Überblick über die Statistik des Gehaltsniveaus für "Project Safety Manager in Baden-Württemberg"

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 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

Team Leader System & Software Development Rail (m/f/x) (Group Leader, Team Leader) [ https://www.think-safe-think-ics.de /] TEAM LEADER SYSTEM & SOFTWARE DEVELOPMENT RAIL (M/W/X) Business Center: Safety or System & Software Locations: Stuttgart, Berlin, Braunschweig, Leipzig YOUR CORE TASKS INCLUDE: Technical and disciplinary management of a team for the development of safety-relevant systems and software according to personal suitability Establishing and maintaining the team culture, challenging and promoting team members, recognizing talents and providing technical support to team members in the project environment Acting independently in development projects in the role of project manager or project team member Technical and sales support for customer inquiries, preparation of offers, as well as cross-team coordination with other team leaders to achieve the best possible utilization in the team WHAT YOU CAN EXPECT FROM US: You will receive a permanent employment contract and a secure job with individual training and career opportunities In-depth training in a professional environment Challenges in the field of safety-critical systems, e.g. in the industrial and rail sectors Enjoy the family atmosphere of an established company, with experienced and motivated colleagues You will receive performance-related remuneration with a 13th monthly salary and results-oriented bonus Organize your working hours freely and benefit from a lot of flexibility - mobile work was part of our offer even before Covid Benefit from our attractive company pension scheme Secure tax-free employer subsidies that you can use for various health offers Take advantage of our offer for an e-bike on a leasing basis with a significant employer subsidy Develop yourself through appreciative feedback and become part of a team where your ideas are welcome WHAT WE WANT FROM YOU: Completed diploma or master's degree in computer science, electrical engineering, transport engineering or similar with a specialization in railroad systems, e.g. ETCS, control and safety technology (LST) or rail vehicles Several years of professional experience or extensive practical experience in the field of rail systems, ideally with management responsibility and a project manager certificate Analytical and solution-oriented thinking as well as an open-minded and communicative manner Fluent German and good English skills Ideally experience in agile system or software development of highly complex technical solutions in the railroad environment INTERESTED? Then we look forward to receiving your application, stating your earliest possible starting date and your salary expectations. Please use the \"Apply now\" button below. ICS - Informatik Consulting Systems GmbH (THINK SAFE THINK ICS) Stefanie Herrmann People and Culture career(at) ics-gmbh.de T +49 711 21037-00 Data protection can be found in our privacy policy [ https://www.ics-gmbh.de/datenschutz/#bewerber ] under point 7 ff. [ https://bewerbung.maxime-media.de/unternehmen/ics-informatik-consulting-systems-gmbh-1994/job/13052 ]

Test Engineer Validation and Verification (m/f/d) The expertum Group offers technical and commercial specialists and managers attractive tasks and career opportunities in the industry. We are a reliable and fair partner for our employees - take the path to new professional challenges with renowned and appreciative customers with expertum! THIS IS WHERE YOU WILL WORK: Recommended by candidates, employees & customers, expertum offers exciting jobs in attractive sectors with appreciative global market leaders in industry. Originating from industry, expertum has been placing qualified specialists and managers in technical and commercial professions for more than 30 years. With almost 50 locations in Germany and Europe, expertum is one of the market leaders with its industry and job profile specialization in the metal, electrical, pharmaceutical, aviation and logistics industries. Become part of our brand family and shape the future with us. We are looking for you as a Test Engineer Validation & Verification (m/f/d) at the Pforzheim site with immediate effect and look forward to receiving your application! THESE ARE YOUR TASKS: Developing and reviewing project-specific V&V strategies and creating test specifications Defining verification methods and tools and specifying the required test environment Writing error messages and creating validation and verification matrices Working closely with the project team to ensure that tests are carried out on time Analyzing and evaluating test results and creating test documentation WHAT YOU BRING WITH YOU: Degree in computer science, electrical engineering, mechanical engineering or a comparable qualification with an understanding of the V-model for software development Experience in software testing, also acquired through internships and theses Independent preparation, execution and follow-up of tests Programming experience in at least one of the following languages is desirable: Matlab, Python, C++, Java Basic knowledge of message transmission and data bus protocols (e.g. CAN, ARINC, serial protocols) Willingness to work closely with the development departments Due to the safety-critical systems, a quick grasp is required Good written and spoken English skills WE GUARANTEE YOU: Vacation and Christmas bonus Company pension scheme Corporate benefits Regular team and company events The chance to work in an open-minded team with ambitious goals Company values that are practiced every day at work Agile working methods and an open feedback culture CV IS ENOUGH: It only takes a few minutes to apply online at expertum. Simply upload your CV, check the transferred data and send the application - done. We look forward to hearing from you!

