Senior Research Scientist
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Are you eager to be part of our voyage towards establishing a small molecule analytical laboratory and expertise area to support he break-through formulation, development and production of novel pharmaceutical products? Are you an enthusiastic scientist with interest within analytical development, project management and collaboration with multiple stakeholders? Then this might be just the right career move for you.In our Small Molecules & Side Chains team, we are looking for a senior scientist with a background in analysis and characterisation to support the growing pipeline of small molecule APIs and side chain projects, many of which are performed externally by CMOs (contract manufacturing organisations) that we collaborate with. Our area is in massive growth and our team is always open for new ideas, knowledge, and competences. The team consists of 4 laboratory technicians, 8 scientists, and 2 specialists.Apply now and join us in building a new strategic area of expertise in Novo Nordisk!The position
You will be responsible for:Scientific responsible and overseeing analytical method development, coordination and project management of CMO activities. Challenging, evaluating and troubleshooting on analytical work in collaboration with the CMOs including document review. Analytical development and validation of a wide variety of analytical methods e.g. NMR, LC-MS, UHPLC, GC, IR and more. Contributing actively to ensure that the documentation of the analytical work from the CMO lives up to current guidelines and industry standards. Contributing to the daily analytical development work in the team in our own laboratories. In this role, you will have a close collaboration with the project managers responsible for outsourcing, API production and analysis, who are responsible for the daily coordination between Novo Nordisk as well as the CMOs and with all our internal and external stakeholders. For you to succeed in the role, it is crucial that you have strong stakeholder management skills as well as an ability to understand the cultural and technical challenges linked to collaboration with external partners across the world.Qualifications
Our ideal candidate has:Master’s degree within Life Sciences (Natural sciences, Chemistry, Pharmacy, Engineering or other relevant discipline) and a PhD or similar experience. Understanding of the pharmaceutical business from a CMO or smaller pharmaceutical company, preferably within small molecule, peptide or protein production and have GMP experience. Practical experience within a variety of analytical methods preferably within the pharmaceutical industry and knowledge, e.g. HPLC, LC-MS, GC, NMR or other relevant techniques. Good knowledge of general chemistry/biochemistry and a natural flair for thinking in new solutions and automation. On a personal level you expect you to be:A team player who also enjoys driving own area of responsibility. You are not afraid to lead the way for your colleagues and stakeholders. You are eager to see things moving forward in a dynamic environment where projects and processes vary and therefore require you to be flexible and willing to adapt. You are a strong communicator and able to communicate complex content to people with different backgrounds and skills, motivating them to hear and follow your ideas and suggestions. We expect you to be fluent in written and spoken English. Fluency in a Scandinavian language is an advantage. Our team thrives with collaboration and a positive attitude. We communicate openly and work towards a shared goal. We see challenges as opportunities, and we celebrate our results together. We support and have a genuine interest in each other, which make our team and work more efficient and meaningful.About the department
The department, CMC Analytical Support, is organised into four highly skilled analytical teams with a total of 80 employees. The department is responsible for developing analytical methods, validation, documentation and delivering analytical results for new drug substances and drug product. The department acts as a link between the research unit and the production, spanning early development to marketed products. As part of Novo Nordisk PSQIT organisation, Chemistry, Manufacturing and Control (CMC) Development & Scaling makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for clinical trials and have a strong culture with a “can do” mind-set.
Working at Novo NordiskAt Novo Nordisk we use our skills, dedication, and ambition to help people with chronic diseases and change their lives. By working with us you will have the opportunity to do the same in a global business environment. We offer great career opportunities based on your personal skills and journey of development.Contact
For further information, please contact Associate Manager Louise Juhl Skov at +45 3077 6570Deadline
15 April 2024. Applications will be reviewed continuously, and interviews will be conducted during the posting period, so please do not hesitate to apply.
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 will be responsible for:
Our ideal candidate has:
The department, CMC Analytical Support, is organised into four highly skilled analytical teams with a total of 80 employees. The department is responsible for developing analytical methods, validation, documentation and delivering analytical results for new drug substances and drug product. The department acts as a link between the research unit and the production, spanning early development to marketed products. As part of Novo Nordisk PSQIT organisation, Chemistry, Manufacturing and Control (CMC) Development & Scaling makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for clinical trials and have a strong culture with a “can do” mind-set.
Working at Novo NordiskAt Novo Nordisk we use our skills, dedication, and ambition to help people with chronic diseases and change their lives. By working with us you will have the opportunity to do the same in a global business environment. We offer great career opportunities based on your personal skills and journey of development.Contact
For further information, please contact Associate Manager Louise Juhl Skov at +45 3077 6570Deadline
15 April 2024. Applications will be reviewed continuously, and interviews will be conducted during the posting period, so please do not hesitate to apply.
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 21.3.2024, 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.
- Forretningsudvikler
- Måløv
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