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Job in Deutschland (Hamburg): Corporate HSE Director (m/f/d)
HELM AG, Innere Stadt, Wien
Corporate HSE Director (m/f/d) Location: Hamburg Business Unit: Corporate Units Employment type: permanent Contact person for this position: Juliane Heunemann 49 40 2375 1875 Experience HELM as a unique family business and an attractive employer. Through a constant exchange of ideas, our ultimate goal is to offer our customers future-oriented solutions within our global network. At any time, in any place. This allows us to work proactively and think long-term - in operations, quality management, process optimization, product development and distribution. We are innovation drivers, possibility makers and a reliable partner, all in one. Corporate Operations at HELM is responsible for "Production & Maintenance", "Engineering, Procurement, Construction", and "Production Controlling" in addition to HSE. A dedicated interface management as well as a close cooperation between these areas is given globally. To support our team in Hamburg, we are looking for an experienced Corporate HSE Director (m/f/d) to start as soon as possible. Your tasks: In this role, you will be responsible for implementing and maintaining effective global HSE frameworks and processes and act as the central point of contact for Health & Safety Environment (HSE) within HELM Group. You will technically lead the external HSE specialist for the Head Office in Hamburg and provide support for re-certifications within HELM (ISO 14001; ISO 45001; ISO 50001). The identification and definition of improvement potentials in audits or inspections also falls within your scope of duties. Motivated and structured, you actively participate in international teams in the design and implementation of global HELM safety programs. You will provide support in the investigation of any accident incidents that may occur and offer advice on the implementation of technical and organizational safety measures to improve our global safety culture. You will be independently responsible for the execution and consulting of risk analyses, hazard assessments, root cause analyses and ideally have experience in PHA, HAZOP, LOPA. In addition, you will take over the function "Responsible Care Leader EMEA" and work closely with the Head of Corporate Operations, the global Responsible Care Leader and the regional HSE Managers of our international sites - focus points here include plant safety, health & safety, as well as the implementation of standards. You will be responsible for developing and measuring global HSE KPIs and driving the implementation of consistent global reporting and dashboards across HELM. Participation in projects and M&A's regarding HSE relevant issues and topics completes your scope. Your profile: You have successfully completed your studies as a safety engineer or possess a comparable qualification. You have also trained as an occupational safety specialist and have extensive professional experience in the area of occupational and plant safety - preferably in the chemical industry. You have relevant knowledge of optimizing processes and workflows in the area of HSE and are keen to help shape company processes and workflows in a changing organizational environment and implement them with a "hands-on mentality". In addition, you are characterized by a quick grasp of new ideas, a self-reliant and structured way of working, and a high degree of moderation and communication skills. Various stakeholders appreciate you as a team-oriented and resilient personality, as you have a distinct entrepreneurial mindset. In addition, you are open to new topics. You enjoy working in an international environment, even on business trips lasting several days, and you are business fluent in English and German. Apply now What we offer At HELM, we are proud of our history and our international economic success. We know how important a healthy working atmosphere and satisfied employees are for this success. We offer among other things: Professional trainings and language courses Company kindergarten for children between 3 and 7 years of age 30 days of holiday 4 holiday apartments Company pension scheme - increased allowance for direct insurance offered by the Company and/or pension fund Advance towards season ticket for public transport HELM's company restaurant CHEMICALS FERTILIZER CROP PROTECTION PHARMA Every day, each one of us contributes to HELM's success with competence, the highest expertise and unique service. We reward this commitment - not only with international opportunities, possibilities for seminars and further training but also with benefits that offer optimal conditions to reach the perfect work-life balance. Interested? Then please apply with all necessary documents via our application portal. If you have questions, feel free to contact the contact person for this position. Reference Number: YF9694837 (please quote in the application) Apply now
Capital Steering Manager (f/m/x)
