Novartis AG

Job ID REQ-10032566 Mar 05, 2025 Switzerland Summary Location: Basel. #LI-Hybrid We are seeking a highly skilled and experienced Associate Director Scientific Business Analysis to support our Project Insights product line within Novartis Biomedical Research Informatics as a Business Analyst and Product Line Partner. The ideal candidate will have a strong background in drug discovery processes, expertise in cheminformatics or bioinformatics, and a keen understanding of data science and process improvement in the context of machine learning operations and data pipelines. In this role, you will execute on every aspect of planning, design, development, and delivery of system solutions for a specific business or technology area, in alignment with design and architectural standards and business requirements. Our Associate Director Scientific Business Analysis will lead the overall business analysis effort on complex scientific products across products, product lines, and sites. You'll strengthen the collaboration with a wide community of research scientists to analyze, understand, ideate, and define solutions, which will be used in the drug discovery domain within exploratory research. About the Role Major accountabilities: Lead all aspects of Business Analysis activities across products, product lines, and sites. Establish best Business Analysis practices and help to embed these into the existing product execution framework. Responsible for elicitation, definition, and documentation of all types of requirements [functional/non-functional/transitional/business] from all types of stakeholders with an integrated approach to design from initial planning through execution and production release. Interviewing stakeholders at all levels of the organization to determine goals, objectives, parameters, and processes to understand the problems to be solved. Identifying and qualifying new demand and assisting with steering proposals through the early phases of product approval. Create a shared product vision by participating in product visioning workshops executing planning, visioning, and prioritization. Work closely with cross-functional groups (User Researcher, UX Design, Product Management), in a highly matrixed organization to build constructive and effective relationships throughout the whole organization. Facilitating the use of cheminformatics, bioinformatics, AI, and machine learning technologies within the product line and across scientific drug discovery workflows, including mapping and improving processes, particularly in the context of machine learning operations (ML OPS). Supporting data science environments and processes with business analysis, contributing to the development and improvement of computational science environments and tools. Ensuring adherence to Novartis global Information Security and Quality standards and policies for all products/services, and ensuring Regulatory Compliance (e.g., GLP & GCP) standards and policies for GxP products/services. If applicable, ensure Regulatory Compliance (e.g. GLP & GCP) standards and policies for GxP products/services. Minimum Requirements: Advanced degree in biology, biotechnology, bioinformatics, cheminformatics or other science discipline and/or computer science, ideally exposed to the drug discovery domain. At least 5 years- experience in a scientific or biotech environment for design and implementation of software systems at enterprise level. Formal experience as a Business Analyst or professional certification as Business Analyst, including demonstrated process improvement capability, capability to map customer needs through strong stakeholder management and ability to liaise with technical teams on requirements. Strong understanding of the drug discovery process, including initial inception to validated targets and from hits with tool compounds to drug candidates. Proficiency with data science tools and systems such as R, Python or other statistical analytics tools, which lead to data-driven decision making within product lines. Desired: Knowledge of cutting-edge data and computing systems. Understanding of embedding AI in various stacks and leveraging large language models (LLMs) to improve workflows. Knowledge in tools such as Spotfire or PowerBI to represent and visualize data effectively. Experience in User Experience to enhance user journeys and workflows in a Unix research environment. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10031499 Mar 11, 2025 Switzerland Summary Location: Basel, Switzerland Role Purpose: Defines, leads and manages the analytical project strategy including the overall analytical control strategy for Drug Substance(s) and Drug Product(s) in line with the overall CMC project development plan; ensures project specific high quality analytical submission documents and ready for inspection status at all time; support/coach analytical team members and thereby contribute to the overall Technical Research & Development strategy and objectives. About the Role As part of the Analytical Research and Development group, this is a new role waiting for you to put your own stamp on it. The position is located at the Novartis Headquarter site in Basel within the Technical R&D (TRD) department of Global Drug Development. Your responsibilities Your responsibilities include but are not limited to : Formulating, developing and driving an overall science, quality and regulatory driven analytical project strategy including contingency plans and risk evaluations in the course of clinical development (API and formulated drug product, essentially small molecules intended for oral administration). Leading and overseeing analytical activities throughout drug development within a global project team such as specification setting, method development and validation, stability and release testing. Activities may cover pre-clinical support, early/late phase clinical development as well as transfer to commercial operations and registration. Being a core member of the technical development sub-team, representing Analytical Research & Development; co-owning the technical development in partnership with Chemical and Pharmaceutical Development; contributing actively to the elaboration of the overall CMC technical development plan and driving state of the art control strategy. Accountability to meet quality, timelines and budget for assigned projects, defining clear analytical project plans Managing interactions with internal and external stakeholders, including potential outsourced activities Proactively identifying potential scientific, technological and GMP gaps, proposing creative solutions and ensuring appropriate communication within and across units Providing input into CMC documents to support regulatory submissions Acting as the analytical project representative in peer reviews as well as internal and external audits Supporting the analytical project teams with quality awareness, strategic input, scientific and technical expertise in a phase dependent manner Strong contribution to advance science, technology and innovation within Analytical R&D What you-ll bring to the role: Minimum BS / MS in analytical chemistry with relevant experience in industry, PhD in analytical chemistry or equivalent desirable Minimum 3-5 years- experience in the pharmaceutical industry, preferably in analytical development and/or quality control Experience in managing projects ideally in a global matrix environment Strong quality focus, experience in a GMP environment Understanding of regulatory expectations and profound scientific knowledge in analytical development (e.g. Chromatography, dissolution rate, titration, physical state etc...) Fluent in English (oral and in writing) Ability to perform in a highly dynamic environment You-ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10041855 Mar 28, 2025 Switzerland Summary We-re a dedicated team united by a drive to deliver significant value to Novartis. You will plan, execute and deliver high quality audits that meet Novartis Internal Audit (IA) methodology standards, strategies and directives. To lead audit teams in activities including assessment of business/information technology risks and evaluation of related internal controls. About the Role Key Responsibilities: Conduct Audits : Lead and perform detailed audits of pharmaceutical supply chain processes, including procurement, manufacturing, distribution, and inventory management. Establish and maintain strong relationship with Novartis internal stakeholders, in particular build strong collaboration to work effectively and seamlessly across our businesses. Risk Assessment : Identify, assess and review potential risks within the supply chain and associated mitigation strategies. Regulatory Compliance : a working knowledge of relevant manufacturing operations regulations, including FDA, EMA, and other global pharmaceutical standards. Process Improvement : Evaluate current processes and recommend improvements to enhance efficiency, reduce costs, and maintain high-quality standards. Reporting : Prepare comprehensive audit reports, summarizing findings, recommendations, and corrective actions for senior management and stakeholders. Data Analysis : As part of the audit or advisory, utilize advanced data analytics and AI where appropriate to identify trends, anomalies, and areas for improvement within the supply chain. Collaboration : Work closely with cross-functional teams, including procurement, logistics, quality assurance, and regulatory affairs, in the understanding and execution of audits and advisories. What you'll bring to the role: Essential Criteria: Degree in a technical or scientific area that contains manufacturing and/or supply chain management, logistics and/or planning. Work experience in technical operations manufacturing and/or supply chain management, planning, logistics and inventory management. Knowledge of pharmaceutical regulations and standards including GMP, GDP and other guidelines. Experience and ability to act in a complex and rapidly changing business environment. Knowledge of process management and/or business process optimization. Fluent in spoken and written English. Willingness to travel (up to 15%) Desirable Criteria: Additional Certifications: Additional relevant certifications such as Certified Supply Chain Professional (CSCP) or Certified in Production and Inventory Management (CPIM), relevant risk management ISO standards, including continuity management experience. Experience with SAP environments. Global Experience: Experience with end-to-end global pharmaceutical supply chains and familiarity with international regulations. Why Novartis? Our purpose is to reimagine medicine to improve and extend people-s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network(link is external) Commitment to Diversity & Inclusion: The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Corporate Business Unit Corporate Location Switzerland Site Basel (City) Company / Legal Entity C010 (FCRS = CH010) Novartis International AG Functional Area Audit & Finance Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

<div class="content-box"><div class="post-178796 post type-post status-publish format-standard hentry tag-chefredaktor-in tag-jounalistin-in tag-onlineredaktor-in tag-redaktor-in tag-datenjournalist-in tag-crossmedia-journalist-in ctx_prof_group-medien-journalismus-verlage ctx_work_location-nord-ostschweiz-fl ctx_flake_location-schoenengrund" id="post-178796" itemprop="description"><div class="company-logo"><img alt="reha löwen schönengrund ag logo" src=" https://medienjobs.ch/content/uploads/2025/03/reha_loewen-1.png"/&gt;&lt;/div&gt;&lt;div class="add-post-on add-post-on--mobile"><div>Anzeige vom:</div><div><time datetime="2025-03-15">15.03.2025</time></div></div><div class="intro"><p>LEU ist die Hauszeitung der reha löwen schönengrund. Er ist auch ein Forumsblatt. Mehr zum LEU in seiner elektronischen Form unter <a href=" https://www.leu-cs.ch " target="_blank">www.leu-cs.ch</a>.</p></div><h1>Redaktor / Redaktorin (ca. 10%)</h1><div class="description"><p>Machen Sie sich vom LEU ihr Bild. Schicken Sie uns Ihre Unterlagen. Gerne nehmen wir gegebenenfalls mit Ihnen Kontakt auf, um alles Nähere zu klären, vorzugsweise zunächst per Mail.</p></div><div class="job-benefits"><h3 class="heading">Mitarbeiter-Benefits</h3><ul class="vacancy-benefits-list"><li>Homeoffice nach Absprache möglich </li></ul></div><div class="job-location"><h3 class="heading">Arbeitsort</h3><p class="arbeitsort-location">Schönengrund <a class="arbeitsort-location-link" href=" https://map.search.ch/Reha%20L%C3%B6wen%20Sch%C3%B6nengrund%20AG%2C%20Sch%C3%B6nengrund%2C%20Oberdorf%2047 " target="_blank">Kartenansicht <span class="icon-arrow"></span></a></p><p class="home-office">Homeoffice (gemäss internen Richtlinien)</p></div><div class="cols-1 address-block"><div class="col-1"><h3 style="margin-bottom: 0">reha löwen schönengrund ag</h3><p> Gustav Kaufmann</p><p>Oberdorf 47</p><p>9105 Schönengrund</p><p><a class="job-phone-deatils" href="tel:071 361 11 31">071 361 11 31</a></p><p><a class="job-phone-email" href=" E-Mail schreiben "> E-Mail schreiben </a></p> </div> <!--/.col-1--><div class="col-2"><h3 style="margin-bottom: 0">Links</h3><p> <a class="job-phone-website" href=" https://www.leu-cs.ch " target="_blank">Website</a></p> </div> <!--/.col-2--></div></div><div class="meta"><hr/><p>Finden Sie alle Stellenangebote von <a href=" https://medienjobs.ch/arbeitgeber-firma/reha-loewen-schoenengrund/"&gt;reha löwen schönengrund ag</a> aus <a href=" https://medienjobs.ch/arbeitsort/schoenengrund/"&gt;Schönengrund&lt;/a&gt;&lt;/p&gt;&lt;/div&gt;&lt;/div&gt ;

Job ID REQ-10039111 Feb 11, 2025 Switzerland Summary 6000! This is the number of associates in the Novartis BioMedical Research (BR). This division is the innovation engine of Novartis, focusing on new technologies that have the potential to help produce therapeutic breakthroughs for patients. The Biologics Research Center (BRC) is accommodated within the BR. BRC, in collaboration with the disease areas (DA) and technical expert groups, builds the future biologics therapy pipeline of Novartis through the discovery and creation of new antibody, protein, nucleic acid and virus-based molecules. We are seeking a highly motivated scientist and leader to join the Project and Portfolio Management group within Biologics Research Center (BRC) at our Basel site in Switzerland. We are looking for experience in early research project leadership in the field of Biotherapeutics, with an emphasis on mAbs, multispecific Abs and therapeutic proteins. Our group is driving successful execution of a wide range of biologics projects. This starts with early strategic and operational discussions on therapeutic concept and drug candidate generation, assembly of internal teams and execution of desired strategy, up to technical leadership of early process development and the developability assessment of candidate compounds. You will be reporting to a group leader of BRC-s Project and Portfolio Management. About the Role What you-ll be doing (key responsibilities, but not limited to): Work collaboratively with cross-functional and multidisciplinary teams, spanning multiple NVS global sites to discover and develop efficient Biotherapeutic- based therapies. Co-lead projects with DA project lead; formulate and execute on project strategy, manage interfaces with DAs, including timelines, priority, board presentations. Build and lead internal BRC teams of experimental scientists. Seek technical and operational input from key BRC / BR / Novartis stakeholders to build the project execution plan. Lead BRC internal project meetings. Collect and interprets data to advance project, adapts strategy, and addresses the right scientific questions. Ensure team discussions and decisions are summarized in minutes. Ensure that key milestones and go / no go criteria are data driven and clearly defined. Own quality of project information and make sure project information is accurate and included in the system(s) in a timely matter. Guide projects with respect to biotherapeutic approaches for discovery, formats, modalities and technologies, and leads corresponding efforts. Lead developability assessment, manufacturing cell line development and early process development. Track and oversee projects by maintaining an overview of the project goals, activities and commitments, and timelines of project teams, in line with strategic priorities. Manage and optimize project plans and resource assignments with the aim to manage/mitigate risks. Align with BRC LT and BRC DA rep on project strategy and resourcing. Regular project/portfolio updates to BRC LT. Represent BRC in and actively contribute to BR core project team. Represent BRC in TRD CMC sub-team up to Gate 2. Manages interfaces to TRD TPLs, BRC and EPD LFs on aspects of project management (timelines, strategy, priority). Conducts planning and resource alignments (e.g. from final vector onwards). Manage and communicate project status, issues, and options for resolution to ensure optimal and timely information flow to all stakeholders (BR and TRD). Foster effective, proactive and open communication within and across project teams, build trust among team members to achieve transparency and clarity of program goals, progress and issues. Mentor less experienced team members. Contribute to vendor/CRO evaluations, coordination of outsourcing requests, budget monitoring and communication, evaluation of external collaborations and due diligence. Ensure best practices, knowledge exchange and continuous mentoring and training of our team members. Minimum requirements: PhD with a strong background in Biotherapeutics. 5+ years of relevant biotech/pharma experience, including focus on biotherapeutic design, production, characterization and delivery. Previous track record of success in leadership position, working with international and multidisciplinary drug development teams. Ambitious, yet highly collaborative and fully committed to team-s and project success. Result- and quality oriented. Able to deal with conflicting interests and willing to make compromises to ensure project progress. Excellent project management skills, organizational and team management skills, interpersonal communication, strong verbal and written communication. Creativity with demonstrated critical thinking and problem-solving skills, ability to pay attention to detail but also see a bigger picture. Comfortable with ambiguity and change, eager and fast learner willing to adopt new tools and processes. Ability to operate in a fast-paced dynamic environment and effectively process multiple avenues of communication and requests in parallel. Why Novartis: Our purpose is to reimagine medicine to improve and extend people-s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

