Formulation Engineering Responsible
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Gentofte
Do you have expertise within formulation and looking to offer your experience within formulation equipment for the development of the future Aseptic Processing facilities? Are you looking for a global position where you can drive formulation processes globally?
If so, then you might be the Formulation Engineering Responsible we are looking for. Read on to find out more!
The position
As Formulation Engineering Responsible, you will have a key position in specifying the future equipment standards for the weighing and formulation equipment to support the current and future portfolio of products. The technical scope of the formulation package include weighing isolator (For handling of OEB4 materials), filter testers, formulation and buffer vessels and well as single use sets for filtration and transfer.
The key tasks will include:
In this position, you will work in collaboration with a wide network of stakeholders on a local and global level! This will include the Formulation Work Package Owner (WPO), Formulation Specialists, our Central Manufacturing Development team, and Subject Matter Experts.
You will have the opportunity to travel to our global sites which includes sites based in Denmark, France, US and China. 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. With a visionary and innovative outlook, you are able to look to the future to help promote process optimisation and digitalisation alongside colleagues.
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 Bo Hove Vanting Andersen (Senior Manager Formulation and W&S) on: +45 30790408.
Deadline
4 December 2022. 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 Formulation Engineering Responsible we are looking for. Read on to find out more!
The position
As Formulation Engineering Responsible, you will have a key position in specifying the future equipment standards for the weighing and formulation equipment to support the current and future portfolio of products. The technical scope of the formulation package include weighing isolator (For handling of OEB4 materials), filter testers, formulation and buffer vessels and well as single use sets for filtration and transfer.
The key tasks will include:
- Defining the future standards for the equipment and technical solutions required to achieve a best in class formulation process.
- Support the design roadmap towards a completely closed system for formulation
- Drive a technical setup that enable control of critical process parameters and support obtaining a deeper understanding of impact on product critical quality attributes.
- Development of qualification approach that will enable a streamlined implementation of the standard solution
In this position, you will work in collaboration with a wide network of stakeholders on a local and global level! This will include the Formulation Work Package Owner (WPO), Formulation Specialists, our Central Manufacturing Development team, and Subject Matter Experts.
You will have the opportunity to travel to our global sites which includes sites based in Denmark, France, US and China. 20% travel is expected for the position.
Qualifications
- You hold an academic degree within Engineering or Natural Sciences or similar.
- 5+ years’ experience with equipment used in the formulation process in pharma or other GMP regulated industry.
- Project execution experience, from design through to implementation
- Knowledgeable some of the following systems: Instruments e.g., vessels. Electrical, Mechanical, Control/SCADA/PLCs, Process Improvement Methodologies, Root Cause Analysis (RCA).
- Good understanding of maintenance and calibration processes in pharma or other GMP regulated industry
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. With a visionary and innovative outlook, you are able to look to the future to help promote process optimisation and digitalisation alongside colleagues.
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 Bo Hove Vanting Andersen (Senior Manager Formulation and W&S) on: +45 30790408.
Deadline
4 December 2022. 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
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 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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