Novartis AG

LEHRSTELLENALS FACHFRAU/-MANN GESUNDHEIT3-jährige Ausbildung (EFZ) per 1. August 2025DEIN ARBEITGEBERDas Heim Weiermatte beherbergt gut 60 ältere und pflegebedürftige Gäste. Wir bieten ihnen ein angenehmes zu Hause und leisten individuelle Pflege und Betreuung. Dank unseren rund 90Mitarbeitenden ist es uns möglich, den Heimbetrieb sicherzustellen und zum Wohle unsererBewohnenden zu handeln.DEINE HAUPTAUFGABENPflege und Betreuung der Heimbewohner/innenUnterstützung in der AlltagsgestaltungMedizinische Verrichtungen wie Blutentnahmen, Verbandswechsel, Medikamenten richten und verabreichenHauswirtschaftliche AufgabenAdministrative und logistische DienstleistungenDEINE KOMPETENZENFreude und Verständnis im Umgang mit älteren MenschenHohes Verantwortungsbewusstsein und SelbständigkeitFreundliche und aufmerksame PersönlichkeitSinn für praktische TätigkeitenÜbrigens: Die Zeugnisse aus der Sekundarstufe wollen wir zwar sehen, aber für uns zählt deineArt und dein Auftreten mindestens genau so viel. Und noch was: beim Einarbeiten in die fachlich wichtigen Themen lassen wir dich nicht allein.UNSER ANGEBOTBegleitung und Betreuung durch eine BerufsbildnerinInteressante und abwechslungsreiche TätigkeitMotiviertes und gut eingespieltes TeamInnovative und wertschätzende BetriebskulturVergünstigte VerpflegungWeitere attraktive Anstellungsbedingungen (z.B. zusätzliche J&S Ferienwoche)KONTAKTWeitere Auskünfte erteilt dir Tamara Giger, Verantwortliche Bildung Pflege, unterTel. 041 / 494 99 68 oder E-Mail schreiben . Bist du interessiert?Dann freuen wir uns auf deine Bewerbung per E-Mail an E-Mail schreiben

Job ID REQ-10027634 Nov 26, 2024 Switzerland Summary "We-re a team of dedicated and smart people united by a drive to achieve together" The ED, Public Affairs WEC (Austria, Belgium, Netherlands, Portugal, Nordics) will spearhead policy thought leadership for the WEC cluster, staying ahead of emerging trends and aligning with cross-functional teams to drive local and regional policy priorities in WEC cluster countries. The role entails fostering collaboration between countries, providing strategic guidance, and executing advocacy initiatives tailored to the cluster's needs. Building strong networks with stakeholders will be crucial in advancing Novartis' objectives across the region. About the Role Key Responsibilities Represent Public Affairs in International WEC LT Drive policy thought leadership for Novartis in WEC cluster countries on key areas, aligned with overall Region Europe PA policy priorities Proactively monitor emerging policy and regulatory topics across the cluster Partner and align with cross-functional partners (e.g. V&A, patient advocacy, communications, medical, healthcare systems) to drive RE policy priorities locally Align with direct reporting countries (AU, BE, NL, PO, Nordics) on local policy priorities and interface with WEC cluster country PA leads to calibrate local view and inputs on key policy areas Work in close alignment with WEC cluster countries PA leads and provide leadership on key issues in WEC cluster and strategic country plans Align with regional PA Portfolio Advocacy leads to drive regional and local execution of advocacy activities in the WEC cluster Build and maintain strong network and partnerships with defined stakeholders across the WEC cluster Essential Requirements Extensive experience in Public Affairs and/or other corporate functions in a pharmaceutical company Proven track record of impactful public affairs, policy, strategy and/or commercial roles at country, regional and/or global levels Strong understanding of the legislative environment in the EU and key national markets. Experience in crisis and issues management Strong communication skills to convey advocacy contents clearly and facilitate alignment among stakeholders across the organisation Ability to work across different parts of the organisation, build networks and share information with key stakeholders Critical thinking, predictive and enterprise mindset and outcome-focused performance management Desirable Requirements Master's degree (e.g. MSc) / University Diploma or equivalent in relevant discipline 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 any order to receive more detailed information about 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 Corporate Affairs Business Unit Corporate Location Switzerland Site Basel (City) Company / Legal Entity C010 (FCRS = CH010) Novartis International AG Functional Area Communications & Public Affairs 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-10027636 Nov 26, 2024 Switzerland Summary "We-re a team of dedicated and smart people united by a drive to achieve together" The ED, Public Affairs SERCE will spearhead policy thought leadership for the SERCE cluster, (Czech Republic, Hungary, Poland, Russia, ECC) staying ahead of emerging trends and aligning with cross-functional teams to drive local and regional policy priorities in SERCE cluster countries. The role entails fostering collaboration between countries, providing strategic guidance, and executing advocacy initiatives tailored to the cluster's needs. Building strong networks with stakeholders will be crucial in advancing Novartis' objectives across the region. About the Role Key Responsibilities Represent Public Affairs in International SERCE LT Drive policy thought leadership for Novartis in SERCE cluster countries on key areas, aligned with overall Region Europe PA policy priorities Proactively monitor emerging policy and regulatory topics across the cluster Partner and align with cross-functional partners (e.g. value & access, patient advocacy, communications, medical, healthcare systems) to drive RE policy priorities locally Align with direct reporting countries (CZ, HU, PL, RU, ECC) on local policy priorities and interface with SERCE cluster country PA leads to calibrate local view and inputs on key policy areas Work in close alignment with SERCE cluster countries PA leads and provide leadership on key issues in cluster and strategic country plans Align with regional PA Portfolio Advocacy leads to drive regional and local execution of advocacy activities in the SERCE cluster Build and maintain strong network and partnerships with defined stakeholders across the SERCE cluster Essential Requirements Extensive experience in Public Affairs and/or other corporate functions in a pharmaceutical company Strong advocacy, influence and communication skills Proven track record of impactful public affairs, policy, strategy and/or commercial roles at country, regional and/or global levels Strong understanding of the legislative environment in the EU and key national markets. Experience in crisis and issues management Strong communication skills to convey advocacy contents clearly and facilitate alignment among stakeholders across the organisation Ability to work across different parts of the organisation, build networks and share information with