Expert in GMP Compliance and Quality Improvement

2 days ago


Hillerød, Hillerød Kommune, Denmark Novo Nordisk AS Full time

At Novo Nordisk A/S, we are seeking a highly skilled Senior GMP Expert to join our Device Manufacturing Development (DMD), Product Control and Global Support department.

The successful candidate will have a strong understanding of Good Manufacturing Practices (GMP) regulations and requirements, with practical experience in the pharmaceutical industry. They will be responsible for managing various quality-related activities across the department, including leading and coordinating root cause investigations, driving quality improvements, and preparing for authority inspections and internal audits.

In this role, you will have the opportunity to work closely with a diverse team of highly skilled professionals, specialists, and project managers who share their expertise and collaborate on future challenges. Our dynamic environment offers significant responsibility and guidance to foster your personal and professional growth.

To succeed in this position, we imagine you:

  • Hold a master's degree in pharmacy, biochemistry, production engineering or similar with practical experience in the pharmaceutical industry with GMP.
  • Possess a strong understanding of GMP regulations and requirements.
  • Have practical experience with investigations, inspections, and deviations, along with a solid LEAN mindset and experience in using LEAN tools.
  • Demonstrate strong stakeholder management skills, setting direction and guiding/coaching.
  • Showcase professional proficiency in both spoken and written English.

We offer a challenging and rewarding career path, where you can make a meaningful impact on our mission to ensure that people can lead a life independent of chronic disease.



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