MSC Production Specialist

Location: On-site

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 an MSC Production Specialist, you’ll manufacture GMP-grade MSCs and support the production process from cell isolation through final product formulation. Your work will directly support our clinical and commercial pipelines.

You’ll also contribute to ongoing process improvement and support the development of new MSC technologies and protocols.

Key Responsibilities

  • Manufacture mesenchymal stromal cells (MSCs) in GMP conditions

  • Perform cell isolation, expansion, harvest, and formulation steps

  • Complete GMP documentation for each batch (logbooks, batch records, deviations)

  • Collaborate with Quality and Operations for batch release and troubleshooting

  • Assist in technology transfer and scale-up activities

  • Support cleanroom operations and aseptic technique adherence

  • Participate in internal training and validation of production protocols

What We’re Looking For

  • Degree in cell biology, biotechnology, or related field

  • Practical experience working with cell cultures, ideally in a GMP or cleanroom environment

  • Familiarity with aseptic techniques, cleanroom practices, and sterile media handling

  • Understanding of GMP principles and documentation workflows

  • Hands-on, reliable, and committed to product quality

  • Team player who thrives in a structured and high-impact setting

What We Offer

  • Competitive salary (>1500 Eur Gross) based on experience and qualifications

  • Private health insurance

  • Personal time off

  • Relocation support

  • Annual training support for technical and regulatory certifications

  • Access to cutting-edge GMP manufacturing systems and cleanrooms

  • Real involvement in clinical-stage product development

  • Exposure to European and global trial activities

Why Join Us

  • Your hands will produce the therapies that go directly to patients.

  • You’ll work at the center of a GMP facility with live clinical and commercial products.

  • You’ll learn from real-world manufacturing while helping build the protocols for tomorrow.

  • You’ll be trusted, trained, and challenged—every batch, every day.

  • You’ll shape the future of cell therapy with a team that moves fast and builds precisely.

To Apply

Send your CV and a short note of interest to: global@keli.eu