key stakeholders Critical thinking, predictive and enterprise mindset and outcome-focused performance management Desirable Requirements Master's degree (e.g. MSc) / University Diploma or equivalent in relevant discipline 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 any order to receive more detailed information about 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 Corporate Affairs Business Unit Corporate Location Switzerland Site Basel (City) Company / Legal Entity C010 (FCRS = CH010) Novartis International AG Functional Area Communications & Public Affairs 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-10030058 Dec 03, 2024 Switzerland Summary Novartis has the ambition to change the lives of millions of people worldwide with inflammatory skin diseases and immunological conditions The Immunology Research Disease Area at the Novartis Institutes for Biomedical Research (NIBR) is investing in the discovery of novel and transformative therapies to improve the life of affected patients. As part of this effort, we are seeking an innovative and highly motivated Principal Scientist or Senior Principal Scientist to initiate and guide drug discovery programs in immunology/dermatology/allergy. About the Role Your Responsibilities: You will be responsible for leadinga state-of-the-art laboratory of BSc/MSc level scientists to discover and develop novel therapiesfor the treatment of immunological diseases of the skin and to progress translational research to understand the pathophysiology of a broad range of dermal diseases. You will: Establishin vitro andin vivoassays as well as translational models to assess the innovative potential of novel therapeutic approaches in these diseases. Lead or contribute toearly drug discovery projects within multidisciplinary teamsup to clinical proof-of-concept studies in patients Define and execute on innovative scientific strategies, test novel disease-relevant hypothesesand propose transformative therapies Closely collaborate with scientists, clinicians, data scientists and technology experts across different departments in the global organization. What you-ll bring to the role: PhD degree in immunology, autoimmunity, molecular biology or related field + a minimum of 5 years of relevant research experience in an academic setting and/or in the pharmaceutical/biotech sector In-depth knowledge of human and mouse immunology, most preferably cutaneous immunologyor allergy, proven by significant scientific accomplishments and successful collaborations documented by publications in high-impact journals Experience withcutting-edge technologies, novel therapeutic approaches and assay development Analytical thinking and excellent skills inorganization of complex tasks, communication and presentation Strong team spirit and a collaborative mindset Desirable requirements: Experience in drug discovery and assay development for profiling of novel therapeutics in a biotech or pharmaceutical setting is a great plus. Experience in leading associates and cross-functional teams is desirable Background of working in an industry setting is advantageous *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 Regulär Shift Work No

Job ID REQ-10033476 Dec 10, 2024 Switzerland Summary The postdoctoral candidate will independently design and perform in vitro experiments with murine and human samples and also in vivo experiments to investigate the role of skin resident memory T cells in inflammatory skin diseases. About the Role Major accountabilities: Independently design and execute in vitro experiments using both murine and human immune cells from skin Independently perform murine in vivo experiments in mechanistic mouse models Generate multi-omics (e.g. protein, sequencing) data sets on cells from skin tissue (murine and human) Analyse multi-omics data sets and continuously evolve analysis skills. Conduct innovative, interdisciplinary translational research to publish results in leading journals Minimum Requirements: PhD in immunology or cellular biology (PhD students in the last year of their thesis work, are eligible to apply) Strong publication record in the area of immunology and/or resident memory T cells Excellent analytical, communication, presentation and organizational skills Candidates must be able to work independently as well as with interdisciplinary teams Experience and knowledge in the field of tissue resident memory T cells, T cell fate and T cell exhaustion Skills: Strong expertise in flow cytometry, murine and human immune cell isolation and manipulation (culture, stimulation, analysis) Experience with murine and/or human skin, as well as basic molecular biology techniques First experience and computational skills (e.g. R, Python, analysis of big data) to analyze own data sets Languages : 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 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. 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 Others Job Type Full time Employment Type Early Career (Fixed Term) Shift Work No

<div class="job-description"><h3><span style="color: #dd3333">Heizungsinstallateur EFZ (m/w/d) in Zollikofen </span><span style="color: #dd3333">gesucht</span></h3><p>Wir die Personal24 sind eine führende Personalvermittlung für temporäre und Dauerstellen in der Deutschschweiz. Wir suchen derzeit für einen unserer Kunden einen erfahrenen Heizungsinstallateur EFZ (m/w/d) für eine Anstellung in Zollikofen.</p><p>Als Heizungsinstallateur EFZ (m/w/d) sind Sie verantwortlich für die Installation, Wartung und Reparatur von Heizungsanlagen sowie für die Durchführung von Servicearbeiten bei unseren Kunden. Sie bringen eine abgeschlossene Berufsausbildung als Heizungsinstallateur EFZ (m/w/d) mit und verfügen über mehrjährige Berufserfahrung in der Branche.</p><h3><span style="color: #dd3333">Ihre Aufgaben:</span></h3><p>– Installation, Wartung und Reparatur von Heizungsanlagen<br>– Montage von Heizkörpern und Rohrleitungssystemen<br>– Prüfung und Instandhaltung von Heizungs- und Klimaanlagen<br>– Fehlerdiagnose und Behebung von Störungen<br>– Umsetzung von sicherheits- und umweltrelevanten Vorschriften</br></br></br></br></p><h3><span style="color: #dd3333">Ihr Profil:</span></h3><p>– Abgeschlossene Berufsausbildung als Heizungsinstallateur EFZ<br>– Erfahrung in der Installation und Wartung von Heizungsanlagen<br>– Handwerkliches Geschick und technisches Verständnis<br/>– Führerschein der Klasse B<br/>– Selbstständige und zuverlässige Arbeitsweise<br/>– Teamfähigkeit und hohe Kundenorientierung<br/>– Gute Deutschkenntnisse</br></br></p><h3><span style="color: #dd3333">Wir bieten:</span></h3><p>– Eine anspruchsvolle und abwechslungsreiche Tätigkeit<br/>– Attraktive Vergütung und Sozialleistungen<br/>– Weiterbildungsmöglichkeiten und berufliche Entwicklungsperspektiven<br/>– Ein dynamisches Arbeitsumfeld in einem etablierten Unternehmen<br/>– Ein motiviertes Team und gute Arbeitsatmosphäre</p><p>Wenn Sie an dieser Herausforderung interessiert sind und die Anforderungen erfüllen, senden Sie uns bitte Ihre vollständigen Bewerbungsunterlagen per E-Mail an <a href=" E-Mail schreiben " rel="noopener" target="_new"> E-Mail schreiben </a>. Wir freuen uns darauf, von Ihnen zu hören!</p><p> </p><p> </p></div>

