Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Senior Associate QC will work under minimal supervision, responsible for one or more of the following activities in QC including analytical testing in process, stability, and finished products. In-depth HPLC experience with Empower Software, some protein concentration testing background with strong GMP lab environment experience. Duties: Testing of in process, stability and finished product samples. eg HPLC, CE, SDS-PAGE, IEF analytical testing, characterization and sample and data management. Review and authorisation of Lab Data Support Analytical Technical Transfer activity testing reports and documentation. Document review/updates when required. Equipment Calibration, Maintenance and Trouble Shooting. Method Validation/Verification. Training of QC Chemistry Laboratory colleagues. Laboratory Investigation support Laboratory Housekeeping and maintaining GMP standards. Assisting in regulatory audits. Education and Experience: Hold a third level qualification (Degree/Diploma) in Biochemistry, Chemistry, Biology Biotechnology or similar Scientific Subject. 5+ years relevant experience in a pharmaceutical/healthcare environment. Have strong technical writing skills. Be detail oriented, self-motivated with good troubleshooting and problem solving abilities. Experience with analytical techniques such as HPLC, CE, SDS-PAGE, IEF testing would also be advantageous. If interested in this posting please feel free to contact Avishek Singh at Avishek.sing or for further information.