<p>Bist du in der Produktionswelt zu hause? Möchtest du deine vorzüglichen Prozess- und Systemkenntnisse im dynamischen Umfeld der Migros-Industrie einbringen? Dann melde dich! Wir haben eine vielseitige Aufgabe, die das Potenzial für eine spätere Führungsrolle mit sich bringt.</p><br/><h2>Was Sie bewegen</h2><p><ul><li>Weiterentwicklung sämtlicher mit der Produktion der Fresh Food & Beverage Group zusammenhängenden Haupt- und Teilprozesse und der MES-Systeme</li><li>Durchführen, Leiten oder Mitarbeiten in IT-nahen Projekten (Projektmanagement, -organisation, -koordination, -dokumentation und Testen)</li><li>Durchsetzen und Kontrollieren der definierten Produktionsprozesse und Abläufe über alle Werke hinweg</li><li>Definieren und Standardisieren der werksübergreifenden Geschäftsprozesse für die Fresh Food & Beverage Group im Bereich der systemtechnischen Produktionsprozesse</li><li>Sicherstellen der Befähigung aller relevanten internen Stakeholdern aus dem Bereich Produktion</li></ul></p><br/><h2>Was Sie mitbringen</h2><p><ul><li>Abgeschlossene Berufslehre (EFZ) · mit Weiterbildung im Bereich Produktion, Supply Chain, Betriebswirtschaft</li><li>Mehrjährige Praxiserfahrung · von Vorteil aus dem Bereich der operativen Produktion und der Anwendung von MES-Systemen, idealerweise in der Lebensmittelindustrie</li><li>Deutsch (fliessend), Englisch (gute Kenntnisse), Französisch (von Vorteil) · </li><li>Sehr gute SAP/S4 Kenntnisse (Modul PP-PI) mit mehrjähriger Erfahrung</li><li>Erfahrung im IT-Projektmanagement (inkl. Spezifizieren, Dokumentieren und Testen)</li><li>Bereitschaft zu örtlich (verschiedene Projekte an verschiedenen Standorten in der Schweiz) wie zeitlich flexiblen Arbeitseinsätzen (Release ca. 4x/Jahr)</li><li>Interesse und Potenzial für eine Weiterentwicklung in eine Führungsrolle</li><li>Kommunikationsstarke, initiative und flexible Persönlichkeit mit Organisationstalent und einem betriebswirtschaftlichen, konzeptionellen Denken</li><li>Laterale Führungserfahrung</li></ul></p><br/><h2>Was wir Ihnen bieten</h2><p><ul><li>Mobil-flexibles Arbeitsmodell · Gleitende Arbeitszeiten mit Möglichkeit zum Homeoffice.</li><li>Faire Löhne · FFB-Group zahlt ihren Mitarbeitenden einen fairen und marktgerechten Lohn auf Basis unseres Personalentlöhnungssystems.</li><li>Berufliche Vorsorge · Versichert in der Migros-Pensionskasse mit deutlich höheren Leistungen als gesetzlich vorgeschrieben; 2/3 übernimmt die Firma.</li><li>Mitarbeiterangebote · Mitarbeiterpunkte Cumulus, Vergünstigte Mobileabos, Höhere Zinssätze Migros Bank, Beiträge Klubschule/Fitness und mehr.</li><li>Du-Kultur · Hoi, hoi zämä, sali - wir sind per Du!</li></ul></p><br/><h2>Bewerbung & Kontakt</h2><p>Monika Alder<br/>HR Business Partner <br/>+41 58 575 34 61<br/> E-Mail schreiben </p>

Job ID REQ-10044268 Mar 26, 2025 Switzerland Summary Location: Basel, Switzerland Full time, onsite, #LI-onsite As a senior principal scientist within Biomarker Development Molecular & Cellular Sciences group you will partner with biomarker, disease area, translational medicine experts to define and execute robust -fit for purpose- clinical biomarker strategy that address key scientific and clinical questions for programs in early and late clinical development phases. About the Role Your responsibilities will include, but not limited to: As Molecular & Cellular Sciences (MCS) biomarker lead and member of the biomarker and diagnostic strategic team (BDST), you will provide scientific and technical insights, contribute to the overall clinical study biomarker strategy and plan to enable proof of mechanism, proof of biology, safety and efficacy understanding and patient selection. As MCS biomarker lead in clinical studies, you will work with biomarker experts to define and lead the execution of cellular and soluble biomarker plan and the successful implementation of internal and external -fit for purpose- biomarker assays. Develop, validate and implement cellular and soluble biomarker assays by working with internal labs as well as external lab partners Manage activities and supervise laboratory in compliance with Novartis guidelines and Good Clinical Practice. Select and evaluate new innovative soluble and cellular biomarker technologies to cover biomarker needs and gaps in early and late projects. Partner with outsourcing functions to evaluate new CROs, drive transitioning and monitoring of internally developed assays to external vendors. Generate and interpret data to enable proof of mechanism, dose selection & proof of biology across early clinical programs and present results at internal meetings Ensure high quality and timely delivery of results Contribute/write quality reports and laboratory manuals. Cross train a variety of biomarker modalities and technologies What you will bring to the role: PhD in Biology, Immunology or cell biology or equivalent related experience and 5+ years of industry experience in biomarker assay development and validation or related fields Extensive understanding and experience in high dimensional flow cytometry (conventional and spectral flow cytometry) and multiplex ligand binding assay technologies (e.g. MSD, Ella, NULISA, Olink) and related software/bioinformatic tools for data analysis is required Extensive experience in technical development, validation, and implementation of cellular and soluble biomarker assays in clinical studies according to international guidelines Experience in outsourcing and leading activities at CROs (e.g. technical troubleshooting) Good Computer skills (Excel, Word, PowerPoint, Soft MaxPro, SMART Book, Spotfire, GraphPad Prism, Watson LIMS) Solid understanding of tools, practices and processes employed in clinical trial settings and drug development Understanding of regulatory requirement relevant to Biomarker Development (e.g. GCLP, ICH) Proven ability to work and lead in a global matrix organizational and scientific environment Experience working in a global organization and matrix-resourcing model Good communication skills for oral and written in English *Restrictions on flexible working arrangements may apply and will be discussed at interview if applicable Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10038818 Feb 05, 2025 Switzerland Summary Our Immunology Disease Area in Biomedical Research division in Novartis is dedicated to world-class research and finding breakthroughs in treatments for millions of patients worldwide suffering from Immunological conditions and diseases. We are currently seeking a senior level Molecular Pathologist with either a Medical or Veterinary doctoral background and a Pathology certification, to join our teams and lead a lab in the Immunology Disease area and help us tackle some of the most challenging unmet needs. About the Role Job Description You will be part of a cross-disciplinary team, working with various labs in Immunology. A strong emphasis for this role is placed in effective teamwork, networking across teams, and development of successful partnerships with academic leaders worldwide. Your responsibilities will include but not be restricted to: Lead an experimental pathology lab within the Molecular Pathology group, in Immunology Translational Research. Use tissue samples from healthy humans, patients suffering from immunological diseases and corresponding animal models for: - Disease understanding - Target validation - Biomarker discovery (pathway-based and pharmacodynamic) Implement spatial omics technologies Use of state-of-the-art imaging modalities and digital image analysis to address key scientific questions Provide pathology expertise for tissue biomarkers in clinical studies Work closely with multidisciplinary project teams in discovery and translational research. Minimum requirements - What you will bring to the role: MD or DVM with relevant human or veterinary pathology experience; plus PhD-level research background You must be a Board-certified Pathologist or Veterinary Pathologist strong Experimental Pathology background/expertise Experience in animal mechanistic and disease models as well as human biosamples Strong background and hands-on expertise in immunohistochemistry and in-situ hybridization, including method development Strong leadership skills - experienced team leader with direct reports, including professional development of team members Excellent presentation and communication skills in English (oral and written), innovative thinking and project management skills Desirable: Prior experience in spatial omics will be an advantage Knowledge of or interest in autoimmune and dermatological diseases is highly desirable *Restrictions on working flexibility may apply to this position and can be discussed at interview as required Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

<p>Die Klubschule Migros ist die grösste Anbieterin für Erwachsenenbildung in der Schweiz. Die Genossenschaft Migros Ostschweiz betreibt sieben Klubschulen, in denen unseren Kunden über 400 verschiedene Kurse und Lehrgänge in einer angenehmen Unterrichtsatmosphäre angeboten werden. Für unsere Klubschule im Herzen der Altstadt von Schaffhausen suchen wir eine/-n Bildungsberater/in /-koordinator/in.</p><br/><h2>Was Sie bewegen</h2><p><ul><li>Professionelle Beratung und Verkauf des gesamten Angebotes der Klubschule am Schalter und Telefon (über 400 Kurse)</li><li>Planung und Organisation von Kursen und Lehrgängen, inkl. Lehrmittelbewirtschaftung</li><li>Erste Ansprechperson für Teilnehmende und Lehrpersonen im Center</li><li>Mithilfe bei Marketingaufgaben und Mitverantwortung für die Infrastruktur</li></ul></p><br/><h2>Was Sie mitbringen</h2><p><ul><li>Abgeschlossene Grund- oder Weiterbildung · im kaufmännischen Bereich</li><li>Mehrjährige Berufserfahrung · im kaufmännischen Bereich mit Kundenkontakt</li><li>Deutsch (sehr gute Kenntnisse) · </li><li>Initiative, teamfähige Persönlichkeit mit ausgeprägter Verkaufs- und Kommunikationskompetenz sowie einer positiven Ausstrahlung</li><li>Selbständige Arbeitsweise, gutes Prozessverständnis und lösungsorientierte Handlungsweise</li><li>Sensibilität für andere Kulturen</li><li>Fremdsprachenkenntnisse erwünscht</li><li>Gute Office-Kenntnisse sowie Kenntnisse SAP von Vorteil</li></ul></p><br/><h2>Was wir Ihnen bieten</h2><p><ul><li>Zentraler Arbeitsort · Gut mit öffentlichen Verkehrsmitteln erreichbar</li><li>Klubschule Migros · Grosszügige finanzielle Beteiligung an selbst ausgewählten Kursen</li><li>Freizeit- und Kulturangebote · Diverse Vergünstigungen auf Ferienangebote und Events</li><li>Sport- und Fitnessangebote · Vergünstigung bei Abonnements der Freizeit- und Fitnessanlagen</li><li>Versicherungen · Vorteilskonditionen bei diversen Versicherungsgesellschaften</li></ul></p><br/><h2>Bewerbung & Kontakt</h2><p>Thomas Hauser<br/>Centerleiter Schaffhausen<br/>+41 58 712 42 75</p>

