Transformation der Reporting-Landschaft: Du begleitest die weitere Transformation unserer bestehenden Reporting-Landschaft hin zu state-of-the-art Power BI ReportingSQL-Datenabfragen und -Reports: Du nutzt Deine fundierten SQL-Kenntnisse für effiziente Datenabfragen und die Erstellung darauf basierender ReportsDatenmodellierung: Gemeinsam mit Deinem Team bist Du verantwortlich für die fachliche (Weiter-)Entwicklung von Datenmodellen in unserer bestehenden SystemlandschaftAufbau und Weiterentwicklung des Data Management Systems: Du wirkst maßgeblich am Aufbau und an der Weiterentwicklung des Data Management Systems und der zugehörigen Prozesse mitDatenqualität und -konsistenz: Du stellst sicher, dass Informationen und Daten im Unternehmen korrekt und konsistent angelegt und gepflegt werdenOperative Lösungen und Data Governance: Du entwickelst operative Lösungen zur Verbesserung der Datenqualität in unserem Unternehmen und entwickelst die dahinterliegende Governance aktiv weiterAnsprechpartner für Fachbereiche: Du unterstützt Deine direkten Controlling-Kollegen bei der Beschaffung und Analyse von Daten und fungierst als zentraler Ansprechpartner für andere Fachabteilungen Ein erfolgreich abgeschlossenes Studium der Betriebswirtschaftslehre, Mathematik, Wirtschaftsinformatik, Informatik oder eines vergleichbaren Studiengangs mit Schwerpunkt Data Analytics, Data Science oder Data ManagementMehrjährige, einschlägige Berufserfahrung im Data Management oder im Bereich Data Analytics, idealerweise im Finanzdienstleistungs- oder Leasing-UmfeldNachweislich sehr gute und praxiserprobte Kenntnisse in der Entwicklung, Implementierung und Wartung von Power BI Reports und Dashboards (DAX, Power Query)Profunde und anwendungsbereite Kenntnisse in SQL für komplexe Datenabfragen, Datenmanipulation und die Arbeit mit relationalen DatenbankenTiefgehendes Verständnis und praktische Erfahrung in der Konzeption und Optimierung von Datenmodellen, Datenstrukturen und ETL-ProzessenMehrjährige Erfahrung in der Definition, Analyse und Weiterentwicklung von ProzessenSehr gute Kenntnisse in Microsoft Excel, insbesondere Power Query sowie Microsoft Power BIErfahrung im Umgang mit Master-Data-Management- und Data-Governance-Tools Sie profitieren von dem exklusiven Zugang zu interessanten Unternehmen und spannenden Projekten in Zusammenarbeit mit Hays als einem soliden und stabilen PartnerWir geben Ihnen wertvolle Tipps und Feedback zu Ihren Bewerbungsunterlagen und VorstellungsgesprächenWir erstellen ein Bewerberprofil mit Ihren Stärken und Potentialen und sorgen dadurch für eine hohe VermittlungsquoteIndividuelle Rundum-Betreuung: Unterstützung in der kompletten Bewerbungsphase Ihr Kontakt Referenznummer 862723/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Act as a Senior Finance Business Partner for R&D, Quality/Regulatory, and Medical Affairs, providing financial insights and decision support to senior stakeholdersLead project controlling for R&D projects and clinical studies, including budgeting, forecasting, cost tracking, and performance analysisEnsure transparency of project costs, resource utilization, and key cost drivers to enable effective financial steering of development activitiesDrive the standardization and continuous improvement of controlling processes, KPIs, and reporting tools across the organizationServe as SAP Key User for CO and PS, supporting project structures, cost allocation logic, and reporting, as well as contributing to SAP ECC6 and S/4HANA implementation and optimization initiatives Degree in Business Administration, Finance, Controlling, or a related fieldRobust experience in controlling, preferably within the Life Sciences, MedTech, or Pharmaceutical industryStrong background in project controlling for R&D projects or clinical studies, including business case evaluation and financial performance managementAdvanced SAP expertise, particularly in SAP CO and PS, with experience using SAP BW / Analysis for Office and advanced Excel reportingProven business partnering and stakeholder management skills, with the ability to challenge senior leaders in a constructive manner; fluent English and solid German skills required Challenging and varied tasks in a promising and innovative industry Flat hierarchies Individual development opportunities Ihr Kontakt Referenznummer 865253/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Das bieten wir DirUnbefristeter Arbeitsvertrag30 Tage UrlaubFlexibles Arbeiten & EigenverantwortungIndividuelle Förderung, Coaching & Weiterbildung (GMP, GAMP, CSV etc.)JobRad (Für Dich und Deinen Partner), betriebliche AltersvorsorgeBenefit Plattform mit mehr als 1.000 VergünstigungenWellhub FitnessFirmenhandy und Option auf Firmenwagen oder BahnCard (auch privat nutzbar)Moderne Unternehmenskultur mit kurzen EntscheidungswegenKollegiales, offenes und unterstützendes TeamSpannende Kundenprojekte im Rhein‑Neckar‑RaumKontakt Arbeitsort: Großraum Mannheim (Dienstsitz Frankenthal) Umfang: Vollzeit oder Teilzeit Start: ab sofort Reporting Line: Berichtet an Gruppenleitung GMP Engineering & CSV Auswahlprozess: „45 min Fachinterview, Kurzes Telefon‑Recap, 60–90 min 2. Fachinterview, Kurzes Telefon‑Recap, → Angebot oder Absage“ Weitere Informationen zu VESCON findest Du unter www.vescon.com.
