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Research Scientist Pharma Roche (m/w/d)
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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
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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, 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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, 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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, 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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 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SOX, SPC- CCDS, Spectroscopy, S-Plus, SPSS, SQL, Start-up activities, statistical analysis, Statistics, Study Management, Study Medication Labelling, Sunshine Act, Supplier Qualification, Supply Chain Distribution, Supply Chain Management, Supply Chain Planning, Supply Planning, SUSAR, SUSARs, TMF, Toxicogenomics, Toxicology, Trackwise, Training, Transport Management, Unicorn Purification System, UPLC, Upstream, UV-Vis Spectroscopy, validation, Veeva, Vendor Management, Venipuncture, VISIO, Western Blot, ZINC, Bratislava, Slovakia, Afrikaans, Argentinian, Armenian, Belgian, Bosnian, Bulgarian, Cambodia, Cantonese, Catalonian, Chinese, Croatian, Czech, Danish, Dutch, English, Flemish, French, Greek, Gujarati, Hebrew, Hungarian, Italian, Japanese, Korean, Latvian, Lithuanian, Luxembourgish, Macedonian, Malayalam, Mandarin, Montenegrin, Norwegian, Persian, Punjabi, Romanian, Russian, Serbian, Slovak, Slovene, Slovenian, Spanish, Swedish, Thai, Turkish, UkrainianLocation: GloballyShare: 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Schülerpraktikum im technischen Bereich/Trainee
771 nora systems GmbH, DE-Weinheim
Schau doch mal rein! Du möchtest mal in ein Unternehmen reinschnuppern? Schauen, wie es ist für ein produzierendes Unternehmen zu arbeiten, dessen Produkt weltweit vertrieben und verlegt wird? Nutze die Chance, beim Weltmarktführer für Kautschuk-Bodenbeläge, Einblick in einen global agierendes mittelständisches Unternehmen zu nehmen. Lerne die ganze Bandbreite von der Forschung über die Produktion bis hin zum Vertrieb und zur Administration kennen. Bei nora kannst du dir als Schüler oder Schülerin einen Eindruck machen in einem Praktikum im technischen Bereich • in der Betriebswerkstatt als Elektroniker/in oder Industriemechaniker/in oder • als ein/e Verfahrensmechanikers/in in unserer Lehrwerkstatt oder • im Lager im Ausbildungsberuf Fachkraft für Lagerlogistik. Wir zeigen dir gerne, welche deiner Interessen und Fähigkeiten zu einem der Ausbildungsberufe passen, die wir bei nora anbieten. NEUGIERIG GEWORDEN? Dann bewirb dich mit einem kurzen Anschreiben, Lebenslauf und deinem letzten Schulzeugnis gleich hier über den Button: Apply. Für weitere Fragen steht Dorothea Hartmann unter der Tel. Nr. 06201 802977 gerne zur Verfügung. Wir freuen uns auf deine Bewerbung. Als Teil der international agierenden Unternehmensgruppe Interface, die weltweit mehr als 4.000 Mitarbeiter beschäftigt, ist die nora systems GmbH der global führende Hersteller von Kautschuk-Bodenbelägen für den Objektbereich. Mit der Registrierung im nora Karriereportal oder dem Zusenden Ihrer Bewerbungsunterlage stellen Sie nora freiwillig Ihre persönlichen Daten zur Verfügung und willigen ausdrücklich in die Erfassung, Verarbeitung und Nutzung der Informationen gemäß der einschlägigen Gesetze und dieser Datenschutzerklärung sowie den allgemeinen nora Datenschutzbestimmungen. At Interface, we believe that flooring is more than what you walk on. We help our customers create interior spaces that support well-being, productivity, and creativity, as well as the sustainability of the planet. As a global leader in modular flooring, we design and manufacture an integrated collection of carpet tiles and resilient flooring, including luxury vinyl tile (LVT) and nora rubber flooring. We’re designers, engineers, scientists, problem-solvers, dreamers, trailblazers and everything in between. Spread all over the world, we are one team with a shared vision and values. Image  Christopher Payne / Esto For us, sustainability is a journey. We're constantly working to improve the quality of our products and lessen the impact they have on human health and the environment. Design leads everything we do. Our team of designers continuously explores trends, textures, colors, and materials to ensure every pattern and detail is thoughtfully crafted.Über das Unternehmen:771 nora systems GmbH
Research Scientist (m/f/d)
Symanto Research, Nürnberg, DE-BY, Valencia, ES-VC
Do you like Natural Language Processing (NLP)? Do you enjoy solving scientific problems? Are you passionate about creating deep learning models using cutting edge technology? For supporting our Research (AI) team in our Valencia office we are currently looking for a Research Scientist (m/f/d). You will work on innovative projects in different NLP areas: opinion mining, author profiling, psycholinguistic profiling, under-resource NLP, relation extraction, etc. In addition, your work will NOT only focus on the company's products and customers. At Symanto we will encourage you to explore your research ideas aligned with our business needs and to publish in blogs, fora, and reputable research conferences and journals. Join our team and you will have the opportunity to work with MSc and PhD researchers from different nationalities, with a record of more than 80 research publications. Please take a look at the papers published at Symanto Read NLP Research from Industry Experts I SymantoDo you like Natural Language Processing (NLP)? Do you enjoy solving scientific problems? Are you passionate about creating deep learning models using cutting edge technology? For supporting our Research (AI) team in our Valencia office we are currently looking for a Research Scientist (m/f/d). You will work on innovative projects in different NLP areas: opinion mining, author profiling, psycholinguistic profiling, under-resource NLP, relation extraction, etc. In addition, your work will NOT only focus on the company's products and customers. At Symanto we will encourage you to explore your research ideas aligned with our business needs and to publish in blogs, fora, and reputable research conferences and journals. Join our team and you will have the opportunity to work with MSc and PhD researchers from different nationalities, with a record of more than 80 research publications. Please take a look at the papers published at Symanto Read NLP Research from Industry Experts I SymantoYour profileEducation, Required Skills and ExperienceBachelor’s degree in computer science, telecommunication technologies, or similarMaster’s degree in NLP, deep learning, or similar+2 years experience as a researcher in NLP and deep learning-related tasks Fluency in EnglishAdvanced knowledge of the following technologies: python, keras, and tensorflowKnowledge of the following technologies: git and dockerExperience with text classification, sequence labeling, model selection, evaluation and result analysisRespectfulness; teamwork skills; organizational and planning skills; communication skills; creativity; proactivity; problem solving; autonomy Preferred Skills and ExperiencePhD in natural language processing, deep learning, or similar+5 years experience as a researcher in NLP and deep learning-related tasks, having a minimum of 2 years as a researcher in a non-academic environmentExperience in publishing research materialSpanish and/or German are a plusKnowledge of multi-class and multi-task classification; adversarial architectures; online learning methodologies; model compression (pruning, quantization, distillation…)Knowledge of the following technologies: pytorch, bash, ssh, linux terminal, kubernetes, and NVIDIA Triton Inference ServerKnowledge of and/or experience with API and web service development in python; agile methodologies; Microsoft Azure DevOps Services; cloud computing solutions; Your job will beDesigning and implementing machine and deep learning-based NLP workflows and algorithms in alignment with the business objectivesPublish articles in blogs, fora, and prestigious NLP/AI conferences and journalsDeliver scalable and maintainable solution using the latest & greatest technologyCollaborate in the different research NLP projectsIdentification and evaluation of strategic innovations (concepts, tools/languages, technologies, services) in the field of NLP and deep learningConstant personal development in the new technologiesRepresent the company in the research communitySupport other teams on research-related mattersWhat we offerWork on Innovative projects and solutionsPossibility to publish in blogs, fora, and reputable research conferences and journalsTraining in new technologies and domainsFlexible working timeA company laptop plus access to cloud GPU servers to conduct your researchHome Office possibilityGreat people to work with in an international environmentChance to develop and grow with the companyOut of office eventsAre you interested?We are looking forward to receiving your application (English CV & motivation letter).Verantwortlichkeiten:Designing and implementing machine and deep learning-based NLP workflows and algorithms in alignment with the business objectivesPublish articles in blogs, fora, and prestigious NLP/AI conferences and journalsDeliver scalable and maintainable solution using the latest & greatest technologyCollaborate in the different research NLP projectsIdentification and evaluation of strategic innovations (concepts, tools/languages, technologies, services) in the field of NLP and deep learningConstant personal development in the new technologiesRepresent the company in the research communitySupport other teams on research-related mattersQualifikationen:Education, Required Skills and ExperienceBachelor’s degree in computer science, telecommunication technologies, or similarMaster’s degree in NLP, deep learning, or similar+2 years experience as a researcher in NLP and deep learning-related tasks Fluency in EnglishAdvanced knowledge of the following technologies: python, keras, and tensorflowKnowledge of the following technologies: git and dockerExperience with text classification, sequence labeling, model selection, evaluation and result analysisRespectfulness; teamwork skills; organizational and planning skills; communication skills; creativity; proactivity; problem solving; autonomy Preferred Skills and ExperiencePhD in natural language processing, deep learning, or similar+5 years experience as a researcher in NLP and deep learning-related tasks, having a minimum of 2 years as a researcher in a non-academic environmentExperience in publishing research materialSpanish and/or German are a plusKnowledge of multi-class and multi-task classification; adversarial architectures; online learning methodologies; model compression (pruning, quantization, distillation…)Knowledge of the following technologies: pytorch, bash, ssh, linux terminal, kubernetes, and NVIDIA Triton Inference ServerKnowledge of and/or experience with API and web service development in python; agile methodologies; Microsoft Azure DevOps Services; cloud computing solutions; Über das Unternehmen:Symanto ResearchBranche:Research and developmentWebsite:https://www.linkedin.com/company/symanto>>>>>https://www.facebook.com/SymantoAI/>>>>>https://twitter.com/SymantoAI