Westhouse is one of the leading international recruitment companies for the placement of highly qualified professionals in areas such as IT Life Cycle, SAP, Engineering, Commercial and Technical Consulting. Westhouse Job: Developer - Systems for Automated Driving / Functional Safety (m/f/d) Your tasks: Development of driver assistance functions in the field of highly automated driving Development of functional requirements for redundant braking systems for highly automated driving commercial vehicles (SAE Level 4) in cooperation with customers and internal function and software development teams in the role of 'Requirements Engineer' Planning, coordination and support of safety-relevant projects with the help of ISO 26262, e.g. carrying out hazard analyses (HARA), developing functional and technical safety concepts, FMEA, FTA Consideration of safety objectives in the system architecture, interfaces and components Supporting project teams with functional safety issues, such as effort estimation, moderation and safety assessments Implementation and further development of safety methodologies Application of the SysML and UML description languages for architecture design Your qualifications: Degree in automotive engineering, mechatronics, electrical engineering, computer science, mechanical engineering or similar Experience with methods such as FMEA and FMEDA Expert knowledge in the fields of vehicle dynamics, trucks, control engineering and signal processing an advantage Practical experience in carrying out the following tasks: Carrying out hazard analyses Hazard Analysis and Risk Assessment (HARA), Development of functional and technical safety concepts Analysis and derivation of safety requirements Failure Mode and Effects Analysis (FMEA) and Failure Tree Analysis (FTA) Relevant user knowledge in the area of functional safety Knowledge of common methods and tools for system design and requirement management Process knowledge in the areas of IATF 16949, ASPICE and ISO26262 What you can expect: General conditions will be discussed personally. We look forward to receiving your informative application documents in electronic form.

Quality & Information Security Manager (m/f/d) (ISO 9001 & ISO 2700x) IT Transformation Management What you can expect Process management: You will analyze, develop and monitor quality and security management processes in accordance with ISO 9001, ISO 2700x, BSI basic protection and NIS-2. Auditing: you carry out internal audits and support external audits Employee training: You train and support employees in quality and safety-related topics. Continuous improvement: You continuously improve processes to increase the efficiency and effectiveness of the quality management system (QMS) and the information security management system (ISMS). IT transformation projects: To ensure that project objectives meet quality and security standards, you plan, monitor and manage IT transformation projects, What you bring with you Educational qualification: Completed business studies or IT-related/commercial vocational training. Specialist knowledge: Knowledge of the ISO 9001 and ISO 2700x standards. Audit experience: First experience in conducting audits and ideally in dealing with auditors. Project management: First experience in project management. Additional qualifications: Certifications in quality management and/or information security management are an advantage. Analytical skills: Ability to process and structure complex information. Communication and language skills: Very good written and verbal communication skills as well as very good German and good written and spoken English skills. Organizational skills: Strong organizational skills. Team motivation: Ability to convince project teams of the importance of ISO standards and IT security. Your benefits Permanent employment contract: Look forward to a permanent employment contract in a modern working environment that offers you stability and security. You will also receive a home office allowance of u20ac500 and the opportunity to work flexibly from home. Secure job: work in a growing company that offers you long-term prospects and job security. Intensive induction and further training: Get off to a successful start with an intensive induction and take advantage of individual further training opportunities at the SOLCOM Academy. An accompanying mentoring program continuously supports you in your professional development. Learning organization: At SOLCOM, we promote continuous learning and knowledge sharing at all levels. Our corporate culture encourages you to actively share your knowledge, develop new skills and come up with innovative solutions. We create an open and flexible working environment where your ideas and perspectives are valued. SOLCOM loves you: Enjoy numerous team events such as team lunches and summer parties. We also offer health checks, employee discounts and many other little treats to enrich your working day. LocationSOLCOM GmbH Schuckertstrasse 1 72766 Reutlingen Start dateBy arrangement Contact person Virginia Walker HR Manager Phone: 07121/1277-344

