Quality Partner

Are you passionate about Quality and have experience with Quality Systems and processes? Are you ready to engage, support, and mobilize colleagues to make a difference for people living with serious chronic diseases? If so, we have an exciting opportunity for you to join us as a Quality Partner.

The Position

As our new Quality Partner, you will be responsible for strategic quality improvement initiatives in our ET API MSAT department. The role holds significant compliance and business impact. You will have the opportunity to influence the role and contribute to building the quality coordination network across the CVP area of ET API MSAT & QC. In cooperation with subject matter experts, you will support management in setting the direction for the department on quality challenges and opportunities to ensure the highest quality for patients. You will:

• Act as a one-point-of-entry for audits and inspections in the department and drive the planning and execution. Additionally, you ensure overall inspection readiness.
• Support and drive the yearly planning of quality activities to be performed across the department. Strengthen and maintain the training setup in the department in collaboration with department specialists.
• Be the “go-to” person on quality subjects; you actively identify and drive quality improvement projects, and support as needed by applying systematic problem solving, process mapping, or other Lean methodologies.

Qualifications

To thrive and succeed, we expect you to have:

• An academic degree as a Pharmacist, Engineer, Scientist, or similar, or equivalent knowledge through relevant practical experience.
• Minimum of 2 years’ experience within GxP guidelines and regulations and current legislation.
• Proficiency in both spoken and written English.

As a person, we expect that you take responsibility, work independently, and make decisions that balance quality requirements, authority expectations, and business needs; demonstrate a Lean mindset, curiosity, and possess some project management skills or experience. You need to have excellent communication and collaboration skills and motivate colleagues with a positive and proactive attitude while actively engaging in decision-making processes.

About the Department

As part of Novo Nordisk’s Product Supply organization, you will be assigned to Emerging Technologies API Manufacturing Development (ET API MDev). We work at the interface between CMC and full-scale manufacturing with a focus on process understanding, implementation, optimization, and life cycle management.  

We offer a very interesting and varying job with the opportunity to work with other highly qualified and motivated colleagues in a multidisciplinary project environment. 

The department is newly established, presenting a unique opportunity to join at the beginning of an exciting journey, while benefiting from the established way of working in Novo Nordisk.

Contact

For further information, contact Sr. Manager Camilla Christensen, cmsc@novonordisk.com

Deadline

08 April 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 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. 

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.