Novo Nordisk
Quality Coordinator with focus on Project Management
Do you want to play a central role in ensuring the best quality system and make a difference for people living with diabetes and other chronic diseases? Do you have a background in science and are familiar with GMP from a production environment? Are you curious and eager to take on tasks and projects complex in nature and gain influence? Then this opportunity might be for you!
For an introduction to our area - CMC API Pilots - please visit our career page
The position
As our Quality coordinator, you will drive the quality agenda of the department as well as monitor and ensure that the department complies with the Novo Nordisk Management System. Your primary role will be to act as a Project Manager on various projects with focus on quality. We offer you the opportunity to work with:
Setting quality goals for the department and ensuring that the quality system is compliant with regulatory requirements
Identifying and taking active part in solving quality improvements across the department to achieve simplicity and build quality into the on-the-floor work flows and processes
Being the department’s go-to person for cross-functional quality projects where you are coordinating and implementing the changes
Trend reporting of deviations
Having an overview of our raw material handling, and act as the link between daily production and the overall production planning
You will get the opportunity to gain solid insights into, and also be able to influence, the workflow and procedures. In the role there is also the possibility to become a deviations expert, and to assume a role of facilitator in systematic problem-solving. As a person it comes natural for you to build relations and contribute to a great collaboration with the colleagues at the facilities. Furthermore, it is vital to gain a thorough understanding of processes and to build good relations with our stakeholders. The role will entail a mix of practical and administrative tasks. As a department Quality coordinator, you will support the management team and collaborate greatly with the department director.
Qualifications
To succeed in this role, you have:
A minimum a MSc in Engineering, Pharmacy, Chemistry or similar
GMP experience within a production environment
Expertise in Quality systems
Fluency in English, understanding of Danish would be a plus
We imagine that you show initiative, and are curious, action- and goal-oriented. You are good at planning and execution, and you are also structured and systematic in your approach to tasks. You like project management, and you are ready to play an active role in improving the department as a whole, nor do you hesitate to take on new tasks of a complex nature.
The department
The position is in the department Cultivation Pilot Plants and part of Chemistry Manufacturing and Control (CMC) API Pilots. CMC API Pilots is the part of the organisation with responsibility to produce active drug substances for the clinical trials and optimize processes for market production.
Cultivation Pilot Plants is a department that cultivates and purifies proteins and peptides, for use in clinical and non-clinical trials. The department consists of two separate production facilities with four production lines in total.
The department is located in Bagsværd, Denmark.
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