Du suchst eine vielseitige Tätigkeit? familea ist ein sozial engagierter Verein mit über 120-jähriger Tradition im Raum Basel. Wir führen über 40 Kitas und eine Tagesstruktur, Kinder- und Jugendheime, das Zentrum Pflegekinder Nordwestschweiz und eine Frauenberatungsstelle. Bei uns stehen Kinder, Familien, Chancengleichheit und Integration im Mittelpunkt.Wir suchen in der familea Kita Horburgpark per 1. März 2025 eine Fachperson Betreuung EFZ mit einem Startpensum von 70%Hast du Freude daran, Kinder in ihrer Entwicklung zu begleiten und ihnen die Welt zu zeigen? Dann bist du bei uns genau richtig! Das sind deine AufgabenBetreuung und Förderung von altersgemischten Kindergruppen (3 Mt. - 9 Jahre)Begleitung von Mitarbeitenden in AusbildungKundenorientierte, offene und vertrauensvolle Zusammenarbeit mit den ElternPlanung und Umsetzung eines abwechslungsreichen Tagesablaufs, abgestimmt auf die Individualität des KindesDas bringst du mit:Abgeschlossene Grundbildung als Fachperson Betreuung Kinder, abgeschlossenes Studium als Sozial- oder Kindheitspädagoge oder ähnliche pädagogische AusbildungBerufs- und Ausbildungserfahrung mit ausgeprägter Selbst-, Fach- und SozialkompetenzFreude und Geduld im Umgang mit KindernEngagement, Zuverlässigkeit, Belastbarkeit und FlexibilitätDu bringst gerne neue Ideen ein und hast Spass an kreativen Aktivitäten wieSingen, Tanzen, Geschichten erzählen…Das erwartet dichEin motiviertes Team mit offener Du-KulturEin kreatives Arbeitsumfeld mit GestaltungsspielraumEigene Weiterentwicklung mit regelmässigen WeiterbildungsmöglichkeitenInteressiert?Sende deine vollständigen Bewerbungsunterlagen direkt online an uns. Für weitere Fragen steht dir Simone Dannmeyer, Kitaleiterin, Tel +41 61 260 85 95 gerne zur Verfügung

<h2>Whatre a big company with a family-owned feel. You will be given the opportunity to make big changes that will ripple throughout the industry while feeling right at home with the Hilti family.<h2>What do we offer?</h2><span style=" display:block;"> In addition to a competitive base salary and bonus potential, we offer a robust benefits package including a generous paid time off policy that includes vacation, personal days, health & wellness, and 2 days per year to give back in your local community, paid family leave, educational reimbursement and student loan assistance, 401(k) matching, medical/dental/vision coverage, and a variety of other benefits to fit the needs of our employees. </span> <br> <span style=" display:block;"> We will give you the tools you need to succeed through hands-on integration training and will support your continued professional development through ongoing training and mentoring, targeted leadership programs, and opportunities for international assignments in any of the 120+ countries in which we operate. </span>

Job ID REQ-10034884 Jan 07, 2025 Switzerland Summary We are seeking a motivated and detail-oriented Research Scientist Intern (Master, pre-Master) to join our dynamic team. The successful candidate will work closely with our experienced scientists, utilizing molecular biological and cell biological methods to contribute to cutting-edge research projects. This internship offers a unique opportunity to gain hands-on experience in a professional laboratory setting, develop technical skills, and contribute to meaningful scientific discoveries. Preferred start date: ASAP Duration: 6-8 months About the Role Major accountabilities: Conduct experiments using molecular and cell biological techniques. Analyze and interpret data, maintaining accurate and detailed records. Collaborate with team members to design and optimize experimental protocols. Present findings in team meetings and contribute to scientific discussions. Essential requirements: Education: Currently pursuing or graduated from a Master's degree in Biology, Molecular Biology, Cell Biology, or a related field. Experience/Professional requirements: Basic knowledge of molecular and cell biological methods. Strong analytical and problem-solving skills. Excellent communication and teamwork abilities. Languages : English. 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 Biomedical Research Business Unit Pharma Research 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

Job ID REQ-10023256 Dec 09, 2024 Switzerland Summary We are looking for a GCP Bioanalysis Senior Scientist in the Translational Medicine Drug Disposition Bioanalytical group. The role involves using bioanalytical knowledge and lab/instrument skills to develop, validate, and analyze clinical samples for the company's novel modality biologics portfolio. Responsibilities include independently designing and validating assays, performing sample analysis, processing data, and evaluating results. As Senior Scientist you will also contribute to health authority documents, maintain lab equipment and records, and mentor team members. The ideal candidate has a college/university degree in biological sciences, experience in regulated biologics bioanalysis, proficiency in various biological techniques, and the ability to work independently and meet deadlines. About the Role In the Senior Scientist role, you will use your knowledge of bioanalytics and lab/instrument skills to develop, validate and analyze clinical samples focusing on our novel modality biologics portfolio. Key responsibilities: Independently designing, developing, and validating assays, and performing sample analysis using biological techniques for PK, PD and immunogenicity following SOPs and guidelines. Being responsible for all assigned study/lab/project activities, and providing input to bioanalytical strategies. Data processing, evaluating results, interpreting data, and drawing relevant conclusions. Critically analyzing data on study and project levels. Conducting lab activities and keeping timely raw data records in accordance with company and health authority guidelines. Preparing study protocols, reports, and contributing to health authority documents. Maintaining high level of competence on routinely used laboratory equipment and/or LIMS systems. Evaluating and setting up new technologies as they are introduced to the lab. Contributing to the general lab environment, including instrument maintenance, writing/updating templates and SOPs, software validation activities, ordering supplies, etc. Coaching and mentoring in a matrix team environment. Essential requirements: College/university degree in biological related sciences or equivalent, with 3+ (Masters) or 5+ (Bachelors) years of experience. Experience in regulated biologics bioanalysis preferred. Strong laboratory skills with proficiency in several biological