Project Engineers/Scientists for New Aseptic Expansion Project
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Måløv
Are you motivated by working in project organisation? Would you like to be involved in a new capacity expansion project, in which you can influence and impact the future of Aseptic production facilities? If yes, we offer a great opportunity to become part of a team, where we turn ideas into actions. Apply today! The Position
In Biotech & Rare Diseases (BDR) expansion project in Måløv, we are planning to expand our production facilities. The aim of this new expansion project is to build a completely new world class manufacturing facility, with cutting edge technology. This new facility aims to innovate our processes and to broaden our perspective, which is why this position requires a candidate with a good innovative mindset and the ability to adapt.
Your main job tasks will be:
• Contributor to either Clean Utility, Formulation, Environmental Monitoring or one of the other enticing work packages
• Whether you are familiar with processes or equipment we need you to help validate and develop the processes and training.
• Work with LEAN mindset, being innovative and open minded along the way.
• Incorporate Quality and Compliance throughout all your work processes and ensure that internal quality demands comply to Current Good Manufacturing Practice (CGMP).
Though the project is located in Måløv, interaction with the AP Expansion project on other sites is needed. Qualifications To be considered for this position you have:
• An academic degree or similar acquired skills
• Solid understanding of Current Good Manufacturing Practice (GMP)
• Some years’ of experience with either process or equipment, related to pharmaceutical production.
• High verbal and written communication skills in English, plus good presentation skills. As a person, you are good at handling complex assignments, and you possess the ability to constantly seeing opportunities rather than limitations. You should also be comfortable with working in an environment in constant change, and be able to optimize, create and implement new working practices. Moreover, it is important that you have excellent cooperation and communications skills. About the Department Our department is currently a part of the Biotech & Rare Disease (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. 500 colleagues who are the end-to-end station for product and process development for all BRD production facilities. The department is under development and therefor you colleagues will gradually grow and there will be amble opportunity to evolve during this journey.
Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we
seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact If you would like to know more about the position, please contact Director Alex Linnemann, on +45 34488105 Deadline 1 August 2023.
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.
In Biotech & Rare Diseases (BDR) expansion project in Måløv, we are planning to expand our production facilities. The aim of this new expansion project is to build a completely new world class manufacturing facility, with cutting edge technology. This new facility aims to innovate our processes and to broaden our perspective, which is why this position requires a candidate with a good innovative mindset and the ability to adapt.
Your main job tasks will be:
• Contributor to either Clean Utility, Formulation, Environmental Monitoring or one of the other enticing work packages
• Whether you are familiar with processes or equipment we need you to help validate and develop the processes and training.
• Work with LEAN mindset, being innovative and open minded along the way.
• Incorporate Quality and Compliance throughout all your work processes and ensure that internal quality demands comply to Current Good Manufacturing Practice (CGMP).
Though the project is located in Måløv, interaction with the AP Expansion project on other sites is needed. Qualifications To be considered for this position you have:
• An academic degree or similar acquired skills
• Solid understanding of Current Good Manufacturing Practice (GMP)
• Some years’ of experience with either process or equipment, related to pharmaceutical production.
• High verbal and written communication skills in English, plus good presentation skills. As a person, you are good at handling complex assignments, and you possess the ability to constantly seeing opportunities rather than limitations. You should also be comfortable with working in an environment in constant change, and be able to optimize, create and implement new working practices. Moreover, it is important that you have excellent cooperation and communications skills. About the Department Our department is currently a part of the Biotech & Rare Disease (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. 500 colleagues who are the end-to-end station for product and process development for all BRD production facilities. The department is under development and therefor you colleagues will gradually grow and there will be amble opportunity to evolve during this journey.
Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we
seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact If you would like to know more about the position, please contact Director Alex Linnemann, on +45 34488105 Deadline 1 August 2023.
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 Måløv.
Jobbet er oprettet på vores service den 25.5.2023, 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.
- Øvrige
- Måløv
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