For our client, an international company based in Stein, we are looking for a Process Automation Engineer to support growth projects and ensure the successful delivery of automated systems. The Process Automation Engineer plays a key role in the delivery of growth projects by bridging process expertise and engineering execution. Acting as the technical link between Manufacturing, MSAT, and Engineering, this role ensures automation strategies and system
For our client, an international company based in Stein, we are looking for a Process Automation Engineer to support growth projects and ensure the successful delivery of automated systems. The Process Automation Engineer plays a key role in the delivery of growth projects by bridging process expertise and engineering execution. Acting as the technical link between Manufacturing, MSAT, and Engineering, this role ensures automation strategies and system
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
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &