Biomedical professional with academic preparation oriented to the design, construction of tools
and technologies, and production process implementation such as medical equipment, medical devices, and orthotics devices. I am focused on leveraging my experience and knowledge to fill an engineering position. Proactive with problem-solving skills, strong decision-making, leadership, and work ethic. Committed to continuously improving product quality and process flow.
Responsible for registering products on the server and assembling the first parts to start the device.
▪ Inspect all material prior to assembly.
▪ Verify that the manufactured products comply with the company's specifications and quality standards.
▪ It works with PLC, MES, CFR regulations, manufacturing manuals, criteria, and validations.
▪ Report to your supervisor any situation that affects the quality of the product.
▪ Compliance with company policy and regulations.
▪ Special works:
o Completion of Type C PCA for a new tool o Execution of Special Work Order/Special Work Request
o Edit a Manufacturing Instruction (Method Instruction)
o Completion of a Tool Qualification Form for a new tool o Preparation of a Chance Notice Request Form
o Conducting training for Product Builders on a new tool
o Participation in a pre-read on Regulatory
o Performing a Drug Triage Form and Safety Triage Form
o Completion of a Pull Test
▪ Working with proposals.
▪ Internal Audit on Unreceived Payment Adjustments
▪ Internal Audit on Employee Asset Management
▪ Permit Management Procedures
▪ Payroll Processing
▪ Allocation of Projects to Employees
▪ Communicating with suppliers to make estimates.
▪ Taking inventory
▪ Scheduling shifts and locations of workers.
▪ Responsible for preparing the payroll and check of the employees.