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International business requires an international corporate philosophy. Are you open to new ideas and do you value cultural diversity? At Raiffeisen Bank International, we are pleased to have more than 16 million customers in 13 CEE countries. And our journey continues - with exciting new issues for us to tackle such as digitalisation and changing customer needs. Join us on our journey.Capital Steering Manager (f/m/x)Capital Steering is a key stakeholder in the management of the capital position of RBIGroup and of RBI AG. The team monitors the development of the capital structure of thenetwork banks and offers consultancy regarding its optimization. Moreover, Capital Steering issupervising strategic capital steering concepts including the management of major capitaltransactions within RBI Group and the management of the structural FX position.What you can expect:Take over the responsibility for RBI AG capital planning and ensure proper & timely regulatory submissionsDevelop further MREL planning and monitoring for Resolution Group AustriaOptimize the capital position of RBIs network banks by aligning with local teams on target capital structures, plans for capital transactions, dividend policy and other structural measuresAct as a SPOC for network units on all relevant topics for capital- and MREL- planning and ensure proper consideration in RBI Group's capital planning and budgeting processProvide regulatory capital and MREL impact assessments for regulatory applicationsContribute to RBI Group's budgeting and forecast process by ensuring proper reflection of all capital- and MREL-relevant topics in the final budgetsDevelop further and implement appropriate monitoring and reporting tools for above mentioned tasksWhat you bring to the table:University degree in business administration, banking & finance, information systems or similar education3-5 years working experience in Banking Controlling, Accounting, Treasury or related roleGood knowledge of current regulatory framework with focus on capital topics would be an advantageExcellent analytical skills, experience in data processing and a self-motivated mindset as well as the ability to work within an agile environmentExperienced user of MS Office, Bloomberg, Tagetik, Qlik, Power BIExcellent verbal and written communication skills in English and German, CEE language is an advantageWhat we offer:You'll work in an international team at a leading bankYou'll benefit from flexible working arrangements and determine your own work-life balanceYou'll benefit from the very latest in tailored professional developmentYou'll earn an appropriate salary starting at EUR 46.500,00 gross p.a. excluding overtimeRBI AG is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ethnicity, race or color, national origin, religion, political or other opinion, gender, sexual orientation or disability.We are looking forward to receiving your online application!https://jobs.rbinternational.com
Job in Deutschland (Ratingen): Supplier Country Manager Scandinavia (m/w/d)
DKV EURO SERVICE GmbH + Co. KG, Innere Stadt, Wien
Supplier Country Manager Scandinavia (m/w/d) There are many ways to success with DKV Euro Service. Fleets in over 40 countries rely on our smart and future-oriented mobility solutions. Become part of a dedicated and enthusiastic team that helps shape commercial mobility throughout Europe. Your tasks About the Job As a Supplier Country Manager Scandinavia, you will be acquiring new business relationships with fuel station networks in Scandinavia. Moreover, you will be managing existing business relationships helping our business partners to solve operational challenges and optimizing commercial agreements. You will use an entrepreneurial approach to proactively identify business opportunities with strategic relevance for DKV. Equipped with your growth mindset and goal-getter mentality you will be striving for performance excellence. Finally, you will be embracing the DKV idea of team of teams and working closely with our sales department to provide best in class products for DKV customers. About your responsibilities Country responsibility in Scandinavia for acquisition of new fuel station partners (Gasoline, Diesel, LNG, CNG, Hydrogen), car washing and parking networks Negotiation of commercial contracts based on market requirements with new and existing partners Management of existing business relationships with fuel station partners Complete processing of service station (fuel, parking, washing) inquiries and offers as well as supplier inquiries regarding the admission decision to the DKV fuel card acceptance network Supporting technical departments in onboarding business partners for DKV fuel card acceptance Negotiation on implementing mobile payment solutions in the fuel station networks Monitoring fuel volume targets and optimization of gross profit Participation in and support of necessary sales promotion measures such as the preparation of basic data for the creation of cartographic aids (road maps and single station displays) Supervision and management of projects with procurement relevance, also across departments Processing of supplier complaints and involvement in customer complaints Your profile Your profile Driven and goal-oriented personality Strong communicator with great negotiation skills - Peoples skills and team player - Entrepreneurial, proactive, solution oriented and goal getter mindset You thrive in fast-paced environment Working experience in at least one of the following industries is preferred but not a must: fuel business, mobility, energy, logistics, automotive, travel industry Working experience in at least one of the following functions preferred: sales, acquisition manager, partner/supplier management, business development, purchasing Required : Professional experience of 3-5 years or more University degree (at least Bachelor’s degree, Master’s degree is a plus) Very good written and spoken English, German language skills is a plus Your benefits With us you will find the best prerequisites for shaping the future. Our international team is dedicated to new challenges. With us, you will find room for your own ideas, attractive remuneration with performance-related bonuses and many other extras. If you have any questions, please contact Sabine Kalthoff by dialling 021025517213. Apply now
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Quality Control and Quality System and Improvement Manager or Expert (f/m/d)
Takeda, Vienna, Wien