Act as a Senior Finance Business Partner for R&D, Quality/Regulatory, and Medical Affairs, providing financial insights and decision support to senior stakeholders Lead project controlling for R&D projects and clinical studies, including budgeting, forecasting, cost tracking, and performance analysis Ensure transparency of project costs, resource utilization, and key cost drivers to enable effective financial steering of development activities Drive the standardization and continuous improvement of controlling processes, KPIs, and reporting tools across the organization Serve as SAP Key User for CO and PS, supporting project structures, cost allocation logic, and reporting, as well as contributing to SAP ECC6 and S/4HANA implementation and optimization initiatives Degree in Business Administration, Finance, Controlling, or a related field Robust experience in controlling, preferably within the Life Sciences, MedTech, or Pharmaceutical industry Strong background in project controlling for R&D projects or clinical studies, including business case evaluation and financial performance management Advanced SAP expertise, particularly in SAP CO and PS, with experience using SAP BW / Analysis for Office and advanced Excel reporting Proven business partnering and stakeholder management skills, with the ability to challenge senior leaders in a constructive manner; fluent English and solid German skills required Challenging and varied tasks in a promising and innovative industry Flat hierarchies Individual development opportunities Ihr Kontakt Referenznummer 865253/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Für nähere Auskünfte zum Aufgabengebiet steht Ihnen in den Chemisch-Biologischen Laboratorien Andrea Hintzmann, Telefon 0211 89-97422, gerne zur Verfügung. Für Fragen zum Bewerbungsverfahren wenden Sie sich gerne an unser Bewerbenden-Büro, Telefon 0211 89-99900 Landeshauptstadt Düsseldorf, Moskauer Straße 25, 40227 Düsseldorf
Own, author, record and investigate Deviations across operationsCollaborate with Subject Matter Experts and key stakeholders to determine root causes and assess product or system impactApply structured investigational tools such as Fault Tree Analysis, Event & Causal Factors Chart, Fishbone Diagram and similar methodologiesDefine effective CAPAs and associated effectiveness checks to prevent recurrenceEnsure full cGMP compliance throughout the investigation lifecycleDrive quality records to timely and accurate completionSupport continuous improvement activities within operationsContribute to enhancing investigation quality, consistency and efficiencyMaintain strong documentation standards and technical writing qualityCommunicate investigation progress and outcomes to relevant stakeholders Bachelor’s degree in chemistry, biotechnology, life sciences or a related fieldExperience with Deviations and cGMP in a regulated pharmaceutical or API environment is a strong advantageKnowledge of biotech manufacturing processes and analytical methods is an advantageExperience with Human and Organizational Performance and risk management approaches is beneficialFluency in English in both written and spoken form; German is an advantageStrong technical writing, analytical and communication skillsStructured, focused and well-organised working styleOpen-minded, agile, highly motivated and adaptable to changeStrong interpersonal and collaboration skills with a proactive mindsetAbility to manage multiple investigations simultaneously in a dynamic environment Opportunity to work in a state-of-the-art large-scale mammalian manufacturing environmentExposure to cross-functional teams and complex deviation management processesImpactful role with high visibility in quality and operations functionsInclusive, international and collaborative workplace culture Ihr Kontakt Referenznummer 863146/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Performs testing of samples linked to operations, validation, utilities and environmental monitoring samplesCoordinate and work on the transfer, development and validation of analytical methods including qualification of equipment needed for analysisCoordination in maintenance, calibration and use of laboratory equipmentActively contribute to the GMP Inspection Readiness of QC to ensure the fully compliance of relevant Quality System and Procedural documentsActively contribute to the QC operational readiness managing projects (external and internal) and the assigned to ressources (including coordination of people daily tasks)Participates in the transfer, development and validation of analytical methods including qualification of equipment needed for analysisCreation and revision of guidance documents such as SOPs/ WIs and other related documents Master’s degree or higher in Life Sciences, Chemistry, Biochemistry, or a related scientific field (lower