JOB REQUIREMENTS: Your Job The Phillips-Medisize Global Technical Services Team is seeking a Validation Engineering Technician to support operations in our Hudson and Menomonie, Wisconsin sites. This role will Assist Validation Engineers and Quality Engineers and/or teams in the completion of validation projects for our MPS division. Support manufacturing in the effort to ensure optimum validation of projects/programs to meet customer, regulatory and manufacturing requirements. Our Team Phillips-Medisize, a Molex Company is an end-to-end provider of innovation, development, and manufacturing solutions to the pharmaceutical, diagnostics and medical device industries. What You Will Do Work with project teams to draft protocol and test case documents. Help to qualify manufacturing equipment to be used in validated processes. Draft deviations and develop summary reports for project wrap ups. Lead low-complexity validation projects. Manage multiple projects and/or challenging projects. Learn and deploy SAP related tools and deliverables associated with validation deviations, customer approvals, and document approval workflows. Suggest creative validation process improvement opportunities. Provide statistical analysis support to sites and Validation Engineers. Assist with creating, updating, and training on WI, SOP and other necessary documents needed to perform validation work. Support global rollout of Global Validation requirements and on-site or desk audits of Phillips-Medisize sites to ensure compliance to the global standards. Set up and manage SharePoint as a global point of contact containing validation best practices information and examples of executed validations. Develop content for the site as needed. Travel to other Phillips-Medisize and vendor sites (up to 10%). Other duties as assigned Safety/Environmental: Where applicable, individual is pre-planning safety into work activities to improve performance, proactively identifies safety concerns, complies with Environmental Management System Program SOP\'s/WI, policy & Program elements and encourages responsible use of resources Who You Are (Basic Qualifications) Associates or technical degree from an accredited college or university OR 3 + years in a regulated manufacturing environment 1-year minimum experience working in a regulated manufacturing environment What Will Put You Ahead Bachelor\'s degree Experience working in a medical manufacturing environment Strong organizational, and problem-solving skills Excellent communication skills and ability to create technical documents Competence with Microsoft Outlook, Word, Excel, and PowerPoint Good project management skills Leadership skills and self-motivation Working knowledge of medical device assembly and inspection equipment Drive to complete projects on time every time This position does not qualify for VISA Sponsorship In order to comply with U.S. export... For full info follow application link. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/4B291CFC29984C5F