QA Professional for operational readiness (Denmark, Odense)

Jobbeskrivelse
Placering
Odense, Denmark

Jobkategori
Quality

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Are you our new operational readiness responsible QA? Are you interested in embarking on an excit-ing journey within a newly established quality assurance organization for our new production site in Tietgenbyen, Odense? We support the expansion of the assembly and packaging capacity for Novo Nordisk and are looking for a QA Professional to join our QA department in Odense and help us suc-ceed. Apply today!

The position
As operational readiness responsible QA, you will become part of a newly established QA department supporting the new production site for assembly and packaging of finished products in Tietgenbyen, Odense, Denmark.
We value a great working environment, team spirit and empowerment as well as good development opportunities for you to succeed in your new role. In this role you will have the responsibility of driv-ing the tasks related to QA operational readiness, for us to be ready to produce products of high quality to millions of patients all over the world. Once the facilities have been constructed, final ap-provals obtained and we start up production, you will help ensure a smooth transition of our proce-dures and documents towards production to bring products to market.
As a part of your role, you will perform QA reviews and oversight of different types of documents and procedures related to both future production and current validation. You will help assure quality and compliance with the current GMP rules and guidelines. Furthermore, you will participate in dif-ferent forums as our local QA representative for operational readiness.
You will collaborate with a variety of stakeholders on developing procedures and implementing sys-tems locally at the site in Odense, for us to live up to both the internal and external requirements in our Quality Management System (QMS).

Qualifications
To succeed in this role, you should:

• Hold an MSc in Pharmacy, Biology, Chemistry, Engineering or similar.
• Preferably have knowledge and experience within quality assurance and/or production in a GMP regulated area.
• Preferably have experience within assembly and packaging processes and the pharmaceuti-cal industry.
• Be proficient in English.

As a person, you are ambitious and ready to be part of our on-going effort to improve the high standards of Novo Nordisk. You dare to challenge us in our way of working and has the desire to take initiative as well as being responsible for your own learning. You are self-driven and have a pro-active approach towards your daily tasks. You are an honest and dedicated team player who inspires and builds trust and respect amongst colleagues and partners. We are cooperating broadly, also across countries, with many different stakeholders, and therefore excellent collaboration and com-munication skills are needed.

About the department
Novo Nordisk is expanding our global manufacturing footprint in Tietgenbyen in Odense, Denmark, to meet the increasing demand for current and future treatments in serious chronic diseases. This presents an exciting challenge and an opportunity to make a lasting impact.
As a member of this Fill & Finish Expansions QA department, you will be key player for ensuring qual-ity in designing, planning, and building our manufacturing footprint in Odense.
Once the facility in Odense is in operation and final approvals have been obtained, it will become part of Novo Nordisk's global network of manufacturing facilities of finished products delivering medi-cine to millions of patients worldwide. To succeed, a high level of commitment from the Quality As-surance department is required to assure the highest quality for our patients, even when challenged during project execution and daily operation.

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 Department Manager Lars Høg Mittag at [email protected]

Deadline
15 January 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 pro-cess, 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.