Scientist for oral product development
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Måløv
Do you want to be a true pioneer? Do you thrive to develop manufacturing processes? Do
you enjoy working in a dynamic environment where teamwork is at the top of the agenda? If yes, you could be our new Scientist in the Oral DP Process Development team in Måløv.
Apply today and join us in developing next generation of innovative oral products in Novo Nordisk and at Contract Development and Manufacturing Organizations (CDMOs). The position We are looking for a colleague who shares our passion for the development of solid dosage forms containing therapeutic proteins or small drug molecules. As responsible for developing manufacturing processes for new oral drug products, you will prepare, execute, and evaluate development studies to ensure the transition of new oral projects from research to clinical trials.
With your experience from the pharmaceutical industry, you will: Represent the department in multi-disciplinary project groups Work closely with experts from a wide range of areas and CDMOs Plan project activities in close collaboration with the project- and line management
Your main task will be to contribute with your knowledge in oral drug delivery technologies and drug formulation. Furthermore, you will be responsible for developing processes, including documentation of production processes for GMP.
For the collaboration with CDMOs you play a crucial role in supporting and advising the CDMOs that we are collaborating with. In addition, you will plan and execute project tasks according to a QbD setup (e.g., DoE) to support our cutting-edge development and have digital transformation in mind. Qualifications To succeed in this role, you have: A Master’s degree within Life Sciences (e.g., engineering, pharmaceutical sciences) or similar Experience from the pharmaceutical industry or academia Know pharmaceutical formulation and/or (medical) engineering with a focus on drug delivery Experience with small molecule development Experience with formulation and process optimisation of solid dosage forms We expect you to be fluent in spoken and written English.
Experience with outsourcing and GMP manufacture at CDMO is an advantage but not a requirement. As an individual you enjoy working in a dynamic environment where teamwork is at the top of the agenda. You are a self-starter taking responsibility for your tasks. You set realistic deadlines and reach them together with the rest of the team. We expect you to have excellent collaboration skills and great communication skills while focusing on stakeholder management. You can set direction scientifically and be a role model for your junior colleagues. About the department The department “Oral DP Process Development” is part of CMC Oral Product Development (OPDev). The main task of the department is to develop manufacturing processes for products in clinical development. For new oral drug products developed in house, the manufacture takes place in our pilot plants (sister department), while products developed at CDMOs are manufactured by the CDMO, ensuring that we bring best-in-class treatments to the market. Oral DP Process Development consists of 50+ colleagues organised in 3 teams, responsible for developing and manufacturing oral drug products and comparators for pre-clinical and clinical trials from phase I to phase III.
The team, Oral DP Process Development, consists of +10 dedicated and enthusiastic colleagues. In our team, the ambition is to develop oral drug product formulations and processes both internally and in collaboration with CDMOs, depending on the molecule. The team covers development of clinical phase II and III. Working at Novo Nordisk Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our careers is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.
Contact For further information please contact Senior Formulation Scientist Anne Zimmermann at +45 3077 6848 or Emil Meng-Lund at +45 3075 7649 , or Associate Manager Sanne Søgaard Nielsen at +45 3079 6937. Deadline 10 April 2023. Please note that applications are screened on an ongoing basis, so you are encouraged to apply as soon as possible. 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.
you enjoy working in a dynamic environment where teamwork is at the top of the agenda? If yes, you could be our new Scientist in the Oral DP Process Development team in Måløv.
Apply today and join us in developing next generation of innovative oral products in Novo Nordisk and at Contract Development and Manufacturing Organizations (CDMOs). The position We are looking for a colleague who shares our passion for the development of solid dosage forms containing therapeutic proteins or small drug molecules. As responsible for developing manufacturing processes for new oral drug products, you will prepare, execute, and evaluate development studies to ensure the transition of new oral projects from research to clinical trials.
With your experience from the pharmaceutical industry, you will:
Your main task will be to contribute with your knowledge in oral drug delivery technologies and drug formulation. Furthermore, you will be responsible for developing processes, including documentation of production processes for GMP.
For the collaboration with CDMOs you play a crucial role in supporting and advising the CDMOs that we are collaborating with. In addition, you will plan and execute project tasks according to a QbD setup (e.g., DoE) to support our cutting-edge development and have digital transformation in mind. Qualifications To succeed in this role, you have: A Master’s degree within Life Sciences (e.g., engineering, pharmaceutical sciences) or similar
Experience with outsourcing and GMP manufacture at CDMO is an advantage but not a requirement. As an individual you enjoy working in a dynamic environment where teamwork is at the top of the agenda. You are a self-starter taking responsibility for your tasks. You set realistic deadlines and reach them together with the rest of the team. We expect you to have excellent collaboration skills and great communication skills while focusing on stakeholder management. You can set direction scientifically and be a role model for your junior colleagues. About the department The department “Oral DP Process Development” is part of CMC Oral Product Development (OPDev). The main task of the department is to develop manufacturing processes for products in clinical development. For new oral drug products developed in house, the manufacture takes place in our pilot plants (sister department), while products developed at CDMOs are manufactured by the CDMO, ensuring that we bring best-in-class treatments to the market. Oral DP Process Development consists of 50+ colleagues organised in 3 teams, responsible for developing and manufacturing oral drug products and comparators for pre-clinical and clinical trials from phase I to phase III.
The team, Oral DP Process Development, consists of +10 dedicated and enthusiastic colleagues. In our team, the ambition is to develop oral drug product formulations and processes both internally and in collaboration with CDMOs, depending on the molecule. The team covers development of clinical phase II and III. Working at Novo Nordisk Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our careers is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing.
Contact For further information please contact Senior Formulation Scientist Anne Zimmermann at +45 3077 6848 or Emil Meng-Lund at +45 3075 7649 , or Associate Manager Sanne Søgaard Nielsen at +45 3079 6937. Deadline 10 April 2023. Please note that applications are screened on an ongoing basis, so you are encouraged to apply as soon as possible. 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.
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 20.3.2023, 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
- Måløv
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