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Bagsværd

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!

The position

As our new 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 quality projects. 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 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
  • Establishing and driving processes around data archiving
  • Ensuring archives and archives systems are compliant

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 / or 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.

Qualifications

You hold as a minimum a bachelor’s degree in Engineering, Pharmacy, Chemistry or similar. Alternatively, you could also be a process engineer, dairy technologist, technician with production experience or similar. It is an advantage if you have GMP experience within a production environment.

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.

You will be working with various departments, so good collaboration and communication skills are essential. It is an advantage that you understand Danish and are fluent in English.

The department

The position is in the department of Purification Pilot Plants and part of Chemistry Manufacturing and Control (CMC) API Pilots. CMC API Pilots is a part of the R&D organization, that manufactures and controls new drug substance candidates for the development portfolio at Novo Nordisk. Currently, 67 staff make up the department, and are split into four teams, three facilities and two locations (Gentofte and Bagsværd). Our core tasks include the upscaling of processes and purification of proteins for toxicological and clinical studies. Our department consists of academics, specialists, interns and technicians.

As a department Quality coordinator, you will report to the department director and be supporting the management team.

Working at Novo Nordisk

At Novo Nordisk, we recognise that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world, and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. Therefore, we are committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve, and the communities we operate in.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We are happy to discuss flexible working, depending on the role and subject to business needs.

Contact

For further information, please contact Charlotte le Fevre on +45 3075 1148.

Deadline

6 November 2022

Interviews will be conducted on an ongoing basis, so we encourage you to apply as soon as possible. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

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Information og data

Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

Arbejdsstedet er beliggende i Bagsværd.

Jobbet er oprettet på vores service den 20.10.2022, men kan have været deaktiveret og genaktiveret igen.

Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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  • Bagsværd

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