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Who we are Helsing is a defence AI company. Our mission is to protect our democracies. We aim to achieve technological leadership, so that open societies can continue to make sovereign decisions and control their ethical standards. As democracies, we believe we have a special responsibility to be thoughtful about the development and deployment of powerful technologies like AI. We take this responsibility seriously. We are an ambitious and committed team of engineers, AI specialists and customer-facing programme managers. We are looking for mission-driven people to join our European teams – and apply their skills to solve the most complex and impactful problems. We embrace an open and transparent culture that welcomes healthy debates on the use of technology in defence, its benefits, and its ethical implications. The role You will own how we prove that our aircraft are hard to detect. While design teams shape geometry and materials, you will show whether those choices hold up under measurement. You will set the low observability (LO) testing roadmap, specify and build our own radar cross-section (RCS) and infrared (IR) test facilities, and define the procedures by which signature performance is verified. You will also scope and supervise the work of external measurement laboratories, then scrutinise the data they return. Your standards will become the reference point for every LO measurement we make, and your evidence will inform design decisions on a flagship aircraft programme. The day-to-day • Build and maintain the multi-year LO testing roadmap, so that measurement capability is in place before each programme milestone requires it • Specify, design and commission in-house LO test facilities, such as anechoic chambers, compact or far-field ranges, pylon systems and radar hardware, including calibration regimes that hold measurement uncertainty within agreed limits • Write master verification and validation test plans for RCS and IR signature measurement at component, subsystem and full-aircraft level • Produce detailed test procedures that deliver consistent, repeatable results across campaigns, sites and suppliers • Define statements of work for subcontracted testing, guide those suppliers technically, and accept or reject delivered measurement data on evidence You should apply if you • Have planned and run RCS measurement campaigns, and can trace a signature result back to the physics and the test set-up that produced it • Have specified, built or operated antenna or RCS test facilities, including near-field, far-field or compact ranges • Work fluently with high-frequency measurement equipment such as vector network analysers, signal generators and spectrum analysers • Apply systems engineering practice to verification and validation, from requirements through test plans to signed-off test reports • Communicate technical reasoning clearly in written and spoken in English and German, to customers as well as engineering colleagues • Hold, or are willing and able to obtain, an extended German security clearance (erweiterte Sicherheitsüberprüfung, Ü2 or Ü3) Note: We operate in an industry where women, as well as other minority groups, are systematically under-represented. We encourage you to apply even if you don't meet all the listed qualifications; ability and impact cannot be summarised in a few bullet points. Nice to have • Experience measuring infrared signatures alongside radar cross-section What we offer • Competitive salary and VSOP options • Relocation support: up to €2,500 and 4 weeks temporary accommodation • Learning: €500/£450 yearly allowance • Health & wellness: gym membership and mental health support (Nilo.health) • Social: regular company events and monthly social allowances • Enhanced parental leave: 22 weeks fully paid for primary caregivers & 6 weeks for secondary caregivers • Family support: 5 days of paid family emergency leave, 100% remote work option during pregnancy and phased return to work These are the core benefits across all locations; there may be additional benefits in specific sites. Helsing is an equal opportunities employer. We are committed to equal employment opportunity regardless of race, religion, sexual orientation, age, marital status, disability or gender identity. Please do not submit personal data revealing racial or ethnic origin, political opinions, religious or philosophical beliefs, trade union membership, data concerning your health, or data concerning your sexual orientation. Helsing's Candidate Privacy and Confidentiality Regime can be found here .

Who we are Helsing is a defence AI company. Our mission is to protect our democracies. We aim to achieve technological leadership, so that open societies can continue to make sovereign decisions and control their ethical standards. As democracies, we believe we have a special responsibility to be thoughtful about the development and deployment of powerful technologies like AI. We take this responsibility seriously. We are an ambitious and committed team of engineers, AI specialists and customer-facing programme managers. We are looking for mission-driven people to join our European teams, and apply their skills to solve the most complex and impactful problems. We embrace an open and transparent culture that welcomes healthy debates on the use of technology in defence, its benefits, and its ethical implications. The role As Systems Engineer for our Armament Control System (ACS), you take end-to-end technical responsibility for a safety-critical system: hardware, software, testing, qualification and safety. You will shape the concept for armament control across the aircraft, the ground station and the data links, then translate that concept into specifications suppliers can build against. At every stage of development, you will upgrade the system to incorporate new weapons and introduce new features. The day-to-day • Take technical responsibility for the full ACS lifecycle, from concept and architecture through hardware and software development, integration and test, to qualification and safety release. • Ensure compliance with industry standards and regulations such as MIL-STD-1760, ARP-4754A, or MIL-STD-882. • Collaborate with cross-functional teams, including hardware, software, and systems integration, to ensure a cohesive and robust system design. • Author and coordinate ACS specifications for suppliers and interfaces for other systems, as well as description documents and user manuals. • Act as the technical point of contact in supplier management, ensuring the right delivery of the ACS items. • Define, model, test and integrate the ACS software, using Matlab Simulink and Speedgoat target machines. You should apply if you • Have strong background and experience in the development of complex, safety-critical