THOR GmbH sucht in eine/n Regulatory Affairs Manager (m/w/d) Fachgruppe Reach & Regulatory Services (ID-Nummer: 13685251)
Lead, Develop and Empower the Team Provide strong technical leadership, foster professional development and ensure continuous growth and engagement of your team. Manage External Service Providers Effectively manage external service providers acting on behalf of CHEPLAPHARM, ensuring quality, compliance and performance.
Zu unseren Kernkompetenzen gehören: Praxisgruppe Regulatory, Governmental Affairs & Investment Control AußenwirtschaftsrechtEuropa- und VerfassungsrechtImmissions- und UmweltrechtGovernmental AffairsÖffentliches Bau- und PlanungsrechtPlanung- und Genehmigung von InfrastrukturprojektenPublic Sector ComplianceProzessführungVergaberecht Praxisgruppe Financial Services Regulation Versicherungs- und Versicherungsaufsichtsfragenfinanzaufsichtsrechtliche ComplianceTransaktionen und ProjekteDigitalisierung Was wir Dir bieten: Ein offenes dynamisches Team, das für Dich da ist, wenn es darauf ankommt Spannende internationale Mandate mit enger Einbindung und unmittelbaren Mandantenkontakt, damit Du von Beginn an wachsen kannstVielfältige Karriereperspektiven und individuelle EntwicklungsmöglichkeitenEin umfassendes Aus- und Weiterbildungsprogramm, das Dir ermöglicht, Deine persönlichen Stärken und fachlichen Interessen weiter auszubilden und zu vertiefenDie Möglichkeit eines mehrmonatigen Auslands-Secondments Was Du mitbringen solltest: Hervorragende juristische Qualifikationen und sehr gute EnglischkenntnisseZusatzqualifikationen wie ein LL.M. oder eine Promotion sind uns willkommenInteresse an wirtschaftlichen FragestellungenNeugierde und Spaß an internationalen HerausforderungenLust auf Teamwork und Eigenverantwortung Contact: Claudia Olthoff - HR-Business Partner - +49 (69) 971477 -213
ADM EMEA Corporate Services GmbH sucht in Hamburg eine/n Financial Regulatory Analyst (f/m/d) EMEA (ID-Nummer: 13721623)
Zu unseren Kernkompetenzen gehören: Praxisgruppe Energy Energieerzeugung und – netzeEnergielieferung und EnergiehandelErneuerbare EnergienKilmaschutz und Emissionshandel Praxisgruppe Financial Services Regulation Versicherungs- und Versicherungsaufsichtsfragenfinanzaufsichtsrechtliche ComplianceTransaktionen und ProjekteDigitalisierung Was wir Dir bieten: Ein offenes dynamisches Team, das für Dich da ist, wenn es darauf ankommt Spannende internationale Mandate mit enger Einbindung und unmittelbaren Mandantenkontakt, damit Du von Beginn an wachsen kannstVielfältige Karriereperspektiven und individuelle EntwicklungsmöglichkeitenEin umfassendes Aus- und Weiterbildungsprogramm, das Dir ermöglicht, Deine persönlichen Stärken und fachlichen Interessen weiter auszubilden und zu vertiefenDie Möglichkeit eines mehrmonatigen Auslands-Secondments Was Du mitbringen solltest: Hervorragende juristische Qualifikationen und sehr gute EnglischkenntnisseZusatzqualifikationen wie ein LL.M. oder eine Promotion sind uns willkommenInteresse an wirtschaftlichen FragestellungenNeugierde und Spaß an internationalen HerausforderungenLust auf Teamwork und Eigenverantwortung Contact: Claudia Olthoff - HR-Business Partner - +49 (69) 971477 -213
EY Deutschland sucht in eine/n (Senior) Consultant Regulatory, Risk & Compliance Transformation Hub (Financial Services) (w/m/d) (ID-Nummer: 13117925)
As family-owned company Dawn Foods drives a culture of global growth, diversity, service to others and continuous learning and fun. Key company values are passion, integrity, relationships, progress and optimism. One of its business regions is Europe & AMEAP (Africa, Middle East and Asia Pacific), with 900 people and head office in Amstelveen (The Netherlands).