techniques (ELISA, ECL, PCR, etc.) and their associated software. Ability to work with minimal supervision and organize work across multiple projects to meet timelines Eagerness to take on additional responsibilities when required; flexibility to adapt to changing priorities and strategies. A collaborative spirit and willingness to mentor/coach peers 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 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 & 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 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-10033326 Dec 09, 2024 Switzerland Summary As our Associate/Senior Clinical Development Medical Director in our Immunology Development Unit you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. The Assoc/Senior Clinical Development Medical Director (CDMD) is the clinical leader of defined program level activities (e.g., submission activities, briefing books etc.), or a large, complex trial, under the leadership of the (Sr.) GPCH. May lead a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase) About the Role Please submit your application to join our Clinical Development Medical Director (Associate/Senior) Talent Pool. Clinical Development Medical Director* (Associate/Senior) **80-100% The (Associate/ Senior) Clinical Development Medical Director (CDMD) is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As (Associate / Senior) CDMD, you will have oversight of the clinical development for the assigned programs and drive execution of the clinical development plan. In addition, you will enable an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs. Your responsibilities will include: Provide clinical leadership and medical strategic input for deliverables in the assigned project/program. Deliverables may include sections of individual protocols consistent with the IDP, data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., IBs, Brochures, briefing books, safety updates, submission dossiers, and responses to Health Authorities) Drive execution of the section of the program in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates Oversee/conduct medical and scientific review of trial data with Clinical Scientific Expert(s). May be the Program Manager of other associates (e.g.., CSE). May function as study medical monitor Support SR/GPCH in ensuring overall safety of the molecule. May be a core member of the Safety Management Team (SMT), and supports program safety reporting (e.g., PSURs, DSURs, and safety related documents) in collaboration with Patient Safety Support the Therapeutic Area Head (TAH) by providing medical input into IDP and CTP reviews and contributing/driving development of disease clinical standards for disease areas. Provide support to the (Sr.) GPCH or TAH in interactions with external partners (e.g., regulatory authorities, KOLs, data monitoring boards, AD Boards, patient advocacy groups), internal partners (e.g., CTT, Research, Translational Medicine, GMA, Marketing, HE&OR), and decision boards) Work with NIBR (Novartis Institute of Biomedical Research)/ Translational Medical Sciences) to drive transition of pre-PoC projects to DDP and with BD&L including target identification and due diligences together with additional matters Ensure career development of Program reports and clinical colleagues through active participation in performance management and talent planning processes. Provide on-boarding, training, & mentoring support Contribute to medical/scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for franchise. May serve on or lead global initiatives (e.g., process improvement, training, SOP development, other Clinical Development line function initiatives) What you'll bring to the role: MD or equivalent medical degree is required*** in addition to advanced knowledge and clinical training in medical/scientific area; Clinical practice experience - 4 years (including residency) preferred Fluent oral and written English Minimum requirement of years of experience in clinical research or drug development will be commensurate with level: Assoc. CDMD - 3 years, CDMD - 5 years, Snr CDMD - 7 years Working knowledge of one of the above listed disease areas is desirable, with proven ability to interpret, discuss and present efficacy & safety data relating to clinical trial(s) Demonstrated ability to establish effective scientific partnerships with key stakeholders Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes Previous global people management experience is preferred, though this may include management in a matrix environment. * Final job title (Associate Clinical Development Medical Director, Level 5/ Clinical Development Medical Director, Level 6 / Senior Clinical Medical Development Director, Level 6) and associated responsibilities will be commensurate with the successful candidates- level of expertise. **Some restrictions to flexible working models may apply and will be discussed at interview if applicable *** For PharmD & PhD qualified applicants, please refer to our posting for Clinical Development Director 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. 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 Barcelona Gran Vía, Spain 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 Dec 09, 2024 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-10030880 Dec 06, 2024 Switzerland Summary In the Senior Scientist role the candidate will apply practical expertise to the design, development, qualification, and implementation of bioanalytical assays for pharmacokinetic (PK), pharmacodynamic (PD) and immunogenicity (IG) studies across all phases of the drug discovery & development pipeline in a non-regulated and GCP environment. About the Role Job specific responsibilities will include but are not limited to: Design, develop, qualify, and implement bioanalytical assays for PK, TK, PD and IG assessment supporting various modalities such as biologics, cell and gene therapy and oligonucleotides platforms using adequate technics following SOPs and guidelines for GCP analysis. Deliver high quality data within defined timelines and aligned to current industry expectations. Complete study sample analysis and draft the bioanalytical report in support of project requests. Support in representing the bioanalytical function on project teams and present results, data interpretation, timelines etc. at project team meetings. Collaborate with internal and external stakeholders to evaluate new bioanalytical technologies and solutions to support challenging project requests. Being responsible for all assigned study/lab/project activities and providing input to bioanalytical strategies. Independently or with the help of a team lead designing and developing, validating assays, and performing sample analysis. Data processing, evaluating results, interpreting data, and drawing relevant conclusions. Critically analyzing data on study and project levels. Conducting lab