Experience

Valdes Architecture & Engineering

• Design Services
• 100 - 200 Employee

• Senior Process Engineer at Valdes Engineering Company

  • Mar 2021 - Present

  Process Engineering Continuous Improvement on API manufacturing. Product transfer, cleaning improvement, efficiency improvement for existing products. Process Engineering Continuous Improvement on API manufacturing. Product transfer, cleaning improvement, efficiency improvement for existing products.



Low & Bonar

• United Kingdom
• Textile Manufacturing
• 200 - 300 Employee

• Process Technology Development Engineer

  • Sep 2018 - Mar 2021



Cytec Solvay Group

• Chemical Manufacturing
• 700 & Above Employee

• Senior Process Engineer II

  • Apr 2005 - Jul 2018

  Solvay Composite Materials, Greenville TX Process Engineer II/Product Steward - 2007 to present Manufacturing Engineer – (2005 – 2007) - Enable increase in sales revenue developing manufacturing/testing processes for the introduction of new products. - Provide training, support and mentoring of Manufacturing Engineers and operations personnel - Initiate and manage capital projects in the range of $0.5M. Drive innovation and continuous improvement through capital project management. - Act as Process Engineer subject matter expert in support of major capital projects. - Create testing processes documents and systems as well as internal specifications - Lead process improvement projects to enhanced safety and quality resulting in safety incidents reduction on the area of over 50%. - Lead process hazard analysis - Conduct root cause investigations and failure analysis for material quality and processes - Create and implement new processes and procedures to increasing process efficiency by 30%. - Support the quality function to ensure quality metrics are satisfied - Enhance the manufacturing process control and throughput by reducing process costs, supporting product quality and production objectives. - Understanding and translating process capability through statistical tools and analysis.



Henkel Loctite

• Sr Process Enginner

  • Nov 1998 - Jun 2004

  New facility start-up. Process optimization. Equipment specification and implementation of new technology. Product transfer and scale-up. Quality documentation support. Quality lab and production area support. New facility start-up. Process optimization. Equipment specification and implementation of new technology. Product transfer and scale-up. Quality documentation support. Quality lab and production area support.



Loctite PR Inc

• Manufacturing Technology Enginner

  • Aug 1996 - Nov 1998

  Operations troubleshooting and products and process improvement. New products implementation and support. Manufacturing process efficiency improvement. Quality and Process documentation. Operations troubleshooting and products and process improvement. New products implementation and support. Manufacturing process efficiency improvement. Quality and Process documentation.



Ivax Pharmaceuticals s.r.o.

• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Process Engineer Technical Services

  • 1994 - 1995

  Responsible for developing validation plans and protocols for process change and new products resulting in improved product integrity. Developed new drug clinical and stability batches manufacturing directions, process monitoring and troubleshooting. Prepared validation protocols for existing and new equipment to comply with FDA regulations. Responsible for developing validation plans and protocols for process change and new products resulting in improved product integrity. Developed new drug clinical and stability batches manufacturing directions, process monitoring and troubleshooting. Prepared validation protocols for existing and new equipment to comply with FDA regulations.



Ayerst-Wyeth Pharmaceuticals, Inc

• Guayama, PR

• Staff Process Engineer

  • Jul 1990 - Apr 1994

  Responsible for developing validation plans, installation qualification, operation qualification and performance qualification of processing and packaging equipment as well as utilities and facilities. Develop and execute cleaning validation protocols and technical reports for manufacturing and packaging equipment. Experienced in product and process validation of solid dosage forms. Also responsible for developing new drugs clinical and stability batches manufacturing directions, process monitoring and troubleshooting.