Matthew Busby Email & Phone Number | Matthew D Busby - Loveland, CO Writing illustrated and orderly technical revision controlled documents. - Developing and maintaining technical revision controlled documentation. - Update technical documents with changes to the process. - Revise technical documents for improved process. Process validation to meet FDA requirements for medical device manufacturing. - Member of group defining content and format for protocols and reports. - Technical Writer developing Process Validation protocols, in MS Word, for medical device production. - Technical Writer for Process Validation reports, in MS Word, for medical device production. - Gather, compile and analyzes data in MS Excel. Engineering Change Orders in Agile PDM - Champion ECOs in Agile PDM to submit and process controlled documents, release new product features and product lifecycle management (PLM). - Implement ECO changes including changes to the manufacturing floor, document updates and purchasing new tooling. Process Engineer Supporting the manufacturing of medical devices. - Provide technical solutions for manufacturing issues. - Provide answers for process related questions that arise. - Purchase and integrate new tooling on the manufacturing floor. New product introduction. - Review new designs for issues that affect producibility. - Restructure BOM, in Agile PDM, to match manufacturing work flow. - Setting up new lines with workstations, tooling and RIP bins. Digital Photography - Cropping and resizing photographs to include only relevant content. - Add annotation to provide additional information and point of focus. - Use desaturation to highlight important areas while giving a wider view for orientation. Specialties: Writing Technical Revision Controlled Documentation – Technical Writer for Process Validation Protocols for Medical Device Manufacturing – Technical Writer for Process Validation Reports for Medical Device Manufacturing – Process Validation for Medical Device Manufacturing – Agile PDM – Product Lifecycle Management (PLM) – Engineering Change Order – Process Engineer – Manufacturing Medical Devices – New Product Introduction – Digital Photography – HTML – CSS – Perl

Matthew Busby

Matthew D Busby - Loveland, CO Writing illustrated and orderly technical revision controlled docume...
Loveland, Colorado, United States

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Matthew Busby’s Email matthew.busby@emerson.com

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Matthew Busby’s Location Loveland, Colorado, United States

Matthew Busby’s Current Industry Micro Motion

Matthew Busby’s Prior Industry Beckman Coulter | Dako | Volunteer For Nonprofit | Agilent Technologies

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Work Experience

Micro Motion

Product Structure Analyst

2011-10-01 00:00:00 - Present

Beckman Coulter

Writing Technical Doumentation - Configuration Management - Process Engineering

2010-08-01 00:00:00 - 2010-11-01 00:00:00

Dako

Senior Technical Operations Technician - Technical Writer for Process Validation Documentation

2003-08-01 00:00:00 - 2007-12-01 00:00:00

Volunteer For Nonprofit

Website Administrator - HTML - CSS - Perl - Website Design

2002-03-01 00:00:00 - 2004-06-01 00:00:00

Agilent Technologies

Custom System Engineer

2000-12-01 00:00:00 - 2001-04-01 00:00:00

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FAQ About Matthew Busby

Matthew Busby is located at
Loveland, Colorado, United States

Matthew Busby is a Matthew D Busby - Loveland, CO Writing illustrated and orderly technical revision controlled documents. - Developing and maintaining technical revision controlled documentation. - Update technical documents with changes to the process. - Revise technical documents for improved process. Process validation to meet FDA requirements for medical device manufacturing. - Member of group defining content and format for protocols and reports. - Technical Writer developing Process Validation protocols, in MS Word, for medical device production. - Technical Writer for Process Validation reports, in MS Word, for medical device production. - Gather, compile and analyzes data in MS Excel. Engineering Change Orders in Agile PDM - Champion ECOs in Agile PDM to submit and process controlled documents, release new product features and product lifecycle management (PLM). - Implement ECO changes including changes to the manufacturing floor, document updates and purchasing new tooling. Process Engineer Supporting the manufacturing of medical devices. - Provide technical solutions for manufacturing issues. - Provide answers for process related questions that arise. - Purchase and integrate new tooling on the manufacturing floor. New product introduction. - Review new designs for issues that affect producibility. - Restructure BOM, in Agile PDM, to match manufacturing work flow. - Setting up new lines with workstations, tooling and RIP bins. Digital Photography - Cropping and resizing photographs to include only relevant content. - Add annotation to provide additional information and point of focus. - Use desaturation to highlight important areas while giving a wider view for orientation. Specialties: Writing Technical Revision Controlled Documentation – Technical Writer for Process Validation Protocols for Medical Device Manufacturing – Technical Writer for Process Validation Reports for Medical Device Manufacturing – Process Validation for Medical Device Manufacturing – Agile PDM – Product Lifecycle Management (PLM) – Engineering Change Order – Process Engineer – Manufacturing Medical Devices – New Product Introduction – Digital Photography – HTML – CSS – Perl – Website Design