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- Review and approval of ICP analyses.
- Support to QC for deviations, out-of-specification results, and laboratory investigations.
- Support to Production (Deviations, studies, stability-project etc.).
- Maintenance of equipment and methods for ICP analysis (ICP-MS and ICP-OES).
- Method development and validation of new ICP analytical methods.
- Qualification and implementation of new equipment to support the ICP laboratory. You will be part of a team where ideas, problems and solutions are discussed in an open, positive, and forthcoming atmosphere. Humour and helpfulness are key characteristics of our team, and we care for the wellbeing of each other. Depending on your interest the job can develop in different directions over time. 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 sciences.
- You have theoretical and practical experience with analytical chemistry.
- You have a strong proficiency in both written and spoken English.
- A high GMP and compliance mind-set is required. Prior experience with ICP-OES / ICP-MS and with working in a GMP environment is preferred. 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 The ICP &Quality team is a part of Material Manufacturing Development in Sourcing Operations, that is responsible for the quality of all raw materials at Novo Nordisk. We are 110 employees, located in Hillerød and Bagsværd. You will join the ICP & Quality team, in Hillerød, which is responsible for analysing Elemental Impurities, analytical support and release testing of raw materials and excipients. 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.