• Member of he development team to launch first fully powered stapler in the world.• Responsible for evaluating and addressing all the Power Devices field returns.• Involved on expanding the sterilization parameters of the Powered Surgical Staplers that is expected to generate $50 Million incremental revenue over a 1 year period.• Responsible for evaluating all supplier change requests, performing studies, modifying design and tracking the implementation.• Attended numerous surgical procedures involving multiple surgeons to understand how the devices are being used and any potential issues with them.• Performed engineering and financial analysis relating to proposed designs.• Responsible for reliability testing of Powered Surgical Staplers.• Developed, implemented and sustained a cross-functional team with the main focus to address training, process or machine related opportunities.• SWI Improvements, implementation and training to over 100 operators across all 3 shifts of operations.•Assist and act as a consultant during numerous troubleshooting processes with machine specific documentation.• Supported equipment upgrades and new equipment installation during the validation process.• Supported the overseas equipment transfer to the North Haven facility.• Test, debug and submitted suggestions of new machinery for improvements in quality, efficiency and safety.• Responsible for setups, adjustments and troubleshooting critical manufacturing equipment (mechanical, pneumatics, vision, robotics).• Responsible for training the manufacturing technicians and junior engineers on new technology and/or processes.• Developed and reviewed existing JSAs for every task performed on various areas of operations.• Collaborated on the design and implementation of new machine maintenance standards procedures (Autonomous Maintenance) for various equipments.

• Managed 12 packing operators and 2 Mechanical Supports on the third shift with excellent results.• Achieved two years without investigation of human errors on the manufacturing process.• Review and translate (English and Spanish) all the new SOP’s for the new Packing Lines.• Notified and discussed any production quality problems with the packing manager and engineers to recommend corrective actions to be taken to avoid recurrences.• Verified the correct count, labeling, and printing before the packing operation started and running the process to assure that the quality controls were maintained.• Supervised the packing process setting up, insured consistent operations, monitoring and cleaning packing lines, sampling production and closing production orders.• Prepared packing process reports after the end of the shift in order to keep all personnel involved in the process informed.• Collaborated with the Industrial Engineers to establish a data recollection system in order to review all the manufacturing standards.• In charge of all the graphic designs of Roche Diagnostic (Ponce) to provide corporate information thought different media channels.• Executed Pre-Fat’s, FATs, MSAs, CQs, OQs and PQs for all new packing machinery and processes introduced to the manufacturing environment.• Collaborated on the transfer of the complete packaging line from its original locations to the final destination. The line included machinery such as: Case Packer (Serpa), Bundler (Pester), Cartoner (Bosh), Labeler (Weiler), etc.

• Supervised 45 construction employees on site with excellent results.• Managed to implement the use of Microsoft Project for a more accurate project schedules and budget analysis.• Created an electronic certification procedure for each task done on every mayor project.• In charge of making take-offs and estimates for each new project.