Überblick über die Statistik des Gehaltsniveaus für "Laboratory Scientist in Deutschland"

Speculative application  Skills: Acne, Actinic Keratosis, Acute Myelogenous Leukemia (AML), AIDS, Allergic Rhinitis, Allergy, Alzheimer's, Anaesthetics, Antibiotics, Anti-infectives, Anxiety, arrhythmia, Asthma, Autoimmune diseases, Autoimmune Disorder, Bacterial Vaginosis, Breast Cancer, Cardiology, Cardiovascular, chemotherapy, Chronic Lymphocytic Leukaemia, Chronic Myeloid Leukemia, Chronic Obstructive Pulmonary Disease, Clinical Pathology, CLL, Congestive Heart Failure, COPD, Cosmetics, Cystic Fibrosis, Dementia, Dentistry, Depression, Dermatology, Diabetes, Diagnostics, Dietetics, Endocrine, Endocrinology, Epilepsy, Family Medicine, Fibromyalgia, Gastroenterology, gastrointestinal, Genetic Diseases, GI, Glioblastoma Multiforme (GBM), Gynaecologic, Gynaecology, Gynecology, Haematology, Haemophilia, Heart Disease, Hematology, Hemopure Anemia, Hepatitis, Hepatology, HIV, Hodgkin's disease, Hypertension, IBD, Immunogenicity, Immunopharmacology, Infections, Infectious Diseases, Influenza, Internal Medicine, Joint Replacement, Lymphoma, Mantle Cell Lymphoma, Melanoma, Menopause, Metabolic, Migraine, Multiple Sclerosis, Musculoskeletal, Myelodysplastic Syndrome, Neonatology, Nephrology, Neurodegenerative disorders, Neurology, Neuroscience, NEUROSURGERY, non small cell lung cancer, Non-Hodgkin Lymphoma, nutraceuticals, Nutrition, OA, Obstetrics, Oncology, Ophthalmology, Oral Health, Orphan Diseases, Orphan drug, Orthobiologic Bone graft, Orthopedic Surgery, Orthopedics, Osteoarthritis, Otitis Externa, Otolaryngology, Ovarian Cancer, Paediatric, Pain, Painful Diabetic Neuropathy, Parkinson’s Disease, Physiology, Podiatry, Post-Menopausal Osteoporosis, Primary Immune Deficiency, Primary Sjogren’s Syndrome, Prostate cancer, Prostatic hyperplasia, Psychiatry, Psychology, Pulmonary, Pulmonology, RA, Rare Disease, Respiratory, retinopathy, Rheumatoid Arthritis, Rheumatology, Rhinitis, Rosacea, Schizophrenia, Seasonal Allergic Rhinitis, Severe Hemophilia, Skin Melanoma, Sleep Disorder, Sleep Medicine, Small Lymphocytic Lymphoma, Small Molecule, Smoking Cessation, Solid Tumors, surgery, Systemic Lupus Erythematosus, Systemic Sclerosis, Tissue Ablation, Transplant, Trauma, Traumatology, Type 2 Diabetes Mellitus, Urology, Vaccine, Vaccines, Vascular Diseases, Weight Loss, Women’s Health, Administrative Assistant, Agile Project Manager, Artwork Coordinator, Associate Director Clinical Operations, Associate Project Manager, Auditor, Biomedical Engineer, Biometrics Manager, Biosample Operations Manager, Biostatistician, Biostatistics Associate Director, Brand Team Lead, Business Administration Associate, Business Administration Manager, Business Analyst, Business Development Associate, Business Development Director, Business Development Manager, CEO, Change Manager, Chemical Project Manager, Chemist, Chemistry, Manufacturing & Control Lead (CMC), Chief Financial Officer, Chief Operating Officer, Chief Technical Officer, Clinical Data Associate, Clinical Data Manager, Clinical Data Specialist, Clinical Development Manager, Clinical Engineer, Clinical Lead, Clinical Operations Director, Clinical Operations Manager, Clinical Pharmacologist, Clinical Programmer, Clinical Project Manager, Clinical Research Associate, Clinical Research Director, Clinical Research Manager, Clinical Research Physician, Clinical Research Specialist, Clinical Study Coordinator, Clinical Study Manager, Clinical Supply Coordinator, Clinical Supply Manager, Clinical Trial Assistant, Clinical Trial Educator, Clinical Trial Manager, Clinical Trial Specialist, CMC Manager, Commercial Manager, Communication Manager, Compliance Associate, Compliance Manager, Computer System Validation Specialist, Contract Associate, Contracts Manager, Country Manager, Customer Service Associate, Data Analyst, Data Analytics Assistant, Data Engineer, Data Management Associate Director, Data Management, Manager, Database Programmer_Designer, Demand Planner, Demand Manager, Developer, Diagnostic Specialist, Director of Contracts & Licensing, Dispensary Assistant, Document Specialist, Drug Safety Associate, Drug Safety Director, Drug Safety Manager, Early Access Project Manager, EHS associate, Electronic Data Capture Manager, Electrophysiologist, Employer Engagement Manager, Engineer (out of industry), Epidemiologist, Exploratory Project Manager, Feasibility Manager, Freelance, FSP Clinical Manager, Global Clinical Data Manager, Graduate, Head of Clinical Data Management, Head of Clinical Operations, Head of Risk Management, Health Economist, Health Information Associate, Healthcare Compliance Manager, HR Associate, HR Manager, Imaging Operations Lead, Inhouse Clinical Research Associate, Intern, Investigator, IT Project Manager, Junior Clinical Data Manager, Junior Clinical Research Associate, Junior Pharmacovigilance officer, Junior SAS Programmer, KOL, Laboratory Assistant, Laboratory Manager, Legal Advisor, Licensing Coordinator, Logistics Associate, Logistics Manager, Logistics Supervisor, Manufacturing Manager, Manuscript Editor, Market Access Manager, Market Access Specialist, Market Insights Specialist, Market Research Associate, Marketing Associate, Material Coordinator, Medical Advisor, Medical Assistant, Medical Devices Project Manager, Medical Director, Medical Information Assistant, Medical Information Associate, Medical Information Manager, Medical Manager, Medical Monitor, medical publisher, Medical Representative, Medical Research Associate, Medical Reviewer, Medical Science Liaison, Medical Technologist, Medical Writer, Medico-economic affairs, Meeting Coordinator, MHRA Pharmacovigilance Inspector, Microbiologist, Occupational Therapist, Office Manager, Ophthalmologist, Packaging Associate, Packaging Coordinator, Patient Recruitment Coordinator, Payroll Specialist, Pharmaceutical Physician, Pharmacist, Pharmacokineticist, Pharmacology Director, Pharmacovigilance Manager, Pharmacovigilance Officer, Physiotherapist, Planning analyst, Policy Officer, Post Doctoral Researcher, Preclinical Project Manager, Principal Biostatistician, Principal Scientist, Privacy Officer, Product manager, Production Manager, Production Specialist, Program Development Manager, Programmer Analyst, Programming Associate Director, Project Assistant, Project Manager (other industry), Proposal Developer, Psychiatrist, Psychologist, Publications Manager, QPPV, Qualified Person, Quality Assurance Assistant, Quality Assurance Complaint