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description The Quality Control and Quality System & Improvement Manager within External Supply Plasma Quality will lead and act as the subject matter expert on technical aspects of the QC and strategy development areas including method transfer/validations, quality events, change control, strategy/planning tools and cross-functional. In addition to that the interaction with various teams to enable appropriate overall QC and strategy development support at the CMOs /CTLs on projects and programs is the key. The position will also support and/or lead quality activities related to oversight of Contract Manufacturing Operations (CMO) performed on behalf of Takeda and will support any GMP, Quality and Compliance activities as required. Your New Opportunity Manage critical issues and timely resolution, developing solutions to complex problems Monitor the performance of CMOs/ CTL’s & suppliers to ensure that they remain in a state of control and are aligned to management metrics/ expectations, and leading the effort to drive improvement Support method development and innovations / technical transfers / projects/ validation / launch activities related to CMO activities Author and review documents such as protocols, memos, data summaries, reports and procedures and contributes publications in field of expertise and relevant CMC sections of regulatory filings Support preparation team development and succession plan, team meetings, workshops and trainings Support preparation of annual product (quality) reviews (APR/APQR), complaint investigations, change controls as assigned deviations Technical expert in multiple analytical technologies, establishing recognition outside the company Provide in-depth know-how of theories, concepts, principles and techniques of relevant scientific areas - proficiency in industry practices, techniques, and standards Your Skills and Qualifications Bachelor’s degree in sciences or Engineering (Chemistry, Biology, Pharmacy, Microbiology, etc.) at least, or a higher degree +5 years’ experience in a QC related position within the pharmaceuticals industry, strong knowledge of cGMP Knowledge and understanding of EU and US cGMP regulations with respect to the production and testing of pharmaceutical and/or biological products Experience in interacting with health authorities including hosting/direct involvement with agency inspections Knowledge and understanding of management/planning and financial tools (Capex, Opex) Knowledge of project management and development tools - excellent time management & prioritization and strong organizational skills Strong track record of identifying and correcting compliance issues and implementing process improvements Practical knowledge of working with QMS databases like TrackWise and Microsoft Office tools, experience with pharmaceutical quality and compliance management systems highly desired Clear, demonstrated proficiency in scientific writing Proactive at keeping current with literature and latest technologies Reliable, quality-conscious, self-driven team player Ability to think “out of the box” and to come with innovative approaches to improve cycle time and quality of results Effective communicator at all levels internally and externally; excellent written, oral, and interpersonal communication and presentation skills (English is required / German is beneficial) At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Takeda encourages and supports its employees by trainings, job rotations and mentoring. A balanced work – life ratio (recognition for work and family, company kindergarten) and numerous benefits (fitness center, cafeteria, etc.) complete our profile as a top employer. For more insights into Takeda click here. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Gender, age, skin color, background or sexual orientation play no role in this as we actively promote diversity. We equally address people with disabilities. In the course of a recruitment process which is as free of barriers as possible, we encourage you to mention all relevant information in this context in your application. Motivated employees must be remunerated appropriately. The minimum salary for this important and responsible position is € 4 527,78 gross per month (full time, collective wage agreement for the chemical industry). The actual remuneration package will be guided by your professional experience and your qualifications, so increased payment is possible. Please submit your detailed CV and letter of motivation! Locations AUT - Austria Remote Worker Type Employee Worker Sub-Type Regular Time Type Full timeBy clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description The Quality Control and Quality System & Improvement Manager within External Supply Plasma Quality will lead and act as the subject matter expert on technical aspects of the QC and strategy development areas including method transfer/validations, quality events, change control, strategy/planning tools and cross-functional. In addition to that the interaction with various teams to enable appropriate overall QC and strategy development support at the CMOs /CTLs on projects and programs is the key. The position will also support and/or lead quality activities related to oversight of Contract Manufacturing Operations (CMO) performed on behalf of Takeda and will support any GMP, Quality and Compliance activities as required. Your New Opportunity Manage critical issues and timely resolution, developing solutions to complex problems Monitor the performance of CMOs/ CTL’s & suppliers to ensure that they remain in a state of control and are aligned to management metrics/ expectations, and leading the effort to drive improvement Support method development and innovations / technical transfers / projects/ validation / launch activities related to CMO activities