Senior CQV Lead - GMP/Regulatory Facility Upgrades

A leading recruitment firm is seeking a CQV Lead to oversee the CQV plan for a pharmaceutical manufacturing upgrade in Athlone. The successful candidate will coordinate cross-functional teams and ensure regulatory compliance. Applicants should have a degree in Engineering and at least 5 years of experience in C&Q within the Life Sciences, along with strong problem-solving and communication skills. This role offers an exciting opportunity to work in a dynamic environment and contribute to significant upgrades.