Project Scientist - Chromatographic Tests and Method Validation

Are you passionate about chromatographic analysis and method validation? Do you thrive in a dynamic environment where your expertise in GMP and analytical techniques can drive real impact? Are you ready to be part of a team that not only optimizes production but also contributes to sustainability efforts? 

If this sounds like you, apply now to be our new Project Scientist for Chromatographic Tests and Method Validation and take your career to the next level with Novo Nordisk! 

The Position 

We are seeking an independently working Project Scientist to join our team at the Kalundborg site. The ideal candidate will have a deep knowledge of chromatographic tests and a thorough understanding of Good Manufacturing Practice (GMP), including method validation.  

This role is part of a team of highly specialized individuals with expertise in GC/GC-MS, LC-MS, IT, and equipment management. Having become familiar with the work process, you will be assigned cross-organization project as a member of an analytical project group e.g online GC 

As a Project Scientist for Chromatographic Tests and Method Validation, the Key Responsibilities are  

• Participate in manufacturing projects aimed at production optimization to improve resource use and reduce our environmental footprint. 
• Conduct chromatographic tests and ensure compliance with GMP standards, including method validation. 
• Collaborate with a multidisciplinary team to achieve project goals and ensure know-how from the analytical lab is communicated to the project. 
• Take part in decision-making processes and contribute to the overall success of the project. 

Qualifications 

On a personal level, you are a self-driven individual with a strong desire to continuously learn and grow. You thrive both independently and as part of a team, valuing collaboration while also taking initiative in your work. You are comfortable making important decisions in partnership with your project team, ensuring that challenges are met with confidence and strategic thinking. Above all, you are passionate about contributing to a greater purpose—being a key player in projects that drive innovation, sustainability, and positive change. 

The ideal candidate should have: 

• M.Sc. or Ph.D. in natural sciences or engineering (e.g., chemistry, biotechnology, or equivalent). 
• Strong background in chromatographic tests and GMP from the pharmaceutical industry 
• Experience with method validation. 
• Passionate about being a small part of a bigger picture and contributing to sustainability efforts. 
• Fluency in English to collaborate effectively in a dynamic, international environment. 

About the Department 

You will be joining a diverse team of experts in GC/GC-MS and LC-MS, along with IT and equipment specialists. We have an informal tone and many unforeseen exciting tasks. We are part of Manufacturing Science and Technology (MSAT) analytical technology in the PS API MSAT organization 

PS API MSAT Analytical Support is specialized in analytical methods and support functions related to the development, implementation, and maintenance of a broad range of analytical methods. The department plays a vital role in supporting the production and QC laboratories in PS API. 

PS API MSAT Analytical Support is located in Kalundborg and is comprised of approximately 70 engaged employees organized into four teams.  

Working at Novo Nordisk 

At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. 

Contact 

For further information, please contact Manager Karen Duus at +45 3077 6696 or Area Specialist Peter Sloth +45 3075 5648 

Deadline 

23 February 2025 

Applications are reviewed continuously, so please submit your application as soon as possible, and please add a link to your LinkedIn profile in your electronic application, if possible. 

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 process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all job applicants 

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.