GMP Consultant - NNE

Employer: Novo Nordisk Engineering (NNE)

Are you experienced working with Good Manufacturing Practice (GMP) in projects or operations? Would you like to be part of a team of skilled colleagues, ensuring GMP compliance in engineering projects shaping the pharma facilities of the future? And do you thrive on engaging with customers? Then you’ll fit right in!

We are experts in end-to-end pharma engineering, and we design and build pharma facilities that are essential for millions of patients all over the world. Our success is built on our relationships, both with our colleagues and our customers. If you are passionate about working for a noble cause on projects shaping the future of sustainable and intelligent pharma facilities, NNE is the place to be. 

Locations: Kalundborg and/or Virum

The Role & Department
We are seeking GMP Consultants to join our GMP Design & Support department. Our team tackles innovative and complex projects that will challenge and engage you. Why do we need you? Our mission is to help our customers bring well-designed GMP facilities into operation quickly and predictably. Your role will be pivotal in delivering the best possible service to our clients, making your broad knowledge and expertise in GMP regulations and compliance essential.

Responsabilities
As a GMP Consultant, you’ll be:

• Supporting our customers in setting the GMP design strategy for engineering projects, and verifying compliance with the strategy throughout the project.
• Facilitating the interpretation of cGMP to ensure that the solutions delivered to our customers are GMP compliant.
• Focusing on customer needs for an innovative and efficient pharma business operation, without compromising GMP compliance.

Requirements
We care about who you are as a person. In the end, how you work, and your energy, is what impacts the results we achieve as a team.

As a person, you are:

• Passionate about bringing well-designed GMP facilities into operation.
• Enthusiastic, results-oriented, and have a desire to learn and act as a mentor to others.
• Enjoying variation and flexibility in your projects.
• Demonstrating technical curiosity as well as a sense of quality and service.
• Responsible when solving tasks, and you thrive in a dynamic and global work environment where you can work independently as well as in teams.
• Approaching projects and customers with a can-do attitude, and you can listen and ask questions to understand their needs.
• Understanding and respectful of your colleagues’ individual and cultural differences.

We believe these qualifications are needed for you to do well in this role:

• You have experience working in a GMP-regulated environment.
• You are knowledgeable about GMP regulations and how to apply them in your work.
• You are familiar with terminologies like Quality Risk Management, Room Classifications, and Science and Risk-based approaches to validation
• You value having fruitful dialogues with colleagues and customers.
• You speak and write fluent English.
• You have a diploma or master’s degree in life sciences or other relevant education.

If you do not check all the boxes, you are welcome to offer alternative experience that you think would be valuable in this role.