Sr. Research Scientist for analytical development

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  • Måløv

As part of Novo Nordisk’s R&D family, Chemistry, Manufacturing and Control (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.
In the department, CMC Analytical Support, for our “Raw Materials, Side Chains and Residues Analyses” team, we are looking for a senior research scientist with a background in analysis and characterisation to contribute to the analytical development work in the team.

About the department
The department, CMC Analytical Support, is organised into five highly skilled analytical teams with a total of 65 employees. 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.

The position

In this position you will be a part of our Raw Materials, Side Chains and Residues team, which is specialised in development and validation of methods for the analysis of raw materials, residues and side chains as well as analysis of corresponding samples for a wide range of Novo Nordisk stakeholders, hence our tasks spans both GMP and GSP.

As senior analytical scientist, you will be responsible for development and validation of analytical methods including chromatographic methods, e.g. High Pressure Liquid Chromatography (HPLC) / Ultra Performance Liquid Chromatography (UPLC) as well as other analytical techniques used for identification and quantification of small molecules and peptides. Your responsibility will include planning, evaluating and troubleshooting on analytical work in collaboration with laboratory technicians and scientists and you will contribute actively to ensure documentation of the analytical work and in maintaining the right quality level in the team.

Additionally, the position holds the opportunity to be involved in development projects, working in close collaboration with the project team, giving input and participating in establishing the project’s analytical control strategy and subsequent method development.

Qualifications

You hold a Master’s degree within Life Sciences (chemistry, pharmacy, engineering or another relevant discipline) and a PhD or similar experience. You have several years of experience from working in the pharmaceutical industry, where you have gained a thorough understanding of the business, preferably within API or drug product production - hence, you have GMP experience combined with a high compliance mindset.

You have a background within organic/inorganic chemistry and knowledge of protein chemistry and you have practical experience within HPLC/UPLC and LC-MS analytical development - knowledge of additional LC techniques such as e.g. ion chromatography is an advantage. You have a natural flair for thinking in new solutions and automations and in this respect additional programming and mathematic modelling skills are preferred.

On a personal level, you are a team player who also enjoys driving own area of responsibility. You are dedicated towards meeting our common goals and 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. You master English and preferably a Scandinavian language (Swedish, Danish or Norwegian).

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 Gry Ravn Jespersen at +45 3079 6452.

Deadline
April 19th 2020

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.


Information og data

Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Måløv.

Jobbet er oprettet på vores service den 1.4.2020, 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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