Quality Specialist - Recalls, Inspection Office

The position

You will get the opportunity to work within an area with high management attention in Novo Nordisk. The deliverables of our team are significant in ensuring quality for our patients and the job will surely challenge and develop your business understanding. Your primary responsibility will be : Lead the coordination of recalls or potential recall situations for Novo Nordisk products. Oversee recalls in close cooperation with relevant health authorities and stakeholders across Novo Nordisk. You will be part of a team of six dedicated colleagues and report to the Recalls Senior Manager and the team is a part of Novo Nordisk Quality Inspection Office. Qualifications To be successful in this role, you need the following: An academic degree in engineering, pharmaceutical sciences, or a related natural science discipline. Experience with quality assurance or production in the pharmaceutical industry within e.g. filling, assembly or packaging, Strong communication skills; both verbal and written communication across all levels of the organization both internally and externally. Fluency in English - both written and spoken, and be an experienced user of MS Office. Preferably you have experience with: Novo Nordisk organisation and prouduct portfolio. Handling change requests, deviations and systematic problem solving. Being a part of a potential recall case or responsible for escalated deviations. Communication to Health Authorities. As a person you are analytical, with a calm and professional authority and have a flexible working attitude. You thrive with working across business areas, facilitating various groups and with business-critical tasks and project with short deadlines. We expect you to be a team player and have a natural interest in quality processes, authority requirements and our obligations to patients world-wide. About the department Located in Bagsværd, Denmark, the department, Inspection Office is a highly specialised area where you will join a team of 22 highly skilled, ambitious, and motivated specialists with the responsibility for handling Recalls, GMP inspections and notified bodies audits in Novo Nordisk as well as responsibility for the corporate recall, batch records, review and release processes. We have a close collaboration with our stakeholders globally in Novo Nordisk spanning across manufacturing sites, affiliate offices and regulatory affairs, as well as with health authorities around the world. 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.