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    2 Jobs gefunden für Operations in Wien, Wien

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      • Wien, Wien
      • Festanstellung
      • Randstad Professionals Austria
      Our client, a big player in the e-commerce sector, is searching for a Senior Software Engineer (m/f/x)Your tasks:The product development team implements tasks that are specified in cooperation with Product ManagementAs a team player, you will be the driving force concerning all technical matters within the cross-functional Tribe and the Software Engineering division as a whole.You will further develop our high-performance server and web applications.Working with the team, you enjoy taking over responsibility for the development, operation and maintenance of services in our system landscape.You are ready to take on product responsibility and to support the Product Management team in planning and carrying out projects.You will take care of code quality and further develop our coding and architecture guidelines within the team.Your profile:You are an excellent Java developer and have very good knowledge of the JVM platform.You have an in-depth understanding of software design patterns and ideally have experience with domain driven design and event-based architecture.You have experience in developing secure, scalable and maintainable REST interfaces.You are familiar with Spring Boot, Spring MVC, Spring Data or a similar framework as well as with relational databases.You are experienced in backend operations, you are also interested in frontend services (HTML, JavaScript, CSS, React or Angular) and motivated to acquire knowledge in this field.You have basic knowledge of the German language or are eager to learn it (by taking language courses during working hours).Your working environment:You will work mostly autonomous within your Tribe.Use of modern technologies (Java 11, Spring Boot 2, Kotlin, React, Kafka).Co-determination in the selection of frameworks and programming languages within the Tribe.Personal budget for conferences and trainings.Selection of preferred working laptop and operating system (Windows, Linux, MacOS), private use is allowed. Our client offers competitive salaries and additional benefits based on your performance, experience and qualifications. The minimum salary for this position is 46.500 EUR gross per year in the collective agreement (IT-Kollektivvertrag 2021). 
      Our client, a big player in the e-commerce sector, is searching for a Senior Software Engineer (m/f/x)Your tasks:The product development team implements tasks that are specified in cooperation with Product ManagementAs a team player, you will be the driving force concerning all technical matters within the cross-functional Tribe and the Software Engineering division as a whole.You will further develop our high-performance server and web applications.Working with the team, you enjoy taking over responsibility for the development, operation and maintenance of services in our system landscape.You are ready to take on product responsibility and to support the Product Management team in planning and carrying out projects.You will take care of code quality and further develop our coding and architecture guidelines within the team.Your profile:You are an excellent Java developer and have very good knowledge of the JVM platform.You have an in-depth understanding of software design patterns and ideally have experience with domain driven design and event-based architecture.You have experience in developing secure, scalable and maintainable REST interfaces.You are familiar with Spring Boot, Spring MVC, Spring Data or a similar framework as well as with relational databases.You are experienced in backend operations, you are also interested in frontend services (HTML, JavaScript, CSS, React or Angular) and motivated to acquire knowledge in this field.You have basic knowledge of the German language or are eager to learn it (by taking language courses during working hours).Your working environment:You will work mostly autonomous within your Tribe.Use of modern technologies (Java 11, Spring Boot 2, Kotlin, React, Kafka).Co-determination in the selection of frameworks and programming languages within the Tribe.Personal budget for conferences and trainings.Selection of preferred working laptop and operating system (Windows, Linux, MacOS), private use is allowed. Our client offers competitive salaries and additional benefits based on your performance, experience and qualifications. The minimum salary for this position is 46.500 EUR gross per year in the collective agreement (IT-Kollektivvertrag 2021). 
      • Wien, Wien
      • Festanstellung
      • Randstad Austria
      Our client Takeda Pharmaceutical Company Limited is a leading global, value-driven, research-based biopharmaceutical company headquartered in Japan. In Austria, Takeda operates along the entire pharmaceutical value chain: research & development, plasma application, manufacturing and distribution. Takeda is the largest pharmaceutical employer in Austria. Every day, around 4,500 employees help to ensure that medicines from Austria reach the whole world and that patients in Austria have access to innovative medicines from Takeda. The Austrian product portfolio helps patients in the fields of oncology, hemophilia and genetic diseases, gastroenterology and immunology, among others. In 2020 and 2021, Takeda was recognized as a Top Employer and Great Place to Work in Austria.To further strengthen the local team for Medical Affairs, PDT, at the site in 1220 Vienna, Takeda is seeking for a Evidence Generation Operations Manager - GMA PDT (f/m/x)who manages assigned aspects of Takeda Medical Affairs Research (TMAR) program including Medical Affairs Company Sponsored Studies (MACS), Investigator Initiated Research (IIR), and Externally Sponsored Collaborative Clinical Research (CCR) studies for Plasma Derived-Therapies (PDT) Business Unit. The position is composed of 3 core responsibilities:1. Act as a Study Operations Manager for assigned PDT GMA-led MACS:Manage the observational/Real World Evidence (RWE) studies in assigned programs in compliance with quality standards (including ICH GCP or GPP as applicable, local regulations and Takeda SOPs)Oversee the Study CROs and other 3rd party vendors including contract negotiation and proper guidance of performance for all activities assigned to a CRO/vendor and escalation of issues2. Management of the TMAR