Summary from listing
Guerbet is hiring a Validation Team Lead to lead the Validation Department and manage validation activities for manufacturing, laboratory, utilities, facilities, cleaning, and computer systems. The role oversees IQ/OQ/PQ and revalidation programs, validation protocols and documentation, audits, change controls, risk assessments, regulatory compliance, project planning, and internal and external validation staff and contractors. It requires a BS degree in engineering or life sciences, 10 years of pharmaceutical validation experience, 8 years of supervisory experience, and knowledge of cGMP, FDA, ICH, EMEA, and related regulations.
