field Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a lo... Standort Amazon Europe, Hermeskeil

DESCRIPTION Amazon EU Customer Fulfillment Operations is seeking a Research Scientist to leverage statistical analysis and machine learning expertise in understanding complex problem statements, driving fast and confident data-driven decisions. If you are passionate about answering some of the most complex dilemma in EUCF Operation, Learning and Development, this is your chance to make history. At Amazon we believe that every day is day one. If you thrive in a challenging, fast-paced, highly analytical and result-oriented environment, you'll meet your match: we don't like to sit still, which is why we treat every day like the first. It's as simple as this: Work Hard. Have Fun. Make History. Key job responsibilities Apply rigorous and scientific approaches to collect, analyze, and provide recommendations on critical business questions, enabling confident and swift decision-making in EU CF Operations Advocate technical solutions to business stakeholders, engineering teams, and executive-level decision makers Develop and execute experiments, including A/B and hypothesis testing, to assess the effectiveness and impact of various business strategies and initiatives Conduct financial analysis, determine ROI, and assess the economic impact of decisions, emphasizing trade-offs, risks, and benefits through robust statistical methodologies. Access, comprehend, and manipulate diverse datasets, constructing analytical models and performing measurements to extract meaningful insights and guide informed decision-making. Foster a culture of knowledge-sharing, actively collaborating with peers and professionals across disciplines to exchange expertise and stay at the forefront of statistical advancements. Utilize statistical analyses, including experimental design and hypothesis testing, to develop cutting-edge machine learning solutions that address complex business queries. Foster knowledge-sharing and actively learn from peers, collaborating with a diverse range of professionals, including hiring, coaching, and training. We are open to hiring candidates to work out of one of the following locations: Luxembourg, LUX BASIC QUALIFICATIONS Masters or PhD in STEM (science, technology, engineering or mathematics) related field Ability to communicate orally and in writing to present business cases and scientific models with rigorous analyses that support results/conclusions to influence important decisions. Advanced technical skills in Excel (PowerQuery, Data Analysis, Pivot Tables), Postgre SQL, Python (Pandas, Numpy). Experience in design of experiment, A/B and hypothesis testing, statistical modeling. Experience investigating the feasibility of applying scientific principles and concepts to business problems and products (eg apply statistical analysis to solve complex business problem statements). Strong understanding of standard machine-learning algorithms (supervised, unsupervised). Experience working in a dynamic, agile environment within a geographically distributed technical and non-technical teams. Technically curious, self-motivated, versatile and solution oriented. Ability to effectively prioritize projects, manage multiple competing priorities simultaneously, and drive projects to completion under tight deadlines. Proven track record of strong verbal/written communication & data presentation skills, including an ability to effectively communicate with both business and technical teams across the world. PREFERRED QUALIFICATIONS In-depth knowledge using Excel (PowerQuery, Data Analysis,Pivot Tables ), PostgreSQL, and Python for data analysis (Pandas, Numpy), visualization (Matplotlib, Seaborn) and modeling (Scikit-learn, Scipy, PyTorch, TensorFlow, and Keras). Experience managing science projects e2e on AWS stack Strong understanding of Amazon operations and Learning and Development metrics. Outstanding communication skills, translating complex technical knowledge into actionable recommendations for directors and VPs and ability to tailor communication to different audiences and stakeholders. Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a lo... Standort Amazon Europe, Idar-Oberstein

Job Description Nordberg Medical is seeking a Medical Affairs Manager DACHAs a Medical Affairs Manager DACH, your role involves providing medical and scientific support for Nordberg Medical’s product. You will act as a subject matter expert for external stakeholders, including key opinion leaders, healthcare professionals, regulatory bodies, and patient advocacy groups. Reporting to the European Medical Affairs Director (with a dotted line to the VP Commercial Operations Central Europe) you will play a pivotal role in supporting the company's growth and expansion efforts. Key Responsibilities include but are not limited to:Strategic and Tactical LeadershipReview scientific literature (mostly medical aesthetics) to inform company strategy, consolidating actionable medical insights. Develop regional medical affairs goals, translating them into tactics for optimal scientific exchange. Manage Key Opinion Leader (KOL) relationships and support faculty development activities. Support clinical research (ISS and SIS) by identifying investigators, managing protocols, and reviewing study data. Ensure compliance with local regulations and review promotional materials. Medical and Scientific LeadershipProvide local scientific perspective to Regional Medical Affairs team.Build relationships with external scientific community and scientific societies. Attend and present at scientific meetings and conferences. Support development of medical educational programs and advisory boards.Regulatory SupportCollaborate with regulatory affairs for submissions and product approvals.Maintain knowledge of regulatory guidelines and assist in resolving regulatory issues.