Analytical Chemist

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Would you like to work on the validation of analytical methods for the future Diabetes and Obe-sity products? Do you want to be involved in validating of analytical methods of the future? Are you interested in joining a dynamic department responsible for validation, site support and im-plementation of new technology?

If so, you could be our new Analytical Chemist based in Bagsværd. Read on to find out more and apply today and join us for a life changing career! The position
We are seeking an experienced Analytical Chemist to join us on a permanent basis. As the new Analytical Chemist, you will join the Validation team and will be ensuring the optimisation, vali-dation, and implementation of analytical methods. The team's focus is on refining and validating new analytical methods for Diabetes and Obesity products. This involves optimizing of analytical methods in close collaboration with CMC (Chemistry, Manufacturing and Control), validation, and documentation in internal reports, and giving input to submission to documents for the au-thorities. You will play a leading role in: • Solving scientific and technical challenges during method optimisation, validation, and implementation.
• Validation of methods for UPLC but also for TOC, pH, Raman and other UV methods. Furthermore, new analytical methods with the purpose of real time release testing will be intro-duced, and our new analytical chemists will have a role in validation and implementation of these technologies. Main stakeholders will include colleagues in the department, Quality Assurance (QA), Regulatory Affairs, and our Quality Control (QC) laboratories. Qualifications To succeed in this role you have: • An academic degree in Pharma, Science, Chemical Engineering or similar, combined with years of working experience within the pharmaceutical manufacturing industry or other highly regulated industries.
• Very experienced within analytical chemistry, troubleshooting, optimisation, and valida-tion of analytical methods. Worked in a laboratory environment, subject to Good Manu-facturing Practise (GMP) preferably with experience with Container Closure Integrity methods.
• Preparing and writing reports for regulatory authorities.
• Working cross functionally and building strong collaborations.
• Strong communication skills in spoken and written English; ability to communicate in Danish is a plus, with an expectation of willingness to learn the language if not already spoken. As a Chemist, you thrive in a dynamic environment and collaborate with colleagues to meet am-bitious deadlines. Additionally, you are a team player, open-minded and possess excellent communication skills to inspire and motivate colleagues. About the department
Analytical Competence Centre is a department in Injectable Finished Products (IFP) Manufactur-ing Development and consists of around 65 employees organised into 5 teams. We are the cen-tral function for analysis of Novo Nordisk Injectable Finish Products during late-stage develop-ment, as well as for marketed products. The department is responsible for validation of analyti-cal methods before process validation in the production, and for the subsequent transfer and ownership of those methods to our QC laboratories across the world.
Additionally, the department is involved in testing, validation and implementing of new analyti-cal techniques to reduce the lead time for analysis, with the ambitious long-term goal of real time release testing of diabetes and obesity finished products. We strive to do all of this in a collaborative environment of joy and curiosity. You will be part of a team consisting of a specialist, academics, and laboratory technicians. Working at Novo Nordisk
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities, and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energize us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life in-dependent of chronic disease. Contact
For further information, please contact Palle Kristensen, Manager, Analytical Validation at +45 30 79 30 25. Deadline
9 June 2024. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your
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.


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Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

Arbejdsstedet er beliggende i Bagsværd.

Jobbet er oprettet på vores service den 22.5.2024, 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.
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