Let’s talk! Your work: • Explore and exploit new technologies • Design and develop Minimum Viable Products / Proof of Concepts to demonstrate technology potential • Tap into our on-prem or public cloud solutions (GCP/Azure) to spin up any infrastructure you need • Work with colleagues from our Centers of Excellence to support their AI/ML roadmaps • Potentially develop new products, together with other Digital Lab colleagues • Keep an eye out for emerging technologies coming up • Communicate with colleagues across the world, lead presentations, workshops and trainings • Proactively look for improvements that take the robot out of the human and help server our customers better • Contribute to further initiatives within Digital Lab (e.g.
Mein Arbeitgeber Fire Point Rocket Technology (FPRT) is a defense technology company at the intersection of advanced chemistry and modern rocket propulsion. We design and manufacture solid rocket fuel and propulsion components that power next generation defense systems, with a strong focus on safety, quality, and compliance.
Mein Arbeitgeber Fire Point Rocket Technology (FPRT) is a defense technology company at the intersection of advanced chemistry and modern rocket propulsion. We design and manufacture solid rocket fuel and propulsion components that power next generation defense systems, with a strong focus on safety, quality, and compliance.
Your Profile Bachelor's degree in Engineering, Physics, Materials Science, or related technical discipline; Master's degree preferred.7+ years of experience in application engineering, product engineering, or technical customer support for medical, optical, or high-reliability components.10+ years of experience supporting medical device OEMs or optical/photonics customers preferred.Strong experience with customer interaction, specification management, and technical communication.Ability to interpret drawings, tolerances, and material/process requirements; hands-on lab and testing experience preferred.Experience with cross-functional collaboration (Sales, Engineering, Product Management, Quality, Operations).Excellent written/verbal communication, presentation skills, and problem-solving capability.Experience supporting verification, validation, and application testing preferred.Some familiarity with medical product standards, regulatory documentation expectations, and design control practices.Experience with DOE, statistical tools, and structured problem-solving (e.g., 8D) preferred.Experience in global, matrixed organizations preferred.Must be able to read, write, and speak EnglishEffective verbal and written communication skills.Self-motivated and results oriented.Due to the nature of work performed at this facility, US Person status may be required.
Dies bedeutet insbesondere: Mitwirkung an der Weiterentwicklung der Codebasis via GitHub (Feature-Entwicklung, Code Reviews und Bearbeitung von Issues) Unterstützung bei der Entwicklung eines Designs und der Implementierung neuer Konzepte, um die Funktionalität und Skalierbarkeit zu erweitern Mitarbeit an der Integration neuer Datensätze und Modelle in die bestehende Bibliothek Wenn wir Ihr Interesse geweckt haben, senden Sie uns bitte ein kurzes Anschreiben, einen aktuellen Lebenslauf, ein Transcript of Records und - falls vorhanden - Referenzen zu relevanten Softwareentwicklungsprojekten, an denen Sie in der Vergangenheit mitgearbeitet haben, vorzugsweise auf Englisch und bevorzugt per E-Mail an timo.stoll@log.rwth-aachen.de .
Dies bedeutet insbesondere: Mitwirkung an der Weiterentwicklung der Codebasis via GitHub (Feature-Entwicklung, Code Reviews und Bearbeitung von Issues) Unterstützung bei der Entwicklung eines Designs und der Implementierung neuer Konzepte, um die Funktionalität und Skalierbarkeit zu erweitern Mitarbeit an der Integration neuer Datensätze und Modelle in die bestehende Bibliothek Wenn wir Ihr Interesse geweckt haben, senden Sie uns bitte ein kurzes Anschreiben, einen aktuellen Lebenslauf, ein Transcript of Records und - falls vorhanden - Referenzen zu relevanten Softwareentwicklungsprojekten, an denen Sie in der Vergangenheit mitgearbeitet haben, vorzugsweise auf Englisch und bevorzugt per E-Mail an timo.stoll@log.rwth-aachen.de.
