Cell Therapy Scientist
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Måløv
Do you want to play a significant role in developing protocols for stem cell derived cell therapy for clinical use and ensuring suitable and compliant raw materials for cutting edge cell therapies? If your answer is positive, then this job will be just right for you!
Apply now and join us for a life-changing career!
The Position
As a Scientist / Senior Scientist in Cell Therapy Process Technology and Clinical Supplies you will be responsible to ensure the appropriate quality of raw materials for Advanced Therapeutic Medicinal Products (Cell therapy) manufacture. Examples of cell therapy raw materials are culture media, supplements, growth factors, enzymes and single use plastic materials. You will coordinate the exchange of not suitable raw materials by testing higher quality alternatives in the cell production process in our development lab. You will provide scientific support and coordinate the GMP raw materials qualification, following internal procedures and regulatory guidelines, and work closely with the Novo Nordisk CMC raw materials team, analytical departments, virologists, microbiologists and QA.
Few key tasks will include but are not limited to:
You will also be part of the relevant CMC teams where you will identify and communicate raw materials and project-related challenges and work on finding solutions with project member and other stakeholders (raw material team, analysis, microbiology, virology).You will ensure the appropriate use of raw materials in the GMP production of stem cell products and closely interact with our manufacturing team based in Fremont, CA or one of our many partners around the world e.g. Sweden, UK, Japan and USA. Finally, you will play an essential role in supporting the writing of the clinical trial application for the cell therapy projects to reach to the patients worldwide.
Qualifications
You must hold a scientific academic degree in Life Sciences, e.g. biology, biochemistry, pharmaceutical sciences or other relevant discipline. Master level or above, preferably combined with 3-5 years relevant experience or a PhD within a relevant area and preferably some years of relevant experience.
The ideal candidate has experience within the following:
As a person, you are open-minded and a good communicator by nature. You have a high level of energy that drives you and inspires your colleagues. You thrive in a changing and dynamic work environment and in a job that requires you to take initiatives and think out of the box when challenges occur. You are a true team-player who enjoys working in close collaboration with colleagues in and out of the laboratory.
About the department
The department Cell Therapy Process Technology and Clinical Supplies is part of Novo Nordisk’s newly established Cell Therapy Research & Development unit, where we develop novel cell replacement therapies for the treatment of serious chronic diseases, together with the rest of Novo Nordisk and with external collaborators. Our department focuses on the development of manufacturing processes and related analysis and setting up clinical supplies for our upcoming clinical trials.
Diabetes mellitus type 1, Parkinson’s disease and chronic heart failure are only some of the indications we are currently working on.
You will join an international and dedicated group of around 70 employees, including scientists, technical coordinators, laboratory technicians and student workers who are part of the CMC and Manufacturing business area in Cell Therapy R&D. We truly believe that stem cell therapies will make a difference in the lives of patients suffering from chronic diseases. If this awakens your interest, please apply and support us in progressing our cell therapy projects into the clinic.
Working in 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 career 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 Ida Kjær, Lead RM Coordinator +45 3077 7010 or Kristoffer Tømmeraas, Director + 45 3075 2648
Deadline
Application deadline: 11 December 2022.
Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified.
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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Apply now and join us for a life-changing career!
The Position
As a Scientist / Senior Scientist in Cell Therapy Process Technology and Clinical Supplies you will be responsible to ensure the appropriate quality of raw materials for Advanced Therapeutic Medicinal Products (Cell therapy) manufacture. Examples of cell therapy raw materials are culture media, supplements, growth factors, enzymes and single use plastic materials. You will coordinate the exchange of not suitable raw materials by testing higher quality alternatives in the cell production process in our development lab. You will provide scientific support and coordinate the GMP raw materials qualification, following internal procedures and regulatory guidelines, and work closely with the Novo Nordisk CMC raw materials team, analytical departments, virologists, microbiologists and QA.
Few key tasks will include but are not limited to:
- Understanding and communicating about the use and criticality of the raw materials in the specific processes
- Risks assessment
- Document review
You will also be part of the relevant CMC teams where you will identify and communicate raw materials and project-related challenges and work on finding solutions with project member and other stakeholders (raw material team, analysis, microbiology, virology).You will ensure the appropriate use of raw materials in the GMP production of stem cell products and closely interact with our manufacturing team based in Fremont, CA or one of our many partners around the world e.g. Sweden, UK, Japan and USA. Finally, you will play an essential role in supporting the writing of the clinical trial application for the cell therapy projects to reach to the patients worldwide.
Qualifications
You must hold a scientific academic degree in Life Sciences, e.g. biology, biochemistry, pharmaceutical sciences or other relevant discipline. Master level or above, preferably combined with 3-5 years relevant experience or a PhD within a relevant area and preferably some years of relevant experience.
The ideal candidate has experience within the following:
- Stem cell culturing and differentiation
- Screening and testing raw materials for GMP production
- Knowledge of the regulatory framework of Advanced therapeutic medicinal products (ATMPs)
- Previous experience or relevant courses within project management will be an asset
- Proficiency in English, both written and spoken
As a person, you are open-minded and a good communicator by nature. You have a high level of energy that drives you and inspires your colleagues. You thrive in a changing and dynamic work environment and in a job that requires you to take initiatives and think out of the box when challenges occur. You are a true team-player who enjoys working in close collaboration with colleagues in and out of the laboratory.
About the department
The department Cell Therapy Process Technology and Clinical Supplies is part of Novo Nordisk’s newly established Cell Therapy Research & Development unit, where we develop novel cell replacement therapies for the treatment of serious chronic diseases, together with the rest of Novo Nordisk and with external collaborators. Our department focuses on the development of manufacturing processes and related analysis and setting up clinical supplies for our upcoming clinical trials.
Diabetes mellitus type 1, Parkinson’s disease and chronic heart failure are only some of the indications we are currently working on.
You will join an international and dedicated group of around 70 employees, including scientists, technical coordinators, laboratory technicians and student workers who are part of the CMC and Manufacturing business area in Cell Therapy R&D. We truly believe that stem cell therapies will make a difference in the lives of patients suffering from chronic diseases. If this awakens your interest, please apply and support us in progressing our cell therapy projects into the clinic.
Working in 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 career 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 Ida Kjær, Lead RM Coordinator +45 3077 7010 or Kristoffer Tømmeraas, Director + 45 3075 2648
Deadline
Application deadline: 11 December 2022.
Please note that applications will be reviewed continuously, and interviews will be planned as soon as a suitable candidate is identified.
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 23.11.2022, 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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