Quality coordinator with focus on Project Management
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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 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
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. You will also have an overview of our raw material handling, and act as the link between daily production and the overall production planning
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 work in the teams, support the management team, and report to the department director.
Qualifications
You hold as a minimum a MSc in Engineering, Pharmacy, Chemistry or similar. It is required to 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 can communicate in both Danish and English.
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 a part of the R&D organisation, that manufactures and controls new drug substance candidates for the development portfolio at Novo Nordisk. 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.
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 Tine Kranker +45 30755156 or Henning H Dall +45 30759798
Deadline
19. February 2023
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.
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 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
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. You will also have an overview of our raw material handling, and act as the link between daily production and the overall production planning
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 work in the teams, support the management team, and report to the department director.
Qualifications
You hold as a minimum a MSc in Engineering, Pharmacy, Chemistry or similar. It is required to 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 can communicate in both Danish and English.
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 a part of the R&D organisation, that manufactures and controls new drug substance candidates for the development portfolio at Novo Nordisk. 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.
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 Tine Kranker +45 30755156 or Henning H Dall +45 30759798
Deadline
19. February 2023
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.
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 26.1.2023, 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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