Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Your role As Digital Products Quality Engineering Lead, you will shape the quality strategy for digital products developed and maintained in an Agile environment. You will lead and develop a team of software quality engineers, ensuring that digital products meet the quality standards required by customers in regulated life-science environments. Working with global, cross-functional teams, you will champion built-in quality, shift-left practices, and continuous verification throughout the product lifecycle. You will oversee end-to-end quality assurance and quality control activities, applying the four-eyes principle, managing escalations, and resolving issues with pace and clarity. You will establish and continuously improve software development processes, quality workflows, templates, and key quality indicators. By influencing engineering teams and strengthening their quality mindset, you will help turn complex challenges into practical actions that support faster go-to-market delivery. You will ensure that product engineering artifacts, traceability, testing evidence, and operational controls are inspection-ready and aligned with customer expectations and applicable regulations. Your expertise will help advance risk-based quality management, software test automation, DevOps, and continuous integration and delivery practices. - You hold a bachelor’s or higher degree in Computer Science, an Engineering discipline, Information or Operational Technology, Digital and Data Management, Information Science or Management, Biomedical Science, Life Sciences, or a related field. - You bring at least 10 years of combined experience in software development or engineering, digital transformation, software quality assurance or control, and software quality management, ideally in a life-science or pharmaceutical environment. - You have experience managing or supervising teams and building quality engineering capabilities through coaching, mentoring, and competency development. - You have a strong command of the software product lifecycle, change management, Agile product development, DevOps, Lean, Plan-Do-Check-Act, software test automation, cloud platforms, and risk-based quality management systems; experience with Computer Software Assurance is an advantage. - You understand GAMP 5 supplier-focused principles and relevant software-related ISO standards, as well as quality expectations in regulated environments, including GMP, GCP, GLP, and 21 CFR Part 11 compliance. - You have a proven track record in software operational controls, including change and incident management, audit support, supplier quality, periodic reviews, deviations, and corrective and preventive actions. - You are experienced in design reviews, verification activities, reviewing software engineering artifacts and testing evidence, managing defects, maintaining product traceability, and supporting audits or inspections. - You communicate clearly in writing and verbally, are confident using tools such as Word, Excel, PowerPoint, SharePoint, and project-planning applications, and are willing to travel globally when required. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Your role: As Senior Project Manager (all genders) you will be responsible for planning, coordinating and implementing M&A projects (acquisition and sale processes, joint ventures and strategic investments). You will use your expertise to support the divisions and companies of our Group at all stages of the M&A process. You will manage interdisciplinary project groups comprising experts from both the divisions and central functions and external consultants. You will develop project plans, organize project meetings and will report on the progress of these projects on a regular basis. Your tasks will include analyzing and evaluating companies and transactions according to quantitative and qualitative criteria. You will work closely with the Business Development units within the divisions. You will support Controlling in producing company valuation models (DCF models) and will back the results with other valuation approaches. You will also organize and manage due diligence processes and will summarize the results. You will conduct negotiations and will work closely with both the legal department and external legal advisors to create the relevant legal documentation, taking into account the input from all the relevant specialist departments. Last but not least, you will prepare decision papers, present these to top management and coordinate key activities following the successful completion of transactions. Who you are: - Degree in business administration with specialization in