Author and review documents such as protocols, memos, data summaries, reports and procedures and contributes publications in field of expertise and relevant CMC sections of regulatory filings Support preparation team development and succession plan, team meetings, workshops and trainings Support preparation of annual product (quality) reviews (APR/APQR), complaint investigations, change controls as assigned deviations Technical expert in multiple analytical technologies, establishing recognition outside the company Provide in-depth know-how of theories, concepts, principles and techniques of relevant scientific areas - proficiency in industry practices, techniques, and standards Your Skills and Qualifications Bachelor’s degree in sciences or Engineering (Chemistry, Biology, Pharmacy, Microbiology, etc.) at least, or a higher degree +5 years’ experience in a QC related position within the pharmaceuticals industry, strong knowledge of cGMP Knowledge and understanding of EU and US cGMP regulations with respect to the production and testing of pharmaceutical and/or biological products Experience in interacting with health authorities including hosting/direct involvement with agency inspections Knowledge and understanding of management/planning and financial tools (Capex, Opex) Knowledge of project management and development tools - excellent time management & prioritization and strong organizational skills Strong track record of identifying and correcting compliance issues and implementing process improvements Practical knowledge of working with QMS databases like TrackWise and Microsoft Office tools, experience with pharmaceutical quality and compliance management systems highly desired Clear, demonstrated proficiency in scientific writing Proactive at keeping current with literature and latest technologies Reliable, quality-conscious, self-driven team player Ability to think “out of the box” and to come with innovative approaches to improve cycle time and quality of results Effective communicator at all levels internally and externally; excellent written, oral, and interpersonal communication and presentation skills (English is required / German is beneficial) At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Takeda encourages and supports its employees by trainings, job rotations and mentoring. A balanced work – life ratio (recognition for work and family, company kindergarten) and numerous benefits (fitness center, cafeteria, etc.) complete our profile as a top employer. For more insights into Takeda click here. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Gender, age, skin color, background or sexual orientation play no role in this as we actively promote diversity. We equally address people with disabilities. In the course of a recruitment process which is as free of barriers as possible, we encourage you to mention all relevant information in this context in your application. Motivated employees must be remunerated appropriately. The minimum salary for this important and responsible position is € 4 527,78 gross per month (full time, collective wage agreement for the chemical industry). The actual remuneration package will be guided by your professional experience and your qualifications, so increased payment is possible. Please submit your detailed CV and letter of motivation! Locations AUT - Austria Remote Worker Type Employee Worker Sub-Type Regular Time Type Full time
Senior Finance Manager (m/f/d)
Hays Österreich – Recruiting Experts Worldwide, Wien
True financial experts are rare - and in great demand. They also command a high price on the job market. We open doors for financial specialists in fields such as accounting, controlling, corporate banking, interim management, risk management and treasury. By drawing on your interests and experience, we will find the right job for you, because with us, specialists find their ideal working environment - all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience. My employerOur client is a very successful international company, a global player in its field of industry and is listed on the US stock exchange. You will be part of a dynamic working environment with significant potential for further development.Central Finance function for the Suisse and Austrian entitiesResponsible for Accounting activities, the year end closing and financial statements of the groupLeading and developing a team of up to 17 peopleControl of daily Accounting operations and GAAP complianceCentral point of contact for external auditors, the tax director and the CFOCoordination of various different finance projects and communication hub to internal and external stakeholderGroup-wide support of process optimization and development of the Accounting departmentProfound knowledge in Accounting and an University degree in Business Administration or Finance (or similar)SOX knowledge and experience with consolidation would be preferableDeep knowledge in taxesExcellent written and verbal communication skills in EnglishExperience in change and process management is a nice to haveSolution- and process-oriented approach, analytical thinking, hands-on mentality and high degree of flexibilityWorking experience in an international company environmentWe are looking for senior candidates with an in-depth knowledge in finance and hands-on experience in an international environment. If you are able to think outside the box, are proactive and also roll up your sleeves than you are the perfect candidate for this position. In this exposed role you will be able to shape the strategy of the company with your team and take the Finance agendas on a higher level.Salary informationThe compensation for this position is at least 70.000 € gross per year. An overpayment is possible, depending on qualifications and experience.
