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Global Quality ManagerINEOS has an exciting opportunity for a Global Quality Manager to join our Composites business. INEOS has 13 global sites: 6 in the US, 1 in Brazil, 4 in the EU, and 2 in China, with our main offices in Dublin, OH, US, and Barcelona, Spain. This position would be based out of one of our main locations: Dublin, OH, US, or Barcelona, Spain.
Job FunctionThe Global Quality Manager is considered a global expert, senior-level individual contributor for INEOS Composite to manage, maintain, and improve all Quality activities related to ISO9000 certification, technology implementation, complaint management, and implementation of improvement plans incorporating best practices. This role involves evaluating and implementing improvements to the Global Quality process to achieve the agreed safety, quality, and business targets within the financial budgets and applicable laws. The Global Quality Manager reports to the Vice President, Operations.
Key ResponsibilitiesMaintain the Global ISO9000 Certification by evaluating and improving the overall certification process, including the Management Review.Develop relationships with all Regional Managers, Plant Managers, Quality Managers, and Business Managers to determine local Quality goals, work through local Quality issues, and develop Global Quality Goals and Objectives.Provide leadership, Quality, and operational guidance on Quality issues.Be the point of contact for all customer complaints and issues.Establish working relationships with global customers as the lead global quality contact.Evaluate and improve the complaint system and process for the future.Manage all Quality-related databases (IDMS, QMS, QIM, etc).Evaluate database systems and processes and improve for the future.Using the Culture of Prevention mindset, evaluate all Global Quality systems and processes within INEOS Composites to improve and/or implement quality, business, and operational excellence across sites.Work with regional leadership and technology group(s) on the implementation of the latest technology for safer and lower-cost manufacturing.Become a resource for the coordination and execution of AsCare and 20P Auditing.All new hires will be required to become fully vaccinated against COVID-19 prior to their first day.
QualificationsBachelor's degree required; Master's preferred.Quality certification(s) preferred.ISO9000 experience/certification(s) required.Manufacturing experience required; strongly preferred chemical or related industry experience.Proficient computer skills required.Analytical and problem-solving skills.Ability to influence across the organization and accomplish through others.Demonstrated ability to collaborate effectively with and lead cross-functional teams.Ability to effectively prioritize and manage multiple projects.Strong communication (written and verbal) and interpersonal skills are a must.Detail-oriented and organized.This job will have expected travel that at times could be up to 25%, including international travel.
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