Job ID REQ-10032015 Mar 21, 2025 Switzerland Summary Location: Basel, Switzerland Role Purpose: Novartis holds a rich development portfolio of small molecules ready to develop into innovative, patient centric, oral dosage forms. As a Drug Product Project Leader (DPPL) working on oral dosage forms, you will lead and manage formulation and manufacturing activities linked to pharmaceutical development for small molecules (New Chemical Entities; NCE). For this position, specific emphasis lies on bringing in-depth experience of pharmaceutical unit operations and related late-phase experience including scale-up and transfer to the commercial site. You will lead drug product teams during all stages of development with a specific focus on late clinical phases. You will be working on oral Small Molecules and in particular on enabling formulation approaches. You will use your strong communication, stakeholder management and influencing skills to effectively lead the drug product sub team and the transfer team in a matrix organization. Your expertise will facilitate the planning and execution of smart DoE and scale-up / transfer campaigns to establish robust manufacturing processes and stable drug products suitable for human trials and commercial supplies following ICH principles. About the Role Your responsibilities will include but are not limited to: You lead and manage all Drug Product (DP) related technical development activities for assigned projects and you represent DP project teams in Technical Research and Development (TRD) sub-teams based on your strong scientific and pharmaceutical development expertise. You lead, manage and support the DP and the transfer teams in line with Novartis values and behaviors. You build strong team spirit and promote knowledge exchange within and between teams. You motivate and coach team members for high performance. You formulate a sound DP project strategy incl. contingency planning and risk assessments as appropriate, involving functional experts, and you ensure alignment with Pharmaceutical Development department and other departments and functions inside and outside of TRD and 3rd parties as applicable. You ensure adherence to the scientific and project review process and through relevant scientific and project management governance boards You ensure creation of high quality and scientifically sound DP development documents enabling a strong CMC submission package, and act as author, reviewer or approver for development documents in accordance with operational procedures and guidelines. You contribute to the generation of registration dossiers, answer DP related questions in internal and external audits, and support Health Authority requests. What you-ll bring to the role: PhD in Pharmaceutical Sciences or relevant scientific field (e.g., Pharmaceutical Technology, Chemical Engineering). Minimum 3 years of relevant technical experience in Development of oral Pharmaceutical Drug Products with proven experience in leading project teams in a matrix organization. Strong expertise in pharmaceutical oral dosage form development, manufacturing, and scale-up for formulations for Small Molecules including enabling formulations, manufacturing and IPC technologies, and scale-up principles. An understanding of material science principles, as applied to oral dosage forms, including the impact of physico-chemical properties of API and excipients on the drug product process and quality. Experience with application of Quality by Design and Quality risk management principles and tools as well as good working knowledge of regulatory guidelines relevant to Drug Product Development, validation, risk management, testing and stability, and new drug applications, together with technical writing and presentation skills. Ideally experience in applying data science, statistics, and DoE to enhance pharmaceutical development by providing a robust framework for data analysis, experimental design, and decision-making, leading to more effective and efficient drug development processes and documentation. Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10032919 Mar 24, 2025 Switzerland Summary In our Pharmaceutical Development (PHAD) unit, we are dedicated to advancing and applying cutting-edge pharmaceutical technologies to positively impact patients worldwide through the ongoing creation of novel commercial products. About the Role We are currently seeking a skilled intern with a background in programming to contribute to the development to create a digital platform to support product design within PHAD. This role entails automating data processes, integrating data from diverse data sources, and constructing visualizations to support business decisions. The ideal candidate will be an innovative problem-solver with experience in data integration, automation, and visualization, and possess programming abilities. We are looking for a student studying data sciences, computer sciences, bioinformatics or a related degree. Preferred start date: May 2025 Duration: 6 months Please attach a cover letter explaining your motivation for this position and let us know when you are available. Thank you very much. Key responsibilities: Utilization of various applications, services, or connectors (e.g., Power Apps) to enable data flow automation. Develop and implement data integration processes to aggregate data from multiple sources into a unified tool for a comprehensive overview. Ensure efficient data management and effective analysis/reporting to support business goals. Application of programming for data visualization to visualize data from multiple sources within a single platform. Development of digital tools to support activities related to environmental sustainability. Essential requirements: Education: Recent graduate (B.Sc./M.Sc.) or enrolled Master Student Languages: Proficiency in English Experience/Professional requirements: Programming skills (e.g. Python): Knowledge in software for data visualization (e.g. Power Bi, Spotfire etc) Ability to work in multidisciplinary teams in an international environment, strong communication skills Desirable requirements: Programming skills and experience with handling and connecting data pools (e.g. Power App, Alteryx) Why Novartis: Our purpose is to reimagine medicine to improve and extend people-s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Others Job Type Full time Employment Type Early Career (Fixed Term) Shift Work No

<h3>Wir haben laufend - auch kurzfristig - freie Praktikumsstellen zu vergeben:</h3><br><br><p><div>Ihre Aufgaben</div><br><ul><li>Tägliche OP-Assistenz bei einem breiten Spektrum an Eingriffen verschiedener Fachdisziplinen</li><li>Unterstützung der Assistenzärzte u. Assistenzärztinnen bei der Stationsarbeit</li><li>Aufnahme / Statuserhebung stationärer Patientinnen und Patienten</li><li>Mithilfe auf der interdisziplinären Notfallstation</li></ul></p><br><p><div>Ihr Profil</div><br><ul><li>Engagierte Persönlichkeit mit Bereitschaft zur interdisziplinären Zusammenarbeit</li><li>Teamorientiertheit, Belastbarkeit sowie Kommunikationsfähigkeit</li><li>Sie sind EU/EFTA-Bürgerin/Bürger oder verfügen bereits über eine gültige Aufenthalts- und Arbeitsbewilligung in der Schweiz (bitte Kopie beilegen)</li></ul></p><br><p>Das Asana Spital Menziken ist das innovative Gesundheitszentrum der Region aargauSüd. In familiärer Atmosphäre gewährleisten wir die qualitativ hochstehende medizinische Grundversorgung der Region.<br/><br/>Dabei sind wir ein familienfreundlicher und attraktiver Arbeitgeber mit fortschrittlichen Anstellungsbedingungen für rund 300 Mitarbeitende.</p><br><p>Interessiert? Gerne erwarten wir Ihre Online-Bewerbung unter jobs.asana.ch</p><br>

Job ID REQ-10043278 Mar 24, 2025 Switzerland Summary The TMF Oversight Manager is responsible for ensuring delivery and oversight of high quality and timely TMF Quality Review activities for a portfolio of internal, outsourced or BD&L studies. You will drive implementation of Clinical Document Governance Management initiatives, projects and process improvement activities to enhance clinical document management systems, processes and standards at Novartis. About the Role This is a hybrid role and can be based in Basel, Dublin or London offices. The expectation is to be in the office 12 days/month Your responsibilities include, but are not limited to Responsible for timely assessment of quality and completeness of TMFs for an assigned portfolio of studies. Identify and communicate TMF risks/trends/patterns and works with key stakeholders to define and implement pragmatic remediations. Execute vendor oversight plan, monitors service metrics, and identifies opportunities for improvement to the operating model. Acts as point of escalation for issues. Serve as Subject Matter Expert on TMF training materials, formal and informal processes and tracking tools for TMF oversight activities in collaboration with CDM Process team and other key stakeholders Provide Audit/Inspection readiness support by driving TMF quality reviews in preparation for audits/inspections, contributes to root cause analysis identification and creation/delivery of CAPAs. Identify and implement improvements to document management processes to improve quality of TMFs. May act as business lead for innovation projects to enhance TMF quality assessment. Support the forecasting and tracking of TMF Quality Review resource needs including proactive identification of resources to support TMF Quality Review activities for high-risk and priority projects. Support definition and refinement of TMF management strategy for assigned portfolio of studies. Ensures clear expectations for TMF set up and maintenance, including contractual agreement with third parties, for outsourced studies. Minimum requirements Bachelor-s degree or equivalent and relevant industry experience Minimum of 5 years working in clinical research and development in the pharmaceutical industry (and/or Contract Research Organisations) with specific experience in clinical documentation and/or records & information management. Demonstrated success in planning and executing cross functional projects. Strong influencing and presentation skills. Ability to communicate effectively at all levels. High organisational awareness, including experience working in multi-disciplinary teams, across cultures and geographies. Good negotiation, problem solving and conflict resolution skills; experience establishing trusted relationships with internal and external stakeholders. Why Novartis? Our purpose is to reimagine medicine to improve and extend people-s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture&nbsp ; You-ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Alternative Location 1 Dublin (NOCC), Ireland Alternative Location 2 London (The Westworks), United Kingdom Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10043086 Mar 06, 2025 Switzerland Summary As a Product Operations Manager of Applied Generative Artificial Intelligence solutions, you play a key role in the co-leadership team that will define, build, and support Generative Artificial Intelligence (GenAI) capabilities for drug discovery. In the co-lead context, you are accountable for all aspects of the software operations from supporting adoptions & integrations, user-support, maintaining stable and secure systems, to increasing the value and operational excellence on the team. As a co-lead and a member of a cross-functional, matrixed team, which may consist of software and data engineers, business analysts, designers and user supporters, your primary responsibilities include but not limited to: About the Role Owning all operational aspects for one or more Agentic AI solutions within the product team, including stable operations and infrastructure- Oversee the end-to-end operations of the Agentic AI platform, ensuring continuous, uninterrupted operation of AI systems, data integrations, cloud infrastructure, and associated services Implement and maintain monitoring tools to track platform health, AI model performance, and system resource usage, proactively identifying performance bottlenecks and work with technical teams to optimize system efficiency and reduce redundancy Mitigating operational risks and manage incident detection and resolution You collaborate closely with the external technology partner to support integration needs, driving solutions for common user community issues Engaging with user communities to understand their scientific needs and questions and identify/guide ways of leveraging the existing platform You effectively connect to, and collaborate with, product teams managing our core data platforms required by the GenAI platform to ensure stability and data accuracy You contribute to vision and opportunities for GenAI to speed-up, streamline and innovate drug discovery by supporting your co-leads by bringing user insights into requirements for, and facilitating data access to technology experts and partners. Manage incidents and troubleshooting, including investigating and solving recuring incidents Providing end-user support, communication, knowledge-base documentation, and trainings Leading Vulnerability management efforts, ensuring security, compliance, usability, performance, and sustainability requirements are met Ensuring license compliance, applying patches, and managing roll-out and upgrades Guiding and coordinating small teams of external application supporters, ensuring effective prioritization of operational activities, Ensuring adherence to Novartis global Information Security and Quality standards and policies for all products/services Ensuring regulatory Compliance (e.g., GLP & GCP) standards and policies for GxP products/services, if applicable Ensuring operational activities and outcomes are reflected on product roadmaps Engaging with other product teams within and across product lines to leverage operational synergies Experience : +5 years of experience in managing AI platform, cloud services, or technical operations Experience in IT or informatics Familiarity with drug discovery research or life sciences Bachelor's degree in a technology or scientific subject Knowledge of AI principles and familiar with Agentic AI frameworks (LangChain or similar).- Familiarity with cloud platforms and their AI-related services Prior experience of operations and support in cloud environment, working with cloud services and AI-related services Strong proficiency with API calls and API data Proficiency with scripting and automation tools (e.g. Python, Terraform, Jenkins) for operational tasks Experience in incident management, troubleshooting and resolving issues related to AI model performance, cloud infrastructure, and platform services Strong analytical skills with the ability to diagnose and resolve complex technical issues related to AI services, infrastructure, or integrations Experience in software support, IT operations or software development in complex business environments Strong communication skills Highly collaborative, proven experience as a team player Familiarity with Agile software development and SDLC Knowledge of Information Technology Service Management (ITSM) Familiarity with DevOps tools Experience in a drug discovery or scientific research setting preferred Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Commitment to Diversity & Inclusion : Novartis is committed to building an outstanding, inclusive work environment and diverse team-s representative of the patients and communities we serve. Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Alternative Location 1 Cambridge (USA), Massachusetts, USA Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10043089 Mar 07, 2025 Switzerland Summary Location: Basel, Switzerland Full time, onsite, #LI-Onsite At Novartis we are reimagining medicine to improve and extend people's lives. We use innovative science and technology to address some of society's most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. How can we continue to advance our science to help patients in need? We believe the answers are found when curious, courageous, and collaborative people are empowered to ask new questions, make bolder decisions, and take smarter risks. In Global Discovery Chemistry (GDC) in Basel, Switzerland, we are at the core of Novartis- purpose. We are looking for a highly motivated, passionate researcher with a strong scientific background in radiochemistry, a curious mind-set, and cultural agility to work in a highly dynamic team to identify new targeting vectors for radioligand therapies (RLT). Join us and help reimagine medicine! About the Role Your responsibilities will include, but are not limited to: You will independently plan and execute the synthesis of radioligands (low molecular weight (LMW), peptide and/or protein vectors) with various radionuclides (Lu-177, Ga-68 and F-18), as part of a dynamic team of radiochemists according to a program defined by the project team. You will propose, evaluate, interpret and validate new radiolabeling procedures with radioisotopes including the use of automation and advanced formulation development. You will collect and perform the quality control of radioligands by High Performance Liquid Chromatography (HPLC), Thin Layer Chromatography (TLC) and Size Exclusion Chromatography (SEC) in the radiochemistry lab environment and release the radioligands for in vitro and in vivo preclinical studies. You will be responsible for following implemented radiation safety regulations (e.g. trainings, dosimetry, release and disposal of radioactive waste). You will evaluate novel technologies including possibilities for automation to increase daily work efficiency. You will collaboratively work with pharmacologists, cell biologists, and project teams to characterize novel radioligand therapies in the upsurging oncology disease area. Minimum requirements What you will bring to the role: A passion for hands-on chemistry experimentation in the laboratory with the ability to critically interpret results, build new experimental hypotheses, and take smart decisions. A bachelor-s degree or apprenticeship in chemistry, pharmacy, or related discipline with previous experience in radiochemistry and radiolabeling techniques. Please note that this position does not require a PhD. Must have a minimum of 2-3 years practical experience in radiochemistry experimentation in the laboratory, including working with Radiometals Comprehensive knowledge of standard IT applications (e.g. E-Notebook, ChemDraw, software-controlled lab equipment). Experience in the use of automated synthesizer for production and purification of radiolabeled molecules is an asset. A mind-set of curiosity, creativity, collaboration and openness to diverse thinking, with an enthusiasm to develop yourself also beyond your current comfort zones. An organized working style, eye for detail, flexibility and commitment to high quality. A desire to collaborate with a highly dynamic team, discuss science and contribute to the next generation of RLTs. Good oral and written communication in English. Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. *Please note that restrictions on flexible working may apply and will be discussed at interview stage if applicable Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10043483 Mar 07, 2025 Switzerland Summary Location: Basel, Switzerland Full time, onsite, #LI-Onsite We are seeking a highly motivated and curious lab-based Senior Scientist I whose focus will be on siRNA discovery in the xRNA Team within Biomedical Research in Basel. The team develops next-generation xRNA therapeutics in a collaborative and innovation driven environment, aiming to transform the lives of millions of patients with unmet medical needs. The successful candidate will have a background in biology research with ideally a focus in RNA biology. The ideal candidate will have strong experience in medium - to high throughput screening using automation, cell culture techniques, assay development and technologies such as liquid handlers. About the Role Key Responsibilities: Design, plan and conduct routine siRNA screening in cell-based transfection assays using qPCR and reporter-based systems Perform novel assay development and optimization for cell-based assays with a focus on improving throughput with automation Contribute to designing, and developing automated workflows Operate automated liquid handling robotics platform Work collaboratively in a matrix-oriented environment and present work on a regular basis in unit meetings Acting as a point-of-contact in the team of day to day activities Document experiments in lab notebook, conduct data analysis, interpretation and present findings to team in a timely manner Role Requirements: A higher degree in biology (such as Bachelor-s or Master-s), or Apprenticeship with equivalent industry experience in biochemistry, cell biology or related scientific discipline A minimum of 5 years of research experience gained ideally in a lab environment in a pharma and/or biotech industry setting Expertise in cell culture and conducting expression read outs (e.g. qPCR, Western Blot, ELISA) Experience with liquid handlers and automation of cell based assays Strong competence in MS office applications, expertise in Excel and maintenance of electronic Lab Notebooks Strong multi-tasking, organizational, attention to detail, verbal/written communication skills Ability to collaborate and thrive in fast-paced, team-oriented environment Desired Requirements: Primary cell culture experience Expertise in Spotfire and/or GraphPad PRISM Expertise with BioMek or Opentrons liquid handlers *Restrictions on flexible working may apply and are discretionary and can be discussed at interview, if applicable Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10043484 Mar 07, 2025 Switzerland Summary Location: Basel, Switzerland Fulltime, onsite, #LIonsite We are seeking a highly motivated and curious Principal Scientist whose focus will be on siRNA discovery in the xRNA Team within Biomedical Research based in Basel. The team develops next-generation xRNA therapeutics in a collaborative and innovation driven environment, aiming to transform the lives of millions of patients with unmet medical needs. The successful candidate will have strong experience in siRNA biology and/or therapeutics and will have a key role in driving the development of the xRNA platform and mentoring Lab team members. About the Role Key Responsibilities: Lead matrix-oriented platform teams for the development of siRNA therapeutics Experience with end-to-end NGS experiments including library preparation, sequencing, and analysis Drive innovation based on data mining form hypothesis generation to conduct studies in a collaborative environment across Biomedical Research Design, plan and supervise siRNA cell-based screening activities Perform novel assay development and optimization for cell-based assays with a focus on improving throughput with automation With supervision lead junior scientists in the lab and with data analysis Represent xRNA team on cross-functional project teams to advance siRNA programs through the development pipeline Document experiments in lab notebook, conduct data analysis, interpretation and present findings to team in a timely manner Role Requirements: PhD in biochemistry or biology or related scientific discipline 3 - 5 years of post-PhD research experience gained in academia as a Postdoc and/or in industry Research experience in siRNA biology. Knowledge of siRNA therapeutics would be an advantage. Strong genomics background with expertise in RNA-Seq from experiment to data processing Able to run R scripts independently Expertise in mammalian cell culture from immortalized to primary cells Experience with cross functional teams and ability to serve as a point of contact for the team with minimal supervision Strong multi-tasking, organizational, attention to detail, verbal/written communication skills Ability to collaborate and thrive in fast-paced, team-oriented environment Desired Requirements: Expertise with BioMek or Opentrons liquid handlers Proficient in R and/or Python. Machine Learning experience a plus. *Restrictions on working flexibility may apply to this position and can be discussed at interview as required Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10042625 Mar 20, 2025 Switzerland Summary Our ambition is to be recognized as the #1 Oncology company in international markets and Pluvicto, is central to this ambition. The Executive Director International, Pluvicto, plays a pivotal role in leading the end-to-end brand strategy, encompassing the vision, development, orchestration, implementation, and evaluation of integrated Pluvicto strategies across major international markets. As an enterprise leader, the ED will focus on the top three countries (Germany, Japan, and China) and Regions, driving the successful launch and growth of Pluvicto to achieve blockbuster status with over $2 billion in sales and double-digit growth, thereby making a significant impact on patients' lives. The incumbent will collaborate closely with Global Drug Development (GDD), International Medical Affairs, Value & Access, and Customer & Market Activation teams to drive consistent strategy development and execution. This role also leads the commercial team, fostering a culture of innovation, collaboration, and execution excellence. The role reports to Disease Commercial Head for Radioligand Therapy (RLT). About the Role Major accountabilities: Collaborate closely with GDD to influence TPP & Integrated Evidence Plan and maximize commercialization & patient access potential for Pluvicto-s new indication and LCM in key markets in international. Analyze market trends and conduct extensive market research, capturing perspective from customers, deeply understanding market dynamics, competition. Use data-driven insights to inform strategic decisions. Lead the development and execution of comprehensive marketing strategies, including, product positioning, differentiation, and scientific message to maximize market penetration and Pluvicto growth. Develop and partner with the top 3 countries (China, Japan, and Germany) to create robust strategic plans, ensuring meticulous execution and performance measurement. Continually collect and integrate feedback from leading countries and regions to refine and enhance brand strategy, positioning, and communication efforts. Effectively communicate Pluvicto-s vision and strategic goals to senior leaders, including the International Leadership Team, General Managers, and regional heads. Lead Pluvicto International Commercialization Excellence (ICE) initiatives, driving best practices in customer engagement strategies. Foster a customer-centric mindset within the international and country teams, focusing on personalizing experiences to extend patient reach and commercial impact. Attract, lead, and develop top talent within the Pluvicto brand team, fostering cross-functional collaboration and innovation. Essential Requirements: +15 years of commercial experience across various functions, demonstrating a broad and deep understanding of the commercial landscape. Proven track record of successful international launches, with commercial leadership experience and therapeutic area (TA) leadership in large markets. Extensive commercial experience in oncology, especially in managing solid tumors, with a preference for expertise in the prostate market Proficient in translating scientific data into differentiated brand value propositions, enabling impactful launches across pre-launch through lifecycle management (LCM) stages Experience with high-performing/high-growth brands or markets, with a clear understanding of key drivers that influence shifting customer and patient behaviors to ensure successful asset launches Strong track record in collaborating and partnering with cross-unit, cross-functional & key markets to achieve strategic and performance targets. Leadership Capabilities: Proven ability to manage and drive performance, ensuring targets are met and exceeded in challenging markets Demonstrated ability to lead and inspire teams, drive cross-functional collaboration, and think strategically in dynamic environments. Focuses on larger, longer-term issues, and creates plans and strategies. Comfortable in navigating the matrix and people related organizational dynamics. Establish credibility & influence across diverse stakeholders and able to navigate in an environment of shared outcomes and cross-business accountabilities. Demonstrates enterprise leadership, balance diverse stakeholders and conflicting priorities to drive results. Empowered teams to execute efficiently, through the layers of organization and across geographies. Clearly and effectively communicates with senior stakeholders (both internal &external)- to align on vision, purpose & goals. Generates trust, builds credibility and drives engagement with people and stakeholders. Location: Basel, Switzerland. Benefits: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: Novartis Life Handbook Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, be-cause of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis? Our purpose is to reimagine medicine to improve and extend people-s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network (link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division International Business Unit Universal Hierarchy Node Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Commercial & General Management Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

<p><strong><h1>Berufsbildner Pflege (m/w/d)</h1></strong></p><p><strong>Ihre Vorteile</strong></p><p><ul><li>Eine interessante, vielseitige und anspruchsvolle Tätigkeit Rahmen der Grundausbildung (FaGe) sowie Tertiärausbildung (dipl. Pflegefachfrau/-mann HF)</li><li>Kleines, aufgestelltes und motiviertes Berufsbildnerteam</li><li>Moderne Anstellungsbedingungen und gutes Arbeitsklima</li><li>Interessante Benefits</li><li>Attraktives Angebot zur Fort- und Weiterbildung, welches wir grosszügig unterstützen</li></ul></p><p><strong>Ihre Aufgaben</strong></p><p><ul><li>Unterstützung und Förderung bei der Erreichung der Lernziele</li><li>Schaffung von Lernsituationen im Rahmen von Lernbegleitungen und Unterstützung der Lernenden / Studierenden bei der selbständigen Anwendung und Vertiefung von Fachwissen sowie in der Reflexion von Pflegesituationen</li><li>Förderung der Lernkompetenz der Lernenden / Studierenden sowie Überprüfung des Lernerfolgs</li><li>Fortlaufende Kontrolle und Führung der Dokumentation des Lernprozesses</li><li>Erteilung von Lernaufträgen im Rahmen der Ausbildungsgänge</li><li>Führen der Zwischen – und Schlussqualifikation der Lernenden und Studierenden </li></ul></p><p><strong>Ihr Profil</strong></p><p><ul><li>Eine abgeschlossene Ausbildung als dipl. Pflegefachperson HF</li><li>Erfahrung im Akutbereich sowie in der Berufsbildung von Vorteil</li><li>Vorhandener Berufsbildnerkurs oder SVEB 1 von Vorteil</li><li>Bereitschaft für die interdisziplinäre Zusammenarbeit mit anderen Abteilungen</li><li>Bereitschaft für Flexibilität bezüglich Einsatzbereich</li><li>Hohe Sozial- und Fachkompetenz sowie hohes Verantwortungsbewusstsein</li><li>Gute PC-Anwenderkenntnisse</li></ul></p>

<h3>Weitblick für Reha und meine Karriere – das ist das Lebens- und Arbeitsgefühl bei den Kliniken Valens. Austausch, Fortschritt, interdisziplinäres Teamwork und gute Aussichten werden hier gross geschrieben.<br/><br/>Wir vergeben nach Vereinbarung ein</h3><br><br><p><div>Deine Aufgaben</div><br><ul><li>Bedienen und Betreuen unserer Patienten und Gäste im Speisesaal, im Room Service, in der Cafeteria und im à la carte Restaurant Zanai</li><li>Sicherstellen der Gästezufriedenheit</li><li>Mise en place Arbeiten</li><li>Bestellwesen</li><li>Ausführen von Reinigungsarbeiten</li></ul></p><br><p><div>Dein Profil</div><br><ul><li>Du studierst an einer Schweizer Hotelfachschule</li><li>Interesse an einer Arbeit mit Gästen und Patienten</li><li>Motivierte, kontaktfreudige und zuverlässige Persönlichkeit</li><li>Hands-on-Mentalität</li><li>Verantwortungsbewusstsein, Flexibilität und hohe Dienstleistungsorientierung</li><li>Gute Deutschkenntnisse</li></ul></p><br><p><div>Deine Zukunft bei uns</div><br><ul><li>Interessante und herausfordernde Tätigkeit in einem innovativen und zukunftsorientierten Unternehmen</li><li>Interne und externe Fort- und Weiterbildungsmöglichkeiten</li><li>Grosszügige Nebenleistungen sowie attraktive <a href=" https://www.kliniken-valens.ch/jobs-karriere/ihre-vorteile/ " target="_blank">Anstellungsbedingungen</a></li></ul></p><br><p><div>Kontakt</div><br>Martina Zimmermann</p><br><p><div>Über uns</div><br>Die Kliniken Valens, gemeinsam mit den Zürcher RehaZentren, sind eine innovative Klinikgruppe mit sieben stationären und drei ambulanten Standorten. Mit über 900 Betten und 2200 Mitarbeitenden ist die Gruppe der grösste Rehabilitationsanbieter der Schweiz. Als Träger der Labels „Friendly Work Space“ und „Beste Arbeitgeber Schweiz“ unterstützen wir unsere Mitarbeitenden bei ihrer Work-Life-Balance und pflegen eine Kultur des Miteinanders.</p><br>

