LSC have a great opportunity for a Senior QA Specialist to join a South Dublin-based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 7+ years of experience in construction management / engineering within the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you! ABOUT THE PROJECT Key Responsibilities : Provide QA leadership during facility design, and layout Provide overall quality direction for processes and procedures associated with project Lead QA review and approval of URS, DS, QRAEs, and IQ / OQ / PQ protocols and reports. Act as the Quality point of contact and decision-maker during validation execution activities, ensuring all activities comply with regulatory and company standards. Ensure Computerised System Validation (CSV) meets regulatory and data integrity standards. Ensure validation documentation is robust, traceable, and inspection-ready. Drive risk assessments and mitigation strategies for new equipment and processes. Provide QA oversight for Change Controls, CAPAs, and Deviation Investigations. Ensure all activities align with Amgen's safety standards, SOPs, and regulatory expectations. Support a safe working environment by adhering to all environmental health and safety practices, rules, and regulations. Preferred Qualifications :
Senior Qa Specialist • Dublin, Leinster, Republic of Ireland