systems within the aerospace or defence industry. • Have experience in developing and managing system specifications and interface control documents. • Proficiency with systems engineering tools for requirements management, modelling, and simulation, such as Jama, Gitlab, Simulink. • Have applied airworthiness and safety standards, for example ARP4754A, MIL-STD-882 or MIL-STD-1760. • Communicate technical reasoning clearly in written and spoken English, to customers and suppliers as well as engineering colleagues. • Hold, or are willing and able to obtain, an extended German security clearance (erweiterte Sicherheitsüberprüfung, Ü2 or Ü3). Note: We operate in an industry where women, as well as other minority groups, are systematically under-represented. We encourage you to apply even if you don't meet all the listed qualifications; ability and impact cannot be summarised in a few bullet points. Nice to have • Have integrated stores or weapons onto an airborne platform, whether crewed or uncrewed. • Have a software development experience in aeronautical and military embedded systems (on Real-Time Operating Systems, applying DO-178C standard, with MIL-STD-1553 sequencing, etc.). What we offer • Competitive salary and VSOP options • Relocation support: up to €2,500 and 4 weeks temporary accommodation • Learning: €500/£450 yearly allowance • Health & wellness: gym membership and mental health support (Nilo.health) • Social: regular company events and monthly social allowances • Enhanced parental leave: 22 weeks fully paid for primary caregivers & 6 weeks for secondary caregivers • Family support: 5 days of paid family emergency leave, 100% remote work option during pregnancy and phased return to work These are the core benefits across all locations; there may be additional benefits in specific sites. Helsing is an equal opportunities employer. We are committed to equal employment opportunity regardless of race, religion, sexual orientation, age, marital status, disability or gender identity. Please do not submit personal data revealing racial or ethnic origin, political opinions, religious or philosophical beliefs, trade union membership, data concerning your health, or data concerning your sexual orientation. Helsing's Candidate Privacy and Confidentiality Regime can be found here .

Who we are Helsing is a defence AI company. Our mission is to protect our democracies. We aim to achieve technological leadership, so that open societies can continue to make sovereign decisions and control their ethical standards. As democracies, we believe we have a special responsibility to be thoughtful about the development and deployment of powerful technologies like AI. We take this responsibility seriously. We are an ambitious and committed team of engineers, AI specialists and customer-facing programme managers. We are looking for mission-driven people to join our European teams, and apply their skills to solve the most complex and impactful problems. We embrace an open and transparent culture that welcomes healthy debates on the use of technology in defence, its benefits, and its ethical implications. The role As an Systems Engineer for Weapon Integration, you will drive all weapon integration activities for our advanced aerial platforms. In this role, you will be responsible for leading the end-to-end integration of a diverse range of weapon systems across multiple domains, ensuring seamless functionality with the core mission and avionics systems. You will act as technical authority for weapon integration, providing guidance and mentorship to a dedicated team of engineers, and driving the successful delivery of this critical capability. The day-to-day • Own the weapon integration programme across all relevant domains, delivering a coherent system-of-systems that meets agreed performance, safety and schedule commitments • Define and maintain the weapon integration roadmap, taking capabilities from concept definition through ground test, flight test and final qualification • Integrate weapons with the aircraft's mission system and avionics architecture, covering data buses, stores management, software interfaces and safe-separation requirements • Author the technical specifications, interface control documents (ICDs) and statements of work that govern delivery by internal teams, suppliers and subcontractors • Shape the verification and validation strategy, and mentor engineers across the team so that integration knowledge is shared rather than concentrated You should apply if you • Have integrated weapons such as missiles, bombs or rockets onto fixed-wing or rotary-wing aircraft, and seen that capability through to qualification • Understand mission systems, avionic architectures and the data bus and stores-management standards that connect them, including MIL-STD-1760 or equivalent • Have worked across the full engineering lifecycle, from requirements capture through verification to in-service support • Use engineering tools for requirements management, modelling and simulation as part of your everyday practice • Communicate technical findings clearly to colleagues, customers and suppliers, in writing and in person • Meet the conditions for an extended German security clearance (Ü2/Ü3), given the sensitive nature of the programme, and communicate comfortably in English and German as the working language Note: We operate in an industry where women, as well as other minority groups, are systematically under-represented. We encourage you to apply even if you don't meet all the listed qualifications; ability and impact cannot be summarised in a few bullet points. Nice to have • Have contributed to flight test campaigns and the associated safety and certification evidence What we offer • Competitive salary and VSOP options • Relocation support: up to €2,500 and 4 weeks temporary accommodation • Learning: €500/£450 yearly allowance • Health & wellness: gym membership and mental health support (Nilo.health) • Social: regular company events and monthly social allowances • Enhanced parental leave: 22 weeks fully paid for primary caregivers & 6 weeks for secondary caregivers • Family support: 5 days of paid family emergency leave, 100% remote work option during pregnancy and phased return to work These are the core benefits across all locations; there may be additional benefits in specific sites. Helsing is an equal opportunities employer. We are committed to equal employment opportunity regardless of race, religion, sexual orientation, age, marital status, disability or gender identity. Please do not submit personal data revealing racial or ethnic origin, political opinions, religious or philosophical beliefs, trade union membership, data concerning your health, or data concerning your sexual orientation. Helsing's Candidate Privacy and Confidentiality Regime can be found here .

