Job Title: QC Analyst – Quality Operations LaboratoryLocation: Carlow-Onsite, IrelandRole Overview:As a QC Analyst, you will perform and review a range of analytical techniques as part of routine and non-routine testing to ensure that processes and products comply with regulatory and quality standards, facilitating product release. You will report to the QC Manager and work closely with cross-functional teams to maintain high-quality standards and compliance.Key Responsibilities:Execute day-to-day laboratory-based duties as part of the QC team.Review and approve batch documentation, deviations, and investigation reports.Support audit readiness and compliance with cGMP, GDP, and regulatory requirements.Participate in internal and external audits and inspections.Perform and review analytical testing including HPLC, immunoassays, cell-based assays, and compendial methods.Support laboratory investigations, trend analysis, method validation, and equipment qualification.Drive continuous improvement, conduct root cause analysis, and resolve system or equipment issues using standard methodologies (e.g., FMEA, Fishbone, 5 Whys).Ensure effective communication of testing progress, deviations, and results within QC team meetings.Work collaboratively to foster a safe, compliant, and high-performing laboratory environment.Qualifications & Skills:Bachelor's degree or higher in a science-related discipline preferred.2-3 years of experience in a QC laboratory within the pharmaceutical industry.Knowledge of cGMP, GDP, and other regulatory requirements.Familiarity with laboratory quality systems and electronic tools (LIMS, SAP, MES).Strong attention to detail, communication, and teamwork skills.Immunoassay and cell culture experience is desirable.Understanding of Lean Six Sigma methodology is a plus.Additional Requirements:Onsite role only (remote or hybrid not applicable).Must be willing to work a 4-cycle 12-hour shift pattern.