Overview     At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.   We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams.    We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you.    At QIAGEN, every day is an opportunity to make a real-life impact.    Join us, grow with us, and together, let's shape the future of biological discovery.  ‎ Your Tasks * You define and maintain the IAM strategy and governance framework, including SOPs and policies, ensuring you align business and IT and comply with standards and regulations * You collaborate with business units to design IAM processes and oversee their execution, including Joiner-Mover-Leaver (JML) workflows and audit-ready access reviews * The development and approval of authorization concepts and access management is led by you, setting scope, frequency, and timelines for recertifications, while you oversee PAM and privileged accounts in complex environments * To coordinate the integration of new applications into IG&A solutions, ensuring you apply standardized access models and support role governance and job profile alignment in systems like Workday is part of your tasks * You ensure adherence to IAM policies and SOPs, provide audit support, and deliver regular reporting to key stakeholders Your Profile * You hold a Bachelor’s or Master’s degree in IT, Computer Science, Information Security, or a related field, combined with at least 3 years of professional experience in IAM or IT security; certifications such as ITIL, ISO 27001, CISSP, or CISM are a plus * Proven expertise in IAM strategy and governance, with experience defining frameworks, SOPs, and policies will help you align business and IT while meeting compliance requirements * You have a strong background in IAM process and lifecycle management, including designing processes with business units and managing end-to-end execution such as JML and access reviews * Deep knowledge of authorization concepts, access management, and privileged account setups (PAM), including oversight of recertification scope, timelines, and OT environments that you handle confidently is part of your expertise * You bring experience integrating applications into IG&A solutions, ensuring standardized access and supporting role governance and job profile alignment in platforms What we offer     * Bonus/Commission   * Local benefits    * Referral Program   * Volunteer Day   * Internal Academy (QIALearn)    * Employee Assistance Program    * Hybrid work (conditional to your role)    Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.      QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.  

Overview     At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.   We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams.    We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you.    At QIAGEN, every day is an opportunity to make a real-life impact.    Join us, grow with us, and together, let's shape the future of biological discovery.  ‎ Your Tasks * You will shape the future of IAM by designing and maintaining a robust technical architecture aligned with our strategy and policies. * Regarding hands-on implementation of IAM solutions you work closely with internal IT teams and trusted service partners. * Your collaboration with Cyber Risk Management experts ensures every design and integration is secure and future-ready. * Seamless integrations of new applications into our Identity Governance & Administration landscape, ensuring consistent IAM practices across IT and OT environments, with a strong focus on SSO is lead by you * You own the architecture of the identity lifecycle management and support IAM rollouts, PAM coverage, SSO adoption and other key IAM aspects from cyber security architecture perspective Your Profile * You hold a Bachelor’s or Master’s degree in IT, Computer Science, Information Security, or a related field, combined with at least 3 years of professional experience in IAM or IT security architecture and design; certifications such as ITIL, ISO 27001, CISSP, or SABSA SCF are a plus  * Your proven expertise in IAM strategy and architecture and hands-on experience with tools such as Microsoft Entra Suite, Sailpoint, Okta, and Ping-Federate are your strengths * You are known for a deep knowledge of authorization, access management, and privileged account management concepts as well as of protocols such as SAML, OAuth, OIDC and SCIM.  What we offer     * Bonus/Commission   * Local benefits    * Referral Program   * Volunteer Day   * Internal Academy (QIALearn)    * Employee Assistance Program    * Hybrid work (conditional to your role)    Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.      QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.  