About Apheris At Apheris, we are building the future of how AI is applied in pharmaceutical R&D. We enable leading pharmaceutical teams to discover and develop drugs faster. We host the industry’s largest federated data networks for drug discovery AI, spanning co-folding, ADMET, and antibody developability. Across these networks, models are trained on proprietary industry datasets to achieve higher performance and broader applicability while keeping data control and IP protected. We deliver these superior models through drug discovery applications that enable teams to run them at scale, further customize them, and integrate them into existing R&D workflows. • AI Structural Biology (AISB) Network : Pharmaceutical companies collaborate in the field of co-folding, structure-based binding affinity predictions and antibody design. • ADMET Network: Pharmaceutical and biotech companies collaborate to improve small-molecule property prediction and expand to further drug modalities. • Antibody Developability Network: Pharma partners collaborate to federate historical and purpose-built antibody developability datasets for secure ML training, without data leaving each partner’s environment. About the role We are looking for an ML Engineer to join our large molecule ML team and build the models behind our antibody, co-folding and developability programs. This is a hands-on role at the intersection of foundation models, structural biology, protein engineering and federated learning. You will build, train and evaluate ML systems for antibody modeling, co-folding, developability prediction and biologics discovery, working on proprietary pharma data across our federated networks. You will own substantial parts of our model programs end to end. That means taking research-led or open-source prototypes and turning them into models that can be evaluated, released and used in real drug discovery workflows. About you You're an ML engineer who works close to the science. You've trained and evaluated models on biological data, and you can take a paper or an open-source model and make it work on a new problem. You care about whether a model actually holds up, not just whether the numbers look good, and you want your work to end up in real use by pharma R&D teams. What you will do • Build, fine-tune and extend large biomolecular models such as OpenFold, Boltz-2 and ESM for antibody modeling, co-folding, binder prediction and developability. • Turn research code and prototypes into reliable components that run in our federated training and evaluation pipelines. • Design evaluations and benchmarks, and deliver results packages for consortium partners. • Own workstreams through to release against agreed milestones, raising risks and trade-offs early. • Work with product, engineering, research and consortium members to make sure the model work meets real application needs. What we expect from you • An MSc, PhD or equivalent experience in machine learning, computational biology, bioinformatics, physics or a related field • Strong Python and PyTorch, and hands-on experience training or fine-tuning deep learning models on biomolecular data. • Hands-on experience with co-folding models or protein language models, such as OpenFold, AlphaFold, Boltz, ESM or similar, beyond just running inference. • Good evaluation habits and solid engineering practice: fair benchmarks, reproducible experiments, and code other people can build on. Nice to have • Experience with Kubernetes-based training, evaluation or deployment, or other MLOps and ML infrastructure tooling. • Experience with federated learning, privacy-preserving ML, or distributed and multi-GPU training. • Experience in pharma, biotech or other regulated or high-trust environments. • Publications in ML, computational biology or structural biology venues such as NeurIPS, ICML, ICLR or similar. What we offer you • Industry-competitive compensation, incl. early-stage virtual share options • Remote-first working – work where you work best, whether from home or a co-working space near you • Great suite of benefits, including a wellbeing budget, mental health benefits, a work-from-home budget, a co-working stipend and a learning and development budget • Regular team lunches and social events • Generous holiday allowance • Quarterly All Hands meet-up at our Berlin HQ or a different European location • A fun, diverse team of mission-driven individuals with a drive to see AI and ML used for good • Plenty of room to grow personally and professionally and shape your own role

• Analysis, modelling and conception of processes for clients in the Discrete Manufacturing Industry in the area of production & planning (PP, Supply Chain, Integrated Planning). • Implementation of a complete project cycle (Design, Build, Test, Run). • Design of discrete manufacturing-specific End-to-end scenarios with focus on Supply chain capabilities. • Conduct Fit-Gap analysis workshops with the client. • Analyze SAP business best practices and make suggestions for improvements or new potential. • Deliver advisory services on how SAP technologies enable a modern and digital production planning function. • Research key business issues to identify improvements across the value chain and support implementation of technology solutions for clients around SAP solutions. • Present effectively the solutions to the client and get their buy-in before moving into Implementation mode. • Elaborate innovative potentials of the new S/4HANA solution, staying relevant and in sync with market changes and innovations. • Contribute to the Nagarro practice growth through innovative spirit. • Functional advisory and support of team members. • Integrated module and process understanding in the Discrete Manufacturing (Maschinen- und Anlagenbau). In-depth Knowledge of at least one SAP Module (PP with QM, PP/DS, IBP). • Experience with some project methodologies (Agile, Hybrid-agile or Waterfall); experience in full life cycle implementation of SAP projects. • Ideally already have experience in S/4HANA projects. • Be self-motivated in learning new concepts and willing to share knowledge & skills with other team members. • Ability to work in global environment, co-ordinate with virtual teams. • Intercultural understanding is an important feature. • Ability and willingness to travel, depending on the project requirements. • Solid written, verbal and interpersonal communication skills in German (C1). • 30 days of paid vacation, internal and external training opportunities, attractive company car and company bicycle arrangements, company-funded accident insurance policy, modern office space at central locations with high-tech equipment, sports programs, access to the corporate benefits portal, free fruit and drinks. • Plenty of room for innovation in a high-growth environment with the latest technologies and products. With us, you can get involved and make a difference. • Flat hierarchies and a workplace with attractive opportunities for growth. In the SAP division of Nagarro, we bundle our expertise for critical business applications, complex ERP landscapes & end-to-end solutions. As a leading force in innovation, we stand as the go-to full-service SAP partner for both medium-sized enterprises and large international corporations. Nagarro helps future-proof your business through a forward-thinking, fluidic, and CARING mindset. We excel at digital engineering and help our clients become human-centric, digital-first organizations, augmenting their ability to be responsive, efficient, intimate, creative, and sustainable. Today, we are 18,500 experts across 40 countries including 2300+ dedicated SAP specialists, forming a Nation of Nagarrians, ready to help our customers succeed.

