Ambitious Validation QA professional

Are you an equipment or QA Professional, who is eager to set direction and to ensure compliance, in close work with your stakeholders? Do you thrive in a constantly changing environment with various challenges and growth opportunities to handle? Do you believe in working together is better than working on your own? Then keep reading.

The position
As an advanced QA professional, you will be working closely with QA colleagues and stakeholders on tasks related production, IPC and computerized equipment in both the tablet productions and finished product productions. QA plays a crucial role in all the tasks, as we set the direction for quality and compliance, thereby ensuring the highest quality for patients in a changing and challenging environment. 

You will be a part of the Qualification of Bulk and Pack team in Emerging Technologies QA Denmark (ET QA DK), where you will be working with qualification of the production equipment and support the daily operation by handling deviations, change requests and SOPs. 
You will ensure that the qualification documentation for implementation and maintenance of equipment complies with internal and external requirements. You will also contribute to finding solutions for ad hoc questions and challenges within compliance of cGMP. 

You will influence and set directions in setting the right level of compliance, optimizing our processes by applying LEAN mindset and establishing new processes. 

In this role, you can expect the following: 

• Have an overview of what is happening in production and participate in relevant projects.
• Approval of documentation, such as qualification, deviations, change control, SOP, trend reports etc. 
• Being a trustworthy partner with stakeholders and setting the quality direction.
• Setting the necessary QA direction in various tasks. 

Qualifications
We seek a colleague who fits our team both professionally and personally. As a person you are open minded, have an outgoing attitude and have strong communication and collaboration skills with both your colleagues in QA and stakeholders.

Also:

• You hold a Master’s degree in chemical engineering, pharmacy or other relevant MSc. 
• Preferably you have minimum 2 years of experience within the pharmaceutical industry and/or qualification experience.
• You dare to challenge us in our way of working and have a desire to take initiative as well as responsibility for your own learning.
• We operate both in a national and international environment, so you must speak and write Danish and English fluently.

As a person, you are a role model for behaviour, a dedicated team player who inspires trust and respect among colleagues and partners. You are open-minded, with a high-quality mindset, and work with a high level of energy, an outgoing attitude, and natural networking skills. These qualities combine to make you an individual who is poised to contribute effectively within a professional setting.

About the department
ET QA DK is an area with approximately 100 skilled and motivated colleagues. We work with assuring quality and compliance of all areas regarding tablets and finished products for the market. We are proud to work in a fast-growing and ambitious part of Novo Nordisk.
ET QA DK consists of three departments and this position is situated in the department named ET FP QA DK with approximately 25 skilled and motivated colleagues. Since this team also covers equipment for tablet production it is pivotal to also collaborate with the ET QA SDF DK department, as they are responsible for the tablet processes and release, but also facilities and cleaning.

Working at Novo Nordisk 
We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease.
 

Contact
For further information, please contact QA Manager Malene Mejer Pedersen at +45 3075 8618.

Deadline
5 February 2025. 

Applications will be evaluated continuously, when received and candidates may be called for interview before the deadline.

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.