In unseren Regulatory-Teams beraten wir Unternehmen und Investoren aus der ganzen Welt bei hochkomplexen internationalen Transaktionen und wirtschaftlich bedeutenden Fragestellungen– Unsere Expertise umfasst die folgenden Schwerpunkte - wo liegt Dein größtes Potenzial? Antitrust & CompetitionEnergy & InfrastructureFinancial Services RegulationProduct RegulationRegulatory, Governmental Affairs & Investment Controls Wir freuen uns auf Deine aussagekräftige Bewerbung!
Serve as a key resource and participating in strategic business development activities, including presentations to prospective clients, professional meetings, or other business development activities for IQVIA Strategic Drug Development Provide internal and external therapeutic and pharmaceutical development-related educational services in support of all branches of IQVIA business. Attend key scientific meetings/conferences and keeping abreast of relevant scientific publications to maintain awareness of current scientific developments and progress in drug development methodology.
Eintritt in neue Europäische Märkte oder in der Initiierung neue Business linesPartner für andere Bereiche und Abteilungen innerhalb der Stellantis Financial Services in Bezug auf regulatorische Fragestellungen (Accounting, Legal, ALM etc.)Austausch und regelmäßige Kommunikation mit der Aufsichtsbehörde in Deutschland (Bundesbank/BaFin/OeNB), Internal & External Audit Ausgewiesener Spezialist im bankenaufsichtsrechtlichen Meldewesen (KWG, CRR)Hochschulstudium der Betriebswirtschaftslehre oder gleichwertiger BildungsstandardProfunde Berufserfahrung in ähnlichen PositionenErfahrungen mit Standard Software Tools im Meldewesen idealerweise in BAIS or FREX (AT)Flexibilität innerhalb des AufgabenbereichsIT- AffinitätIdealerweise Erfahrungen im Leasing BusinessExzellente Kenntnisse in MS Excel und Grundlagen in MS AccessExzellente analytische Fähigkeiten Aus- und WeiterbildungBetriebliche AltersvorsorgeEssenszulageFahrzeugleasingFlexible ArbeitszeitenGesundheitsmaßnahmenHomeofficeKostenlose GetränkeMitarbeitereventsMitarbeiterprämienMitarbeiterrabatteParkplatzVermögenswirksame Leistungen Gehaltsinformationen 80.000 - 100.000 Euro je nach Erfahrungslevel Ihr Kontakt Ansprechpartner Katarzyna Lorenowicz Referenznummer 862838/1 Kontakt aufnehmen Telefon:+49-(0)69-3008821291 E-Mail: katarzyna.lorenowicz@hays.de Anstellungsart Festanstellung durch unseren Kunden
In unseren Regulatory-Teams beraten wir Unternehmen und Investoren aus der ganzen Welt bei hochkomplexen internationalen Transaktionen und wirtschaftlich bedeutenden Fragestellungen– Unsere Expertise umfasst die folgenden Schwerpunkte - wo liegt Dein größtes Potenzial? Antitrust & CompetitionEnergy & InfrastructureFinancial Services RegulationProduct RegulationRegulatory, Governmental Affairs & Investment Controls Wir freuen uns auf Deine aussagekräftige Bewerbung!