Machine Operator (Maschinen- und Anlagenführer) (m/f/d)
Germany - Ritter GmbH, DEU-Schwabmünchen
The Opportunity: Machine Operator (Maschinen- und Anlagenführer) Ritter, ein Teil von Avantor sucht nach einem engagierten Maschinen- und Anlagenführer (m/f/d) in Schwabmünchen, um unsere Operative zu optimieren. Hierbei handelt es sich um eine Vollzeitstelle, bei der Sie im 3-Schichtsystem arbeiten: Früh-, Spät-, Nachtschicht und vollste Verantwortung über die Maschinen tragen werden. Sie haben die Möglichkeit, Teil eines engagierten Teams zu sein. Wenn Sie Erfahrungen in der Mechanik mitbringen – melden Sie sich jetzt! Das bringen Sie mit: Mechanisches und technisches Verständnis Mindestens 3 Jahre Erfahrung in einer ähnlichen Produktionsumgebung Bereitschaft zur Schichtarbeit Deutsch in Wort und Schrift Diese Aufgaben erwarten Sie: Verantwortung für die Ordnung und Sauberkeit der Maschinen Überprüfung des Fertigungsprozesses während der Produktion Eigenständiges Erkennen und Beheben von Fehlern an der Fertigungslinie Arbeiten mit den Betriebsdatenerfassungsprogrammen Eigenverantwortlich für Mengen und Qualität unter Berücksichtigung festgelegten Parametern arbeiten Wer sind wir ? Ritter, ein Teil von Avantor, stellt Kunststoffprodukte von ausgezeichneter Qualität her - Kartuschen für Dicht- und Klebstoffe. Bei Ritter ist Innovation der Schlüssel zu unserem Erfolg, seit fast 60 Jahren entwickeln wir maßgeschneiderte Produkte für unsere geschätzten internationalen Kunden. Mit unserem eigenen Werkzeugbau, moderner Technologie, einschließlich Digitaldruck und einer eigenen Grafikabteilung, ist unsere Zukunft ehrgeizig und spannend. Unser Produktionsstandort im bayerischen Schwabmünchen verfügt nicht nur über ein preisgekröntes Energiekontrollsystem, sondern wir verwenden auch ungiftige Kunststoffe, wieder verwertbare Kunststoffe und setzen auf biobasierte, biologisch abbaubare und kompostierbare Materialien. Wir arbeiten daran, eine großartige Zukunft zu schaffen, und laden Sie ein, Teil unserer Reise zu sein. Wir verpflichten uns, Sie auf diesem Weg durch unsere vielfältige, gleichberechtigte und integrative Kultur zu unterstützen, die Lernerfahrungen zur Förderung Ihrer beruflichen Entwicklung und Ihres Erfolgs beinhaltet. #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
Senior Director, Proteomics Research, Germany
OmicEra Diagnostics GmbH, Germany - Planegg
Help us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview The Senior Director, Proteomics Research works on multiple projects that are extremely complex in scope, often across multiple groups and sites. As a technical expert and a leader, the Senior Director, Proteomics Research is responsible for providing overall directions, technical insights, guidance, and mentoring to a large group of scientists to ensure successful planning, design, and execution of proteomics research-related projects. Specifically, the Senior Director, Proteomics Research is responsible for determining the scope, technical difficulty, plan, time, resources, and risks associated with new assignments and projects geared toward protein biomarkers discovery and validation. He/she will be providing leadership and guidance to a team of scientists in Planegg, Germany with the focus on leveraging mass spectrometry to discover biomarkers that help advance cancer diagnosis and treatment. The Senior Director will also be managing the Planegg research facility in which the mass spectrometry research will be performed. This includes day to day operational management, budgeting, and forecasting which are an integral part of the overall research and technology development budgeting and plans. Essential Duties Include, but are not limited to, the following: Provide leadership and technical guidance and mentorship to a team of research associates and scientists. Work on significant and unique issues where analysis, situations, or data requires an evaluation of intangible variables and may impact future concepts, products, or technologies. Work on multiple projects that are extremely complex in scope, often across multiple groups and sites. Determine the scope, technical difficulty, plan, timeline, resources, and risks associated with new assignments and projects. Present and clearly communicate findings of research at data meetings, group meetings, and project team meetings to determine the next steps and the path forward for successful outcomes. Identify, adapt, and advance new technology initiatives. Exercise latitude and independent judgement to determine methods and procedures or technologies on new assignments and provide ideas for new techniques. Maintain thorough knowledge of technological industry developments; provide technical assessment, guidance, and help with Go/No Go decisions when evaluating or developing technologies, methods, and procedures. Provide deep scientific leadership and technical input and help guide decisions affecting project planning and experimental design or product development. Prepare, provide, and present information and data for scientific abstracts, industry conferences, project meetings, or publications. Perform complex analyses and present results and data driven outcomes to Senior Management, as well as to a variety of audiences throughout the organization. Contribute to the intellectual property portfolio by implementing innovative and creative ideas to solve problems or improve on current methods, as well as guide and shape nascent ideas that are presented by the scientists and team members. Provide help with IP disclosure and assist in answering questions related to IP filings. Prepare, review, and approve detailed technical procedures, protocols, and reports. Prepare reports and documentation and provide highly technical analysis or summarization of experimental results and project/study outcomes, next steps and provide future direction of the project, and help senior management/project teams with determining Go/No Go decisions. Share ideas and be receptive to new ideas when collaborating within and across departments. Question the status quo and seek and evaluate improvements to existing technologies, processes, or methods. Undertake independent and collaborative research to meet department and project objectives. Promote an open, collaborative environment built on trust to foster positive teamwork that allows for free exchange of ideas. Invest in developing talent to meet both career goals and the organization's goals. Build strength-based teams; apply diverse skills and perspectives to achieve current and future business needs. Create and deliver high quality presentations that effectively communicate and tie into a cohesive story the project status and/or experimental results. Effectively manage, support, and guide your team, including, but not limited to delegating tasks and responsibilities, assess employee performance and provide helpful feedback and training opportunities. Consistent demonstration of exceptional leadership qualities, including, but not limited to the ability to attract and retain the best team, foster a culture of high performance, lead with integrity, humility, accountability, and courage, and set a clear vision to energize teams towards the future. Ability to effectively work on several varied projects at one time, with frequent changing priorities. Excellent analytical, problem solving, and decision-making skills. Exercise technical proficiency, scientific creativity and rigor, and independent thought when challenging and debating scientific ideas. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company’s Quality Management System policies and procedures. Maintain regular and reliable attendance. Ability to act with an inclusion mindset and model these behaviors for the organization. Ability to work nights and/or weekends, as needed. Ability to lift up to 20 pounds for approximately 5% of a typical working day. Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 50% of a typical working day. Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height. Ability to comply with any applicable personal protective equipment requirements. Ability to use various types of laboratory equipment; including microscopes, microtomes, blades, strainers, and pipettes for extended periods of time. May perform repetitious actions using lab tools. Ability to use near vision to view samples at close range. May be exposed to hazardous materials, tissue specimens, and instruments with moving parts, lasers, heating and freezing elements, and high-speed centrifugation. Ability to travel 10% of working time away from work location, may include overnight/weekend/international (to USA) travel. Minimum Qualifications Ph.D. in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position; or Master’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position and 4 years of related experience in lieu of a Ph.D.; or Bachelor’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position and 6 years of related experience in lieu of Ph.D. 16+ years of industry or academia experience in biology and/or chemistry. 14+ years of experience in medical device/IVD, biotech, life science, or pharmaceutical industry. 5+ years of experience leading or directing people and/or project teams. Demonstrated experience in mass spectrometry and protein research. Advanced understanding of GMP, ISO, and Quality Systems. Proficient in Microsoft Office to include Excel, Word, and PowerPoint. Demonstrated ability to perform the essential duties of the position with or without accommodation. Preferred Qualifications 20+ years of experience in medical device/IVD, biotech, life science, or pharmaceutical industry. 7+ years of experience leading or directing people and/or project teams. Experience in protein testing platforms, mass spectrometry as a protein discovery tool, and protein research/assay development methods. Experience in developing and running protein ELISA assays. Knowledge of statistical models for data analysis and results reporting. #LI-JR1 Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, email **********. We’ll work with you to meet your accessibility needs. Not ready to apply? Join our talent community and stay up to date on what’s new at Exact Sciences. We are Exact Sciences, and we're changing lives together through earlier detection and smarter answers. https://vimeo.com/660680929Über das Unternehmen:OmicEra Diagnostics GmbH
Clinical Research MD, Belgium - L
TalentSource Life Sciences,
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
Edge Devices Systems Administration Intern @ Deltia (Berlin)
Merantix, Berlin
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
Lagerlogistik/Fachlagerist (m/f/d)
Germany - Ritter GmbH, DEU-Schwabmünchen
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
Business Development Intern @Deltia (Remote)
Merantix, Berlin
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
Field Application Engineer
Opal-RT, Nuremberg, Germany