activities and keeping timely raw data records in accordance with company and health authority guidelines. Maintaining high level of competence on routinely used laboratory equipment and/or LIMS systems. Evaluating and setting up new technologies as they are introduced to the lab. Leading to the general lab environment, including instrument maintenance, writing/updating templates and SOPs, software validation activities, ordering supplies, etc. Coaching and mentoring in a matrix team environment Experience: College/university degree in biological related sciences or equivalent, with 3+ (Masters) or 5+ (Bachelors) years of experience. Experience in biologics bioanalysis preferred. Strong laboratory skills with expertise in cell activation assays using reporter systems, ligand binding assays (e.g. ELISA, MSD or other), drug potency assays. Proficiency in protein purification, immunoprecipitation and antibody pull down assays will be an advantage. Ability to work with minimal supervision and organize work across multiple projects to meet timelines. Eagerness to take on additional responsibilities when required; flexibility to adapt to changing priorities and strategies. A collaborative spirit and willingness to mentor/coach peers Additional accountabilities: Skilled in collaboration across project team labs. May suggest/build new network connections within existing project teams. Routinely trains members of lab and broader project team in familiar techniques. Expected (if needed) to undertake organizational responsibility (such as equipment power user, lab safety rep). Accountable for increasingly complex experiments; key contributor to the success of drug discovery, technology, and/or early development projects. Brings ideas from a concept or question to a decision in experimental design, based on previous observations. 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: Discoveries -Developments -Experimental methods -Adherence to Novartis policy and guidelines -Project & stakeholder feedback Additional skills: Collaborating across boundaries. Project Management. Collaboration. Curiosity. Drug Development. Flexibility. Pipeline (Software). Teamwork. 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 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-10030648 Dec 06, 2024 Switzerland Summary We-re looking for an enthusiastic and motivated recent recipient of a PhD in a pharmaceutical sciences-related field (e.g., pharmacy, biology, chemistry, biotechnology), preferably with general experience and knowledge in biologic / protein products. We offer a 3 years- Postdoctoral Research position in our Biologics Drug Product Development department in Basel (Switzerland), supporting an innovative project in the context of ultra-highly concentrated novel formulations for monoclonal antibodies. Preferred start date: Q1 2025 Latest start date: April 2025 Duration: 2 years #LI-Onsite About the Role Major accountabilities: Addressing manufacturing technology questions in collaboration with a technology partner. Process optimization and detailed product characterization using various non-standard methods. Optimization of rheology, injectability, and compatibility of antibody suspensions. Connection with the compatibility and bioavailability of the suspensions in vivo. Development of in vivo and in vitro tests for product evaluation. Supervision of two PhD students whose research topics fall within the postdoc-s area of expertise. Minimum Requirements: Work Experience: Good knowledge of laboratory and/or technical tools for biologic drug product development and process optimization Interest in problem-solving and optimization strategies Strong skills in mentoring and guiding junior researchers. Teamwork and willingness to collaborate. Skills: PhD in a related field (e.g., pharmaceutical sciences, biology, chemistry, biotechnology, etc.) - graduation no longer than 1 year ago General experience and knowledge in biologic / protein products, ideally experiences on high dose protein formulations Languages : English. 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 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 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

Job ID REQ-10033631 Dec 16, 2024 Switzerland Summary The Executive Director, Omnichannel Enablement Products, is a key member of the Marketing Technology team within the Commercial and Launch Strategy, International organization. The MarTech team is dedicated to defining, delivering, and scaling the right technology products that empower international countries and regions to create and deploy high-value customer experiences and engagement. This role involves overseeing the strategic direction, team management, and optimization of web products, content enablement capabilities, and AI-powered content solutions. It bridges product management, ecosystem integration, and innovation leadership to deliver scalable, efficient, and impactful content strategies globally. In this role, you will adopt a customer-first mindset and possess a strong understanding of Omnichannel and Content Enablement technologies and strategies for Pharma. This includes incorporating AI to develop high-quality content creation in both Commercial and Medical functions, with Medical and Legal Review (MLR). The ideal candidate will have expertise in these capabilities, along with excellent analytical, organizational, and communication skills to translate business problems and insights into strategies for commercial excellence. About the Role Major Accountabilities: Develop, deliver, and maintain internal and external omnichannel, web, and content solutions that enable best-in-class user productivity. Support day-to-day operations by developing scalable processes and ensuring best practices are maintained. Critical to success is the ability to understand and optimize the movement of data across these systems. Ensure a feedback loop with Marketing, Sales, Analytics, and Technology stakeholders to understand goals and gaps, and develop new engagement strategies that advance goals. Partner with enterprise IT and US product owners to fully leverage internal tools and platforms; ensure adoption, utilization, and change management across all International markets. Define KPIs and metrics in complexity reduction, improved customer experience delivery, and speed to market. Evangelize and elevate the role of omnichannel marketing to fuel customer experience excellence. Define the strategic roadmap for web platforms, aligning with broader MarTech objectives. Ensure platforms deliver exceptional user experiences and align with global and local needs. Oversee content enablement strategies (DAM, Content Planning, AI Approval/MLR, AI Generation and Authoring) to accelerate the creation, localization, and personalization of content. Enable seamless collaboration and integration across platforms to build a unified content ecosystem. Drive AI-powered