finance or a university degree in another subject with an additional business qualification (e.g. MBA) - At least five years of professional experience working in M&A at a company, at a Private Equity firm, in investment banking or in relevant fields within the pharmaceutical, biotechnology or chemical industries - Experience in project management and ideally in an international environment - Highly structured working style and analytical mindset - Team-oriented and strong communication skills - Ability to motivate teams - Strong organizational skills and ability to cope with pressure - Reliability and flexibility - Willingness to travel on business - Ability to conduct negotiations in English What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Your Role Data and AI are reshaping the way global organizations operate, and this role sits at the heart of that transformation. As a Software Engineer within our Enabling Functions Data Office, you will design and deliver high-impact data and AI solutions that power smarter ways of working across the organization. You will be part of a collaborative, internationally distributed team of engineers and architects, working within a Product-Oriented Delivery model to bring Analytics, AI, and data products to life at scale. In this role, you will: - Design, build, and maintain scalable applications, data pipelines, and platform components that translate complex business requirements from enabling functions such as HR, procurement, and legal into future-ready technical solutions. - Develop robust applications and interfaces that replace manual processes with seamless, intuitive user experiences. - Take ownership of data platforms, ensuring cost efficiency, governance, security, and compliance across the full data lifecycle. - Partner closely with stakeholders across your delivery pod to understand business needs and shape the technical direction of solutions. - Shape the future of data engineering within Enabling Functions, leveraging platforms such as Snowflake, AWS, and Palantir Foundry. - Contribute to a growing Spain-based hub within a team , with the opportunity to work on diverse and high-visibility AI use cases spanning automation, carbon footprint analytics, procurement intelligence, and more. Who You Are - You bring several years of proven expertise and experience in software engineering, including application design, development, and delivery within enterprise environments, with a strong foundation in writing clean, maintainable, and secure code. - You are proficient in development platforms and languages such as Python and Spark, and you apply modern engineering practices including version control, CI/CD pipelines, and automated testing as a matter of course. - You have hands-on experience with data platform technologies such as Palantir Foundry, Snowflake, and PySpark, and you are confident designing and delivering end-to-end data pipelines. - You have a solid understanding of data pipeline architecture, data governance, data lineage, privacy and security controls, and compliance standards in enterprise-scale environments. - You communicate complex technical concepts clearly and confidently to non-technical stakeholders, and you are comfortable translating business requirements into actionable technical solutions. - Familiarity with AI workflows, MLOps, AI safety and guardrails, or CI/CD for AI components is a plus - You hold a university degree or equivalent qualification in a relevant technical or engineering discipline. - You are comfortable working in a distributed, international team environment and are open to occasional travel within Europe. - Strong communication skills in English ; proficiency in German is a plus. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Your Role: As a Director Integration & Carve-Out, you will own the end-to-end integration and carve-out execution for our small to mid-size strategic deals. Reporting to the Head of Portfolio Execution (VP), you will be joining a highly energetic, mission-driven team of experienced integration and carve-out leaders managing these strategic initiatives across the three sectors. Key Responsibilities - Represent integration interests during due diligence. - Own and lead assigned integration or carve-out projects end-to-end – serving as the primary point of contact with full accountability across all workstreams. - Design and drive a structured, disciplined implementation strategy – from project set-up and timeline planning through milestone delivery – dynamically adapting and recalibrating plans as the situation evolves. - Build trusted partnerships and align with key stakeholders and business leaders, mobilizing necessary cross-functional