*English follows*Field Application Engineer – NürnbergDas ehrgeizige Ziel von OPAL-RT ist es, die Echtzeitsimulation zu demokratisieren, indem sie für jeden Ingenieur und Forscher erschwinglich und zugänglich gemacht wird. Schließen Sie sich der OPAL-RT-Familie an und gestalten Sie die Zukunft der Technologie mit. Als weltweit führendes Unternehmen in verschiedenen Anwendungsbereichen werden unsere Simulationswerkzeuge in einer Vielzahl von Bereichen eingesetzt, z. B. in der Automobilindustrie, der Luft- und Raumfahrt, dem Energiesektor, dem Transportwesen, der industriellen Fertigung und vielen anderen. OPAL-RT wurde in Quebec gegründet und hat eine wachsende weltweite Präsenz - OPAL-RT hat den Wind in den Segeln!Die Stelle beschreibt sich wie folgt:In dieser technischen Schlüsselposition sind Sie dafür verantwortlich, unserem Kundenstamm ein Höchstmaß an Unterstützung zu bieten, was bei Bedarf Besuche beim Kunden für Inbetriebnahmen, Demonstrationen, Schulungen und Fehlerbehebungen erfordert. Dazu hilft ein FAE im Verkauf potentiellen Kunden unsere Anwendungen zu verstehen und technische Details zu erklären. Daneben unterstützt ein FAE die Entwicklung neuer Produkte, insbesondere durch die Erfassung und Analyse von Kundenanforderungen. Ein FAE muss regelmäßig reisen, hauptsächlich in Deutschland, Österreich und der Schweiz, aber auch zu unserem Hauptsitz in Montreal, Kanada.Von der sich bewerbenden Person erwarten wir gute Arbeitsbeziehungen zu Kund*innen und Teammitgliedern, ausgezeichnete Problemlösungsfähigkeiten, effektive mündliche und schriftliche Kommunikationsfähigkeiten, Interesse an einer gründlichen Dokumentation und ausgeprägtes technisches Fachwissen auf dem Gebiet der Leistungselektronik, der Energiesysteme oder der Entwicklung eingebetteter Systeme, vorzugsweise mit Erfahrung in der Echtzeitsimulation auf Plattformen wie OPAL-RT, RTDS, dSPACE, Typhoon, NI usw.Die Arbeit bei OPAL-RT ist spannend und herausfordernd. Werden Sie das neueste Mitglied in unserem dynamischen Support-Team!Ihre Hauptaufgaben werden sein:Schulungen und Inbetriebnahmen: Vorbereiten und Durchführen von Kundenbesuchen.Entwicklung von Modellen: Ausarbeitung schlüsselfertiger Lösungen für bestimmte Kunden.Kundenbetreuung: Unterstützung vor Ort, per E-Mail oder Telefon-Support.Vertriebsunterstützung: Technische Validierung von Angeboten, Präsentation von Demonstrationen.Entwicklung von Demos: Pflege der bestehenden Demodatenbank und Vorbereitung von Demos für neue Anwendungen.Dokumentation: Erstellung von technischen Präsentationen und Schulungsmaterial.Reisen: Reisebereitschaft; 25% bis 33% pro Monat oder je nach Bedarf.Um ausgewählt zu werden, müssen Sie das folgende Profil aufweisen:Bachelor- oder Master-Abschluss in Elektrotechnik oder einer anderen einschlägigen Ingenieurdisziplin;Vorzugsweise 0,5 bis 2 Jahre einschlägige Erfahrung im Bereich Echtzeitsimulation (Praktika und Abschlussarbeiten werden angerechnet);Kenntnisse von Matlab/Simulink;Gute mündliche und schriftliche Kenntnisse in Deutsch und Englisch.Gründe, warum wir Ihre Bewebung bevorzugen würden:Sie beherrschen die Programmiersprachen VHDL, Python, C++;Sie haben Kenntnisse in einem oder mehreren der folgenden Software-Tools: MATLAB Simulink, Hypersim, RSCAD, PowerFactory;Sie verfügen über gute Kenntnisse der folgenden Betriebssysteme: LinuxSie haben Spaß an DIY-Projekten mit Mikrocontrollern wie Arduino oder Raspberry PiSie sind in der Lage, sich auf Französisch zu verständigen (unser Hauptsitz ist in Montreal)Eine Karriere bei OPAL-RT passt zu Ihnen, wenn Sie:Sie sind auf der Suche nach anregenden Herausforderungen, die Sie ständig zu Höchstleistungen anspornen.Sie träumen von einem familiären Umfeld, das gleichzeitig professionell, kooperativ und freundlich ist.Sie mögen flexible Arbeitszeiten, um Arbeit und Privatleben miteinander zu vereinbaren.Sie wollen Ihr Wissen und Ihre Kenntnisse weiter ausbauen, indem Sie Seite an Seite mit Forschern, Innovatoren und Wissenschaftlern arbeiten, die eines teilen: Leidenschaft.Sie lösen gerne Rätsel, stürzen sich in neue Themen und sind bereit für Abenteuer.Sie haben sich entschieden, einen wichtigen Beitrag zum technologischen Fortschritt in einer Vielzahl von Branchen zu leisten.Sie wollen für Ihre Ideen, Kreativität und Talente anerkannt werden.Sie kennen Ihren Wert und streben ein weltweit wettbewerbsfähiges Gehalt an.Sie wollen nicht nur einen Job, Sie wollen Karriere machen!_________________________________________OPAL-RT Germany is looking for a Field Application Engineer – Nürnberg OfficeAbout OPAL-RT Technologies:Imagine working for a company with customers including NASA, Bombardier, ABB, EMBRAER, MIT, GE, Ford, GM, NREL and Hydro-Québec! OPAL-RT’s ambitious challenge is to fully democratize simulation, making it affordable and accessible to every engineer and researcher. Joining the OPAL-RT family means you will be helping to develop the technology of the future.OPAL-RT is recognized leader in diverse and powerful applications. The company's tools are used in a wide variety of fields, including, automotive, aerospace, energy, transportation and industrial manufacturing. Established in Quebec and bolsteredby a global presence, OPAL-RT is always looking to the future.Achievements and stimulating challenges:In this key technical position you will be responsible to deliver the highest level of support to our customer base, which requires visiting customer premises for installation, demonstrations, trainings, troubleshooting when needed. In addition, the FAE provides technical know-how in developing new business, specifically by capturing and analyzing customer requirements to propose complete solutions. The FAE is required to travel on a regular basis largely in Germany, Austria and Switzerland but also to our headquarters in Montreal, Canada. The candidate we seek is expected to have strong working relationships with customers and team members, excellent problem-solving skills, effective verbal and written communication skills, concern for thorough documentation and strong technical expertise in the area of power electronics, power systems or embedded system development with preferably some real-time simulation experience on platforms such as OPAL-RT, RTDS, dSPACE, Typhoon, NI etc.Working for OPAL-RT is exciting and challenging. Become the latest member of our dynamic Support team!Main Duties:Training/Commissioning: Prepare, execute and report customer visits Model development: Prepare turnkey solutions for specific customers.Customer Support: On-site support, e-mail / phone support and maintain customer relations.Sales Support: Technical validation of quotations, present demos and participate at trade shows,conferences etc.Documentation: Create and maintain technical presentations and training material.Demo development: Maintain existing demos database and prepare demos for new applications.Travel: Willingness to travel; 25% to 33% per month or need based.Requirements:Education: Bachelor’s or Master’s degree in electrical engineering or other relevant engineering discipline;Expérience: Preferably 0.5 to 2 years of relevant experience (internships and thesis qualify);Technical aspect: Knowledge of Matlab/Simulink;Soft skills: Strong oral and written skills in German and English. Significant assets: You know how top program in VHDL, Python, C++; You have a knowledge of one or more of the following software tools: Hypersim, RSCAD, PowerFactory; You have a good knowledge of these operating systems: Linux You have fun doing DIY projects with Microcontrollers like Arduino or Raspberry Pi You are able to communicate in French (Our headquarters are in Montreal)A career with OPAL-RT will suit you if:You are seeking stimulating challenges that will constantly push you to do your best.You dream of a family environment that is also professional, cooperative and friendly.You need a flexible schedule and the ability to telecommute in order to balance work and home life.You want to continue to expand your knowledge and knowhow by working side-by-side with researchers, innovators and scientists who share one thing: Passion.You have chosen to be an important contributor the technological progress in a multitude of industries.You want to be recognized for your ideas, creativity and talents.You know your worth and seek a globally competitive salary.You do not just want a job; you want a career!*The use of the masculine gender includes the feminine and is employed solely to facilitate reading.*Creating meaningful work means embracing different perspectives. We are an equal opportunity employer and do not discriminate. Embracing difference is what makes OPAL-RT what it is — we wouldn’t have it any other way.Über das Unternehmen:Opal-RT
Genetic Services Specialist
Genus PLC, Hannover, Niedersachsen(Homeoffice)
Business Overview:Genus strives to provide beef, dairy and pork producers with superior breeding stock to enable the production of affordable and nutritious animal protein for consumers. PIC is the swine division with a mission to pioneer animal genetic improvement to help nourish the world. PIC currently supplies over 70% of the world’s top pork producers. We directly employ people in 18 countries worldwide and our products are available in more than 50 countries across the globe. We are a diverse team, ranging from scientists to sales teams, production personnel to customer service, and are all united by a passion for producing nutritious, affordable pork and a commitment to continuous improvement. Corporate Vision - Pioneering animal genetic improvement to help nourish the world. PIC – Our goal is to enable customers to become the most successful pork producers in the world.Role Overview:Reporting to European Genetic Services Director with a dotted line to Commercial Director in Germany.Based in Germany (preferably Hannover) - Supporting Customers and business partners in Germany and across Western Europe. Objective – Provide Genetic Services to PIC customers and business partners; Support genetic management in customer systems by accurately monitoring, identifying opportunities, and implementing action plans targeting maximum commercial level merit in our customer systems. Essential Duties and Responsibilities: Participates in development, enhancement, and execution of routine genetic services to customers includingCommunication of the PIC breedingProduct performance forecasting through modellingPre- and post- sales supportDam-line dissemination within customer systemsOn-farm execution of breeding programsRoutine reporting to customer and account teams with key focus on execution Builds knowledge of the company, processes and customers by solving a range of straightforward problemsAnalyses possible solutions using standard proceduresDevelop training and support materials on PIC products and genetic programs; explain the benefits of new technologies and enhancements to PIC products and genetic programs Requirements:University degree in Animal Breeding or Quantitative Genetics or equivalent degree with Genetics component; advanced degree preferred with at least 5 years’ experience in this field.Understanding of the technologies/techniques that are used to make genetic improvementExcellent organizational and interpersonal skills are requiredExcellent technical writing and presentation skills with the ability to communicate in an organized and concise mannerAbility to work both autonomously and collaborate across teams and functional areasAbility to work in and maintain performance expectations in diverse cultural contexts and fast-paced environmentWork requires continual attention to detail and ability to establish priorities and meet deadlinesDemonstrated ability to analyze and solve problems in an empowered, self-directed/managed work environmentProficient in Microsoft Office and other relevant software applicationsDomestic and some International travel a key part of the roleBackground knowledge of the pig industry preferred essentialWritten and verbal proficiency in German and English a requirement HomeofficeÜber das Unternehmen:Genus PLC
