GMP Coordinator, Athlone

Are you passionate about maintaining high-quality manufacturing standards? Can you ensure compliance with Good Manufacturing Practices and drive continuous improvement? Do you thrive in a dynamic, quality-focused environment, supporting teams and managing audits?

Apply now and join Novo Nordisk as a GMP Coordinator and make an impact in quality and compliance!

The position

As a GMP Coordinator, you will play a key role in maintaining high-quality standards and ensuring compliance with regulatory requirements. You'll work closely with management to drive continuous quality improvement, promote simplicity, and harmonize processes across departments. Your expertise will support daily operations, audits, and the implementation of new procedures.

Your key responsibilities are:

• Managing Quality in own department and adherence to QMS
• Quality Performance Monitoring
• Contribute to Operational Process Development Quality related deliverables
• Responsible for audit & inspection coordination in own department
• Support to local project activity

Qualifications

To succeed in this role, you will need the following qualifications and experience:

• Bachelor’s degree with at least 5 years of relevant experience
• Strong quality mindset with a focus on excellence and continuous improvement
• Proactive and innovative, always looking for creative solutions
• Detail-oriented with a commitment to simplicity and efficiency
• Excellent communicator, adaptable, and able to collaborate across stakeholder groups
• Organized, structured, and results-driven, thriving as a reliable team player

About the department

Located in Athlone and part of the global CMC development team, Oral Product Development Athlone will play a leading role in Novo Nordisk’s oral solid dosage expansion, with an ambition to develop world class tablet products for patients living with chronic diseases. You will be part of a cross functional and global team that works on early and late development, clinical supply and scale up of oral products. We foster a collaborative and supportive atmosphere, where your contributions will make a significant impact on our organisational goals.

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 necessarily 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

Please click on "apply now" to submit your resume in English.

Deadline

Please submit your application via our online application tool by 10th of April 2025.

Please note that we are reviewing applications on ongoing basis, therefore the position will be filled as soon as the successful candidate has been found. Internal candidates are kindly requested to inform their line manager before applying. 

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.