Enthusiastic scientist for development of Drug Product formulation
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Måløv
Do you have what it takes to break new ground and develop injectable pharmaceutical products during clinical development? Are you eager to act in a team linking research and production during clinical development and generate formulation and processes documentation for new injectable products? If yes, then please keep reading!
About the department
Injectable Formulation Development is part of CMC Development, and we are organised in R&D. We are responsible for developing formulations and production processes for injectables of new biopharmaceutical products. The department is organised in 4 teams and has approximately 65 employees in total from diverse backgrounds and is situated in Måløv. In our daily work we link research and final production for Launch and drive the entire variety of injectable projects from early stage (phase 1-2) to late-stage (phase 3/PV) development. The development projects in the department include all injectables across all therapeutic indications comprising GLP-1 products, insulins, haemophilia products, monoclonal antibodies, and RNAi.
The job
We offer you a position, where you have the responsibility for product and process development to secure optimal pharmaceutical characteristics and stability.
In the team you help set a clear scientific direction and inspire your colleagues with your positive and can-do attitude.
Your responsibilities will be:
In return we offer you a flexible workplace with a warm, inclusive, passionate, and welcoming atmosphere where we care about each other, and your opinion is valued.
Qualifications
You hold a PhD or a M.Sc. within Pharmacy, Chemistry, Biophysics, Engineering of related field of study preferably backed by 2-3 years of working experience within drug product development.
Preferably, you have:
As a person you show drive and have a positive can-do mind-set, you enjoy working in a team with highly motivated people dedicated to developing the next generation of pharmaceuticals in a continuously developing environment. At the same time, you work systematically and can adhere to strict documentation and quality standards. You have excellent collaborative skills, and agility and flexibility are a natural part of your approach to interact with colleagues in the department and with your stakeholders.
Working at Novo Nordisk
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management and growth hormone therapy, we offer a fantastic opportunity to join our department with a lively and collaborative culture. Novo Nordisk encourages continuous growth and provides opportunities to build great careers.
Contact
For further information, please contact Associate Manager Mette Willer at +45 3075 1662.
Deadline
11th of December 2022.
Applications will be reviewed on an ongoing basis.
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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About the department
Injectable Formulation Development is part of CMC Development, and we are organised in R&D. We are responsible for developing formulations and production processes for injectables of new biopharmaceutical products. The department is organised in 4 teams and has approximately 65 employees in total from diverse backgrounds and is situated in Måløv. In our daily work we link research and final production for Launch and drive the entire variety of injectable projects from early stage (phase 1-2) to late-stage (phase 3/PV) development. The development projects in the department include all injectables across all therapeutic indications comprising GLP-1 products, insulins, haemophilia products, monoclonal antibodies, and RNAi.
The job
We offer you a position, where you have the responsibility for product and process development to secure optimal pharmaceutical characteristics and stability.
In the team you help set a clear scientific direction and inspire your colleagues with your positive and can-do attitude.
Your responsibilities will be:
- Collaborate with project teams, and be responsible for designing, interpreting, and reporting studies on drug products.
- Take ownership of writing documentation for internal and external use including clinical trial applications and submission documents.
- Interact with a wide variety of internal stakeholders, e.g., Product Supply, Regulatory affairs, Quality Assurance, Research- and Analytical Development.
- Together with your colleagues you take initiative, encourage, and contribute to the on-going optimisation of processes and systems with LEAN as the guiding principle.
In return we offer you a flexible workplace with a warm, inclusive, passionate, and welcoming atmosphere where we care about each other, and your opinion is valued.
Qualifications
You hold a PhD or a M.Sc. within Pharmacy, Chemistry, Biophysics, Engineering of related field of study preferably backed by 2-3 years of working experience within drug product development.
Preferably, you have:
- Experience in formulation and/or process development and documentation, including regulatory and quality aspects of drug development projects.
- Ability to promote collaboration with other parts of the organisation as the position requires close interaction with a variety of stakeholders.
- Knowledge within data handling and high attention to detail.
- You possess strong communication skills both verbally and written in English and it is an advantage but not a requirement to handle spoken and written Danish.
As a person you show drive and have a positive can-do mind-set, you enjoy working in a team with highly motivated people dedicated to developing the next generation of pharmaceuticals in a continuously developing environment. At the same time, you work systematically and can adhere to strict documentation and quality standards. You have excellent collaborative skills, and agility and flexibility are a natural part of your approach to interact with colleagues in the department and with your stakeholders.
Working at Novo Nordisk
At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management and growth hormone therapy, we offer a fantastic opportunity to join our department with a lively and collaborative culture. Novo Nordisk encourages continuous growth and provides opportunities to build great careers.
Contact
For further information, please contact Associate Manager Mette Willer at +45 3075 1662.
Deadline
11th of December 2022.
Applications will be reviewed on an ongoing basis.
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 17.11.2022, 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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