Location: Fully remote (EMEA timezone) Start date: ASAP Languages: Fluent English required Industry: Cloud Computing / AI / European Deep-Tech SaaS ABOUT THE ROLE Pragmatike is recruiting on behalf of a European deep-tech company building a sovereign, energy-efficient cloud platform for modern AI and high-performance workloads. The company operates a distributed, highly automated infrastructure and is scaling rapidly across a multi-entity, international footprint. As part of this growth, building an AI-native finance organization is a strategic priority. We are seeking a Group Financial Controller to own and scale group accounting, consolidation, reporting, and controls across multiple legal entities. Reporting directly to the CFO, this is a senior, hands-on leadership role for a finance professional capable of structuring, automating, and modernizing accounting operations in a deep-tech environment. Strong, proven experience leveraging AI in accounting workflows is mandatory. This role is not about maintaining legacy processes, but about designing and operating an AI-first accounting function. YOUR RESPONSIBILITIES • Own the monthly, quarterly, and annual group close and consolidation processes across all entities. • Deliver accurate management accounts, as well as board and investor reporting. • Ensure IFRS and local GAAP compliance across multiple jurisdictions. • Define, document, and enforce group accounting policies and internal controls. • Lead, optimize, and scale the NetSuite ERP across the group (NetSuite experience is mandatory). • Drive automation and AI adoption in accounting operations, including reconciliations, anomaly detection, journal automation, and close acceleration. • Manage audits, statutory filings, intercompany accounting, and transfer pricing processes. • Partner closely with the CFO on strategic initiatives, scaling efforts, and financial governance. • Build robust, scalable accounting infrastructure suited to a high-growth, deep-tech organization. REQUIRED QUALIFICATIONS • 8–12+ years of experience in accounting, financial control, or similar senior finance roles. • Strong experience operating in multi-entity, international environments. • Background in SaaS, cloud, infrastructure, or deep-tech companies. • Expert-level NetSuite experience (+++). • Hands-on experience implementing AI tools in accounting workflows (mandatory). • Strong knowledge of IFRS and/or local GAAP, with solid consolidation expertise. • Qualified accountant (CPA, ACA, ACCA, or equivalent). • Proven ability to build finance infrastructure and processes from the ground up. • Comfortable operating in fast-paced, high-growth environments with high ownership. PREFERRED QUALIFICATIONS • Experience supporting rapid international expansion or group restructuring. • Exposure to automation-first or data-driven finance organizations. • Prior involvement in audit transformation or finance system implementations at scale. • Strong stakeholder management skills with executive leadership and investors. WHY JOIN US You will take on a key leadership role within a European AI and cloud deep-tech company, with the opportunity to design and scale a best-in-class, AI-native accounting function. This role offers high autonomy, strategic influence, and direct exposure to the CFO, within a fully remote EMEA setup and limited travel (~10–15%). Pragmatike is committed to a fair, transparent, and inclusive recruitment process. We do not discriminate based on age, disability, gender, gender identity or expression, marital or civil partner status, pregnancy or maternity, race, religion or belief, sex, or sexual orientation. In accordance with GDPR, your personal data will be processed lawfully, fairly, and securely, and used solely for recruitment purposes, including sharing it with our client(s) for employment consideration. You may request access, correction, or deletion of your data at any time. We are committed to maintaining the confidentiality and security of your information throughout the recruitment process.

Your mission Als Steuerberater oder Bilanzbuchhalter (m/w/d) übernimmst du eine zentrale Rolle in unserem Finanz- und Rechnungswesen. Du verantwortest die termingerechte und korrekte Erstellung von Monatsauswertungen, prüfst Kosten und Geschäftsvorgänge und stellst eine verlässliche finanzielle Berichterstattung sicher. Darüber hinaus kümmerst du dich um steuerliche Themen und Meldungen, insbesondere die Umsatzsteuervoranmeldungen (USt-VA), und bist zentrale Ansprechperson für Finanzämter und weitere Behörden. Du begleitest steuerliche Fragestellungen, bereitest relevante Unterlagen und Auswertungen vor und stellst die Einhaltung entsprechender Fristen sicher. Als kompetente Ansprechperson stehst du bei allen Fragen rund um Bilanzierung, Rechnungswesen und Steuern zur Verfügung und arbeitest eng mit internen Ansprechpartnern sowie externen Partnern zusammen. Wenn Du deine Karriere beschleunigen möchtest und Interesse für den Digital Health Bereich hast, dann schreibe uns. Deine Mission: • Du bist die zentrale Ansprechperson für alle steuerlichen Fragestellungen im Unternehmen und berätst Geschäftsführung und Fachbereiche in steuerrechtlichen Themen. • Du verantwortest die Erstellung bzw. fachliche Prüfung von Jahresabschlüssen und Steuererklärungen und koordinierst bei Bedarf die Zusammenarbeit mit externen Partnern. • Du verantwortest die Umsatzsteuervoranmeldungen (USt-VA) sowie weitere steuerliche Meldungen und stellst die Einhaltung aller relevanten steuerlichen Fristen sicher. • Du übernimmst die Kommunikation mit Finanzämtern und anderen Finanzbehörden, beantwortest steuerliche Anfragen und begleitest Betriebsprüfungen. • Du prüfst und bewertest steuerrechtliche Sachverhalte und entwickelst praxisorientierte Lösungen für das Unternehmen. • Du berätst bei steuerlichen Gestaltungs- und Optimierungsfragen und bewertest die steuerlichen Auswirkungen unternehmerischer Entscheidungen. • Du stellst die steuerliche