Technicon
We are looking for a

QUALITY & VALIDATION ENGINEER FOR PROJECT COMPLIANCE

TECHNICAL WRITER

About the position

We are experiencing increased demand from our clients for structured project execution, strong quality processes, and clear requirement traceability. That’s why we’re expanding our team with a Quality & Validation Engineer who can ensure clarity, consistency, and compliance across our project documentation and validation activities.

You’ll be working closely with our existing Quality & Validation Engineer and will be part of our Compliance department, ensuring strong alignment between project execution, quality standards, and regulatory requirements. You’ll always have a sparring partner who shares your passion for structure, quality, and well-executed projects.

Your main task will include:

This is a varied and hands-on role with great potential to shape your own work and responsibilities. You will play an important role in strengthening the quality and validation aspects of our projects.

Who are you

There are many ways into this role. What matters most is that you have technical understanding and an interest in quality, structure, and compliance.

You might come from a background in engineering, automation technology, quality assurance, compliance, validation, project assistance or similar fields. You may already have experience with documentation and validation from automation projects or regulated industries such as pharma – but you might also be earlier in your career and motivated to learn. At Technicon, we value curiosity and willingness to grow just as much as prior experience.

You may be familiar with documentation frameworks and standards. For example, we work with GAMP 5 and ISO standards – but if you don’t know them in depth yet, we will help you learn. You work in a structured and methodical way and can keep track of tasks and details, even when you’re involved in several projects at once.

You communicate clearly and precisely in both Danish and English. You enjoy creating structure, ensuring quality, and seeing requirements translated into concrete, testable solutions. You thrive when things are well-organized, aligned, and compliant.You are comfortable taking ownership and helping drive validation activities forward. You’re confident in asking questions and constructively challenging when needed to ensure quality and compliance.

What do we offer

At TECHNICON, we offer a flexible workday with a high degree of freedom and influence over your tasks. We work in project-based teams and value knowledge sharing and strong collaboration.

In short:

Who are we

At TECHNICON, we are driven by the ambition to create intuitive and user-friendly automation solutions for the pharma industry. We believe the best solutions emerge from the synergy between people and technology – and between skilled, committed colleagues.

You’ll join a passionate, interdisciplinary team where there’s room to be yourself and grow both personally and professionally.

How to apply

Please send your application and CV to: application@technicon.dk. Remember to write the position you are applying for in the subject line. We’re conducting interviews on a rolling basis, so don’t hesitate to get in touch. If you have any questions about the position, feel free to contact our HR department at +45 29161012 or email ldv@technicon.dk

We look forward to hearing from you!

Send your application and CV to: application@technicon.dk

You can also download the job description as a PDF.

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