Research Scientist
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Måløv
Do you have what it takes to develop innovative injectable pharmaceutical products during clinical development? Are you eager to proactively collaborate in a team linking research, production processes and product formulation during clinical development? If yes, then keep reading!
The position
We offer you a position, where you have the shared responsibility for product and process development to secure optimal pharmaceutical characteristics and stability.
Your responsibilities will be:
• Work in close collaboration with a project team, and be responsible for designing, interpreting, and reporting studies on drug products.
• Write documentation for internal and external use including clinical trial applications and submission documents for market approval.
• Interact with a wide variety of internal and external stakeholders, e.g., Production, Regulatory Affairs, Quality Assurance, Contract Manufacturing Organisations, Research- and Analytical Development.
• Together with your colleagues you take initiative, encourage, and contribute to continually optimise the way we work with LEAN mindset as the guiding principle.
In the team you help set a clear scientific direction and inspire your colleagues with your positive and can-do attitude.
Qualifications
You hold a M.Sc. within Pharmacy, Chemistry, Biophysics, Engineering or related field within protein chemistry, preferably supported with working experience within drug product development or the pharmaceutical industry.
Preferably, you have:
• Interest in and knowledge of biopharmaceutical formulation, stability and/or manufacturing processes.
• Ability to promote collaboration with other parts of the organisation as the position requires close interaction with a variety of stakeholders.
• Experience with data handling software and how to convey key findings.
• You possess strong communication skills both verbally and written in English.
As a person you take responsibility for your tasks and collaborate with stakeholders to reach project deliverables. You enjoy working in an environment that continuously develops and how we did things yesterday, is not necessarily how we do them today. Therefore, you should have the ability to learn things fast and implement them in your daily work.
Due to your flexible mindset, you thrive with new tasks and have a systematic and challenging approach which ensures the right quality output. Hereby, bringing the project and department to the next level. You embrace your central role, because our overall responsibility is that the product is of high quality and documented at the right level.
About the department
Injectable Formulation Development is part of CMC (chemistry, manufacturing and control) within Research & Development. We are responsible for developing and optimising drug formulations and production processes for injectables of new biopharmaceutical products. The department is organised in 4 teams and has approximately 65 employees and situated in Måløv. We work across teams to link research and final production for market and drive the entire variety of injectable projects from early stage (phase 1-2) to late-stage (phase 3) development. The projects in the department include all injectable products comprising biopharmaceutical molecules as GLP-1’s, insulins, monoclonal antibodies, and RNAi.
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
For further information, please contact Associate Manager Jens Toft Hummelshøj at
+45 3077 5768.
Deadline
1 of January 2023
Applications will be reviewed on an ongoing basis so earlier applications are encouraged.
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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The position
We offer you a position, where you have the shared responsibility for product and process development to secure optimal pharmaceutical characteristics and stability.
Your responsibilities will be:
• Work in close collaboration with a project team, and be responsible for designing, interpreting, and reporting studies on drug products.
• Write documentation for internal and external use including clinical trial applications and submission documents for market approval.
• Interact with a wide variety of internal and external stakeholders, e.g., Production, Regulatory Affairs, Quality Assurance, Contract Manufacturing Organisations, Research- and Analytical Development.
• Together with your colleagues you take initiative, encourage, and contribute to continually optimise the way we work with LEAN mindset as the guiding principle.
In the team you help set a clear scientific direction and inspire your colleagues with your positive and can-do attitude.
Qualifications
You hold a M.Sc. within Pharmacy, Chemistry, Biophysics, Engineering or related field within protein chemistry, preferably supported with working experience within drug product development or the pharmaceutical industry.
Preferably, you have:
• Interest in and knowledge of biopharmaceutical formulation, stability and/or manufacturing processes.
• Ability to promote collaboration with other parts of the organisation as the position requires close interaction with a variety of stakeholders.
• Experience with data handling software and how to convey key findings.
• You possess strong communication skills both verbally and written in English.
As a person you take responsibility for your tasks and collaborate with stakeholders to reach project deliverables. You enjoy working in an environment that continuously develops and how we did things yesterday, is not necessarily how we do them today. Therefore, you should have the ability to learn things fast and implement them in your daily work.
Due to your flexible mindset, you thrive with new tasks and have a systematic and challenging approach which ensures the right quality output. Hereby, bringing the project and department to the next level. You embrace your central role, because our overall responsibility is that the product is of high quality and documented at the right level.
About the department
Injectable Formulation Development is part of CMC (chemistry, manufacturing and control) within Research & Development. We are responsible for developing and optimising drug formulations and production processes for injectables of new biopharmaceutical products. The department is organised in 4 teams and has approximately 65 employees and situated in Måløv. We work across teams to link research and final production for market and drive the entire variety of injectable projects from early stage (phase 1-2) to late-stage (phase 3) development. The projects in the department include all injectable products comprising biopharmaceutical molecules as GLP-1’s, insulins, monoclonal antibodies, and RNAi.
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
For further information, please contact Associate Manager Jens Toft Hummelshøj at
+45 3077 5768.
Deadline
1 of January 2023
Applications will be reviewed on an ongoing basis so earlier applications are encouraged.
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 "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Måløv.
Jobbet er oprettet på vores service den 30.11.2022, 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.
- Forretningsudvikler
- Måløv
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