Process Scientist

Jobbeskrivelse
Placering
Kalundborg, Denmark

Jobkategori
Quality

Are you ready to make a difference for people with diabetes and other chronic diseases? Do you feel ready to expand on your knowledge and/or experience with High-Performance Liquid Chromatography (HPLC) and other chemical tests performed in a GMP-regulated environment? Do you dream about new challenges and potentially greater responsibility?

If so, you might be our new Process Scientist for Quality Control (QC) laboratory in Kalundborg. Read on and apply today

The Position
As a Process Scientist for QC laboratory, you will be securing the best medicine for our patients in a team of 20 colleagues of both other scientists and laboratory technicians. You will be the main go-to person for the HPLC analyses of our products and collaborate with other QC laboratories in Active Pharmaceutical Ingredients (API) production.

The main tasks will be to:

1. Coordinate cross-departmental tasks on behalf of the department.
2. Provide support to the lab technicians.
3. Optimize processes, implement changes and handle deviations.
4. Work with Lean and data analysis.

The position is temporary for a period of 1.5 years.

Qualifications
The qualifications we value include having:

1. A min. master’s degree in natural sciences, engineering, pharmacology or similar.
2. GMP experience and knowledge about cLEAN.
3. Experience with HPLC analysis in the laboratory from the pharmaceutical industry or another GMP-regulated environment, as well as QC compliance experience, which is considered a plus.
4. Professional proficiency in written and verbal English and Danish.

On a personal level, you possess a great sense of curiosity, humour, and an open, positive mindset. Being able to work independently in a structured way whilst still being a strong team player – both within the team but also in work relations across the department and area is key to succeed in this role.

Having the ability to thrive in a dynamic environment with a proactive approach and to take on responsibility, while seeing possibilities instead of limitations is crucial part of our daily tasks. To be successful in the position, it is of highest importance to juggle priorities easily and independently, without disrupting the flow of tasks.

About the Department
In Active Pharmaceutical Ingredients (API), located in Kalundborg, we produce insulin and GLP-1 to help people living with chronic diseases like diabetes and obesity.

The QC department in IM1 consists of 5 teams and approximately 60 colleagues all in all. We develop best in a safe working environment hence we continuously focus on well-being and a positive as well as engaging workplace.

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.

Contact
For further information, please contact Associate Manager Christine Bruun Edling at +45 3079 4737.

Deadline
8 September 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 CV.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.