Management Assistant (m/f/d)
Germany - Ritter GmbH, DEU-Schwabmünchen
The Opportunity: Wir – Ritter, part of Avantor- suchen eine/n Personal Assistant (m/w/d), in dieser spannenden Vakanz unterstützen Sie unter anderem unseren Geschäftsführer mit regelmäßig anfallenden Assistenzaufgaben. Sie haben die Möglichkeit, in einem internationalen Umfeld mit flexiblen Arbeitszeiten Ihre Fähigkeiten unter Beweis zu stellen. Wenn Sie Erfahrung im Bereich der Assistenz und organisatorisches Geschick 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: Ein erfolgreich abgeschlossenes administratives Studium oder eine Berufsausbildung im kaufmännischen Bereich Einschlägige, relevante Berufserfahrung als Assistenz (Erfahrung in der Geschäftsführungsassistenz von Vorteil) Fließende Deutsch und Englischkenntnisse (in Wort und Schrift) Versierter Umgang mit Outlook, MS Office, insbesondere Word und Power Point Ausgezeichnetes Zeitmanagement und die Fähigkeit Prioritäten zu setzen Hohes Maß an Eigeninitiative und Stress Resilienz Organisationstalent, Detailorientierung sowie Kommunikationsgeschick und Diskretion Ihre Aufgaben:  Allgemeine Assistenzaufgaben, Verwaltung der Postaufträge, Meetingräume, Besucherparkplätzen etc. Organisation von Unternehmensveranstaltungen (Townhall, Sommerfest etc.) einschließlich der Erstellung von Präsentationen Reisebuchungen, inklusive Flugbuchungen, Hotel- und Restaurantreservierungen Enge Zusammenarbeit mit der Finanzabteilung, zu Bestandsaufzeichnungen sowie Erstellung von Reiseberichten und weiteres monatliches Reporting Verwaltung und Organisation des Büromaterials und Aufbau & Pflege der entsprechenden Lieferantenbeziehungen Kommunikation mit der Gebäudeverwaltung zu Schäden und Änderungen an Büroräumen Archivierung von Unternehmensdokumenten, Führung, Aufzeichnung zu Ein- und Ausgangsdokumenten und deren Registrierung Unterstützung beim Onboarding neuer Mitarbeiter:innen, inklusive Koordinierung mit der IT-Abteilung bezüglich der Büroausstattung : Zugangskarte, Schlüssel, Büromaterial usw. Organisation von Vorstellungsgesprächen und Verantwortung für die Evakuierung in Notfällen Unterstützung bei der Verteilung der Transportabonnements, Geschenkkarten und Urlaubsgutscheinen 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-Hybrid 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
International Medical Science Liaison
PreventionGenetics, Cologne
Help us change livesAt Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others.Company OverviewExact Sciences is dedicated to delivering patient critical answers across the cancer journey from early detection to treatment decision making. With a strong focus on people and an empathetic spirit, which fuels the company’s culture, driving them to create and deliver solutions rooted in the needs of patients, providers, and families.From earlier cancer detection to treatment guidance and monitoring, Exact Sciences are helping people get the answers they need to make more informed decisions across the cancer continuum. With a leading portfolio of products for earlier detection and treatment guidance, they help people face the most challenging decisions with confidence with a dedication to continuously innovate, combining scientific rigor with an open-minded approach to deliver the next big thing.Exact Sciences is continuously expanding the pipeline with the aim of tackling a wider array of cancer tests through the following measures:Expanding the Oncotype IQ platform to include liquid and tissue-based tests, all with the goal of making cancer care smarter.Adapting biomarker-based technologies create a liquid biopsy capable of detecting cancers and precancers from a blood sample.Using their proven multi-marker approach to achieve analytical sensitivity needed to discriminate between normal and cancerous samples.Collaborating with world-class clinicians and scientists at Mayo Clinic to identify biomarkers associated with the 15 deadliest cancers.Building a cancer detection platform upon learnings from the development of Cologuard (commercially available in the US only).By 2020, Oncotype DX will have been used to guide treatment decisions for more than 1 million cancer patients worldwide in breast, prostate and colon cancer.In July 2019 Exact Sciences acquired Genomic Health, a genetic cancer detection company based in Redwood City, California, for USD 2.8 billion, creating the leading global cancer diagnostics company.In 2020 Exact Sciences acquired Thrive Earlier Detection Corp., a Massachusetts-based healthcare company, in a multi-billion-dollar deal, and Base Genomics, which has technology for DNA methylation analysis.In February 2021 Exact Sciences announced the acquisition of Ashion Analytics, LLC (Ashion) from The Translational Genomics Research Institute (TGen), an affiliate of City of Hope. Ashion is a CLIA-certified and CAP-accredited sequencing lab based in Phoenix, Arizona with the genomics testing capabilities necessary to address the increasingly complex needs of clinical, academic, and biopharma customers focused on precision cancer treatments.The company is based in the United States, with International headquarters in Zug, Switzerland. Position SummaryRepresenting the medical function, the MSL will act as a medical/clinical education liaison to external and internal stakeholders, while supporting commercial business and reimbursement objectives for the portfolio of products, most notably for breast and colorectal cancers. This role will engage with customers and colleagues across medical affairs and commercial groups to provide medical and scientific support for our on-market as well as help launch newer products into the international region.Near term business objectives include supporting growth of the Oncotype DX Breast Recurrence Score assay by providing medical information and education through scientific exchange in a fair-balanced manner to Medical Oncology, Surgeons, and Pathology Key Opinion Leaders as well as other healthcare professionals. In addition, the role supports the company’s R&D and investigator-initiated studies in the development and commercialization of genomic assays that lead to improved treatment decisions for oncology patients.To be an effective business partner MSLs develop and maintain outstanding knowledge of Exact Sciences products, competitor products, and other diagnostic options within therapeutic areas. MSLs must also maintain an in-depth understanding of the medical strategy and broader Exact Sciences strategy to ensure their own activities are coordinated and aligned. MSLs must be professionals with integrity and scientific creditability to interact with thought leaders, government health authorities, and medical centers of excellence.This position is based in Germany.Essential DutiesInclude, but are not limited to, the following:Inline Product & Team SupportDeliver education of the broad healthcare provider (HCP) community, such as key opinion leaders (KOL’s), oncologists, pathologists, surgeons, nurses, and payors regarding Exact Sciences products as permissible by local laws and regulations.Serves as external, credible scientific expert on disease area and Exact Sciences products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings.Responds to unsolicited requests for medical information on Exact Sciences products in a credible, balanced/objective manner.Participate in the development and execution of a KOL outreach plans.Identify and map KOL, other stakeholder, key accounts as well as patient referral patterns and pathways.Maintain and develop synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities.Support medical-marketing initiatives, such as conference planning and support, medical education content development, faculty speaker training, sales training, reimbursement initiatives.Work with medical directors to take complex medical messages and position them to enable clear and concise understanding by both external audiences and partners within Exact Sciences.Stay abreast of new clinical developments, publications, and market trends to be a conduit for the greater medical team and other internal teams for review of these developments.Assist with set up and delivery of advisory boards, speaker trainings, and external payor reviews, as needed.Support preparation and presentation of medical review slides and materials at national sales meetings, pre-conference meetings, and field sales conference calls.Attend, develop summaries of, and present key medical findings from scientific congresses.Gather and interpret new clinical data from conferences and literature, as well as competitive intelligence, and report back on findings to medical affairs and marketing stakeholders.Pipeline & Clinical Trials SupportIdentify physicians currently managing patients with breast and colorectal cancer and cultivate a network of experts at academic and community centers to identify new trial sites and/or drive patient referrals and rapid enrolment.Delivers medical / scientific training to clinical study sites and provide input to key internal stakeholders on training materials for clinical trials, products in development, therapeutic areas, and disease state as outlined by the trial sponsor.Establishes and maintain strong working relationships with Principal Investigators (PIs) and clinical trial sites to support the enrollment and conduct of Exact Sciences clinical studies. Facilitate escalation of investigator questions/concerns, recruitment/retention initiatives and clinical site & investigators meetings as it relates to recruitment strategies.Minimum QualificationsAdvanced degree in clinical specialty (PharmD, PhD, MD) with clinical experience.3-5+ years’ experience as an MSL/CTL or senior clinical development role.3+ years Oncology experience required.3+ years of experience in pharmaceutical industry with knowledge of clinical research design and conduct.Preferred QualificationsExperience in Diagnostics or Biotech industry is a plus.SkillsExcellent oral, written and presentation communication skills. Excellent English, multiple languages preferred.Proficient use of Microsoft Office Suite and other IT systems.Experience with VEEVA systems is a plus.Ability to independently deliver quality results in a timely manner.Ability to work as part of a team.Cultural ImpactHighest integrity and ethical behavior.Mutual respect for colleagues.Collaborative within teams, uses resources carefully and can build a great place to work and grow.Ability to interact within culturally diverse teams.Business acumen and innovative mindset. Ability to manage though complexity and ambiguity, while focusing on the end goal.Discretion with sensitive and confidential information.OtherAbility to travel 60-70% % of working time away from work location, may include overnight/weekend travel.#LI-TK1Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, email E-Mail anzeigen. We’ll work with you to meet your accessibility needs.Not ready to apply? Join our talent community and stay up to date on what’s new at Exact Sciences. Standort PreventionGenetics, Cologne
