Job Description

Are you passionate about ensuring compliance with the highest quality standards? Do you have a knack for driving quality activities and coordinating Good Manufacturing Practice (GMP) efforts? We are looking for a QC GMP Coordinator to join our team at Novo Nordisk’s Koriyama Factory in Fukushima. If you’re ready to take the next step in your career, read on and apply today for a life-changing opportunity.

About the department

Novo Nordisk is a global healthcare company with over 100 years of innovation in diabetes care. This heritage has equipped us to help people defeat obesity, haemophilia, growth disorders, and other serious chronic diseases. Headquartered in Denmark, Novo Nordisk employs over 77,000 people in 80 offices and markets our products in more than 170 countries.

The Quality Control department at Novo Nordisk’s Koriyama Factory in Fukushima is dedicated to ensuring the highest standards of quality for our products and processes. Our team is responsible for ensuring compliance, driving quality activities, and coordinating GMP efforts. We support the GMP/Quality Management System (QMS)-related tasks and ensure inspection/audit readiness. With a dynamic and collaborative atmosphere, the department is committed to excellence and continuous improvement.

The position
As a QC GMP Coordinator, you will:

• Support the Manufacturing Supervisor in aligning Koriyama Factory’s QMS/GMP with J-GMP to ensure compliance.
• Oversee compliance checks on the shop floor within the Quality Control department.
• Stay updated on GMP requirements and apply the latest information to the organization’s GMP/QMS.
• Facilitate quality activities and contribute input to the QC management team for quality target setting.
• Serve as the main contact for GMP audits/inspections, coordinating training and addressing deviations and audit findings.

Qualifications

• Bachelor’s degree or higher in Pharmacy (preferably as a pharmacist), Sciences, or Pharma Engineering.
• Demonstrated solid experience in the pharmaceutical industry, with a focus on production, quality control laboratories or quality assurance.
• Strong understanding of international standards and local regulations related to the pharmaceutical industry.
• Experience in quality-related tasks and knowledge of relevant regulatory requirements and procedures.
• Business-level English proficiency (reading, writing, and speaking) coupled with strong personal skills, including the ability to work independently, take initiative, and communicate effectively with stakeholders.

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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