16 set - Monza
Experteer Italy
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 processesImplement and manage documentation (protocols, reports, methods) per GMP/SOPs/guidelinesSupport instrument calibration according to SOPs and protocolsDegree in Biotechnology / CTF or other Scientific fieldPrevious laboratory experienceGMP QC lab experience is a plusProficiency in biotech/biochemical analyses (PCR/qPCR, sequencing, ELISA, SDS-PAGE)Experience with HPLC and CGE is a plusEnglish and Italian professional knowledge#J-18808-Ljbffr
18 set - Italia
Sitly
18 set - Porcia
Synergie Italia
18 set - Italia
Sitly
18 set - Italia
Altro