LSC have an exciting contract opportunity for QC Analyst to join a leading biotechnology company based in Dublin and make a real impact in the field of quality control. The Sr Associate QC position is perfect for those who have 3+ years biopharmaceutical QC experience with product testing in a GMP laboratory setting.. ABOUT THE ROLE: Perform a wide variety of assays, including routine and non-routine methods Evaluate and approve analytical data, ensuring compliance with cGMP standards Troubleshoot issues and communicate effectively with stakeholders Participate in audits, initiatives, and cross-functional projects ARE YOUR SKILLS A MATCH: Bachelor's degree in a Science-related field 3+ years of biopharmaceutical QC experience or related GMP laboratory experience Experience with analytical techniques such as pH, clarity, and osmolality testing Detail-oriented with excellent problem-solving abilities Self-motivated and capable of working independently Proven track record of meeting deadlines and working effectively in a team Apply today directly through this advert or contact Kathy Gillen on for further information. All applicants must hold a valid work permit and visa for at a least 12 months. LSC cannot provide work permit sponsorship.