team members and providing clear direction and oversight for accountabilities and assignments. - Drive creation and sign-off of the future target operating model. - Ensure smooth delivery at country level. - Orchestrate high-impact workstream governance – establishing meeting cadence, creating and deploying common frameworks for feedback, inputs, and deliverables within a business unit and across our company – keeping all teams laser-focused on value drivers and key enablers across the company. - Drive fast decision-making – proactively identifying and resolving risks and pivoting course decisively to protect deal success. - Ensure full compliance with legal and regulatory requirements throughout the transaction lifecycle, safeguarding our organizational and financial interests. - Plan and manage overall integration / separation cost budget. - Ensure people and organizational aspects (culture, org design, retention and engagement, capability identification and preservation) are appropriately considered and managed in integrations. - Lead the end-to-end definition, implementation, and delivery of post-closing services (incl. Manufacturing Supply Agreements (MSAs) and Transitional Service Agreements (TSAs) in carve-out projects. Lead and manage timely and effective post-closing agreement exit in integrations. - Understand and communicate concerns, motivations and needs of all entities to ensure maximum benefit is realized and business momentum is maintained / increased. - Track and report performance against agreed-upon milestones and deliverables (as well as top- and bottom-line synergy / value creation targets in integrations). - Maintain a structured approach for keeping all relevant stakeholders informed – reporting integration / carve-out progress against financial and non-financial targets, surfacing roadblocks, and driving timely escalation to senior leadership. - Create a clear roadmap and transition plan for handover and ongoing ownership. - Actively coach and develop junior team members. - Continuously evolve transaction execution-related best practices and engage in best-practice building. Who You Are: Minimum Qualifications: - Master’s degree, e.g., in Business Administration, Economics, Finance or related fields - 6+ years of experience with global, matrixed organizations - 6+ years of experience in management consulting or similar positions, with demonstrated success in steering large, cross-functional teams and overseeing substantial resources in complex environments - Demonstrated 2+ years of leading operational post-merger integrations and / or carve-outs across various deal types (e.g., share deals, asset deals, standalone / incubator integrations, spin-off). - 2+ years of leadership experience - Broad-based knowledge and project experience in the industries in which our company operates (Life Science / Healthcare and / or Electronics) – with curiosity about the technologies shaping our future - Strong analytical and problem-solving skills, with attention to detail - Good balance of strategic and operational strength - Exceptional organizational skills, with ability to work in an agile manner and change course as required; able to systematically work through ambiguity - Skilled at building credibility and networks – from working teams to C-suite – both internally and with external partners - Strong business acumen – deep understanding of business processes / operating models, with knowledge of financial analysis, ROI analysis and key performance indicators - Continuous learning orientation and ability to quickly acquire new skills and domain knowledge in evolving business contexts - Strong drive, especially in fast-paced, complex and high-pressure environments, showing resilience and adaptability - Proven ability to make sound, data-driven decisions with confidence and minimal need for escalation - Culturally and politically savvy, strong in change management and communications Preferred Qualifications: - MBA degree - Proficient financial literacy and experience in financial due diligence, valuation, and M&A lifecycle - Multi-year experience in strategy, business development, portfolio management, investment banking, or related field is a plus - AI literacy or interest in AI – including critical thinking and experience with AI tools, concepts and prompt engineering to accelerate project execution and drive synergies What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Als Pharmakant bzw. Chemikant in unserer Herstellung für feste Arzneiformen übernehmen Sie die Bedienung und Überwachung unserer Produktionsanlagen und stellen einen reibungslosen Ablauf im Herstellprozess sicher. Sie arbeiten zuverlässig, bringen sich aktiv ins