**This is a 12 month onsite role in Limerick with full Stryker benefits.**Previous industry experience desired. Experience in interacting with regulatory agencies (FDA, MoH, TUV, etc.) desired. Familiarity with ISO 13485, GDP, GMP desired. Strong knowledge of Quality Concepts (e.g. Risk Management, CAPA, Audits, Statistics). Must possess strong communication, project management and influencing skills as well as have the ability to manage multiple tasks simultaneously.Ability to represent Quality function with project teams.Strong interpersonal skills, written, oral communication and negotiations skills. Highly developed problem-solving skills. Strong analytical skills.Demonstrated ability to work independently and as part of cross-functional teams. Experience in working in a compliance risk situation. Support and Drive Human Factor practices, familiarity in the science of Human Factor identification, reduction, and mitigation. Develop understanding of risk management practices and concepts and applies knowledge to manufacturing operations. * Level 8 Degree in Science or Engineering* 2 years experience in Quality
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