Luis Ramirez Email & Phone Number | Electronic Engineering degree with 20 plus years of experience working in the Quality and Manufacturing Engineering Fields. Bilingual, Self motivated and focused toward improvement using a team concept. Experienced in Quality Management, Quality and Manufacturing Engineering level positions. Skilled in developing and implementing a well structured Quality System program based on FDA’s Quality Systems Regulation CFR Part 820, ISO 13485 Quality System for Medical Devices, ISO9001 standards, Canadian Medical Device Regulations (SOR 98-282) and Japans MO 169, 2004. Certified by ASQ as a Quality Manager (CQM), Certified Quality Engineer (CQE) and Quality Auditor (CQA). Certified by AAMI (Association for the Advancement of Medical Instrumentation) on FDA’s Quality System Regulation and as ISO 9000/2000 Lead Auditor of Quality Systems accredited by ANSI-RAB National Accreditation Program for the training of QMS (Quality Managment System) Auditors. Writing and performing equipment and process validations. Specialties: Liaison (Management Representative) during third party audits/inspections (FDA, ISO, customers and Corporate). Quality Systems Lead Auditor for obtaining or maintaining certification to industry regulations and standards.

Luis Ramirez

Electronic Engineering degree with 20 plus years of experience working in the Quality and Manufactur...
12040 El Greco Circle, El Paso, United States

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Luis Ramirez’s Location 12040 El Greco Circle, El Paso, United States

Luis Ramirez’s Current Industry Cardinal Health

Luis Ramirez’s Prior Industry Biosense Webster A Johnson And Johnson | Business Exellence Professional Consulting

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Quality Assurance Engineer

2016-10-01 00:00:00 - Present

Staff Manufacturing Engineer

2013-03-01 00:00:00 - 2016-10-01 00:00:00

Validations Engineer

2011-01-01 00:00:00 - 2013-03-01 00:00:00

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Luis Ramirez is a Electronic Engineering degree with 20 plus years of experience working in the Quality and Manufacturing Engineering Fields. Bilingual, Self motivated and focused toward improvement using a team concept. Experienced in Quality Management, Quality and Manufacturing Engineering level positions. Skilled in developing and implementing a well structured Quality System program based on FDA’s Quality Systems Regulation CFR Part 820, ISO 13485 Quality System for Medical Devices, ISO9001 standards, Canadian Medical Device Regulations (SOR 98-282) and Japans MO 169, 2004. Certified by ASQ as a Quality Manager (CQM), Certified Quality Engineer (CQE) and Quality Auditor (CQA). Certified by AAMI (Association for the Advancement of Medical Instrumentation) on FDA’s Quality System Regulation and as ISO 9000/2000 Lead Auditor of Quality Systems accredited by ANSI-RAB National Accreditation Program for the training of QMS (Quality Managment System) Auditors. Writing and performing equipment and process validations. Specialties: Liaison (Management Representative) during third party audits/inspections (FDA, ISO, customers and Corporate). Quality Systems Lead Auditor for obtaining or maintaining certification to industry regulations and standards.

Luis Ramirez has prior
experience in the following industries:
Biosense Webster A Johnson And Johnson | Business Exellence Professional Consulting

Luis Ramirez has the following professional experience:
Cardinal Health | Biosense Webster A Johnson And Johnson | Business Exellence Professional Consulting