Senior validation IT QA

The position

As IT QA Professional you will become part of a newly established QA team supporting a new production site for assembly and packaging of finished products. We value a great working environment, team spirit and empowerment as well as good development opportunities. Along with the rest of the team you will have the responsibility of QA review and oversight of many types of documents, primarily related to validation and qualification. You will also ensure quality and compliance with the current GMP rules and guidelines. Your main tasks will be to: Collaborate with stakeholders to develop and execute test plans, test cases, and test scripts to ensure the quality of our products and services. Review different types of documents, mainly validation and qualification in the beginning. Collaborate with development teams to identify and resolve defects and issues. Participate in design and code reviews to ensure quality standards are met. You will work with stakeholders to document requirements and acceptance criteria, develop and maintain test documentation, including test plans, test cases, and test scripts as well as participate in performing functional, regression, and performance testing. Qualifications The ideal candidate will have: Bachelor’s degree in computer science, Software Engineering, or a related field. Experience in QA, with a focus on automation and AI & familiarity with artificial intelligence and machine learning concepts. Min. 2 years of experience with GMP guidelines and regulations, and a good understanding of regulatory compliance requirements. Understanding of IT infrastructure, including networking, databases, and operating systems. Proficiency in English. As a person you are ambitious and ready to be part of our on-going effort to improve our high standards. You dare to challenge us in our way of working and has the desire to take initiative as well as being responsible for your own learning. A proactive mindset is key to succeeding in this role. You are an honest and dedicated team player who inspires and build trust and respect amongst colleagues and partners. We are cooperating broadly with many stakeholders and therefore excellent collaboration and communication skills are needed. About the department Novo Nordisk is seeking to expand our global manufacturing footprint in Odense, Denmark to meet the increasing demand for current and future treatments in serious chronic diseases. This presents an exciting challenge and an opportunity to make a lasting impact. As a member of this Fill & Finish Expansions QA team, you will be key player for ensuring quality in designing, planning, and building our manufacturing footprint in Odense. Once the facility in Odense is in operation and final approvals have been obtained, it will become part of Novo Nordisk's global network of manufacturing facilities. To succeed, a high level of commitment from the Quality Assurance department is required to ensure the highest quality for our patients, even when challenged during project execution and daily operation. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.