Quality Control Professional, Koriyama Factory

Are you passionate about ensuring the highest quality standards in pharmaceutical products? Do you thrive in a collaborative environment where precision and continuous improvement are key? If so, we invite you to join our Quality Control team at Novo Nordisk in Koriyama Factory, Fukushima. Read on and apply today for a life-changing career!

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 our Koriyama Factory in Fukushima is dedicated to ensuring the highest standards of product quality and compliance. Our team systematically manages QC projects and activities according to product specifications and Quality Control Standard Codes. We stay updated on the latest Japanese regulations to maintain compliance and foster strong relationships with QC stakeholders. With a focus on continuous improvement, we strive to enhance efficiency in our routine tasks, all while supporting the stable supply of high-quality products. Join a dynamic and collaborative team where your contributions will make a tangible impact.

The position

As a Quality Control Professional, you will play a pivotal role in maintaining and enhancing the quality of our products. Your key responsibilities will include :

• Guiding and supervising QC technicians to conduct quality control tests, providing training and support to enhance their skills and performance.
• Identifying opportunities to improve the efficiency and effectiveness of routine quality control tasks, implementing process improvements, and monitoring their impact.
• Driving key local and global QC improvement projects, utilising IT systems such as LIMS (Laboratory Information Management System) to optimise QC processes and enhance operational efficiency.
• Ensuring compliance with Japanese regulations, global SOPs, and Novo Nordisk internal rules by reviewing and incorporating specific compliance methods into QC processes.
• Coordinating QC method transfers activities and managing launch-related tasks to support the seamless introduction of new products while maintaining quality standards.

Qualifications