educational background acceptable with relevant experience)Solid experience in chemical or biochemical laboratories, including work in a regulated GMP environmentExperience performing analytical testing of samples related to operations, validation, utilities, and environmental monitoringStrong expertise in analytical method transfer, development, and validationExperience with qualification, maintenance, and calibration of analytical laboratory equipmentSolid understanding of GMP regulations, quality systems, and inspection readiness within QC laboratoriesExperience in creating and revising SOPs, work instructions, and other quality documentationAbility to coordinate QC activities and support operational readiness projects in laboratory environmentsStrong collaboration and communication skills, working effectively across cross functional teamsDemonstrated ability to drive results, adapt quickly to changing situations, and maintain a strong business and quality focus Renowned pharmaceutical company Attractive salary package HAYS Benefits Ihr Kontakt Referenznummer 864632/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Design, conduct, and analyze in vivo studies involving intravenous injections, blood collection, and bleeding/thrombosis modelsExecute full end-to-end in vivo workflows, from study preparation to sample processing and documentationCharacterize gene therapy candidates using molecular and biochemical assays such as ELISA, thrombin generation, and chromogenic assaysHandle, prepare, and evaluate patient-derived blood and plasma samples for in vitro and ex vivo experimentsPerform data analysis, interpret results, and present findings to the research teamMaintain accurate, complete, and compliant documentation across all experimental stepsContribute to lab operations, including safety standards, inventory, equipment handling, and general organizationCollaborate with cross-functional team members to ensure smooth coordination and progress on gene therapy studies Academic background in life sciences (MSc or BSc) or completed scientific apprenticeship with hands-on laboratory experienceActive certification for animal experimentation (e.g., LTK1, FELASA, or equivalent)Proven hands-on experience with rodent work, including intravenous injections and blood samplingAbility to independently design, execute, and manage in vivo studies from start to finishExperience with molecular or biochemical assays relevant to hemostasis, thrombosis, or gene therapyStrong ability to plan experiments, analyze data, and interpret scientific resultsFluency in English with clear communication skillsHighly organized, proactive, and team-oriented mindset with strong reliability and attention to detail Opportunity to contribute directly to translational gene therapy research with high scientific impactHands-on work with a combination of in vivo, ex vivo, and molecular biology techniquesCollaborative environment with close teamwork and modern laboratory infrastructureDiverse and meaningful daily tasks involving both preclinical models and human biological samples Ihr Kontakt Referenznummer 865654/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Schritt 1: Bewerbung - Eingangsbestätigung Schritt 2: Sichtung Ihrer Bewerbungsunterlagen Schritt 3: Einladung zum Telefon- oder Videointerview Schritt 4: Feedback Ihr Ansprechpartner: Sina-Marie Dachs, Telefonnummer: +49 15119501574
Wir freuen uns über Ihre Bewerbung, die Sie bitte über den untenstehenden Button "Jetzt online bewerben" bis spätestens 31.03.2026, Kennziffer 2026-001-FA_III-B einreichen. Ansprechperson Prof. Dr. Margareta Müller Telefon: +49.7720/307-4231 margareta.mueller@hs-furtwangen.de
Dein Ansprechpartner - Nadine Kolling, Senior Expert People Management #Telefon 069566083050 #E-Mail bewerbung@infomotion.de
Initiate and formulate proposals / business cases for quality improvement projects including deliverables and planning for the development and implementation of proposed improvements Create and maintain supplier records in the qualification system Assess material changes and drive required quality change controlsSupport supplier qualification activities and coordinate supplier auditsManage supplier relationships to ensure value delivery and site performanceDevelop material specifications to support qualification and releaseCoordinate material release schedules to secure on-time production supplyCollaborate with tech transfer, procurement, quality, and manufacturing on supplier and material selectionEnsure materials meet required quality grades for clinical manufacturingAlign purchase orders and material planning with lead times, safety, quality, cost, and production schedulesSupport quality investigations, risk assessments, and continuous improvement initiatives including business case development.Bachelor’s or Master’s degree in engineering, pharmacy