Team ein und tragen dazu bei, dass unsere Abläufe effizient umgesetzt werden. Wir sind ein mittelständisches Pharma-Produktions-Unternehmen im Südwesten Deutschlands und sind Teil der Shenzhen Xingyin Pharmaceutical Unternehmensgruppe. Mit unserem Venenpräparat Aescuven sind wir Marktführer in China. Umfangreiche Entwicklungstätigkeit, höchste Qualität und moderne Fertigungsmethoden, garantieren unseren gleichbleibend hohen Standard. Ihre Aufgaben - Bedienung und Überwachung unserer Produktionsanlagen für Arzneimittel - Einrichten und Rüsten der Anlagen - Verwiegung und Verarbeitung von Rohstoffen - Granulieren, Sieben und Tablettieren von Materialien - Durchführung von Inprozesskontrollen - Reinigung der Anlagen sowie Unterstützung bei der vorbeugenden Instandhaltung der Maschinen - Sorgfältige Dokumentation der Herstellprozesse Ihr Profil - Abgeschlossene Ausbildung als Pharmakant bzw. Chemikant - Erfahrung in der Herstellung von Arznei- oder Lebensmitteln - Gute Deutschkenntnisse - Bereitschaft zur Schichtarbeit - Sorgfältige, zuverlässige Arbeitsweise, Teamfähigkeit sowie gute Selbstorganisation Unsere Benefits - Tarifgebundene Vergütung (Chemie-Tarif) inkl. Urlaubs- und Weihnachtsgeld sowie weiteren tariflichen Leistungen - Betriebliche Altersvorsorge - Strukturierte Einarbeitung mit Einarbeitungsplan und festem Ansprechpartner - Arbeitsmedizinische Betreuung inkl. Vorsorgeuntersuchungen - Zuschuss zum Fitnessstudio und Dienstrad - Essenszuschuss - Gute Erreichbarkeit sowie Mitarbeiterparkplätze - Regelmäßige Teamevents (z. B. Sommerfest und Weihnachtsfeier) - Arbeiten in einem stabilen, etablierten Pharmaunternehmen Wir freuen uns auch über Bewerbungen aus dem (EU-)Ausland!/ We also welcome applications from (EU) abroad! Für Bewerber/Bewerberinnen, die Ihren festen Wohnsitz im Ausland haben: Die Zentrale Auslands- und Fachvermittlung (ZAV) hilft Ihnen bei der Arbeitssuche in Deutschland. Wir sind Teil der staatlichen Arbeitsagentur. Unser Service ist kostenlos. Wir informieren Sie gerne: +49 (0) 228 713 1313 Registrieren Sie sich gern für unseren Service: https://www.arbeitsagentur.de/int/en/advice-and-support For applicants who have their permanent residence abroad: The International and Specialized Services will help you find a job in Germany. We are a department of the German Federal Employment Agency. Our service is free of charge. We will be happy to inform you: +49 (0) 228 713 1313 For our service please register yourself: https://www.arbeitsagentur.de/int/en/advice-and support IncomingZAV Ergänzende Informationen: Anforderungen an den Bewerber: Erweiterte Kenntnisse: Lebensmittelchemie, Arzneimittelproduktion, Qualitätsprüfung, Qualitätssicherung, Dokumentation (technisch), Sieben, Maschinenführung, Anlagenführung, -bedienung

Wir suchen zur Verstärkung unseres Teams zum nächstmöglichen Zeitpunkt: eine/n Zahntechniker/in (m/w/d) in Vollzeit oder Teilzeit. Sie bringen mit: - vielseitige Kenntnisse sind wünschenswert - ergebnisorientiertes, sorgfältiges und motiviertes Arbeiten Ihr Einsatzort ist das Dentallabor in der Großen Brauhausstraße 3 in Halle/Saale. Haben wir Ihr Interesse geweckt haben, dann senden Sie Ihre Bewerbung an: B&B Dentalservice GbR Große Brauhausstraße 3 06108 Halle (Saale) Sachsen-Anhalt

Wir sind ein produzierendes und entwickelndes Biotechnologieunternehmen mit rund 130 Mitarbeitenden an den Standorten Ahrensburg bei Hamburg und Vancouver, Kanada und gehören zur DFB Pharmaceuticals Gruppe. Mit umweltfreundlichen und nachhaltigen biologischen Prozessen betreiben wir in Ahrensburg die weltweit größte Fermentationsanlage für pflanzliche Zellkulturen, entwickeln innovative biotechnologische Prozesse und stellen pharmazeutische Wirkstoffe für die Krebstherapie her. An unserem Entwicklungs- und Produktionsstandort in Ahrensburg betreiben wir auf ca. 5.000 m² komplexe und automatisierte Anlagen für pharmazeutisch-biotechnologische Prozesse vom Labor- bis zum Produktionsmaßstab. Produktionsmitarbeiter Biotechnologie (m/w/d) Bedienung und Überwachung der Anlagen zur Fermentation und Aufreinigung pharmazeutischer Wirkstoffe unter GMP-Bedingungen Steuerung und Kontrolle komplexer Herstellungsprozesse vom Labormaßstab bis zur Produktion im 75.000 l Bioreaktor mittels Prozessleitsystemen Durchführung von Wartungs-, Instandhaltungs- und Reinigungsarbeiten Herstellung von Nährmedien und Rohstoffverwiegungen Durchführung von Probenahmen und Inprozesskontrollen GMP-gerechte Dokumentation aller Prozessschritte Teilnahme an der Rufbereitschaft (nach entsprechender Einarbeitung) Abgeschlossene Ausbildung zum Chemikanten, Pharmakanten, Brauer, Mälzer, zur Fachkraft für Lebensmitteltechnik (m/w/d) oder vergleichbare Qualifikation aus der