<div class="job"><div class="row displayDT marginTopLarge" role="img" style=" "><div class="col-xs-12 center scaled backgroundimagedbd1e678-59de-4723-81d5-6 large-image-component" style="height: 230px;"></div></div><div class="row displayM" role="img" style=" "><div class="col-xs-12 center scaled backgroundimagedbd1e678-59de-4723-81d5-6 large-image-component" style="height: 95px;"></div></div><div class="joblayouttoken rtltextaligneligible displayDTM"><div class="inner fontcolorfb08899fd87c1d95" style="font-family:custom81d021cd635b49158dea7; font-size:12px;"><div class="row"><div class="col-xs-12 fontalign-left"><span class="rtltextaligneligible" data-careersite-propertyid="description" itemprop="description" lang="en-US" xml:lang="en-US"><span class="jobdescription"><div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:18.0px;word-wrap:break-word"><h2 style="font-size:1.0em;margin:0.0px"><b>#WeAreCamelot</b></h2> </div><div><p style="text-align:justify"></p><p style="text-align:center"><span style="font-size:28.0px"><b>(Senior) Business Process Consultant SAP PM/ EAM (all genders)</b></span></p><p style="text-align:center"></p><p><span style="font-size:16.0px">As a strategic advisor, digital innovator and trusted implementation partner, Camelot's Data & Analytics division is a leader in advising data-driven organizations. We drive digital transformation and help our clients to increase the value of their data by developing innovative concepts and solutions in data management. Our project results are of uncompromising quality. We create a solid foundation for world-class analytics based on high-quality data that enables companies to make informed and sustainable decisions. Join us in transforming enterprises!</span></p><p></p></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:18.0px;word-wrap:break-word"><h2 style="font-size:1.0em;margin:0.0px"><b>Make a difference.</b></h2> </div><div><p style="text-align:justify"></p><ul><li style="text-align:justify"><span style="font-size:16.0px">You will develop concepts, strategies and implementation plans for our clients in the area of SAP maintenance, with a focus on data as the basis for all processes</span></li><li style="text-align:justify"><span style="font-size:16.0px">You will implement these plans within an international and interdisciplinary team</span><span style="font-size:16.0px"></span></li><li style="text-align:justify"><span style="font-size:16.0px">Given the necessary experience, you can take on the role of a stream lead</span></li><li style="text-align:justify"><span style="font-size:16.0px">You will contribute to the development of innovative solutions in the area of Enterprise Asset Management (EAM)</span></li><li style="text-align:justify"><span style="font-size:16.0px">You will support acquisition and development of the division as well as maintain contact with external partners</span></li></ul><p></p></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:18.0px;word-wrap:break-word"><h2 style="font-size:1.0em;margin:0.0px"><b>Bring your experience.</b></h2> </div><div><p style="text-align:justify"></p><ul><li style="text-align:justify"><span style="font-size:16.0px">You have already successfully participated in consulting projects, preferably with first experience as Stream Lead</span></li><li style="text-align:justify"><span style="font-size:16.0px">You have experience in the areas of Maintenance and Data Management</span></li><li style="text-align:justify"><span style="font-size:16.0px">You have knowledge of SAP S/4HANA, ideally also SAP PM or SAP EAM</span></li><li style="text-align:justify"><span style="font-size:16.0px">You enjoy working in a team as well as with clients and are open to traveling</span></li><li style="text-align:justify"><span style="font-size:16.0px">Working in a team and being in contact with clients is exciting to you</span></li><li style="text-align:justify"><span style="font-size:16.0px">Fluent communication in German <u>and</u> English is no problem for you (must have)</span></li></ul><p style="text-align:justify"></p><p style="text-align:justify"></p><p><span style="font-size:18.0px"><b> MANNHEIM– COLOGNE– HAMBURG– MUNICH– BASEL</b></span></p><p></p><p><span style="font-size:18.0px"><b>Ready to join? <a href=" https://www.linkedin.com/in/heidrun-lehnert-68421932/"&gt;Heidrun Lehnert</a> is your contact at Camelot.</b></span></p><p></p></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:18.0px;word-wrap:break-word"><h2 style="font-size:1.0em;margin:0.0px"><b>Your benefits – what we offer.</b></h2> </div><div><p></p><ul><li><p><span style="font-size:16.0px"><b>We continuously support you in your successful career growth</b> through cross-functional onboarding, mentoring, regular feedback, and target-oriented development through a versatile, high-profile, and personalized training catalog.</span></p></li><li><p><span style="font-size:16.0px"><b>Become an innovation leader</b> leveraging the company-wide innovation spirit and implement your visions with blueprints and prototypes.</span></p></li><li><p><span style="font-size:16.0px"><b>Work flexibly</b> from the customer site, our office locations, or your home – in short: <b>benefit from our FlexWork concept</b>. Recharge your batteries by taking a sabbatical.</span></p></li><li><p><span style="font-size:16.0px"><b>Take care of yourself, others, and our planet</b> by participating in our CSR & Diversity Community and Wellbeing & Resilience Center initiatives.</span></p></li><li><p><span style="font-size:16.0px"><b>Benefit from various, sustainable corporate discounts</b>, sports options, and different mobility concepts, such as a company bicycle. Receive an attractive bonus for each employee you recruit as part of our employee referral program. Make provisions for your future with our capital formation program and take out a company pension plan supported by us.</span></p></li><li><p><span style="font-size:16.0px"><b>Experience the Camelot Spirit</b> through regular company, social, or sports events. Network, get into professional discussions, and stay informed through our internal communication platforms and formats, e.g., Lunch Roulettes, Knowledge Nuggets, and Townhall Meetings.</span></p></li></ul><p></p><ul></ul></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:18.0px;word-wrap:break-word"><h2 style="font-size:1.0em;margin:0.0px"><b>Camelot – Strategy. Innovation. Solution.</b></h2> </div><div><p></p><p><span style="font-size:16.0px">We are a global management and technology consulting firm focusing on value chain management. Our mission: turning our clients’ value chains into a competitive advantage and creating lasting impact where our clients need it most. By combining our industry focus, value chain process expertise, and technology know-how, we guide our clients from strategy to sustainable technology adoption.</span></p><p></p><p><span style="color:#808080"><span style="font-size:16.0px"><em>Camelot is committed to diversity. DEIB is firmly anchored in our corporate values, CSR activities and entrepreneurial actions. As proudsignatories of the Diversity Charter, our doors are open to all talent – regardless of gender, nationality, ethnicity, religion, physical ability, age,sexual orientation, and identity. At Camelot, we welcome you for who you are.</em></span></span></p><p></p><p><span style="font-size:16.0px"><span style="color:#808080"><em><b>Be different. Be you. Be Camelot.</b></em></span></span></p><p><span style="font-size:16.0px"><span style="color:#ffffff">#LI-HL1</span></span></p></div></div></div></span></span></div></div></div></div><p class="job-location"><span class="jobmarkets"></span></p></div>

<div class="box" id="inserat-details"><h1>globegarden Alpenquai, Kindertagesstätte in Luzern</h1><div><div class="categories"><div class="display-field-container"><div class="display-label">Kategorie</div><div class="display-field"><a href="/kinderbetreuung">Kinderbetreuung</a> › <a href="/kinderkrippen">Kinderkrippen, KiTas</a> </div></div></div><div class="locations"><div class="display-field-container"><div class="display-label">Standort</div><div class="display-field"> 6005 St. Niklausen LU, <a href="/luzern">Kanton Luzern</a><br/>Alpenquai 28b </div></div></div><div class="description">Moderne Kinderoase direkt am See. Optimale und ruhige Lage in dem beliebtem Wohn- und Arbeitsquartier Alpenquai, Nähe der Kantonsschule.<br/><br/>In unserer Kindertagesstätte betreuen wir Kinder von 3 Monaten bis zum Primarschuleintritt. Unsere globegarden Kinderkrippe arbeitet nach einem eigenen Programm Discovering the world step by step©, welches Kinder spielerisch fördert und jeden Tag für Spass und Spannung sorgt! Vom Säugling bis zum Kindergartenkind bieten wir Kindern eine aktive Lernumgebung mit Möglichkeiten zum Rollenspiel, Kneten, Basteln oder auch einfach zum Zurückziehen und Kuscheln.<br/><br/>Kontaktieren Sie uns für mehr Informationen und um einen Besuch in einer unserer Kinderkrippen zu vereinbaren, denn ein persönlicher Besuch sagt mehr als jede Broschüre.<br/><br/>Kontaktieren Sie uns direkt unter: +41 44 536 55 32 oder E-Mail<br/><a href="/inserate/133145/umleitung?u=CfDJ8EDJWQJ_AGNPiFWQKPQtWBAg6HmW-LKgKnlEd7lAsLyZFXvn39xarcG0H4A6N8W5YGdVnaSHGfiuypgYuGmoZUkRQMhLmg5SmibjwtxPX2yyzkZG4wBfpgIk9vb7PWZNZAmqAev2MlGdDzoi8AUac3s_LB8c-ostLry-eVlS11IJ" rel="nofollow" target="_blank">www.globegarden.ch/locations/alpenquai</a><br/><br/>Finden Sie einen globegarden in Ihrer Nähe:<br/><a href="/inserate/133145/umleitung?u=CfDJ8EDJWQJ_AGNPiFWQKPQtWBDuNNheRwfOCIMLPQNQfLHm3ljuOHrtccJPI8-x-p00TcTUKjaORjpm5rMuLgSjR1THUpmh1sTXhuz7xj20GJuD7gLWmburws1nOAZ_ll1T3XEZI9xRj9Qd1GlB9fDAxgM" rel="nofollow" target="_blank">www.globegarden.ch</a><br/><br/>Oder erfahren Sie mehr über die globegarden Kinderkrippen Zürich, Zug, Schaffhausen, Luzern, Basel auf: <a href="/inserate/133145/umleitung?u=CfDJ8EDJWQJ_AGNPiFWQKPQtWBC1DFg2pxbaq7C7NMpg0qhyc72vQNo-dtWUpqlzU_ktFppc5dxQkb4vYMKKJZwP14E0FDJ4A6Z5ufHS5GlS9CDirbHQjrC3iyIRtj9vUG4TTpb4QmoWQwZi3xB5GWjnITg" rel="nofollow" target="_blank">www.facebook.com/globegarden</a><br/><br/>--------------------------------------------<br/>Modern childrenll look closely, ask a lot of questions, bring along grandparents or friends, compare us to other centers and take the time you need to feel confident in this important decision.<br/><br/>Contact us directly: +41 44 536 55 32 or E-Mail<br/><a href="/inserate/133145/umleitung?u=CfDJ8EDJWQJ_AGNPiFWQKPQtWBBzcf9FQOeSA135ylnLf3hyJkAmBU9l3eUQxiRBSNPPN3BttKskSihN44mE-zG1L39hokj5FbeXakCCpb43jaaUEO48iiSBvZn5KqDWZZhSIbLJtzRKnJk0V0TxCTFMMdb6a91jJNXbis0l_GQbizYB" rel="nofollow" target="_blank">www.globegarden.ch/locations/alpenquai</a><br/><br/>Find a globegarden childcare center in your neighborhood:<br/><a href="/inserate/133145/umleitung?u=CfDJ8EDJWQJ_AGNPiFWQKPQtWBALiqQx64mH9gIBDj-2MYfKfUZr6WK8PSlnaMVXvloa9NEM0Q_PPmQ2LCpdIHjCup4sZ4azJfA9qhaFcHE75mV6Ub10CGP36nTIrcywHj-2n3UL5H65dWvC_kFLut6kL50" rel="nofollow" target="_blank">www.globegarden.ch</a><br/><br/>Take a peek at daily activities at the nursery and preschool:<br/><a href="/inserate/133145/umleitung?u=CfDJ8EDJWQJ_AGNPiFWQKPQtWBCiYyg7iQE6Ds-eAwwasWpams4QThs9JYXbQWKY7OF3D6RAJ8270HLREZiElpU7tXxLoYVWfFFN4XGzHSOPhfRPGEdJW0M-WTJmPhSn74B4tZcAO85zrMGm8377IYR2fwU" rel="nofollow" target="_blank">www.facebook.com/globegarden</a></div> <div class="pictures"><img alt="Bild 1: globegarden Alpenquai, Kindertagesstätte in Luzern" src="/inserate/133145/bilder/1"/></div><div class="toolbar"><ul><li> Inserat 133145 vom 03.03.2025 </li></ul></div></div></div>

<h3>Einleitung</h3><p>Das Park Hotel Vitznau - Eine Oase für alle Sinne! Die exquisiten Räumlichkeiten bestechen durch hohen Komfort, die luxuriöse Ausstattung mit erlesenen Materialien, modernsten technischem Equipment und einer einmaligen Wohlfühlatmosphäre. Verschiedene Themenwelten verleihen jedem Raum seine individuelle Geschichte – so individuell wie seine Gäste. Für kulinarische Höhenflüge sorgen unsere mit Michelin Sternen und Gault Millau Punkten ausgezeichneten Restaurants. </p> <p>Die Neuro-Rehabilitationsklinik cereneo ist direkt mit dem Park Hotel Vitznau, am Vierwald-stättersee, verbunden. Hier trifft modernste Wissenschaft auf einfühlsame, individuell abgestimmte Behandlungskonzepte. Mit innovativen Ansätzen und massgeschneiderten Therapien sorgt cereneo dafür, dass jeder Patient in einer Umgebung der Ruhe und Regeneration wieder neue Lebensqualität gewinnt.</p> <p><strong>Deine kulinarische Reise beginnt in unserem Recruiting Video:</strong><strong> </strong>HVLL (@hvll_official) | TikTok</p> <p> </p> <p><strong>Gut zu Wissen:</strong><br /> - Teilzeitpensen sind möglich</p> <p>- Spannende Arbeitszeitmodell mit variabler Dienstplangestaltung</p> <p>- Trinkgeld: Du wirst am Trinkgeld des Hotelbereichs beteiligt, denn es gilt : One Team one Dream</p><h3>Deine Skills</h3><ul><li>Du hast Freude am Umgang mit Menschen und verfügst über ein professionelles und freundliches Auftreten</li> <li>Du besitzt ausgezeichnete, sowie breit aufgestellte handwerkliche Fähigkeiten</li> <li>Du hast Leidenschaft für Deinen Beruf und die Arbeit am Gast</li> <li>Kommunikationsstärke, sowie vielseitiges Interesse zeichnet Dich aus</li> <li>Kalkulation, Preisvergleiche und Einkaufsmanagement gehört zu deinen Stärken</li> <li>Du hast ein gutes Gefühl für die Weiterentwicklung einer Guest Experience und bist aufgestellt gegenüber Neuerungen und Technologien</li> <li>Du bringst Erfahrung mit in einem ähnlichen Betrieb, einer komplexen Grossküche oder einer zentralen Produktionsküche</li> <li>Du besitzt gute Deutsch- und Englischkenntnisse, weitere Fremdsprachen sind von Vorteil</li> <li>Sichere EDV Kenntnisse sind für Dich eine Selbstverständlichkeit</li> <li>Du denkst und handelst unternehmerisch mit dem Schwerpunkt Mitarbeiter- und Warenkosten und bringst gute betriebswirtschaftliche Kenntnisse mit</li> <li>Du besitzt «hands-on» Mentalität und bist ein Organisationstalent</li> </ul><h3>Deine Mission</h3><ul><li>Du bist verantwortlich für die operative Leitung der Klinik cereneo Küchen (Park Hotel Vitznau und Campus Hotel Hertenstein)</li> <li>Du bist verantwortlich für die Führung, Anleitung, Motivation und Schulung von 2 Mitarbeitern</li> <li>Du pflegst den direkten Patientenkontakt und eruierst deren Bedürfnisse</li> <li>Du fungierst als Ansprechpartner für die Klinik und bist für die reibungslose Kommunikation zwischen Klinikpersonal und Küche zuständig</li> <li>Du nutzt Ressourcen effizient und schöpfst Synergien im Team aus</li> <li>Du entwickelst ein innovatives und gästeorientiertes Verpflegungsangebot für ca. 30 Patienten der cereneo Klinik</li> <li>Du führst Schulungen und Coachings für die Küchen-Mitarbeiter durch und unterstützt deren Entwicklung</li> <li>Du optimierst Produktionsabläufe und kalkulierst die Gerichte in einer stets aktuellen Rezeptdatenbank, um ein effizientes Cost-Controlling sicherzustellen</li> <li>Du pflegst eine vorbildliche Lagerbewirtschaftung und erfasst die Lagerbestände regelmässig</li> <li>Du stellst Qualitäts- und Hygienevorgaben sicher und bist für dessen Einhaltung zuständig</li> <li>Du pflegst einen engen Austausch mit den anderen Küchenchefs der Gruppe und unterstützt die HVLL Küchen zu Spitzenzeiten punktuell</li> </ul><h3>Deine Goodies</h3><ul><li><u>Unterkunft & Parkplatz:</u> Unsere möblierten und preiswerten Personalzimmer sowie auch Mitarbeiterparkplätze befinden sich in unmittelbarer Nähe zum Hotel. </li> <li><u>Finanzielles:</u> Wir bieten positionsgerechte Entlöhnung, überobligatorische Pensionskassenleistungen und beteiligen Dich am Unternehmenserfolg. </li> <li><u>Entwicklung:</u> Wir unterstützen Deine persönliche und berufliche Entwicklung mit einer Vielzahl an internen und externen Schulungen durch unsere «be different Academy».</li> <li><u>Rabatte/Prämien:</u> Du profitierst von Employee & Family Raten in unseren Hotels, Vermittlungsprämie für angeworbene Mitarbeitende, Teildienst-Prämie, Zuschuss für die KiTa in Vitznau und vieles mehr… </li> <li><u>Gesundheit/Freizeit:</u> Verwöhne Dich täglich mit leckeren Speisen im preiswerten Mitarbeiterrestaurant und geniesse den Freizeitbereich inkl. Gym in unserem «Schiff Ahoi». Wir bieten ein breitgefächertes Angebot für Aktivitäten in der Region und organisieren jährlich tolle Mitarbeiterevents.</li> <li>... und viele weitere Benefits findest Du hier: HVLL – Hospitality Visions Lake Lucerne AG</li> </ul>