or science related field or profound experience working in a relevant academic or industry field Renowned pharmaceutical companyLong term contractAttractive salary package25 Days Holiday Ihr Kontakt Referenznummer 863542/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Mai 2026 Weitere Auskünfte vorab sind ausdrücklich willkommen bei Leon Budde (Telefon: +49 (0) 152 37620564, E-Mail: leon.budde@imes.uni-hannover.de). Bitte reichen Sie folgende Unterlagen ein: Lebenslauf, einschließlich bisheriger Erfahrungen in der Betreuung von Studierenden und Promovierenden, in der Antragstellung (Drittmittel) sowie in der Lehre Ein einseitiges Statement, in dem Sie Ihre Forschungsinteressen sowie Ihre Motivation und Zielsetzung für den Aufbau und die Leitung einer eigenen Forschungsgruppe darlegen Zeugnisse und Leistungsübersichten (inklusive Noten) zu Promotions-, Master- und Bachelorabschluss (sofern vorhanden) Zwei ausgewählte Publikationen, bei denen Sie Hauptautor*in bzw. maßgeblich federführend beteiligt waren Senden Sie Ihre Unterlagen bis zum 31.03.2026 entweder digital an E-Mail: sekretariat@imes.uni-hannover.de oder alternativ postalisch an: Gottfried Wilhelm Leibniz Universität Hannover Institut für Mechatronische Systeme An der Universität 1, Geb. 8142, 30823 Garbsen Informationen nach Artikel 13 DSGVO zur Erhebung personenbezogener Daten finden Sie unter: https://www.uni-hannover.de/de/datenschutzhinweis-bewerbungen/
Weitere Hinweise Für Auskünfte steht Ihnen Herr Prof. Dr. Jakob Franke (Telefon: 0511 762-2628, E-Mail: jakob.franke@botanik.uni-hannover.de) gerne zur Verfügung. Bitte richten Sie Ihre Bewerbung mit den üblichen Unterlagen bis zum 29.03.2026 in elektronischer Form als einzelnes PDF-Dokument an E-Mail: jakob.franke@botanik.uni-hannover.de oder alternativ postalisch an: Gottfried Wilhelm Leibniz Universität Hannover Institut für Botanik Prof.
Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectivesDesign and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regionsBuild and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutionsConduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiativesContribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical dataOversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL DirectorAct as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentationPlan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical OfficerRepresent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencersServe as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic communityCollaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities Solid direct experience working with Key Opinion Leaders, ideally within the ophthalmology sector Exceptional communication and interpersonal skills, with the ability to build trust-based relationships across diverse stakeholder groupsFull professional proficiency in English, both spoken and writtenStrong business acumen and a demonstrated ability to effectively manage timelines, processes, and procedural workflowsExperience with product launches, advisory boards, and post-approval studies is highly advantageousRelevant academic background required (e.g., life sciences, healthcare, business, or a related field) A very renowned companyOther Locations: Oberkochen/Jena/Berlin Ihr Kontakt Referenznummer 865508/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectives Design and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regions Build and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutions Conduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiatives Contribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical data Oversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL Director Act as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentation Plan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical Officer Represent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencers Serve as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic community Collaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities Solid direct experience working with Key Opinion Leaders, ideally within the ophthalmology sector Exceptional communication and interpersonal skills, with the ability to build trust-based relationships across diverse stakeholder groups Full professional proficiency in English, both spoken and written Strong business acumen and a demonstrated ability to effectively manage timelines, processes, and procedural workflows Experience with product launches, advisory boards, and post-approval studies is highly advantageous Relevant academic background required (e.g., life sciences, healthcare, business, or a related field) A very renowned company Other Locations: Oberkochen/Jena/Berlin Ihr Kontakt Referenznummer 865508/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH