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Senior Associate Consultant AD (m/f/d), Germany
ITL Germany, Stuttgart
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Praktikum International Sales & Sales Efficiency
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Influencer Marketing Manager (German Speaking) (f/m/d)
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About the jobUNOQUIP was founded on a simple idea: Expert Solutions to improve patient care. With experienced international partners, we are marketing and selling medical devices in the field of fluid management, respiratory care, airway management and nursing care.Are you ready to take on this mission? Reporting to the Commercial Head of DACH, you’ll take care of UNOQUIP's Clinical Sales and Business Development in Germany. The purpose of this position is to deliver real clinical value to health care professionals and business partners – go beyond product to improve patient outcomes.1. Who are we?Founded in October 2022, UNOQUIP is a fast-growing global marketer of high-quality single-use medical devices. We are dedicated to equipping healthcare professionals with solutions to provide optimal patient care in acute care settings.We are an international, experienced, and highly committed team with a passion for what we do. 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You have / you are:Bachelor’s degree in Life Science or Business-related subjects or other relevant education.A strong clinical understanding, preferably a clinical nursing background in acute care.Strong, empathic presentation skills including presentations in front of clinical stakeholders.A talent to interact with healthcare professionals and operating in complex clinical environments like intensive care units.Proven ability to work within a team with a can-do attitude, being open for new experiences and changes.Good selling skills, while not necessarily being a sales expert.A talent for identifying trends and future requirements and being able to share and distribute the knowledge in a wider organisation.Experience of working in the Medical Device Industry will be an advantage.Through effective decision-making, planning, and implementation, deliver superior business results within tight deadlines.Analytical & IT skills, including ability to efficiently work with excel calculations and databases.Confident personality with an engaging positive mindset and attention to detail.Work with minimal supervision, good initiative, and follow-up, focus on details, while understanding how work fits into the larger picture.100% proficient in your local language (German), written and spoken, and in English.Other requirements:Ability to travel 50% of the working time.References from at least 2 senior managers and from 2 reputable customers.Desired:Experience in working in international organisations and/or project groups.Preferred experience in using MS Dynamics 365.5. What can we offer you?Engage in building an international medical device start-up with a strong patient focus and international colleagues.Be part of an energetic, collaborative, and positive culture.Basic and ongoing training in our product range and market trends, to enable competent exchanges with suppliers and customers.Become involved in a very meaningful project in the healthcare industry.Company car.Up to 28 days of vacation.Ability to work 100% remotely.6. Interested?Complete the LinkedIn application.We aim to give you an initial response within 2 weeks. Next steps are communicated in the phone call with recruiters.As a candidate, you consent to UNOQUIP storing your CV and application for the purpose of recruiting for the specific positions advertised here. We will keep the data for a maximum of 6 months, during which time you can also ask us to delete your data by writing us through Linkedin with subject “GDPR - Your full Name”. Standort UNOQUIP, Stuttgart
Clinical Study Nurse
Pharmiweb, Tübingen
Clinical Study Nurse at ClinChoice (View all jobs) Tübingen, Germany Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds.... ClinChoice is searching for a Clinical Study Nurse to join one of our clients, where you will work on-site at a hospital in Tübingen, initially 0.5 FTE for a 12 month contract. ClinChoice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts. Main Job Tasks and Responsibilities: Measure vital signs (i.e. blood pressure, pulse rate, BMI, etc.), perform ECG’s, draw blood and perform infusions including putting infusion tubes and clinical monitoring during/after the infusion. Ship blood and laboratory samples to the central labs. Check questionnaires, perform database screening and discuss study information with subjects to aid with informed consent. Support the Principal Investigator with subject eligibility. Maintain Investigator Site File. Assist project teams with study-specific documentation as appropriate. Complete Case Report Forms (CRFs/eCRFs) and Data Clarification Forms (DCFs). Track, quality check and maintain drug accountability records. Ensure completion of site status reports. Ensure source documents (e.g. laboratory reports) are reviewed