Filling Engineering Responsible
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Do you have strong expertise with filling lines and looking to offer your experience in the development of the future Aseptic Processing facilities? Are you looking for a global position where you can drive the technical filling processes globally?
If so, then you might be the Filling Engineering Responsible we are looking for. Read on to find out more!
The position
As our new Filling Engineering Responsible, you will be key in helping specify and define the filling and isolator solution. This will involve ensuring all requirements are documented and reviewed according to GMP standards, quality, and subsequently tested globally. The position offers a unique opportunity to design a “fleet” of identical isolator filling lines, that is required to deliver a consistent high OEE, while being flexible to support the future demands.
Specifically, some of your tasks will include:
The team is working as a central design team for 4 aseptic production sites all over the world, thus, you will be collaborating closely together with stakeholders both locally and globally. This will include collaborating with the Filling Work Package Owner (WPO), Filling Specialists, our Central Manufacturing Development team, and Subject Matter Experts within the filling process track across the AP Expansion programme.
Furthermore, you will have the opportunity to travel to our global sites which includes sites based, in Denmark, France, US and China. Up to 20% travel is expected for the position.
Qualifications
As a person, you have a focus on quality, have a problem-solving approach and the drive to create new solutions and challenge the status quo. Furthermore, you have excellent communication skills to build relations cross functionally and globally. For this position, you are required to be fluent in spoken and written English. As you will be working globally with the Danish sites, France and China, language skills within these areas would be advantageous.
About the department
Technology Standards is a department in the newly created area of AP Expansions which is anchored within Product Supply, which globally accounts for +19,000 of Novo Nordisk’s +44,000 employees.
The responsibility of AP Expansion is to plan and execute the establishment of new aseptic filling capacity across the global manufacturing network within BioTech and Rare Diseases (BRD) and Injectable Finished Products (IFP) for new filling platforms while ensuring harmonisation and global standards.
Across the different roles there is a distinct global aspect as the end goal is a global standard and best practice, and working with multiple sites, cultures and traditions will be a key element.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here – to ensure that people can lead a life independent of chronic disease.
Contact
For further information please contact Deepak Krishnakumar (Senior Project Manager, Tech Standards) on: +45-34481145
Deadline
8 January 2023. Please note, we will review applications and conduct 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.
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If so, then you might be the Filling Engineering Responsible we are looking for. Read on to find out more!
The position
As our new Filling Engineering Responsible, you will be key in helping specify and define the filling and isolator solution. This will involve ensuring all requirements are documented and reviewed according to GMP standards, quality, and subsequently tested globally. The position offers a unique opportunity to design a “fleet” of identical isolator filling lines, that is required to deliver a consistent high OEE, while being flexible to support the future demands.
Specifically, some of your tasks will include:
- Development of new technical filling standard, design and test of technical solutions with vendor, troubleshooting and ramp up globally.
- Development of future process flow and processes according to the aseptic standards and authority requirements.
- Development of a technical filling platform that enables ongoing monitoring and improvements based on collected data and predictive models.
- Design and definition of a “fleet based” CQV (Commissioning, Qualification and Validation) program (FAT, SAT, IQ/OQ).
The team is working as a central design team for 4 aseptic production sites all over the world, thus, you will be collaborating closely together with stakeholders both locally and globally. This will include collaborating with the Filling Work Package Owner (WPO), Filling Specialists, our Central Manufacturing Development team, and Subject Matter Experts within the filling process track across the AP Expansion programme.
Furthermore, you will have the opportunity to travel to our global sites which includes sites based, in Denmark, France, US and China. Up to 20% travel is expected for the position.
Qualifications
- You hold an academic degree within Engineering or Natural Sciences or similar.
- 5+ years’ technical experience within with filling lines for aseptic products. Knowledge in filling lines using isolator technology is advantageous.
- Technical aptitude in terms of machine design and experience with CAE tools
- Production/ aseptic production, GMP or CMC (Chemistry, Manufacturing and Controls) experience in the pharmaceutical, biotechnology or similar industry is preferred.
- Knowledge/ and interest in exploring and driving new technologies.
As a person, you have a focus on quality, have a problem-solving approach and the drive to create new solutions and challenge the status quo. Furthermore, you have excellent communication skills to build relations cross functionally and globally. For this position, you are required to be fluent in spoken and written English. As you will be working globally with the Danish sites, France and China, language skills within these areas would be advantageous.
About the department
Technology Standards is a department in the newly created area of AP Expansions which is anchored within Product Supply, which globally accounts for +19,000 of Novo Nordisk’s +44,000 employees.
The responsibility of AP Expansion is to plan and execute the establishment of new aseptic filling capacity across the global manufacturing network within BioTech and Rare Diseases (BRD) and Injectable Finished Products (IFP) for new filling platforms while ensuring harmonisation and global standards.
Across the different roles there is a distinct global aspect as the end goal is a global standard and best practice, and working with multiple sites, cultures and traditions will be a key element.
Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here – to ensure that people can lead a life independent of chronic disease.
Contact
For further information please contact Deepak Krishnakumar (Senior Project Manager, Tech Standards) on: +45-34481145
Deadline
8 January 2023. Please note, we will review applications and conduct 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
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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 16.11.2022, 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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