Brandon Eckert

Product Regulatory Affairs Analyst @ Fort Wayne Metals

About Brandon Eckert

Brandon Eckert is a Product Regulatory Affairs Analyst with expertise in regulatory strategy and compliance in the biomedical device industry. He holds a Bachelor's degree in Chemistry from Butler University and a Master of Science in Law from Northwestern University Pritzker School of Law.

Work at Fort Wayne Metals

Brandon Eckert has been employed at Fort Wayne Metals as a Product Regulatory Affairs Analyst since 2020. In this role, he focuses on regulatory strategy and compliance within the biomedical device industry. His responsibilities include ensuring that products meet regulatory standards and facilitating the approval process for medical devices. Eckert's expertise in regulatory affairs is informed by his educational background and previous work experience.

Education and Expertise

Brandon Eckert holds a Bachelor's degree in Chemistry from Butler University, which he completed from 2015 to 2019. He furthered his education at Northwestern University Pritzker School of Law, earning a Master of Science in Law in 2020. His academic background in both chemistry and law enables him to effectively navigate the complexities of regulatory affairs in the biomedical sector.

Background

Brandon Eckert has a diverse background that combines experience in healthcare and law. Before his current role, he worked at Zimmer Biomet as a Lab Technician for three months in 2019. He also served as an Environmental Programs Assistant at Butler University from 2018 to 2019 and as a Laboratory Assistant from 2017 to 2018. These roles provided him with practical insights into laboratory operations and environmental compliance.

Regulatory Strategy and Compliance Experience

Brandon Eckert possesses significant experience in regulatory strategy and compliance within the biomedical device industry. His role as a Product Regulatory Affairs Analyst involves integrating his knowledge of chemistry and law to enhance regulatory processes. This combination of expertise allows him to contribute effectively to medical device manufacturing and ensure adherence to industry regulations.

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