Associate Manager in Raw Materials
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Associate manager to set direction within Raw Materials safety
Do you have the skills and the experience to set a clear direction and inspire an experienced scientific team to produce great results? Are you eager to work with complex problem-solving related to Raw materials safety both within standard and novel therapy areas? If yes, then you may be our new Associate manager in Virology and Raw Materials.
The position
This position is a great opportunity to lead a team of experienced scientists (~14 and growing) and contribute to the establishment of Raw material qualification of materials for Cell Therapy production to clinical trials. Furthermore, you will drive optimisations and projects to improve our standard working processes.
The leadership team you will be part of consists of one Director and two more Associate managers. We meet weekly and discuss specific topics on a daily basis.
As Associate manager, you set direction for your team by being approachable and communicating clearly and effectively both with the team and with your internal and external stakeholders. You ensure that your team lives up to current and future organisational goals. You monitor and evaluate the progress of projects and support the team’s continuous development of innovative methods and ideas.
In this job you will have opportunities to grow personally and professionally by developing your leadership competencies at the same time as you increase your scientific and business insight.
Qualifications
Ideally, you hold an MSc or PhD in Molecular Biology, Pharmaceutical Science, Chemistry, or related discipline and have practical leadership experience, where you have successfully motivated and developed team performance. You have experience within API process safety, GMP, QC analysis and outsourcing to CMOs.
You thrive working in a changing environment and are not afraid to set direction. You like to involve and motivate your team members and have great collaboration skills.
About the department
As part of Novo Nordisk’s R&D family, Chemistry, Manufacturing and Control (CMC) Development makes a significant difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for non-clinical and clinical trials with the help from approximately 1400 CMC employees. We develop and formulate all new protein processes, coming out of our research unit and through that we ensure best-in-class treatments to the market. CMC Development is organised in six areas of expertise supporting the entire drug development pipeline.
The Virology and Raw materials Department is a newly established part of CMC API Development. In our department, you will find 45+ highly skilled and motivated colleagues with a “can-do” attitude divided into 3 teams.
In our Virology teams, our main responsibility is to ensure a robust downstream process able to remove/inactivate viruses and coordinate activities such as viral testing to ensure the virus safety of mammalian expressed protein products in Development. In the Raw Materials team, the main focus is on raw materials safety to ensure that the suitability of materials is properly evaluated.
We receive projects from our research organization and transfer them to our manufacturing organisation. We work in close collaboration with multiple internal and external stakeholders.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better. In exchange, we offer unique possibilities for professional and scientific development in an informal working environment, and the chance to integrate into a dynamic team of highly qualified and enthusiastic colleagues.
Contact
For further information, please contact Kristine B. Uldahl, Director, at +45 30775640.
Deadline
18th November 2022
Candidates will be evaluated continuously.
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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Do you have the skills and the experience to set a clear direction and inspire an experienced scientific team to produce great results? Are you eager to work with complex problem-solving related to Raw materials safety both within standard and novel therapy areas? If yes, then you may be our new Associate manager in Virology and Raw Materials.
The position
This position is a great opportunity to lead a team of experienced scientists (~14 and growing) and contribute to the establishment of Raw material qualification of materials for Cell Therapy production to clinical trials. Furthermore, you will drive optimisations and projects to improve our standard working processes.
The leadership team you will be part of consists of one Director and two more Associate managers. We meet weekly and discuss specific topics on a daily basis.
As Associate manager, you set direction for your team by being approachable and communicating clearly and effectively both with the team and with your internal and external stakeholders. You ensure that your team lives up to current and future organisational goals. You monitor and evaluate the progress of projects and support the team’s continuous development of innovative methods and ideas.
In this job you will have opportunities to grow personally and professionally by developing your leadership competencies at the same time as you increase your scientific and business insight.
Qualifications
Ideally, you hold an MSc or PhD in Molecular Biology, Pharmaceutical Science, Chemistry, or related discipline and have practical leadership experience, where you have successfully motivated and developed team performance. You have experience within API process safety, GMP, QC analysis and outsourcing to CMOs.
You thrive working in a changing environment and are not afraid to set direction. You like to involve and motivate your team members and have great collaboration skills.
About the department
As part of Novo Nordisk’s R&D family, Chemistry, Manufacturing and Control (CMC) Development makes a significant difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for non-clinical and clinical trials with the help from approximately 1400 CMC employees. We develop and formulate all new protein processes, coming out of our research unit and through that we ensure best-in-class treatments to the market. CMC Development is organised in six areas of expertise supporting the entire drug development pipeline.
The Virology and Raw materials Department is a newly established part of CMC API Development. In our department, you will find 45+ highly skilled and motivated colleagues with a “can-do” attitude divided into 3 teams.
In our Virology teams, our main responsibility is to ensure a robust downstream process able to remove/inactivate viruses and coordinate activities such as viral testing to ensure the virus safety of mammalian expressed protein products in Development. In the Raw Materials team, the main focus is on raw materials safety to ensure that the suitability of materials is properly evaluated.
We receive projects from our research organization and transfer them to our manufacturing organisation. We work in close collaboration with multiple internal and external stakeholders.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better. In exchange, we offer unique possibilities for professional and scientific development in an informal working environment, and the chance to integrate into a dynamic team of highly qualified and enthusiastic colleagues.
Contact
For further information, please contact Kristine B. Uldahl, Director, at +45 30775640.
Deadline
18th November 2022
Candidates will be evaluated continuously.
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 Bagsværd.
Jobbet er oprettet på vores service den 15.8.2022, 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.
- Forretningsudvikler
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