Jobs in Turkey

Stembio (a Koc Holding/Koc Healthcare company) is a cutting-edge cGMP laboratory specializing in the production and preparation of cellular products such as MESenchymal Stem Cells (MSCs), exosomes, immunotherapy products, cord blood banking and tissue grafts. We are committed to delivering high-quality, regulatory-compliant cell therapy products through rigorous quality control and validation processes.

We are seeking a motivated and detail-oriented Junior CAR-T Manufacturing Expert (GMP) for Stembio to support the production of CAR-T cell therapies in a GMP-compliant environment.

This role involves executing and optimizing cell therapy manufacturing processes, ensuring adherence to cGMP regulations, and collaborating with cross-functional teams to maintain high-quality standards. This position offers an opportunity to contribute to cutting-edge cancer treatments while gaining experience in a fast-evolving field.

If you are passionate about CAR-T cell manufacturing and have the expertise to uphold the highest standards, we encourage you to apply!

• Master’s degree in Biology, Molecular Biology, Immunology, or a related scientific discipline.
• Minimum 2 years of experience in academia or industry; experience in a GMP laboratory is a plus.
• Strong understanding of GMP testing operations with expertise in T-cell biology.
• Previous experience in CAR-T cell manufacturing (R&D); GMP experience is preferred.
• Ability to work independently in problem-solving, conducting lab investigations, and implementing corrective and preventive actions (CAPA).
• Strong teamwork and communication skills, with the ability to thrive in a fast-paced, collaborative environment and quickly learn new technical skills.

• Perform routine CAR-T cell manufacturing operations under GMP conditions, ensuring adherence to quality and regulatory standards.
• Understand, evaluate, and ensure GMP compliance at every stage of the manufacturing process.
• Play an active role in establishing and optimizing GMP lab operations, contributing to process development and compliance improvements.
• Support and/or oversee method qualification, transfer, and validation, including protocol development and execution.
• Conduct routine sample testing (in-process, release, and stability) under GMP or non-GMP conditions, ensuring laboratory maintenance and data integrity.
• Analyze, review, and trend analytical results to ensure consistency and compliance with quality standards.
• Author, review, and revise SOPs, method validation/transfer protocols, and technical reports in alignment with regulatory and internal requirements.
• Maintain strict adherence to GMP/GLP regulations, ensuring high-quality manufacturing standards and compliance.

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