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 the management team and other local GMP Coordinators. You will be responsible for supporting management and colleagues across the site 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 preparation for and follow-up on authority inspections and internal audits.
• Coach supporters and team leaders in GMP behaviour and understanding.
• Ensure high-level GMP overview, and report quality trends to management.
• Lead and coordinate critical quality issues and compliance activities in department and cross site coordination if necessary.

You will also work in Quality Management System (QMS) – Delivery of Quality Management Review (QMR) and you will support daily operation with quality and ensure high-level of GMP on shopfloor.

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.
• Validation experience.
• Professional proficiency in English.
• A broad and holistic perspective thinking, seeing the big picture without losing sight or interest in key details.

You are proactive and a fast learner. You are a people person that can interact and communicate at all levels of the organisation, from operator to management, 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
1st December 2024
 

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.