.About UsSpellman High Voltage Electronics Corporation, a family owned business for over 75 years, takes pride in powering progress in health, security and quality of life. We are key partners with the world's leading medical devices, semiconductor, scientific analytics and industrial systems manufacturers. When they want to push the limits of what's possible with high voltage applications, they turn to us to make it happen.While Spellman is not a household name, our products are used to make and often power many of the most advanced technologies that make modern life possible. With design and manufacturing sites in North America, Europe and Asia, we have become the preferred provider of high voltage power solutions for OEMs pushing the boundaries of technology around the world by designing and producing the products they need to power progress.Objective / Purpose of the Function:Be accountable to the Quality Management System and ensure compliance with the latest versions of industry, customer, ISO's standards, statutory and regulatory applicable requirements.Update and maintain the site's Quality Management System and the Management Review process, including coordinating and leading the meetings between all interested parties to resolve concerns, issues and reaching agreements. Continuously update, improve and develop internal QMS enhancing processes, protocols and procedures as necessary.Acting customer liaison for all customer visits and audits to the site, including the review and assessment of customer satisfaction derived from these.Develop and execute strategic plans to provide support needed to all functional departments and continuously improve knowledge, skills and learning.Strategically develop the product, process, 6s, ESD audit plans to monitor the effectiveness of the Spellman Quality Management system. Lead the CAPA verification process.Continuously oversee the Global/industry requirements and proactively communicate to the top management any deviation or risk identified.Review, establish and assess department key process indicators and provide actions when these are not achieved.Submission and execution of site level continual improvement projects (e.G., product, process, controls, procedures, software, systems, tools, trainings, social, psychological, environmental, etc.)Principal Responsibilities:Plan and execute internal and external audits, addressing findings promptly.Identify inefficiencies and implement improvements to optimize quality processes.Lead quality initiatives and cross-functional teams effectively.Anticipate potential issues and develop solutions before they impact quality.Collaborate effectively with internal and external stakeholders to support quality objectives.Ensure staff are trained on QMS procedures and understand their role in maintaining quality.Stay updated on industry trends and adapt the QMS accordingly