Eintritt in neue Europäische Märkte oder in der Initiierung neue Business lines Partner für andere Bereiche und Abteilungen innerhalb der Stellantis Financial Services in Bezug auf regulatorische Fragestellungen (Accounting, Legal, ALM etc.) Austausch und regelmäßige Kommunikation mit der Aufsichtsbehörde in Deutschland (Bundesbank/BaFin/OeNB), Internal & External Audit Ausgewiesener Spezialist im bankenaufsichtsrechtlichen Meldewesen (KWG, CRR) Hochschulstudium der Betriebswirtschaftslehre oder gleichwertiger Bildungsstandard Profunde Berufserfahrung in ähnlichen Positionen Erfahrungen mit Standard Software Tools im Meldewesen idealerweise in BAIS or FREX (AT) Flexibilität innerhalb des Aufgabenbereichs IT- Affinität Idealerweise Erfahrungen im Leasing Business Exzellente Kenntnisse in MS Excel und Grundlagen in MS Access Exzellente analytische Fähigkeiten Aus- und Weiterbildung Betriebliche Altersvorsorge Essenszulage Fahrzeugleasing Flexible Arbeitszeiten Gesundheitsmaßnahmen Homeoffice Kostenlose Getränke Mitarbeiterevents Mitarbeiterprämien Mitarbeiterrabatte Parkplatz Vermögenswirksame Leistungen Gehaltsinformationen 80.000 - 100.000 Euro je nach Erfahrungslevel Ihr Kontakt Ansprechpartner Katarzyna Lorenowicz Referenznummer 862838/1 Kontakt aufnehmen Telefon:+49-(0)69-3008821291 E-Mail: katarzyna.lorenowicz@hays.de Anstellungsart Festanstellung durch unseren Kunden
Kommunikation mit Benannten Stellen, Behörden und externen Partnern Erstellung moderner, nachvollziehbarer technischer Dokumentationen und Risikobewertungen Steuerung regulatorischer Aufgabenpakete in enger Zusammenarbeit mit Entwicklung, Produktion und Service Planung, Durchführung und Nachbereitung interner und externer Audits Aktive Mitarbeit in einem interdisziplinären Umfeld, das Robotik, KI, Medizin und Engineering verbindet Abgeschlossenes Studium im (medizin-)technischen oder naturwissenschaftlichen Bereich Idealerweise beruflicher Start in der Softwareentwicklung und spätere Spezialisierung in Qualitätsmanagement oder Regulatory Affairs Fundierte Kenntnisse relevanter Normen und regulatorischer Vorgaben (MDR, FDA, ISO 13485, IEC 60601 ff.)
Kommunikation mit Benannten Stellen, Behörden und externen PartnernErstellung moderner, nachvollziehbarer technischer Dokumentationen und Risikobewertungen Steuerung regulatorischer Aufgabenpakete in enger Zusammenarbeit mit Entwicklung, Produktion und Service Planung, Durchführung und Nachbereitung interner und externer Audits Aktive Mitarbeit in einem interdisziplinären Umfeld, das Robotik, KI, Medizin und Engineering verbindet Abgeschlossenes Studium im (medizin-)technischen oder naturwissenschaftlichen Bereich Idealerweise beruflicher Start in der Softwareentwicklung und spätere Spezialisierung in Qualitätsmanagement oder Regulatory Affairs Fundierte Kenntnisse relevanter Normen und regulatorischer Vorgaben (MDR, FDA, ISO 13485, IEC 60601 ff.)
Key Responsibilities: Leadership: Serve as a biostatistical consultant for other members of the department and staff members from other Biostatistics departments within the company Represent sponsors at meetings with regulatory agencies or other regulatory meetings, may participate as a member of a Data and Safety Monitoring Committee Participate in independent research activities, teaching opportunities, presentations, and preparation of manuscripts for publication Participate as high level lead biostatistician on major projects, including developing/reviewing protocols, preparing analysis plans, and writing sections of joint clinical/statistical reports, integrated summaries and/or NDA sections Leading studies at an operational level Provide expert review and initiate methodology development work with regards to statistical standards and validation procedures Consult on operational/statistical/therapeutic area topics Knowledge Sharing: Maintain knowledge and awareness of developments in biostatistics and clinical trial methodology, and regulatory requirements that impact on analyses Performs as subject matter expert (SME) Risk Management: Identifies risks to project delivery and/or quality, leads in a way to minimize risks Anticipates risks to avert need for study level escalations, supports lead in implementing risk mitigation actions Lock and Unblinding Process: Leads the database lock and unblinding process for the statistical team Participate on the biostatistics randomization team (drafts randomization specifications and/or perform quality control (QC) review of randomization schedules) Statistical Expertise: Provide expert statistical input into review of statistical deliverables (i.e. statistical section of a protocol, statistical analysis plans, table shells, programming and table specifications, data review, tables, listings, figures, and statistical sections for complex and/or integrated reports) Provide expert input into data management deliverables (i.e. database design, CRF design, validation checks and critical data) Provide expert review of ADaM reviewers guide (ADRG) and metadata Perform senior biostatistical review (SBR) Produce or perform quality control review of sample size calculations for complex studies Requirements: Masters or PhD degree in Biostatistics or a related field with relevant experience within the life-science industry Expert in a broad range of complex statistical methods that apply to Phase 2-3 clinical trials Expert in strategically collaborating with clinical and drug development expertsExperience in serving as statistical lead for regulatory submissions, including preparation of submission datasets, eCTD support, meeting with regulatory teams, and responding to regulatory queries In-depth knowledge of applicable clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Strong working knowledge of SAS or RExcellent knowledge of CDISC Data Standards Superb communication and collaboration skills Independent and pro-active problem solving skills IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Please apply with your English CV and motivation letter as well as your education certificates and job reference letters (Arbeitszeugnisse). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Please apply with your English CV and motivation letter as well as your education certificates and job reference letters (Arbeitszeugnisse). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Key Responsibilities: Ensure all deliverables are inspection-ready and compliant with regulatory and internal guidelinesMaintain central planning for document writing and QC deliverablesProvide recommendations for process improvements to enhance collaboration between CPP and document service teamsDrive document shell creation, QC processes, and timeline management Skills & Experience: Strong experience in writing full CSR for Phase 1 clinical pharmacology studies.