Overview     At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.   We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams.    We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you.    At QIAGEN, every day is an opportunity to make a real-life impact.    Join us, grow with us, and together, let's shape the future of biological discovery.  ‎ Your Tasks * You will shape the future of IAM by designing and maintaining a robust technical architecture aligned with our strategy and policies. * Regarding hands-on implementation of IAM solutions you work closely with internal IT teams and trusted service partners. * Your collaboration with Cyber Risk Management experts ensures every design and integration is secure and future-ready. * Seamless integrations of new applications into our Identity Governance & Administration landscape, ensuring consistent IAM practices across IT and OT environments, with a strong focus on SSO is lead by you * You own the identity lifecycle management for human and non-human accounts in Entra ID and AD, while steering IAM rollouts based on critical KPIs like recertifications, PAM coverage, and SSO adoption. Your Profile * You hold a Bachelor’s or Master’s degree in IT, Computer Science, Information Security, or a related field, combined with at least 3 years of professional experience in IAM or IT security architecture and design; certifications such as ITIL, ISO 27001, CISSP, or SABSA SCF are a plus  * Your proven expertise in IAM strategy and architecture and hands-on experience with tools such as Microsoft Entra Suite, Sailpoint, Okta, and Ping-Federate are your strengths * You are known for a deep knowledge of authorization, access management, and privileged account management concepts as well as of protocols such as SAML, OAuth, OIDC and SCIM.  What we offer     * Bonus/Commission   * Local benefits    * Referral Program   * Volunteer Day   * Internal Academy (QIALearn)    * Employee Assistance Program    * Hybrid work (conditional to your role)    Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.      QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.  

Company Description Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to market and ensuring the safety of our pharmacological developments at all stages. Job Description As Group Leader – Clinical Operational Excellence, you will lead a team of experts and take ownership of driving operational excellence across our European Clinical Development organization. In this strategic role: - You will lead and coordinate clinical operational excellence initiatives including inspection readiness initiatives across Clinical Development EU, ensuring compliance with GCP, SOPs, and regulatory requirements while driving efficiency and high-quality standards. - Together with your team you will oversee TMF services, trial oversight- and training requirements for clinical studies, including Key Peformance Indicator management, TMF vendor oversight, and proactive risk mitigation. - In addition, you will drive innovative approaches with focus on clinical trial oversight-, TMF-, and trial training strategy and ensure best‑practice implementation. - Next to this together with your team, you will identify and implement process improvements, lead cross-functional initiatives to standardize clinical operations, and ensure proper Training Coordination to maintain accurate training records. - You will support the ClinDev EU team with audits and regulatory inspections by preparing documentation, tracking CAPAs, and reviewing trial-related manuals and plans to communicate quality requirements. - In this leadership position, you will collaborate closely with Clinical Trial Management, Data Management, QA, and vendors, providing structured leadership through goal setting, coaching, and performance reviews. - Finally, you develop effective relationships with internal and external stakeholders and work in a dynamic environment to continuously improve operational processes and compliance standards. Qualifications - You hold a university degree in Life Sciences, Natural Sciences, or a related healthcare field and bring proven experience in clinical operations within the pharmaceutical or biotech industry. - You have a strong track record in sponsor oversight for Phase II/III trials and hands-on TMF (eTMF) management, with measurable improvements in quality, completeness, and timeliness. - You possess in-depth knowledge of ICH E6(R2/R3), EU CTR, EMA/FDA inspection behaviors, SOP governance, and trial-specific oversight plans, and you are skilled at prioritizing multiple tasks to meet timelines. - You are a strong and experienced leader with proven disciplinary and functional management skills, demonstrating excellent organizational abilities and fostering collaboration across clinical teams and vendors. - You communicate effectively in English (German is a plus), enjoy working in a dynamic environment, and demonstrate pragmatic, risk-based decision-making with a solution-oriented mindset. - You are a motivated and open-minded team player with strong interpersonal skills and the ability to thrive in complex, fast-paced settings. Additional Information What we offer - Working with free and self-determined time management, also mobile working - An intercultural environment characterized by diversity and flat hierarchies - Freedom to contribute creatively and play an active role in shaping the company - Individual further training in our Miltenyi University as the core of the Miltenyi DNA - 30 days of vacation, discounted ticket to Germany, (e)-bike leasing, capital-forming benefits, company pension plan, disability insurance, canteen, and much more. Diversity is the bedrock of our creativity Our mission: To innovate treatments and technologies and tackle the world’s most serious health challenges. And that’s why we connect the dots –across various disciplines, linking different perspectives, skills, and abilities. You and your talent are welcome here in our inclusive and collaborative environment. So come as you are. Regardless of gender, sexual identity, age, ethnicity, religion or disability. Become part of our team and focus on pushing the borders of medicine. We look forward to your application If you want to work in an open, creative and supportive team, this is the place for you. We look forward to receiving your application along with your salary expectations and availability.

