Primetals Technologies Germany GmbH sucht in eine/n Senior Project Design Engineer (m/w/d) (ID-Nummer: 13660313)
PwC Strategy& (Germany) GmbH sucht in eine/n Werkstudent Social Media Grafik Design (w/m/d) (ID-Nummer: 13673709)
Responsibilities: Development, monitoring and improvement of engineering quality processes, methods, procedures and relevant quality KPICoordination, reviewing for consistency and assist in writing of all additional processes, procedures and standards owned by the Design Organisation; particular contribution to definition of engineering standardsDevelopment and monitoring of quality criteria of engineering deliverables, design documents, checklists and similarCreation of interface documents required for control of engineering services suppliers (DOID, DO-DO agreements)Planning and execution of internal and external audits to ensure compliance to the DOH and its Design Management System (Process Audits, Product Audits, engineering services suppliers audits)Contribution, planning and support to audits performed by entities independent/external to the Design Organisation (EASA, LBA, HISM)Support of root cause analysis for internal and external engineering quality issuesActive participation in continuous improvement processes and lessons learnedCreation and coordination of Supplier Quality Control Plans, including management of alternativesSupport Supply Chain Quality with audits of manufacturing suppliersContribution to Aircraft Program Milestones Development GatesSupport of risk management activitiesPlanning and execution of training sessions on quality tools, practices and proceduresSupport to engineering trainings Requirements: Good understanding of quality principlesGood understanding of engineering quality aspects of an aircraft OEMPreferably Engineering degree (BA Eng/Sc) in aeronautics / aviation or mechanical or quality degree> 3 year of professional expertise in aircraft industry or in relevant adjacent fieldBasic knowledge of airframe certification requirements, design criteria, materials, methods and toolsNew aircraft development experience would be a plusAbility to prioritise, manage and execute multiple simultaneous tasks What we offer: Future prospects in an innovative, growing, and agile companyAn exciting work environment with diverse career opportunitiesA tariff/above-tariff salaryFlexible working hours and the option for remote work30 vacation days per year and special leave for special occasions upon employment at Xtended EngineeringBonus programs for referrals and employee recruitmentTeam events Xtended Engineering GmbH bringt qualifizierte Ingenieure mit Unternehmen aus der Industrie und Wirtschaft zusammen.
Company description 💧 Aliaxis is a leading technology company that designs sustainable, easy to install, and innovative fluid management solutions. Over 15,000 people have selected to work for us in more than 40 countries, meeting our customers’ most demanding needs for pipes and fitting systems in building, infrastructure, industrial and agriculture sectors.
Your Profile Master or PhD degree of Optics, Materials or Engineering.Min. 10 years work experience in opto-electronics industry；min. 5 years with management role.Good knowledge in optical materials, especially on high index wafers, blue glass, filter glass etc.Good knowledge of application of optical glass and/or wafer, and optical module design. Knowledge of metrology system.The ability of analysis and problem solving with creative thinking.The ability of project development, follow-up and management.Fluently spoken and written English and Mandarin.Good communication skills and teamwork spirit.
Das Unternehmen bedient Kunden und Plattformen auf der ganzen Welt und konzentriert sich dabei auf die technologische Expertise und die Zusammenarbeit mit Kunden in den Bereichen Design und Engineering. TECHNIPLAS unterhält langfristige Beziehungen zu vielen der weltweit führenden Automobilherstellern und Industrieunternehmen.
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.
Knowledge of ME Methods & Tools: Methods: WPR, industrial process design, industrialization, Jigs & Tools (J&T), time studies and calculation (e.g. PERT, MTM-STV Airbus). Tools & Systems: SAP (PP/PM), PLM systems (Zamiz, TiCon, TAKSY, DocMaster/ECM), Delmia/Apriso, Google Workspace, Microsoft Office.
Knowledge of ME Methods & Tools: Methods: WPR, industrial process design, industrialization, Jigs & Tools (J&T), time studies and calculation (e.g. PERT, MTM-STV Airbus). Tools & Systems: SAP (PP/PM), PLM systems (Zamiz, TiCon, TAKSY, DocMaster/ECM), Delmia/Apriso, Google Workspace, Microsoft Office.
