Quality Management System Partner

4 weeks ago


Ballerup, Ballerup Kommune, Denmark Novo Nordisk Full time
About the Role

We are seeking a highly skilled Quality Management System Partner to join our team at Novo Nordisk. As a key member of our Quality Assurance team, you will be responsible for ensuring the highest standards of quality and compliance across our department Oral Product Development.

Key Responsibilities
  • Develop and implement quality management strategies to drive compliance and improve quality
  • Collaborate with cross-functional teams to identify and drive quality improvement initiatives
  • Ensure high-level GMP overview and report quality trends to management
  • Participate in and follow-up on authority inspections and internal audits
  • Support daily operations and ensure the relevant level of GMP and training
Requirements
  • Master's degree in pharmacy, biochemistry, production engineering or similar
  • Extensive experience from the pharmaceutical industry, in roles related to QMS, manufacturing, QC or QA
  • Strong understanding of GMP regulations and requirements
  • Experience with project management, and preferably are LEAN certified
  • Full professional proficiency English, while Danish is an advantage, but not required
About the Department

The team QMS, Training & Health and Safety is responsible for ensuring the highest standards of quality, training and health and safety across our department Oral Product Development (OPDev) in Novo Nordisk Emerging Technologies. Our team is one of 3 teams in Project Office, which primary purpose is to set the direction for OPDev.

Working at Novo Nordisk

We are a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them.



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