Analytical Scientist with Validation experience for Biopharma Analytical Manufacturing Development

Do you want to be part of a dynamic department with a diverse range of tasks within transfer of methods and validation of Biopharm’s portfolio of haemophilia and growth hormone products? Then this position will suit you.

The department

In Biopharm Analytical MDev we validate and optimise analytical methods for new products within e.g. haemophilia and growth hormone. We have innovation in focus, and we implement new technology continuously. Working with various kinds of tasks and professional challenges we use our professional skills combined with systematic problem solving.  We are 50 employees in the department, organized in three teams and a staff function that takes care of activities across the department. In the department we have a good and informal atmosphere, a good work-life balance and sharing of knowledge across teams and professions.

The position

You will be part of a group of validation scientists in the team with responsibility for transfer, optimization and validation of analytical methods for new products according to current regulatory requirements. You will prepare protocols, reports and analytical procedures and you will assist the laboratories in Biopharm with the implementation of the methods in close collaboration with the group of laboratory technicians in the team. Furthermore, you will drive projects to optimize and improve the current analytical methods in Biopharm QC and support the rest of the department with preparation of documentation for the authorities. You will have contact to a lot of colleagues outside the team and will be in close dialogue with the development departments, Biopharm QC and Quality Assurance (QA). All in all, it is a challenging and stimulating job that requires energy, drive and flexibility.

Qualifications

• You hold a Master’s degree in Science within Pharmacy, Chemistry or a similar field
• You have experience from a laboratory environment subject to GMP with one or several analytical techniques such as ELISA, clotting assays, SPR, CE-SDS, HPLC and/or iCIEF.
• You have experience within validation and standardization of analytical methods and knowledge of equipment qualification is also an advantage
• You thrive in a busy environment with an unpredictable workday where you are faced with difficult issues and also have to keep focus on the adjustment of small details
• You are good at creating an overview and prioritizing your tasks; even when deadline approaches.
• You never compromise on quality and at the same time you are good at completing your tasks in time and move on to new tasks with energy and enthusiasm.
• You are a team player – openminded, engaged and able to inspire and motivate your colleagues. We expect you to possess good communication skills in both oral and written Danish and English.

Working at Novo Nordisk

At Novo Nordisk your skills, dedication and ambition help us change lives for the better. In exchange we offer you to work with extraordinary talent and give you the opportunity to get an insight into a complex business area where culture, politics, a broad product range and various manufacturing sites are part of the daily business.

Contact

For further information, please call associate manager Lasse Lollike on +45 3079 5435.

Candidates will be interviewed concurrently with our receipt of the applications.

Deadline for applications: 24 March 2021

Millions rely on us

To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronic diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

Application: https://careers.novonordisk.com/job/Gentofte-Analytical-Scientist-with-Validation-experience-for-Biopharma-Analytical-Manufacturing-Development-Capi/658033401/?locale=en_GB