Lebensmittel- oder Kosmetikindustrie Erste Berufserfahrung im pharmazeutischen Umfeld wünschenswert, idealerweise in der biotechnologischen Herstellung Technisches Verständnis und handwerkliches Interesse Strukturierte und zuverlässige Arbeitsweise sowie ausgeprägtes Qualitätsbewusstsein Teamfähigkeit sowie hohes Sicherheits- und Verantwortungsbewusstsein Bereitschaft zu gelegentlicher Wochenendarbeit und Rufbereitschaft sowie vereinzelten Schichttagen Sehr gute Deutschkenntnisse (mind. C1) Führerschein Klasse B Einen unbefristeten Arbeitsplatz in einer zukunftsorientierten Branche Ein abwechslungsreiches und anspruchsvolles Arbeitsumfeld Eine 38,75-Stunden-Woche 30 Urlaubstage plus Urlaubsgeld Ein flexibles Arbeitszeitmodell (im Rahmen der betrieblichen Erfordernisse) Zuschuss zu Vermögenswirksamen Leistungen Flache Hierarchien und kurze Entscheidungswege Ein kollegiales Team mit wertschätzender Unternehmenskultur Raum für Eigenverantwortung und persönliche Weiterentwicklung

Wir sind ein produzierendes und entwickelndes Biotechnologieunternehmen mit rund 130 Mitarbeitenden an den Standorten Ahrensburg bei Hamburg und Vancouver, Kanada, und gehören zur DFB Pharmaceuticals Gruppe. Mit umweltfreundlichen und nachhaltigen biologischen Prozessen betreiben wir in Ahrensburg die weltweit größte Fermentationsanlage für pflanzliche Zellkulturen, entwickeln innovative biotechnologische Prozesse und stellen pharmazeutische Wirkstoffe für die Krebstherapie her. An unserem Entwicklungs- und Produktionsstandort in Ahrensburg betreiben wir auf ca. 5.000 m² komplexe und automatisierte Anlagen für pharmazeutisch-biotechnologische Prozesse vom Labor- bis zum Produktionsmaßstab. Elektroniker mit Schwerpunkt Betriebstechnik (m/w/d) Sicherstellung der Funktionsfähigkeit der elektrotechnischen Installationen, elektrischer sowie informationstechnischer Steuerungs- und Versorgungssysteme Betreuung der EMSR-Technik unserer kontinuierlich betriebenen Prozessanlagen sowie unserer Betriebstechnik durch Kontrollen, Störungsbeseitigung und Instandhaltungsmaßnahmen Projektunterstützung bei Neuinstallationen, Anlagenmodernisierungen sowie Optimierungen unserer Prozessleitsysteme Koordination, Durchführung und Dokumentation von Kalibriertätigkeiten an unseren Prozessanlagen Dokumentation im elektrotechnischen Umfeld Koordination und Betreuung externer Dienstleister im Bereich der Elektrotechnik Teilnahme an der Rufbereitschaft (nach erfolgreicher Einarbeitung) Abgeschlossene Ausbildung als Elektroniker / Elektriker für Betriebstechnik oder einer ähnlichen Fachrichtung mit einschlägiger Berufserfahrung Mindestens 5 Jahre Erfahrung in der Betreuung elektrotechnischer und automatisierter Anlagen in der Prozessindustrie, wie Biotechnologie, Pharmazie, Chemie, Kosmetik oder Nahrungsmittel Kenntnisse in der industriellen Elektro- und MSR-Technik Erfahrungen in Kalibriertätigkeiten sind von Vorteil Kenntnisse im GMP-Umfeld wünschenswert Kommunikative, teamorientierte sowie verantwortungs- und qualitätsbewusste Arbeitsweise Flexibilität, Einsatzbereitschaft Sehr gute Deutschkenntnisse Einen unbefristeten Arbeitsplatz in einer zukunftsorientierten Branche Ein abwechslungsreiches und anspruchsvolles Arbeitsumfeld Individuelle und fachliche Entwicklungsmöglichkeiten in einem wachsenden Unternehmen Eine 38,75-Stunden-Woche 30 Tage Jahresurlaub plus Urlaubsgeld Ein flexibles Arbeitszeitmodell ohne Schichtarbeit Zuschuss zu Vermögenswirksamen Leistungen Ein kollegiales und motiviertes Team mit flachen Hierarchien und Raum für Eigeninitiative Eine von Dialog, Gemeinschaft und Qualitätsorientierung geprägte Unternehmenskultur

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. This position can be filled either in Switzerland (Eysins) or Germany (Darmstadt) in a hybrid format. Your role Real-world evidence is reshaping how medicines are developed, approved, and valued — and in this role, you will be at the forefront of that transformation. As a Director Real-World Evidence Scientist in Oncology, you will own and drive the end-to-end RWE strategy for one or more complex, high-priority oncology programs, operating as a recognized scientific authority across the organization and beyond. You will define and lead the integration of RWE into clinical development and regulatory strategies, working directly with global program teams and cross-functional partners across clinical, regulatory, market access, and commercial functions. You will design, initiate, and oversee non-interventional studies — from protocol development through to study reporting — and ensure the selection of fit-for-purpose real-world data sources that address critical research questions. Your scientific judgment will directly inform