Dies bedeutet insbesondere: Mitwirkung an der Weiterentwicklung der Codebasis via GitHub (Feature-Entwicklung, Code Reviews und Bearbeitung von Issues) Unterstützung bei der Entwicklung eines Design und der Implementierung neuer Konzepte, um die Funktionalität und Skalierbarkeit zu erweitern Mitarbeit an der Integration neuer Datensätze und Modelle in die bestehende Bibliothek Wenn wir Ihr Interesse geweckt haben, senden Sie uns bitte ein kurzes Anschreiben, einen aktuellen Lebenslauf, ein Transcript of Records und - falls vorhanden - Referenzen zu relevanten Softwareentwicklungsprojekten, die Sie in der Vergangenheit durchgeführt haben, vorzugsweise auf Englisch und bevorzugt per E-Mail an timo.stoll@log.rwth-aachen.de.
Register with us and reap the benefits of interesting job offers that match your skills and experience. Design, conduct, and analyze in vivo studies involving intravenous injections, blood collection, and bleeding/thrombosis models Execute full end-to-end in vivo workflows, from study preparation to sample processing and documentation Characterize gene therapy candidates using molecular and biochemical assays such as ELISA, thrombin generation, and chromogenic assays Handle, prepare, and evaluate patient-derived blood and plasma samples for in vitro and ex vivo experiments Perform data analysis, interpret results, and present findings to the research team Maintain accurate, complete, and compliant documentation across all experimental steps Contribute to lab operations, including safety standards, inventory, equipment handling, and general organization Collaborate with cross-functional team members to ensure smooth coordination and progress on gene therapy studies Academic background in life sciences (MSc or BSc) or completed scientific apprenticeship with hands-on laboratory experience Active certification for animal experimentation (e.g., LTK1, FELASA, or equivalent) Proven hands-on experience with rodent work, including intravenous injections and blood sampling Ability to independently design, execute, and manage in vivo studies from start to finish Experience with molecular or biochemical assays relevant to hemostasis, thrombosis, or gene therapy Strong ability to plan experiments, analyze data, and interpret scientific results Fluency in English with clear communication skills Highly organized, proactive, and team-oriented mindset with strong reliability and attention to detail Opportunity to contribute directly to translational gene therapy research with high scientific impact Hands-on work with a combination of in vivo, ex vivo, and molecular biology techniques Collaborative environment with close teamwork and modern laboratory infrastructure Diverse and meaningful daily tasks involving both preclinical models and human biological samples Ihr Kontakt Referenznummer 865654/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Register with us and reap the benefits of interesting job offers that match your skills and experience. Design, conduct, and analyze in vivo studies involving intravenous injections, blood collection, and bleeding/thrombosis modelsExecute full end-to-end in vivo workflows, from study preparation to sample processing and documentationCharacterize gene therapy candidates using molecular and biochemical assays such as ELISA, thrombin generation, and chromogenic assaysHandle, prepare, and evaluate patient-derived blood and plasma samples for in vitro and ex vivo experimentsPerform data analysis, interpret results, and present findings to the research teamMaintain accurate, complete, and compliant documentation across all experimental stepsContribute to lab operations, including safety standards, inventory, equipment handling, and general organizationCollaborate with cross-functional team members to ensure smooth coordination and progress on gene therapy studies Academic background in life sciences (MSc or BSc) or completed scientific apprenticeship with hands-on laboratory experienceActive certification for animal experimentation (e.g., LTK1, FELASA, or equivalent)Proven hands-on experience with rodent work, including intravenous injections and blood samplingAbility to independently design, execute, and manage in vivo studies from start to finishExperience with molecular or biochemical assays relevant to hemostasis, thrombosis, or gene therapyStrong ability to plan experiments, analyze data, and interpret scientific resultsFluency in English with clear communication skillsHighly organized, proactive, and team-oriented mindset with strong reliability and attention to detail Opportunity to contribute directly to translational gene therapy research with high scientific impactHands-on work with a combination of in vivo, ex vivo, and molecular biology techniquesCollaborative environment with close teamwork and modern laboratory infrastructureDiverse and meaningful daily tasks involving both preclinical models and human biological samples Ihr Kontakt Referenznummer 865654/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Dies bedeutet insbesondere: Mitwirkung an der Weiterentwicklung der Codebasis via GitHub (Feature-Entwicklung, Code Reviews und Bearbeitung von Issues) Unterstützung bei der Entwicklung eines Design und der Implementierung neuer Konzepte, um die Funktionalität und Skalierbarkeit zu erweitern Mitarbeit an der Integration neuer Datensätze und Modelle in die bestehende Bibliothek Wenn wir Ihr Interesse geweckt haben, senden Sie uns bitte ein kurzes Anschreiben, einen aktuellen Lebenslauf, ein Transcript of Records und - falls vorhanden - Referenzen zu relevanten Softwareentwicklungsprojekten, die Sie in der Vergangenheit durchgeführt haben, vorzugsweise auf Englisch und bevorzugt per E-Mail an timo.stoll@log.rwth-aachen.de.