Specialist, Quality Assurance Director, Quality Assurance Manager, Quality Assurance Specialist, Quality Control Associate, Quality Control Manager, Quality Control Specialist, Quality Engineer, Quality Manager, Quality Specialist, R&D Manager, R&D Project Manager, Record Specialist, Recruitment & Screening Co-ordinator, Registration Specialist, Regulatory Affairs Administrator, Regulatory Affairs Associate, Regulatory Affairs Director, Regulatory Affairs Manager, Regulatory Affairs VP, Regulatory Documentation Scientist, Regulatory Information Specialist, Regulatory labelling specialist, Regulatory Program Manager, Regulatory Site Activation Manager, Remote Site Monitor, Senior, Research Coordinator, Research Funding Manager, Research Team Manager, Resources Manager, Respiratory Physiotherapist, Sales Manager, Sales Rep, Sample Manager, SAS Programmer, Scientific Advisor, Scientific Affairs Associate, Scientist, Senior Associate Supply Chain (GMP), Senior Biostatistician, Senior Clinical Lead, Senior Clinical Research Associate, Senior Clinical Supply Chain Associate, Senior Clinical Team Manager, Senior Clinical Trial Manager, Senior Epidemiologist, Senior Medical Affairs Officer, Senior Nutrition Scientist, Senior Regulatory Affairs Manager, Senior Scientist, Site Engagement Manager, Site Visit Report Reviewer, SOFTWARE DEVELOPER, Software Engineer, Start Up Director, Start-up Manager, Start-Up Specialist, Strategy Lead, Study Authorisation Associate, Study Delivery Operational Specialist, Submissions Manager, Supply Chain Coordinator, Supply Chain Manager, Supply Chain Planner, Surgical Technician, Systems Administrator, Technical Project Leader, Technical Services Specialist, Training Associate, Training Manager, Translator, Validation Engineer, Vendor Manager, Veterinary Nurse, Warehouse Associate, Warehousing & Distribution Leader, BSc, CQA, GMC, MBA, MBChB, MD, MPhil, MRCPsych, MSc, No CRA Certificate, PGDip, Ph.D Statistics, Pharm D, PhD, PRINCE2, Registered Nurse, SAP, Six Sigma, SolTRAQs, Veterinary, 3PL, ADaM, Administration, Adverse Event management, Advocacy plans, Agile, AKTA, Analytical SEC, Animal Health, APICS, Applicant Tracking System Management, APS, ARISg, auditing, Batch release, Batch Review, BHV, Bioequivalence, Bioinformatics, Biologic, Biomarkers, biometrics, Biosamples, Biosimilars, Biostatistics, Biotech, Black Belt, Business Development, C++, Candidate Attraction, CAPA, CDISC, Cell Biology, Cell stem-based therapy, CER, Chemstations, Client communication, Clinical, Clinical Affairs, Clinical Data Management, Clinical Programming, Clinical Research Organisation, Clinical Trial Applications, clinical trials, close out visits, CMC, CMO, Commercialisation, Compassionate Use, Competent Authorities, Computer Systems Validation, Contract, CPIM, CRF Design, CRO, CSR, Data Analysis, data entry, Data Science, Data Warehouse, database design, Datalabs, DHPC, Distribution, Distribution Planning, DMC, Document Management, Downstream, Drug destruction, Drug Development, Drug Safety, DSUR, E2E, Early Access, Early Phase, EC Submissions, ECG, eCRF, EDC, electronic data capture, ELISA, Epidemiology, ePRO, ERP, eTMF, e-TMF, EU Legislation, Eudravigilance, European Federation of Pharmaceutical Industries, Export Management, FDA Audits, Feasibility, Finance, Forecast, FPLC, GCP, GDP, Gene Therapy, Global, Global Regulatory Affairs, GLP, GMP, Government Affairs, GS1 standards, Health Economics, Healthcare, Healthcare Compliance, Healthy Volunteers, Home-based, HPLC, IATA, ICF, ICH-GCP, Imaging, Immunology, IMP, IMPACT, IMPD, Import Management, IND, InForm, Informatics, International, Interviewing, Inventory Management, Investigator Payments, in-vitro, in-vivo, IRB Submissions, IRT, ISO 13485, ISO 13485:2003, ISO 14971, ISO 9001, ISO13485, IVRS, Java, Lab, Labelling, Laboratory, LEAN, Line Management, Logistics, MA-CC, Manufacturing, MAPP, Market Access, Market Insights, Market Intelligence, Market Research, Marketing, Marketing authorizations, Materiovigilance, MedDRA, Medical Affairs, Medical Communication, Medical Devices, Medical Information, Medical Writing, Medidata Rave, Monitoring, Monitoring Visit, MS Office, MS Project, My Trials, NMR, Office-based, Oracle, Outcomes Research, Outsourcing, Packaging, Paediatrics, Patient Outcomes, Permanent, PET scans, Pharma, Pharmaceutical, Pharmacodynamics, Pharmacoeconomics, Pharmacoepidemiology, Pharmacokinetic, Pharmacokinetics, Pharmacology, Pharmacovigilance, Pharmacy, Phase I, pipetting, PMP, Policy, Post Marketing, Postdoctoral research, Post-marketing, Preclinical, Pricing & Reimbursement, Pricing and Reimbursement, PROC, Process Excellence, Procurement, Product Management, Project Leadership, Project Management, PromoMats, Protein Characterisation, protocol development, Protocol writing, PSURs, Public Affairs, publishing, Purchasing, QP, Qualification Visit, Quality Assurance, Quality Control, Quality Management, Quality Management System, Radiology, Randomisation, Randomization, Rave, Reactovigilance, Real World Evidence, Recruitment, Regional Monitoring, Regulatory, Regulatory Operations, Regulatory submissions, Regulatory Systems Management, remote monitoring, RFI, Risk Management, risk-based monitoring, RMA, RMP, SAE, SAE reporting, Sales Inventory, Sample size estimation, Samples, SAS, Scrum, SDS-PAGE, SDTM, Serialisation, Shipments, shipping, Simoa, Site contracts, Site Engagement, site payments, SOX, SPC- CCDS, Spectroscopy, S-Plus, SPSS, SQL, Start-up activities, statistical analysis, Statistics, Study Management, Study Medication Labelling, Sunshine Act, Supplier Qualification, Supply Chain Distribution, Supply Chain Management, Supply Chain Planning, Supply Planning, SUSAR, SUSARs, TMF, Toxicogenomics, Toxicology, Trackwise, Training, Transport Management, Unicorn Purification System, UPLC, Upstream, UV-Vis Spectroscopy, validation, Veeva, Vendor Management, Venipuncture, VISIO, Western Blot, ZINC, Bratislava, Slovakia, Afrikaans, Argentinian, Armenian, Belgian, Bosnian, Bulgarian, Cambodia, Cantonese, Catalonian, Chinese, Croatian, Czech, Danish, Dutch, English, Flemish, French, Greek, Gujarati, Hebrew, Hungarian, Italian, Japanese, Korean, Latvian, Lithuanian, Luxembourgish, Macedonian, Malayalam, Mandarin, Montenegrin, Norwegian, Persian, Punjabi, Romanian, Russian, Serbian, Slovak, Slovene, Slovenian, Spanish, Swedish, Thai, Turkish, UkrainianLocation: GloballyShare: 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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