International Medical Science Liaison
PreventionGenetics, Frankfurt
Help us change livesAt Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others.Company OverviewExact Sciences is dedicated to delivering patient critical answers across the cancer journey from early detection to treatment decision making. With a strong focus on people and an empathetic spirit, which fuels the company’s culture, driving them to create and deliver solutions rooted in the needs of patients, providers, and families.From earlier cancer detection to treatment guidance and monitoring, Exact Sciences are helping people get the answers they need to make more informed decisions across the cancer continuum. With a leading portfolio of products for earlier detection and treatment guidance, they help people face the most challenging decisions with confidence with a dedication to continuously innovate, combining scientific rigor with an open-minded approach to deliver the next big thing.Exact Sciences is continuously expanding the pipeline with the aim of tackling a wider array of cancer tests through the following measures:Expanding the Oncotype IQ platform to include liquid and tissue-based tests, all with the goal of making cancer care smarter.Adapting biomarker-based technologies create a liquid biopsy capable of detecting cancers and precancers from a blood sample.Using their proven multi-marker approach to achieve analytical sensitivity needed to discriminate between normal and cancerous samples.Collaborating with world-class clinicians and scientists at Mayo Clinic to identify biomarkers associated with the 15 deadliest cancers.Building a cancer detection platform upon learnings from the development of Cologuard (commercially available in the US only).By 2020, Oncotype DX will have been used to guide treatment decisions for more than 1 million cancer patients worldwide in breast, prostate and colon cancer.In July 2019 Exact Sciences acquired Genomic Health, a genetic cancer detection company based in Redwood City, California, for USD 2.8 billion, creating the leading global cancer diagnostics company.In 2020 Exact Sciences acquired Thrive Earlier Detection Corp., a Massachusetts-based healthcare company, in a multi-billion-dollar deal, and Base Genomics, which has technology for DNA methylation analysis.In February 2021 Exact Sciences announced the acquisition of Ashion Analytics, LLC (Ashion) from The Translational Genomics Research Institute (TGen), an affiliate of City of Hope. Ashion is a CLIA-certified and CAP-accredited sequencing lab based in Phoenix, Arizona with the genomics testing capabilities necessary to address the increasingly complex needs of clinical, academic, and biopharma customers focused on precision cancer treatments.The company is based in the United States, with International headquarters in Zug, Switzerland. Position SummaryRepresenting the medical function, the MSL will act as a medical/clinical education liaison to external and internal stakeholders, while supporting commercial business and reimbursement objectives for the portfolio of products, most notably for breast and colorectal cancers. This role will engage with customers and colleagues across medical affairs and commercial groups to provide medical and scientific support for our on-market as well as help launch newer products into the international region.Near term business objectives include supporting growth of the Oncotype DX Breast Recurrence Score assay by providing medical information and education through scientific exchange in a fair-balanced manner to Medical Oncology, Surgeons, and Pathology Key Opinion Leaders as well as other healthcare professionals. In addition, the role supports the company’s R&D and investigator-initiated studies in the development and commercialization of genomic assays that lead to improved treatment decisions for oncology patients.To be an effective business partner MSLs develop and maintain outstanding knowledge of Exact Sciences products, competitor products, and other diagnostic options within therapeutic areas. MSLs must also maintain an in-depth understanding of the medical strategy and broader Exact Sciences strategy to ensure their own activities are coordinated and aligned. MSLs must be professionals with integrity and scientific creditability to interact with thought leaders, government health authorities, and medical centers of excellence.This position is based in Germany.Essential DutiesInclude, but are not limited to, the following:Inline Product & Team SupportDeliver education of the broad healthcare provider (HCP) community, such as key opinion leaders (KOL’s), oncologists, pathologists, surgeons, nurses, and payors regarding Exact Sciences products as permissible by local laws and regulations.Serves as external, credible scientific expert on disease area and Exact Sciences products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings.Responds to unsolicited requests for medical information on Exact Sciences products in a credible, balanced/objective manner.Participate in the development and execution of a KOL outreach plans.Identify and map KOL, other stakeholder, key accounts as well as patient referral patterns and pathways.Maintain and develop synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities.Support medical-marketing initiatives, such as conference planning and support, medical education content development, faculty speaker training, sales training, reimbursement initiatives.Work with medical directors to take complex medical messages and position them to enable clear and concise understanding by both external audiences and partners within Exact Sciences.Stay abreast of new clinical developments, publications, and market trends to be a conduit for the greater medical team and other internal teams for review of these developments.Assist with set up and delivery of advisory boards, speaker trainings, and external payor reviews, as needed.Support preparation and presentation of medical review slides and materials at national sales meetings, pre-conference meetings, and field sales conference calls.Attend, develop summaries of, and present key medical findings from scientific congresses.Gather and interpret new clinical data from conferences and literature, as well as competitive intelligence, and report back on findings to medical affairs and marketing stakeholders.Pipeline & Clinical Trials SupportIdentify physicians currently managing patients with breast and colorectal cancer and cultivate a network of experts at academic and community centers to identify new trial sites and/or drive patient referrals and rapid enrolment.Delivers medical / scientific training to clinical study sites and provide input to key internal stakeholders on training materials for clinical trials, products in development, therapeutic areas, and disease state as outlined by the trial sponsor.Establishes and maintain strong working relationships with Principal Investigators (PIs) and clinical trial sites to support the enrollment and conduct of Exact Sciences clinical studies. Facilitate escalation of investigator questions/concerns, recruitment/retention initiatives and clinical site & investigators meetings as it relates to recruitment strategies.Minimum QualificationsAdvanced degree in clinical specialty (PharmD, PhD, MD) with clinical experience.3-5+ years’ experience as an MSL/CTL or senior clinical development role.3+ years Oncology experience required.3+ years of experience in pharmaceutical industry with knowledge of clinical research design and conduct.Preferred QualificationsExperience in Diagnostics or Biotech industry is a plus.SkillsExcellent oral, written and presentation communication skills. Excellent English, multiple languages preferred.Proficient use of Microsoft Office Suite and other IT systems.Experience with VEEVA systems is a plus.Ability to independently deliver quality results in a timely manner.Ability to work as part of a team.Cultural ImpactHighest integrity and ethical behavior.Mutual respect for colleagues.Collaborative within teams, uses resources carefully and can build a great place to work and grow.Ability to interact within culturally diverse teams.Business acumen and innovative mindset. Ability to manage though complexity and ambiguity, while focusing on the end goal.Discretion with sensitive and confidential information.OtherAbility to travel 60-70% % of working time away from work location, may include overnight/weekend travel.#LI-TK1Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, email E-Mail anzeigen. We’ll work with you to meet your accessibility needs.Not ready to apply? Join our talent community and stay up to date on what’s new at Exact Sciences. Standort PreventionGenetics, Frankfurt
International Medical Science Liaison
PreventionGenetics, Munich
Help us change livesAt Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others.Company OverviewExact Sciences is dedicated to delivering patient critical answers across the cancer journey from early detection to treatment decision making. With a strong focus on people and an empathetic spirit, which fuels the company’s culture, driving them to create and deliver solutions rooted in the needs of patients, providers, and families.From earlier cancer detection to treatment guidance and monitoring, Exact Sciences are helping people get the answers they need to make more informed decisions across the cancer continuum. With a leading portfolio of products for earlier detection and treatment guidance, they help people face the most challenging decisions with confidence with a dedication to continuously innovate, combining scientific rigor with an open-minded approach to deliver the next big thing.Exact Sciences is continuously expanding the pipeline with the aim of tackling a wider array of cancer tests through the following measures:Expanding the Oncotype IQ platform to include liquid and tissue-based tests, all with the goal of making cancer care smarter.Adapting biomarker-based technologies create a liquid biopsy capable of detecting cancers and precancers from a blood sample.Using their proven multi-marker approach to achieve analytical sensitivity needed to discriminate between normal and cancerous samples.Collaborating with world-class clinicians and scientists at Mayo Clinic to identify biomarkers associated with the 15 deadliest cancers.Building a cancer detection platform upon learnings from the development of Cologuard (commercially available in the US only).By 2020, Oncotype DX will have been used to guide treatment decisions for more than 1 million cancer