Simulationsergebnisse, Prüfdaten, Forschungsdaten) zur Unterstützung interner Entscheidungsprozesse und regulatorischer Positionierungen Enge Zusammenarbeit mit Engineering, R&D und Produktentwicklung sowie Einbringung wissenschaftlicher und regulatorischer Expertise zur Entwicklung sicherer und zukunftsfähiger Produkte Mitwirkung an Forschungsaktivitäten und Generierung wissenschaftlicher Evidenz zur Verwendung in regulatorischen Diskussionen und Normungsgremien Erstellung technischer Dokumentationen, Berichte und Präsentationen für interne Stakeholder sowie externe regulatorische und wissenschaftliche Zielgruppen Unterstützung der CYBEX-Vertretung in Industrie-, Regulierungs- und Normungsgremien durch datenbasierte fachliche Beiträge Mitwirkung bei der Präsentation wissenschaftlicher Arbeiten von CYBEX auf Konferenzen, Workshops und Expertengremien Dein Weg zu CYBEX: Abgeschlossenes Studium im Bereich Ingenieurwesen, Data Science, Statistik, Biomechanik, Physik oder einer vergleichbaren naturwissenschaftlich-technischen Fachrichtung Fundierte Kenntnisse oder starkes Interesse im Bereich Datenanalyse, Modellierung und virtueller Simulation – idealerweise in einem sicherheitskritischen oder ingenieurwissenschaftlichen Umfeld Erfahrung in der Anwendung von Human Body Models (HBMs) in virtuellen Crashsimulationen zur Verletzungsprognose ist sehr wünschenswert Fähigkeit, komplexe Daten zu analysieren, Muster zu erkennen und Ergebnisse in klare Schlussfolgerungen sowie Handlungsempfehlungen zu überführen Sehr gute schriftliche und mündliche Kommunikationsfähigkeiten mit der Fähigkeit, technische Inhalte adressatengerecht aufzubereiten Interesse oder idealerweise erste Erfahrungen im Bereich Kindersicherheit, Kinderrückhaltesysteme, Insassenbiomechanik oder Verletzungsprävention sind von Vorteil Ausgeprägte Team- und Kommunikationsfähigkeit sowie Freude an der interdisziplinären Zusammenarbeit zwischen Engineering, Forschung, Regulierung und kommerziellen Bereichen Neugierde, Lernbereitschaft und Flexibilität in einem dynamischen internationalen Umfeld Bereitschaft zu gelegentlichen Dienstreisen innerhalb Deutschlands und international Fließende Deutsch- und Englischkenntnisse in Wort und Schrift Wir agieren international und haben Mitarbeiter und Mitarbeiterinnen aus über 29 Nationen.
Main Responsibilities: Drive actions to ensure material availability supporting customer releases and service schedulesWork with internal groups to streamline documentation effortsAssist in updating material master dataSupport management of purchase orders and service work ordersAnalyze inventory data and parametersManage existing data sets and create new data models for metrics and reportingMaintain effective communication with internal and external customersPerform other related duties as assignedTo succeed, you will need Skills / Knowledge / Experience: Education level: Must be a Junior or Senior pursuing a Bachelor’s degree in Supply Chain, Business, or Information Systems at an accredited college or university.
Main Responsibilities: Assist with Internal Audit & Evaluate Findings Assist with Customer Master Data updates Contact Customers to resolve open credits Analysis of freight invoices and analyze for trends Assist Analyst with reporting on various business lines Other duties as assigned To succeed, you will need Skills / Knowledge / Experience: Education level: Must be a Junior or Senior Business Administration, majoring in accounting at an accredited college or university. Knowledge areas/Skills: Microsoft Excel & Outlook proficiency Excellent written and oral communication skills that demonstrate a proven ability to develop relationships with a range of internal and external customers Excellent planning and organizational skills Self-motivates, independent, flexible, organized, and methodical.
Your role Candidate must be fluent in English Mission/Purpose of the Job: The General Audit Intern supports Internal and Financial Audit functions by assisting with control reviews, testing, compliance checks, data validation, and financial analysis.
If you're a creative thinker with a passion for 3D design and event experiences, this role could be a perfect fit for you. Please click "Apply Now." All applicants must submit a portfolio or showreel for consideration. All applications will be handled in strict confidence and used solely for recruitment purposes.
Financial performance, commercial outcomes, and overall clinic risk management remain the ultimate responsibility of the GM. Confidentiality The post holder must maintain confidentiality of information regarding patients, employees, and other Company business in accordance with National and European data protection legislation.
Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
Training, induction and assisting in the performance management of new and junior staff Regulatory Compliance Assisting in the delivery of group level projects Qualifications and Experience: Minimum of a degree in Life Sciences, preferably a MSc or PhD HCPC Registered (or immediately eligible) Minimum of 5 years of clinical experience, some preferably at a senior/management level Fully trained in all clinical laboratory procedures, preferably including biopsy Advanced knowledge of the UK Regulatory Framework Must be self-motivated, eager to learn and resilient. High level of attention to detailed and focused Excellent communication skills Salary: Competitive (Depending on experience) Location: TFP Nurture Fertility - Nottingham Working Hours: 37.5 Monday to Friday Weekend Working at approximately a 1:4 (renumerated with TOIL/overtime) On-Call: Working approximately a 1:4 in coordination with your weekend (remunerated with a daily rate of pay in addition to your basic salary) Pension: Dual contribution pension scheme Holiday Entitlement: 27 Days + Bank holidays (pro rata)
Training, induction and assisting in the performance management of new and junior staff Regulatory Compliance Assisting in the delivery of group level projects Qualifications and Experience: Minimum of a degree in Life Sciences, preferably a MSc or PhD HCPC Registered (or immediately eligible) Minimum of 5 years of clinical experience, some preferably at a senior/management level Fully trained in all clinical laboratory procedures, preferably including biopsy Advanced knowledge of the UK Regulatory Framework Must be self-motivated, eager to learn and resilient. High level of attention to detailed and focused Excellent communication skills Salary: Competitive (Depending on experience) Location: TFP Belfast Fertility Working Hours: 37.5 Monday to Friday Weekend Working at approximately a 1:4 (renumerated with TOIL/overtime) On-Call: Working approximately a 1:4 in coordination with your weekend (remunerated with a daily rate of pay in addition to your basic salary) Pension: Dual contribution pension scheme Holiday Entitlement: 27 Days + Bank holidays (pro rata)
Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
For enquiries or to request a full role profile please contact Louise Dooley, Senior Talent Acquisition Specialist (louise.dooley@oxinst.com) Please note on this occasion we are unable to provide sponsorship for visa applicants for this particular post, as such applicants must hold the right to work in the UK to be eligible. Why Oxford Instruments Andor? Our company values of being Inclusive, Innovative, Trusted and Purposeful are at the core of everything we do for our customers and our teams.