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

Was uns bei Starlab ausmacht. Wir stellen uns gerne vor: Wir verbinden Wissenschaft mit Leidenschaft. Unsere Laborprodukte inspirieren unsere Kunden, wie Forschungseinrichtungen, Krankenhäuser oder Institute, dank modernster Technologie jeden Tag. Wir sind blitzschnell, agil und geben gemeinsam Gas. Unsere Teammitglieder können allein – gehören dennoch zusammen. Was uns ausmacht? Unsere lösungsorientierte Wandelbarkeit. Was dich bei uns erwartet: Neue Erfahrungen: Vom Kick-off bis zum erfolgreichen Projektabschluss bist du bei verschiedenen Marketingkampagnen dabei. Du erfährst, wie du Märkte analysierst, um deine Zielgruppe zu erreichen und entwickelst gemeinsam mit deinem Team kreative Lösungen, die es so noch nie gab. Spannende Tools – du unterstützt bei innovativen Aktionen bis hin zur passgenauen Kommunikationsmaßnahme. Deine Marketing-Skills von morgen sichern unsere strategische Weiterentwicklung und fördern die Umsetzung unserer Unternehmensvision – you are great! Du wirst ein kommunikatives Mastermind, das immer die richtigen Worte findet und andere begeistert. Das bringst du zu uns mit. Deine mittlere Reife oder das Abitur hast du in der Tasche? Bei Deutsch und Englisch konntest du richtig glänzen? Nice to meet you! Du hast ein Grundinteresse an Social Media, Werbung und Wirtschaft im Allgemeinen. In deinem Umfeld wirst du für deine Zuverlässigkeit geschätzt und kannst durch Kommunikationsgeschick, Kreativität und Überzeugungskraft alle mitreißen? Bei uns bist du genau richtig. Nice to have: Vielleicht konntest du bereits erste praktische Erfahrung in Praktika oder Nebenjobs sammeln. So viel bieten wir dir. Ein Mentor oder eine Mentorin steht dir mit Rat und Tat zur Seite – alle anderen Teammitglieder natürlich auch! Auch wenn dich deine Teammitglieder vermissen werden: Du kannst an deinen 30 Urlaubstagen komplett abschalten. Bock zu quatschen? Auf Azubiveranstaltungen triffst du andere Azubis, auch aus dem Mutterkonzern. UK, Frankreich oder Italien: bei einem freiwilligen Auslandseinsatz hast du die Chance, weitere Standorte unserer bunten Welt kennenzulernen. Dank E-Learning und standortübergreifenden Weiterbildungsmaßnahmen kannst du bei uns über dich hinauswachsen. Und es gibt noch mehr zu entdecken: HVV Proficard und zahlreiche Mitarbeitervorteile erwarten dich! Deine Neugier auf Starlab ist geweckt – aber ein paar Fragen sind noch offen? Diese beantwortet Natalie Lindner dir sehr gern! Kontaktier uns gern per Mail (**********) und vergiss deine Telefonnummer nicht, dann rufen wir dich gern zurück. *Bei uns findest du gelebte Chancengleichheit. Starlab ist ein buntes Unternehmen mit einem Sinn für Gemeinschaftlichkeit und gegenseitige Wertschätzung. Wir fördern eine vielfältige Unternehmenskultur und achten daher auf ein tolerantes und respektvolles Miteinander, bei dem es keinen Platz für Diskriminierung gibt. Starlab International GmbH is a group of companies specialising in liquid handling technology and laboratory products. The group comprises subsidiaries in Germany, Austria, France, Great Britain and Italy, as well as distributors worldwide. The product portfolio includes laboratory consumables such as pipette tips, single-channel and multi-channel pipettes, cell culture and PCR consumables, nitrile and latex gloves, as well as instruments for general laboratory use. Starlab's products and services are aimed at research institutions in the public sector such as biological and medical institutes, universities and hospitals, but also at companies active in the life sciences area, as well as workshops and state criminal investigation offices. Our solutions enable bright minds to change the world. We look forward to meeting bright minds with a great attitude and passion for everything they do. Working for Starlab means being part of a community with about 200 colleagues in Europe who are passionate for science and our products. If you are ready to ask the right questions and ready to answer those that have yet to be asked and if you love to enable and inspire passionate scientists in labs around the world - then we need to have a chat with you! Passion is our driving factor at Starlab.Über das Unternehmen:Starlab International GmbH

Associate Director Laboratory Automation – BAS (m/f/x) – R-218041 (Fulltime / permanent/ non-tariff) THE OPPORTUNITY As Laboratory Automation Expert, you will join CSL's Global Bioanalytical Science (BAS) department in Plasma Product Development (PPD) and be responsible for providing globally competitive automation capabilities in this vital international role. You will bring expertise in developing automated end-to-end solutions for complex chemical and biological sample management, analysis, and data pipelines. In this role, you will collaborate with and guide an interdisciplinary international team of scientists and automation specialists. You will be responsible for aligning and integrating PPD BAS automation efforts within CSL’s worldwide automated analytical platform and workflows. THE ROLE Your main responsibility will be to establish laboratory robotics, data analysis, and life science automation workflows focusing on analytical development in BAS in alignment with other functions including Bioprocess Development and Biopharmaceutical Process Development. Ideally you offer experiences with laboratory automation tools, including but not limited to automated liquid handlers, task scheduling software packages, programming of laboratory robotics. You collaborate with subject matter experts in the global CSL network to contribute to the development of a scalable, robust, and reliable robotics and automation framework. Manage the alignment of the Bioanalytical Sciences automation efforts with CSL’s global analytical automation initiatives. You create alignment between the Bioanalytic’s robotics and automation framework, and overall CSL enterprise automation and R&D strategy. Perform gap analysis of existing manual and automated workflows and identify opportunities for efficiency gain via automation. You are an advocate for the application of automation technology in an analytical environment being both an enabler and a source of value creation. Train users and transfer ownership of automated workflows to the analytical execution teams. YOUR SKILLS AND EXPERIENCE Postgraduate degree (preferably PhD) in a quantitative science or engineering and/or extensive experience in relevant industry environment Minimum of 5-10 years of progressively responsible relevant experience in automation, analytical protein chemistry, biophysics, biochemistry, engineering or other pharmaceutically related field Strong problem-solving and managing skills with an emphasis on product development lifecycle (e.g., plan, develop, test, deploy, troubleshoot, iterate) with a drive to learn and master new technologies and techniques. Strong knowledge of programming languages such as Python, R, and cloud computing solutions such as AWS. Knowledge on laboratory automation standards such as SiLa Working knowledge of Regulatory Good Practices (GxP) with regards to laboratory experimentation and documentation. Excellent communication and presentation skills in English. Overnight travel, both nationally and occasionally internationally required up to 10% of the time. WHAT WE OFFER Innovative work-environment at our R&D campus CSL-subsidized company bike leasing We offer childcare for up to 14 children (from 6 months till 3 years old) Access to a free Gym facility onsite Please ensure to apply online with your CV, certifications as well as your salary expectation. We are looking forward to your application. Our Benefits We encourage you to make your well-being a priority. It’s important and so are you. Learn more about at CSL. About CSL Behring CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about . We want CSL to reflect the world around us As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about at CSL. Do work that matters at CSL Behring! Standort CSL Plasma, Marburg

