GMP Auditor
Zentiva Zobrazit všechny práce
- Praha 10
- Trvalý pracovní poměr
- Plný úvazek
We are looking for an experienced GMP Auditor to join our Corporate Quality team. In this key role, you will help govern critical quality incidents, ensure consistent escalation and reporting across Zentiva, and strengthen compliance with global regulatory and GMP requirements. You will act as a trusted quality partner across manufacturing sites, affiliates, and external partners.Main ResponsibilitiesLead and manage quality escalations, including assessment, categorization, mitigation, and Health Authority communicationProvide expert guidance on external audits and regulatory expectationsPlan, conduct, and document independent audits in compliance with Zentiva’s Quality System and applicable regulationsAct as a liaison between Quality and business stakeholders to ensure effective issue resolutionSupport regulatory surveillance and Health Authority reportingDesign and conduct risk-based external audits (CMOs, suppliers, service providers)Drive continuous improvement of quality systems, processes, and documentationContribute to corporate quality governance, training, and knowledge sharingTraveling within Europe up to 70%RequirementsUniversity degree in pharmacy, chemistry, life sciences, engineering, or related field5+ years of experience in GxP / Quality, within the pharmaceutical industry is requiredStrong knowledge of GMP, regulatory requirements, audits, deviations, and change controlExperience with internal and external audits, and inspectionsExperience working in production siteExcellent analytical, communication, and stakeholder management skillsAbility to work independently in a complex, matrix environmentFluent English (written and spoken)