Cirtec Medical
Sue Kramm is an experienced professional in document control and quality assurance within the medical device and technology sectors. Currently serving as an Engineering Document Control Specialist at Cirtec Medical since March 2021, Sue has previously held positions at Abbott and IMRIS, where responsibilities included customer and customs technical roles and quality assurance management. With extensive experience at Cypress Semiconductor, Sue supervised documentation processes, managed electronic documentation systems, and ensured compliance with ISO standards. Early career roles included quality assurance and inspection positions at Printed Circuit Inc. and St. Jude Medical, highlighting a strong foundation in technical writing, training, and production oversight. Education includes completion of studies at Parkview High School.
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Cirtec Medical
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Whether you’re a cutting-edge startup or a leading Class II or III medical device manufacturer, Cirtec is here to help bring life-enhancing therapies to market – quickly and cost-effectively. Our staff of engineers and manufacturing experts can help you succeed at any or every stage of your product development cycle, including design/development, pilot and clinical build, manufacturing and finished device assembly. Cirtec brings three decades of experience in developing medical devices fabricated under 21 CFR 820 and ISO 13485 quality standards. Our dedicated program management experts are here to help you bring your product from concept through commercialization – on time, on budget and as seamlessly as possible.