Wir sind ein siebenköpfiges Team in der Corporate IT, das mit Leidenschaft dafür sorgt, dass unsere Systeme reibungslos laufen und unsere Kolleg:innen optimal arbeiten können. Wir sind verantwortlich für den Betrieb und die Weiterentwicklung der WEINMANN IT-Landschaft und arbeiten partnerschaftlich mit unseren Kolleg:innen aus den Fachabteilungen an prozessualen und technischen Verbesserungen. Uns verbindet die Begeisterung für Technik, Teamwork und praxisnahe Lösungen. Dabei legen wir Wert auf eine offene Kommunikation, gegenseitige Unterstützung und Spaß an neuen Herausforderungen. Starte deine Zukunft ab dem 01.08.2026 bei uns am Standort Hamburg – als Auszubildender Fachinformatiker (m/w/d) für Systemintegration. Dein Aufgabengebiet umfasst: - Einarbeitung in die IT nach Ausbildungsrahmenplan - Betreuung und Unterstützung im User Help Desk - Einarbeitung und Support im Bereich Netzwerkinfrastruktur (LAN/WLAN/WAN) - Unterstützung im Bereich Security auf Basis Microsoft Active Directory und Entra - Mitarbeit in IT-Projekten (Hard-und Software) - Internationaler Support Du bringst folgende Qualifikationen mit: - Du hast einen sehr guten mittleren Schulabschluss oder die (Fach-)Hochschulreife - Du interessierst dich besonders für die Fächer Mathematik, Informatik, Deutsch und Englisch - Du hast Spaß daran im Team zu arbeiten und bist auch in der Lage selbstständig Probleme im IT-Umfeld zu lösen - Du hast idealerweise bereits erste praktische Erfahrung durch Praktika oder im privaten Umfeld im IT Bereich sammeln können Das erwartet dich bei uns: - Nach erfolgreichem Ausbildungsabschluss besteht die Möglichkeit der Übernahme in ein festes Arbeitsverhältnis - Eine angemessene Ausbildungsvergütung, Urlaubs- und Weihnachtsgeld und weitere tarifliche Sonderzahlungen - Projektorientiertes Arbeiten in einem dynamischen Team - Unsere Gesundheitsangebote: Egym Wellpass bietet für jeden das richtige Sport- und Wellnessangebot, über myFürstenberg erhalten du und deine Angehörigen ein Angebot zur individuellen Weiterentwicklung und Stärkung der mentalen Gesundheit - Ein offenes und vertrauensvolles Arbeitsklima und Raum für die optimale Entfaltung deines Potentials - Gemeinschaftliche Aktivitäten in unserer Weinmann Emergency (WE) Community We Simplify Saving Lives. Hast du Lust, gemeinsam mit uns einen Beitrag zur Rettung von Menschenleben zu leisten? Dann verstärke unser Team! Wir freuen uns auf deine Bewerbung! Bitte füge deiner Bewerbung ein Anschreiben, einen Lebenslauf und Kopien der letzten Zeugnisse sowie eventuelle Praktikumsnachweise bei. Für Vorabfragen stehen wir dir telefonisch sehr gerne zur Verfügung.

