Tecnico de Calidad III.

at  Medtronic

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

PHYSICAL JOB REQUIREMENTS

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

• This position will support Post-Market EU MDR remediation and implementation projects, to deliver quality parts, materials, and services, prevent defects, and allow Medtronic to provide customers with the highest quality and reliable products.
• Provides technical guidance and quality compliance for Supplier Quality engagement throughout EU MDR projects’ lifecycle, driving product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified in accordance to applicable industry standards, regulatory requirements, and customer requirements.
• Collaborates with EU MDR project teams to develop Purchasing Controls deliverables for product families being remediated for EU MDR including but not limited to: Supplier Segmentation (i.e., feature/product quality impact assessment), Production Part Approval Process or equivalent (i.e., product qualification), Supplier Change Control, Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, Control Plans, etc.
• This position will also support site Supplier Quality if or when employee’s capacity allows.
• Provides technical support to engineers to achieve improvements in cycle-time, yield, unit cost, quality, safety and compliance of production and operations processes and products.
• Monitors instruments and equipment and collects operating data, including calibration, inspection, testing and repair activities, to assist in making on-line adjustments to instruments, equipment, or products.
• Analyzes and resolves malfunctions and deviations of instruments and control systems to identify and resolve problems.
• Conducts, analyses and prepares reports using metrics from salvage tracking, trending, reporting and root-cause analyses.
• Maintains process designs to optimize process, equipment and facility use while conforming to standard operating procedures (SOPs) and Good Manufacturing Practices (GMPs)