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

Team Leader (m/f/x) - Genetic / Diagnostic Scientist permanent, fulltime, based in Martinsried (by Munich) To support and strengthen our Scientific Services department, we are looking for a motivated and dedicated Team Leader, with a passion for innovation and further development of molecular genetic diagnostics, reporting, and employee development to join our department as soon as possible. Job description: You are leading, developing and fostering a team of scientists. You supervise the process development including optimization & standardization of our routine diagnostics. You will work in national & international projects. You are part of the resource and delivery planning. You participate in reporting of routine diagnostics. You present our medical-scientific contributions at national and international specialized congresses. Your background: Life science degree (biology, molecular diagnostics, or a comparable field of study), advanced degree desirable. Strong social and leadership skills, with at least 2 years of relevant professional experience. Profound knowledge in genetics, molecular genetics and human biology. Experience in human genetic diagnostics is desirable. Responsible, independent and solution-oriented working attitude. Motivation to familiarize yourself with new specialist areas and technologies. Fluent German and very good written and spoken English skills, are a must. Our offering: Interesting and dynamic job in an international company with a range of responsibilities and opportunities for further development. 30 vacation days. Flexible work models including Home Office. Become part of our company, sharing a strong team spirit as well as a collegial atmosphere with motivated colleagues. Freedom to develop your own ideas and work independently with responsibility for your own work. A friendly and respectful departmental and working atmosphere, as well as an open communication culture and team events. Extensive training opportunities. Possibility to bring in your experiences in a cross-functional environment. We promote your health through company fitness with WellPass an offer you discounts, for example travel, fashion, electronics and much more via corporate benefits. Our location has good public transport connections. We are convinced that diversity helps to make our organization more efficient and attractive. We welcome applications from people of all ages, gender identities, ethnic and cultural backgrounds. Disabled people with the equal professional qualifications will be given special consideration. Have we piqued your interest? If so, please send us your application including your salary expectations and starting date directly via the application form. Click here to Apply Adress: MVZ Martinsried GmbH, attn. personnel department, Lochhamer Str. 29; 82152 Planegg-Martinsried,Website: medicover-diagnostics.de; E-Mail: E-Mail anzeigen About us In the more than 25 years of its existence, MVZ Martinsried, which currently has around 300 employees, has developed into an interdisciplinary medical care center whose service portfolio now covers the full range of laboratory diagnostics, including microbiology and virology, in addition to numerous special analyses in the field of human genetic diagnostics and also offers genetic counselling. Since January 2019, the MVZ has been part of the Medicover Group, which successfully offers comprehensive diagnostic services in Germany and abroad. In Germany, numerous specialized analyses in the field of human genetic diagnostics as well as classic laboratory diagnostics are provided for patients, registered doctors and other medical care companies at over 40 locations. Over 44,000 employees in 18 countries around the world work in clinics, practices, blood collection points, laboratories and support areas, all with one thing in common: a passion for good medicine. • INTEGRITY • PASSION FOR QUALITY • ENTREPRENEURSHIP • EMPOWERMENT • TEAMWORK • Standort MVZ Martinsried GmbH, Krailling

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

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

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

Team Leader (m/f/x) - Genetic / Diagnostic Scientist permanent, fulltime, based in Martinsried (by Munich) To support and strengthen our Scientific Services department, we are looking for a motivated and dedicated Team Leader, with a passion for innovation and further development of molecular genetic diagnostics, reporting, and employee development to join our department as soon as possible. Job description: You are leading, developing and fostering a team of scientists. You supervise the process development including optimization & standardization of our routine diagnostics. You will work in national & international projects. You are part of the resource and delivery planning. You participate in reporting of routine diagnostics. You present our medical-scientific contributions at national and international specialized congresses. Your background: Life science degree (biology, molecular diagnostics, or a comparable field of study), advanced degree desirable. Strong social and leadership skills, with at least 2 years of relevant professional experience. Profound knowledge in genetics, molecular genetics and human biology. Experience in human genetic diagnostics is desirable. Responsible, independent and solution-oriented working attitude. Motivation to familiarize yourself with new specialist areas and technologies. Fluent German and very good written and spoken English skills, are a must. Our offering: Interesting and dynamic job in an international company with a range of responsibilities and opportunities for further development. 30 vacation days. Flexible work models including Home Office. Become part of our company, sharing a strong team spirit as well as a collegial atmosphere with motivated colleagues. Freedom to develop your own ideas and work independently with responsibility for your own work. A friendly and respectful departmental and working atmosphere, as well as an open communication culture and team events. Extensive training opportunities. Possibility to bring in your experiences in a cross-functional environment. We promote your health through company fitness with WellPass an offer you discounts, for example travel, fashion, electronics and much more via corporate benefits. Our location has good public transport connections. We are convinced that diversity helps to make our organization more efficient and attractive. We welcome applications from people of all ages, gender identities, ethnic and cultural backgrounds. Disabled people with the equal professional qualifications will be given special consideration. Have we piqued your interest? If so, please send us your application including your salary expectations and starting date directly via the application form. Click here to Apply Adress: MVZ Martinsried GmbH, attn. personnel department, Lochhamer Str. 29; 82152 Planegg-Martinsried, Website: medicover-diagnostics.de; E-Mail: infomedicover-diagnostics.de About us In the more than 25 years of its existence, MVZ Martinsried, which currently has around 300 employees, has developed into an interdisciplinary medical care center whose service portfolio now covers the full range of laboratory diagnostics, including microbiology and virology, in addition to numerous special analyses in the field of human genetic diagnostics and also offers genetic counselling. Since January 2019, the MVZ has been part of the Medicover Group, which successfully offers comprehensive diagnostic services in Germany and abroad. In Germany, numerous specialized analyses in the field of human genetic diagnostics as well as classic laboratory diagnostics are provided for patients, registered doctors and other medical care companies at over 40 locations. Over 44,000 employees in 18 countries around the world work in clinics, practices, blood collection points, laboratories and support areas, all with one thing in common: a passion for good medicine. • INTEGRITY • PASSION FOR QUALITY • ENTREPRENEURSHIP • EMPOWERMENT • TEAMWORK • Standort MVZ Martinsried GmbH, Planegg

The INM - Leibniz Institute for New Materials in Saarbrücken, Germany, is an internationally leading center for materials research, a scientific partner to national and international research institutions, and a provider of research and development for companies worldwide. The INM is an institute of the Leibniz Association with about 250 employees. The INM is looking for aCore Facility Head for Lab Automation (f/m/d)New technologies enable new working methods, and materials science is no exception. INM plans to integrate automated processes and AI to accelerate and enrich the materials discovery cycle. We are establishing a position that will build and provide expertise on automated experimental workflows to lead our accelerated research core facility for combinatorial synthesis and/or high throughput testing. This core facility will be equipped with liquid handling systems for materials synthesis (e.g., hydrogels, colloidal systems), molecular biology (e.g., recombinant DNA and protein synthesis), and materials characterization (e.g., optical transmission, nano-indentation).Your TasksLead the INM Accelerated Research Core Facility, operate and oversee the automated sample handling and analysis systems, including solid and liquid handling robots and analytical instruments.Collaborate closely with INM research groups and support workflow automation and streamlining of laboratory processes.Design and implement data handling and analysis workflows in collaboration with INM researchers integrating statistical analysis and artificial intelligence.Stay updated and implement emerging automation technologies, research trends, and best practices in the facility. Your Profile We seek an interdisciplinary researcher with:Completed Ph.D. in materials sciences, chemistry, biochemistry, molecular biology, or related topics.Ideally, experience in combinatorial synthesis, high-throughput biology, or parallel and multiparametric materials characterization.Experience in conducting projects related to workflow automation, including statistical experimental design and data analysis.Experience in programming languages (e.g., Python, C++).Hands-on experience with solid and liquid handling systems.Proficiency in English.What we offerConceptualize and direct a core facility with:A TV-L 100% contract according to your qualification level. The contract will initially be limited to 2 years with the opportunity for a permanent contract based on transparent performance criteria.A dynamic, interdisciplinary, and international research environment with excellent, state-of-the-art infrastructure.A cooperative environment, with plenty of opportunities to interact with other researchers, also outside the team and the institute.The opportunity for training to support high-quality research and to further develop your profile.An environment with a flat hierarchy that welcomes participation and supports self-driven development.The Leibniz network stimulates creative and entrepreneurial personalities. Standort INM - Leibniz-Institute for New Materials gGmbH, Neunkirchen

