We are currently seeking professionals to fill QA positions at our facility. These roles will be integral to our Quality Assurance team, ensuring that our production processes meet the highest standards of quality and regulatory compliance.
The ideal candidates will demonstrate a strong attention to detail, analytical thinking, and a commitment to excellence.
Responsibilities include:
* C coordinating batch record review and release preparation activities
* E nsuring documentation quality
* S supporting the timely release of products in compliance with GMP and regulatory requirements
Requirements:
* B ackground in life science, pharmacy chemistry, or any related field
* E xperience Level: Open to both early-career professionals and experienced specialists in Quality Assurance, preferably in sterile production
* F luency in English & Italian, both written and spoken
About the Role
This role is part of a global team that develops pharma facilities of the future and works with advanced technology to rethink fill & finish facilities.
Our team is composed of enthusiastic, collaborative, and goal-driven professionals, each bringing a diverse level of experience and expertise.
We thrive in a culture of continuous improvement by collaborating with other departments (production, warehouse, laboratories, MST).
Working at Novo Nordisk
We drive change and strive 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 Information
Please apply via our online platform. We commit to an inclusive recruitment process and equality of opportunity for all job applicants.
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 know this is only possible with talented employees with diverse perspectives, backgrounds and cultures.