Job Title:Quality Auditor – P2Location:Tipperary, IrelandContract Type:Fixed Term Contract- Hybrid/ Day roleRole DescriptionThe contractor will be a member of the Quality Assurance team, supporting GMP compliance and quality activities within a regulated pharmaceutical environment. The role involves reviewing documentation, conducting audits, and ensuring that processes and products meet defined quality standards and regulatory requirements.Key ResponsibilitiesReview and approve production, analytical, and packaging documentation to ensure compliance with SOPs, GMP, and regulatory requirements.Communicate and collaborate with cross-functional teams to resolve issues and facilitate compliance.Support product recalls, stock recoveries, and other quality-related actions as needed.Identify compliance gaps and recommend improvements for continuous quality enhancement.Create, update, and maintain Standard Operating Procedures (SOPs).Perform and review investigations, change controls, deviations, complaints, and CAPAs.Assist with induction or onboarding of new team members, if required.Compile and interpret data for reports and presentations.Conduct audits of procedures, data, facilities, equipment, and systems (including computerized systems) to ensure regulatory compliance.Stay up-to-date with current Good Manufacturing Practice (cGMP) and regulatory requirements.Perform any additional tasks assigned by the manager or supervisor.Experience, Knowledge & SkillsDegree in an Engineering or Science discipline or equivalent industrial experience in a regulated environment.Knowledge of GMP, quality systems, and regulatory requirements.Strong analytical and problem-solving skills.Excellent communication and interpersonal skills for effective cross-functional collaboration.Attention to detail and ability to maintain high-quality standards under strict regulatory requirements.Qualifications & EducationBachelor's degree in Engineering, Science, or a related discipline or substantial relevant industrial experience.Prior experience in a pharmaceutical or regulated manufacturing environment is preferred.