Quality Assurance Associate

Novo Nordisk


Posted 8 days ago

Job Description

Are you highly motivated by being able to make a difference in improving patients’ lives? Are you a high-performing executive who is energized by taking exceptions and able to influence people around you? If so, you should continue reading and applying today.
At Novo Nordisk Pars in Kordan, the position of Quality Assurance Associate provides you the opportunity to work in a high-performing team and contribute directly towards the business results while creating value for diabetes patients.

About the department:

Novo Nordisk (NN) is a global healthcare company with 100 years of innovation and supervision in diabetes care. This heritage has given us experience and capabilities that also enable us to help people defeat obesity, hemophilia, growth disorders, rare diseases, and other serious chronic diseases. Headquartered in Denmark, Novo Nordisk employs over 50,000 people in 80 countries and markets its products in more than 170 countries.

The position:

As a Quality Assurance Associate (QA Associate), you will be responsible for ensuring products and business processes meet GMP, Novo Nordisk A/S, and local requirements.

  • Reception, reconciliation, and QA review and release of incoming material including cartridges and Printed Packaging Material (PPM) and status assignment in SAP.
  • Handle and QA review of deviations.
  • Cooperate with process owners, Production Support (PS), and Head Quarter in any issue impacting Product quality patient safety, and Quality Management System compliance and handle other Quality Monitoring reviews (QMR) training.
  • Responsible for QA for Qualification and validation.
  • Review the PPM Batch Control Report & status assignment in SAP.
  • Cooperate in, QMR, Quality Monitoring Trend, and QAP preparation.


  • 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.

Please send your CV online and only in English (click on Apply and follow the instructions).


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.

To see more jobs that fit your career