Project Quality Coordinator, Koriyama Factory

Are you passionate about ensuring high-quality standards and compliance in project activities? Do you have experience working with quality systems and regulations? We are looking for a Project Quality Coordinator to join our Project Office team in Koriyama Factory (KFA). If you are detail-oriented, analytical, and have strong communication skills, then read on and apply today for a life-changing career.

About the department
At Novo Nordisk we are experiencing a rapid growth in sales over the recent years and along with the wide range of new products to be launched, we are re-enforcing our production capability world-wide.
As our Koriyama Factory (KFA) is also expanding its workforce, this exciting opportunity is now available for a Project Quality Coordinator, KFA in Japan to join one of the largest scale projects of the factory expansion (expanding the building, not just the equipment) by collaborating with the team members. Also, ensuring high level of compliance with all the internal and external regulations/requirements in all activities and readiness for new product launches as per defined milestones.

The position
The Project Quality Coordinator role involves maintaining and updating Quality policies within NN, ensuring adherence to these policies during the expansion of facilities, and contributing Quality perspectives to equipment design. Compliance with internal and external regulations is emphasized throughout project activities, with regular internal inspections to enforce adherence to Quality policies. Additionally, the position entails assisting in the development of processes and procedures for project-related activities while aligning with NNWay, Essentials, and Triple Bottom Line principles.

• Getting involved in the facility expansion, including equipment design, from a quality professional perspective.
• Performing regular inspections and reviews internally in the project to ensure adherence to quality policies.
• Collaborating with the KFA QA team to implement and maintain quality in line with global requirements.
• Acting or supporting as a quality professional during audits or inspections.
• Ensuring new buildings, facilities, and equipment are well qualified and/or confirmed and maintaining them in a verified state from a quality professional perspective.

Qualifications

• Bachelor’s degree in a relevant field.
• More than 2 years of experience as quality assurance at pharmaceutical or medical device company.
• Knowledge of Japanese regulations (GMP/GQP).
• Knowledge of general quality management systems.
• Japanese and English communication skills (email, Teams/Face-to-Face meetings, etc.)

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 energize 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
Upload your CV to our online career page (click on Apply and follow the instructions).

Deadline
Until the completion of recruitment.
Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.
 

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.

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