About the Position

We are now looking for an Engineer – Validation for an international and highly relevant Life Science assignment. This is the initial assignment as a consultant at QRIOS Life Science, where you will work with one of our partners in manufacturing-related operations.

The assignment is part of a strategic project aimed at establishing a new manufacturing site in Muskegon, Michigan (USA), where working methods and processes reflect an existing operation in Uppsala. You will work closely with teams in both Sweden and the USA and play a key role in the validation work on-site.

As a consultant at QRIOS, you will not only have the opportunity to contribute to a complex and exciting assignment – you will also gain a platform for long-term development, with opportunities for more assignments and new challenges within Life Science moving forward.

QRIOS operates throughout the Mälardalen region (from Södertälje to Uppsala), Gothenburg, and Skåne. We always take into account where you as a consultant want to work, and our assignments are usually geographically concentrated – there is no expectation to commute across Sweden.

Start date: February 11 (flexible)
Assignment length: until December 31, 2026
Scope: full-time, 40 hours/week
Location: Uppsala with regular work on-site in Muskegon, Michigan (approx. 40% travel)
Number of positions: 1
Application deadline: January 21

Your Main Responsibilities

Work together with colleagues in Uppsala and Muskegon in the validation work at the new site
Develop and compile validation protocols
Conduct validation tests of equipment on-site in Muskegon
Compile and finalize validation reports
Work both independently and in close collaboration with international project teams
Ensure high quality and traceability with a strong focus on documentation

Who Are You?

Have a bachelor's degree in engineering
Have at least 3 years of experience in the Life Science industry
Have practical experience in equipment validation within manufacturing
Are very strong in documentation and work in a structured and meticulous manner
Communicate fluently in both Swedish and English, both spoken and written
Have the ability and willingness to travel to the USA for 1–2 week periods, up to approx. 40% of the working time

You thrive in an environment where structure meets innovation and where collaboration across borders is a natural part of everyday life. You are curious, responsible, and see the value in contributing to something that is built from the ground up.

About the Business

The assignment is placed with an international partner of QRIOS Life Science, within a project focusing on establishing and validating a new manufacturing facility for resin production in the USA. Working methods, processes, and quality requirements are based on an established operation in Uppsala, creating a dynamic and educational environment where global collaboration is at the center.

About QRIOS Life Science

QRIOS is your reliable partner in the Life Science sector. We are experts in recruitment and consulting solutions for specialist and managerial roles within pharmaceuticals, medical technology, biotechnology, chemical engineering, and food technology. Our strength lies in the fact that our employees have extensive experience in the industry themselves, giving us a unique understanding of our clients' needs and challenges.

As a consultant at QRIOS, you have the opportunity to try out different assignments, develop quickly, and build a broad network within Life Science. Together, we drive innovation and contribute to a better future.

QRIOS MINDS GO FURTHER.