Vacant job

Why this job is for you For those who know that validation is about more than 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, with safe products that enhance the quality of life for users.

With us, you will be part of a strong validation team with broad expertise 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 clients transition to sustainable and safe solutions. We combine expertise in quality, safety, sustainability, and project management – ensuring that our assignments make a real difference, both for our clients and for the people affected.

Responsibilities You will work with validation and qualification of computerized systems, processes, and equipment within the Life Science industry. You will take on early responsibility in projects and can influence everything from design to commissioning – thereby directly contributing 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 finished product.

We believe in collaboration, knowledge sharing, and quality awareness as the way forward. We share experiences, bounce ideas, and support each other throughout the entire project lifecycle. Here, you will 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 help our clients succeed in their validation projects. You have a quality-oriented work approach and a strong desire to develop yourself, as well as to uplift others.

You also have:

• A degree in biotechnology, medical engineering, chemical engineering, computer engineering, or similar

• Experience in 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

• Good knowledge of GxP regulations (experience with GAMP5, 21 CFR Part 11, and Eudralex Annex 11 is a plus)

• Very good Swedish and English, both spoken and written

• If you also have experience in digitalization projects or automation within Life Science, we see it as an asset

We believe in curiosity and learning as a driving force – therefore, we place great importance on your willingness to develop, share knowledge, and contribute to making us all better together.

An exciting journey with Knightec Group Semcon and Knightec have merged to form Knightec Group. Together, we are Northern Europe's leading strategic partner in product and digital service development – how cool is that?

With a unique combination of cross-functional expertise and a holistic understanding of business, we help our clients realize their strategies – from idea to finished solution. At Knightec Group, we have the competence, attitude, and drive needed to take on the most challenging and innovative projects.

For our employees, this means fantastic opportunities to help shape the future through meaningful projects at the forefront of technology. Here, you will not only develop and grow but also become part of something bigger.

Does this sound like the place for you? Join us on an exciting journey!

Practical information This is a permanent position with a six-month probationary period, located at our office at Dragarbrunnsgaten 45 in Uppsala. Travel may occur to our clients. Start date is as soon as possible or by agreement.

Please submit your application as soon as possible, but no later than 2026-01-25. If you have any questions about the position, feel free to contact Lina Orfanidou, Talent Acquisition Partner. Please note that due to GDPR, we only accept applications via our career page.

We look forward to hearing from you!