Postdoc in Molecular Epidemiology/ Data Science (f/m/x)102339 Full time 39 h/week LeipzigWe are Helmholtz Munich. In a rapidly changing world, we discover breakthrough solutions for better health.Our research is focused within the areas of metabolic health/diabetes, environmental health, molecular targets and therapies, cell programming and repair, bioengineering, and computational health. We particularly excel in the fields of basic research, bioengineering, artificial intelligence, and technological development.Through this research, we build the foundations for medical innovation. Together with our partners, we seek to accelerate the transfer of our research, so that laboratory ideas can reach society and improve people’s quality of life at the fastest rate possible.This is what drives us. Why not join us and make a difference? As one of the world’s leading research centers, Helmholtz Munich provides a stimulating international environment for excellent research. The Helmholtz Institute for Metabolic, Obesity and Vascular Research ( HI-MAG )at the University of Leipzig , Germany is part of Helmholtz Munich and aims to uncover the molecular and clinical underpinnings of metabolic, obesity and vascular disorders to enable precision therapies. Together with renowned scientists and supported by state-of-the-art infrastructure, you will have the opportunity to make important contributions towards scientific knowledge and the improvement of people’s quality of life. Our international and dynamic interdisciplinary team is closely integrated with the research structures of the Medical Faculty (https://www.uniklinikum-leipzig.de/en/science-research) of the University of Leipzig, Helmholtz Munich (https://www.helmholtz-munich.de/en) , and leading local as well as national research consortia, such as the Collaborative Research Consortium SFB „ObesityMechanisms“ (https://www.sfb1052.de/) , the future German Center for Child and Youth Health (DZKJ) (https://dzkj.org/) , and our large children’s and adolescent’s cohort LIFE Child (http://www.dzkj.org/) . We have large, well-characterized cohorts up and running with a longitudinal setting: LIFE Child (n~5000) + Leipzig Obesity Childhood Cohort (n~3000) complemented by the Leipzig Adipose Tissue Childhood cohort (n~500), with deep phenotyping allowing for combining clinical, epidemiological, lifestyle and functional omics data.Leipzig is a lively and attractive University City of 630,000 people with a rich cultural and musical history, numerous parks within the city and several lakes at cycling distance. Leipzig has been rated amongst the 100 most livable cities twice in the New York Times rating.Prof. Matthias Tschöp (Dr. Med., Dr. hc.),CEO of Helmholtz Munich:"We believe that excellent research requires a range of different perspectives. Diverse teams reach better solutions and are more innovative in their research topics.Establishing our Diversity Management Strategy demonstrates our commitment to ensuring an appreciative company culture based on mutual respect. We are also implementing diversity-sensitive processes throughout our whole organization."Your tasksModelling the risk for complex disease derived from the interaction of genetic predisposition and environmental factors acting in childhood through longitudinal and cross-sectional analyses in large cohort studiesDeveloping risk scores and prediction modelling, including genetic predisposition and consideration of developmental patternsIdentification of molecular targets for genetic predisposition to obesity and related cardiometabolic disorders in childhood using integrative omics approaches combining functional and computational genomics dataMultiomics analyses: genome, transcriptome, methylome in both blood and adipose tissueCommonalities of gene environment interactions in the origin of common diseases in childhoodLarge scale epidemiological analyses (incl. meta-analyses, trajectories, cluster analyses)Your profileA master degree in bioinformatics, systems biology, biomedicine, nutritional science, physiology, computer science, mathematics OR epidemiology OR any life science degree with a strong interest in data sciencesMD, PhD or experienced PhD student with interest/experience in the fields as outlined aboveSound knowledge of statistics in the context of biological systems (love numbers, stats and models) and basics of epidemiological statisticsExperience with large-scale multi-omics approaches is an advantageGood understanding of the biomedical background and experience with cohort studies is highly recommendedFlexibility, innovative thinking and preparedness to enter new avenues, ideas, questions, creativity and ability to drive and pursue research projectsEnthusiasm and a high level of motivation for scientific work and reproducible researchBenefitsCareer DevelopmentPostdoc program, scientific training & career center with tailored offersRecreation30 days annual leave, flexi days, plus public holidaysInternational Staff ServiceSupport with the relocation and integration process in GermanyHealth PromotionSports, company doctor, mental health initiativesIf you fulfil all the requirements, you may be eligible for a salary grade of up to E 13. Social benefits are based on the Collective Wage Agreement for Public-Sector Employees (TVöD). The position has an (initial) fixed term of 2 years but may be extended under certain circumstances. We are committed to promoting a culture of diversity and welcome applications from talented people regardless of gender, cultural background, nationality, ethnicity, sexual identity, physical abilities, religion or age. Qualified applicants with physical disabilities will be given preference. If you have obtained a university degree abroad, we will require further documents from you regarding the comparability of your degree. Please request the Statement of Comparability for Foreign Higher Education Qualifications as early as possible. (https://www.helmholtz-munich.de/en/career/is-your-foreign-university-degree-recognised-in-germany)Interested in applying?If you have any questions, feel free to contact Antje Körner, [email protected], who will be happy to help.

Research physician for optoacoustic imaging (f/m/x)102250Full timeMunichWe are Helmholtz Munich. In a rapidly changing world, we discover breakthrough solutions for better health.Our research is focused within the areas of metabolic health/diabetes, environmental health, molecular targets and therapies, cell programming and repair, bioengineering, and computational health. We particularly excel in the fields of basic research, bioengineering, artificial intelligence, and technological development.Through this research, we build the foundations for medical innovation. Together with our partners, we seek to accelerate the transfer of our research, so that laboratory ideas can reach society and improve people’s quality of life at the fastest rate possible.This is what drives us. Why not join us and make a difference? The Institute of Biological and Medical Imaging ( IBMI ) at Helmholtz Munich and the Chair of Biological Imaging (CBI) at the Technical University of Munich (TUM) are an integrated, multi-disciplinary research unit, which provide bioengineering solutions to urgent societal needs. IBMI scientists develop next-generation imaging and sensing methods to measure previously inaccessible properties of living systems, hence, catalyzing breakthroughs in biology, medicine, and the environment. Comprising 11 inter-disciplinary laboratories and scientists from more than 25 countries, IBMI offers state-of-the-art infrastructure for innovative research and an ideal environment to accelerate your career. We now seek a highly qualified and motivated Research Physician (f/m/x) to drive the translation of novel optoacoustic imaging systems into the clinics. We are looking forward to receiving your comprehensive online application, including your letter of motivation, CV, and academic transcripts of records, preferably in English.Prof. Matthias Tschöp (Dr. Med., Dr. hc.),CEO of Helmholtz Munich:"We believe that excellent research requires a range of different perspectives. Diverse teams reach better solutions and are more innovative in their research topics.Establishing our Diversity Management Strategy demonstrates our commitment to ensuring an appreciative company culture based on mutual respect. We are also implementing diversity-sensitive processes throughout our whole organization."Your tasksOptoacoustic imaging and sensing can collect structural and functional information about health and disease offering novel ways to monitor health conditions and life-style or medical interventions. Building upon our extensive expertise in developing methods and systems, we are now focusing on the clinical translation of optoacoustic technology in cardio-metabolic medicine.The successful candidate will drive clinical studies that aim to develop novel prevention and prognosis methodology in close collaboration with our clinical partners. The work is expected to pioneer methodology that monitors the development of different cardiovascular and metabolic diseases, including diabetes, in ways that move away from symptoms-based medicine, into the realm of continuous healthcare. This is a field with potential to accelerate your scientific career, greatly impact society, improve the efficiency and cost of healthcare and offer outstanding opportunity for commercial exploitation.Your profileThe successful applicant should be a Physician (medical student or doctor) with great motivation to promote advanced technology and the future of medicine and excellent knowledge of the German language as required for patient recruitment.Preferred (but not necessary) qualifications include:Medical Device Regulation (MDR) certification or interest to become MDR certified.Excellent track record of research achievements and publications in top-ranked journals.Strong motivation, scientific curiosity, and commitment to scientific excellence.Team player skills and enthusiasm to work in a multi-disciplinary, collaborative environment.Command of the English language.BenefitsCareer DevelopmentPostdoc program, scientific training & career center with tailored offersRecreation30 days annual leave, flexi days, plus public holidaysInternational Staff ServiceSupport with the relocation and integration process in GermanyHealth PromotionSports, company doctor, mental health initiativesIf you fulfil all the requirements, you may be eligible for a salary grade of up to E 13. Social benefits are based on the Collective Wage Agreement for Public-Sector Employees (TVöD). The position has an (initial) fixed term of 2 years but may be extended under certain circumstances. We are committed to promoting a culture of diversity and welcome applications from talented people regardless of gender, cultural background, nationality, ethnicity, sexual identity, physical abilities, religion or age. Qualified applicants with physical disabilities will be given preference. If you have obtained a university degree abroad, we will require further documents from you regarding the comparability of your degree. Please request the Statement of Comparability for Foreign Higher Education Qualifications as early as possible. (https://www.helmholtz-muenchen.de/index.php?id=54651&L=1)Interested in applying?If you have any questions, feel free to contact Ivy Curren, [email protected], who will be happy to help.

Staff scientist Bioinformatics (f/m/x) - Next Generation Sequencing102347 Full time 39 hrs./week Neuherberg near MunichHome Office OptionsWe are Helmholtz Munich. In a rapidly changing world, we discover breakthrough solutions for better health.Our research is focused within the areas of metabolic health/diabetes, environmental health, molecular targets and therapies, cell programming and repair, bioengineering, and computational health. We particularly excel in the fields of basic research, bioengineering, artificial intelligence, and technological development.Through this research, we build the foundations for medical innovation. Together with our partners, we seek to accelerate the transfer of our research, so that laboratory ideas can reach society and improve people’s quality of life at the fastest rate possible.This is what drives us. Why not join us and make a difference? The Bioinformatics Platform of the Genomics Core Facility at Helmholtz Munich is looking for a highly motivated Next Generation Sequencing (NGS) Bioinformatician (f/m/x) to join our team of experienced scientists. The bioinformatics team provides primary, secondary and tertiary (custom) bioinformatic analyses, courses and consultation for our core users. The successful candidate will support these activities and perform a wide range of NGS analyses (e.g. bulk and single-cell RNA- and ATAC-Seq, ChIP-Seq, Genomic variation) to support various R&D projects. You will work closely with biologists, clinicians, computational scientists and staff from other core facilities to implement and validate new computational pipelines.If you like to be part of a dynamic team working at the cutting edge of science wanting to make an impact in developing future health solutions, this full time position may be for you.Prof. Matthias Tschöp (Dr. Med., Dr. hc.),CEO of Helmholtz Munich:"We believe that excellent research requires a range of different perspectives. Diverse teams reach better solutions and are more innovative in their research topics.Establishing our Diversity Management Strategy demonstrates our commitment to ensuring an appreciative company culture based on mutual respect. We are also implementing diversity-sensitive processes throughout our whole organization."Your tasksData processing for users of the platform using established computational pipelines or development of individual research pipelines as reusable workflowsBioinformatics consulting for researchers at Helmholtz MunichDesign and implementation of research projects and analysis pipelines for users of the platformLecturer and development of bioinformatics courses for scientists at different levels (beginner, advanced)Your profileMaster or PhD degree in Bioinformatics or related fieldsStrong programming skills (R & RMarkdown, Python, bash, git)Strong scientific track recordTeaching experience in bioinformatics, computational or statistics coursesExperience with various Next-Generation Sequencing technologies and bioinformatic analyses (e.g. bulk and single-cell RNA- and ATAC-Seq, ChIP-Seq, Genomic variation)Experience with Linux systems and the use of high-performance computing environmentsEnglish language proficiencyHighly motivated team player with strong communication skills, a proactive mindset and a service-oriented personalityDesirable qualificationsExperience with the analysis of spatial single cell data (10x Genomics Visium or Xenium)Experience with container technologies (e.g. Docker, Singularity), Conda and workflow languages (e.g. Nextflow)BenefitsCareer DevelopmentPostdoc program, scientific training & career center with tailored offersRecreation30 days annual leave, flexi days, plus public holidaysInternational Staff ServiceSupport with the relocation and integration process in GermanyHealth PromotionSports, company doctor, mental health initiativesWork-Life-BalanceFlexible working hours and flexi-time modelsScientific ResourcesState-of-the-art infrastruture and Core FacilitiesIf you fulfil all the requirements, you may be eligible for a salary grade of up to E 13. Social benefits are based on the Collective Wage Agreement for Public-Sector Employees (TVöD). The position has an (initial) fixed term of 2 years, with the possibility of moving to a permanent contract. We are committed to promoting a culture of diversity and welcome applications from talented people regardless of gender, cultural background, nationality, ethnicity, sexual identity, physical abilities, religion or age. Qualified applicants with physical disabilities will be given preference. If you have obtained a university degree abroad, we will require further documents from you regarding the comparability of your degree. Please request the Statement of Comparability for Foreign Higher Education Qualifications as early as possible. (https://www.helmholtz-munich.de/en/career/is-your-foreign-university-degree-recognised-in-germany)Interested in applying?If you have any questions, feel free to contact Thomas Walzthöni, [email protected], who will be happy to help.

