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Qc analyst

Dublin
Asset Recruitment
Qc analyst
Posted: 17h ago
Offer description

OverviewQC Analyst Our client is a leading pharmaceutical company committed to quality, innovation, and regulatory excellence.Role Overview: The QC Analyst (Analytical Chemistry) plays a key role in ensuring the quality and compliance of manufacturing processes and products outputs through advanced chemical analysis and quality control activities. This position contributes directly to the organization’s commitment to product integrity, regulatory compliance, and continuous improvement by applying deep technical expertise within a GMP-regulated environment.This is a 6-month contract role, with a 16/5 shift schedule and a shift premium.ResponsibilitiesIndependently execute advanced and complex chemical analyses to support quality control activitiesEnsure quality control processes comply with regulatory standards and internal quality systemsLead and support laboratory operations, including equipment qualification, routine maintenance, and troubleshootingProvide technical guidance, mentoring, and support to junior team membersDrive continuous improvement initiatives to optimize laboratory processes, efficiency, and complianceCollaborate across departments to troubleshoot and resolve complex problemsAdditional ResponsibilitiesManage quality control processes to ensure high standards of quality and regulatory complianceEnsure laboratory operations adhere to regulatory requirements, managing documentation and reporting effectivelyMaintain laboratory operations, including routine equipment maintenance and troubleshooting, to ensure smooth and efficient workflowPrepare detailed reports on quality control and manufacturing deviations, collaborating closely with Quality AssuranceEnsure proper functioning of laboratory instruments and equipment by establishing routine maintenance and troubleshooting protocolsImplement process improvements in quality control and laboratory operations to enhance efficiency and complianceMaintain thorough and accurate documentation in compliance with regulatory standardsQualificationsStrong expertise in analytical chemistry with the ability to perform complex analyses independentlySolid understanding of quality control systems and regulatory expectations (e.g., GMP)Advanced technical expertise to independently solve complex problemsExperience preparing technical documentation, deviation reports, and investigation summariesAbility to provide technical guidance, share knowledge, and strengthen team capabilitiesEffective communication and collaboration skills across departments
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