Senior Qa
VivaBioCell S.p.A. in Udine, Italy, is seeking a Senior QA / Regulatory Affairs Specialist to ensure GMP and ISO compliance.
The role is hybrid, reporting to the Quality & Regulatory Department, and requires leading regulatory activities and supporting audits.
You will manage quality documentation, contribute to the ongoing improvement of the quality system, and collaborate with cross-functional teams to maintain compliance with 21 CFR Part 11 where applicable.
#J-*-Ljbffr
The role is hybrid, reporting to the Quality & Regulatory Department, and requires leading regulatory activities and supporting audits.
You will manage quality documentation, contribute to the ongoing improvement of the quality system, and collaborate with cross-functional teams to maintain compliance with 21 CFR Part 11 where applicable.
#J-*-Ljbffr