patients worldwide in breast, prostate and colon cancer.In July 2019 Exact Sciences acquired Genomic Health, a genetic cancer detection company based in Redwood City, California, for USD 2.8 billion, creating the leading global cancer diagnostics company.In 2020 Exact Sciences acquired Thrive Earlier Detection Corp., a Massachusetts-based healthcare company, in a multi-billion-dollar deal, and Base Genomics, which has technology for DNA methylation analysis.In February 2021 Exact Sciences announced the acquisition of Ashion Analytics, LLC (Ashion) from The Translational Genomics Research Institute (TGen), an affiliate of City of Hope. Ashion is a CLIA-certified and CAP-accredited sequencing lab based in Phoenix, Arizona with the genomics testing capabilities necessary to address the increasingly complex needs of clinical, academic, and biopharma customers focused on precision cancer treatments.The company is based in the United States, with International headquarters in Zug, Switzerland. Position SummaryRepresenting the medical function, the MSL will act as a medical/clinical education liaison to external and internal stakeholders, while supporting commercial business and reimbursement objectives for the portfolio of products, most notably for breast and colorectal cancers. This role will engage with customers and colleagues across medical affairs and commercial groups to provide medical and scientific support for our on-market as well as help launch newer products into the international region.Near term business objectives include supporting growth of the Oncotype DX Breast Recurrence Score assay by providing medical information and education through scientific exchange in a fair-balanced manner to Medical Oncology, Surgeons, and Pathology Key Opinion Leaders as well as other healthcare professionals. In addition, the role supports the company’s R&D and investigator-initiated studies in the development and commercialization of genomic assays that lead to improved treatment decisions for oncology patients.To be an effective business partner MSLs develop and maintain outstanding knowledge of Exact Sciences products, competitor products, and other diagnostic options within therapeutic areas. MSLs must also maintain an in-depth understanding of the medical strategy and broader Exact Sciences strategy to ensure their own activities are coordinated and aligned. MSLs must be professionals with integrity and scientific creditability to interact with thought leaders, government health authorities, and medical centers of excellence.This position is based in Germany.Essential DutiesInclude, but are not limited to, the following:Inline Product & Team SupportDeliver education of the broad healthcare provider (HCP) community, such as key opinion leaders (KOL’s), oncologists, pathologists, surgeons, nurses, and payors regarding Exact Sciences products as permissible by local laws and regulations.Serves as external, credible scientific expert on disease area and Exact Sciences products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings.Responds to unsolicited requests for medical information on Exact Sciences products in a credible, balanced/objective manner.Participate in the development and execution of a KOL outreach plans.Identify and map KOL, other stakeholder, key accounts as well as patient referral patterns and pathways.Maintain and develop synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities.Support medical-marketing initiatives, such as conference planning and support, medical education content development, faculty speaker training, sales training, reimbursement initiatives.Work with medical directors to take complex medical messages and position them to enable clear and concise understanding by both external audiences and partners within Exact Sciences.Stay abreast of new clinical developments, publications, and market trends to be a conduit for the greater medical team and other internal teams for review of these developments.Assist with set up and delivery of advisory boards, speaker trainings, and external payor reviews, as needed.Support preparation and presentation of medical review slides and materials at national sales meetings, pre-conference meetings, and field sales conference calls.Attend, develop summaries of, and present key medical findings from scientific congresses.Gather and interpret new clinical data from conferences and literature, as well as competitive intelligence, and report back on findings to medical affairs and marketing stakeholders.Pipeline & Clinical Trials SupportIdentify physicians currently managing patients with breast and colorectal cancer and cultivate a network of experts at academic and community centers to identify new trial sites and/or drive patient referrals and rapid enrolment.Delivers medical / scientific training to clinical study sites and provide input to key internal stakeholders on training materials for clinical trials, products in development, therapeutic areas, and disease state as outlined by the trial sponsor.Establishes and maintain strong working relationships with Principal Investigators (PIs) and clinical trial sites to support the enrollment and conduct of Exact Sciences clinical studies. Facilitate escalation of investigator questions/concerns, recruitment/retention initiatives and clinical site & investigators meetings as it relates to recruitment strategies.Minimum QualificationsAdvanced degree in clinical specialty (PharmD, PhD, MD) with clinical experience.3-5+ years’ experience as an MSL/CTL or senior clinical development role.3+ years Oncology experience required.3+ years of experience in pharmaceutical industry with knowledge of clinical research design and conduct.Preferred QualificationsExperience in Diagnostics or Biotech industry is a plus.SkillsExcellent oral, written and presentation communication skills. Excellent English, multiple languages preferred.Proficient use of Microsoft Office Suite and other IT systems.Experience with VEEVA systems is a plus.Ability to independently deliver quality results in a timely manner.Ability to work as part of a team.Cultural ImpactHighest integrity and ethical behavior.Mutual respect for colleagues.Collaborative within teams, uses resources carefully and can build a great place to work and grow.Ability to interact within culturally diverse teams.Business acumen and innovative mindset. Ability to manage though complexity and ambiguity, while focusing on the end goal.Discretion with sensitive and confidential information.OtherAbility to travel 60-70% % of working time away from work location, may include overnight/weekend travel.#LI-TK1Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, email E-Mail anzeigen. We’ll work with you to meet your accessibility needs.Not ready to apply? Join our talent community and stay up to date on what’s new at Exact Sciences. Standort PreventionGenetics, Munich
International Medical Science Liaison
PreventionGenetics, Düsseldorf
Help us change livesAt Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others.Company OverviewExact Sciences is dedicated to delivering patient critical answers across the cancer journey from early detection to treatment decision making. With a strong focus on people and an empathetic spirit, which fuels the company’s culture, driving them to create and deliver solutions rooted in the needs of patients, providers, and families.From earlier cancer detection to treatment guidance and monitoring, Exact Sciences are helping people get the answers they need to make more informed decisions across the cancer continuum. With a leading portfolio of products for earlier detection and treatment guidance, they help people face the most challenging decisions with confidence with a dedication to continuously innovate, combining scientific rigor with an open-minded approach to deliver the next big thing.Exact Sciences is continuously expanding the pipeline with the aim of tackling a wider array of cancer tests through the following measures:Expanding the Oncotype IQ platform to include liquid and tissue-based tests, all with the goal of making cancer care smarter.Adapting biomarker-based technologies create a liquid biopsy capable of detecting cancers and precancers from a blood sample.Using their proven multi-marker approach to achieve analytical sensitivity needed to discriminate between normal and cancerous samples.Collaborating with world-class clinicians and scientists at Mayo Clinic to identify biomarkers associated with the 15 deadliest cancers.Building a cancer detection platform upon learnings from the development of Cologuard (commercially available in the US only).By 2020, Oncotype DX will have been used to guide treatment decisions for more than 1 million cancer patients worldwide in breast, prostate and colon cancer.In July 2019 Exact Sciences acquired Genomic Health, a genetic cancer detection company based in Redwood City, California, for USD 2.8 billion, creating the leading global cancer diagnostics company.In 2020 Exact Sciences acquired Thrive Earlier Detection Corp., a Massachusetts-based healthcare company, in a multi-billion-dollar deal, and Base Genomics, which has technology for DNA methylation analysis.In February 2021 Exact Sciences announced the acquisition of Ashion Analytics, LLC (Ashion) from The Translational Genomics Research Institute (TGen), an affiliate of City of Hope. Ashion is a CLIA-certified and CAP-accredited sequencing lab based in Phoenix, Arizona with the genomics testing capabilities necessary to address the increasingly complex needs of clinical, academic, and biopharma customers focused on precision cancer treatments.The company is based in the United States, with International headquarters in Zug, Switzerland. Position SummaryRepresenting the medical function, the MSL will act as a medical/clinical education liaison to external and internal stakeholders, while supporting commercial business and reimbursement objectives for the portfolio of products, most notably for breast and colorectal cancers. This role will engage with customers and colleagues across medical affairs and commercial groups to provide medical and scientific support for our on-market as well as help launch newer products into the international region.Near term business objectives include supporting growth of the Oncotype DX Breast Recurrence Score assay by providing medical information and education through scientific exchange in a fair-balanced manner to Medical Oncology, Surgeons, and Pathology Key Opinion Leaders as well as other healthcare professionals. In addition, the role supports the company’s R&D and investigator-initiated studies in the development and commercialization of genomic assays that lead to improved treatment decisions for oncology patients.To be an effective business partner MSLs develop and maintain outstanding knowledge of Exact Sciences products, competitor products, and other diagnostic options within therapeutic areas. MSLs must also maintain an in-depth understanding of the medical strategy and broader Exact Sciences strategy to ensure their own activities are coordinated and aligned. MSLs must be professionals with integrity and scientific creditability to interact with thought leaders, government