Senior Scientist for CMO management and analytical support
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Are you eager to be part of our voyage towards the break-through formulation, development and production of novel pharmaceutical products? Are you an enthusiastic scientist with interest within analytical development and project management coupled with experience working with contract manufacturing organisations (CMOs)? Then this might be just the right career move for you.
In our Raw Materials, Side Chains and Residues Analyses team, we are looking for a senior scientist with a background in analysis and characterisation to support the CMOs that we collaborate with as well as to contribute to the daily analytical development work in the team. Apply now and join us for a life-changing career! The position In this position you will be a part of our Raw Materials, Side Chains and Residues team, where your main responsibility will be oriented towards coordination and project management of CMO activities, combined with analytical development tasks within the team. Our new Senior Research Scientist will be responsible for: Reviewing documentation, evaluating and troubleshooting on analytical work in collaboration with the CMOs Contributing actively to ensure that the documentation of the analytical work from the CMO lives up to current guidelines and industry standards Analytical development and validation of analytical methods including chromatographic methods, e.g. Ultra-High-Pressure Liquid Chromatography (UHPLC) as well as other analytical techniques such as IC, GC, MS, NMR, IR etc In this role, you will have a close collaboration with the Analytical Project Manager who is responsible for the daily coordination between Novo Nordisk as well as the CMOs and with all our internal 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 CMOs. Qualifications Our ideal candidate has: A Master’s degree within Life Sciences (Natural sciences, 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 peptide, small molecule, or protein production and have GMP experience Practical experience within HPLC/UPLC and LC-MS analytical development preferably within the pharmaceutical industry and knowledge of additional techniques such as GC/GC-MS or ion chromatography is an advantage Good knowledge of general chemistry/biochemistry and a natural flair for thinking in new solutions and automation. On a personal level, you are 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. Additionally, 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. Ideally, you master both English and a Scandinavian language (Swedish, Danish or Norwegian).
About the department
The department, Chemistry, Manufacturing and Control (CMC) Analytical Support, is organised into four highly skilled analytical teams with a total of 65 employees. The department is responsible for developing analytical methods, validation, documentation and delivering analytical results for new drug substance, drug product and side chains as well as for raw materials, excipients, and various process related residues and leachable. Furthermore, we are responsible for solid state peptide and protein characterisation including particle characterisation and stability studies. Providing analytical support to all parts of Novo Nordisk, the department acts as a link between the research unit and the production, spanning early development to phase 3 clinical trials and registration. Together we represent many years of scientific experience enabling us to innovate and solve exciting and challenging tasks. In future, we will further strengthen our collaboration with CMO's to expand the product portfolio at Novo Nordisk A/S. As part of Novo Nordisk’s R&D family, CMC Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture, and distribute drug candidates for non-clinical and clinical trials and represent a strong culture with a “can do” mind-set.
Working at Novo Nordisk
At 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. We divide them into three tracks: Specialist, Project Manager or Manager.
Contact
For further information, please contact Associate Manager Louise Juhl Skov at +45 3077 6570
Deadline
18 January 2023. Applications will be reviewed continuously, and interviews will be conducted during the posing 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.
In our Raw Materials, Side Chains and Residues Analyses team, we are looking for a senior scientist with a background in analysis and characterisation to support the CMOs that we collaborate with as well as to contribute to the daily analytical development work in the team. Apply now and join us for a life-changing career! The position In this position you will be a part of our Raw Materials, Side Chains and Residues team, where your main responsibility will be oriented towards coordination and project management of CMO activities, combined with analytical development tasks within the team. Our new Senior Research Scientist will be responsible for:
About the department
The department, Chemistry, Manufacturing and Control (CMC) Analytical Support, is organised into four highly skilled analytical teams with a total of 65 employees. The department is responsible for developing analytical methods, validation, documentation and delivering analytical results for new drug substance, drug product and side chains as well as for raw materials, excipients, and various process related residues and leachable. Furthermore, we are responsible for solid state peptide and protein characterisation including particle characterisation and stability studies. Providing analytical support to all parts of Novo Nordisk, the department acts as a link between the research unit and the production, spanning early development to phase 3 clinical trials and registration. Together we represent many years of scientific experience enabling us to innovate and solve exciting and challenging tasks. In future, we will further strengthen our collaboration with CMO's to expand the product portfolio at Novo Nordisk A/S. As part of Novo Nordisk’s R&D family, CMC Development makes a real difference for patients with chronic diseases across the world. We develop, manufacture, and distribute drug candidates for non-clinical and clinical trials and represent a strong culture with a “can do” mind-set.
Working at Novo Nordisk
At 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. We divide them into three tracks: Specialist, Project Manager or Manager.
Contact
For further information, please contact Associate Manager Louise Juhl Skov at +45 3077 6570
Deadline
18 January 2023. Applications will be reviewed continuously, and interviews will be conducted during the posing 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 22.12.2022, 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.
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