QMS Professional

Are you a dedicated QMS professional looking to make a difference in the production of life-changing diabetes treatments? Do you have a passion for quality management systems and a desire to work in a diverse and inclusive workplace? 

If so, apply today for a life-changing career!
Get introduced to CMC API Pilots and meet our employees by visiting our career site.

The position 
As a Quality Management System (QMS) Professional, you will play a crucial role in driving quality initiatives and projects that will maintain and optimize our high standards of operation.

Your responsibilities will include:

• Participate in audits and inspections
• Write deviations and change requests
• Author SOPs and training material
• Be responsible for the Quality Management Review in the department
• Build and maintain strong relationships with stakeholders across the organization and wider Novo Nordisk to set the strategic direction of QMS and other relevant initiatives.

Qualifications 
To succeed in this role, you should possess the following qualifications:

• An academic degree, preferably in Engineering, Pharmacy, Chemistry, Biology, Biopharmaceutics, or related fields.
• Relevant work experience in the medical device or pharmaceutical industry within QMS, Quality Assurance, production, or similar roles.
• GMP experience.
• Fluency in written and spoken English; Danish language skills are an advantage.
• A strong quality-oriented, proactive, pragmatic mindset, with the ability to thrive in fast-paced environments. Strong stakeholder management skills are also essential.

On a personal level, you are ambitious, curious, proactive and have a strong interest in developing yourself and people in your network. You demonstrate a service-minded attitude, independence, a focus on simplicity and a sense of responsibility for your tasks. Finally, you exhibit excellent communication skills, enabling effective collaboration with individuals from diverse nationalities and cultures. 

About the department 

As part of the Novo Nordisk PSQIT organisation, Chemistry, Manufacturing and Control (CMC) Development & Scaling makes a real difference for patients with chronic diseases across the world. We develop, manufacture, and distribute drug candidates for clinical trials and have a strong culture with a “can do” mindset.

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 Associate Manager Linette Bræmer-Jensen at ltso@novonordisk.com.

 
Deadline 
2 March 2025

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 CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. 
Applications will be evaluated continuously when received, and candidates may be called for interview before the deadline. 
 

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.