Mary George
Quality Manager at Praxis Technology- Claim this Profile
Click to upgrade to our gold package
for the full feature experience.
Topline Score
Bio
Brian Biley
My work with Mary as a project engineer at a medical device manufacturer provided opportunities to collaborate with her regarding validations of equipment and manufacturing processes, change management, and development of QC equipment. I have found her to be extensively knowledgeable in FDA GMP requirements, statistical techniques, and supplier qualifications. Always open to informal discussions, as well as more formal meetings, she was instrumental in timely validations of new products, new manufacturing processes, and QC inspection methods.
Aaron Snyder, MSc, cGMP
Mary is very detailed focused and takes her time making decisions. She is very good at looking through complex validations, DHR’s, Quality System Data, and other quality related items. During my time working with Mary she supported multiple investigation, two new product development projects, multiple product transfers, and a staff of four direct reports. She has a detailed understanding of both quality and compliance. She is diligent and hard working. During the high volume parts of the new product develop projects Mary worked long hours to ensure quality’s deliverables were met in a timely manner. She is very friendly and a great team player. I can confidently recommend Mary for a Quality Engineering or Management role.
Brian Biley
My work with Mary as a project engineer at a medical device manufacturer provided opportunities to collaborate with her regarding validations of equipment and manufacturing processes, change management, and development of QC equipment. I have found her to be extensively knowledgeable in FDA GMP requirements, statistical techniques, and supplier qualifications. Always open to informal discussions, as well as more formal meetings, she was instrumental in timely validations of new products, new manufacturing processes, and QC inspection methods.
Aaron Snyder, MSc, cGMP
Mary is very detailed focused and takes her time making decisions. She is very good at looking through complex validations, DHR’s, Quality System Data, and other quality related items. During my time working with Mary she supported multiple investigation, two new product development projects, multiple product transfers, and a staff of four direct reports. She has a detailed understanding of both quality and compliance. She is diligent and hard working. During the high volume parts of the new product develop projects Mary worked long hours to ensure quality’s deliverables were met in a timely manner. She is very friendly and a great team player. I can confidently recommend Mary for a Quality Engineering or Management role.
Brian Biley
My work with Mary as a project engineer at a medical device manufacturer provided opportunities to collaborate with her regarding validations of equipment and manufacturing processes, change management, and development of QC equipment. I have found her to be extensively knowledgeable in FDA GMP requirements, statistical techniques, and supplier qualifications. Always open to informal discussions, as well as more formal meetings, she was instrumental in timely validations of new products, new manufacturing processes, and QC inspection methods.
Aaron Snyder, MSc, cGMP
Mary is very detailed focused and takes her time making decisions. She is very good at looking through complex validations, DHR’s, Quality System Data, and other quality related items. During my time working with Mary she supported multiple investigation, two new product development projects, multiple product transfers, and a staff of four direct reports. She has a detailed understanding of both quality and compliance. She is diligent and hard working. During the high volume parts of the new product develop projects Mary worked long hours to ensure quality’s deliverables were met in a timely manner. She is very friendly and a great team player. I can confidently recommend Mary for a Quality Engineering or Management role.
Brian Biley
My work with Mary as a project engineer at a medical device manufacturer provided opportunities to collaborate with her regarding validations of equipment and manufacturing processes, change management, and development of QC equipment. I have found her to be extensively knowledgeable in FDA GMP requirements, statistical techniques, and supplier qualifications. Always open to informal discussions, as well as more formal meetings, she was instrumental in timely validations of new products, new manufacturing processes, and QC inspection methods.
Aaron Snyder, MSc, cGMP
Mary is very detailed focused and takes her time making decisions. She is very good at looking through complex validations, DHR’s, Quality System Data, and other quality related items. During my time working with Mary she supported multiple investigation, two new product development projects, multiple product transfers, and a staff of four direct reports. She has a detailed understanding of both quality and compliance. She is diligent and hard working. During the high volume parts of the new product develop projects Mary worked long hours to ensure quality’s deliverables were met in a timely manner. She is very friendly and a great team player. I can confidently recommend Mary for a Quality Engineering or Management role.
Experience
-
Praxis Technology
-
United States
-
Medical Device
-
1 - 100 Employee
-
Quality Manager
-
2017 - Present
-
-
Quality Engineer
-
2014 - 2017
-
-
-
Covidien
-
New York
-
Sr. Quality Engineer
-
2009 - 2013
-
-
-
Boston Scientific
-
United States
-
Medical Equipment Manufacturing
-
700 & Above Employee
-
Manager I, Quality Assurance
-
2003 - 2009
-
-
Education
-
Clarkson University