Vernetta Meyers Email & Phone Number | As a Risk Management Quality Engineer at Philips, I apply my Certified Associate in Project Management (CAPM) credential and my 25+ years of experience in cGMP FDA regulated environments to ensure the quality and safety of medical devices. I collaborate with cross-functional teams to conduct risk assessments to include authoring Product Safety Update Reports (PSURs), Post Market Surveillance Reports (PMSRs), and Post Market Surveillance Plans (PMSPs), audits, complaint investigations, and medical device reporting (MDRs) in compliance with global standards and regulations. My professional mission is to leverage my extensive background in quality assurance, people management, and process improvement to deliver high-quality products and services that meet the needs and expectations of customers and stakeholders. I have successfully led and supported multiple projects, audits, and remediations involving finished suspension dosage, tabletop packaging, and bulk API pharmaceutical facilities, demonstrating my domain expertise and problem-solving skills.

Vernetta Meyers

As a Risk Management Quality Engineer at Philips, I apply my Certified Associate in Project Manageme...
Suffolk, Virginia, United States

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Vernetta Meyers’s Location Suffolk, Virginia, United States

Vernetta Meyers’s Current Industry Philips

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Risk Management Quality Engineer

2021-03-01 00:00:00 - Present

Risk Management Consultant

2019-05-01 00:00:00 - 2021-03-01 00:00:00

Quality & Compliance Consultant/Quality Engineer

2016-10-01 00:00:00 - 2017-08-01 00:00:00

Quality Associate

2015-10-01 00:00:00 - 2016-09-01 00:00:00

Compliance & Quality Manager

2015-03-01 00:00:00 - 2015-07-01 00:00:00

Quality Assurance Representative

2011-06-01 00:00:00 - 2013-05-01 00:00:00

QA Release Lead

2004-12-01 00:00:00 - 2007-12-01 00:00:00

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Vernetta Meyers is a As a Risk Management Quality Engineer at Philips, I apply my Certified Associate in Project Management (CAPM) credential and my 25+ years of experience in cGMP FDA regulated environments to ensure the quality and safety of medical devices. I collaborate with cross-functional teams to conduct risk assessments to include authoring Product Safety Update Reports (PSURs), Post Market Surveillance Reports (PMSRs), and Post Market Surveillance Plans (PMSPs), audits, complaint investigations, and medical device reporting (MDRs) in compliance with global standards and regulations. My professional mission is to leverage my extensive background in quality assurance, people management, and process improvement to deliver high-quality products and services that meet the needs and expectations of customers and stakeholders. I have successfully led and supported multiple projects, audits, and remediations involving finished suspension dosage, tabletop packaging, and bulk API pharmaceutical facilities, demonstrating my domain expertise and problem-solving skills.

Vernetta Meyers has prior
experience in the following industries:
Eg Life Sciences | Maetrics | Biomat Usa | Vmi Office Solutions | Eli Lilly | Monsanto

Vernetta Meyers has the following professional experience:
Philips | Eg Life Sciences | Maetrics | Biomat Usa | Vmi Office Solutions | Eli Lilly | Monsanto