<p>Möchtest du die operative Exzellenz in unserer Logistikzentrale Herdern, Stadt Zürich, vorantreiben? Bist du bereit, deine Expertise im Lean Management einzubringen, um unsere Organisation weiterzuentwickeln und nachhaltige Effizienzsteigerungen zu erzielen? Dann bist du bei uns genau richtig!</p><br/><h2>Was du bewegst</h2><p><ul><li>Fachliche Leitung der Lean Transformation in der Logistikzentrale Herdern </li><li>Einführung und Weiterentwicklung von Lean Methoden (z.B. Shopfloor Management, Zielkaskadierung)</li><li>Training und Coaching von Teams und Abteilungen in der Anwendung der Lean Methoden</li><li>Leitung von Verbesserungsprojekten zur Verschwendungsreduktion (z.B. mittels Prozess- und Potenzialanalysen)</li><li>Planung und Umsetzung von Kommunikationsmassnahmen entlang der Lean Transformationen</li><li>Enge Begleitung von Führungskräften und Mitarbeitenden zur Unterstützung im Veränderungsprozess</li><li>Identifizierung von Handlungsfeldern für Verbesserungen und Ableitung von Massnahmen</li></ul></p><br/><h2>Was du mitbringst</h2><p><ul><li>Abgeschlossenes Studium (Uni/ETH, FH, HF) · oder Ausbildung im Bereich Logistik, Betriebswirtschaft oder einem verwandten Feld</li><li>mehrjährige · Führungs- und Berufserfahrung im Lean Management, in einer Produktions- oder Logistikumgebung</li><li>Deutsch (verhandlungssicher) · </li><li>Erfahrung in der Projektleitung und im Umgang mit Stakeholdern auf verschiedenen Unternehmensstufen </li><li>Fundierte Kenntnisse in der Anwendung von Lean-Methoden und -Prinzipien</li><li>Ausgeprägte Kommunikationsfähigkeiten und Überzeugungsstärke</li><li>Gute laterale Führungs- und Sozialkompetenz</li><li>Hohe Eigeninitiative sowie eine proaktive und systematische Arbeitsweise</li><li>Teamgeist und die Fähigkeit, andere zu motivieren und zu befähigen</li></ul></p><br/><h2>Was wir dir bieten</h2><p><ul><li>Zentraler Arbeitsort · Arbeiten in Zürich West</li><li>Gesund arbeiten · Gesundheitsfördernde Angebote wie Massagen und Gesundheitschecks</li><li>Flexible Arbeitszeit · Private und berufliche Ansprüche vereinbaren</li><li>Kinderbetreuung · In der hauseigenen Kinderkrippe «Wirbelschloss»</li><li>Mobilität · Mit dem einmaligen Freizeitbonus pro Jahr von insgesamt max. CHF 500.– beteiligen wir uns an deinem ÖV-Abo</li><li>Handy-Abo · Du darfst dich auf Sonderkonditionen für das Handy-Abo freuen</li><li>Sozialleistungen · Faire Sozialleistungen</li><li>Berufliche Vorsorge · Hervorragende Pensionskassenleistungen mit hoher Arbeitgeberbeteiligung</li><li>Verpflegung · Vergünstigung im Personalrestaurant</li><li>Cumulus-Punkte · Du erhältst zusätzliche Cumulus-Punkte beim Einkaufen</li><li>Migros Bank · Vorzugszinsen bei Privat- und Anlagekonto, kostenlose Kontoführung, vergünstigte Hypotheken und mehr</li><li>Mitarbeiterangebote · Es warten viele weitere Vergünstigungen bei Migros- und Partnerbetrieben auf dich</li><li>Ferien · Du profitierst von 5 Wochen Ferien pro Jahr</li><li>Klubschule Migros · Beteiligung an den Kurskosten in der Klubschule</li><li>Freizeit- und Kulturangebote · Du profitierst von vergünstigten Tickets bei ausgewählten kulturellen Veranstaltungen</li><li>Sport- und Fitnessangebote · Du kannst einmalig pro Jahr einen Freizeitbonus von insgesamt max. CHF 1000.– z. B. für ein Jahresabo fürs M-Fitnesscenter einlösen</li><li>Gezielte Förderung · GMZ Young Talents Community: du beteiligst dich an spannenden Projekten unserer Community und nimmst an Events teil, die dich weiterbringen</li><li>Aus- und Weiterbildung · Unterstützung bei berufsbezogener Aus- und Weiterbildung, Jährlicher Bildungsbonus im Wert von CHF 1000.–</li><li>Gestaltungs- und Entscheidungsspielraum · Verwirkliche deine innovativen Ideen</li><li>Sozial- und Personalberatung · Interne Sozialberatung</li></ul></p><br/><h2>Bewerbung & Kontakt</h2><p>Laila Ulmann<br/>Leiterin HR Marketing & Rekrutierung<br/>+41 58 561 56 71<br/> E-Mail schreiben </p>

<div class="content-box"><div class="post-177623 post type-post status-publish format-standard hentry tag-chefredaktor-in tag-jounalistin-in tag-onlineredaktor-in tag-redaktor-in tag-datenjournalist-in tag-crossmedia-journalist-in ctx_prof_group-medien-journalismus-verlage ctx_work_location-nord-ostschweiz-fl ctx_flake_location-wittenbach" id="post-177623" itemprop="description"><div class="company-logo"><img alt="Ostschweiz Druck AG logo" src=" https://medienjobs.ch/content/uploads/2024/07/firma15250.jpg"/&gt;&lt;/div&gt;&lt;div class="add-post-on add-post-on--mobile"><div>Anzeige vom:</div><div><time datetime="2025-02-04">04.02.2025</time></div></div><div class="intro"><p>Wir sind ein modernes und familiengeführtes Unternehmen, welches sich mit dem neusten Maschinenpark und einem motivierten Team den Herausforderungen der grafischen Branche stellt.</p><p>Ab Juni 2025 oder nach Vereinbarung, haben wir folgende Stelle neu zu besetzen: </p></div><h1>Korrektor/in ca. 80%</h1><div class="description"><p><strong>Deine Aufgaben:</strong></p><ul><li>Einwandfreies Korrekturlesen von Fach- und Publikumszeitschriften sowie von Texten im Akzidenzbereich hinsichtlich Orthografie, Grammatik, Syntax, Zeichensetzung und Typografie</li><li>Bogenrevisionen auf Vollständigkeit überprüfen</li><li>Arbeitszeiten: tagsüber</li></ul><p><strong>Dein Profil:</strong></p><ul><li>Korrektorenausbildung oder sattelfester Quereinsteiger mit entsprechenden Kenntnissen</li><li>Deutsche Muttersprache, sehr gute Französischkenntnisse</li><li>Italienisch- und Englischkenntnisse von Vorteil, aber nicht Voraussetzung</li><li>Mehrjährige Erfahrung im Korrekturlesen</li><li>Von Vorteil: Kenntnisse der Korrekturzeichen sowie typografisches Grundwissen</li><li>Du arbeitest selbstständig und bewahrst auch unter Termindruck Ruhe und Konzentration</li></ul><p>Gerne erwarten wir deine vollständige Bewerbung per E-Mail an Pietro Lira. <a href=" E-Mail schreiben " target="_blank"> E-Mail schreiben </a></p></div><div class="job-location"><h3 class="heading">Arbeitsort</h3><p class="arbeitsort-location">Wittenbach <a class="arbeitsort-location-link" href=" http://map.search.ch/wittenbach/hofstetstr.%2014 " target="_blank">Kartenansicht <span class="icon-arrow"></span></a></p></div><div class="cols-1 address-block"><div class="col-1"><h3 style="margin-bottom: 0">Ostschweiz Druck AG</h3><p>Herr Pietro Lira</p><p>Hofstetstrasse 14</p><p>9300 Wittenbach</p><p><a class="job-phone-deatils" href="tel:+41 71 292 29 29">+41 71 292 29 29</a></p><p><a class="job-phone-email" href=" E-Mail schreiben "> E-Mail schreiben </a></p> </div> <!--/.col-1--><div class="col-2"><h3 style="margin-bottom: 0">Links</h3><p> <a class="job-phone-website" href=" http://www.ostschweizdruck.ch " target="_blank">Website</a></p><p> <a href=" https://www.facebook.com/ostschweizdruck " target="_blank">Facebook</a></p><p> <a href=" https://www.instagram.com/ostschweizdruck " target="_blank">Instagram</a></p> </div> <!--/.col-2--></div></div><div class="meta"><hr/><p>Finden Sie alle Stellenangebote von <a href=" https://medienjobs.ch/arbeitgeber-firma/ostschweiz-druck-ag/"&gt;Ostschweiz Druck AG</a> aus <a href=" https://medienjobs.ch/arbeitsort/wittenbach/"&gt;Wittenbach&lt;/a&gt;&lt;/p&gt;&lt;/div&gt;&lt;/div&gt ;

Le Garage-Carrosserie Baechler & Fils SA à Corminboeuf, fort dautomobiles 100% H/FTâches principales : Assurer lun CFC de mécanicien, mécatronicien ou équivalent Vous êtes désireux dévoluer avec les dernières technologies de véhicules Flexible et résistant au stress, vous possédez la capacité de travailler en équipe Vous êtes dynamique, mo vé et persévérant Grand sens de la communica on, ap tude à développer une rela on de confiance avec les clients et les collaborateurs Connaissances des véhicules du groupe Stellan s est un grand atout Maîtrise du français à l'oral Cete offre vous intéresse ?Nous atendons votre dossier de candidature complet (letre de mo va on, CV, diplômes et préten ons salariales) par courriel à E-Mail schreiben Garage-Carrosserie Baechler & Fils SA - Route du Centre 7 - 1720 Corminboeuf - www.garagebaechler.ch

<h3></h3><p>Im Migros Take Away Seedamm-Center werden täglich frische und saisonale Speisen angeboten. Aus einer grossen Auswahl können sich unsere Gäste den ganzen Tag über verpflegen. Für unser motiviertes Team suchen wir zur Ergänzung eine dienstleistungsorientierte Persönlichkeit.</p><h3>Ihr Profil</h3><ul><li>Bildung: Abgeschlossene Berufslehre (EFZ) Im Bereich Gastronomie</li><li>Berufserfahrung: 2-3 Jahre Berufserfahrung Im geforderten Bereich</li><li>Berufserfahrung in der Gastronomie/Hotellerie oder im Detailhandel</li><li>Erste Berufserfahrung in der Systemgastronomie</li><li>Flexible Einsatzbereitschaft von Montag bis Samstag in verschiedenen Schichten (Früh- und Spätdienste)</li><li>Effiziente und ordentliche Arbeitsweise </li><li>Motivierte, dienstleistungsorientierte und humorvolle Teamplayer-Persönlichkeit</li><li>Deutsch (sehr gute Kenntnisse)</li></ul><br /><h3>Ihre Aufgaben</h3><ul><li>Kundenbedienung, Beratung sowie aktiver Verkauf</li><li>Kassenbedienung inkl. Inkasso</li><li>Fachliche Verantwortung während der Schicht</li><li>Bewirtschaftung der Buffets und Vitrinen sowie ansprechender Warenpräsentation</li><li>Diverse Mise en Place Arbeiten sowie die Zubereitung von Getränken und Speisen</li><li>Pflege der Maschinen und Arbeitshilfsmittel sowie diverse Entsorgungsarbeiten</li><li>Einhaltung der GMZ-Qualitätsstandards und Richtlinien</li></ul><br /><br /><h3>Wir bieten</h3><br /><ul><li>Handy-Abo: Du darfst dich auf Sonderkonditionen für das Handy-Abo freuen</li><li>Berufliche Vorsorge: Hervorragende Pensionskassenleistungen mit hoher Arbeitgeberbeteiligung</li><li>Sozialleistungen: Faire Sozialleistungen</li><li>Verpflegung: Vergünstigung im Personalrestaurant</li><li>Cumulus-Punkte: Du erhältst zusätzliche Cumulus-Punkte beim Einkaufen</li><li>Migros Bank: Vorzugszinsen bei Privat- und Anlagekonto, kostenlose Kontoführung, vergünstigte Hypotheken und mehr</li><li>Klubschule Migros: Beteiligung an den Kurskosten in der Klubschule</li><li>Freizeit- und Kulturangebote: Du profitierst von vergünstigten Tickets bei ausgewählten kulturellen Veranstaltungen</li></ul><br />