Please apply with your English CV and motivation letter. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Please apply with your English CV and motivation letter as well as your education certificates and job reference letters (Arbeitszeugnisse). IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage Early Phase clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients.
Our highly specialised consultants can cater to your every wish and expectation and will prepare you for interviews and contract negotiations. Give it a try and learn what the market has to offer – our services are free of charge, non-binding and discreet! We look forward to hearing from you. Design and implement a SQL-based landing zone for regulatory data Develop stored procedures for transformation, enrichment, and aggregation Build and operate high-volume batch processing chains for monthly/quarterly cycles Implement SSIS-based ingestion flows and job orchestration Ensure data quality, technical lineage, and full traceability across layers Define and document integration patterns and mapping logic between landing-zone datasets and Tagetik-based reporting templates Perform operational monitoring, troubleshooting, and performance optimization Strong expertise in Microsoft SQL Server and T-SQL Hands-on experience with stored-procedure-driven ETL and complex data models Solid SSIS skills for orchestration and control of processing chains Experience with batch processing, logging, restartability, and performance tuning Knowledge of data lineage, reconciliation, and regulatory processing needs Experience with reporting platforms such as Tagetik is a plus Familiarity with Oracle source systems is advantageous Renowned Client Remote Option Ihr Kontakt Ansprechpartner Eliška Stejskalová Referenznummer 862801/1 Kontakt aufnehmen E-Mail: eliska.stejskalova@hays.at Anstellungsart Freiberuflich für ein Projekt
Our highly specialised consultants can cater to your every wish and expectation and will prepare you for interviews and contract negotiations. Give it a try and learn what the market has to offer – our services are free of charge, non-binding and discreet! We look forward to hearing from you. Design and implement a SQL-based landing zone for regulatory dataDevelop stored procedures for transformation, enrichment, and aggregationBuild and operate high-volume batch processing chains for monthly/quarterly cyclesImplement SSIS-based ingestion flows and job orchestrationEnsure data quality, technical lineage, and full traceability across layersDefine and document integration patterns and mapping logic between landing-zone datasets and Tagetik-based reporting templatesPerform operational monitoring, troubleshooting, and performance optimization Strong expertise in Microsoft SQL Server and T-SQLHands-on experience with stored-procedure-driven ETL and complex data modelsSolid SSIS skills for orchestration and control of processing chainsExperience with batch processing, logging, restartability, and performance tuningKnowledge of data lineage, reconciliation, and regulatory processing needsExperience with reporting platforms such as Tagetik is a plusFamiliarity with Oracle source systems is advantageous Renowned ClientRemote Option Ihr Kontakt Ansprechpartner Eliška Stejskalová Referenznummer 862801/1 Kontakt aufnehmen E-Mail: eliska.stejskalova@hays.at Anstellungsart Freiberuflich für ein Projekt
Sie entwickeln das Informationssicherheitsmanagementsystem weiter und sorgen für die Einhaltung gängiger Standards Sie definieren Sicherheitsrichtlinien, Prozesse und Leitlinien und stellen deren Umsetzung im gesamten Unternehmen sicher Sie bewerten neue Technologien, Services und Systemarchitekturen bezüglich Informationssicherheit, Risiken und Compliance-Vorgaben Sie führen Risikoanalysen durch, erstellen Sicherheitsbewertungen und leiten entsprechende Maßnahmen ab Sie beraten Führungskräfte und Fachbereiche zu Sicherheitsanforderungen, Risikoeinschätzungen und Best Practices Sie steuern und überwachen Sicherheitsziele, Kennzahlen und Reviews, um eine kontinuierliche Sicherheitsverbesserung sicherzustellen Sie erhöhen das Sicherheitsbewusstsein im Unternehmen durch Awareness-Maßnahmen, Schulungen und klare Kommunikation Sie stellen den strukturierten Umgang mit Sicherheitsvorfällen sicher – inklusive Dokumentation, Klassifizierung und Lessons Learned Sie begleiten technische Analysen von Schwachstellen, Penetration Tests und Systemüberprüfungen Sie arbeiten mit dem operativen Cybersecurity-Team zusammen, z.?
