I'm currently recruiting for a Quality Officer role with one of our Athlone based clients.
This is a permanent role with a strong salary and benefits package, and a hybrid working model. Key Responsibilities Quality Assurance responsibility for change control, complaints & CAPA management within the organizationMaintain Quality Management System processes in line with company proceduresMonitor and support the completion of quality tasks e.g.
change control and CAPA actions, internal audits, etc.Document control, including issue and archiving of documentationReport out key process indicators (Change Control, Deviations, Complaints, CAPA, etc.
)Aid in the investigation of deviationsEnsure root causes are appropriately identified, trended and corrective actions are verified for effectivenessMonitoring the quality performance of contract manufacturers and laboratoriesReview records for completeness and compliance with GMP/GDP requirements and internal proceduresTake on any further reasonable responsibilities as assigned to you by your managerQualifications / Experience Bachelor's degree in any Life Science, Biomedical, or related field (or equivalent work experience)Minimum of 2 years' experience quality compliance experience within the pharmaceutical industryGood understanding of cGMP, 21 CFR Part 211, and related regulations associated with pharmaceutical productsAttributes Must possess excellent organizational skills, planning, scheduling, the ability to follow and help drive complex processes, procedures and systemsWillingness and capability to handle multiple responsibilities that are required in a start-up organizationHigh proficiency in MS OfficeMust maintain a high level of professionalismMust have effective verbal, written and interpersonal skillsAbility to work in collaborative and independent work situations and environments with minimal supervision
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