GMP Quality Manager
2 days ago
About the Role
The GMP Coordinator will be responsible for maintaining a high level of compliance with cGMP and Novo Nordisk's Quality Management System. This involves supporting the department in developing and maintaining a robust quality management system, ensuring that all processes and procedures are in place to meet regulatory requirements.
Key responsibilities include:
- Maintaining a high level of compliance with cGMP and Novo Nordisk's Quality Management System
- Supporting continuous improvements of quality performance and processes
- Driving and improving processes that create transparency for key quality indicating parameters
- Identifying trends and proposing areas for improvement
- Acting as one-point of contact for GMP partners and local responsible for coordination of Inspections and Audits
This role requires a dynamic mix of coordination, follow-up and execution of tasks in a focused manner. You must be able to and be motivated by a flexible workstyle and the ability to prioritize your own tasks and time.
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