Quality Control Specialist
Location: On-site | Remote
Type: Full-time
About KELI Therapeutics
KELI Therapeutics is a European clinical-stage biotech company based in Kaunas, Lithuania, at the intersection of science, clinical translation, and global health. We are focused on treating high-burden inflammatory conditions with precision cell/gene and exosome-based therapeutics. Our pipeline includes mesenchymal stromal cells for systemic inflammation, chondrocyte-based products for orthopedic repair, and exosome formulations for the wellness and skincare markets. We operate under a licensed tissue establishment and GMP-ready manufacturing facility. We’ve launched a multicenter clinical trial for Acute Kidney Injury across five EU countries. We're scaling rapidly toward global commercialization, with strategic plans across Europe, the Gulf, Asia, and North America.
The Role
As a Quality Control Specialist, you’ll be the final gatekeeper between production and patient delivery. You will carry out essential release testing and work closely with the manufacturing and quality teams to ensure all products meet strict clinical and regulatory standards.
Key Responsibilities
Perform Process Control, Stability, and Product Quality Control release testing on cell therapy and exosome batches
Maintain and execute validated QC protocols under GMP conditions
Engage in method validation procedures and prepare and update SOPs, validation protocols, and reports in both Lithuanian and English.
Ensure daily maintenance of laboratory equipment and accurately document all performed actions
Analyze data, document results, and support batch release
Collaborate with QA and manufacturing to troubleshoot issues and maintain compliance
Support environmental monitoring and trending activities as needed
Prepare for and support regulatory inspections and audits
What We’re Looking For
Degree in life sciences, biotechnology, or related field
Hands-on experience in a GMP or regulated QC environment
Strong understanding of sterility testing, viability assays, or microbial analysis
Detail-oriented with strong documentation and organizational skills
Able to work independently in a fast-paced, quality-driven setting
What We Offer
Competitive salary (>1500 Eur Gross) based on experience and qualifications
Private health insurance
Personal time off
Relocation support
Flexible work hours where applicable
Annual training and professional development support
Travel opportunities to clinical sites and partner facilities
Work in a licensed, purpose-built GMP facility
Why Join Us
Join a growing company with global ambitions
Be part of a team developing therapies for unmet global medical needs
Work in a purpose-built GMP facility with cutting-edge cell technologies
Gain exposure to clinical-stage operations and international trials
Shape the future of regenerative medicine from the inside out
To Apply
Send your CV and a short cover note to global@keli.eu