​ ​​StellenausschreibungDas Friedrich-Loeffler-Institut gehört zum Geschäftsbereich des Bundesministeriums für Ernährung und Landwirtschaft und zählt zu den weltweit führenden Forschungsinstituten auf dem Gebiet der Tiergesundheit. Es unterrichtet und berät die Bundesregierung auf diesem Gebiet. Es verfügt über modernste Laboratorien und experimentelle Tierhaltungen auch für Großtiere in den Schutzstufen 2-4 sowie über Insektarien im BSL-2- und BSL-3-Bereich.Am Hauptstandort Insel Riems ist zum nächstmöglichsten Zeitpunkt der Dienstpostender stellvertretenden Institutsleiterin / des stellvertretenden Institutsleiters (m/w/d) im Institut für Infektionsmedizin zu besetzen. Derzeit sind im Institut für Infektionsmedizin 10 Arbeitsgruppen angesiedelt. Weitere Informationen zum IMED finden Sie auch unter www.fli.de (http://www.fli.de) . Bei Vorliegen der laufbahnrechtlichen und sonstigen Voraussetzungen ist die Verbeamtung auf Lebenszeit und die Übertragung des Amtes einer Direktorin und Professorin bzw. eines Direktors und Professors in der Besoldungsgruppe B1 der Bundesbesoldungsordnung vorgesehen. Alternativ kann die Einstellung als Tarifbeschäftigte/Tarifbeschäftigter mit außertariflichem Entgelt in Höhe der Dienstbezüge nach Besoldungsgruppe B1 BBesO) erfolgen.Aufgaben:Das Institut für Infektionsmedizin (IMED) betreibt Diagnostik und Forschung zu infektionsbedingten Krankheiten auf den Themenfeldern „Vektoren“ und „Nicht-klassische, landwirtschaftliche Nutztiere“. Einen Schwerpunkt bilden aktuell entsprechende Arbeiten bei Arthropoden als Vektoren im Bereich des Monitorings, der Vektorkompetenz, der Pathogenese, der Virus-Vektor-Wirt-Interaktionen und der Risikobewertung. Die Nutzinsekten sollen zukünftig in diese Fragestellungen einbezogen werden.Die Diagnostik und Forschung zu infektionsbedingten Krankheiten in der Aquakultur bilden einen zweiten Schwerpunkt. Dem Institut sind die Nationalen Referenzlabore für Bienenkrankheiten sowie für verschiedene Fisch-, Muschel- und Krebstierseuchen zugeordnet.Der zukünftig besondere Fokus auf potentielle Vektoren wird sich auch in der erwarteten Leitungstätigkeit im IMED widerspiegeln. Die aktive Förderung der kollegialen Zusammenarbeit mit den anderen Fachinstituten des Friedrich-Loeffler-Instituts (FLI) sowie die Mitarbeit in nationalen und internationalen Gremien ist ebenfalls eine wichtige Aufgabe.Anforderungen:Wir suchen eine hochqualifizierte Wissenschaftlerin/ einen hochqualifizierten Wissenschaftler, insbesondere im Bereich der Veterinärmedizin, Biowissenschaften oder verwandter Wissenschaften. Die erfolgreiche Kandidatin/ der erfolgreiche Kandidat sollte langjährige Erfahrungen auf dem Gebiet der Infektionsforschung in Arthropoden als Vektoren oder Nutzinsekten aufweisen. Im Mittelpunkt sollen dabei Erkrankungen stehen, die durch Übertragung auf andere Tierarten und/oder als Zoonose relevant sind.Darüber hinaus erwarten wir einschlägige Erfahrungen im Leiten einer eigenen Arbeitsgruppe oder Abteilung sowie durch Habilitation oder gleichwertige wissenschaftliche Leistungen nachweisbare Qualifikationen. Erfahrungen mit administrativen Aufgaben und strategischer Teamentwicklung sind erforderlich, um die mit der Position verbundenen Leitungsaufgaben zu erfüllen.Fähigkeiten in der teamorientierten Führung von Mitarbeiter/-innen, ausgezeichnete Kommunikationseigenschaften, in der Einwerbung von Drittmitteln, Erfahrung bei der Mitarbeit in nationalen und internationalen Gremien sowie sehr gute deutsche und englische Sprachkenntnisse werden ebenfalls vorausgesetzt.Die Tätigkeit beinhaltet den Einsatz im Sicherheitsbereich, was eine Überprüfung gem. Sicherheitsüberprüfungsgesetz und besondere Schutzvorkehrungen vor Gesundheitsgefahren erfordert. Die persönliche und gesundheitliche Eignung ist daher Voraussetzung für die Stellenbesetzung.Wir engagieren uns für ein familienfreundliches Arbeitsumfeld durch flexible Arbeitszeiten, die grundsätzliche Möglichkeit zur Teilzeitbeschäftigung und die Unterstützung bei der Suche von Kinderbetreuung. Zu unseren Sozialleistungen gehören ein betriebliches Gesundheits- und Wiedereingliederungsmanagement, eine betriebliche Sozialberatung, sowie vermögenswirksame Leistungen.Das Friedrich-Loeffler-Institut sieht sich der Inklusion verpflichtet. Bewerbungen von Menschen mit Schwerbehinderungen sind daher ausdrücklich erwünscht. Diese werden im Auswahlverfahren bevorzugt berücksichtigt.Das FLI hat sich zum Ziel gesetzt, den Anteil von Frauen in Leitungspositionen zu erhöhen und fordert Frauen ausdrücklich auf, sich zu bewerben. Bei gleicher Qualifikation werden Frauen nach Maßgabe des § 8 BGleiG bevorzugt berücksichtigt.Entsprechend unserer internationalen Ausrichtung begrüßen wir die Bewerbung von Menschen aller Nationalitäten und Ethnien.Nähere Auskünfte erteilen:Frau Prof. Dr. Kühn, Tel.: 038351/ 7-1102; E-Mail: [email protected] oder Frau Dr. Franzke, Tel.: 038351/ 7-1206; E-Mail: [email protected] (mailto:[email protected]) Wir freuen uns auf Ihre Bewerbung. Bitte schicken Sie Ihre Bewerbungen mit aussagefähigen Qualifikationsnachweisen, insbesondere Lebenslauf, Zeugnissen sowie Veröffentlichungs-verzeichnis bis zum 30.06.2024 als ein PDF-Dokument per E-Mail an [email protected] mit dem Betreff „ Stelle 26/24 “. Alternativ können Sie Ihre Bewerbungsmappe auch mit der Post an das Friedrich-Loeffler-Institut, Referat Personal, Postfach 1318 in 17466 Greifswald - Insel Riems schicken. Bitte beachten Sie, dass unvollständige Unterlagen zum Ausschluss aus dem Bewerbungsverfahren führen können. Eine Eingangsbestätigung sowie die weitere Kommunikation erfolgen per E-Mail. Bitte überprüfen Sie Ihre Spamfilter-Einstellungen!Job vacancyThe Friedrich-Loeffler-Institut is part of the Federal Ministry of Food and Agriculture and is one of the world's leading research institutes in the field of animal health. It informs and advises the Federal Government in this field. It has state-of-the-art laboratories and experimental animal facilities, including for large animals in protection levels 2-4 as well as insectaria in the BSL-2 and BSL-3 area.The main site on the island of Riems is seeking candidates for the position ofDeputy Head of the Institute (m/f/d) in the Institute of Infectologyfor appointment as soon as possible. The Institute of Infectology (IMED) currently has 10 research groups. Further information on the IMED can also be found at www.fli.de.If the requirements under career law and other conditions are met, the status of a civil servant as Director and Professor in grade B1 of the Federal Salary Scale with unlimited tenure is intended. Alternatively, the position can be filled as an employee in civil service covered by a collective bargaining agreement with non-tariff pay in the amount of the remuneration according to salary group B1 (BBesO).Tasks:The Institute of Infectology is involved in diagnostics and research on infection-related diseases in the fields of "vectors" and "non-classical farm animals". Main research focus is on arthropods as vectors in the areas of monitoring, vector competence, pathogenesis, virus-vector-host interactions and risk assessment. Beneficial insects are to be included in these investigations in the future.Diagnostics and research into infection-related diseases in aquaculture form a second focus. The National Reference Laboratories for bee diseases and different fish, mussel and crustacean diseases are assigned to the institute.The future special focus on potential vectors will also be reflected in the expected management activities at IMED. The active support of collegial cooperation with the other specialized institutes of the Friedrich-Loeffler-Institut (FLI) as well as participation in national and international committees is also an important task.Requirements:We are looking for a highly qualified scientist, especially in the field of veterinary medicine, biosciences or related sciences. The successful candidate should have years of experience in the field of infection research in arthropods as vectors or beneficial insects. The focus should be on diseases that are relevant in transmission to other animal species and/or as zoonosis.In addition, we expect relevant experience in leading your own research group or department as well as proven qualifications through habilitation or equivalent scientific achievements. Experience with administrative tasks and strategic team development is required to fulfil the management tasks associated with this position.Skills in team-orientated management of staff, excellent communication skills, in the acquisition of third-party funding, experience in working on national and international committees and very good German and English language skills are also required.The job involves working in the security sector, which requires a check in accordance with the Security Inspection Act and special protective measures against health hazards. Personal and health suitability is therefore a prerequisite for the position.We are committed to a family-friendly working environment through flexible working hours, the fundamental possibility of part-time employment and support in finding childcare. Our social benefits include company health and reintegration management, company social counselling and capital-forming benefits.The Friedrich-Loeffler-Institut is committed to inclusion. Applications from people with severe disabilities are therefore specifically encouraged. They will be given preferential consideration in the selection process.The FLI would like to increase the proportion of women in management positions and specifically encourages women to apply. Women with equal qualifications will be treated with priority in accordance with § 8 BGleiG.In accordance with our international orientation, we welcome applications from people of all nationalities and ethnicities.For further information please contactFrau Prof. Dr. Kühn, Phone: 038351/7-1102; E-Mail: [email protected] or Frau Dr. Franzke, Tel.: 038351/71206; E-Mail: [email protected] (mailto:[email protected]) . We look forward to receiving your application. Please send your application with all usual documents, in particular CV, certificates and list of publications by 30 June 2024 as a PDF document by e-mail to [email protected] with the subject "Position 26/24". Alternatively, you can send your application by post to the Friedrich-Loeffler-Institut, Referat Personal, Postfach 1318 in 17466 Greifswald - Insel Riems. Please note that incomplete documents may lead to exclusion from the application procedure.A confirmation of receipt and further communication will be sent by e-mail. Please check your spam filter settings!

