Andrew Kamrowski
About Andrew Kamrowski
Andrew Kamrowski is a Senior Design Engineer at GF Health Products, Inc., where he has worked since 2016. He specializes in product development and design for multiple brands, while also providing support across various operational groups.
Work at GF Health Products, Inc.
Andrew Kamrowski has served as a Senior Design Engineer at GF Health Products, Inc. since 2016. In this role, he provides support to various departments, including manufacturing, quality, and customer service. His responsibilities include evaluating and resolving issues related to production, quality, and customer inquiries. He leads the development and design of products for multiple brands under the company, such as Basic American Medical Products, Lumex, Hausted, Gendron, and Everest & Jennings. His work is crucial in ensuring that products meet both customer needs and regulatory standards.
Previous Experience in Engineering
Before joining GF Health Products, Inc., Andrew Kamrowski worked as a Fabrication Engineer at DRM Industries Corporation from 2014 to 2016. His role involved engineering tasks that contributed to the fabrication processes. Prior to that, he was a Manufacturing Engineering Co-op at Trane Commercial (Ingersoll Rand) for one year, from 2012 to 2013. These positions provided him with valuable experience in engineering practices and manufacturing processes.
Education in Mechanical Design
Andrew Kamrowski earned a Bachelor's Degree in Engineering Technology with a focus on Mechanical Design from the University of Wisconsin-Stout. His studies spanned from 2009 to 2014, during which he gained foundational knowledge and skills relevant to his engineering career. This educational background supports his current role in product design and development.
Technical Expertise and Compliance
In his role as a Senior Design Engineer, Andrew Kamrowski writes detailed product engineering technical specifications that adhere to verification and validation criteria. He maintains a working knowledge of current regulatory and testing requirements, including FDA regulations, ISO 13485, and IEC standards. His expertise allows him to manage projects of medium to high complexity, ensuring compliance with applicable standards while focusing on cost, quality, and risk management.
Product Development in Regulated Environments
Andrew Kamrowski is involved in creating and developing products within an FDA-regulated environment. His work ensures that all products meet the necessary regulatory standards, which is critical in the healthcare and medical device industries. This responsibility highlights his role in maintaining product integrity and safety throughout the design and development process.