and signed by The Investigator. Maintain study files and the databases for assigned projects. Co-coordinate ordering/dispatch and track trial materials. Assist with trial progress tracking and update distribution tasks by updating the Clinical Trial Management systems. Support with tracking and safety reporting of study progress. Provide activity reports, expenses and timesheets as required. Report adverse events (AEs) and serious adverse events (SAEs) to all relevant personnel parties. Enter data into the eCRF. Work with the Clinical Research Associate (CRA) to resolve queries. Adhere to the site and study-specific protocol training whilst undertaking visit duties. Maintain standards of professional competence and current clinical practices under ICG-GCP, EU Clinical Trials Directive EU2001/20EC and German Regulatory Requirements. Complete study visits at the site, in line with the study protocol requirements. Ensure all relevant information regarding subjects is recorded, reported and where necessary, acted upon the communicate any changes to the Investigator study team as appropriate. Work at site and Patient Services team to ensure that all aspects of service for assigned groups of subjects are met, through the adherence to study schedules, protocols and local clinical practice regulations and requirements. Flexible approach to working hours to accommodate the dynamic nature of research visits. Education and Experience: Registered Nurse or Medical Assistant with at least 2 years of post-registration experience. Previous experience as a Research Nurse or Medical Assistant including a recent (within the last 1 year) ICH-GCP update. Experience in neurology is desirable. Skills Requirements: Infusion experience essential. Good phlebotomy skills. ECG recording. Managing infusion reactions. Demonstrated organisational skills. Proven flexibility and the ability to work under pressure. Good communication skills. Proficiency in German mandatory, English desirable. Proactive contribution towards the team by being a flexible team player. Ability to work effectively both in a team & independently in a fast-paced environment. Excellent understanding of the clinical processes. Good knowledge of clinical trials, including EU Clinical Trials Directives, Good Clinical Practice for Clinical Trials, and German regulations is desirable, training can be provided. Excellent computer skills required, MS Office proficiency at a minimum. The Application ProcessOnce you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoiceClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company EthosOur mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. Key words: Study Nurse, Research Nurse, Trial Nurse, Registered Nurse, Clinical Trials, Clinical Research, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated #LI-DNP
Clinical Study Nurse
Pharmiweb, Stuttgart
Clinical Study Nurse at ClinChoice (View all jobs) Tübingen, Germany Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds.... ClinChoice is searching for a Clinical Study Nurse to join one of our clients, where you will work on-site at a hospital in Tübingen, initially 0.5 FTE for a 12 month contract. ClinChoice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts. Main Job Tasks and Responsibilities: Measure vital signs (i.e. blood pressure, pulse rate, BMI, etc.), perform ECG’s, draw blood and perform infusions including putting infusion tubes and clinical monitoring during/after the infusion. Ship blood and laboratory samples to the central labs. Check questionnaires, perform database screening and discuss study information with subjects to aid with informed consent. Support the Principal Investigator with subject eligibility. Maintain Investigator Site File. Assist project teams with study-specific documentation as appropriate. Complete Case Report Forms (CRFs/eCRFs) and Data Clarification Forms (DCFs). Track, quality check and maintain drug accountability records. Ensure completion of site status reports. Ensure source documents (e.g. laboratory reports) are reviewed and signed by The Investigator. Maintain study files and the databases for assigned projects. Co-coordinate ordering/dispatch and track trial materials. Assist with trial progress tracking and update distribution tasks by updating the Clinical Trial Management systems. Support with tracking and safety reporting of study progress. Provide activity reports, expenses and timesheets as required. Report adverse events (AEs) and serious adverse events (SAEs) to all relevant personnel parties. Enter data into the eCRF. Work with the Clinical Research Associate (CRA) to resolve queries. Adhere to the site and study-specific protocol training whilst undertaking visit duties. Maintain standards of professional competence and current clinical practices under ICG-GCP, EU Clinical Trials Directive EU2001/20EC and German Regulatory Requirements. Complete study visits at the site, in line with the study protocol requirements. Ensure all relevant information regarding subjects is recorded, reported and where necessary, acted upon the communicate any changes to the Investigator study team as appropriate. Work at site and Patient Services team to ensure that all aspects of service for assigned groups of subjects are met, through the adherence to study schedules, protocols and local clinical practice regulations and requirements. Flexible approach to working hours to accommodate the dynamic nature of research visits. Education and Experience: Registered Nurse or Medical Assistant with at least 2 years of post-registration experience. Previous experience as a Research Nurse or Medical Assistant including a recent (within the last 1 year) ICH-GCP update. Experience in neurology is desirable. Skills Requirements: Infusion experience essential. Good phlebotomy skills. ECG recording. Managing infusion reactions. Demonstrated organisational skills. Proven flexibility and the ability to work under pressure. Good communication skills. Proficiency in German mandatory, English desirable. Proactive contribution towards the team by being a flexible team player. Ability to work effectively both in a team & independently in a fast-paced environment. Excellent understanding of the clinical processes. Good knowledge of clinical trials, including EU Clinical Trials Directives, Good Clinical Practice for Clinical Trials, and German regulations is desirable, training can be provided. Excellent computer skills required, MS Office proficiency at a minimum. The Application ProcessOnce you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoiceClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company EthosOur mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. Key words: Study Nurse, Research Nurse, Trial Nurse, Registered Nurse, Clinical Trials, Clinical Research, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated #LI-DNP
Supplier Quality Manager (m/w/d) Elektronik
AllatNet Recruiting, Lindau, Ravensburg, Friedrichshafen
Ihr Aufgabenbereich -Sie planen und führen Lieferantenbesuche, Potenzialanalysen und Lieferantenaudits durch-Sie sind für die Betreuung und die strategische Entwicklung von nationalen und internationalen Lieferanten im Rahmen der zugeordneten Materialgruppe zuständig-Sie betreuen die Qualität sowie die Weiterentwicklung der neuen und vorhandenen Lieferanten-Die Vorbereitung, Verhandlung und Abschluss von Qualitätsverträgen sowie die Zulassung und Qualifizierung der Lieferanten liegt in Ihrer Hand-Sie gestalten bei der Umsetzung der Qualitätsanforderungen unter Anwendung gängiger Q-Methoden und Normen (z.B. ISO9001, EN9100, IATF 16949)-Teamleitung zur strukturierten Problemlösungen (QRQC)-Sie sind die Schnittstelle zu Lieferanten sowie intern zu den Bereichen Entwicklung, Produktion und Einkauf Ihr Profil -Sie haben ein erfolgreich abgeschlossenes Studium im Bereich Elektronik, Elektrotechnik oder vergleichbares-Sie besitzen Berufserfahrung im Qualitätsmanagement von Elektronikprodukten-Sie besitzen praktische Erfahrung in der Fertigung von Elektronikprodukten in der Zusammenarbeit mit EMS-Dienstleistern-Sie haben die Zusatzqualifikation sowie die Erfahrung als Auditor (z. B. VDA 6.3, IAFT 16949, ISO 19011)-Sie gehen sicher im Umgang mit Lieferanten und Geschäftspartnern um-Sie besitzen Kommunikationsstärke-Ihre sehr guten Deutsch- und Englischkenntnisse runden Ihr Profil abAuf Ihre Bewerbung freuen wir uns.Tel. +49 (0)751 56 84 97 30E-Mail: [email protected]
IT Project Manager | M/F/D - Ref: SHS/JR-14053
consult16 GmbH, Ulm
consult16 GmbH supports a wide variety of clients. We are an industry-independent and strategic partner for our clients, providing expert advice and placement of specialists and executives up to management level. Our expertise covers the entire value creation process of modern companies, in all disciplines - technical, business or commercial. We work together with our clients on interesting and technologically innovative projects. Our cross-industry experience and consistent focus on customer requirements make us THE trusted partner of many well-known companies - especially when projects, large orders or absences of permanent staff require qualified, flexible or prompt deployment of personnel. On this basis, we can make optimum use of the skills of our employees, whether newcomers or professionals, and present our customers with an individually tailored personnel concept, even in complex cases. Our client is a global market leader in sensor technology for the aerospace industry. For the location in Ulm we are looking for immediately, initially within the scope of temporary employment **** IT Project Manager | M/F/D - Ref: SHS/JR-14053 **** Your tasks: **** Independent management, coordination and implementation of IT projects Ensuring the planning and implementation of IT projects in terms of time, budget and quality on the basis of standardized process models Specification of demands and creation of clear scope, objectives and deliverables Planning and implementation of work packages with the assigned project teams Planning of resources and time, as well as the creation of business cases Monitoring and reporting on project progress Agile project management expertise Interface between the IM areas and the business areas Close coordination