William Briceño Email & Phone Number

Provide direction to employees regarding the quality engineering and quality control processes.Supervise Quality Engineers, also supervise Inspectors and Technicians● Establish an environment focused on continual improvement.● Participate in audits (internal & external) and regulatory agency inspections.● Responsible for maintaining quality systems requirements through procedures, work instructions and documentation including: ○ Quality Engineering○ Quality Control○ Nonconforming materials○ Product Investigation/failure analysis● Quality engineering oversight of finished good activities.● Batch record review/release and review of other documentation from medical device manufacturing and packaging suppliers, and ensure that all activities comply with quality requirements and Nevro procedures.● Follow-up with local suppliers on deviations and non-conformities for materials and components received. Also, will work with supplier quality at headquarter to follow-up on non-local suppliers on deviations and non-conformities.● Quality assessment of changes to manufacturing processes, materials, and procedures and ensure applicable and appropriate documentation are generated.● Provide direction to manufacturing processes and personnel.● Work with cross-functional team to implement comprehensive preventative maintenance work instruction as well as revalidation requirements.● Review and disposition Non-conformance reports. Perform Root Cause analysis in order to determine corrective and preventive action activities.● Evaluate risk, manage risk assessment activities and create associated documentation.● Lead Supplier management and Supplier Quality activities for local suppliers.● Responsible for performing Quality assessment of changes to manufacturing processes, materials, and procedures and ensure applicable and appropriate documentation are generated.

Provide support and subject matter leadership for the production/service controls processes, and measurement/analysis/improvement processes, of the global quality management system. Support and directly participate in the development, implementation, and establishment of global quality system policies, procedures and processes. Facilitate and track various projects in support of global quality system objectivesSupport project execution by participating in, or leading cross-functional teams over multiple sites and time zones.Develop and continuously improve quality processes in the role of process owner. As a process owner, provide stewardship over assigned processes to ensure compliant and effective quality systems and processes. Provide quality engineering technical support for quality processes, for example; data analysis and trending, verification and validation testing, calibration and preventive maintenance, or statistical techniques. Manage monthly/quarterly/annual key process indicators (KPIs) utilizing a business intelligence application, generating metrics, and facilitating data analysis and review. Leading CAPA/ PA Investigation for Quality System Issues & ImprovementPreparing Rework Protocols or memos for NCRs

Costa Rica

Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.Lead the engineering group and technicians, generating strategies to meet the expectations and goals of the company.Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensures processes and procedures are in compliance with regulations.Adapts machine or equipment design to factory and production conditions.Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.

Costa Rica

Engineer responsible to improve Product Quality, Customer Service and reduce Costs by optimizing current Manufacturing Equipment, Manufacturing process or managing new Equipment Development Projects Demonstrate technical knowledge to innovate, develop and/or support processes, procedures, tooling and/or automation in the manufacturing process.Communicate frequently and effectively with core team members, clients and stakeholders. Demonstrating Technical Knowledge for Relocation, Installation, Start-up, Qualification, Training and Sustaining of Equipment related to Product / Process. Creating and understanding documentation as it relates to technical discipline (e.g., specifications, validations, prototypes, technical manuals, equipment drawings/BOMs). Applying Project Management Tools to effectively ensure that projects and goals meet overall performance, schedule and cost requirements. Actively participates in cross-functional business improvement opportunities.

Engineer responsible for improving the manufacturing process and to work collaboratively to develop, transfer and apply new technologies, products, materials, manufacturing processes or equipment. Responsible for collecting and analyzing, testing and research data to establish the technical specifications for designing or modifying products, processes and materials. Analysis methods to control such as (DFMEA, PFMEA), validation plans and verification protocol creation and reporting of validation.Responsible to lead projects constantly evaluate the project in order to verify that they have achieved the expected results.

Planning, coordinating and supervising the work of preparation of route allocation of transportation, distribution of products as well as all staff in charge. Responsible for managing the resources associated with the management including monthly management-annual budget and each of the assigned accounts. Control and monitoring projects Sales Management.

Ingeniero En Electromedicina, Engineering

Bachiller Educación Diversificada