Mike Emeigh - Consultant, Self-employed

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Work Background

AccentureAssociate Manager, Intelligent Engineering

Sep. 2014 - Apr. 2023Phoenix, Arizona Area

Crowe Horwath LLPSenior Consultant, Regulatory Compliance Risk

May. 2014 - Sep. 2014Greater Grand Rapids, Michigan Area

Earthlink BusinessProject Analyst, Commissions Team

Jan. 2011 - Aug. 2013Raleigh-Durham, North Carolina AreaI performed business analysis, data reporting, and QA testing for sales force compensation systems. In this position I was the primary point of contact for the user community in Sales Operations and Commissions, and provided direct application-level expertise as well as data and analytical support. In this position I was asked to: Develop database and system design models Identify interfaces and build APIs between commissions and sales, billing, and account management Perform manual and (minimal) automated testing Create and extract sales, billing, and commissions reports and database queries Develop SQL queries against MySql, Oracle, and DB2 databases Write test code for C#/.Net using nUnit

Earthlink BusinessQA Manager

Oct. 2007 - Aug. 2013Raleigh-Durham, North Carolina AreaI was the first QA hire at Deltacom, which was purchased by Earthlink Business in 2010. In this role I built a QA function within Deltacom IT, and was asked to: Write test plans and procedures Perform manual tests Assist developers with automated unit tests Provide test reports to upper management Implement and manage an issue tracking system Implement and manage a configuration management system Represent QA on project teams, to ensure that the appropriate level of testing and validation was conducted before key systems were released to the users Among the systems on which I performed software testing/QA were: toll-free number rerouting (desktop and mobile) automated provisioning sales force commissioning sales force account assignment

H&R BlockSenior Tax Advisor

Jan. 2007 - Apr. 2014I've been preparing tax returns since 1992. In 2007 while between consulting jobs I began working at H&R Block in Wake Forest. I've continued there part-time during tax season, and last year I obtained specialty certifications in small business and investment income. I am training to become an Enrolled Agent. Feel free to ask me anything you want to know about taxes!

Independent Validation ConsultantSelf Employed

Mar. 2005 - Dec. 2006Raleigh-Durham, North Carolina AreaSelf-employed software validation consultant in FDA-regulated environments.

LiposcienceSQA Coordinator

Mar. 2004 - Mar. 2005I led the team building a software QA capability for a medical device and clinical trials service provider required to comply with US FDA regulatory requirements (21 CFR Part 820, 21 CFR Part 58, 21 CFR Part 11). In that role I was asked to: Implement a Software Development Life Cycle; Write Standard Operating Procedures (SOPs); Develop Corrective and Preventative Action (CAPA) plans; Write requirements and design documents; Participate in audits of our processes and respond to audit observations; Assist in developing a Disaster Recovery Plan.

Baseball Think FactoryScholar

Jan. 2001 - Jan. 2013Jim Furtado asked me to be a contributor to Baseball Think Factory back in the very early days when it was known as Baseball Primer. I've been there ever since. I've contributed feature articles to the site on fielding analysis and relief pitching and post minor league baseball articles to the Notes in a Minor Key portion of the site.

Glaxo Smith KlineProject Leader, IT QA Validation

Sep. 1998 - Mar. 2004As Project Leader at GlaxoSmith Kline, I performed validation activities to ensure regulatory compliance with US FDA requirements for pharmaceutical manufacturing (21 CFR Part 210/211, 21 CFR Part 11). In this environment I was asked to: Write validation plans and protocols for Laboratory Systems (LIMS and equipment validation); Write validation plans and protocols, and conduct qualification tests (IQ/OQ/PQ) for network infrastructure components; Lead regulatory audits of third-party software developers to review their Software Development Life Cycle (SDLC) processes and documents for compliance with FDA regulatory requirements.