Jenn Dinan at Wallace Myers is hiring a QC ANALYST to work on contract at our clients 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 on to discuss further and send your CV via the link provided Contract Length12 Months Desired Start Date: ASAP Pay Rate: per hour) Working hours 8am -4.30pm The 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. MAIN ACCOUNTABILITIES: Executing analytical testing in a timely manner, ensuring adherence to the committed scheduled plans Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and data integrity requirements Ensuring that he/she is trained and qualified to the assigned analytical testing that requires to be qualified Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plans Informing his/her manager of any quality or HSE event (deviations, OOx,) in a timely manner to ensure investigation and impact assessment are performed appropriately Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately Executing assigned CAPAs related to remediation plans, continuous improvements Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately. 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 see Skills: Quality Control Pharmaceutical Laboratory GMP Benefits: paid holidays gym