ABOUT READILY
Readily Diagnostics is an Uppsala-based in vitro diagnostics (IVD) company developing a platform for rapid molecular diagnostics
at the point of care. We are a small, hands-on team of scientists and engineers moving from research and prototyping toward pilot
production and regulated product development under ISO 13485 and IVDR, working closely with Uppsala University, Karolinska
Institutet, SciLifeLab and the Uppsala life science ecosystem.
THE ROLE
We are recruiting an R & D Specialist to join a cross-functional project developing a rapid molecular test for three pathogens and
their antimicrobial resistance (AMR) markers, combining sample preparation, our molecular assay and a point-of-care device.
You will be part of the molecular development team and work through the whole chain: establishing sample preparation, identifying
the best genomic targets for recognition, designing the assay and verifying its performance, and finally bringing the assay
together with sample preparation in the finished product. You will work alongside experienced Readily experts and closely with our
engineering, production and QA/RA colleagues, so that what you develop at the bench is robust, reproducible and ready for transfer
to production.
The role reports to the COO and is placed in our R&D / Product Development team.
WHAT YOU WILL DO
Molecular development
Select and evaluate genomic targets based on literature and discussions with experts in the field
Design and optimize molecular assays against the selected targets
Test performance of the assay in silico and in the wet lab using appropriate genomic materials
Translate bench-based protocols into robust, miniaturized workflows compatible with the finished device
Integration and validation
Combine sample preparation with the molecular assay and the point-of-care device
Plan and execute experiments to verify assay function, sensitivity and specificity through the development phases
Analyze and interpret experimental data, summarize findings and propose next steps
Support iterative development and improvement of protocols together with R&D, Production and QA
Production readiness
Document methods and control points according to quality standards to support technology and design transfer
Contribute to material specifications and QC steps for molecular reagents and device components
Documentation and collaboration
Author protocols, test plans and verification reports in line with our quality management system
Participate in risk assessments from a molecular science perspective
Contribute to project meetings, design reviews and discussions with internal and external partners
WHO YOU ARE
University degree in molecular biology, biotechnology or a related discipline – MSc or PhD is an advantage
Minimum 5 years’ experience of molecular assay development and applied research in an interdisciplinary setting
Solid skills in molecular biology techniques, assay optimization, experimental design and data analysis
Good documentation practice and clear technical writing
Structured, curious and comfortable moving between the literature, the computer and the lab bench
Fluency in both Swedish and English, written and spoken, is required for this position.
It is a merit if you have experience of:
Padlock probes, rolling circle amplification or related nucleic acid detection chemistries
Antimicrobial resistance markers or clinical microbiology
Assay miniaturization, lab-on-chip formats or design transfer to production
Medical device R&D under ISO 13485, IVDR or 21 CFR Part 820, including design control and risk management (ISO 14971)
WHAT WE OFFER
A clearly defined scientific role in a funded project with a concrete goal
Direct influence on a product from target selection to point-of-care test
Short decision paths and an interdisciplinary team of scientists and engineers
The opportunity to build experience in regulated IVD development and technology transfer
APPLICATION
This is a fixed-term project position of 12 months with the possibility of extension, full-time, based in Uppsala.
Please send your CV and a short cover letter no later than 27 september 2026. Interviews are held on an ongoing basis, so we
encourage you to apply as soon as possible.
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