activities, including the review, initiation, tracking, archiving, completion and reporting of any of 3 type of studies, as well as process and system improvement initiatives:Oversee and facilitate receipt, processing, and internal cross-functional review of internal/external study submissionsCoordinate the capture, archiving and reporting of appropriate study level information and documents in the respective systemsManages finance and contract related aspects for globally funded studies3. Act as a Fair Market Value budget evaluator for TMAR Studies and perform the budget evaluation according to Takeda Job Aid Requirements:Master`s degree is required, preferably in a health or natural sciences related fieldMinimum of 2-3 years of pharmaceutical, biotech or CRO industry experience, preferably in clinical operations or medical affairsOperating experience in managing observational/Real World Evidence studies is necessaryExperience in coordinating externally sponsored studies (i.e IIR, CCR) would be an assetKnowledge about the structure of study budgets is essential, preferably know- how about the industry standards related to the fair market value evaluation processUser skills in study management systems and financial systems (f.e. iEnvision, CTMS, ARIBA)Ability to communicate and interact thoughtfully, transparently, and appropriately with a variety of stakeholders both internal and externalOpenminded to create and set up new processes and contribute to improvements for the study management in a cross functional and international environmentExcellent English language skills fluently spoken and written and intermediate German language skillsWorking in a hybrid working modelThe minimum salary for this position is € 4.527,78 gross per month (full time, collective wage agreement for the chemical industry), due to your professional experience and your qualifications an increased payment is intended. The contract will be limited for 1 year, an extension of the contract is possible.If we have inspired your interest, we look forward to receiving your meaningful application via www.randstad.at!We draw your attention to the fact that your application documents in their entirety, including all personal data contained therein, will be forwarded to Takeda for the purpose of carrying out the application procedure and the pre-selection.
      Our client Takeda Pharmaceutical Company Limited is a leading global, value-driven, research-based biopharmaceutical company headquartered in Japan. In Austria, Takeda operates along the entire pharmaceutical value chain: research & development, plasma application, manufacturing and distribution. Takeda is the largest pharmaceutical employer in Austria. Every day, around 4,500 employees help to ensure that medicines from Austria reach the whole world and that patients in Austria have access to innovative medicines from Takeda. The Austrian product portfolio helps patients in the fields of oncology, hemophilia and genetic diseases, gastroenterology and immunology, among others. In 2020 and 2021, Takeda was recognized as a Top Employer and Great Place to Work in Austria.To further strengthen the local team for Medical Affairs, PDT, at the site in 1220 Vienna, Takeda is seeking for a Evidence Generation Operations Manager - GMA PDT (f/m/x)who manages assigned aspects of Takeda Medical Affairs Research (TMAR) program including Medical Affairs Company Sponsored Studies (MACS), Investigator Initiated Research (IIR), and Externally Sponsored Collaborative Clinical Research (CCR) studies for Plasma Derived-Therapies (PDT) Business Unit. The position is composed of 3 core responsibilities:1. Act as a Study Operations Manager for assigned PDT GMA-led MACS:Manage the observational/Real World Evidence (RWE) studies in assigned programs in compliance with quality standards (including ICH GCP or GPP as applicable, local regulations and Takeda SOPs)Oversee the Study CROs and other 3rd party vendors including contract negotiation and proper guidance of performance for all activities assigned to a CRO/vendor and escalation of issues2. Management of the TMAR activities, including the review, initiation, tracking, archiving, completion and reporting of any of 3 type of studies, as well as process and system improvement initiatives:Oversee and facilitate receipt, processing, and internal cross-functional review of internal/external study submissionsCoordinate the capture, archiving and reporting of appropriate study level information and documents in the respective systemsManages finance and contract related aspects for globally funded studies3. Act as a Fair Market Value budget evaluator for TMAR Studies and perform the budget evaluation according to Takeda Job Aid Requirements:Master`s degree is required, preferably in a health or natural sciences related fieldMinimum of 2-3 years of pharmaceutical, biotech or CRO industry experience, preferably in clinical operations or medical affairsOperating experience in managing observational/Real World Evidence studies is necessaryExperience in coordinating externally sponsored studies (i.e IIR, CCR) would be an assetKnowledge about the structure of study budgets is essential, preferably know- how about the industry standards related to the fair market value evaluation processUser skills in study management systems and financial systems (f.e. iEnvision, CTMS, ARIBA)Ability to communicate and interact thoughtfully, transparently, and appropriately with a variety of stakeholders both internal and externalOpenminded to create and set up new processes and contribute to improvements for the study management in a cross functional and international environmentExcellent English language skills fluently spoken and written and intermediate German language skillsWorking in a hybrid working modelThe minimum salary for this position is € 4.527,78 gross per month (full time, collective wage agreement for the chemical industry), due to your professional experience and your qualifications an increased payment is intended. The contract will be limited for 1 year, an extension of the contract is possible.If we have inspired your interest, we look forward to receiving your meaningful application via www.randstad.at!We draw your attention to the fact that your application documents in their entirety, including all personal data contained therein, will be forwarded to Takeda for the purpose of carrying out the application procedure and the pre-selection.

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