Professional in IM1 QA Cleaning – Novo Nordisk A/S – Kalundborg

Are you excited to play an important role in ensuring the quality and safety of our products? Do you want to make a difference within QA? If so, we might have an opportunity in IM1 QA Cleaning for you! The Position As a QA professional, you will play a central role where you need to make decisions for Quality. This demands a solution-oriented approach when collaborating with colleagues both in the QA organisation and in production. The main tasks will be to: Set directions for Quality Ensure that our documentation follows internal and external requirements by reviewing documents from the production sites Work closely with your colleagues in an open-plan office. We have a positive working environment with a desire and a will to solve challenges through open and honest dialogue. We work together as a team because we ensure collaboration across competences and take care of each other. We always work on improving our way of working and we appreciate new ideas and continues improvements. Qualifications To succeed in this role, you have: Master´s degree in Pharmacy or corresponding education (for example MSc. Chem Eng. or MSc. Biology) Ideally, you have knowledge about GMP Preferably, experience with QA CIP (Cleaning in Place) knowledge is a plus Proficiency in English As a person you are open, honest, forthcoming, and inclusive regarding your colleagues in both QA and the production. You enjoy working in a dynamic environment where you can take responsibility and take action. About the Department IM1 QA is a department, consisting of approx. 42 dedicated and engaged employees situated in Kalundborg. The department is divided into 3 teams and the open position is in the QA team responsible for cleaning in place (CIP). Our department ensures a high level of quality in close cooperation with our stakeholders. Our responsibility is to assure product quality and regulatory compliance, perform quality oversight and approve quality documents such as SOPs, change requests monitoring, and validation documents. We participate in systematic problem solving and approve deviations. We expect you to have an eye for detail and understanding of the functionality of our various types of equipment. You will be working in a busy, but socially relaxed and informal environment, where we emphasize collaboration, engagement, well-being, and compliance. We offer you an exciting job in an open and dynamic work environment with good opportunities for professional and personal development.

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