Job ID REQ-10040901 Feb 19, 2025 Switzerland Summary Location: Basel, Switzerland Role Purpose: As Formulation Specialist / Expert Science and Technology in Oral Pharmaceutical Development, you will design, plan, perform, interpret, and report results of scientific experiments to ensure the timely development of drug product formulations and manufacturing processes or innovation projects. Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people-s lives. To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies, data & digital, and building specific therapeutic areas and platform depth and capabilities - all to bring our medicines to patients even faster. We are seeking key talent, like you, to join us and help give people with disease and their families a brighter future to look forward to. About the Role The role: Position purpose The purpose of this role is to develop our growing pipeline of oral products. We are looking for an expert in the area of Oral Solid Dosage Forms (small molecules, NCE). As a member of the team, you will play a key role in the development of formulations and processes for oral dosage forms with end-to-end scope, from first-in-human trials to marketing phase. You will plan, perform and document scientific experiments for formulation- and process development for preparation and timely delivery of drug products incl. support at GMP manufacturing, primarily in the area of Oral Solid Dosage forms. You will participate in scientific teams and contribute to the overall Technical Research and Development strategies and goals. Major accountabilities For the development of oral solid dosage forms we are looking for an experienced associate. Your duties will be to develop formulations of capsules, film coated tablets or sachets, to develop manufacturing processes including scale-up. In addition, you will support the process transfer to GMP Pilot Plant and Novartis Technical Operations (TechOps) sites, and support the manufacture of clinical supplies under a GMP environment. Your responsibilities will be to plan, perform scientific experiments (or pilot plant processes) for formulation- and process development under minimal guidance from team members and to contribute to the interpretation and report results. You have experience in actively applying digital tools e.g. for reporting of experiments, and are experienced and curious to utilize and to further advance data&digital tools. Your accountabilities will include: Plan, coordinate, perform and document scientific experiments in collaboration with functional and project leads Develop phase appropriate formulations for oral drug products Develop efficient and robust processes for oral drug products Utilize data digital tools (e.g. e-Lab Journal, digital IPC data handling, digital data recording, data visualization tools) Provide raw data documentation, evaluation and interpretation of results Propose and provide input for the design of next experiments Transfer procedures/instructions to GMP production facilities (e.g. Pilot Plant, NTO), including troubleshooting Support the manufacture of clinical supplies under a GMP environment Contribute to investment projects and maintenance of infrastructure/equipment. Adherence to quality, quantity, and timelines for all assigned tasks. Adherence to Novartis standards, in particular, quality, ethical, health, safety, and environment (HSE), and information security (ISEC) standards. Reproducibility of experiments and results. Minimum Requirements: Education: Degree in Pharmaceutical Sciences or a related discipline (e.g. MSc, or BSc with 2 years industry experience or a College of Applied Science Diploma or equivalent, lab technician Apprenticeship with 6 years industry experience and relevant on the job training) with strong experience in formulation development and pre-formulation. Experience in manufacturing under GMP is advantageous. Experience Ideally a minimum of 3 to 5 successful years of experience in pharmaceutical development of oral solid dosage forms, e.g. in lab, technicum or Pilot Plant setting, with experience in the most common pharmaceutical technologies und unit operations. Experience in formulation development / pre-formulation incl related experience with (functional) excipients and on enabling formulations is advantageous. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment. Experience and Severity in actively applying data-digital tools alike e-LabNotebook, digital documentation and data recording tools. Additional experience, e.g. from contribution to the development and advancement of those tools is advantageous. Good scientific or technical knowledge in galenics/pharmaceutical technology / formulation- and/or process development at lab, pilot and production. Excellent user experience of software and computer tools (e.g. electronic documentation). Languages. Proficiency in English required (oral & written), German and/or French is an advantage. Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regulär Shift Work No

<div class="box" id="inserat-details"><h1>Liebevolle Betreuung gesucht zur Unterstützung des Alltags</h1><div><div class="categories"><div class="display-field-container"><div class="display-label">Kategorien</div><div class="display-field"><a href="/seniorenbetreuung">Seniorenbetreuung/-Hilfe</a> › <a href="/pflegehilfe">Begleitung/Pflegehilfe</a>, <a href="/kochen">Kochen/Mahlzeitendienst</a> </div></div></div><div class="locations"><div class="display-field-container"><div class="display-label">Standort</div><div class="display-field"> 8008 Zürich Seefeld, Stadtkreis 8, <a href="/zuerich">Kanton Zürich</a></div></div></div><div class="description">Zur Unterstützung des Alltags unserer Eltern, die gerne zu hause leben. <br/>Kochen, Reinigen, Organisation und Unterstützung, Hilfe bei Körperpflege, <br/>Aktivation, Gesellschaft und Begleitung zu Besuchen, Ausstellungen, Konzerten.</div> <div class="toolbar"><ul><li> Inserat 133892 vom 09.03.2025 </li></ul></div></div></div>

Job ID REQ-10043957 Mar 19, 2025 Switzerland Summary -Directs the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies. Interacts and negotiates with regulatory agency personnel in order to expedite approval of pending registration and answers any questions. Serves as a regulatory liaison on the project team throughout the product lifecycle. Ensures rapid and timely approval on of new drugs, biologics/biotechnology and/or medical devices and continued approved status of marketed drugs or medical devices. Serves as regulatory representative to marketing or research project teams and government regulatory agencies. Provides advice to development and/or marketing teams on manufacturing changes, line extensions, technical labeling, appropriate regulations and interpretations. Coordinates, reviews, and may prepare reports for submission. About the Role Major accountabilities: Is responsible for implementing regulatory strategy and managing operational activities for assigned major/ large regions. Provides input into global regulatory strategy and contributes to Regulatory Functional Plan (RFP) and Seed Document, or their equivalents, including identification of gaps or risks in global strategic plan for assigned regions. Partners with regions to align on regulatory strategy in order to fulfil business objectives -Implements RFP across assigned regions. Determines requirements and sets objectives for Health Authority (HA) interactions with DRA GPT representative and/or GTAL. Facilitates preparation and finalization of briefing books and contributes to preparation of summary documents. Develops and implements plans for timely response to HA requests and coordinates responses. May serve as local HA liaison depending on location (e.g., FDA or EMA). Drives coordination, planning, and submission of dossiers in assigned regions worldwide. Review of global dossier summary documents. Develops and implements plans to avoid/minimize clock stops during submission review. Reviews, approves and submits Clinical Trial Applications (CTAs) and Investigational New Drugs (INDs). Reviews and submits Risk Management Plans. May lead negotiations for regional approvals independently or with DRA GPT representative and/or GTAL. Responsible for facilitating timely submission and approval of dossier with HAs under the guidance of the DRA GPT representative and/or GTAL. Contributes to and often leads the development of departmental goals and objectives. Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Key performance indicators: Successful implementation of global regulatory strategy for timely submissions and approvals with the best possible labels based on available data. Identification of main HA issues -Participation in relevant regulatory Boards leading to valuable input from these Boards. Successful Participation in HA interactions to achieve business objectives. Adherence to Novartis policy and guidelines -Project & stakeholder feedback Minimum Requirements: Work Experience: Cross Cultural Experience. Functional Breadth. Project Management. Operations Management and Execution. Representing the organization. Skills: Clinical Trials. Cross-Functional Teams. Detail Oriented. Drug Development. Lifesciences. Negotiation Skills. Problem Solving Skills. Regulatory Compliance. Risk Management. Languages : English. Location: Basel, Switzerland or UK, London Hybrid working requirement 3 days / 12 days per month in office. Why Novartis : Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together?: https://www.novartis.com/about/strategy/people-and-culture&nbsp ; Commitment to Diversity & Inclusion : Novartis is committed to building an outstanding, inclusive work environment and diverse team-s representative of the patients and communities we serve. Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Alternative Location 1 London (The Westworks), United Kingdom Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Job ID REQ-10043044 Mar 19, 2025 Switzerland Summary Responsible for the development and implementation - including adequate training to staff, efficiency, gap assessment and continuous improvement and performance - as well as operational support of assigned regulatory processes, as applicable and in close collaboration with the Process Director and other functions as applicable, to ensure organizational readiness and compatibility with associated systems and technology and compliant with global regulatory requirements and Novartis standards. About the Role Key Responsibilities: For assigned processes: Drive Business process creation, review by Process Review Committee (or equivalent), continuous improvement (including system, technology and automation needs to improve process performance). This includes developing, authoring/writing (as applicable) and maintaining procedural documents, establishing KPI and working with Training & Capability team members to provide associated functional training. Actively shepherd the process documents through the preparation process, self-author/write or provide guidance to author(s) on the content of a procedural document with respect to the process. In partnership with International / Regions and Policy, monitor and review emerging regulations and regulatory guidelines and analyze impact on Novartis regulatory processes Contribute to inspections and internal audits as applicable. Provide direct input and expertise in the areas of process design, risk management, governance, organizational design and compliance. Pressure-tested and risk-mitigate plans for transition from old to new/revised processes Ensure high level of connectivity, alignment, transparency and collaboration with Subject Matter Experts (SME) across RA and with other Development and corporate functions and departments, as required. In partnership with Systems team, incorporate technology portfolio deliverables into integrated transformation roadmap as well as any other non-drug development projects that have bearing on the broader transformation. Contribute to learning/training strategy for regulatory capability building, functional learning and learning technology. Document Control Mastery: Ensure meticulous version control and accessibility of quality documents (eg. SOP, WP, BPG), adhering to industry standards. SOP operational management: Example: (opening and completing the Change request in relevant system, sending draft SOP for QMS review, getting the SOP uploaded in eSOPS, etc). to 'shepherd' the procedure through the procedure creation/update process. Essential Requirements: Life Science Degree or other University degree with equivalent experience Regulatory and drug development experience Strong knowledge on E2E process, supporting system, regulations and business change(s). Strong working knowledge of QMS, SOPs and compliance Strong process authoring/writing capabilities Technology-savvy - ability to leverage and use systems, technology and automation (including digital assistants and AI tools) to derive efficiency in processes Ability to anticipate the impact of any change(s) from external and internal sources to the E2E process, to supporting systems and training Ability to effectively contribute to teams in a matrix environment Analytic, influencing, and communication skills. Ability to define metrics Process simplification and optimization Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? : https://www.novartis.com/about/strategy/people-and-culture Commitment to Diversity & Inclusion : Novartis is committed to building an outstanding, inclusive work environment and diverse team-s representative of the patients and communities we serve. Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

<div class="box" id="inserat-details"><h1>Zentrum für Kinder und Familien im Reusstal</h1><div><div class="categories"><div class="display-field-container"><div class="display-label">Kategorie</div><div class="display-field"><a href="/kinderbetreuung">Kinderbetreuung</a> › <a href="/betreuung">Kinderbetreuung Diverse</a> </div></div></div><div class="locations"><div class="display-field-container"><div class="display-label">Standort</div><div class="display-field"> 5524 Nesselnbach, <a href="/aargau">Kanton Aargau</a><br/>Landstrasse 1a </div></div></div><div class="description">Herzlich willkommen in der Kinderlaube - Dem Begegnungsort für Kinder und Familien im Reusstal.<br/><br/>Wir bieten Kurse, Spielgruppen und Nachmittagsbetreuung für Kinder von 6 Monaten bis 7 Jahre<br/><br/>Bei uns können Sie Ihr Kind für einzelne Angebote anmelden und brauchen sich nicht gleich für ein ganzes Jahr für etwas zu entscheiden. Oder suchen Sie kurzfristig eine pädagogisch, wertvolle Beschäftigung für ihr Kind, weil Sie dringend etwas erledigen müssen? Auch dies ist bei uns möglich. Oder arbeiten Sie spontan im Homeoffice und suchen eine kurzfristige Betreungsmöglichkeit für ihr Kind. Auch da können wir Sie bestimmt unterstützen.<br/><br/>Während den Ferien bieten wir jeweils während einer Woche ein Ferienprogramm an. <br/><br/>Auf unserer Homepage finden Sie alle Angebote und Informationen und können sich natürlich auch einen Platz reservieren.<br/><br/>Wir freuen uns auf Ihren Besuch<br/>Das Kinderlaube-Team<br/><a href="/inserate/131228/umleitung?u=CfDJ8EDJWQJ_AGNPiFWQKPQtWBD4lodTw46tL5sSjTd51qhhP29o14_r1o8I7u7DflLWc7RTr1uXdwB4sd0AMNXqYC_NGcl6bX5ngWNKOPDsDMsQ0DSIpzbc6nxKvpUT-9FGobso6mLz9AmQEqFYvByPOz4" rel="nofollow" target="_blank">www.kinderlaube.ch</a></div> <div class="pictures"><img alt="Bild 1: Zentrum für Kinder und Familien im Reusstal" src="/inserate/131228/bilder/1"/><img alt="Bild 2: Zentrum für Kinder und Familien im Reusstal" src="/inserate/131228/bilder/2"/><img alt="Bild 3: Zentrum für Kinder und Familien im Reusstal" src="/inserate/131228/bilder/3"/><img alt="Bild 4: Zentrum für Kinder und Familien im Reusstal" src="/inserate/131228/bilder/4"/></div><div class="toolbar"><ul><li> Inserat 131228 vom 24.03.2025 </li></ul></div></div></div>

Job ID REQ-10036470 Jan 22, 2025 Switzerland Summary ~ Diese Rolle nutzt chemische Laborfähigkeiten, um Produkte oder Materialien zu testen und zu messen und gleichzeitig sicherzustellen, dass die Analyse gemäß etablierten Standard Operating Procedures (SOPs), Analytischen Methoden und aktuellen Kompendien durchgeführt wird. About the Role Ihre Haupttaetigkeiten: Probenlagerung und -verwaltung Analytische Prüfung/Dokumentation von Arzneimitteln/Fertigprodukten/Reklamationen/Stabilität/Verpackungsmaterialproben nach GxP-Standards Testen/Beispielspeichern und -management . Analytische Dokumentation von Stabilitätsproben nach GxP-Standards Validation Erfahrung: Fundierte technische und wissenschaftliche Kenntnisse der pharmazeutischen/ chemischen Analytik/QC/Äquivalentes Arbeitserfahrung in einer Laborumgebung in der pharmazeutischen Industrie Sprachen : Englisch & Deutsch Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Operations Business Unit Innovative Medicines Location Switzerland Site Basel (Land) Company / Legal Entity C049 (FCRS = CH028) Novartis Pharma Schweizerhalle AG Functional Area Quality Job Type Full time Employment Type Befristet (Befristet) Shift Work No

