Reference Material Coordinator
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Gentofte
Are you ready to apply your project management experience and analytical skills in an exciting organization, where you will get challenged grow, and expand your capabilities to the fullest? Do you want to be a part of the development and implementation of new drugs and make a difference in our vision to change the life of patients with rare diseases?
Then you might be the Reference Material Coordinator we are looking for!
The position
As a Reference Material Coordinator, you will play a key role in managing the reference materials of all the products of the Biotech and Rare Disease (BRD) portfolio. Together with four other reference material coordinators, you will be responsible for coordinating all tasks related to reference materials, such as implementation and maintenance. It can include production and establishment of reference materials, setting specifications, stability studies etc. You will be a part of a group that is well structured and pursues the solid results through good cooperation.
You will cooperate with Reference Material Coordinators in CMC Development on reference materials being transferred from CMC to Product Supply. As part of your job, you will support the internal users of reference material at Novo Nordisk laboratories and productions sites, as well as answering questions and preparing regulatory documentation for various authorities.
You will be working close together with your colleagues in the team as well as with product scientists, product coordinators and statisticians in BRD. You will also interact with several stakeholders across Novo Nordisk such as production, regulatory affairs, QA and QC.
Finally, you will join a harmonious team and department with competent, caring, and positive colleagues. We have a strong foundation of employees with high seniority mixed with newcomers. Novo Nordisk is a great place to work, and in our latest internal engagement survey the department scored well above average.
Qualifications
To succeed in this role, you have:
You enjoy working on long-term projects in implementing new reference materials and processes. You take responsibility and work in an organised way. You are naturally good at communicating with all types of stakeholders both verbally and in writing. This helps you to keep all your stakeholders aligned, informed, and engaged. You are motivated by the opportunity of getting a large network across our area.
About the department
Our team is part of the BRD Manufacturing Development & Quality Control area that has its base in Denmark. What other companies call Manufacturing Science & Analytical Technology (MSAT) we call Manufacturing Development. We are app. 460 colleagues who are the end-to-end station for product and process development for all BRD production facilities, driving innovation both when it comes to industry 4.0 technology and expansion of the product portfolio. Our area also includes the Quality Control unit for all BRD’s products. Together we drive change by always looking for improvements within our processes and in the way we work to make our products reach as many patients as possible.
Working at BRD, Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and in quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are app. 2500 colleagues committed to drive change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we are also striving to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career?
Contact
For further information, please call Associate Manager Julie Kruse Jensen +45 30 77 50 11.
Deadline
18 December 2022. But please apply as soon as possible as we will be conducting interviews on an ongoing basis.
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.
Print job Send to e-mail
Then you might be the Reference Material Coordinator we are looking for!
The position
As a Reference Material Coordinator, you will play a key role in managing the reference materials of all the products of the Biotech and Rare Disease (BRD) portfolio. Together with four other reference material coordinators, you will be responsible for coordinating all tasks related to reference materials, such as implementation and maintenance. It can include production and establishment of reference materials, setting specifications, stability studies etc. You will be a part of a group that is well structured and pursues the solid results through good cooperation.
You will cooperate with Reference Material Coordinators in CMC Development on reference materials being transferred from CMC to Product Supply. As part of your job, you will support the internal users of reference material at Novo Nordisk laboratories and productions sites, as well as answering questions and preparing regulatory documentation for various authorities.
You will be working close together with your colleagues in the team as well as with product scientists, product coordinators and statisticians in BRD. You will also interact with several stakeholders across Novo Nordisk such as production, regulatory affairs, QA and QC.
Finally, you will join a harmonious team and department with competent, caring, and positive colleagues. We have a strong foundation of employees with high seniority mixed with newcomers. Novo Nordisk is a great place to work, and in our latest internal engagement survey the department scored well above average.
Qualifications
To succeed in this role, you have:
- An academic degree within Pharmacy, Chemistry, Engineering or a similar field.
- +2 years of experience in analytical development, drug development, production or QC.
- Experience in managing and executing smaller and larger projects.
- Experience from working with product specifications, analytical methods, production and/or regulatory documentation in the pharmaceutical industry is an advantage.
- Full professional proficiency in English and ability to understand and read Danish.
You enjoy working on long-term projects in implementing new reference materials and processes. You take responsibility and work in an organised way. You are naturally good at communicating with all types of stakeholders both verbally and in writing. This helps you to keep all your stakeholders aligned, informed, and engaged. You are motivated by the opportunity of getting a large network across our area.
About the department
Our team is part of the BRD Manufacturing Development & Quality Control area that has its base in Denmark. What other companies call Manufacturing Science & Analytical Technology (MSAT) we call Manufacturing Development. We are app. 460 colleagues who are the end-to-end station for product and process development for all BRD production facilities, driving innovation both when it comes to industry 4.0 technology and expansion of the product portfolio. Our area also includes the Quality Control unit for all BRD’s products. Together we drive change by always looking for improvements within our processes and in the way we work to make our products reach as many patients as possible.
Working at BRD, Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and in quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are app. 2500 colleagues committed to drive change for people with serious chronic diseases. We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we are also striving to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career?
Contact
For further information, please call Associate Manager Julie Kruse Jensen +45 30 77 50 11.
Deadline
18 December 2022. But please apply as soon as possible as we will be conducting interviews on an ongoing basis.
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.
Print job Send to e-mail
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 1.12.2022, 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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- Gentofte
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