health authorities, and medical centers of excellence.This position is based in Germany.Essential DutiesInclude, but are not limited to, the following:Inline Product & Team SupportDeliver education of the broad healthcare provider (HCP) community, such as key opinion leaders (KOL’s), oncologists, pathologists, surgeons, nurses, and payors regarding Exact Sciences products as permissible by local laws and regulations.Serves as external, credible scientific expert on disease area and Exact Sciences products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings.Responds to unsolicited requests for medical information on Exact Sciences products in a credible, balanced/objective manner.Participate in the development and execution of a KOL outreach plans.Identify and map KOL, other stakeholder, key accounts as well as patient referral patterns and pathways.Maintain and develop synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities.Support medical-marketing initiatives, such as conference planning and support, medical education content development, faculty speaker training, sales training, reimbursement initiatives.Work with medical directors to take complex medical messages and position them to enable clear and concise understanding by both external audiences and partners within Exact Sciences.Stay abreast of new clinical developments, publications, and market trends to be a conduit for the greater medical team and other internal teams for review of these developments.Assist with set up and delivery of advisory boards, speaker trainings, and external payor reviews, as needed.Support preparation and presentation of medical review slides and materials at national sales meetings, pre-conference meetings, and field sales conference calls.Attend, develop summaries of, and present key medical findings from scientific congresses.Gather and interpret new clinical data from conferences and literature, as well as competitive intelligence, and report back on findings to medical affairs and marketing stakeholders.Pipeline & Clinical Trials SupportIdentify physicians currently managing patients with breast and colorectal cancer and cultivate a network of experts at academic and community centers to identify new trial sites and/or drive patient referrals and rapid enrolment.Delivers medical / scientific training to clinical study sites and provide input to key internal stakeholders on training materials for clinical trials, products in development, therapeutic areas, and disease state as outlined by the trial sponsor.Establishes and maintain strong working relationships with Principal Investigators (PIs) and clinical trial sites to support the enrollment and conduct of Exact Sciences clinical studies. Facilitate escalation of investigator questions/concerns, recruitment/retention initiatives and clinical site & investigators meetings as it relates to recruitment strategies.Minimum QualificationsAdvanced degree in clinical specialty (PharmD, PhD, MD) with clinical experience.3-5+ years’ experience as an MSL/CTL or senior clinical development role.3+ years Oncology experience required.3+ years of experience in pharmaceutical industry with knowledge of clinical research design and conduct.Preferred QualificationsExperience in Diagnostics or Biotech industry is a plus.SkillsExcellent oral, written and presentation communication skills. Excellent English, multiple languages preferred.Proficient use of Microsoft Office Suite and other IT systems.Experience with VEEVA systems is a plus.Ability to independently deliver quality results in a timely manner.Ability to work as part of a team.Cultural ImpactHighest integrity and ethical behavior.Mutual respect for colleagues.Collaborative within teams, uses resources carefully and can build a great place to work and grow.Ability to interact within culturally diverse teams.Business acumen and innovative mindset. Ability to manage though complexity and ambiguity, while focusing on the end goal.Discretion with sensitive and confidential information.OtherAbility to travel 60-70% % of working time away from work location, may include overnight/weekend travel.#LI-TK1Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, email E-Mail anzeigen. We’ll work with you to meet your accessibility needs.Not ready to apply? Join our talent community and stay up to date on what’s new at Exact Sciences. Standort PreventionGenetics, Düsseldorf
International Medical Science Liaison
PreventionGenetics, Berlin
Help us change livesAt Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others.Company OverviewExact Sciences is dedicated to delivering patient critical answers across the cancer journey from early detection to treatment decision making. With a strong focus on people and an empathetic spirit, which fuels the company’s culture, driving them to create and deliver solutions rooted in the needs of patients, providers, and families.From earlier cancer detection to treatment guidance and monitoring, Exact Sciences are helping people get the answers they need to make more informed decisions across the cancer continuum. With a leading portfolio of products for earlier detection and treatment guidance, they help people face the most challenging decisions with confidence with a dedication to continuously innovate, combining scientific rigor with an open-minded approach to deliver the next big thing.Exact Sciences is continuously expanding the pipeline with the aim of tackling a wider array of cancer tests through the following measures:Expanding the Oncotype IQ platform to include liquid and tissue-based tests, all with the goal of making cancer care smarter.Adapting biomarker-based technologies create a liquid biopsy capable of detecting cancers and precancers from a blood sample.Using their proven multi-marker approach to achieve analytical sensitivity needed to discriminate between normal and cancerous samples.Collaborating with world-class clinicians and scientists at Mayo Clinic to identify biomarkers associated with the 15 deadliest cancers.Building a cancer detection platform upon learnings from the development of Cologuard (commercially available in the US only).By 2020, Oncotype DX will have been used to guide treatment decisions for more than 1 million cancer patients worldwide in breast, prostate and colon cancer.In July 2019 Exact Sciences acquired Genomic Health, a genetic cancer detection company based in Redwood City, California, for USD 2.8 billion, creating the leading global cancer diagnostics company.In 2020 Exact Sciences acquired Thrive Earlier Detection Corp., a Massachusetts-based healthcare company, in a multi-billion-dollar deal, and Base Genomics, which has technology for DNA methylation analysis.In February 2021 Exact Sciences announced the acquisition of Ashion Analytics, LLC (Ashion) from The Translational Genomics Research Institute (TGen), an affiliate of City of Hope. Ashion is a CLIA-certified and CAP-accredited sequencing lab based in Phoenix, Arizona with the genomics testing capabilities necessary to address the increasingly complex needs of clinical, academic, and biopharma customers focused on precision cancer treatments.The company is based in the United States, with International headquarters in Zug, Switzerland. Position SummaryRepresenting the medical function, the MSL will act as a medical/clinical education liaison to external and internal stakeholders, while supporting commercial business and reimbursement objectives for the portfolio of products, most notably for breast and colorectal cancers. This role will engage with customers and colleagues across medical affairs and commercial groups to provide medical and scientific support for our on-market as well as help launch newer products into the international region.Near term business objectives include supporting growth of the Oncotype DX Breast Recurrence Score assay by providing medical information and education through scientific exchange in a fair-balanced manner to Medical Oncology, Surgeons, and Pathology Key Opinion Leaders as well as other healthcare professionals. In addition, the role supports the company’s R&D and investigator-initiated studies in the development and commercialization of genomic assays that lead to improved treatment decisions for oncology patients.To be an effective business partner MSLs develop and maintain outstanding knowledge of Exact Sciences products, competitor products, and other diagnostic options within therapeutic areas. MSLs must also maintain an in-depth understanding of the medical strategy and broader Exact Sciences strategy to ensure their own activities are coordinated and aligned. MSLs must be professionals with integrity and scientific creditability to interact with thought leaders, government health authorities, and medical centers of excellence.This position is based in Germany.Essential DutiesInclude, but are not limited to, the following:Inline Product & Team SupportDeliver education of the broad healthcare provider (HCP) community, such as key opinion leaders (KOL’s), oncologists, pathologists, surgeons, nurses, and payors regarding Exact Sciences products as permissible by local laws and regulations.Serves as external, credible scientific expert on disease area and Exact Sciences products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings.Responds to unsolicited requests for medical information on Exact Sciences products in a credible, balanced/objective manner.Participate in the development and execution of a KOL outreach plans.Identify and map KOL, other stakeholder, key accounts as well as patient referral patterns and pathways.Maintain and develop synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities.Support medical-marketing initiatives, such as conference planning and support, medical education content development, faculty speaker training, sales training, reimbursement initiatives.Work with medical directors to take complex medical messages and position them to enable clear and concise understanding by both external audiences and partners within Exact Sciences.Stay abreast of new clinical developments, publications, and market trends to be a conduit for the greater medical team and other internal teams for review of these developments.Assist with set up and delivery of advisory boards, speaker trainings, and external payor reviews, as needed.Support preparation and presentation of medical review slides and materials at national sales meetings, pre-conference meetings, and field sales conference calls.Attend, develop summaries of, and present key medical findings from scientific congresses.Gather and interpret new clinical data from conferences and literature, as well as competitive intelligence, and report back on findings to medical affairs and marketing stakeholders.Pipeline & Clinical Trials SupportIdentify physicians currently managing patients with breast and colorectal cancer and cultivate a network of experts at academic and community centers to identify new trial sites and/or drive patient referrals and rapid enrolment.Delivers medical / scientific training to clinical study sites and provide input to key internal stakeholders on training materials for clinical trials, products in development, therapeutic areas, and disease state as outlined by the trial sponsor.Establishes and maintain strong working relationships with Principal Investigators (PIs) and clinical trial sites to support the enrollment and conduct of Exact Sciences clinical studies. Facilitate escalation of investigator questions/concerns, recruitment/retention initiatives and clinical site & investigators meetings as it relates to recruitment strategies.Minimum QualificationsAdvanced degree in clinical specialty (PharmD, PhD, MD) with clinical experience.3-5+ years’ experience as an MSL/CTL or senior clinical development role.3+ years Oncology experience required.3+ years of experience in pharmaceutical industry with knowledge of clinical research design and conduct.Preferred QualificationsExperience in Diagnostics or Biotech industry is a plus.SkillsExcellent oral, written and presentation communication skills. Excellent English, multiple languages preferred.Proficient use of Microsoft Office Suite and other IT systems.Experience with VEEVA systems is a plus.Ability to independently deliver quality results in a timely manner.Ability to work as part of a team.Cultural ImpactHighest integrity and ethical behavior.Mutual respect for colleagues.Collaborative within teams, uses resources carefully and can build a great place to work and grow.Ability to interact within culturally diverse teams.Business acumen and innovative mindset. Ability to manage though complexity and ambiguity, while focusing on the end goal.Discretion with sensitive and confidential information.OtherAbility to travel 60-70% % of working time away from work location, may include overnight/weekend travel.