Overview     At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.   We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams.    We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you.    At QIAGEN, every day is an opportunity to make a real-life impact.    Join us, grow with us, and together, let's shape the future of biological discovery.  ‎ Deine Aufgaben: * Du bist Procurement Business Partner für interne Stakeholder und pflegst strategische Lieferantenbeziehungen. * Du führst Ausschreibungen durch, verhandelst und gestaltest Dienst- und Werkverträge. * Du stellst die Einhaltung von Compliance sicher und unterstützt die kontinuierliche Prozessoptimierung. * Du verantwortest Einsparungen und die Erreichung definierter KPIs. * Du wirkst bei der Umsetzung und Weiterentwicklung der globalen Procurement-Strategie in der Kategorie Professional Services mit. * Du arbeitest in internationalen Projekten, z. B. bei der Implementierung von SAP Ariba. * Du unterstützt aktiv bei der Einführung eines neuen External-Workforce-Moduls und bringst deine IT-Affinität ein (z. B. Konfiguration, Tests, Anwender-Support). Dein Profil: * Abgeschlossenes wirtschaftswissenschaftliches Studium (z. B. BWL, VWL, Wirtschaftsingenieurwesen, Supply Chain Management) oder vergleichbare Ausbildung. * Mehrjährige Erfahrung im indirekten Einkauf, idealerweise in Professional Services. * Erfahrungen im Bereich External Workforce, Zeitarbeit, Arbeitnehmerüberlassung oder Freelancer-Management aus Einkaufssicht oder vergleichbarer Berufserfahrung. * Ausgeprägte Verhandlungsstärke und analytische Fähigkeiten. * Professionelle Kommunikation mit Stakeholdern bis zur Geschäftsführungsebene. * Verhandlungssichere Deutsch- und Englischkenntnisse in Wort und Schrift. * Sicherer Umgang mit MS Office sowie fundierte Erfahrung im Lieferantenmanagement. * Kenntnisse in SAP, idealerweise SAP Ariba ; Erfahrungen in Workday sind ein Plus * IT-Affinität und Bereitschaft, sich in neue Systeme einzuarbeiten.  What we offer     * Bonus/Commission   * Local benefits    * Referral Program   * Volunteer Day   * Internal Academy (QIALearn)    * Employee Assistance Program    * Hybrid work (conditional to your role)    Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.      QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.  

Overview     At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.   We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams.    We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you.    At QIAGEN, every day is an opportunity to make a real-life impact.    Join us, grow with us, and together, let's shape the future of biological discovery.  ‎ Die Global Technical Operations (GTO) Division ist das Zentrum für QIAGENs technologische und ingenieurtechnische Expertise und unterstützt unsere weltweiten Produktionsstandorte. In dieser Rolle arbeitest du im Bereich Process Engineering und gestaltest aktiv die Zukunft unserer Fertigungstechnologien für IVD- und HID-Produkte. Deine Aufgaben: * Du identifizierst und bewertest neue Fertigungstechnologien für deren Einsatz bei QIAGEN für IVD- und HID-Produkte. Darauf basierend spezifizierst du Produktionsanlagen und steuerst eigenständig oder im Team Beschaffungsprojekte. * Du entwickelst Produktionskonzepte und Business Cases auf Basis von Produktionskennzahlen, Fertigungskosten und der Bewertung bestehender Anlagen. * Du leitest Projekte zur Entwicklung automatisierter Fertigungs- und Montageprozesse für IVD- und HID-Produkte mit starkem Fokus auf Sondermaschinenbau. * Du konzipierst, planst, führst durch und dokumentierst Prozess- und Datenanalysen. * Mit deiner technischen Expertise und deinem Netzwerk von Experten und Maschinenlieferanten bist du zentrale Ansprechperson für interne Stakeholder (Produktentwicklung, Einkauf, Produktionsstandorte etc.). Dein Profil: * Du hast ein abgeschlossenes Ingenieurstudium und mehrjährige Berufserfahrung, idealerweise in der produzierenden Medizintechnik- oder Pharmaindustrie, im Bereich Maschinen- oder Anlagenbau oder einer vergleichbaren technischen Rolle; vorzugsweise im Life-Science-, IVD- oder GMP-Umfeld. * Du bringst nachweisbare Erfahrung in technischen Beschaffungsprojekten mit, inkl. Erstellung von Spezifikationen, Lieferantenauswahl und -steuerung, Durchführung von FAT/SAT, Abnahme und Inbetriebnahme, Layout-Design, Zykluszeitberechnung und Optimierung des Durchsatzes. * Du trittst sicher und professionell im Umgang mit Maschinenlieferanten und Integratoren auf. * Du hast fundierte Kenntnisse in Automatisierung und Erfahrung in Projekten zu Automatisierung, Verpackung und/oder Robotik. * Erfahrung mit Papierverarbeitungsmaschinen (z. B. Vakuumfördertechnik, Stanz- und Schneideeinheiten, Falt-, und Klebetechnik) ist ein Plus. * Kenntnisse in regulierten Produktionsumgebungen (ISO 13485, GMP, Maschinenrichtlinie, Change Control, Risikomanagement, Validierungen IQ/OQ/PQ) sind von Vorteil. * Du verfügst über sehr gute Deutschkenntnisse (mindestens C1) und fließende Englischkenntnisse. What we offer     * Bonus/Commission   * Local benefits    * Referral Program   * Volunteer Day   * Internal Academy (QIALearn)    * Employee Assistance Program    * Hybrid work (conditional to your role)    Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.      QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.  