Compliance des Unternehmens sicher und behältst relevante Änderungen der Steuergesetzgebung im Blick. • Du begleitest besondere steuerliche Themen, beispielsweise im Zusammenhang mit Investitionen, Verträgen, internationalen Sachverhalten oder Unternehmensstrukturen. • Du leitest die Buchhaltung und das Controlling und unterstützt bei komplexen Bilanzierungs- und Bewertungsfragen. • Du entwickelst unsere internen Strukturen kontinuierlich weiter und unterstützt dabei, diese effizient und digital aufzustellen. Your profile Was bringst du mit: • Steuerberater oder Bilanzbuchhalterausbildung • Mindestens drei- bis fünfjährige Berufserfahrung • Gute DATEV- und MS-Office-Kenntnisse • Interesse an Digitalisierungs-Themen der Finanzbuchhaltung (DMS) • Selbständiges und verantwortungsbewusstes Arbeiten • Sichere Kommunikation in deutscher und englischer Sprache (weitere Sprachen sind ein Plus) Why us? Das bieten wir dir: • Ein maßgeschneidertes Onboarding-Programm, das es dir ermöglicht, deine Fähigkeiten und Möglichkeiten in deiner Position sehr schnell aufzubauen • Eine agile Arbeitsstruktur, in der Initiative und Kreativität geschätzt werden • Flache Hierarchien und eine offene Feedback-Kultur • Flexible Arbeitszeiten und remote work, damit du Arbeit und Leben optimal vereinbaren kannst • Ein energiegeladenes, motiviertes und gut organisiertes Team • Teamevents und monatliche Workshops für die Entwicklung deiner Fähigkeiten und der mentalen Gesundheit • Dein eigenes Weiterbildungsbudget zu deiner Verwendung • Schnelle Aufstiegsmöglichkeiten • Eine positive, dynamische und offene Unternehmenskultur

Lust auf eine besondere Herausforderung? Bei JobRad® Loop musst du dir keine Erlaubnis holen, um etwas zu bewegen. Eine Datenplattform, die du selbst prägen kannst, statt eine zu verwalten, die andere gebaut haben. Als Senior Data Platform Engineer baust du unsere Snowflake -Plattform mit auf, setzt Standards und führst das Team fachlich. Dein Wort zählt, bis hinauf zur Geschäftsführung und sogar in der gesamten JobRad® Gruppe. Du bringst die Ideen, wir geben dir den Raum dafür. Remote aus Deutschland oder an einem unserer Standorte in München oder Kabelsketal. Let's ride together! Was du brauchst, um erfolgreich zu sein • Snowflake-Praxis: Du hast 2–3 Jahre produktiv mit Snowflake gearbeitet und kennst Performance, Kosten und Best Practices • Data Engineering: Du beherrschst SQL und Python, baust ETL-/ELT-Pipelines (z. B. mit dbt, Airflow oder Talend) und setzt CI/CD und Infrastructure as Code ein • Architektur & Cloud: Du kennst Data Warehouses, Data Lakes und Datenmodellierung und hast Erfahrung mit mindestens einer Cloud-Plattform (AWS von Vorteil, Interesse an Azure) • Eigenverantwortung: Du arbeitest selbstständig, setzt Standards und bringst eigene Ideen für die Weiterentwicklung ein • Stakeholder & Führung: Du kommunizierst sicher bis zur Geschäftsführung, coachst Kolleg:innen und übernimmst fachliche Verantwortung • Sprache: Du sprichst sicher Deutsch (B2/C1/C2-Niveau) und hast gute Englischkenntnisse • Wohnsitz in Deutschland: Du lebst in Deutschland und arbeitest remote oder in München bzw. Kabelsketal (zwischen Halle & Leipzig) Dein Beitrag zu unserer Erfolgsgeschichte • Richtung vorgeben: Du triffst Architekturentscheidungen mit, setzt Standards und überlegst, wohin die Plattform als Nächstes gehen kann • Plattform bauen: Du baust unseren neuen Data Lake auf und machst Snowflake zur Datenbasis des ganzen Unternehmens • BI neu denken: Aus den Daten aller Bereiche entsteht mit dir eine neue BI-Landschaft • Brücken schlagen: Du bringst die Daten unserer Schwesterfirma (JobRad Leasing GmbH) mit unseren zusammen und legst die Basis für Prognosen • Pipelines, die laufen: Automatisiert, performant und stabil, mit CI/CD von Anfang an • Team & Stakeholder: Du coachst das Team fachlich und sprichst auf Augenhöhe mit Geschäftsführung, Head-ofs und Fachbereichen • Leuchtturm werden: Gemeinsam machen wir unsere Abteilung zum Vorbild für die gesamte JobRad® Gruppe Sei nicht überrascht: Diese Stelle findest du ebenfalls unter dem Jobtitel "Senior Data Engineer (m/w/d) – Snowflake" – das ist unsere Art des Split-Tests. Warum JobRad® Loop? • new work: echter Gestaltungsspielraum, wirklich kurze Entscheidungswege, faire JobRad® Loop Gehaltsstruktur in einem modernen Office-Setting (vom kreativen Workshopraum, über die Möglichkeit deinen vierbeinigen Feelgood-Manager mitzubringen bis hin zu Meetingboxen als Rückzugsort) • financial support: Essenszuschuss (46 € monatlich), Sachwertgutschein (50 € monatlich) oder Bezuschussung zu EGYM Wellpass, Mitarbeiterrabatt auf unsere Bikes (1.080 € jährlich) und bei unserem Partner futurebens sowie Jubiläumsgeschenk • work life experience: 30 Tage Urlaub, anteiliges Homeoffice und flexible Arbeitszeiten auf Vertrauensbasis mit fairer Zeiterfassung • green mobility: Übernahme des Deutschlandtickets oder JobRad®-Leasing-Zuschuss für bis zu zwei Bikes (85 € monatlich) • workation: arbeite jährlich an bis zu 40 Tagen aus 50 verschiedenen Ländern weltweit • food & drinks: Obst, Kaffee, Tee und Getränke sind im Office for free • health promotion: Kooperation mit nilohealth.com zur Förderung deiner mentalen Gesundheit • social responsibility: jährlich 2 Sonderurlaubstage für dein ehrenamtliches Engagement • fun & community : regelmäßige Company-Events und private Get-togethers (von Bike-Touren bis hin zum Feierabendbier auf der Wiesn) • personal growth & security: individuelle Entwicklungsmöglichkeiten im Rahmen deines unbefristeten Arbeitsverhältnisses Hinweis: Wir achten sehr darauf, für alle Mitarbeiter:innen passende und faire Benefits zu ermöglichen, dennoch sind nicht alle Benefits bei Full Remote möglich.

Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas. As our company continues we grow we are seeking a Start Up Specialist to join our growing team. For this position, we are open to candidates at all levels, who have acquired some Site Start Up experience gained from within a Clinical Research Organisation. We are open to candidates located in Hungary, Poland, Serbia, Slovakia or Romania with fluency in Hungarian. Essential functions of the job include but are not limited to: • Preparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and amendments/notifications) for submission to Competent Authorities, Ethics Committees, and other applicable local bodies according to local requirements and within required timelines to obtain all necessary authorizations/approvals for the conduct of the Clinical Trial according to international and local/national applicable regulations, company SOPs and principles of ICH-GCP. • Interaction with CA/EC for study purposes and handling responses to the CA/EC. • Providing regular updates about CA and EC submissions to the Start Up Lead and/or Regulatory Lead assigned to the study and to Project Manager/Project Team • Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to assigned responsibilities and to keep Regulatory Leadership • Preparation/Support the development of study specific start-up plans, IMP release requirements and essential document review criteria. • Partner with the assigned site CRA to ensure alignment in communication and secure site • review and manage collection of essential documents required for site activation/IMP release. • Customize country/site specific Patient Information Sheet and Informed Consent Form. • Responsible for/facilitates the translation and co-ordination of translations for documents. • Maintain communication with other key functions participating to country start up e., Feasibility, Clinical Operations, Project Management, Regulatory, and Site Contracts management group on project specific status and deliverables. • Act as SME for collection and maintenance of site level critical path to Site Activation data points, including but not limited to Competent Authority, local IRB/Ethics Committee (EC) timelines, site contracts and budget negotiation requirements for and other required reviews to secure on time site activation for the assigned sites in the country. • When required, participate/support the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee department. • May participate/support feasibility group in site outreach to assess potential interest of investigators to a potential study. • Keep an updated knowledge of the local clinical trial laws, regulations and help distributing their knowledge within PFM to ensure the conduct of Clinical Trials according to international and local/national applicable regulations. • Maintain audit/inspection readiness at all times and file documents as per TMF plan and/ or study specific plans in the relevant TMF • May support the clinical team performing Pre-Study Site Visits. The ideal candidate will have: Minimum Required: • Bachelor’s degree in life sciences or related field (ideally in a scientific or healthcare discipline), or Registered Nurse (RN) or equivalent combination of education, training, and experience. • A qualification in Pharmacy/ work experience as a Pharmacist would be highly beneficial. • Demonstrated experience as a Regulatory or Start Up specialist (or comparable role) in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies. Other Required: • Strong communication and organizational skills. • Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required. • Must be fluent in Hungarian and English, as you will be supporting Hungarian sites Preferred: • Relevant regulatory and site start-up (feasibility, contract negotiations, CA/ EC/ IRB submissions) experience. • Experience using milestone tracking tools/systems. • Ability to prioritise workload to meet deadlines • Advanced degree in medical or life sciences (MD, PhD, PharmD)/RAC certification/Masters in Regulatory Science. LI-OS1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice . Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to …

Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas. As our company continues we grow we are seeking a Start Up Specialist to join our growing team. For this position, we are open to candidates at all levels, who have acquired some Site Start Up experience gained from within a Clinical Research Organisation. We are open to candidates located in Hungary, Poland, Serbia, Slovakia or Romania with fluency in Hungarian. Essential functions of the job include but are not limited to: • Preparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and amendments/notifications) for submission to Competent Authorities, Ethics Committees, and other applicable local bodies according to local requirements and within required timelines to obtain all necessary authorizations/approvals for the conduct of the Clinical Trial according to international and local/national applicable regulations, company SOPs and principles of ICH-GCP. • Interaction with CA/EC for study purposes and handling responses to the CA/EC. • Providing regular updates about CA and EC submissions to the Start Up Lead and/or Regulatory Lead assigned to the study and to Project Manager/Project Team • Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to assigned responsibilities and to keep Regulatory Leadership • Preparation/Support the development of study specific start-up plans, IMP release requirements and essential document review criteria. • Partner with the assigned site CRA to ensure alignment in communication and secure site • review and manage collection of essential documents required for site activation/IMP release. • Customize country/site specific Patient Information Sheet and Informed Consent Form. • Responsible for/facilitates the translation and co-ordination of translations for documents. • Maintain communication with other key functions participating to country start up e., Feasibility, Clinical Operations, Project Management, Regulatory, and Site Contracts management group on project specific status and deliverables. • Act as SME for collection and maintenance of