#LI-TK1Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, email E-Mail anzeigen. We’ll work with you to meet your accessibility needs.Not ready to apply? Join our talent community and stay up to date on what’s new at Exact Sciences. Standort PreventionGenetics, Berlin
International Medical Science Liaison
Genomic Health, Inc., Germany
Help us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Company Overview Exact Sciences is dedicated to delivering patient critical answers across the cancer journey from early detection to treatment decision making. With a strong focus on people and an empathetic spirit, which fuels the company’s culture, driving them to create and deliver solutions rooted in the needs of patients, providers, and families. From earlier cancer detection to treatment guidance and monitoring, Exact Sciences are helping people get the answers they need to make more informed decisions across the cancer continuum. With a leading portfolio of products for earlier detection and treatment guidance, they help people face the most challenging decisions with confidence with a dedication to continuously innovate, combining scientific rigor with an open-minded approach to deliver the next big thing. Exact Sciences is continuously expanding the pipeline with the aim of tackling a wider array of cancer tests through the following measures: Expanding the Oncotype IQ platform to include liquid and tissue-based tests, all with the goal of making cancer care smarter. Adapting biomarker-based technologies create a liquid biopsy capable of detecting cancers and precancers from a blood sample. Using their proven multi-marker approach to achieve analytical sensitivity needed to discriminate between normal and cancerous samples. Collaborating with world-class clinicians and scientists at Mayo Clinic to identify biomarkers associated with the 15 deadliest cancers. Building a cancer detection platform upon learnings from the development of Cologuard (commercially available in the US only). By 2020, Oncotype DX will have been used to guide treatment decisions for more than 1 million cancer patients worldwide in breast, prostate and colon cancer. In July 2019 Exact Sciences acquired Genomic Health, a genetic cancer detection company based in Redwood City, California, for USD 2.8 billion, creating the leading global cancer diagnostics company. In 2020 Exact Sciences acquired Thrive Earlier Detection Corp., a Massachusetts-based healthcare company, in a multi-billion-dollar deal, and Base Genomics, which has technology for DNA methylation analysis. In February 2021 Exact Sciences announced the acquisition of Ashion Analytics, LLC (Ashion) from The Translational Genomics Research Institute (TGen), an affiliate of City of Hope. Ashion is a CLIA-certified and CAP-accredited sequencing lab based in Phoenix, Arizona with the genomics testing capabilities necessary to address the increasingly complex needs of clinical, academic, and biopharma customers focused on precision cancer treatments. The company is based in the United States, with International headquarters in Zug, Switzerland. Position Summary Representing the medical function, the MSL will act as a medical/clinical education liaison to external and internal stakeholders, while supporting commercial business and reimbursement objectives for the portfolio of products, most notably for breast and colorectal cancers. This role will engage with customers and colleagues across medical affairs and commercial groups to provide medical and scientific support for our on-market as well as help launch newer products into the international region. Near term business objectives include supporting growth of the Oncotype DX Breast Recurrence Score assay by providing medical information and education through scientific exchange in a fair-balanced manner to Medical Oncology, Surgeons, and Pathology Key Opinion Leaders as well as other healthcare professionals. In addition, the role supports the company’s R&D and investigator-initiated studies in the development and commercialization of genomic assays that lead to improved treatment decisions for oncology patients. To be an effective business partner MSLs develop and maintain outstanding knowledge of Exact Sciences products, competitor products, and other diagnostic options within therapeutic areas. MSLs must also maintain an in-depth understanding of the medical strategy and broader Exact Sciences strategy to ensure their own activities are coordinated and aligned. MSLs must be professionals with integrity and scientific creditability to interact with thought leaders, government health authorities, and medical centers of excellence. This position is based in Germany. Essential Duties Include, but are not limited to, the following: Inline Product & Team Support Deliver education of the broad healthcare provider (HCP) community, such as key opinion leaders (KOL’s), oncologists, pathologists, surgeons, nurses, and payors regarding Exact Sciences products as permissible by local laws and regulations. Serves as external, credible scientific expert on disease area and Exact Sciences products at HCP field meetings, key medical and scientific conferences, advisory boards, clinical investigator meetings and patient advocacy group meetings. Responds to unsolicited requests for medical information on Exact Sciences products in a credible, balanced/objective manner. Participate in the development and execution of a KOL outreach plans. Identify and map KOL, other stakeholder, key accounts as well as patient referral patterns and pathways. Maintain and develop synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities. Support medical-marketing initiatives, such as conference planning and support, medical education content development, faculty speaker training, sales training, reimbursement initiatives. Work with medical directors to take complex medical messages and position them to enable clear and concise understanding by both external audiences and partners within Exact Sciences. Stay abreast of new clinical developments, publications, and market trends to be a conduit for the greater medical team and other internal teams for review of these developments. Assist with set up and delivery of advisory boards, speaker trainings, and external payor reviews, as needed. Support preparation and presentation of medical review slides and materials at national sales meetings, pre-conference meetings, and field sales conference calls. Attend, develop summaries of, and present key medical findings from scientific congresses. Gather and interpret new clinical data from conferences and literature, as well as competitive intelligence, and report back on findings to medical affairs and marketing stakeholders. Pipeline & Clinical Trials Support Identify physicians currently managing patients with breast and colorectal cancer and cultivate a network of experts at academic and community centers to identify new trial sites and/or drive patient referrals and rapid enrolment. Delivers medical / scientific training to clinical study sites and provide input to key internal stakeholders on training materials for clinical trials, products in development, therapeutic areas, and disease state as outlined by the trial sponsor. Establishes and maintain strong working relationships with Principal Investigators (PIs) and clinical trial sites to support the enrollment and conduct of Exact Sciences clinical studies. Facilitate escalation of investigator questions/concerns, recruitment/retention initiatives and clinical site & investigators meetings as it relates to recruitment strategies. Minimum Qualifications Advanced degree in clinical specialty (PharmD, PhD, MD) with clinical experience. 3-5+ years’ experience as an MSL/CTL or senior clinical development role. 3+ years Oncology experience required. 3+ years of experience in pharmaceutical industry with knowledge of clinical research design and conduct. Preferred Qualifications Experience in Diagnostics or Biotech industry is a plus. Skills Excellent oral, written and presentation communication skills. Excellent English, multiple languages preferred. Proficient use of Microsoft Office Suite and other IT systems. Experience with VEEVA systems is a plus. Ability to independently deliver quality results in a timely manner. Ability to work as part of a team. Cultural Impact Highest integrity and ethical behavior. Mutual respect for colleagues. Collaborative within teams, uses resources carefully and can build a great place to work and grow. Ability to interact within culturally diverse teams. Business acumen and innovative mindset. Ability to manage though complexity and ambiguity, while focusing on the end goal. Discretion with sensitive and confidential information. Other Ability to travel 60-70% % of working time away from work location, may include overnight/weekend travel. #LI-TK1 Our success relies on the experiences and perspectives of a diverse team, and Exact Sciences fosters a culture where all employees can develop personally and professionally with a sense of respect and belonging. If you require an accommodation, email **********. We’ll work with you to meet your accessibility needs. Not ready to apply? Join our talent community and stay up to date on what’s new at Exact Sciences. We are Exact Sciences, and we're changing lives together through earlier detection and smarter answers. https://vimeo.com/660680929Über das Unternehmen:Genomic Health, Inc.
Research Scientist (all genders) Stem Cell
Evotec SE, Hamburg
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