initiatives to improve content efficiency, personalization, and compliance: Assess and prioritize key AI use cases to enhance content workflows and reduce manual efforts. Establish KPIs and analytics frameworks to evaluate the impact and efficiency of AI-driven content solutions. Continuously explore emerging technologies to maintain a competitive edge in digital content strategies. Be a thought leader on omnichannel strategies and performance from a technology perspective; serve as a change agent in delivering International/CLS goals; ensure buy-in from Field on concepts and future-state Field operations. Essential Requirements: Over 12 years of experience in developing end-to-end globally scaled web, content, and omnichannel solutions and services to support business performance, with demonstrated results. Proficiency in lead nurturing, management, and loyalty/adherence to drive connected customer experiences. Previous experience as a Platform/Product Owner for complex global organizations in the Life Sciences industry, with proven results. Expertise in omnichannel and automation systems, including strong working knowledge of web architecture and experience with DAM, MRM (FUSE/Aprimo) workflow tools and processes (production, MLR, etc.). Ability to understand and co-lead technical platform/capability integrations and requirements processes to drive a compliant, competitive approach for the enterprise. Experience in platform strategy and management, with the ability to deliver solutions using Agile methodology and integrate platforms and technologies into core business processes and standards. Desirable Requirements: Passionate about building great solutions and solving customer and business problems. Demonstrated ability to synthesize information to develop recommendations and strategies. Able to navigate and lead through ambiguity with data-driven decision-making. Embraces a collaborative and open partnership mindset. A growth mindset that embraces learning by doing. Organizational savvy and a change enabler. Excellent written and verbal communication skills. Strong analytical, strategic, time management, and negotiating skills. Ability to inspire extended teams to deliver with excellence. Effective at influencing and aligning strategies with markets and stakeholders. Location: This role can be based in Basel CH, Dublin IE or London UK. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. 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 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 Marketing 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-10027245 Nov 15, 2024 Switzerland Summary Diese Position umfasst die Unterstützung der Forschung durch hochwertige Tierpflege und Haltungsstandards, die Unterstützung des Vivarium Betriebs sowie die Sicherstellung gesetzlicher Vorgaben in einem gebäudeübergreifenden, multidisziplinären Forschungsprogramm. About the Role Wichtige Verantwortlichkeiten Zuständig für den Betrieb des Vivariums und die tägliche Pflege von Nagetieren (hauptsächlich Mäuse), Durchführung klinischer Beobachtungen, Eingabe und Pflege relevanter Tierdaten in der Tierhaltungsdatenbank sowie Wartung der Tieranlagen (Reinigung und Desinfektion) und Versand von Tieren. Führt gemäß Anforderungen spezifische Aktivitäten zur Mäusezucht und zur Unterstützung von Forschungsvorhaben durch. Einhalten aller institutionellen und behördlichen Protokolle und Richtlinien. Verantwortlich für die Verfolgung kontinuierlicher Verantwortlich für die Verfolgung kontinuierlicher Lern-/Berufsentwicklungsmöglichkeiten und die Verbesserung/Erweiterung der Fähigkeiten. Wichtige Leistungsindikatoren Gleichbleibende und qualitativ hochwertige Tierpflege und Wartung der Vivarien vor Ort. Teamorientiert und interaktiv. Fördert die Entwicklung und Leistung von Kollegen/Teams. Starke Aufmerksamkeit für die effiziente/konsistente Erledigung von Aufgaben. Kontinuierliche Unterstützung des Vivarium Operations Managements bei der Aufrechterhaltung der Einhaltung aller internen und externen Standards gemäss geltender SOPs. Identifizieren und lösen von betrieblichen Herausforderungen im Vivarium vor Ort. Berufserfahrung Abgeschlossene Tierpfleger Ausbildung EFZ mit Fachrichtung «Versuchstiere» oder eine gleichwertige Ausbildung. Vier Tage anerkannte Fortbildung in den letzten vier Jahren von Vorteil. Fähigkeiten Verfügt über ein gutes Verständnis in der Pflege von Labornagern in einer Forschungsumgebung und kann dieses eigenständig in der Praxis einsetzen. Kann bei Nagern Geschlechter und Alter bestimmen, Absetzen, Biopsieren, Verpaaren und verschiedene Applikationen durchführen. Erkennung typischer/atypischer Verhaltensweisen und Tiergesundheit. Ist mit den relevanten Bestimmungen des Schweizer Tierschutzgesetzes und der Tierschutzverordnung vertraut und wendet diese korrekt an. Kenntnisse in Microsoft Office, Outlook erforderlich. Kenntnisse im Umgang mit der Zuchtdatenbank wünschenswert Verfügt über starke Kommunikationsfähigkeiten in Wort und Schrift. 20 kg heben und schwere Gegenstände bewegen können und längere Zeit stehen und wiederholende Bewegungen ausführen. An Wochenenden und Feiertagen arbeiten. Sprachen Deutsch Englisch (verfügt über gute Englischkenntnisse.) Warum Novartis? Unser Vorsatz ist es, die Medizin neu zu gestalten, um Menschenleben zu verbessern und zu verlängern. Unsere Vision ist es, das wertvollste und vertrauenswürdigste Pharmaunternehmen der Welt zu werden. Wie wir das erreichen werden? Mit unseren Mitarbeitern. Es sind unsere Mitarbeiter, die uns tagtäglich dazu antreiben, unsere Ziele zu erreichen. Werden Sie Teil dieser Mission und dieses großartigen Teams! Erfahren Sie hier mehr: http://www.novartis.com/about/strategy/people-and-culture Was wir bieten: Alle Informationen finden Sie in unserem Novartis Life Handbook (Englisch): https://www.novartis.com/careers/benefits-rewards . Kontaktieren Sie den zuständigen Talent Acquisition Business PartnerIn, wenn Sie für weitere Details Engagement für Vielfalt und Inklusion: Novartis setzt sich für Vielfalt, Chancengleichheit und Inklusion ein. Wir sind bestrebt, vielfältige Teams zusammenzustellen, die für die Patienten und Gemeinschaften repräsentativ sind, denen wir dienen. Wir bemühen uns um die Schaffung eines inklusiven Arbeitsplatzes, der durch Zusammenarbeit mutige Innovationen fördert und unsere Mitarbeiter in die Lage versetzt, ihr volles Potenzial zu entfalten. Unsere Einstellungsentscheidungen basieren auf Chancengleichheit und der besten Qualifikation, ungeachtet von Geschlecht, Religion, Alter, Hautfarbe, Rasse, sexueller Orientierung, Nationalität oder Behinderung. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Position nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber dennoch mit uns in Kontakt bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, dann treten Sie hier dem Novartis Netzwerk bei: http://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 Functional Area Research & Development Job Type Full time Employment Type Regulär Shift Work No