site level critical path to Site Activation data points, including but not limited to Competent Authority, local IRB/Ethics Committee (EC) timelines, site contracts and budget negotiation requirements for and other required reviews to secure on time site activation for the assigned sites in the country. • When required, participate/support the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee department. • May participate/support feasibility group in site outreach to assess potential interest of investigators to a potential study. • Keep an updated knowledge of the local clinical trial laws, regulations and help distributing their knowledge within PFM to ensure the conduct of Clinical Trials according to international and local/national applicable regulations. • Maintain audit/inspection readiness at all times and file documents as per TMF plan and/ or study specific plans in the relevant TMF • May support the clinical team performing Pre-Study Site Visits. The ideal candidate will have: Minimum Required: • Bachelor’s degree in life sciences or related field (ideally in a scientific or healthcare discipline), or Registered Nurse (RN) or equivalent combination of education, training, and experience. • A qualification in Pharmacy/ work experience as a Pharmacist would be highly beneficial. • Demonstrated experience as a Regulatory or Start Up specialist (or comparable role) in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies. Other Required: • Strong communication and organizational skills. • Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required. • Must be fluent in Hungarian and English, as you will be supporting Hungarian sites Preferred: • Relevant regulatory and site start-up (feasibility, contract negotiations, CA/ EC/ IRB submissions) experience. • Experience using milestone tracking tools/systems. • Ability to prioritise workload to meet deadlines • Advanced degree in medical or life sciences (MD, PhD, PharmD)/RAC certification/Masters in Regulatory Science. LI-OS1 #LI-Remote Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice . Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to …

Algolia is the retrieval intelligence layer that turns intent into trusted, decision-grade outcomes. Powering more than 1.7 trillion queries a year for over 18,000 customers with millisecond latency and 99.999% reliability, we are the recognized leader for Search and Product Discovery by top industry analyst firms. The Algolia platform turns a company's products, content, and business rules into data that humans, applications and AI agents can act upon. The result is trusted customer experiences with stronger conversions for measurable business impact. As a Senior Software Engineer on the Connectors Platform Team, you’ll play a key role in building products that help our customers ingest, transform, and enrich their data with AI, making it simple to integrate into Algolia. The Team & Platform The Connectors Platform Team builds and scales the services that bring our customers’ data into Algolia, reliably, securely, and at scale. Our work touches: • E-commerce: powering real-time integrations with Shopify, Commercetools, BigCommerce • Data Connectivity: connecting to sources like JSON, BigQuery, Supabase, MySQL, and beyond • Data Transformations: allow customers to transform their data as it flows into Algolia • AI Enrichment Pipelines: enhancing data to improve search relevance We run on Go, Kubernetes, and Google Cloud, with an engineering culture built around reliability, performance, and simplicity. What You'll Do • Design, build, and scale distributed data ingestion services serving thousands of global businesses • Drive improvements to system reliability, scalability and throughput • Champion engineering excellence in testing, observability, and performance • Mentor teammates and help evolve the engineering culture as we grow You might be a fit if you • Bring proven experience building and operating high-traffic production systems in Go • Have strong hands-on experience with Kubernetes, Terraform, and Google Cloud • Love the challenge of designing resilient systems that handle high-traffic workloads • Care about writing high-quality, tested, maintainable code • Communicate clearly and collaboratively in English LI-Remote Algolia does not discriminate on the basis of race, color, religion, sex, age, national origin, military status, veteran status, disability status, sexual orientation, gender identity, genetic information, or any other characteristic protected by law. The annual base salary compensation range for this role reflects market pay data within this location. The exact compensation offered for this role may vary depending on specific location and job-related knowledge, technical skills, and experience; and is only one part of our Total Rewards philosophy to compensate and recognize employees for their work. Base Salary Pay Range €67.500 — €94.000 EUR FLEXIBLE WORKPLACE STRATEGY: Algolia’s flexible workplace model is designed to empower all Algolians to fulfill our mission to power search and discovery with ease. We place an emphasis on an individual’s impact, contribution, and output, over their physical location. Algolia is a high-trust environment and many of our team members have the autonomy to choose where they want to work and when. We have a global presence with offices in Paris, NYC, London, Sydney and Bucharest, however we also offer many of our team members the option to work remotely either as fully remote or hybrid-remote employees. Positions listed as "Remote" are only available for remote work within the specified country. Positions listed within a specific city are only available in that location - depending on the role it may be available with either a hybrid-remote or in-office schedule. WE’RE LOOKING FOR SOMEONE WHO CAN LIVE OUR VALUES: • GRIT - Problem-solving and perseverance capability in an ever-changing and growing environment. • TRUST - Willingness