Job Description We are looking for Quality Control Technicians to join us in our mission to build the world’s greenest battery. The role is a part of our Revolt Ett team based in Skellefteå / Västerbotten. About the jobWe are looking for driven people with a laboratory experience who preferably have background in the industrial sampling and testing. The persons we are looking for are systematic and eager to learn.In your role, you will work in chemical laboratory performing various analyses and tests of incoming materials as well as production samples.Our production will run 24/7 including weekdays, weekends and all the holidays. The shifts will rotate between morning, evening and nights and we need you to be able to rotate between all the shifts.You will get the chance to have a real impact on our success story in Sweden and see the results of your work! About the teamThe QC team should be the experts, having experience in receiving samples, measuring methods, samples preparation, and result reporting. Your team will play an important role in supporting the production team in measuring and improving our product quality. QC team will be developing, validating, defining, and implementing the inspection methods for all tested materials. Furthermore, the team will be responsible for Measurement System Analysis and work with the R&D group to evaluate and compare product quality (it includes participation in Root Cause Analysis). Key responsibilities include but are not limited to:Perform samplings and prepare material for testing.Perform routine quality control tests and measurements ensuring that incoming material/product meet quality specifications. Operate various analytical techniques including ICP-OES, ICP-MS, XRF, pH measurements, titrations, oven, etc.Interpret data and report the results. Apply with CV and cover letter or your complete LinkedIn profile. Full time employment, fixed salary.Planned starting date is as soon as possible.

Job Description We are looking for an experienced Senior Quality Control Engineer-CT to join us in our mission to contribute to a greener future. The role is a part of our excellent Quality team based in Skellefteå. By joining us, you will be a key player in establishing and one of the first large scale European battery factories. About the jobYou will be responsible for the development, validation, and implementation of the methods used for computed tomography and other non-destructive test methods. Adherence to the principles of Quality Assurance in QC. Proven track record in statistical analysis and measurement system analysis (MSA).Key responsibilities include but are not limited to:•Develop, validate and document methods and procedure for scanning and analyzing intermediate and final products from battery cell production• Performing special scan requests for battery cells and their components on Computed Tomography and X-Ray systems (e.g. Waygate, Nikon, Exacom)• Performing problem solving and improvement activities for scanning activities and its records aswell as updating work instructions• Optimize methods to increase efficiency and turn-around time of the laboratory.• Working with instrument suppliers and machine builders for designing custom fixtures,instruments & automation• Inputs for laboratory planning of expansions and related sourcing of additional equipment andinstruments• Train team members on instrument usage, analysis and troubleshooting activities• Provide guidance and specialist knowledge for product families or processes• any other duties and responsibilities required to deliver on company objectives Accountability/Authorization • Budget responsibility: N• Direct reports: N• Authorized to decide on investments according to role and policy. Apply with CV in English or your complete LinkedIn profile.Full time employment, fixed salary. Planned starting date is asap.

Job Description About the jobThe key responsibilities of the Testing manager is to plan, manage and coordinate the daily activities of a sub-team within the Laboratories Quality team at Northvolt ETT. This includes ensuring the execution of the control plan, both the logistics and successful testing of cells, as well as collaborating with stakeholders from production/quality/logistics/R&D/cell design to support them as best as possible in terms of their daily testing needs and requirements. Additionally, the Testing Manager’s responsibility is to maximise the use of available resources (personnel, equipment, material), build a strong and talented team that can meet the high demands of our internal customers in terms of quality, efficiency, and turn-around time of results. Key responsibilities include but are not limited to:The Quality Control Area Manager has several key types of responsibilities, each with a distinct set of duties and expectations. In addition, this role requires a high degree of flexibility and ability to cope with ambiguity and rapid change in production operations and quality control needs. The main types of responsibilities and expectations thereof are (in no particular order of priority): Direct Management of Employees. This role usually has several direct reports and as such the Area Manager is expected to handle the day-to-day management of these employees, including: Assistance with hiring and onboarding. Attendance. Vacation, holiday, and other time-off management and approvals. Corrective actions for behaviour if required. Ensuring all basic company compliance type training (e.g., safety, company policy) is attended and adhered to. Operations Management of specific QC activities (both employees and throughput). This responsibility is concerned with the actual productivity of the sub-team. Management of the execution of all quality control analyses of the sub-team as per the control plan. Plan and communicate to the team their daily/weekly priorities (immediate to 168-hour timeframe), ensure expectations and responsibilities are clear. Responsible for short-term planning and scheduling of people and resources to achieve optimal throughput, as well as any necessary planning involved with control plan and project changes. Coordinate logistics of incoming/outgoing samples to/from QC lab; immediate collection and reporting of results back to production. Support the team with running analytical testing on a range of instruments. Ensure non-conformities about material deviations are reported and follow up on improvement. Operational Training, Quality, and Safety Compliance of Direct Personnel and Daily Processes. The Area Managers are responsible for ensuring that basic expectations and requirements are met, which includes: Strict adherence to all safety requirements and safe operation/handling of equipment and materials by all team members. ensure the team works in the safest manner possible. Drive continuous improvement of ways of workings and analyses to increase the team’s efficiency and optimize analyses turn-around times. Ensure continuous cross-training within the team; set up training sessions, develop & grow expertise within the team for them to be able to safely and competently perform their tasks. Ensure SOPs and WIs are being followed and continuously updated. This includes strict adherence to Northvolt’s 5S standards. Expect, Plan For, and Manage a Certain Degree of Ambiguity and Constant Change. This job, due to the company still being a start-up environment, requires flexibility and the ability to work well and coordinate with others. It requires the ability to build relationships and trust across boundaries of responsibility, continuously collaborate with all internal customers to ensure to support them as best as needed, so that ultimately the company can operate as a team with a common goal, while still holding each other accountable for their respective expectations.Accountability/AuthorizationBudget responsibility: YesDirect reports: YesAuthorized to decide on investments according to role and policy.The person we are looking for is driven, caring and structured. You thrive by leading others and work towards common goals. You are used to a high paced work environment and got good time management skills. Qualities that we cherish are flexibility, sense of quality, friendliness, motivation to take on new challenges, grit and a sense of humor. Northvolt is an equal opportunity employer. We're a diverse group of individuals, united by a common mission, who recognise that while our actions as individuals have a role to play in driving Northvolt towards its goals, we always seek to move forward as a team. We offer you an open and welcoming atmosphere where we win as a team – and fail as a team. Northvolt is growing at the speed of light and we are a strong believer in internal career development. For us it’s important to look at your skills and potential, please refrain form including your picture and age with your application to help us with this. Apply with CV in english or your complete LinkedIn profile. Full time employment, fixed salary. Planned starting date is asap. Please note that any applications submitted via email or direct messaging will not be considered.