Job Title: QC AnalystLocation: Cashel, Co. TipperaryAbout the CompanyA global leader in pharmaceutical manufacturing, our Cashel site is dedicated to innovation and quality. We ensure the highest industry standards while delivering life-changing products worldwide.Job SummaryWe are hiring a QC Analyst to support laboratory setup, conduct essential testing, and ensure compliance with cGMP standards. This role offers an opportunity to work in a fast-paced environment and contribute to key quality operations.Key ResponsibilitiesSupport laboratory setup and equipment qualification.Prepare and review laboratory procedures, protocols, and reports.Perform QC testing in line with SOPs, cGMP, and regulatory requirements.Conduct method verification, validation, and technical transfers.Manage laboratory consumables and ensure proper tracking.Assist in regulatory audits and maintain audit readiness.Collaborate with cross-functional teams, including technicians, operations, and warehouse staff.Maintain compliance with Good Documentation Practice (GDP) and Quality Management Systems (QMS).Ensure EHS standards are upheld in the laboratory.Liaise with CROs and conduct audits as needed.RequirementsDegree in Chemistry, Biochemistry, Pharmaceutical Science, or related field.Experience in a cGMP-regulated QC or ARD laboratory.Strong understanding of method validation, technical transfer, and regulatory compliance.Excellent documentation, reporting, and communication skills.Ability to manage multiple tasks in a fast-paced environment.BenefitsCompetitive salary & annual bonusFlextime options for work-life balanceLaya Healthcare for employee, partner & dependents5% employer-matched pension planEducational assistance & career development supportInterested? Apply now and be part of an innovative and high-performing team!#L1-DB4
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