Vacant job

Why this job is for you

For you, validation is about more than just documentation – it’s about building trust, safety, and quality at every step. You want to drive change, not just follow it. Here, you will grow as a specialist while contributing to solutions that make a real difference for people and society, delivering safe products that improve users' quality of life.

At our company, you will become part of a strong validation team with broad competence in qualification, computerized systems, and processes. We work together, share knowledge, and help each other grow. There are always colleagues to bounce ideas off, and room for you to take on new types of projects and assignments.

Within our business area Compliance & Management, we help our customers transition to sustainable and secure solutions. We combine expertise in quality, safety, sustainability, and project management – ensuring our projects make a real difference, both for our customers and for the people affected.

Responsibilities

You will work with the validation and qualification of computerized systems, processes, and equipment within the Life Science industry. You will take on early responsibility in projects and influence everything from design to commissioning – thereby contributing directly to safe products and improved quality of life. Your work ensures that every step in the process meets the highest standards – from initial requirements to the finished product.

We believe in collaboration, knowledge sharing, and quality awareness as the path forward. We share experiences, bounce ideas, and support each other throughout the entire project lifecycle. Here, you have the space to take initiative, drive development, and fully utilize your expertise.

Qualifications

We are looking for someone who thrives in an environment where quality, technology, and development meet – and who wants to contribute to our customers' success in their validation projects. You have a quality-oriented approach and a strong desire to develop yourself, as well as to lift others up.

You also have:

• A Bachelor's or Master's degree in Biotechnology, Medical Technology, Chemical Engineering, Computer Science, or similar
• Experience with validation within Life Science, including work with IQ/OQ/PQ phases
• Experience in requirements, deviation, and risk management
• Experience in requirements specification, documentation, and URS (User Requirement Specifications)
• Good knowledge of GxP regulations (experience with GAMP5, 21 CFR Part 11, and Eudralex Annex 11 is a plus)
• Very good Swedish and English skills, both spoken and written
• Experience with digitalization projects or automation within Life Science is considered an asset

We believe curiosity and learning are the driving forces – therefore, we place great emphasis on your willingness to develop, share knowledge, and contribute to us all becoming better together.

An exciting journey with Knightec Group

Today, Knightec Group is one of Northern Europe's leading strategic partners in product and digital service development – how cool is that?

By combining engineering competence, digital expertise, and business understanding, we help our customers transform new technology into real solutions that create value. We work at the intersection of business strategy and technology development, supporting our customers throughout the entire journey – from initial ideas to development, implementation, and further evolution.

At Knightec Group, people with different perspectives, experiences, and specialist areas come together. Together, we create innovation that makes a real difference – for businesses, people, and society at large.

For our employees, this means great opportunities to help shape future solutions through meaningful projects at the absolute forefront of technology. Here, you will not only develop and grow in your role – you will also become part of a team where curiosity, collaboration, and the courage to challenge drive us forward.

Does this sound like the place for you? Join us on our continued journey!

Practical Information

This is a permanent position with a six-month probationary period, located at our office at Dragarbrunnsgatan 45 in Uppsala. Travel to our customers may occur as part of the role. Start date is as soon as possible or by agreement.

Please submit your application as soon as possible, but no later than 2026-06-28. If you have any questions about the position, you are welcome to contact Kicki Björ, Talent Acquisition Specialist. We handle all applications via our career page to ensure safe and secure processing of your personal data in accordance with GDPR.

We look forward to hearing from you!