OverviewJenn Dinan at Wallace Myers is hiring a QC ANALYST to work on contract at our client's Global Biopharma site in WATERFORD. Please only apply if you are ALREADY eligible to work in the ROI. This is a contract vacancy, so a valid work permit is a pre-requisite - you must have 12 months + permission on your valid work permit. Contact Jenn Dinan to discuss further and send your CV via the link provided.Contract Length: 12 MonthsDesired Start Date: ASAPPay Rate: per hourWorking hours: 8am - 4.30pmThe Quality Control (QC) Analyst is responsible for sample receipt, testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations. Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation. The Quality Control Operations group supports Laboratory Investigations, Deviation Investigations, CAPA support, Training, and Change Controls. Quality Control Validation Support consists of the Method Validation Group and the Equipment Qualification Group. Quality Control is also responsible for assisting in site-wide studies and projects.All applications will be treated with the strictest of confidence.At Wallace Myers International Recruitment Agency we specialise in sourcing professionals for key industries and services. See our website for more details.Privacy Policy: By applying for this role you are agreeing that your details will be stored in our database and may be considered for similar future positions. For more info seeSkillsQuality Control, Pharmaceutical, Laboratory, GMPBenefitsPaid holidays, gymMAIN ACCOUNTABILITIES: Executing analytical testing in a timely manner, ensuring adherence to the committed scheduled plansPerforming tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records related to these tasksRecording all expected raw data, calculations, information related to tasks, to comply with cGMP and data integrity requirementsEnsuring that the analyst is trained and qualified to the assigned analytical testing that requires qualificationPerforming the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plansInforming the manager of any quality or HSE event (deviations, OOX, etc.) in a timely manner to ensure investigations and impact assessment are performed appropriatelyParticipating actively in investigations where involved to ensure investigations and impact assessment are performed appropriatelyExecuting assigned CAPAs related to remediation plans and continuous improvements. Ensuring that lab facilities and instruments are kept in a quality and safety status to ensure they can be used appropriately.
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