Your Tasks - as important as our Software:

• Develop innovative software products for the regulated industry, based on our CARA platform
• Analyze new requirements, create appropriate concepts, and implement them by programming
• Take responsibility for the architecture and for all technical aspects of the application. This includes topics like interfaces, security, performance, deployment and high availability
• Coach your colleagues on best practices, perform code reviews and provide guidance on all technical topics
• Organize your work by using tools like git and Confluence
• You are an integral part of the Scrum team, you advise the Product Owner of all technical questions, you propose technical user stories and provide estimates

Your Profile - as good as our Solutions:

• You have a university degree in computer science
• You have relevant experience in working with complex software products and very good knowledge (5+ years) of professional software development using Java/Groovy
• You have a high affinity to DevOps and any kind of automation
• You are well organized, and you are a team player
• You do not like technical debts

What we consider as a Big Plus:

• You have already gained experience in the regulatory environment, preferably in software development for the pharmaceutical industry and therefore you know its specifics/guidelines
• You have sound knowledge of and practical experience in the field of document management systems (DMS)
• You have good knowledge of the configuration of document management systems (DMS), preferably D2/Documentum or CARA
• Knowledge of regulatory standards like eCTD, HL7, FHIR and IDMP
• Knowledge of Data Science
• Your profile is rounded off by a high degree of analytical and conceptual skills as well as a profound understanding of user needs and solution design.

What we offer you:

• 30 Days Vacation
• Mobile Working
• Personal Development
• Pension Scheme
• Overtime Regulation
• Flexible Working Hours
• Canteen
• Free Coffee & Tea