<div class="css-oplht1" data-automation-id="jobPostingDescription"><p>Wer sich für eine Karriere bei <b>Lombard Odier</b> entscheidet, ist für einen renommierten, globalen Vermögensverwalter und Asset Manager tätig, der sich auf nachhaltige Investitionen fokussiert. Wir sind eine unabhängige und innovative Bank erster Wahl für private und institutionelle Kunden. Unsere Gruppe ist eine der bestkapitalisierten weltweit. Wir verwalten rund CHF 300 Milliarden und sind auf vier Kontinenten von über 25 Niederlassungen aus tätig.</p><p></p><p>Mit unserer über 225-jährigen Geschichte sind wir ein Investmenthaus mit umfassendem Angebot an diskretionärer und beratender Portfolioverwaltung sowie <span style="word-break: break-word; word-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto; -webkit-hyphens:auto; -ms-hyphens: auto; -moz-hyphens: auto;">Finanzdienstleistungen.</span> Unsere hochmoderne <span style="word-break: break-word; word-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto; -webkit-hyphens:auto; -ms-hyphens: auto; -moz-hyphens: auto;">Technologie-Plattform</span> vermarkten wir auch erfolgreich an andere Finanzinstitute. Über <b>Lombard Odier Investment Managers</b> bieten wir <span style="word-break: break-word; word-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto; -webkit-hyphens:auto; -ms-hyphens: auto; -moz-hyphens: auto;">Vermögensverwaltungsdienstleistungen</span> und Anlagestrategien an.</p><p></p><p><b>"Rethink Everything" ist unsere Philosophie</b> – sie steht im Zentrum unseres Handelns. Wir sind durch mehr als 40 Finanzkrisen stärker geworden, indem wir die Welt um uns herum ständig neu gedacht haben. So bieten wir unseren Kundinnen und Kunden stets neue Anlageperspektiven.</p><p></p><p></p><p><b>Assistant(e) de Gestion - Lausanne</b></p><p></p><p>Au sein de notre bureau de Lausanne, vous ferez partie dévaluation du portefeuille, les soldes de comptes, les opérations, etc</li><li>Traiter les ordres de transfert, assurer les call-back</li><li>Assurer la liaison avec les fournisseurs de services internes afin douverture de compte et traiter les <span style="word-break: break-word; word-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto; -webkit-hyphens:auto; -ms-hyphens: auto; -moz-hyphens: auto;">ouvertures/fermetures</span> de compte tout en respectant les processus/politiques internes strictes de la banque</li><li>Fournir un soutien pour les présentations PowerPoint, les feuilles de calcul et le matériel de traitement de texte ainsi que pour des projets spécifiques</li><li>Soutenir les activités de marketing de lactivité</li></ul><p></p><p><b>Contribuer aux initiatives commerciales des équipes:</b></p><ul><li>Aider les banquiers privés à produire le matériel de présentation pour les réunions avec les clients et prospects</li><li>Assister les banquiers privés dans lévénements et/ou dy limiter, le manuel de conformité du bureau local et les politiques et procédures de conformité publiées de temps à autre</li><li>Maintenir des connaissances appropriées pour sADN et les valeurs de Lombard Odier et les respecter en tout temps</li></ul><p></p><p><b>Votre Profil :</b></p><ul><li>Formation bancaire (Diplôme de l’Ecole de Commerce, CFC ou équivalent), HEC, HEG</li><li>Maitrise parfaite du français et de l’anglais, toute autre langue est un atout</li><li>Bonne connaissance des services de Banque Privée (Crédits Lombard, Gestion de Portefeuille, Assurance Vie...) et très à l'aise avec Microsoft Office</li><li>Excellente présentation, facilité et intérêt pour les contacts avec la clientèle</li><li>Diligent, autonome, multitâche et ayant la capacité de prioriser votre charge de travail</li><li>Aptitude à travailler en groupe, flexibilité, attitude constructive</li><li>Sens aigu du service, précision, rigueur et notion accrue de confidentialité</li></ul><p></p><p><b>Fünf Werte definieren die DNA unseres Hauses</b>. <b>Exzellenz</b> motiviert uns, die Besten unseres Gebiets zu sein, und <b>Innovation</b> ermöglicht unseren Fortschritt. <b>Respekt</b> ist das Fundament unserer Interaktionen, und <b>Integrität</b> leitet unser Handeln. Gemeinsam sind wir <b>One Team</b>, das sich mit leidenschaftlichem Engagement in den Dienst unserer Kundinnen und Kunden stellt.</p><p></p><p>Wir fördern eine inklusive und integrative Arbeitsumgebung für unsere Mitarbeitenden. <b>Vielfalt, Gleichberechtigung und Inklusion</b> sind fest in unserem Unternehmensleitbild ‘La Maison’ verankert und wir sind bestrebt, dass unsere Mitarbeitenden sowohl ihre beruflichen als auch ihre persönlichen Ziele verwirklichen können. Wir fördern interne Karrierewege durch individualisierte und kompetenzbasierte Trainingsangebote. Wir sind fest davon überzeugt, dass der Aufbau vielfältiger Teams zu unserem nachhaltigen Erfolg beiträgt und daher Fundament unserer <span style="word-break: break-word; word-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto; -webkit-hyphens:auto; -ms-hyphens: auto; -moz-hyphens: auto;">Unternehmensstrategie</span> ist.</p><p></p><p><b>Es ist eine tolle Gelegenheit, um Teil des Teams zu werden. Alle Bewerbungen werden streng vertraulich behandelt.</b></p></div>

Job ID REQ-10043949 Mar 18, 2025 Switzerland Summary -Directs the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies. Interacts and negotiates with regulatory agency personnel in order to expedite approval of pending registration and answers any questions. Serves as a regulatory liaison on the project team throughout the product lifecycle. Ensures rapid and timely approval on of new drugs, biologics/biotechnology and/or medical devices and continued approved status of marketed drugs or medical devices. Serves as regulatory representative to marketing or research project teams and government regulatory agencies. Provides advice to development and/or marketing teams on manufacturing changes, line extensions, technical labeling, appropriate regulations and interpretations. Coordinates, reviews, and may prepare reports for submission. About the Role Major accountabilities: Is responsible for implementing regulatory strategy and managing operational activities for assigned medium regions. Provides input into global regulatory strategy and contributes to Regulatory Functional Plan (RFP) and Seed Document, or their equivalents, including identification of gaps or risks in global strategic plan for assigned regions. Partners with regions to align on regulatory strategy in order to fulfil business objectives -Implements RFP across assigned regions. Determines requirements and sets objectives for Health Authority (HA) interactions with DRA GPT representative and/or GTAL. Facilitates preparation and finalization of briefing books and contributes to preparation of summary documents. Develops and implements plans for timely response to HA requests and coordinates responses. May serve as local HA liaison depending on location (e.g., FDA or EMA). Drives coordination, planning, and submission of dossiers in assigned regions worldwide. Review of global dossier summary documents. Develops and implements plans to avoid/minimize clock stops during submission review. Reviews, approves and submits Clinical Trial Applications (CTAs) and Investigational New Drugs (INDs). Reviews and submits Risk Management Plans. May lead negotiations for regional approvals independently or with DRA GPT representative and/or GTAL. Responsible for facilitating timely submission and approval of dossier with HAs under the guidance of the DRA GPT representative and/or GTAL. Erroneous decisions result in critical delays and modifications to projects or operations; cause substantial expenditure of additional time, human resources, and funds; and jeopardize future business activity -Contributes to and often leads the development of departmental goals and objectives. Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Key performance indicators: Successful implementation of global regulatory strategy for timely submissions and approvals with the best possible labels based on available data. Identification of main HA issues -Participation in relevant regulatory Boards leading to valuable input from these Boards. Successful Participation in HA interactions to achieve business objectives. Adherence to Novartis policy and guidelines -Project & stakeholder feedback Minimum Requirements: Work Experience: Functional Breadth. Cross Cultural Experience. Operations Management and Execution. Project Management. Skills: Clinical Trials. Detail Oriented. Drug Development. Lifesciences. Negotiation Skills. Regulatory Compliance. Languages : English. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients- lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Benefits and Rewards: Read our handbook to learn about all the ways we-ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Development Business Unit Innovative Medicines Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

<p>Um den Erfolg der Migros weiter auszubauen und neue Schritte in die Zukunft zu tun, suchen wir für unseren Direktionsbereich Group IT des Migros-Genossenschafts-Bundes, Business Unit Migros-Industry, eine erfahrene, engagierte sowie unternehmerisch denkende und handelnde Persönlichkeit.</p><br/><h2>Was du bewegst</h2><p><ul><li>Zusammen mit den SAP Berater*innen erarbeitest du Vorschläge für die Erweiterung bestehender Programme zur optimalen Unterstützung der Business Prozesse</li><li>Du entwickelst und wartest SAP-Applikationen aufgrund von fachlichen und betrieblichen Anforderungen</li><li>Du konzipierst und realisierst Change Requests über den gesamten Lebenszyklus von SAP-Anwendungen hinweg</li><li>Du arbeitest eng mit unserem Near- und Offshore Team zusammen</li><li>Du analysierst und behebst bestehende Softwarefehler zur Störungsbehebung betroffener SAP-Anwendungen</li></ul></p><br/><h2>Was du mitbringst</h2><p><ul><li>Abgeschlossenes Studium (Uni/ETH, FH, HF) · in (Wirtschafts-) Informatik oder gleichwertige Ausbildung</li><li>Mehrjährige praktische Berufserfahrung · in der SAP-Entwicklung (ABAP, ABAP OO, HANA DB) </li><li>Deutsch (fliessend), Englisch (sehr gute Kenntnisse) · </li><li>Du bringst Kenntnisse in und Interesse für verschiedene SAP Module und deren Prozesse mit (Logistik, EWM, MFS, PP, FI/CO, PLM, MDG)</li><li>Du bist ein Experte in Technologien wie Fiori, WebDynPro, Adobe Forms, CDS Views, Cloud-Themen und Schnittstellentechnologien</li><li>Du bist es dir gewohnt und schätzt es, in einem internationalen Team zu arbeiten und strebst eine offene, konstruktive Zusammenarbeit an</li><li>Du arbeitest gerne selbständig und eigenverantwortlich</li></ul></p><br/><h2>Was wir dir bieten</h2><p><ul><li>Mobil-flexibles Arbeitsmodell · Zeitliche und räumliche Flexibilität bei der Erfüllung der Funktion (als Orientierung 40% Home Office)</li><li>Zentraler Arbeitsort · Zentraler Arbeitsort in der Stadt Zürich (Limmatplatz oder Nähe Hardbrücke)</li><li>Eigenverantwortung & Freiraum · Abwechslungsreiches Aufgabenfeld mit hoher Eigenverantwortung</li><li>Mutterschaftsurlaub / Vaterschaftsurlaub · 18 Wochen Mutterschafts- und 4 Wochen Vaterschaftsurlaub</li><li>Gezielte Förderung · Förderung unserer Mitarbeitenden mit gezielten Personalentwicklungsmassnahmen</li><li>Freizeit- und Kulturangebote · Als Hauptsponsor bei Läufen und Events bietet Migros den Mitarbeitenden beschränkte Plätze zum halben Preis an. </li></ul></p><br/><h2>Bewerbung & Kontakt</h2><p>Stephanie Hürlimann<br/>Talent Acquisition Partner</p>

<span style="font-size:14px;">Wir die MANPOWER AG sind im Bereich der Personaldienstleistung tätig. Unsere Aufgabe ist es, Kunden bei der Vermittlung von Temporär- und Dauerstellen bei Auftragsspitzen, zur Auftragssteigerung, bei vorrübergehenden Engpässen, als auch bei der Festvermittlung von Fachpersonal professionell zu unterstützen.<br />Mit Standorten in der ganzen Schweiz können Sie mit uns an der Seite alle ihre Projekte erfolgreich realisieren.<br /><br />Für unseren Kunden in der Region suchen wir eine/n:</span><h2><strong><span style="font-size:18px;">Reifenpraktiker 100% (w/m/d)</span></strong></h2><h2><span style="font-size:16px;"><strong>Deine Aufgaben</strong></span></h2><ul><li><span style="font-size:14px;">Reifenmontage – Aufziehen der Reifen auf die Felgen</span></li><li><span style="font-size:14px;">Allgemeiner Reifen- und Radwechsel</span></li><li><span style="font-size:14px;">Auswuchten</span></li><li><span style="font-size:14px;">Wartungsarbeiten an Personenwagen</span></li></ul><p></p><h2><span style="font-size:16px;"><strong>Dein Profil</strong></span></h2><ul><li><span style="font-size:14px;">Motivierte und speditive Arbeitsweise</span></li><li><span style="font-size:14px;">Körperliche Belastbarkeit</span></li><li><span style="font-size:14px;">Gute Deutschkenntnisse</span></li><li><span style="font-size:14px;">Führerausweis Kat. B</span></li></ul><br /><p></p><span style="font-size:14px;">Marcel Fladrich gibt Ihnen sehr gerne weitere Auskünfte über diese Stelle bekannt. Sie erreichen ihn unter Tel. Nr.+41 58 307 29 24 oder per E-Mail auf <a href=" E-Mail schreiben "> E-Mail schreiben </a><br /><br />In wenigen Schritten können Sie sich auch direkt auf <a href=" http://www.manpower.ch"&gt;www.manpower.ch&lt;/a&gt ; als Gast registrieren und Ihre Bewerbungsunterlagen einreichen.<br /><br />Unser Team freut sich auf Ihre Persönlichkeit.</span>