JOB REQUIREMENTS: Your Job 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. Our Global Technical Services Team is seeking a Quality Engineering Technician to support operations in our Hudson, WI. Travel between the other WI sites will be expected based on where the resources are needed. Mileage reimbursement will be provided per the Molex policy. This role will Assist Validation Engineers and Quality Engineers in the completion of Quality and Process Validation projects. It will also support manufacturing in the effort to ensure optimum completion of programs to meet customer, regulatory and manufacturing requirements. Our Team Phillips Medisize, a privately owned, global CDMO, collaborates with industry leaders and innovators to design and manufacture drug delivery systems, medical devices and diagnostic tools that save and improve the quality of life for millions of patients annually. With our dedicated team of 6,000+ employees and 29 development and manufacturing sites across three continents, Phillips Medisize shares our customers\' mindset that every product is critical to a healthcare provider and their patients somewhere in the world. What You Will Do * Support the Quality team and all AQP processes by developing product quality criteria and defining new product deliverables. * Work with project teams to draft validation documentation. * Help qualify manufacturing equipment to be used in validated processes. * Use SAP for quality and validation document approval workflows. * Suggest creative quality and validation process improvement opportunities. * Support on-site or desk audits of Phillips-Medisize sites to ensure compliance to our global Validation 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%). Who You Are (Basic Qualifications) * Associate\'s or Technical Degree * 1+ year experience working in a regulated manufacturing environment; medical or pharmaceutical manufacturing preferred What Will Put You Ahead * Strong organizational and problem-solving skills * Excellent communication skills and ability to create technical documents * Good project management skills * Leadership skills and self-motivation * Competence with Microsoft Outlook, Word, Excel, and PowerPoint * Working knowledge of medical device assembly and inspection equipment * Statistical analysis experience This position does not qualify for VISA Sponsorship. At Koch companies, we are entrepreneurs. This means we openly challenge the status quo, find new ways to create value... For full info follow application link. Equal Opportunity Employer, including disability and protected veteran status. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/EDBDD521B46648AE