Vacant job

Why this job is for you

At Knightec Group, we understand that validation is more than just documentation. It is about achieving common goals together – delivering a safe product and improving the quality of life for users. You enjoy seeing the big picture, from requirements at the beginning to a fully validated process, equipment, or system at the end. You are meticulous and enjoy documenting.

You will become part of our competency area within Validation Management, where you will participate in workshops, mentorship programs, and discussion forums that promote knowledge sharing and collaboration. You will also become part of our national initiative within Medtech Compliance, where professional development and collaboration are in focus.

Within our business area Compliance & Management, we support an efficient transition to digital, sustainable, and secure solutions through expert knowledge in areas such as quality, safety, sustainability, and project management.

Responsibilities

You will take on varied roles where you support our customers and where your expertise comes into play. You will work with:

• Validation and qualification of processes, equipment, and computerized systems within the Life Science industry.
• Participation in requirements setting, design, procurement, and commissioning, which gives you the opportunity to influence results and outcomes.

Qualifications

We are looking for you who are quality-conscious and enjoy learning new things and sharing knowledge with others. You have a technical interest and are receptive. In addition to your personal qualities, we want you to have:

• A quality-oriented approach and a desire to develop yourself and your colleagues.
• An engineering degree in biotechnology, medical technology, chemical engineering, computer engineering, or similar.
• At least three years of experience independently driving process validation work within Life Science and being responsible for the DQ/IQ/OQ/PQ phases, with a focus on CSV equipment, packaging, and cleanroom environments.
• Experience in requirements and deviation management.
• Good knowledge of GxP regulations, especially GAMP5, 21 CFR Part 11, and Eudralex Annex 11 and/or ISO13485.
• Fluency in both Swedish and English.

An exciting journey with Knightec Group

Knightec Group is today 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 and support our customers throughout the journey – from the first ideas to development, implementation, and further development.

At Knightec Group, people with different perspectives, experiences, and specialist areas come together. Together, we create innovation that makes a real difference – for companies, 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 not only develop and grow in your role – you also become part of a team where curiosity, collaboration, and the courage to challenge drive us forward.

Practical Information

This is a permanent position with a six-month probation period, located at our office in Malmö, Ångbåtsbron 1, or at our office in Helsingborg, Stortorget 11. Travel to our customers may occur as part of the role. Start date is by agreement.

Please submit your application as soon as possible, but no later than 2026-08-10. If you have any questions about the position, you are welcome to contact Oliver Rydberg, Talent Acquisition Specialist. Please note that due to GDPR, we only receive applications via our career page.

We look forward to hearing from you!