Requirements
- Bachelor’s or Master’s degree in Science relevant disciplines (e.g. Chemistry, Chemical Engineering, or Biotechnology).
- 2 to 3 years of quality assurance experience in the pharmaceutical industry. Freshers are also encouraged to apply.
- Demonstrate knowledge of quality assurance and GMP compliance.
- Experience in reviewing batch records, quality control data, and regulatory inspections.
- Ability to manage multiple priorities with a deadline and have a highly organized and detail-oriented mindset.
- Upper intermediate level of English in both written and oral skills.
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:
Please send your CV online and only in English (click on Apply and follow the instructions).
Deadline:
30/05/2023
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 in 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 the communities we operate in. Together, we’re life-changing.