Senior Development Scientist in Downstream Development, Virus Safety
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Gentofte
Do you love and live for virology? Do you thrive with handling and completing diverse tasks for numerous projects under restricted timelines? And do you possess an inherent curiosity towards virus safety and ATMP’s and to improve the development of your assays and processes? Then you are on the right path to become our new colleague. We are looking for an experienced Senior Development Scientist for our Virus Safety team in Downstream Development.
The position
As a Senior Scientist, you will provide scientific leadership within virology and drive development projects within virus safety and ATMP projects. The position is a balanced mix of viral safety assay development, with regards to the downstream purification process and its virus clearance capacity and to support our exciting ATMP projects, such as cell therapy, with your virus safety expertise.
As a Senior Development Scientist, you will:
Apart from that, you will participate in cross organizational project groups, collaborate with other departments both in Research Units and in manufacturing (Product Supply) and combine hands-on experience from the virus safety world with modern aspects e.g. automation.
You can look forward to a broad range of exciting challenges feeding into your personal and professional development. Our working environment is dynamic and informal with a lot of drive and with a strong culture of cross-functional collaboration.
Qualifications
You hold a PhD. in a related field (e.g. virology), or as a minimum, a M.Sc. in immunology, pharmacy, (bio-)chemical engineering, protein chemistry or a related discipline preferably with 3+ years of industrial experience. You have experience within virology, virus safety and are aware of the regulatory landscape surrounding this. Having experience with ATMPs is considered a clear advantage. You may have theoretical understanding as well as practical experience from the laboratory, preferably with protein purification techniques such as chromatography including hands-on experience with e.g. ÄKTA systems.
We operate in a fast-changing environment, with an increasing level of automation and digitalization. It is therefore considered an advantage to be an innovative individual with ability and experience within areas of automation and digitalization. Knowledge within molecular detection techniques e.g. qPCR is beneficial but not a requirement.
As a person, you enjoy collaborating, learning, and sharing information with others. You are driven by achieving great results together with fellow colleagues. Further, you thrive in an environment with many stakeholders and cross-organizational projects.
About the department
The job is within the Virology and Raw Materials Department in CMC Development, R&D, located in Gentofte. The Virology and Raw Materials Department has 40+ employees which are divided in three teams. Our main responsibility in the Virus Safety team is to contribute to the development of manufacturing processes for new drug substances all the way from research to market authorisation focusing on evaluating the raw materials and the downstream process for its virus clearance capacity as well as providing regulatory expertise within virus safety on ATMP’s. This is performed in close collaboration with the Downstream Development department, the Raw Materials team, research and manufacturing units, quality assurance and pilot facilities.
Contact
For further information, please contact Development Scientist Charlotte Ernstsen at +45 3077 7950.
Applications will be reviewed on an on-going 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 on your CV.
Deadline
January 22nd 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.
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The position
As a Senior Scientist, you will provide scientific leadership within virology and drive development projects within virus safety and ATMP projects. The position is a balanced mix of viral safety assay development, with regards to the downstream purification process and its virus clearance capacity and to support our exciting ATMP projects, such as cell therapy, with your virus safety expertise.
As a Senior Development Scientist, you will:
- Perform and develop virus safety assays for early-stage projects to Phase II projects
- Support our Research Units regarding virus safety regulations on ATMP projects
- Drive innovation and continuously incorporate new ideas into our daily way of working
- Work across teams in our department
Apart from that, you will participate in cross organizational project groups, collaborate with other departments both in Research Units and in manufacturing (Product Supply) and combine hands-on experience from the virus safety world with modern aspects e.g. automation.
You can look forward to a broad range of exciting challenges feeding into your personal and professional development. Our working environment is dynamic and informal with a lot of drive and with a strong culture of cross-functional collaboration.
Qualifications
You hold a PhD. in a related field (e.g. virology), or as a minimum, a M.Sc. in immunology, pharmacy, (bio-)chemical engineering, protein chemistry or a related discipline preferably with 3+ years of industrial experience. You have experience within virology, virus safety and are aware of the regulatory landscape surrounding this. Having experience with ATMPs is considered a clear advantage. You may have theoretical understanding as well as practical experience from the laboratory, preferably with protein purification techniques such as chromatography including hands-on experience with e.g. ÄKTA systems.
We operate in a fast-changing environment, with an increasing level of automation and digitalization. It is therefore considered an advantage to be an innovative individual with ability and experience within areas of automation and digitalization. Knowledge within molecular detection techniques e.g. qPCR is beneficial but not a requirement.
As a person, you enjoy collaborating, learning, and sharing information with others. You are driven by achieving great results together with fellow colleagues. Further, you thrive in an environment with many stakeholders and cross-organizational projects.
About the department
The job is within the Virology and Raw Materials Department in CMC Development, R&D, located in Gentofte. The Virology and Raw Materials Department has 40+ employees which are divided in three teams. Our main responsibility in the Virus Safety team is to contribute to the development of manufacturing processes for new drug substances all the way from research to market authorisation focusing on evaluating the raw materials and the downstream process for its virus clearance capacity as well as providing regulatory expertise within virus safety on ATMP’s. This is performed in close collaboration with the Downstream Development department, the Raw Materials team, research and manufacturing units, quality assurance and pilot facilities.
Contact
For further information, please contact Development Scientist Charlotte Ernstsen at +45 3077 7950.
Applications will be reviewed on an on-going 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 on your CV.
Deadline
January 22nd 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.
Print job Send to e-mail
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 4.1.2023, 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.
- Forretningsudvikler
- Gentofte
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