GMP Coordinator

Do you have passion for GMP, and are you motivated by setting the right quality and compliance direction? Do you get energy from having a large contact base and the possibility to work with highly qualified colleagues within your field? 

If so, you might be the new GMP Coordinator we are looking for. Apply now for a life-changing career!
  
The position
As GMP Coordinator for Production Support in Bagsværd, you will work closely with our project team and management. We are supporting a production site which is undergoing major expansions throughout the coming years with implementation the newest technologies within aseptic production. You will be responsible for supporting management and colleagues in maintaining and developing a high GMP-level. You will be positioned in Production Support and report to the Senior Manager.
 

Your main responsibilities will include: 

• Drive a high level of GMP in reconstruction and validation documentation 
• Prepare for and follow-up on our frequent authority inspections and internal audits
• Coach supporters and team leaders in GMP behaviour and understanding.
• Ensure high-level GMP overview within our projects and overall compliance level and report compliance risks to management.  
• Lead and coordinate critical quality issues and compliance improvement 

You will also work in partnership with other local GMP coordinators on cross-site compliance improvement and participate in setting direction for the GMP-level across the entire site. 

Qualifications
You will be a great asset to our team because you have: 

• An academic degree within Chemistry, Pharmacy, Engineering or similar.
• Minimum 2 years experience working in the pharmaceutical industry.
• Complex production processes experience within GMP regulated areas.
• Professional proficiency in English.
• A broad and holistic perspective thinking, seeing the big picture without losing sight or interest in key details.
• Validation experience is an advantage.

You are proactive and a fast learner. You are a people person that can interact and communicate at all levels of the organisation and you take pride in solving your tasks and challenges as close to the process as possible, with close involvement of your key stakeholders.

About the department 
Production Support, Bagsværd is responsible for the operation, maintenance and development of our facilities and utility equipment including associated systems and processes. We produce insulin and obesity products for patients around the world for market and clinical trials. 

Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessary 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. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.
 
Contact 
For further information, please contact: Senior Manager, Peter Martin Andersen at +45 30 79 62 64

Deadline
5th January 2025
 

We will review applications and conduct interviews on an ongoing basis.
 

You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV (Curriculum Vitae). 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.