Job Title:QC Material Management Analyst – ContractDuration:12 monthsLocation:Cruiserath, Dublin – HybridHourly Rate:€19.72 per hour – PAYE engagementThis role does not offer sponsorship.Job Description:The QC Material Management Analyst will join the QC Site Operations team at a leading biopharmaceutical facility in Cruiserath, Dublin. Reporting to the QC Material Management Supervisor, this role is responsible for performing raw material testing, in-process sample analysis, and laboratory duties in compliance with cGMP regulations.Responsibilities:Perform QC testing of water samples (TOC, pH, Conductivity).Conduct raw material analysis using techniques including HPLC, KF, UV, IR, and wet chemistry.Complete laboratory documentation accurately and on time.Ensure compliance with Standard Operating Procedures (SOPs) and registered specifications.Author and review laboratory documentation, including SOPs.Perform batch paperwork reviews and reconcile laboratory analyses.Investigate and document out-of-specification results in line with site procedures.Support technical transfer of new projects.Assist with deviation and out-of-specification investigations using the Infinity system.Manage samples, maintaining chain of custody using CIMS and LIMS.Stay up to date with corporate and industry compliance requirements for laboratory operations and aseptic manufacturing.Carry out any additional duties as directed by the Lab Supervisor.Requirements:Third level qualification (Degree) in Chemistry, Biology, or a related discipline.2–3 years' experience in a pharmaceutical/healthcare laboratory or related technical function.Strong written and verbal communication skills.Ability to work effectively in a collaborative, team-based environment.