Denmark Job Openings

Novo Nordisk
GMP Coordinator
Gentofte
November 6, 2024
As GMP coordinator, you will be part of management and have close collaboration with the local Warehouse teams. The dynamic workday consists of problem solving, risk assessments, audit and inspections and input to project across site GE.
- Set the standard for the GMP compliance level in the local WH.
- Prepare, handle and coordinate audit and inspections together with GMP coordinators in the CVP area.
- Drive and implement major operational tasks - e.g. requirements from authorities, new equipment, major change cases and deviation handling, with a focus on continuous improvement and optimizations.
- Participate in and conduct risk assessment for WH activities for projects.
- A min. bachelor`s degree in manufacturing, pharmaceutical engineering or similar field.
- Extensive, proven knowledge of GMP and work experience as a supporter or GMP coordinator in production or Warehouse, preferably with minimum 4 years of experience.
- Knowledge or experience from operations and development within Warehouse, production, supply chain, or other relevant functional areas.
- Fluency in written and spoken Danish and English.
Thriving on working with processes, problem solving, data in Excel, and give input to validations/qualifications, all while bringing strong quality and compliance mindset is crucial in this role.
You will be part of Warehouse leadership where we prioritize time for sparring, knowledge sharing and are always willing to give each other a helping hand if needed. We are a social team that makes room for diversity and sees the strength in each other's differences
In the department we are ambitious and strive to deliver the best possible services to our production departments. To help you do this, we will guarantee you a lot of sparring and development feedback. And we make sure to have fun while we drive the business forward.
Aseptic Manufacturing site Gentofte is part of the global Product Supply Aseptic Manufacturing network. At our sites across Gentofte, we are more than 700 colleagues responsible for the aseptic manufacturing where we are transforming the API (Active Pharmaceutical Ingredient) into finished products for people living with serious chronic diseases. We work with advanced processes such as formulation, filling, and freeze- drying in a sterile environment. We bring value to our patients by delivering high-quality products in compliance with GMP (Good Manufacturing Practice) in a timely and cost-effective manner as we constantly optimize our processes and invest in new technology.
For further information, please contact Serap Sahin (Senior Manager) OPSI@novonordisk.com
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