Company description

AFRY offers services in engineering, design, digitalization and consulting. We are dedicated experts in industry, energy and infrastructure, creating value for future generations. AFRY has a global reach with deep roots in the Nordics. Together we accelerate the transition to a more sustainable society.

AFRY's Life Science segment is a leading player in Scandinavia and our team in Gothenburg collaborates with clients in pharmaceuticals, biotechnology and medical technology to create innovative and sustainable solutions.

We have a wide variety of assignments, you will work cross-functionally and have colleagues working with everything from quality and process to automation.

At AFRY, we believe in the power of differences and collaboration. Ideas and knowledge are shared, and there is a culture of challenging and supporting each other to develop further. A large network of competent colleagues and customers is available to develop together with, while a supportive and coaching manager is at hand.

Job description

Who are you?

We believe that you have experience working with quality assurance and validation as well as regulatory work. We attach great importance to your personal qualities and would like you to be a flexible person with good interpersonal skills. To be suitable for this role, we believe that you are driven, meticulous and like to keep track of all the details. You are a good organizer, able to plan work efficiently and good at documenting.

For you, it is a matter of course to work in a structured and quality-conscious manner. You enjoy and have the ability to quickly familiarize yourself with new projects and customer needs.

Qualifications

To be relevant for this role, we wish you to have:

• A minimum of 5 years of work experience in quality assurance and validation work in the Life Science industry.
• An engineering or science degree in chemistry, biotechnology, medical technology or similar relevant field.Experience in validation of equipment, processes, cleaning, sterilization, computerized systems, media systems and/or cleanrooms
• Good knowledge of GxP (GMP, GLP, GCP and GDP) and ISO standards (ISO 9001 and ISO 13485).
• Good knowledge of regulatory requirements for medical devices and medical devices for in vitro diagnostics.
• Ability to express yourself fluently in English and Swedish, both in speech and in writing
• Flexible and able to travel in the service if necessary

Additional information

The deadline for applications is November 10, but we work with continuous recruitment. Welcome with your application!

At AFRY we drive change in everything we do. We believe that change happens when bold ideas come together, when we collaborate, innovate and embrace creative solutions, that is how we create the future. We are constantly looking for qualified candidates to join our inclusive teams around the world. Join us and accelerate the green transition