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Posts by Jesseca Lyons

Get the latest updates and best practices in the MedTech industry from our blog. Join 200,000+ other MedTech professionals outperforming their peers.
Establishing a QMS
Etienne Nichols
February 2, 2024

FDA Publishes Final Rule on QMSR

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Establishing a QMS

Guide to Managing Your Medical Device on the Market and Scaling Manufacturing

Laura Maher
January 3, 2024
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Ultimate Guide to ISO 14155:2020 for Medical Devices

Jon Bergsteinsson
September 15, 2023
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About the Author

Jesseca Lyons is a Senior Medical Device Guru at Greenlight Guru and a Mechanical Engineer by trade who loves working with cross functional teams, including both engineering and non-engineering disciplines. She’s spent most of her career gathering and defining requirements for new product design and development in the medical device industry. She believes the best part of being an engineer and working at greenlight.guru is that she can use her skills to help customers and make a positive impact in their lives.

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Product Development

Fundamentals of Supplier Management for Medical Device Companies

Jesseca Lyons
March 19, 2017
As a manufacturer of medical devices, it is your responsibility to be on top of the entire system that sees your product go from the idea stage to when it is available for... Read More
Product Development

Why Use ISO 14971 vs. FMEA (Template Included)

Jesseca Lyons
August 1, 2016
This may be stating the obvious, but engineers are generally very analytical. One of the areas where engineers are analytical is in evaluating all the ways things can go... Read More
Establishing a QMS

5 Places Paper Might Be Hiding in Your Medical Device Company

Jesseca Lyons
July 11, 2016
A few weeks ago you left a big pile of paperwork (also known as your Document Change Order (DCO/ECO) in the hands of the master of the universe (also known as your document... Read More
Establishing a QMS

What It Means to Join the Greenlight Guru Family

Jesseca Lyons
June 27, 2016
When your medical device company makes the decision to go with Greenlight Guru, you might think that you’re simply getting access to our award-winning eQMS software... Read More
Product Development

5 Medical Device Project Management Tips That Will Help You Complete Your Project On Time

Jesseca Lyons
June 13, 2016
If you’re an engineer at a small medical device company, chances are, at some point, you’re going to be asked to manage a project. Read More
Post-Market Surveillance

4 Lessons I Learned Going Through an FDA / ISO Audit for the First Time as an Engineer

Jesseca Lyons
May 24, 2016
As an engineer, there’s not a lot that makes me nervous. Going through an FDA / ISO audit? That makes the top of the list in my book. Read More

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