Quality Engineer

at  PhillipsMedisize

Your Job
Phillips Medisize, a Molex company, is currently seeking a Quality Engineer to support the development, validation and manufacturing of injection molded parts and assembly at our Hudson location.
Our Team
At Phillips Medisize, our goal is to create value for others. We empower every team member to hear, feel and see the quality in every action we take. By incorporating quality into the design of products and processes and predicting potential quality problems before manufacturing and delivering the product, we can create mutual benefit. The leading task of quality control involves enforcing the use of specified processes and materials, ensuring the qualification of operators and equipment, and making a series of planned measurements to determine if quality standards are being met.

WHO YOU ARE (BASIC QUALIFICATIONS)

• Bachelor’s degree in an Engineering related field OR 4 + years of direct Quality experience
• 1+ years Quality/Regulatory experience
• Legally authorized to work permanently in the United States for any employer without requiring a visa transfer or visa sponsorship

• Development and implementation of statistical incoming and in-process sampling/control plans
• Manage the qualification of processes performed by Phillips-Medisize suppliers; troubleshoot and lead corrective actions relating to supplier performance
• Initiate and manage customer/internal corrective actions using data based, structured, problem-solving methodology.
• Participate in AQP meetings representing quality, where appropriate
• Leverage their comparative advantage to actively participate in continual improvement/innovation, corrective action, and internal/external customer satisfaction
• Support quality functions of day-to-day manufacturing operations.
• Acknowledgment and understanding of all customer General Quality Agreements, General Quality Requirements and standards, as set by each customer
• Responsible for being a communication liaison between the customer and manufacturing facility
• Be a technical resource for the initiation and implementation of cost improvement plans on new and existing programs
• Manage acceptance of product & deliverables
• Coordinate new process techniques that improve overall job efficiencies
• Contribute to the design and development of components, assemblies, and devices for various industries
• Responsibility for Risk Management Process, including coordinating activities (PFMEA)
• Manage the design and process validation activities for development program