Job ID REQ-10029829 Dec 04, 2024 Switzerland Summary The Neuroscience Department within BioMedical Research at Novartis Pharma AG in Basel, Switzerland, is searching for a motivated and experienced Research or Senior Scientist. This individual will assume a hands-on role within the in vivo neuroinflammation team and contribute to several research projects focused on the development of new therapies for neurodegenerative disorders, potentially helping improve the lives of millions of patients worldwide suffering neurodegenerative illnesses and conditions. The main focus will be on novel neuroimmune cell pathways to elucidate the mechanisms at the molecular, cellular and ex vivo/in vivo level. Joining our team you will independently but with close collaboration with the other members of the Neurosciences group plan, execute, document, analyze and interpret experiments. *Please note that this is a part time job share position with a maximum 70% working time About the Role Your responsibilities will include: Designing, conducting and protocolling independently in vivo studies with specific focus on neuroinflammatory pathways Establishment of new in vivo models for neuroinflammatory/neurodegenerative diseases Performing and interpreting ex vivo analyses with emphasis on histology, biochemistry, FACS and molecular biology Development and execution of in vitro cellular assays for assessing inflammatory processes Presenting data and putting it in a complex context Supporting general laboratory duties Your profile: University degree (MSc) or equivalent qualification, preferably in neuroscience, immunology, cell biology. *Please note that PhD candidates will not be considered for this position* Minimum 2-3 years relevant lab based work experience in an industrial or academic setting Previous experience in neuroscience drug discovery area would be an advantage. 60-70% job position Strong expertise in in vivo rodent work e.g. different routes of dosing, surgery, stereotactic brain injections, behavior, perfusion. Relevant animal experiment course available (e.g. LTK1) Experience in different histological methods, microscopy and image analyses Experience in RNA/DNA technologies and biochemistry, e.g. qPCR technologies, Westernblot Good knowledge of immunology and immunological methods such as flow cytometry, HTRF, ELISA Good knowledge in cell culture work, e.g. primary cells, iPSCs Used to evaluating large datasets, strong documentation capabilities and interest to use new informatics analysis tools Eager to learn and combine new techniques and concepts, to present results within the lab, to use and apply literature data, to perform exploratory activities and to work independently and as a team member Scientific curiosity, initiative, commitment, flexibility and good organization skills Track record of successful collaborations, open communication with different stakeholders, strong team player and networker Excellent oral and written 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. 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 Part time Employment Type Regulär Shift Work No

Job ID REQ-10027151 Dec 19, 2024 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 Formulation Project Leader 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 assigned projects. For this position, specific emphasis lies on bringing in-depth experience in applied data science, mechanistic modelling and simulation of pharmaceutical unit operations. About the Role Your responsibilities will include but are not limited to: You drive the modeling and simulation in the formulation and process development activities. You are accountable to develop and implement data-driven and physics-based models. You role-model applying data-centric ways of working by leading and implementing digital transformation initiatives in development activities. You role-model advanced data processing and handling. You support the design and development of (enabling) formulation and manufacturing process deliverables. You contribute to the creation and updating of formulation project plans aligned with the overall Drug Product (DP) and TRD project plans and internal guidance. You closely collaborate with DP sub-team members. You understand, identify and manage with them together critical aspects around DS, DP, packaging, device and analytics. You ensure authoring of correct, comprehensible, structured, complete and legible scientific development reports and GMP Supply documents to allow timely start of development trials, process transfers and supply activities. You contribute to the generation of filing dossiers, answer DP related questions in inspections and support Health Authority requests. What you-ll bring to the role: Advanced degree (minimum PhD) in a relevant scientific field Minimum 2-4 years of successful industry experience applying data science and modeling & simulation in the development of pharmaceutical products Experience in implementing computational models to guide formulation and/or manufacturing processes development of drug products. For example, quantum chemistry/cheminformatics for formulation development including solubility prediction and/or energy and mass balances for manufacturing process development including granulation, blending, compression etc. Good knowledge of data science and data visualization Strong background in programming and/or machine learning Excellent scientific skills Interdisciplinary thinking and interest in collaboration with other functions Successfully demonstrated track record of creativity and problem solving in projects. Good communication, organizational, planning and negotiation skills (German language skills desired). 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-10031992 Dec 16, 2024 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 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 assigned projects. For this position, specific emphasis lies on bringing in-depth experience in applied data science, mechanistic modelling and simulation of pharmaceutical unit operations. You will lead drug product teams during all stages of development but with a focus on initial clinical phases. You will be working on oral Small Molecules and in particular on enabling formulation approaches. You will use your strong communication and influencing skills to effectively lead the drug product subteam. Your expertise will facilitate the creation of innovative and stable drug products suitable for human trials and commercial supplies. 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 team 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. Provide input on performance of team and team members. 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 othefrmulatr departments and functions inside and outside of TRD and 3rd parties as appropriate. You assess, consolidate and negotiate resource needs and timelines for assigned projects within the DP project team and ensure resources are accurately reflected in the planning systems. 