Quality Control and Quality System and Improvement Manager or Expert (f/m/d)
Takeda, Wien, Vienna
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description The Quality Control and Quality System & Improvement Manager within External Supply Plasma Quality will lead and act as the subject matter expert on technical aspects of the QC and strategy development areas including method transfer/validations, quality events, change control, strategy/planning tools and cross-functional. In addition to that the interaction with various teams to enable appropriate overall QC and strategy development support at the CMOs /CTLs on projects and programs is the key. The position will also support and/or lead quality activities related to oversight of Contract Manufacturing Operations (CMO) performed on behalf of Takeda and will support any GMP, Quality and Compliance activities as required. Your New Opportunity Manage critical issues and timely resolution, developing solutions to complex problems Monitor the performance of CMOs/ CTL’s & suppliers to ensure that they remain in a state of control and are aligned to management metrics/ expectations, and leading the effort to drive improvement Support method development and innovations / technical transfers / projects/ validation / launch activities related to CMO activities Author and review documents such as protocols, memos, data summaries, reports and procedures and contributes publications in field of expertise and relevant CMC sections of regulatory filings Support preparation team development and succession plan, team meetings, workshops and trainings Support preparation of annual product (quality) reviews (APR/APQR), complaint investigations, change controls as assigned deviations Technical expert in multiple analytical technologies, establishing recognition outside the company Provide in-depth know-how of theories, concepts, principles and techniques of relevant scientific areas - proficiency in industry practices, techniques, and standards Your Skills and Qualifications Bachelor’s degree in sciences or Engineering (Chemistry, Biology, Pharmacy, Microbiology, etc.) at least, or a higher degree 5 years’ experience in a QC related position within the pharmaceuticals industry, strong knowledge of cGMP Knowledge and understanding of EU and US cGMP regulations with respect to the production and testing of pharmaceutical and/or biological products Experience in interacting with health authorities including hosting/direct involvement with agency inspections Knowledge and understanding of management/planning and financial tools (Capex, Opex) Knowledge of project management and development tools - excellent time management & prioritization and strong organizational skills Strong track record of identifying and correcting compliance issues and implementing process improvements Practical knowledge of working with QMS databases like TrackWise and Microsoft Office tools, experience with pharmaceutical quality and compliance management systems highly desired Clear, demonstrated proficiency in scientific writing Proactive at keeping current with literature and latest technologies Reliable, quality-conscious, self-driven team player Ability to think “out of the box” and to come with innovative approaches to improve cycle time and quality of results Effective communicator at all levels internally and externally; excellent written, oral, and interpersonal communication and presentation skills (English is required / German is beneficial) At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Takeda encourages and supports its employees by trainings, job rotations and mentoring. A balanced work – life ratio (recognition for work and family, company kindergarten) and numerous benefits (fitness center, cafeteria, etc.) complete our profile as a top employer. For more insights into Takeda click here . We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Gender, age, skin color, background or sexual orientation play no role in this as we actively promote diversity. We equally address people with disabilities. In the course of a recruitment process which is as free of barriers as possible, we encourage you to mention all relevant information in this context in your application. Motivated employees must be remunerated appropriately. The minimum salary for this important and responsible position is € 4 527,78 gross per month (full time, collective wage agreement for the chemical industry). The actual remuneration package will be guided by your professional experience and your qualifications, so increased payment is possible. Please submit your detailed CV and letter of motivation Locations AUT - Austria Remote Worker Type Employee Worker Sub-Type Regular Time Type Full time By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description The Quality Control and Quality System & Improvement Manager within External Supply Plasma Quality will lead and act as the subject matter expert on technical aspects of the QC and strategy development areas including method transfer/validations, quality events, change control, strategy/planning tools and cross-functional. In addition to that the interaction with various teams to enable appropriate overall QC and strategy development support