CQV Engineer | Life Sciences (H/F)

La mission

As a CQV Engineer, you will play a key role in ensuring the quality, compliance, and validation of critical systems and processes within the Life Sciences industry. In this role you will play a key role in: - Developing and executing validation protocols (IQ, OQ, PQ) for equipment, utilities, and manufacturing systems in accordance with GMP guidelines and regulatory requirements. - Leading and supporting commissioning, qualification, and validation (CQV) activities across a range of projects, from new facility builds to equipment upgrades, ensuring timely and compliant delivery. - Collaborating with cross-functional teams including engineering, quality assurance, and operations to ensure validation activities are aligned with project timelines and client expectations. - Preparing and reviewing technical documentation such as validation master plans, risk assessments, deviation reports, and summary reports to ensure full regulatory compliance. - Supporting regulatory inspections and audits by providing technical expertise and ensuring all CQV documentation is audit-ready and meets the standards of bodies such as the FDA, EMA, and FAMHP.