Du betreust unser Portfolio an Cannabis-Vollextrakten und begleitest aktiv die Markteinführung unseres neuen Fertigarzneimittels VER-01.Du konzeptionierst und pflegst Marketing‑ und Vertriebsunterlagen für Ärzte und Apotheker in enger Abstimmung mit QS, Außendienst und Grafik.Du planst, steuerst und realisierst unsere Messeauftritte – von Konzept und Layout über Standbaukoordination bis hin zu Budget‑ und Zeitplanung - gemeinsam mit Messebauern, Scientific Marketing und Grafik.Du entwickelst, betreust und optimierst das Schulungskonzept für den Außendienst (Präsenztrainings, eLearning) – inklusive Inhaltserstellung, Moderation und Erfolgskontrolle.Du betreust unsere eLearning-Plattform und verantwortest Kursmanagement, Contentpflege, Nutzerverwaltung, Reporting und die kontinuierliche Verbesserung der Lernpfade.Du entwickelst unsere Web- und Fachkreisseite laufend weiter und hältst diese aktuell.Du konzipierst unsere Fachpressekampagne, setzt PR‑Maßnahmen in Abstimmung mit Agenturen um und pflegst aktiv Pressekontakte.Du steuerst externe Dienstleister (PR‑ und Mediaagenturen, Messebauer, Druckereien) und übernimmst Briefings, Auswahl und Budgetkontrolle.Du arbeitest eng mit unseren Fachabteilungen im Bereich Quality Assurance, Operations/Supply Chain, Scientific Marketing, Clinical Trials, Grafik und Web Development zusammen.Du kannst ein erfolgreich abgeschlossenes (Fach-)Hochschulstudium, vorzugsweise im Bereich Marketing, BWL, Kommunikationswissenschaften, Naturwissenschaften oder Pharmazie, vorweisen.Du bringst mind. 2 Jahre Berufserfahrung im Produktmanagement mit — idealerweise im Healthcare/Pharma‑Umfeld.Du koordinierst cross-funktionale Teams sicher und verfügst über eine strukturierte und selbstständige Arbeitsweise: Stakeholder Management und Priorisierung sind für Dich Routine.Du verfügst über eine schnelle Auffassungsgabe und ein hohes Maß an Eigeninitiative.Du hast ein Gespür für Kreativität, Gestaltung / Design und Text und besitzt eine hohe Sprach- und Kommunikationskompetenz.Du bringst ein ausgeprägtes Business Mindset mit, hast Spaß an aktivem Austausch und kreativer Lösungsfindung über alle Unternehmensebenen hinweg und Lust, in einem dynamischen Umfeld viel zu bewegen und Großes zu schaffen.Du bringst verhandlungssichere Deutsch- und Englischkenntnisse (mind.
Uniplan vereint heute alle kreativen Disziplinen von Strategie, Kreation, Design und Projekt- und Eventmanagement bis hin zum Engineering und der Produktion. Dabei begleiten wir unsere Kunden von der ersten Idee bis zum letzten Handgriff: Über 300 Uniplaner an weltweit acht Standorten erwecken visionäre Ideen mit hohem Anspruch an die Machbarkeit zum Leben – alles für den einen Moment, der das Markenerlebnis einzigartig macht.
Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectives Design and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regions Build and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutions Conduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiatives Contribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical data Oversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL Director Act as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentation Plan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical Officer Represent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencers Serve as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic community Collaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities Solid direct experience working with Key Opinion Leaders, ideally within the ophthalmology sector Exceptional communication and interpersonal skills, with the ability to build trust-based relationships across diverse stakeholder groups Full professional proficiency in English, both spoken and written Strong business acumen and a demonstrated ability to effectively manage timelines, processes, and procedural workflows Experience with product launches, advisory boards, and post-approval studies is highly advantageous Relevant academic background required (e.g., life sciences, healthcare, business, or a related field) A very renowned company Other Locations: Oberkochen/Jena/Berlin Ihr Kontakt Referenznummer 865508/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Als Team Lead E-Commerce (w/m/d) berichtest Du direkt an die Geschäftsführung.Du verantwortest unsere digitalen Flagship Stores in allen Ländern.Du treibst mit Deinem Team unsere geographische Expansion voran und expandierst unsere digitalen Flagship Stores in weitere Länder.Dein Team umfasst Country Manager, CRM, Developer, Designer und unseren Customer Support – als Team Lead übernimmst Du Personalverantwortung für ca. 15 Mitarbeiter.Du entwickelst unseren E-Commerce-Auftritt und unser CRM kontinuierlich weiter damit wir unserer Mission jeden Tag ein Stück näherkommen: Make Probiotics the Foundation for a longer and healthier life, for all.Deine zentralen KPIs sind die Conversion Rate unserer Online-Stores, welche Du durch konsequentes A/B Testen kontinuierlich steigerst, und unsere Umsätze und Kosten aus CRM-Aktivitäten wie E-Mail, WhatsApp und Print.Du und Dein Team setzen Maßstäbe in den Bereichen E-Commerce und CRM, die unsere Position als best-in-class player in diesen Bereichen weiter ausbauen.
This role requires a highly experienced biostatistician capable of working independently, representing the Biostatistics function within cross‑functional teams, and delivering high‑quality statistical input throughout study design, execution, and analysis. Key Responsibilities Statistical Leadership & Study Support Serve as the primary statistical lead and main point of contact on the Clinical Trial Team (CTT), representing Biostatistics with confidence and professionalism.Work independently to support clinical teams, providing proactive statistical guidance throughout the study lifecycle.Lead statistical strategy discussions, including endpoint definitions, analysis methods, risk mitigation, and regulatory expectations.
Das Unternehmen bedient Kunden und Plattformen auf der ganzen Welt und konzentriert sich dabei auf die technologische Expertise und die Zusammenarbeit mit Kunden in den Bereichen Design und Engineering. TECHNIPLAS unterhält langfristige Beziehungen zu vielen der weltweit führenden Automobilherstellern und Industrieunternehmen.
At Nordex, rotor blade aerodynamic design is a key differentiator in our wind turbine technology. We are seeking an experienced engineer who can lead complex design projects and contribute to the continuous improvement of our aerodynamic capabilities.
Experience in set-up and conduct of Phase II clinical trials including in depth knowledge of early phase study designs, protocol writing and clinical pharmacology. Additional experience in conduct of Phase I and Phase III trials would be an advantage.
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.
At Nordex, rotor blade aerodynamic design is a key differentiator in our wind turbine technology. We are seeking an experienced engineer who can lead complex design projects and contribute to the continuous improvement of our aerodynamic capabilities.
Comfortable interpreting commercial / financial trends and results, with ability to guide teams to design and execute research and analysis and translate outputs into strategic implications for investorsWell-developed written and verbal communication skills including presentations, chairing meetings / Q&A sessions and report writingKnowledge of key issues and current developments in the biopharma / life sciences industryEvidence of career progression in consulting and/or transaction advisory roles In addition to the skills and experience above, a Manager should have: Bachelor’s degree or equivalent.
In addition to the responsibilities listed above, the Therapeutic Strategy VP will be expected to: Lead and support clinical trial design and all associated aspects for various clients. Provide strategic and therapeutic area guidance for clinical development plans in compliance with applicable regulatory, medical, and ethics guidelines.
Das Unternehmen bedient Kunden und Plattformen auf der ganzen Welt und konzentriert sich dabei auf die technologische Expertise und die Zusammenarbeit mit Kunden in den Bereichen Design und Engineering. TECHNIPLAS unterhält langfristige Beziehungen zu vielen der weltweit führenden Automobilherstellern und Industrieunternehmen.
Vorbereitung und Erstellung regelmäßiger (monatlicher) Baufortschrittsberichte. Organisation und Protokollierung aller Arten von Projekt-, Design- und Bau-Meetings. Verantwortung für die Projektdokumentation und Übergabe beim Projektabschluss. Du wirst systematisch an mehreren Projekten gleichzeitig unter der Aufsicht eines erfahrenen Projektmanagers und in Zusammenarbeit mit verschiedenen Teammitgliedern - auch aus anderen Geschäftsbereichen - arbeiten.
