Summary: Our client is a biopharmaceutical company based in Waterford, seeking a Project Manager who will be responsible for their Automated Visual Inspection implementation project. Responsibilities: mAbs and LYO Automated Visual Inspection PPQs and Regulatory Submission Lead cross-functional, multi-site teams, in the introduction and business integration of the project. Translate customer needs into defined, approved project scope statements Work with functional managers to quantify resource requirements. Establish detailed project plans and drive execution of project tasks in line with agreed scope, schedule, and cost. Establish and execute a communication plan for the project and facilitate information flow between stakeholders and sites. Drive project risk identification, analysis, response, and implement & monitor mitigations to minimise impact to the project or wider business. Facilitate cost estimation to determine project budget and drive adherence to budget and forecast submission Project Stakeholder Management to analyze stakeholder expectations and their impact on the project, and to develop appropriate management strategies for effectively engaging stakeholders in project decisions and execution. The project manager is responsible for some project GMP documents in line with Waterford site procedures. Qualifications & Experience: Deree in Science, Engineering or equivalent Experience in biopharma industry, in a project leadership role Demonstrated experience in project/program management in drug substance or drug product Project Management certification, PMI, etc Working knowledge of cGMPs, GLP etc