CQV Engineer: Pharma Validation
CAI is seeking a qualified CQV specialist in Italy to support commissioning, qualification, and validation of pharmaceutical facilities, utilities, and equipment.
You will write and execute protocols, develop summary reports at client sites, and manage the CQV documentation lifecycle from SLIA to OQ, while providing cGMP leadership for our Life Sciences clients. Travel to sites in Italy and abroad is expected.
You will write and execute protocols, develop summary reports at client sites, and manage the CQV documentation lifecycle from SLIA to OQ, while providing cGMP leadership for our Life Sciences clients. Travel to sites in Italy and abroad is expected.