Are you detail-oriented, engaged, and enjoy working in a structured environment? We're looking for a Laboratory Engineer (Microbiology) who wants to contribute to high quality and secure processes in our GMP-certified operations.
Our facility in Karlskoga specializes in manufacturing and packaging semi-solid and liquid products. The Karlskoga site offers a broad range of services, including terminal sterilization and WFI production. The facility also has specialized infrastructure designed to meet the high requirements for manufacturing controlled pharmaceuticals, ophthalmic solutions, and sterile semi-solid preparations.
About the Role
As a laboratory engineer, you'll become an important part of our analytical quality control team. The position involves broad and independent work where you participate in planning, performing, and prioritizing microbiological analyses. The role also includes reporting and reviewing analysis results as well as working with production hygiene, including planning and conducting production hygiene analyses.
Further, the position encompasses:
Issuing and investigating deviations
Ordering laboratory materials
Developing and updating SOPs/analysis methods
Instrument responsibility
Issuing and compiling analysis and laboratory reports
Working on projects related to microbiological operations
We're Looking for You If You:
Are positive, responsible, and collaborate easily
Have higher education in microbiology, molecular biology, biomedicine, or BMA
Have experience working in a microbiological laboratory, including aseptic work, filtration, agar plate casting, and handling of sterile and non-sterile processes according to GMP
Have good knowledge of Swedish and English, both spoken and written
Welcome to become part of our team – where your expertise makes a difference!
About Meribel Pharma Solutions
Meribel Pharma Solutions was founded in 2024 and is a niche, mid-sized CDMO specializing in providing customized pharmaceutical solutions to pharmaceutical companies. With headquarters in the United Kingdom and 11 facilities in Sweden, France, and Spain, we offer specialized expertise in sterile multidose, freeze-drying, sachets, and blister packaging, as well as services to support development from concept to commercialization. We are dedicated to elevating pharmaceutical services to new heights and delivering comprehensive support through every step of a product's journey, whether the product is an oral solid dose, liquid, or semi-solid. Want to know more about us? Visit our website: https://meribelpharma.com/.
What We Offer You:
With us, you'll become an important part of a company on an exciting journey. Here you get to work in an environment where improvement work truly makes a difference—both for the business and for your colleagues.
A clean and structured GMP environment with stable processes.
A team that values collaboration and development.
A workplace where quality and safety are central, and where you have the opportunity to grow and make an impact.
Favorable terms with collective agreement, ATK days, and wellness benefits, plus time off on all pinch days.
Does This Sound Interesting to You?
For questions about the position, contact:
Quality Manager QA/QC Chamilla Chahin, mailto:[email protected]
For questions about the recruitment process, contact:
HR Generalist Sandra Lindell, mailto:[email protected]
Application:
Selections are made on an ongoing basis with the final application deadline 2026-09-13
We look forward to receiving your application!