decision-making at the most senior levels of the organization. Beyond program delivery, you will represent the organization in interactions with health authorities, contribute to peer-reviewed publications, and present at international conferences — actively shaping the external scientific landscape. You will also champion methodological innovation, drive process improvements, and serve as a scientific mentor to colleagues within the function, contributing to a culture of rigor, collaboration, and continuous learning. Who you are - You hold a Master’s degree or PhD in Epidemiology, Public Health, Health Economics and Outcomes Research, Biostatistics, or a related discipline, and bring 8 or more years of RWE experience gained in a pharmaceutical, biotechnology, or contract research organization setting. - You have deep expertise in studies based on secondary data use — including claims data, electronic medical records, and registries — across multiple healthcare environments (Europe, US, and/or Asia), as well as experience in primary data collection. - You are proficient in working with federated data networks and familiar with data standards such as OMOP CDM or FHIR, and bring strong methodological skills spanning epidemiology, pharmacology, and pharmacovigilance. - You have a proven track record of leading RWE strategy at a global program level, navigating complex, matrixed organizations and collaborating effectively across clinical development, regulatory affairs, and market access functions. - You bring experience in regulatory and/or payer submissions and interactions, and a thorough understanding of the evolving regulatory environment for RWE. - You communicate with clarity and confidence — translating complex scientific content for diverse audiences, including senior leadership and external stakeholders — and you are fluent in English. - Ideally, you also bring experience with AI/ML applications in RWE (including NLP), patient-reported outcomes (PRO), health technology assessment, and a track record of thought leadership through publications, conference presentations, or advisory roles. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

IHRE AUFGABEN Bearbeitung, Kontierung und Verbuchung sämtlicher Geschäftsvorgänge Prüfung und Buchung von Eingangs- und Ausgangsrechnungen Vorbereitung und Durchführung des Zahlungsverkehrs Betreuung des Mahnwesens Mitwirken/ Verantwortung bei der/ für die Erstellung von Monats-, Quartals- und Jahresabschlüssen Mitwirken bei der Erstellung der Budgetplanung und des Forecasts Durchführung von Wirtschaftlichkeits- und Profitabilitätsanalysen sowie Ad-hoc-Auswertungen Währungssicherung Ansprechpartner für Wirtschaftsprüfer, Banken und Steuerberater Erstellen von Umsatzsteuer-Voranmeldungen Intrastat-Meldungen Betreuung der Anlagenbuchhaltung ZM-Meldungen DAS BRINGEN SIE MIT Erfolgreich abgeschlossene Berufsausbildung mit dem Schwerpunkt auf Finanz- und Rechnungswesen Einschlägige Berufserfahrung in der Buchhaltung Gute MS-Office-Kenntnisse Kenntnisse im Umgang mit einem ERP-System Ausgeprägtes Zahlenverständnis und analytisches Denkvermögen Schnelle Auffassungsgabe und strukturierte Arbeitsweise Englischkenntnisse von Vorteil DAS ERWARTET SIE Eine optimale Verkehrsanbindung des Standortes an Bus (1 Minute Fußweg), Bahn (5 Minuten Fußweg) und Autobahn (8 Minuten Fahrzeit) Sie sind von Anfang Teil des Teams und übernehmen Verantwortung Flache Unternehmenshierarchie und kurze Entscheidungswege 30 Tage Erholungsurlaub pro Jahr Eine attraktive betriebliche Altersvorsorge, bei der die Umwandlung von Entgelt großzügig vom Arbeitgeber bezuschusst wird Zeiterfassung auf Vertrauensbasis in einem Gleitzeitmodell Erfolgsbeteiligung in Form einer variablen Jahressonderzuwendung Ergänzende Informationen: Homeoffice: Umfang: Nach Vereinbarung Anforderungen an den Bewerber: Grundkenntnisse: Quartalsabschlüsse, Textverarbeitung Word (MS Office), Deckungsbeitragsrechnung, E-Mail-Programm Outlook (MS Office), Lohn-, Einkommensteuer, Umsatzsteuer, Rechnungslegung nach HGB, Mahn- und Klagewesen, Revision, Gewinn-und-Verlust-Rechnung, Kalkulation, FIBU-Programme, Ausgangsrechnung bearbeiten, Fakturieren, Finanzbuchhaltung, Kassenführung (Bargeld), Kosten- und Leistungsrechnung, Lohn- und Gehaltsbuchhaltung, -abrechnung, Monatsabschluss, Reisekostenabrechnung, Spesenabrechnung, Sachkontenbuchhaltung, Statistische Meldungen (Buchhaltung, Finanzwesen), Zahlungsverkehr, Jahresabschluss, Berichtswesen, Information, Abrechnung, Anlagenbuchhaltung, Bilanzierung, Debitorenbuchhaltung, Steuerrecht, Organisation, Rechnungsprüfung, Terminplanung, -überwachung, Controlling, Buchführung, Buchhaltung Erweiterte Kenntnisse: Kaufmännische Kenntnisse