Markem-Imaje is a trusted world manufacturer of product identification and traceability solutions, offering a full line of reliable and innovative inkjet, thermal transfer, laser, print and apply label systems. Markem-Imaje delivers fully integrated solutions that enable product quality and safety, regulatory and retailer compliance, better product recalls and improved manufacturing processes. The Role Our Pre-Sales Engineer designs and configures in close collaboration with our sales team solutions, based on customer specific requirements and agreed specifications, performs testing of the configured solution, creates solution technical documentation and stores in internal shared drives. The Pre-Sales Engineer supports the Solution Delivery Engineers during installations until completion of the customer agreed configured solution. What you will do: Design based on customer feedback and requirements ideal application solutions based on our product portfolioUtilize Standard Solution Packages as the starting point for configuration or project engineering work on all customer projectsManage the demand process for special items (non MI standard parts) with local suppliersProvide a competitive price calculation based on solution requirements Responsible for performing in house verification of the configured solutionsBuild the Detailed Design Specification documentation required based on project deliverablesSupport installation of the configured solution for after customer validationCreation and delivery of the hand off package for Service Delivery TeamSupport escalated installation, FAT and SAT issues Install CoLOS solutions at customer sites or remotelyAct as Project Manager, being the customers´ main point of contact, as well as internal point of contact from start, roll out and execution. What you need to have: Engineering background including PC and PLC based systemsKnowledge in Vision (product inspection) would be a plusComputer Skills and aptitude for quickly learning new software tools and computer hardwareKnowledgeable in packaging industry and supply chain automationActs in a professional manner and enhances customer satisfaction.Excellent verbal and written communication skills at all levels for the organizationAbility to work in a multi-tasked environmentDirect customer interface experience preferredDocumentation skills is a MUSTBachelor or comparable degree in Engineering (Electrical, Software, Computer, or Automation)Experience with packaging line equipment, preferably in pharmaceutical and/or food packaging industriesProven track record of fault finding and problem solving.Project Management skillsMS SQL Databases and ODBCCommunication with PLC systems and OPCTCP/IP - Experience with IP Addressing and SubnettingMS SQL OS/Windows OSSQL ReportsMust be fluent in English, multi-lingual is preferredThe position involves approximately 60% of travel, on average, mostly domestic travel. This involves traveling to customer sites, possibly involving air travel. You’ll only be the right candidate if you are aligned to our values and culture: Collaborative entrepreneurial spirit Winning through customers High ethical standards, openness and trust Expectations for results Respect and value people #LI-DNI If you believe you match our values and have the experience we’re looking for, then apply! We can’t wait to hear from you. #-INDEED #SWEWork Arrangement : Hybrid All qualified applicants will receive consideration for employment without discrimination on the basis of race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other factors prohibited by law.Fraudulent Recruiting Disclaimer: Dover Corporation and our affiliated operating companies want to alter applicants to internet job posting fraud, where parties posing as Dover employees, recruiters, or other agents, try to engage with online practices that involve payment or personal information outside of our official application and hiring process. Please verify the authenticity on an invitation to apply for a job, or for a job offer contacting us directly through our Dover and affiliated operating company websites at https://careers.dovercorporation.com/. To learn how you can protect yourself, review our Recruitment Fraud Notice on our careers site. This position may be located in : EMEA : Germany : Stuttgart : StuttgartSub Division: Direct Distribution GermanyJob Requisition ID: 54948Job Function : Engineering

For over 70 years, the Pneuhage Group has been a successful service and trading company in the tire and wheel industry with several tire retreading companies. We employ more than 2,400 people (m/f/d) throughout Germany. In central management, we see ourselves as a partner, consultant and service provider for our more than 160 branches, the wholesale trade and tire retreading. For our WWS team in Karlsruhe we are looking for you as Process and application manager (m/f/d) Your tasks: You will work in technical and application support and be largely responsible for the further development of our merchandise management system (SAP ERP) You will manage projects and implement requirements in various processes You take on customizing activities, test, document and train the SAP target processes including the coordination of external consultants You are responsible for planning and conducting target group-oriented training courses on site and / or at the head office As part of the telephone user support, you will support our specialist departments on technical and functional issues Your profile: You have a keen interest in mapping processes in merchandise management Ideally, you have basic commercial knowledge and process knowledge in the technical retail sector You have experience in project work Your basic SAP knowledge is based on good knowledge that you have acquired through your studies or work experience You are strong in argumentation and communication and know how to combine a willingness to make decisions with a willingness to cooperate We offer: Varied and challenging activities in an innovative and dynamic team the possibility of flexible working hours and home office by prior arrangement Short decision-making processes and a wide range of design options A familiar working atmosphere characterized by fairness and appreciation intensive induction and a wide range of further education and training opportunities Employee discounts, profit-sharing, bike leasing and other additional benefits. Your contact person We welcome you and look forward to receiving your complete application documents, stating your salary expectations. For initial information, please contact our head of department Johannes Mu00fcller (Tel.: 0173/6293375) or our personnel officer Ebru Yurdakul (Tel.: 0721/6188-856). We are consistently striving to improve our targeted approach to applicants. Please help us to do this by indicating in your application where you discovered our job advertisement. Pneuhage Management GmbH & Co KG Human Resources Department Ms. Ebru Yurdakul An der Rossweid 23-25 | 76229 Karlsruhe www.pneuhage.de [email protected] Additional information: Requirements for the applicant: Basic knowledge: WebDynpro (SAP) interface tool, SAP ERP, information and communication management, SAP Netweaver integration and application platform, process management, information technology, computer technology. Advanced knowledge: Project management