About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
Role OverviewWe are seeking an experienced Privileged Access Management (PAM) Subject Matter Expert (SME) to lead the design, implementation, and operational maturity of PAM capabilities across a complex enterprise environment.This role is responsible for establishing and enforcing robust security controls for privileged identities, ensuring compliance with regulatory and security standards, and embedding PAM as a core enterprise security capability.The
Role OverviewWe are seeking an experienced Privileged Access Management (PAM) Subject Matter Expert (SME) to lead the design, implementation, and operational maturity of PAM capabilities across a complex enterprise environment.This role is responsible for establishing and enforcing robust security controls for privileged identities, ensuring compliance with regulatory and security standards, and embedding PAM as a core enterprise security capability.The
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