Do you want to take part in development and validation, release testing and support of ICP analysis for raw materials, excipients, drug substances and finished drug products? In that case you should apply for the new position as ICP Analytical Chemist in Material Manufacturing Development. If you are as ambitious as we are, you can look forward to an exciting job in an environment where we seek to be best in class in everything we do.
The position
As ICP Analytical Chemist your primary tasks will include:
Maintenance of equipment and methods for ICP analysis (ICP-MS and ICP-OES). QC support to deviations, out-of-specification results, and laboratory investigations Support to Product supply (Deviations, studies, stability-project etc.) Method development and validation of new ICP analytical methods. Qualification and implementation of new equipment to support the ICP laboratory QC control of ICP analyses As part of our department, you will also be involved in the diverse assignments we deliver to other parts of Novo Nordisk. This will give you a variety of challenges, and therefore strong collaboration with your colleagues is essential. You will be part of a team where ideas, problems and solutions are discussed in an open, positive and forthcoming atmosphere.
Qualifications
To be successful in this role it is required that:
You hold a Master´s Degree in Chemistry, Pharmacy, Engineering, or another relevant field within the natural science. Strong practical and theoretical background within analytical chemistry will be required. You have experience with ICP-OES and ICP-MS You have a strong proficiency in both written and spoken English A high GMP and compliance mind-set is required. Additionally, it would be an advantage if you also have knowledge within systematic problem solving, and a good eye for processes and optimization. As a person, you enjoy working in project groups and have a high level of energy to drive yourself and your colleagues forward to deliver on milestones. You work in a structured manner and find solutions that are robust and will ensure the correct quality level. You motivate your colleagues with a positive, forthcoming attitude.
About the department
You will join Material Manufacturing Development in Product Supply Sourcing Operations. We consist of 100 employees, located in Hillerød and Bagsværd. We are responsible for the quality of all raw materials at Novo Nordisk. You will join the ICP group within the analytical support team, which is responsible for analysing Elemental Impurities for Product Supply, release testing of raw materials and excipients and support to PS. We cooperate with a variety of functions, including development, production, Quality Control and Quality Assurance as well as Novo Nordisk sites all over the world.
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