Sie entwickeln das Informationssicherheitsmanagementsystem weiter und sorgen für die Einhaltung gängiger StandardsSie definieren Sicherheitsrichtlinien, Prozesse und Leitlinien und stellen deren Umsetzung im gesamten Unternehmen sicherSie bewerten neue Technologien, Services und Systemarchitekturen bezüglich Informationssicherheit, Risiken und Compliance-VorgabenSie führen Risikoanalysen durch, erstellen Sicherheitsbewertungen und leiten entsprechende Maßnahmen abSie beraten Führungskräfte und Fachbereiche zu Sicherheitsanforderungen, Risikoeinschätzungen und Best PracticesSie steuern und überwachen Sicherheitsziele, Kennzahlen und Reviews, um eine kontinuierliche Sicherheitsverbesserung sicherzustellenSie erhöhen das Sicherheitsbewusstsein im Unternehmen durch Awareness-Maßnahmen, Schulungen und klare KommunikationSie stellen den strukturierten Umgang mit Sicherheitsvorfällen sicher – inklusive Dokumentation, Klassifizierung und Lessons LearnedSie begleiten technische Analysen von Schwachstellen, Penetration Tests und SystemüberprüfungenSie arbeiten mit dem operativen Cybersecurity-Team zusammen, z.?
Qualifications & Experience Advanced degree in Biostatistics, Statistics, or a related field (PhD preferred; Master’s accepted with significant experience).Proven experience working independently as a study statistician in late-phase (Phase II/III) clinical trials.Experience in pharmaceutical industry strongly preferred; CRO experience is a plus.Hands‑on expertise with clinical outcomes studies, including cardiovascular events, symptomatic endpoints, and quality‑of‑life measures.Demonstrated ability to implement complex statistical methods and guide cross‑functional teams through analytical decision‑making.Proficiency in SAS; working knowledge of R is advantageous.Experience with regulatory submissions and interaction with health authorities is a plus. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
As the world’s largest contract logistics specialist, we create competitive advantage for our customers by tailoring logistics solutions based on our globally standardized warehousing, transportation and integrated services modular components. We bring together sector expertise, global scale and local knowledge to design and manage supply chains from raw materials and manufacturing through to the delivery of finished goods and return services.
We support you and our customers in all areas of structural and civil engineering, facility management, large-scale industrial construction, technical building equipment and real estate management. As a national and international personnel services provider, we can offer you both short-term projects and long-term opportunities in your local area, nationwide and around the world – all free of charge to you.
Requirements Chief Engineer / Second Engineer license or degree in Naval Architecture / Marine Engineering Minimum 5 years seagoing or relevant technical experience, including at least 1 year in a shore-based role Strong knowledge of international maritime regulations and vessel technical systems Fluent English skills and confident use of common IT tools Analytical mindset, strong communication skills, and structured working style Willingness to travel internationally on a regular basis Valid work authorization for / residence in Germany is advantageous Benefits Diverse technical role within a global maritime environment at one of the market leaders Modern office environment in central Hamburg Career development opportunities within an international organisation Public transport contribution and additional, individual employee benefits Responsibilities Monitor the technical and operational performance of assigned container vessels Initiate inspections, define repair scopes, and coordinate procurement in line with class and regulatory requirements Supervise technical interventions and liaise with shipyards, classification societies, and service providers Review technical incidents, challenge root cause analyses, and implement continuous improvement measures Act as primary contact for captains, chief engineers, internal stakeholders, and external partners Prepare and control vessel budgets and support cost optimisation initiatives Maintain vessel documentation, certificates, and compliance with international maritime regulations Monitor fuel, oil, and technical consumption and support efficiency improvements Travel to vessels, ports, and project sites as required Informationen über den Arbeitgeber Our client is a global maritime organisation managing a modern fleet of container vessels.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with one single client and to manage clinical research projects in different therapeutic areas.
