Development Scientist
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Bagsværd
Are you a skilled protein purification professional with a strong interest in optimization and support? Are you excited to work where development meets manufacturing, helping to improve processes and ensure consistent production? Do you thrive in a self-directed environment, where prioritising tasks and taking ownership of your work assignments are key to success? Whether you possess extensive experience or are just starting your career, we have an exciting opportunity for you! Join our team as a Development Scientist and pave the way towards a life-changing career! Apply today!
The position
In this position, you will get a unique chance to work at the crossroad between development and GMP manufacturing. The “Process Support” organisation in PS API (Product Supply, Active Pharmaceutical Ingredients), provides support to production departments such as: Process optimisation, troubleshooting, and transfer of new processes from development to production. As we support the API production, your role will be to contribute to continuous stable operations and quality in the production of marketed insulins and GLP-1 analogues.
Your fields of work will be:
• Process optimisation
• Support to production facilities including problem-solving.
• Planning and evaluation of experiments
• Preparation of protocols and reports and maintenance of development documentation.
Furthermore, you will be supporting the production departments with scientific data and engaging in professional discussions. Since the job is self-organized to a large extent, it is very important that you can prioritize work assignments. In this job you can look forward to gaining personal as well as professional development.
Qualifications To be successful in this role, we imagine that you hold a degree within Science, Pharma, Engineering, or other relevant field complimented with some years of overall experience with protein purification including practical experience from industry.
Preferably, you also have experience or knowledge within one or more of the following:
• Separation techniques such as filtration, chromatography, and precipitation
• Organic chemistry and chemical modifications
• Experience from a GMP regulated production is an advantage.
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 are 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 with responsibility 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 scientists and laboratory technicians. We thrive on professional challenges and work independently with great individual responsibility and a high level of commitment. We collaborate with diverse 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. The department is in Bagsværd, 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 possibly 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 Arda Yildiz at +45 30756676 or Michael Nissen at +45 30775233.
Deadline
19 May 2024.
Applications will be reviewed on an ongoing basis, so please do not hesitate to apply.
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.
The position
In this position, you will get a unique chance to work at the crossroad between development and GMP manufacturing. The “Process Support” organisation in PS API (Product Supply, Active Pharmaceutical Ingredients), provides support to production departments such as: Process optimisation, troubleshooting, and transfer of new processes from development to production. As we support the API production, your role will be to contribute to continuous stable operations and quality in the production of marketed insulins and GLP-1 analogues.
Your fields of work will be:
• Process optimisation
• Support to production facilities including problem-solving.
• Planning and evaluation of experiments
• Preparation of protocols and reports and maintenance of development documentation.
Furthermore, you will be supporting the production departments with scientific data and engaging in professional discussions. Since the job is self-organized to a large extent, it is very important that you can prioritize work assignments. In this job you can look forward to gaining personal as well as professional development.
Qualifications To be successful in this role, we imagine that you hold a degree within Science, Pharma, Engineering, or other relevant field complimented with some years of overall experience with protein purification including practical experience from industry.
Preferably, you also have experience or knowledge within one or more of the following:
• Separation techniques such as filtration, chromatography, and precipitation
• Organic chemistry and chemical modifications
• Experience from a GMP regulated production is an advantage.
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 are 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 with responsibility 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 scientists and laboratory technicians. We thrive on professional challenges and work independently with great individual responsibility and a high level of commitment. We collaborate with diverse 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. The department is in Bagsværd, 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 possibly 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 Arda Yildiz at +45 30756676 or Michael Nissen at +45 30775233.
Deadline
19 May 2024.
Applications will be reviewed on an ongoing basis, so please do not hesitate to apply.
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 6.5.2024, 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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