Vacant job

Why this job is right for you

At Knightec Group, we understand the importance of improved quality of life for patients through safe medical technology products. With a focus on quality and regulatory compliance in the product development process, you play a key role in enabling new technology and more efficient medical technology solutions on the market.

As a consultant with us, you will become part of our Center of Excellence within Medtech Compliance. Here, you will have the opportunity to develop through training, knowledge sharing, and varied customer assignments within medical technology. You will work closely with both colleagues and customers on projects that contribute to safe and sustainable products.

We offer an environment where you have the opportunity to grow in your role, influence your work, and develop your skills together with experienced colleagues.

Responsibilities

In this role, you may work with:

• Contributing to the development and quality assurance of medical technology products throughout the entire product lifecycle.
• Participating in projects with both startups and established international companies within medical technology.
• Working within Design Control, technical documentation, Quality Assurance, and regulatory affairs.
• Supporting customers in working with quality management systems and compliance with regulatory requirements.
• Collaborating cross-functionally with development teams, quality functions, and other stakeholders.
• Contributing to knowledge sharing and experience exchange with colleagues within Medtech Compliance.

Qualifications

We believe you have experience in Compliance or quality work within medical technology and thrive in a role where you can combine structure, collaboration, and problem-solving. You have a burning interest in quality and regulatory issues, while appreciating working closely with both technology and business operations.

Furthermore, we would like you to have:

• A degree in Biotechnology, Medical Technology, Chemical Engineering, or a similar field.
• At least 2-3 years of experience working in the medical technology industry, for example within Design Control, CE marking, Quality Assurance, Regulatory Affairs, or quality management systems.
• A good understanding of relevant standards and regulatory requirements such as MDR, ISO 13485, ISO 14971, and IEC 62304.
• Good communication skills in Swedish and English.
• Ability to work systematically and collaborate in various types of organizations and project environments.

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, supporting our customers throughout the journey – from initial 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 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 probation period, located at our office in Gothenburg, Lindholmsallén 2. 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 2026-08-16. If you have any questions about the position, you are welcome to contact Talent Acquisition Specialist, Oliver Rydberg. Please note that due to GDPR, we only accept applications via our career page.

We look forward to hearing from you!