to trust our co-workers and to take ownership. • CANDOR - Ability to receive and give constructive feedback. • CARE - Genuine care about other team members, our clients and the decisions we make in the company. • HUMILITY - Aptitude for learning from others, putting ego aside. We’re looking for talented, passionate people to help build the world’s best search and discovery technology. We value autonomy, diversity, and collaboration. We’re committed to creating an inclusive workplace where everyone is respected and supported—regardless of race, age, ancestry, religion, sex, gender identity, sexual orientation, marital status, color, veteran status, disability, or socioeconomic background. IMPORTANT NOTICE FOR CANDIDATES - Recruitment Fraud Notice We’ve recently seen an increase in recruitment scams targeting job seekers. To help protect yourself, please keep the following in mind: • Our open positions may appear on third-party job boards, but the best way to apply safely is directly through our careers page . • All genuine communication from Algolia will come from an @algolia.com email …

Vous souhaitez piloter des projets IT internationaux ayant un impact concret sur les pratiques hospitalières et la qualité des soins ? Nous recherchons un(e) Chef de Projet Implémentation Logicielle International – Healthcare IT (H/F) pour accompagner le déploiement européen de solutions de santé numérique. Vous interviendrez sur des logiciels destinés à améliorer l'utilisation des traitements antimicrobiens et à renforcer la surveillance des infections dans les établissements de santé. Au cœur de cette mission, vous assurerez la coordination des équipes techniques, des interlocuteurs hospitaliers et des différentes parties prenantes internationales. Vos principales missions Pilotage des projets d'implémentation • Piloter simultanément plusieurs projets de déploiement de solutions logicielles auprès d'établissements hospitaliers européens. • Construire les plannings, définir les jalons et organiser les différentes phases d'implémentation. • Superviser l'avancement des projets et anticiper les risques susceptibles d'affecter les engagements. • Garantir la coordination des activités jusqu'à la mise en production. Coordination des clients internationaux • Accompagner les chefs de projet des établissements hospitaliers dans la préparation et la réalisation des déploiements. • Animer les réunions opérationnelles et assurer une communication régulière avec les interlocuteurs locaux. • Coordonner les interventions des différentes équipes afin de sécuriser les étapes clés. • Maintenir une relation de confiance avec les clients tout au long des projets. Coordination des équipes internes • Collaborer avec les équipes d'intégration de données, de développement, de support applicatif et les équipes commerciales locales. • Organiser les interventions des différents contributeurs. • Faciliter la résolution des difficultés techniques et organisationnelles. • Assurer la circulation des informations entre les équipes internationales. Mise en production et accompagnement • Participer aux ateliers de cadrage et aux étapes de validation des solutions. • Coordonner les opérations de mise en production. • Accompagner les premières semaines d'exploitation et organiser le transfert vers les équipes de support. • Contribuer à l'amélioration continue des processus de déploiement. Environnement technique et fonctionnel • Healthcare IT / Digital Health • Clinical Decision Support Systems (CDSS) • Electronic Health Records (EHR / EMR) • Hospital Information Systems (HIS) • Interopérabilité hospitalière • HL7 • Antimicrobial Stewardship • Infection Surveillance Les technologies et standards ci-dessus correspondent au domaine des solutions et aux connaissances appréciées pour la mission. Aucun outil précis de gestion de projet ou langage de développement n'est imposé. Formation Formation supérieure en informatique, systèmes d'information, ingénierie ou gestion de projet, ou expérience professionnelle équivalente. Expérience Vous justifiez d'au moins 5 années d'expérience en gestion de projet IT, idéalement dans le déploiement de solutions logicielles chez des clients internationaux. Vous avez déjà assuré la coordination de projets d'implémentation jusqu'à leur mise en production. Une expérience auprès d'établissements hospitaliers, d'éditeurs de logiciels médicaux ou d'acteurs de la santé numérique représente un avantage significatif. Compétences clés • Gestion de projets d'implémentation logicielle. • Coordination de plusieurs projets simultanés. • Planification, suivi des risques et gestion des dépendances. • Animation de comités projet et de pilotage. • Gestion des relations clients et des parties prenantes. • Coordination d'équipes techniques internationales. • Accompagnement des mises en production. Une certification PMP ou PRINCE2 constitue un plus. Langues indispensables • Français courant. • Anglais courant. • Italien courant. La maîtrise de l'espagnol constitue un atout supplémentaire. Qualités personnelles Vous êtes reconnu(e) pour votre autonomie, votre sens du service et votre capacité à fédérer des interlocuteurs variés. Votre rigueur, votre diplomatie et votre communication vous permettent d'évoluer efficacement dans des environnements multiculturels. Vous appréciez les responsabilités, savez gérer plusieurs priorités et adoptez une approche proactive pour faire avancer les projets. Les + du poste Projets internationaux à l'échelle européenne. Solutions innovantes dans le domaine de la santé numérique. Impact concret sur les pratiques hospitalières. Collaboration avec des équipes techniques et métiers multiculturelles. Responsabilités de pilotage de bout en bout. Interactions directes avec les établissements de santé. Télétravail majoritaire depuis un pays européen. Environnement associant innovation technologique et enjeux de santé publique. Pourquoi rejoindre Citech ? Rejoindre CITECH, c'est intégrer une ESN à taille humaine qui …