Overview     At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.   We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams.    We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you.    At QIAGEN, every day is an opportunity to make a real-life impact.    Join us, grow with us, and together, let's shape the future of biological discovery.  ‎ Deine Aufgaben: * An unserem Standort in Hilden (bei Düsseldorf) übernimmst du mit unserem Instandhaltungsteam die Anlagenwartungen sowie die Anlagenreparaturen * Du bist verantwortlich für die Störungssuche und die dazugehörige Dokumentation der Störungsbeseitigung * Du wirkst aktiv bei der Optimierung von Produktionsanlagen und -prozessen mit und trägst dadurch zur Verbesserung der Anlagenverfügbarkeit und Prozesssicherheit bei * Du koordinierst und betreust Fremdfirmeneinsätze * Du erstellst erforderliche Dokumenten für die Instandhaltungsmaßnahmen und arbeitest im 3-Schicht Betrieb unter Reinraumbedingungen im GMP Umfeld Dein Profil: * Du besitzt eine abgeschlossene Berufsausbildung im Bereich Elektriker/Elektroniker/Mechatroniker * Du konntest bereits Erfahrungen im Bereich der Störungssuche an Produktionsanlagen sammeln wie z.B. von elektrischen / pneumatischen Störungen * Idealerweise kennst du die Qualitäts- sowie Sicherheitsvorschriften der Life Science Industrie und bringst Kenntnisse in der Automatisierungstechnik, Antriebstechnik und Feldbussysteme mit * Du besitzt Praxiserfahrung in der Fehlersuche mit Kenntnissen in dem System S7 sowie Grundkenntnisse in der Mess- und Regelungstechnik und darüber hinaus Kenntnisse in den Netzformen und der 5 Sicherheitsregeln VDE * Mit deinem starkem Fokus auf Kommunikation und Service zu deinen internen Kunden bewegst du dich sicher im Deutschen; Englisch ist ein Vorteil * Deine guten Kenntnisse in MS Office unterstützt deine strukturierte, eigenverantwortliche und dabei teamorientiere Arbeitsweise What we offer     * Bonus/Commission   * Local benefits    * Referral Program   * Volunteer Day   * Internal Academy (QIALearn)    * Employee Assistance Program    * Hybrid work (conditional to your role)    Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.      QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.  

Company Description Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to the market. Job Description As a Senior Clinical Trial Physician, you will play a pivotal role in providing medical leadership and scientific expertise to ensure the successful planning, execution, and supervision of clinical trials in hemato-oncology. You will contribute to study design, regulatory submissions, data review, and publications, while collaborating closely with cross-functional teams to maintain the highest standards of patient safety and regulatory compliance. As a valuable member of the Medical Science team: - You will lead the design and implementation of clinical trial protocols, ensuring adherence to ICH-GCP, ethical standards, and regulatory requirements. - You will provide medical supervision of ongoing trials, working closely with Clinical Operations and vendor Medical Monitors, and support protocol amendments as needed. - You will review and analyze clinical trial data, contributing to Clinical Study Reports (CSRs), MAA/BLA submissions, and other regulatory documentation. - Next to this, you will support the development of scientific publications and presentations, serving as a medical and scientific interface to internal and external stakeholders, including KOLs. - You will ensure regulatory compliance, providing medical guidance on safety, adverse events, and study conduct, and contributing to the preparation of regulatory submission packages. - In addition, you will work closely with cross-functional teams, including Clinical Operations, Regulatory Affairs, Biostatistics, and external partners, to ensure the smooth execution of clinical programs and foster a culture of scientific excellence and accountability. Qualifications As a Senior Clinical Trial Physician, you ideally hold a medical degree (MD) with valid license to practice; board certification in hemato-oncology is strongly preferred. - You bring a strong medical and scientific background in hemato-oncology, with proven experience in clinical trial design, execution, and supervision. - You have experience with regulatory submissions (MAA/BLA) and scientific publications. - You have industry experience in Pharma/Biotech, ideally in a cross-functional, global clinical development setting. - You are highly organized, detail-oriented, and proactive, with the ability to take ownership and make decisions in a fast-paced environment. - You are an excellent communicator and collaborator, able