LSC have a great contract opportunity for a QC Senior Analyst to join a biopharmaceutical company in Dublin focused on serving patients with severe and ultra-rare disorders through the innovation, development and commercialization of life-transforming therapeutic products. If you have 4 years of experience working in the biochemistry, pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: Perform all lab functions in compliance with cGMP. Follow written procedures for the following tests, as trained and qualified: Gel electrophoresis (SDS-PAGE, IEF). ELISA and plate-based assays (potency and residual assays such as HCP and ProA). Stability scheduling and testing. Recognize and report aberrant test results and sample conditions. Provide QC SME and day to day technical guidance to QC biochemistry analysts. Lead and complete execution of investigations/CAPAs in a timely manner. Provide lab support including reagent preparation, cleaning, and routine equipment maintenance. ABOUT YOU - ARE YOUR SKILLS A MATCH? BSc in Chemistry or a biological science 4-7 years' experience with experience in gel electrophoresis (SDS-PAGE, IEF), ELISA and plate-based assays A working knowledge of the cGMP QC laboratory environment, and equipment associated with testing of biopharmaceutical products. Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply! Apply via this advert or contact Kathy Gillen at LSC on if you have any more questions about this role! Skills: QC Senior