Warehouse QA Specialist (Fixed Term - 12 Months)

End of 2024, Novo Nordisk acquired the manufacturing site Catalent Anagni S. r. l. with the ambition to expand our capacity to meet the needs of millions of patients. You will be part of a global team that will develop the pharma facilities of the future and work with advanced technology to rethink our fill &finish facilities.

       

Are you passionate about quality assurance in warehousing and ensuring compliance with GMP and GDP regulations? Do you thrive in a dynamic environment where you can drive the quality agenda and collaborate with diverse stakeholders? Join us as a Ware-house QA Specialist and play a key role in securing optimal quality standards across our external warehouses, apply now!

 

The position

As Warehouse QA specialist, you will be responsible for ensuring the right quality level in the warehouse and setting direction in relation to requirement mapping. In the role, you will have to gain deep insight into the processes at warehouses, ensure compliance with local regulatory requirements and be able to communicate with a vast variety of people.

 

Your key responsibilities will be to:

· Drive the Quality agenda and ensure compliance with regulatory requirements and Novo Nordisk QMS during implementation external warehouses

· Ensure Good Manufacturing Practice (GMP) &Good Distribution Practise (GDP) compliance

· Continuously secure that warehouses operate with the right and optimal quality level. This includes their Quality Management system, licenses/certificates, ware-house validation, etc.

· Write, review, and approve quality related documents, such as Quality Agree-ments, etc.

· Participate in relevant audits with external suppliers and internally in Novo Nordisk

 

We offer a dynamic and stimulating environment with opportunities for professional growth and continuous development. The initial contract will be a 12-months fixed term contract.

 

Qualifications

To succeed in this role, you:

· Hold an academic degree in e. g. , supply chain, logistics, chemistry, biology, engi-neering, pharmacy, or similar

· Have proven experience within quality assurance roles, preferably with a focus on warehousing

· Have gained said experience in a GMP regulated industry (i. e. . Pharmaceuticals, medical devices, food…)

· Are fluent in English both written and spoken

· Preferably have knowledge within facility validation

 

On a personal level you are ambitious, curious, proactive and have a great interest in developing yourself and people in your network. Your attitude is service minded, inde-pendent with an eye for simplicity and take responsibility for your tasks.

Finally, you demonstrate great communication skills, this includes being able to com-municate and collaborate with different nationalities and cultures.

 

About the department

The Technical Production Excellence is a team of around 30 young professionals that plays a key role in improving, optimizing and ensuring compliance in our manufacturing processes. We promote a collaborative working environment where we celebrate team-work and continuous learning.

 

By joining this team, you will have the opportunity to manage critical documentation, in-cluding SO Ps, Master Batch Records, Change Controls, and Work Instructions, to im-prove operational efficiency and quality. Additionally, we lead the digitalization of manu-facturing processes and the implementation of the Manufacturing Execution System (MES) to enhance productivity, traceability, and data-driven decision-making. Finally, you will take part in cross-functional projects related to new products, processes and manufacturing lines implementation.

 

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 ex-perimentation, 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

If you believe you are qualified, and cannot wait to take the challenge, please upload your CV directly via our online application tool.

 

Deadline

15 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.