Drying Scientist, Manufacturing Development
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Bagsværd
Do you have interest, knowledge and maybe experience with spray drying and/or freeze drying? If so, we are searching for a talented scientist to join our team and lead PS API Process Support to new heights.
Apply today for a life-changing career and unlock your potential in optimization and support! The position
In this position, you will have a unique opportunity to work at the intersection of development and GMP manufacturing. As a member of the Product Supply, Active Pharmaceutical Ingredient (PS API) Process Support team, you will provide valuable assistance to production departments in various areas, including process optimization, troubleshooting, and the transfer of new processes from development to production. Your primary responsibility will be to contribute to the continuous stability, delivery, optimization, and quality of API production. Your main focus will be on:
• Process optimization
• Support to production facilities incl. problem-solving and scientific deviation input
• Planning and evaluation of experiments
• Preparation and review of protocols and reports
• Preparation and maintenance of development documentation. Furthermore, you will be supporting the production departments with scientific data and engage in professional discussions. Given the self-organized nature of the role, effective prioritization of work assignments is crucial. By taking on this position, you can expect personal and professional growth opportunities, allowing you to enhance your skills and knowledge in the field. Qualifications
To be successful in this role, we imagine that you have an engineering degree or a master’s degree in chemistry, pharmacy, or a similar field.
You must be interested in working with drying techniques on a scientific level, specifically, spray drying and freeze drying. Furthermore, one or more of the following qualifications are relevant:
• Knowledge or experience with spray drying
• Knowledge or experience with freeze drying
• Experience from a GMP regulated production is an advantage
• Experience with collaboration with contract manufacturing organisations (CMO’s) may also be an advantage It is possible that you have already used your competencies to solve various practical challenges within spray drying and/or freeze drying and have a solid understanding of the processes. You can use your scientific knowledge to troubleshoot and identify optimization initiatives that can contribute to the continuous improvement of our manufacturing processes. As a person, you work independently, can handle a complex workday, and enjoy a close and friendly collaboration with your team and department. You are responsible, flexible, and have the courage and drive to engage in new assignments and stick to them until the job is finished. It is important that you are a good communicator, since you will be in daily contact with other scientists, technicians, production employees, project managers, analytical laboratories, and others. A positive mindset will suit our working environment where a good laugh is appreciated even when things are getting hectic. About the department In PS API, we produce the pharmaceutical backbone of our many quality products. PS API Process Support is part of Manufacturing Development, and we have six teams responsible for the timely support of the many processes that create our products. You can look forward to becoming part of a dynamic and well-functioning team consisting of 10 scientists and 6 laboratory technicians. We thrive on professional challenges and work independently with great individual responsibility and a high level of commitment. We collaborate with various stakeholders in the organization including production departments, research, regulatory affairs, and QA. We, therefore, enjoy being part of a wide range of activities and projects within the organization. We also have external collaboration with contract manufacturing organisations (CMO’s). The department is located in Bagsværd, which will be your primary location, but also has offices in Kalundborg. Our primary objective is to support the production facilities in Kalundborg and USA. You should therefore expect some activities in Kalundborg and occasionally travel to our site in USA. 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 Bolette Kragholm at +45 30797681 or associate manager Casper Mørck at +45 30798657. Deadline
23 July 2023.
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.
Apply today for a life-changing career and unlock your potential in optimization and support! The position
In this position, you will have a unique opportunity to work at the intersection of development and GMP manufacturing. As a member of the Product Supply, Active Pharmaceutical Ingredient (PS API) Process Support team, you will provide valuable assistance to production departments in various areas, including process optimization, troubleshooting, and the transfer of new processes from development to production. Your primary responsibility will be to contribute to the continuous stability, delivery, optimization, and quality of API production. Your main focus will be on:
• Process optimization
• Support to production facilities incl. problem-solving and scientific deviation input
• Planning and evaluation of experiments
• Preparation and review of protocols and reports
• Preparation and maintenance of development documentation. Furthermore, you will be supporting the production departments with scientific data and engage in professional discussions. Given the self-organized nature of the role, effective prioritization of work assignments is crucial. By taking on this position, you can expect personal and professional growth opportunities, allowing you to enhance your skills and knowledge in the field. Qualifications
To be successful in this role, we imagine that you have an engineering degree or a master’s degree in chemistry, pharmacy, or a similar field.
You must be interested in working with drying techniques on a scientific level, specifically, spray drying and freeze drying. Furthermore, one or more of the following qualifications are relevant:
• Knowledge or experience with spray drying
• Knowledge or experience with freeze drying
• Experience from a GMP regulated production is an advantage
• Experience with collaboration with contract manufacturing organisations (CMO’s) may also be an advantage It is possible that you have already used your competencies to solve various practical challenges within spray drying and/or freeze drying and have a solid understanding of the processes. You can use your scientific knowledge to troubleshoot and identify optimization initiatives that can contribute to the continuous improvement of our manufacturing processes. As a person, you work independently, can handle a complex workday, and enjoy a close and friendly collaboration with your team and department. You are responsible, flexible, and have the courage and drive to engage in new assignments and stick to them until the job is finished. It is important that you are a good communicator, since you will be in daily contact with other scientists, technicians, production employees, project managers, analytical laboratories, and others. A positive mindset will suit our working environment where a good laugh is appreciated even when things are getting hectic. About the department In PS API, we produce the pharmaceutical backbone of our many quality products. PS API Process Support is part of Manufacturing Development, and we have six teams responsible for the timely support of the many processes that create our products. You can look forward to becoming part of a dynamic and well-functioning team consisting of 10 scientists and 6 laboratory technicians. We thrive on professional challenges and work independently with great individual responsibility and a high level of commitment. We collaborate with various stakeholders in the organization including production departments, research, regulatory affairs, and QA. We, therefore, enjoy being part of a wide range of activities and projects within the organization. We also have external collaboration with contract manufacturing organisations (CMO’s). The department is located in Bagsværd, which will be your primary location, but also has offices in Kalundborg. Our primary objective is to support the production facilities in Kalundborg and USA. You should therefore expect some activities in Kalundborg and occasionally travel to our site in USA. 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 Bolette Kragholm at +45 30797681 or associate manager Casper Mørck at +45 30798657. Deadline
23 July 2023.
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 "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 16.5.2023, 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.
- Øvrige
- Bagsværd
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