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 YOU WILL DO Be a key influencer to our business colleagues in resolving significant or potential issuesUnderstand your customer by gathering requirement, presenting concepts and proposal, providing updates on deliverables and negotiating issue resolution when neededAct as a coordinator across projects to monitor performance to ensure delivery of quality application on timeWork with external parties in assembling the system components with standardized modulesCustomizeCommercial Off-The-Shelf (COTS)based on pre-determined parameters, and execute customizing testsEnsure works are documented according to required standards, methods and toolsAssist in the define, initiate and design of architecture in projects/ program WHAT YOU SHOULD HAVE: Working experience and knowledge in Software Development Life Cycle (SDLC) with relevant qualification in IT fieldPassion in developing a high quality softwareInquisitive and analytical mind Strong IT and business acumenProven ability to work in a multi-cultural and multi-functional environmentCustomer and end-user focusedExcellent oral and written communications skills WHAT IS THE PLUS POINT(S) Minimum 6+ Years of experience with proven Analytical, Programming and Technical consultancy skills in Enterprise Application Integration, Technical integration Design Solution, Providing production support, delivering build and implementation services, Configuring Testing Environments and support end to end testing with customers and 3rd party vendors and familiar with transition to production project documentation and deployment process Expertise in development of Flow Services, Java services, Administration, Troubleshooting, Validations, Broker, UM, Triggers, Notifications, JDBC adapter, Java API, Trading Networks, FTP management, configuration, maintenance and installation, Axway GXS AI , Webmethods, Java, C++, BAM, BPMS, API, Web flow services, Unix Scripting , XML PI WebMethods o webMethods 6.5/7.1.2/8.0.2/9.5/9.8 Integration Platform o Trading Networks 6.1 o webMethods Adapters JDBC, SAP, Web Sphere MQ, XSLT, JMS o Messaging Systems Broker and UM, JMS o Adapter Configuration Tool, Upgrade Utility Tool, Document Tracker o BAM and BPM implementation o Cognos Reporting Web Services, XML and Industry Standards o HTTP, XSLT, REST, SOAP, WSDL, XQL, MQTT, JNDI o EDI (Electronic Data Interchange), EDIFACT, XML, JSON, RossettaNet, ANSI X12 standards, transmission protocols, data structures and Mappings for 810, 850,855 and 997 document types.
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.
Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, logistics challenges, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
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.
You can expect to use your strong design background to broaden your experience across the full development cycle, ensuring continued professional and technical development.
Responsible for the inclusion of Cardiovascular elements into proposals.Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.Support preparation of customer and bid defense meetings, e.g. training and preparation of the assigned project team; provide specific content; ensure presentation focus and content effectively conveys Cardiovascular strategy.
Provide scientific, clinical, and operational advice to internal stakeholders developing proposals: this may include, but is not limited to, providing the strategy to protocol design/clinical development plan, mining data to address important clinical questions relevant to the study, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
Mein Arbeitgeber Fire Point Rocket Technology (FPRT) is a defense technology company at the intersection of advanced materials science and modern rocket propulsion. We design and manufacture solid rocket propellant and propulsion components that power next-generation defense systems, with an uncompromising focus on safety, quality, and compliance.
Mein Arbeitgeber Fire Point Rocket Technology (FPRT) is a defense technology company at the intersection of advanced materials science and modern rocket propulsion. We design and manufacture solid rocket propellant and propulsion components that power next-generation defense systems, with an uncompromising focus on safety, quality, and compliance.
Principal Accountabilities: Collaboration in projects of the European Data Science & Advanced Analytics Team.Concept, design, development and execution of complex innovative AI/Machine Learning solutions as well as execution and implementation of concept studies using advanced statistical methods.Development of deep learning models for structured medical concept extraction from unstructured data.Productionalization of machine learning algorithms in Big Data platforms.Application of modern data mining and machine learning techniques in connection with Healthcare Big Data to identify complex relationships and link heterogeneous data sources.Advanced usage of Large Language Models for summarization, chatbot, entity extraction etc.Develop foundational Deep Learning Models for assets and patients.Builds and trains new production grade algorithms that can learn from complex, high dimensional data to uncover patterns from which machine learning models and applications can be developed.