Process Standardization Specialist

2 weeks ago


Bagsværd, Gladsaxe Municipality, Denmark Novo Nordisk Full time
About the Role

The position of Documentation Supporter at Novo Nordisk is a key role in ensuring the quality and integrity of our processes. As a member of the FPM Engineering team, you will be responsible for coordinating and deploying the process for development and maintenance of global QMS standards together with the process managers. This involves working within all Finish Product production processes, delivery processes and the related Q processes.

Key Responsibilities

As a Documentation Supporter, your responsibilities will include supporting and guiding process managers and project managers within QMS and change request handling, coordinating and supporting the process for updating and developing global standards, collaborating with cross-site Process Groups to ensure the incorporation of best practices in the standards, drafting, structuring, and finalizing documents and related training material in a clear and easy-to-understand language, and overseeing documentation handling in the department.

Requirements

We are looking for someone who thrives in an ever-changing environment while keeping the high quality of their work. Our ideal candidate enjoys collaborating with various stakeholders from different cultural backgrounds and has a practical knowledge of finished product production. To succeed in this role, you will have a Master's degree or equivalent in engineering or a related field, at least 2 years of experience within Finish Product manufacturing, experience within GxP regulated pharmaceutical manufacturing environment, and professional proficiency in English. Additionally, you will have experience with cLEAN and be a team player with a great ability to collaborate, have a 'can-do' attitude, and be interested in finding new and improved ways to make our processes more efficient.

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