Novo Nordisk A/S
Gladsaxe, 1 stilling
- Regulatory Affairs
- Denmark - Søborg
Our growth is your opportunity. Being part of Novo Nordisk Research & Development means working at one of the world’s largest and most successful biopharmaceutical companies. Our R&D organisation is vital to Novo Nordisk's continued growth and we always welcome talented people who would like to grow with us.
Are you ready to join a dedicated team of 6 skilled and motivated colleagues responsible for development and maintaining of graphic design for all printed packaging material in Novo Nordisk A/S. Then we have an exciting job for you in Graphic Design & Support, Global Labelling Operations in Søborg.
About the department
Graphic Design and Support is part of Global Labelling Operations in Global Regulatory Operations (part of Regulatory Affairs). Regulatory Affairs is a fast-changing field, and the 450 employees serve as Novo Nordisk’s advocates around the world by ensuring rapid regulatory approval in all markets. In Graphic Design and Support we are responsible for all the art work in regards to the development and support of the printed packaging materials and new product launches for all Novo Nordisk A/S products and devices. We are currently 6 graphic designers working closely together with our graphic designers in Bangalore.
The job
As a Graphic Professional you will have three areas of responsibility: Coordinate Graphic activities with Product Supply incl. graphic artwork, Join our graphical development support set-up incl. graphic artwork, Ensure high level of GMP-compliance for the Graphic Design and Support team.
You will be responsible for coordinating graphic activities within Regulatory Operations related to packaging material maintenance and development activities, for example new packaging lines, optimisation of packaging lines, changes related to packaging concepts affecting the graphic artwork and strategic development projects related to i.e. new global requirements or continuous process optimisation activities. The activities are cross-organisational, and you will be responsible for providing and coordinating artwork and other relevant input from an end-to-end perspective. In addition, you will ensure timely deliverables between the relevant stakeholders from Product Supply including Packaging department’s, packaging production lines, Sourcing and Strategic development and Regulatory Affairs.
You will participate in the graphical development support set-up, ensuring that the needs of our many stakeholders – i.e. production, affiliates and marketing – are meet in the best possible way. This requires both development of artwork and coordination of tasks.
Last but not least, you will secure and support GMP-compliance in Graphic Design and Support, by planning and execution of more complex quality tasks including non-conformities and Change Request cases. You will be responsible for the establishment and implementation of relevant quality improvements, and challenge the actions planned in order to solve problems with focus on GMP and quality, while completing the tasks in a timely manner.
In addition to the above, the position also includes responsibility for composing artwork either alone or with graphic designers from the team. The relevant artwork and/or documentation for activities and decisions must be created, stored and archived according to Good Documentation Practices and internal procedures.
Qualifications
You have a relevant academic education, i.e. Engineer, MA in design or equivalent, and are an advanced user in both Adobe InDesign and Adobe Illustrator and preferably have skills within Quark. You have a very strong quality mind-set and solid experience with GMP and or the pharmaceutical industry. You are known for your positive mind-set, structured approach and analytical and strategic skills. You enjoy working in a dynamic environment with changing priorities that demands you work proactively and independently with a high level of drive, initiative, flexibility and persistence. You are fluent in English, both written and spoken.
As stakeholder management is an important part of the job, we expect you to be comfortable interacting with stakeholders at any organisational level and are used to working across organisational and geographical boundaries. You are result-oriented, ambitious, and like to be challenged. You are comfortable working both as part of a team and independently with responsibility for your own tasks.
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
For further information, please contact Karen Elisabeth Winther at +45 3079 2546.
Deadline
25 October 2015.