and cooperation with our IM portfolio management **** Your profile: Successfully completed studies (at least Bachelor) in the field of business informatics, industrial engineering, business administration or comparable qualification Several years of professional experience as a project manager or IT consultant, both in classic and agile project management Knowledge of multi-project management advantageous Proven track record of large-scale projects (ideally with a project volume in the millions, a project team of at least 10 people and a duration of over 20 months) MS-Office at least in detail. specialized knowledge German and English at least business fluent Very good analytical and conceptual skills, as well as high quality awareness Strong communication skills in an international context Structured, systematic and detail-oriented way of working High sense of responsibility, ability to work under pressure and organizational talent Willingness to travel on business is a prerequisite Are you interested? Then send us your informative application documents, stating your starting date and salary expectations, exclusively by e-mail to [email protected] (https://mailto: [email protected] ) or give us a call! Discretion is a matter of course. Additional information: Requirements for the applicant: Expert knowledge: IT organization, agile project management, security systems (IT), data security, project management, IT coordination
Internship Customer Engagement Master Data Management (M/F/D)
HUGO BOSS, METZINGEN, Baden-Württemberg
Our vision is to establish HUGO BOSS as the leading premium tech-driven fashion platform worldwide and to be one of the top 100 global brands. At HUGO BOSS, we work as a team to apply our knowledge, skills and experience together and create a diversity of ideas and solutions. What unites us? We love fashion, we change fashion!At HUGO BOSS, you have the opportunity to contribute your personality, ideas and creativity - because only when we break new ground together can we create something unique. Become part of our team of more than 17.000 employees worldwide and shape your future at HUGO BOSS!Have you always wanted to know what the future of Customer Engagement, system-based central processing of customer data and data analysis looks like in practice? Then take a look behind the scenes with us and get stuck in. We are responsible for managing programs such as CRM, Personalization and Data Science and the operational implementation of global projects. As an interface between Data, IT and business impact, we work in a very diverse and international environment. We offer an internship (m/f/d) for 6 months, starting mid-October 2024 - Use your university knowledge to apply it in practice and get a comprehensive insight into the multi-faceted Customer Engagement world at HUGO BOSS.What you can expect: You support the conception, implementation, testing and roll-out of global projects and their implementation in the CMDM system (e.g. Guest Customers, WeChat). You are in direct exchange with our specialist departments (including IT, Data Analytics, ECOM...) Continuous optimization of customer data quality across processes, functions and systems Developing and implementing concepts for data quality rules for sustainable data quality management Execution of data analyses and planning of data processes Independently assume responsibility for tasks and sub-projects Your profile: You are studying or have already completed a degree in economics or a comparable course of study You count analytical skills and conceptual thinking among your strengths You work in a structured and careful manner You have a very good command of written and spoken English You have a sound knowledge of MS Office (especially Excel) and ideally have a basic understanding of IT applications (CRM system, campaign management system) You enjoy working in a team, have good communication skills and are committed to your workI-CH1 Your benefits: Made for Me: three days in Metzingen and two days working remotely. Our hybrid working model "Threedom of work" is as individual as your personal needs. Sustainability is one of our key values, and more than just a trend. We are committed to environmental, animal and climate protection, and human rights. Does innovation drive you? Same for us! We have digitized most of our workflows and almost fully automated our logistics centres. Exclusive discounts for shopping and arts: benefit from discounts for family and friends along with free entrance to more than 15 international art museums. High-performing people need a healthy balance. Take advantage of the employee gym, the beach volleyball field or yoga classes on the rooftop terrace. As a fashion company, we value good taste in everything - including food. Welcome to our own restaurant and café, Times. We are a global company with our employees representative of the world at large. Our inclusive culture embraces each person's authenticity and individuality. We are committed to equal employment opportunity. And we believe our equitable work environment helps unleash your full potential and inspires you to thrive.
Clinical Trial Manager
Pharmiweb, Stuttgart
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. Roles & Responsibilities of the position: The Trial Manager (m/f/d) is responsible for the management of clinical sites including the site identification and qualification, the timely delivery of clinical trial enrollment in accordance with scientific objectives, timely delivery of database locks, issues management at clinical trial sites, and ensuring inspection readiness at all times for assigned therapeutic areas within a region or country. You will also be responsible for the oversight of vendor monitoring activities at clinical trial sites, including the identification, mitigation and escalation of significant findings and trends. Key Responsibilities: You will be responsible for all activities required at clinical trial sites and by investigators and site staff participating in the client’s trials; including the site identification and qualification, enrollment planning and execution, to database lock and close out You will also perform management and issue mitigation, identification and resolution The development of strategic institutional/site relationships will be a main focus You will develop and implement site risk plans, ensure site and country level inspection readiness at all times, leverage metrics to inform site/country/regional level for their decision making and provide vendor oversight for site monitoring activities at site/country level It will be a goal to establish and develop strong professional relationships with clinical investigators All in all you will be the communication “bridge” between sites, third party vendors and the client Job Requirements: You have a Bachelor’s degree or equivalent in a scientific or health-related field You also bring experience in clinical research as well as good GCP knowledge Demonstrated leadership behavior, strong communication skills as well as the willingness to travel are also required About 4 + years of experience in clinical trial monitoring or similar experience in the industry A very good professional knowledge of German and English
Mathematician / Software Developer C++ (m/f/d)
Brunel GmbH NL Mannheim, Mannheim
Mathematician / Software Developer C++ (m/f/d) Your tasks We are looking for a software developer with expertise in meshing and computational geometry. Degree in mathematics, computer science or similar field required. Practical experience in C++, multithreading and object-oriented software development desired. We look forward to receiving your application! Development of new functions for determining component characteristics Design of innovative geometric algorithms for triangulated meshes and point clouds Extension of components for the registration and meshing of 3D point data Optimization of process steps to improve measurement duration Implementation of improvements for more efficient data acquisition and processing Integration of new technologies to increase the accuracy and reliability of measurements Collaboration with other teams to coordinate and integrate new functions Carrying out tests and validations to ensure the quality and functionality of new features Your qualifications Completed studies in mathematics, computer science or a similar field Comprehensive knowledge in the fields of meshing, computational geometry and/or computer graphics, both theoretical and practical Competence in C++ and experience in multithreading Solid knowledge of object-oriented software development and software design patterns Fluency in German Your advantages We offer you a corporate culture that is characterized by the diversity of our employees and mutual appreciation - between employees and at all levels of the company. In addition to varied get-togethers with the local Brunel teams, this also includes regular feedback discussions with your account manager about your challenges and prospects. You will be optimally supported and prepared for future projects with individual further education and training. Open-ended employment contracts, 30 days' vacation, work account regulations and a company-financed pension scheme are a matter of course with us. What Brunel stands for Working at Brunel means: attractive work tasks, exceptional career prospects, the security of an expanding engineering service provider and the full diversity of engineering and IT. In the DACH-CZ region alone, we have more than 40 locations and development centers with accredited test laboratories and more than 120 locations worldwide with more than 12,000 employees in over 40 countries. More than 45 years of international success and over 25 years in Germany. Standing still means going backwards - with Brunel you can make a difference!
GROUP IT Manager (m/f/d)
Dietz GmbH, Karlsbad
GROUP IT Manager (m/f/d) The companies of the DIETZ GROUP are united by their focus on a common goal: To support people with physical disabilities in their participation in life by increasing their mobility and comfort. As a leading national and international manufacturer of innovative rehabilitation and care aids, we are committed to a well thought-out, sustainable product world every day. Are you looking for a meaningful, responsible role in a modern working environment and in a great team? Then we are looking for you! We look forward to receiving your application. What are your tasks as GROUP IT Manager? Management and strategic development of the IT department at Group level for all locations Ensuring a stable and efficient IT infrastructure and its continuous optimization Responsibility for IT security strategy and its implementation at Group level You will be responsible for planning, implementing and monitoring IT projects to support the business objectives Coordinating and setting up existing IT projects, such as NetSuite, Microsoft 365u00b0, Configure One and Joint Roadmap Working with various departments to understand their IT requirements and develop solutions Compliance with data protection and security guidelines across Europe What do you bring to the table as a GROUP IT Manager? Completed studies in the field of computer science, business informatics or a comparable qualification Several years of professional experience in a managerial IT position, ideally in an international company Sound knowledge of IT infrastructure, networks, cloud computing and IT security standards Experience in managing and implementing IT projects Business fluent communication and presentation skills in German and English Strong communication and problem-solving skills Mobility, flexibility and willingness to travel throughout Europe Your benefits with us: Dynamic team in a pleasant working environment that focuses on collaboration, innovation and diversity Familiar atmosphere in which team cohesion and collegial support are emphasized We offer flexible working hours with mobile working for a good work-life balance We guarantee intensive training and a wide range of further training opportunities Long-term job security in a meaningful and innovative industry Attractive company benefits, including company pension scheme, health promotion and employee discounts Referral bonuses such as \"employees recruit employees\" High-quality two-wheeler use through business bike leasing Sustainable action and environmental awareness are part of our corporate culture Charging facilities for electric vehicles on our company premises We look forward to receiving your application stating your earliest possible starting date and your salary expectations, either by e-mail to [email protected] (https://mailto: [email protected] ) or to the DIETZ GmbH // Stefanie Schneider // Reutu00e4ckerstrau00dfe 12 // 76307 Karlsbad.
IT System Administrator (m/f/d) (Business IT Specialist (Fachschule))
Colordruck Baiersbronn W. Mack GmbH & Co. KG, Baiersbronn
IT System Administrator (m/f/d) (Business IT Specialist (technical college)) As a medium-sized family business with state-of-the-art technology, we are one of the leading folding carton producers in Europe. With expert advice, innovative developments, comprehensive performance potential and certified quality, we are an ideal partner for demanding branded goods manufacturers and industrial companies. They value our market orientation, innovative strength and technical expertise. Due to our successful company development, we are looking for you as a new IT System Administrator (m/f/d) As an IT system administrator, you ensure the smooth operation of our IT infrastructure and are the key to an efficient and secure working environment for our entire team. Your responsibilities: Support of hardware and software throughout the company Development, care and maintenance of the individual software used MIS/ERP administration Interface programming and monitoring Application support and user support Your know-how: Degree in business informatics (FH, DH) or training with many years of experience and further training in IT in an industrial company Experience in Microsoft and Linux server architecture and detailed knowledge of Microsoft Office and Lotus Notes General programming knowledge (VB, Notes Script, Delphi, Java, PHP) is desirable Structured, systematic, responsible and independent way of working, even with a high workload Your working environment & your prospects: Place of work: Administration Team size: 5 Individual further training opportunities Opportunities to participate in training courses and seminars Your benefits: 37.5-hour week, 30 vacation days, profit sharing, company pension plan, canteen and meal allowance, occasion-related benefits, free drinks & fruit, discounts, company bicycles, vacation and Christmas bonus, free parking, flexible parental leave arrangements, company events, flexible working hours Would you like more information in advance? Our HR Manager, Mr. Ju00fcrgen Kilgus, will be happy to answer your questions directly on 07442/830-230 or by email at [email protected]. Qualified on-the-job training is guaranteed. colordruck Baiersbronn W. Mack GmbH & Co KG Saarstrasse 2-10 | 72270 Baiersbronn Phone +49 7442 / 830-0 www.colordruck.net Would you like more information in advance? Our HR Manager, Mr. Ju00fcrgen Kilgus, will be happy to answer your questions directly on 07442/830-230 or by email at [email protected]. Qualified on-the-job training is guaranteed. colordruck Baiersbronn W. Mack GmbH & Co KG Saarstrasse 2-10 | 72270 Baiersbronn Phone +49 7442 / 830-0 www.colordruck.net Additional information: Requirements for the applicant: Advanced knowledge: Network administration, management, organization, programming language PHP, system support, system administration, system management, user consulting, user support (IT), business informatics, operating system Linux, programming language Java, programming language Delphi, programming language VB.NET, software engineering, software engineering, system administration Lotus Notes/Domino, security systems (IT), data security, system software (development, programming, analysis), client-server technology, user interfaces, user interfaces, programming, enterprise resource planning (ERP), hardware installation, software installation
Head of the data center (m/f/d)
Pu00e4dagogische Hochschule Heidelberg, Heidelberg
Heidelberg University of Education is a center of excellence in educational science with a regional, national and international impact. Around 5,300 students and researchers are active at the university each semester. We owe our success to the professional collaboration of around 650 people from research, teaching, science and administration. The Computer Center ensures smooth and secure IT operations by planning technological changes and ensuring their implementation and operation. As of October 1, 2024, the position of Head of the data center (m/f/d) (100%, up to EG 13 TV-L) to be filled on a permanent basis. Depending on the number of applicants, an additional specialist allowance may be paid. Your tasks Strategic management and further development**:** As head of our data center, you will be responsible for personnel, financial and resource planning. You will continuously develop the system infrastructure with a strong focus on IT security. Project management and cooperation: You will lead important IT projects and work closely with external partners. Your expertise plays a key role in drafting and negotiating contracts. Ensuring first-class services for different users:* You ensure an excellent service that meets the diverse requirements of our different user groups. You attach particular importance to compliance with legal norms and standards in IT security and data protection. Operational processes: You will support our day-to-day business with your technical expertise and ensure that operations run smoothly. Reporting and quality assurance: You are responsible for reporting and ensure the quality and compliance of our processes through precise documentation. Your profile / recruitment requirements Professional qualification: Degree in computer science or business informatics or a comparable degree with relevant professional experience Leadership skills: proven management experience in the IT sector, ideally in a data center Technical know-how: in-depth knowledge of server administration, virtualization technologies, network architecture, firewalls, Active Directory, IT security and data protection Personal profile: You have a strong analytical mindset, are characterized by a systematic way of working and are always eager to familiarize yourself with new technological areas. You also have very good written and verbal communication skills in German and English. We offer you an interesting and varied field of activity An attractive workplace in a dynamic university environment flexible working hours Wide range of training and development opportunities Good transport connections (public transport) and subsidized job ticket (Germany ticket) For more information on the job profile, please contact Prof. Dr. Christian Spannagel ( [email protected] ). The Heidelberg University of Education aims to increase the proportion of women in those areas in which women are currently underrepresented. Severely disabled applicants will be given preferential consideration if they are suitable. We look forward to receiving your application by 30.06.2024. Please submit it together with the usual documents (cover letter, CV, certificates) exclusively via the BITE applicant management system. You can find our applicant management system here: https://bewerbermanagement.net/de/jobposting/b3444a8faec7a11b06b8d22e2360d55aba11c8d00/apply?ref=homepage ( https://bewerbermanagement.net/de/jobposting/b3444a8faec7a11b06b8d22e2360d55aba11c8d00/apply?ref=homepage )
IT Portfolio Manager (m/f/d)
STRATO Personal GmbH, Stuttgart
IT Portfolio Manager (m/f/d) As a dynamic and modern personnel service provider, we offer our many years of experience and our comprehensive market know-how in a wide range of different industries exciting positions with interesting and innovative companies. Benefit from from our national and international networks and take advantage of STRATO personal as your personal springboard. We offer you comprehensive support and take care of all the administrative processes relating to your application - for you, of course free of charge. STRATO personal GmbH Temporary employment/employment agency/outsourcing/head hunting/onsite Management As your track assistant, we bring you into exciting projects in the field of Automotive. At the earliest possible date, we are looking for motivated employees for a renowned sports car manufacturer. Your tasks: Collaboration in the implementation and further development of lean portfolio management as part of the digital transformation Implementation and further development of IT reporting (cost reporting, etc.) with regard to method and tool Planning, preparation and implementation of (committee) meetings incl. preparation of documents Collaboration in ensuring conformity in IT/SW development and operation Collaboration in the development of methods, standards and tools for quality assurance of digital solutions Your profile: Degree in computer science, project management or a comparable qualification More than one year of professional experience in a comparable work environment, ideally in the automotive sector Experience in portfolio management / multi-IT project management Understanding of SAFe and/or agile working in the context of IT, SAP Business fluent German language skills Ability to structure We offer you: Permanent employment contract above-tariff remuneration plus vacation and Christmas bonuses + performance bonuses Prospect of being taken on Company pension scheme with employer subsidy Employee referral program with attractive bonuses Personal, local support and advice Assumption of costs for work clothing and health checks Contribution to travel tickets, if applicable Flexible working hours and partly mobile working Innovative and leading companies in the automotive industry Interested? Then please apply with your complete application documents (current CV and references from your last three professional positions). Please understand that your documents must consist of cannot be returned for organizational reasons. Therefore, please refrain from sending expensive folders and photos, and original documents. Please note that we will store your data in our IT system in accordance with the provisions of the Federal Data Protection Act or store it when you apply. With your application you agree to the electronic processing/storage of your data. The storage at any time.