The Role: The Clinic Operations Manager is responsible for the overall day-to-day operational leadership of the clinic, ensuring safe, efficient, high-quality, and patient-centred service delivery. Reporting directly to the General Manager (GM), the role leads all clinic operational teams (Patient Support, Nursing, and Lab) and is accountable for workforce performance, operational effectiveness, patient experience, complaints management, and service standards.
Strong clinical research skills and commitment to evidence-based and patient-centered clinical development. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
Develop and execute scalable go-to-market strategies for (embedded) cybersecurity products and services. Build sales structures, CRM processes, and reporting frameworks from the ground up. Lead the full sales cycle from first contact to contract signature.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas.
Maintains a positive outlook at work; handles criticism well and learns from itAbility to establish and maintain effective working relationships with a wide network of individuals e.g. co-workers, managers and customersEffective mentoring and training skills, fostering learning and knowledge sharing with colleagues IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
#LI-Remote #LI-HARJINDERBHUMVRA IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
#Health : Your health matters to us – benefit from health days, company sports activities, office yoga, and free support from the pme Family Service. #Holiday: We offer you 30 days of vacation per year based on a full-time position, plus December 24th and 31st off. #OneCompany : Stronger together – with over 10,000 employees from 95 nations, we promote an international and collegial corporate culture.
#Health: Your health matters to us – benefit from health days, company sports activities, office yoga, and free support from the pme Family Service. #Holiday: We offer you 30 days of vacation per year based on a full-time position, plus December 24th and 31st off. #OneCompany: Stronger together – with over 10,000 employees from 95 nations, we promote an international and collegial corporate culture.
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas in Germany or the DACH region.
Refund Services Product Manager (gn) - Location Romania Your job at DKV Mobility? As part of a leading European B2B platform for on-the-road payment solutions, you will work in an exciting environment.
As well as contributing to the clinical workload, the successful candidate will have opportunities to be involved in training junior embryologists, service development, research, quality management, donor recruitment and project work. The Deputy Laboratory Manager will support the Laboratory Manager in the delivery of the service and management of the laboratory team.
As well as contributing to the clinical workload, the successful candidate will have opportunities to be involved in training junior embryologists, service development, research, quality management, donor recruitment and project work. The Deputy Laboratory Manager will support the Laboratory Manager in the delivery of the service and management of the laboratory team.
Your assignments Producing designs, both initial outlines and full plans, of sewerage, water treatment and flood defence structures such as pump systems and pipe networksPresenting project details and technical information to colleagues and clientsWriting reportsManaging project budgetsKeeping up to date with changes in regulatory legislation and guidelinesWriting and advertising tender documents and managing contractsLiaising with clients, contractors, government agencies, local authorities and suppliersSupervising local staff and site workersUsing a variety of specialist computer applications/simulation softwareMaintain effective relationships with members of all divisions and departments responsible for performing services related to the projectPrepare construction cost estimates, perform construction monitoring and coordinate field activities Your profile University degree (M.Sc.) in civil engineer, mechanical engineer, process or environmental engineer or other suitable qualification Experience in the preparation of master plans, feasibility studies, tender documents and construction planning, and/or experience with construction supervision, project management and/or commissioning of water supply and/or wastewater treatment facilities.Preferably 5 years of professional experience in international consulting/engineering in the field of urban water management, preferably in projects financed by bilateral and multilateral donor organisations and development banksStructured approach to work a high degree of flexibility, initiative, persuasiveness and negotiation skills as well as the ability to work in a team Willingness to travel extensively Good knowledge of written and spoken English and preferably an additional business language (French, Spanish, etc.)
FoodChain ID has offices in the US, Europe, Asia, and South America and serves customers in the food industry in over 100 countries with services in analytics, certification, and consulting (data solutions for risk management and regulatory databases etc.). YOUR NEW CHALLENGE You lead the sale of FoodChain ID services across key customers and prospects in the DACH region You are responsible for developing and maintaining high value customer relationships and for acquisition of customers and prospect businesses to maximize the opportunity You actively cooperate with internal stakeholders to guide in the development of strategic plans You provide “Voice of the Client” feedback on market needs and company service delivery WHAT TO BRING Some years of experience as a Key Account Manager in B2B sales in the DACH region, selling products that require explanation (preferably digital services) to big and medium sized food companies You are preferably knowledgeable in quality subjects, such as Food Safety, Testing and Certification You bring experience in managing complex customers and a network of decision makers as a plus You are a “hunter” personality with strong communication and negotiation skills, able to understand your customer needs, open-minded as well as with a proactive approach, self-confidence and resilience THE OFFER FOR YOU FoodChain ID relies on personal responsibility and ownership.
