Oscar Borrelli Email & Phone Number

Miami Lakes, Florida, United States

Generate detailed design and drawings, concepts and new products mechanisms in 2D and 3D. Resolve issues to meet required goals. Maintain and update 3D models, blueprints and Manufacturing Documentation. Develop the required documentation and work order instructions (Assembly Instructions, BOM) to every new product development. Ensure correctives actions for mechanical designs issues are addressed appropriately and implemented in a timely manner. Research, evaluate, confirm and approve the technology and/or systems to be used in the product development process meets product requirements. Collaborate with a multidisciplinary team to design conception through verification testing of the systems to ensure designs are feasible, dependable and scalable. Develop methods and procedures for testing products or systems to ensure they conforms to engineering and customer requirements.

Hialeah, Florida, United States

Plans, coordinates, and directs Quality Management Systems (QMS). ISO 9001-2015 Oriented. Rail, Defense (MIL-STD / MIL-SPEC) and Aerospace Manufacturing Environment (MRO).ISO AS 9100 knowledge. Incoming raw material inspection. First Piece Inspection (Evaluate and Understand mechanical drawings, confirm dimensions, material and finish to assure customer requirement before to release programming and manufacturing. In process inspection. Blueprint interpretation and GD&T. Familiar with many measurement instruments such as Calipers, Micrometers, Height Gage, Thread Gages, Radii Gages, Pin Gages. Performance of Certificates of Compliance (COC), First Article Inspection Reports (FAIR) FAA (Parts 21), Strong attention to details, Visual inspection routine, Identify and troubleshoot problems and issues, Implement and improve quality control operating procedures, Visual Welding Inspection and WPS development. Quarantine, Non- Conformance, Corrective Action and Deviation Report. Documentation Review. Lean Manufacturing Knowledge. Internal Quality Audits. Equipment Traceability and Calibration. Statical Control Process.

Miami, Florida, United States

FDA regulation, cGMP’s. Daily checks, assist to QA Manager reviewing documents and QC Specialist in receiving and inspecting raw materials and packaging supplies. Assist in issuing batch records, Cutting Records, Packaging Records and Labels. Responsible for Production Line releases, daily monitoring production for any quality issues. Assist QC Specialist in inspecting quality of finished products. Responsible for inspection and maintain compliance with cGMP’s, water sampling for external lab testing, sampling food batches for testing, assist QA in documents reviews and control. Daily use of 7 Quality Tools.

Valencia, Venezuela.

Data Collect and analysis. Monitoring of Preventive and Corrective work orders, Document Review, Assign WO to mechanical or electricians, prepares and adjust schedule for preventive maintenance. Generation of Management Indicators, Critical spare parts inventory control, Development, Improvements and Projects within the Department, Design of Parts and Elements of Machines by SolidWorks Software 2014, Reverse Engineering. Root Causes Analysis, Realization of FMEA's, National and International Purchases of Critical Spare Parts

Bachelor Of Engineering - Be, Mechanical Engineering, Mechanical Engineer

Education record