An excellent opportunity for a QC Analyst with 1 - 2 years analytical testing experience within a cGMP regulated pharmaceutical lab. significant experience performing HPLC, KF, FTIR required. Experience working with raw materials within a pharmaceutical company is preferred.** 12 month contract located in North Dublin.Responsibilities will include (but not limited to):Performing QC testing (TOC, pH Conductivity) of water samples. Performing analysis of Raw Materials including HPLC, KF, UV, IR and wet chemistry techniques. Completion in a timely and accurate manner of laboratory documentation as directed by the QC Manager.Assisting in updating and issuing documentation, including SOPs, as required.Performing routine data analysis, assist in the investigation of OOS results, perform trending analysis and writing investigation reports.Accurately documenting laboratory work.Execute and assist in technical transfer and co-validation activities.Sample management activities- ensuring chain of custody is maintained using CIMS and LIMSAssisting with qualification of laboratory instruments.Data review based on demonstrated proficiency on assays.Qualifications and Experience required:Previous experience performing QC testing within a regulated pharmaceutical or biopharmaceutical laboratory is required.experience performing HPLC, KF, FTIR, wet chemistry tests within the pharmaceutical industry.Proficient user of Empower software.BSc. in Science/Chemistry/Biochemistry or related discipline.The successful candidate must demonstrate an ability to work independently and recognize anomalous trends or results.Must demonstrate problem solving ability, as well as the ability to prioritize objectives from multiple projects and adhere to scheduled timelines.Excellent communication and the ability to work in a team based collaborative environment are required.