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 scientific sound DP development documents enabling a strong CMC submission package and act as author, reviewer or approver role for development documents in accordance to the operational procedures and guidelines. You contribute to the generation of filing dossiers, answer DP related questions in inspections and support Health Authority requests. You lead, manage and support the DP team 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. What you-ll bring to the role: Advanced degree in relevant scientific field (e.g. Pharmaceutical Technology, Chemistry) Minimum 2-4 years of successful industry experience in the development of pharmaceutical formulations in a matrix organization. Successfully demonstrated expertise in a specific scientific/technical area of Biopharmaceutical sciences, understanding of physical-chemical properties of molecule and impact on in-vivo performance. Knowledge on oral biopharmaceutics, biopharmaceutical modeling and defining bridging strategies is desirable. Strong project management skills, ability to solve complex problems in a matrix system with good communication, organizational, planning and negotiation skills (German language skills desired). Interdisciplinary thinking and interest in collaboration with other functions. Broad and profound understanding of development activities and processes in pharmaceutical sciences. Good knowledge of laboratory and/or technical tools as well as knowledge of relevant GLP, GMP regulations and policies. Strong presentation skills and scientific/technical writing skills. 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-10033601 Jan 09, 2025 Switzerland Summary The IT Site Business Partner / Business Analyst for Operations to be based in Schweizerhalle represents the IT function, IT strategy and technology roadmap at the site, captures IT demand, collaborates with IT functions, and supports the implementation of digital strategies at the ChemOps Schweizerhalle and Biological Drug Substance Supply (BDSS) site in Klybeck, Basel. The role contributes to the product roadmap, supports global rollouts and change management, and works with the Schweizerhalle and BDSS DDIT OPS IT team. The role leads IT projects, gathers requirements, creates demand, and prioritizes IT projects and features. Additionally, it ensures adherence to Good Manufacturing (GMP) and Information Security and Compliance (ISC) standards. About the Role Job Description Role Responsibilities: · Drive innovation in tech-driven business capabilities and processes, leading conversations with a consulting mindset. · Partner with Business to drive Data and Digital Programs, co-owning transformation outcomes. · Measure and drive business value of Operations Data and Digital Programs. · Improve the 'ease of engagement' with IT. · Serve as a key business partner for ChemOps Switzerland and BDSS. Own the technology roadmap, handle escalations and key decisions and ensure business continuity. · Ensure adherence to Security & Compliance policies for Operations IT systems at the Schweizerhalle and BDSS sites. · Represent the sites in audits and inspections. Role Requirements: · Bachelor-s degree in Computer Science, IT, or a related field. · Track record of interactions with senior management and leveraging digital technology/big data. · Strong relationship management skills. · Project management and change management experience. · Fluency in English and German. · 8+ years in regulated manufacturing environment or IT global industry. · Ability to work and lead cross-functional teams in a matrix environment. · Experience collaborating across boundaries and influencing without authority. · Proven track record in delivering global digital plant solutions. 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. 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 CTS Location Switzerland Site Muttenz (with Canteen) Company / Legal Entity C049 (FCRS = CH028) Novartis Pharma Schweizerhalle AG Functional Area Technology Transformation Job Type Full time Employment Type Regular Shift Work No

AEXIN est une société suisse spécialisée dans les services IT, reconnue pour ses solutions complètes dinnovation et à la sécurité des systèmes dintégration de nouvelles technologies réseau et des migrations sécurisées. Documenter les configurations, les interventions et les incidents, et fournir des rapports réguliers aux équipes concernées. Assurer une veille technologique pour anticiper les évolutions et les risques liés à la sécurité réseau. Documenter ses interventions, fournir un feedback régulier, et entretenir une relation client de qualité avec un esprit de service professionnel et orienté client.Profil recherché : Expérience déquipe, autonomie, et capacité à documenter ses interventions et à donner un feedback constructif. Français, Anglais, Allemand un plusCe que nous offrons : Un environnement de travail stimulant et des projets variés. La possibilité de travailler dans une entreprise axée sur l'innovation et la sécurité des infrastructures IT. Un lieu de travail flexible, entre Vessy, Marin ou Renens

<span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">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></span><br /><strong><span style="font-size:16pt;">Qualitätsfachmann/-fachfrau (m/w/d) 100 %</span></strong><span style="font-size:11pt;"><span style="font-family:Calibri, sans-serif;"><strong><span style="font-size:14pt;">Ihre Aufgaben</span></strong></span></span><ul><li><span style="font-size:14px;">Aufdecken und melden von Produkte- und Produktionsfehlern durch Sichtprüfung</span></li><li><span style="font-size:14px;">Datenerfassung und Umgang mit Daten im ERP System</span></li><li><span style="font-size:14px;">Produkt- und produktionsgerechte Anwendung diverser Prüfmethoden</span></li><li><span style="font-size:14px;">Professioneller Umgang mit Prüf- und Messmitteln</span></li></ul><p><span style="font-size:11pt;"><span style="font-family:Calibri, sans-serif;"><strong><span style="font-size:14pt;">Kenntnisse / Fähigkeiten</span></strong></span></span></p><ul><li><span style="font-size:14px;">Technische Berufslehre und Erfahrung in der Qualitätssicherung von Vorteil</span></li><li><span style="font-size:14px;">Hohes Qualitätsbewusstsein sowie exakte Arbeitsweise</span></li><li><span style="font-size:14px;">Ausgeprägte Feinmotorik</span></li><li><span style="font-size:14px;">Freude an Teamarbeit</span></li><li><span style="font-size:14px;">Englischkenntnisse von Vorteil</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.<br /><br />In wenigen Schritten können Sie sich auch direkt auf www.manpower.ch als Gast registrieren und Ihre Bewerbungsunterlagen einreichen.<br /><br />Unser Team freut sich auf Ihre Persönlichkeit.</span><br />