to work effectively with Clinical Operations, Regulatory, Biostatistics, KOLs, and other stakeholders. - You are committed to patient safety, regulatory compliance, and scientific integrity in all aspects of your work. Additional Information What we offer - Working with free and self-determined time management, also mobile working - An intercultural environment characterized by diversity and flat hierarchies - Freedom to contribute creatively and play an active role in shaping the company - Individual further training in our Miltenyi University as the core of the Miltenyi DNA - 30 days of vacation, discounted ticket to Germany, (e)-bike leasing, capital-forming benefits, company pension plan, disability insurance, canteen, and much more. Diversity is the bedrock of our creativity Our mission: To innovate treatments and technologies and tackle the world’s most serious health challenges. And that’s why we connect the dots –across various disciplines, linking different perspectives, skills, and abilities. You and your talent are welcome here in our inclusive and collaborative environment. So come as you are. Regardless of gender, sexual identity, age, ethnicity, religion or disability. Become part of our team and focus on pushing the borders of medicine. We look forward to your application If you want to work in an open, creative and supportive team, this is the place for you. We look forward to receiving your application along with your salary expectations and availability.

Hennig Arzneimittel is looking for a young professional passionate about digital communication and online marketing to strengthen its activities in the German market, with a specific focus on pharmaceutical marketing. The selected candidate will support branding, content creation, and performance marketing initiatives, contributing to the design and implementation of social media campaigns and e-commerce activities (including Amazon and pharmaceutical online channels). They will also be involved in the creation of digital content (newsletters, DEMs, informational materials) aimed at healthcare professionals and corporate stakeholders. Proficiency in Italian and English (B2 level or higher) is considered a plus, to facilitate collaboration with international teams and partners. Main responsibilities: - Operational management of social media channels (LinkedIn, Facebook, Instagram), with a focus on editorial planning, copywriting, and performance analysis - Support for digital advertising campaigns, including Amazon activities and promotions through online pharmacies - Creation and localization of digital content: emails, informational materials, graphic assets, and newsletters - Cross-functional collaboration with marketing, sales, and compliance teams for content validation - Monitoring of campaign performance and preparation of concise reports Requirements: - Degree in Marketing, Economics, Communication, or Business Administration, preferably obtained at a German Hochschule or equivalent institution, with a specialization in digital marketing - Good knowledge of social media platforms, key digital marketing tools and AI LLM platforms. - Familiarity with graphic tools (e.g., Canva, Adobe Express) for the creation of simple yet effective visual content - Team-oriented mindset, strong organizational skills, and attention to detail - Excellent communication skills, precision, and result-oriented approach - Proficiency in German (native or C1 level) and a good command of Italian (B2 or higher) Preferred qualifications: - Previous experience (even brief) in similar roles (e.g., digital marketing internships) - Basic knowledge of platforms such as Amazon Seller/Vendor Central - Interest in the pharmaceutical sector and its digital dynamics What we offer: - A concrete opportunity for growth in the pharmaceutical digital marketing field - The chance to explore tools, formats, and languages in an international context - Support in training and the acquisition of advanced digital skills Further benefits at Hennig Arzneimittel: - Flexible working time models - Vacation and Christmas bonuses and anniversary payments - Competitive salary reflecting qualifications, experience, and responsibilities - 30 vacation days as well as special leaves for personal occasions - Free on-site parking - Subsidized meals in our company cafeteria - Free coffee, mineral water and fruits - Back exercise classes led by a qualified physiotherapist - Access to our corporate benefits program - Daily breakfast van on site - Annual events (e.g. summer party) - Voluntary training possibilities - and more Contact: If you have any questions regarding this position, please feel free to contact us at +49 6145 508 0