Our highly specialised consultants can cater to your every wish and expectation and will prepare you for interviews and contract negotiations. Give it a try and learn what the market has to offer – our services are free of charge, non-binding and discreet! We look forward to hearing from you. You develop concepts and participate in feasibility studies to meet technical requirements You perform and take ownership of specific software development tasks, ensuring reviews using checklists and templates You lead work package definition, estimation, and planning, and enhance or document SW unit specifications and designs You review designs and contribute to the SW architecture, defining quality attributes and staying updated with technology trends You conduct root-cause analysis of complex issues and provide bug fixes for post-market software releases You ensure compliance with processes, propose improvements, and stay informed about regulatory and market standards Education in a software related field such as software or electrical engineering Industry experience Proven experience as a Software Engineer with a strong focus on Rust development Solid understanding of Rust's core concepts, including ownership, borrowing, and lifetimes Experience with asynchronous programming in Rust (e.g., using async/await) Familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx) Experience with Linux and Dockers Internal career opportunities World renowned pharmaceutical company International and diverse environment Ihr Kontakt Referenznummer 865359/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Our highly specialised consultants can cater to your every wish and expectation and will prepare you for interviews and contract negotiations. Give it a try and learn what the market has to offer – our services are free of charge, non-binding and discreet! We look forward to hearing from you. You develop concepts and participate in feasibility studies to meet technical requirementsYou perform and take ownership of specific software development tasks, ensuring reviews using checklists and templatesYou lead work package definition, estimation, and planning, and enhance or document SW unit specifications and designsYou review designs and contribute to the SW architecture, defining quality attributes and staying updated with technology trendsYou conduct root-cause analysis of complex issues and provide bug fixes for post-market software releasesYou ensure compliance with processes, propose improvements, and stay informed about regulatory and market standards Education in a software related field such as software or electrical engineering Industry experienceProven experience as a Software Engineer with a strong focus on Rust developmentSolid understanding of Rust's core concepts, including ownership, borrowing, and lifetimesExperience with asynchronous programming in Rust (e.g., using async/await)Familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx) Experience with Linux and Dockers Internal career opportunities World renowned pharmaceutical companyInternational and diverse environment Ihr Kontakt Referenznummer 865359/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Due to the passion, expertise and reputation of our team, the clinic has grown into a leading fertility clinic and offers a full suite of treatment and diagnostic services, including PGT. Providing treatment to both NHS and private patients, Oxford Fertility performs approximately 1000 fresh cycles and 1000 frozen cycles per year.
#LI-remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Our highly specialised consultants can cater to your every wish and expectation and will prepare you for interviews and contract negotiations. Give it a try and learn what the market has to offer – our services are free of charge, non-binding and discreet! We look forward to hearing from you. Develop and maintain software solutions by applying in-depth technical knowledge and problem-solving skills, while ensuring compliance with regulatory standards for medical softwareEnsure the timely delivery of high-quality software for medical devices that meets both the company's standards and customer needs, influencing the success of the team and broader project outcomesCommunicate complex technical concepts effectively, fostering an environment of collaboration and continuous learning within and across diverse and intercultural teamsEmpower your team members to take ownership of their work and leading by example to foster teamwork and mentorship Degree or equivalent practical experience in a specialized field related to software development or engineeringProven experience in software development, with a demonstrated passion and hands-on professional experience working with Rust incl. a solid understanding of Rust's core concepts (ownership, borrowing, and lifetimes), experience with asynchronous programming in Rust (e.g., using async/await) and familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx).Capable of solving complex issues creatively and effectively, using a multi-faceted approach based on thorough analysis to resolve complex technical challengesExcellent communication skills with the ability to foster an inclusive and diverse environment as well as collaborate effectively within and across teamsEnglish fluency is a prerequisite, German is advantageous Internal career opportunitiesWorld-renowned medical devices company Ihr Kontakt Referenznummer 858105/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt