GMP Coordinator Lead

2 days ago


Hillerød, Hillerød Kommune, Denmark Novo Nordisk AS Full time

We are looking for a highly skilled GMP Coordinator Lead to join our team in API Manufacturing 4, 25K Multi-Product Facilities. This is an exciting opportunity for a seasoned professional with expertise in Good Manufacturing Practice (GMP) to drive quality-related improvements and lead audit and inspection setup within the four departments.

Responsibilities:
  • Lead and coordinate quality improvements in 25K, ensuring compliance with GMP regulations and industry best practices.
  • Plan, prepare, handle, and follow up on authority inspections and internal audits in 25K.
  • Responsible for GMP training and contributing to the understanding of GMP in 25K, fostering a culture of continuous learning and improvement.
  • Analyze data to support production KPIs, identifying areas for optimization and implementing corrective actions.
  • Collaborate with cross-functional teams to optimize quality processes in 25K and across the CVP area.
  • Fulfill the role as Data Integrity Steward in the ongoing Novo Nordisk Data integrity project.
About the Team:

You will be part of a dynamic team that manufactures innovative products for patients living with diabetes, hemophilia, hormonal imbalances, and other impactful chronic diseases. We have around 200 employees split into different teams and staff functions.

Requirements:
  • A degree in natural science, engineering, or a similar field.
  • At least 5 years of experience from a similar position within Novo Nordisk.
  • Experience with ISO and/or LEAN is an advantage, as it is an integral part of our everyday work.


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