IT Validation Engineer - NNE

Employer: Novo Nordisk Engineering (NNE)

Does the idea of working with validation of complex data engineering solutions excite you? And do you thrive on close collaboration with great colleagues? 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: Virum or Kalundborg

The Role 

We are looking for a Validation Engineer to join our team of highly skilled colleagues in Manufacturing Intelligence. As a team, we are working on providing full-service intelligence solutions for pharma manufacturing, covering all aspects of data engineering and science, including cloud deployment, app development, data implementation, data management, GxP validation, and advanced analytics.

We specializes in data connectivity solutions that enable data-driven decision-making, process automation, and faster access to critical production data.

Why do we need you? Our goal is to grow our Danish team providing our customers with skilled resources for their projects and strategic challenges. Your role will be key in developing solutions for customers, ensuring proper testing and documentation of solutions, and continuously give input to our department’s skillset and delivery models.

Responsabilities
As an IT Validation Engineer, you’ll be:

• Part of setting the standard for testing and qualification of the developed solutions
• Coordinating with engineers across disciplines in close collaboration with our customers
• Participate in IT risk assessments and requirement setting
• Monitoring the quality of the validation work and supporting engineers during test activities
• Working with Science and Risk based validation with high focus on quality of data and data integrity

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:

• Enthusiastic about IT and data quality and interested in learning
• Outgoing who actively seek advice and share knowledge among colleagues and peers
• Result-oriented and have a well-structured work ethic
• Efficient and keep your promises and deadlines
• Comfortable with direct Customer interaction and relationship building

In all positions there are some things that are needed, and others a bonus. We believe these qualifications are needed for you to do well in this role:

• Experience in the Lifesciences and/or Biotech Industry preferably particularly in Commissioning, Qualification and Validation of automation systems, software, or IT
• Have worked with GAMP5, SRV, IT risk assessments and GMP test documentation is an advantage
• Knowledge of/or experience working with MS Azure DevOps or eTIMS (HP ALM)
• Knowledge of/or experience in basic coding languages, markdown editing etc
• You have a degree in engineering or other relevant work experience
• You speak and write English fluently and optionally Danish

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