at the CMOs /CTLs on projects and programs is the key. The position will also support and/or lead quality activities related to oversight of Contract Manufacturing Operations (CMO) performed on behalf of Takeda and will support any GMP, Quality and Compliance activities as required. Your New Opportunity Manage critical issues and timely resolution, developing solutions to complex problems Monitor the performance of CMOs/ CTL’s & suppliers to ensure that they remain in a state of control and are aligned to management metrics/ expectations, and leading the effort to drive improvement Support method development and innovations / technical transfers / projects/ validation / launch activities related to CMO activities Author and review documents such as protocols, memos, data summaries, reports and procedures and contributes publications in field of expertise and relevant CMC sections of regulatory filings Support preparation team development and succession plan, team meetings, workshops and trainings Support preparation of annual product (quality) reviews (APR/APQR), complaint investigations, change controls as assigned deviations Technical expert in multiple analytical technologies, establishing recognition outside the company Provide in-depth know-how of theories, concepts, principles and techniques of relevant scientific areas - proficiency in industry practices, techniques, and standards Your Skills and Qualifications Bachelor’s degree in sciences or Engineering (Chemistry, Biology, Pharmacy, Microbiology, etc.) at least, or a higher degree 5 years’ experience in a QC related position within the pharmaceuticals industry, strong knowledge of cGMP Knowledge and understanding of EU and US cGMP regulations with respect to the production and testing of pharmaceutical and/or biological products Experience in interacting with health authorities including hosting/direct involvement with agency inspections Knowledge and understanding of management/planning and financial tools (Capex, Opex) Knowledge of project management and development tools - excellent time management & prioritization and strong organizational skills Strong track record of identifying and correcting compliance issues and implementing process improvements Practical knowledge of working with QMS databases like TrackWise and Microsoft Office tools, experience with pharmaceutical quality and compliance management systems highly desired Clear, demonstrated proficiency in scientific writing Proactive at keeping current with literature and latest technologies Reliable, quality-conscious, self-driven team player Ability to think “out of the box” and to come with innovative approaches to improve cycle time and quality of results Effective communicator at all levels internally and externally; excellent written, oral, and interpersonal communication and presentation skills (English is required / German is beneficial) At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Takeda encourages and supports its employees by trainings, job rotations and mentoring. A balanced work – life ratio (recognition for work and family, company kindergarten) and numerous benefits (fitness center, cafeteria, etc.) complete our profile as a top employer. For more insights into Takeda click here . We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Gender, age, skin color, background or sexual orientation play no role in this as we actively promote diversity. We equally address people with disabilities. In the course of a recruitment process which is as free of barriers as possible, we encourage you to mention all relevant information in this context in your application. Motivated employees must be remunerated appropriately. The minimum salary for this important and responsible position is € 4 527,78 gross per month (full time, collective wage agreement for the chemical industry). The actual remuneration package will be guided by your professional experience and your qualifications, so increased payment is possible. Please submit your detailed CV and letter of motivation Locations AUT - Austria Remote Worker Type Employee Worker Sub-Type Regular Time Type Full time
Test- and Application Manager (f/m/x) - in Agile IT Delivery Regulatory Reporting
Raiffeisen Bank International AG, Wien, AT
International business requires an international corporate philosophy. Are you open to new ideas and do you value cultural diversity? At Raiffeisen Bank International, we are pleased to have more than 16 million customers in 13 CEE countries. And our journey continues - with exciting new issues for us to tackle such as digitalisation and changing customer needs. Join us on our journey. Test- and Application Manager (f/m/x) - in Agile IT Delivery Regulatory ReportingAs a member of a motivated cross-functional team, working in an agile setting, you will support operating our Regulatory Universe - the ecosystem for all required regulatory data with the goal to enable reporters to reach material compliance with regulatory requirements with least effort. We are searching for a proactive test and application manager to shape and operate our product.What you can expect:Act primarily as an application manager for the regulatory universe (maintain, configure and run the systems)Perform the incident managementImplement service- and application management processes and IT controlsImplement continuous improvements of our servicePerform and optimize the release and test management.Furthermore, help organize the knowledge sharing and upskilling activities between the teams for testingSupport testers with deviation analysisCoordinate the Go Live ActivitiesWhat you bring to the table:You have 3 + years of experience working as a test and/or application managerExperience with ABACUS GMP or similar regulatory reporting software solutionsYou love to work with data and people.You have solid skills in SQL and data modelling.Knowledge of Banking Products and Processes Know-how of Regulatory Reporting Requirements and Processes is an advantageAffinity to develop small implementations and support with bug fixing by using mainly your SQL skillsFluent in English; German is a plus and we help you improve itWhat we offer:You'll work in an empowered agile team at a leading international bankYou'll benefit from flexible working arrangements and determine your own work-life balanceYou'll benefit from the very latest in tailored professional developmentYou'll earn an appropriate salary starting at EUR 47.000,- gross p.a. excluding overtimeRBI AG is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ethnicity, race or color, national origin, religion, political or other opinion, gender, sexual orientation or disability.We are looking forward to receiving your online application!https://jobs.rbinternational.com
Job in Deutschland (Geschwand): Leiter (m/w/d) Business Development für eine unserer Beteiligungsgesellschaften
Schmetterling International GmbH & Co. KG, Innere Stadt, Wien
Leiter (m/w/d) Business Development für eine unserer Beteiligungsgesellschaften (als Nachfolge für einen der Geschäftsführer in den nächsten zwei Jahren) Wer sind wir? Schmetterling International ist das größte unab­hängige und inhaber­geführte Touristik-Vertriebs­unter­nehmen Europas. Ihre Aufgaben Operative Steuerung des Unter­nehmens Key-Account-Management Neukundengewinnung Steigerung der Kundenzufriedenheit und ­bindung Marketingunterstützung und -beratung Strategische Entwicklung Projektleitung Ihre Qualifika­tionen Studium der Betriebswirtschaft bzw. vergleichbar oder Ausbildung zum kaufmännischen Betriebswirt (m/w/d) Hohes kaufmännisches Ver­ständnis und Entscheidungs­wille Langjährige Erfahrung mit Kundenbindungs­instrumenten (Mehrwert­systemen) Sehr gute Kenntnisse im Projekt­management für Key-Accounts Mehrjährige Erfahrung im Vertrieb bzw. Marketing Smartes, sehr gepflegtes und souveränes Auftreten Begeisterungsfähigkeit, Überzeugungs­kraft sowie Kommunikations- und Verkaufs­stärke Unser Angebot Mittel- bis langfristige Perspektive in einem erfolg­reichen Unter­nehmen Umfassende Aufgaben­stellung Strukturierter Einstieg und intensive Ein­arbeitung Gestaltungs- und Entscheidungs­freiräume Interessiert? hier bewerben Schmetterling International GmbH & Co. KG Geschwand 131 91286 Obertrubach bewerbung[AT]schmetterling.de www.schmetterling.de
Job in Deutschland (Kirchdorf an der Iller): Project Manager Sales (m/f/d) for Global Network
Firmengruppe Liebherr, Innere Stadt, Wien
 One Passion. Many Opportunities. www.liebherr.com/karriere Liebherr-Logistics GmbH, based in Kirchdorf an der Iller, is responsible for global spare parts logistics for various Liebherr product areas. To this end, Liebherr-Logistics GmbH operates a state-of-the-art logistics center for the dispatch of Liebherr original parts on over 47,000 m². Project Manager Sales (m/f/d) for Global Network Job-ID 37330 Your Responsibilities: Coordination and independent processing of tasks in the "Sales" area in cross-company projects in the "Global Network" area Implementation and documentation of the resulting content and measures Process recording, analysis and optimization Coordinating and supporting function in the implementation of new systems, methods and processes Analysis activities including data acquisition and processing Independent work in day-to-day business and in project tasks Your Profile: Successfully completed studies with content in business administration, logistics or project management. Alternatively, a comparable training with relevant professional experience Knowledge of common ERP systems and how they work Knowledge of known project management and process optimization methods Very good knowledge of English Good understanding of business and logistical processes Independent, structured and analytical way of working Self-confident appearance as well as communication and teamwork skills Flexibility and willingness to travel Unser Angebot Sie sind auf der Suche nach neuen beruflichen Herausforderungen? Die Firmengruppe Liebherr bietet Ihnen als international erfolgreiches Familienunternehmen einen sicheren Arbeitsplatz, eine einzigartige Vielfalt an Aufgaben und spannende Entwicklungsmöglichkeiten. Werden Sie noch heute Teil unseres starken Teams und lernen Sie die Firmengruppe Liebherr als zuverlässigen Partner kennen. Anschrift: Liebherr-Logistics GmbH Oberopfingen St. Vitus 1 88457 Kirchdorf an der Iller Kontakt: Andrea Klöcker Tel.: 49 7354 80-7325 Jetzt bewerben Bitte bewerben Sie sich ausschließlich online unter www.liebherr.com/karriere