In this role you will join the GMP QC lab focused on mRNA processes, performing analyses on samples and ensuring compliance with GMP and SOPs. You will support instrument calibration and documentation, contributing to quality control in a fast-moving biotech environment. The position is on a two-shift system (1st/2nd) with Monday–Friday work and occasional flexibility to meet business needs. You will work closely with cross-functional teams to uphold product quality. This is a hands-on opportunity to contribute to critical biopharma workflows.
- Perform GMP-compliant analysis on incoming, in-process, and release samples for mRNA manufacturing processes
- Implement and manage documentation (protocols, reports, methods) per GMP/SOPs/guidelines
- Support instrument calibration according to SOPs and protocols
- Degree in Biotechnology / CTF or other Scientific field
- Previous laboratory experience
- GMP QC lab experience is a plus
- Proficiency in biotech/biochemical analyses (PCR/qPCR, sequencing, ELISA, SDS-PAGE)
- Experience with HPLC and CGE is a plus
- English and Italian professional knowledge
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