The Study Physician ensures state-of-the-art medical oversight from the Trial Design Outline (TDO) kickoff through to the Clinical Trial Report (CTR) and serves as a core member of both the Trial Team and the Evidence Network Team.
BudgetkontrolleBegleitung der Ausschreibung und Vergabe von Bau- bzw. Generalunternehmerleistungen (Design & Build)Qualitäts-, Risiko- und Claim-Management durch regelmäßiges Reporting Beratung & Konzeption Technische und planerische Beratung beim AnmietungsprozessEntwicklung individueller Belegungskonzepte mit internen PlanungstoolsKreative Entwurfskonzepte (mit dem Design Team)Beratung zu technischen, baustrukturellen und genehmigungsrechtlichen FragestellungenBegleitung bei Farb-, Material- und Möblierungskonzepten Ihr Profil Ausbildung & Erfahrung Abgeschlossenes Studium: Architektur, Innenarchitektur, Bauingenieurwesen oder ProjektsteuerungBerufserfahrung in Planungsbüro oder Bau-/ProjektmanagementErfahrung mit Büro- oder Retail-Fit-outs von Vorteil Fachkompetenz Kenntnisse in Planung, Koordination und Überwachung von InnenausbaumaßnahmenKenntnisse von Bauvorschriften, Brandschutz und ArbeitsstättenrichtlinienGrundverständnis für TGA, Elektroinstallationen und Workplace-TechnologienSicherer Umgang mit Kosten- und Zeitplanungstools sowie MS Office/Excel Persönliche Stärken Selbstständige, strukturierte und ergebnisorientierte ArbeitsweiseExzellente Kommunikations- und Präsentationsfähigkeiten (Deutsch und Englisch mind.
Mein Arbeitgeber Fire Point Rocket Technology (FPRT) is a defense technology company operating at the intersection of advanced chemistry and modern rocket propulsion. We design and manufacture solid rocket fuel and propulsion components that power next-generation defense systems, with uncompromising focus on safety, quality, and compliance.
Mein Arbeitgeber Fire Point Rocket Technology (FPRT) is a defense technology company operating at the intersection of advanced chemistry and modern rocket propulsion. We design and manufacture solid rocket fuel and propulsion components that power next-generation defense systems, with uncompromising focus on safety, quality, and compliance.
What makes you stand out You hold a master’s degree in Computer Science, Software Engineering, Mathematics, Statistics, or a related quantitative field.You have at least 3 years of professional experience in ML Engineering or MLOps, with a proven track record of building, deploying, and operating tailored AI/ML solutions in production.You bring deep expertise in Python and SQL, hands‑on experience with cloud platforms (ideally Azure), and familiarity with data warehouses such as Snowflake; foundational knowledge of Infrastructure‑as‑Code tools like Terraform is a plus.You are proficient with CI/CD tools (e.g., Azure DevOps), containerization technologies (Docker/Kubernetes), and apply modern software design patterns confidently.You thrive in a dynamic, agile, and innovative environment, working effectively both independently and as part of a team.You possess excellent English communication skills, both written and spoken; German language skills are considered a plus.