Biocomposites Keele is seeking a Quality Compliance Lead to own the QMS/eQMS and ensure regulatory compliance with ISO 13485, MDSAP, GMP and FDA standards. You will lead internal audits and drive continuous improvement.
You will manage a quality team, develop training, review documentation, and support supplier and regulatory audits. Some travel is required to support global operations in a fast‑moving medical devices environment.
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Quality Compliance Lead — Medical Devices (ISO13485 & Audits) in Keele employer: Biocomposites
Biocomposites is an exceptional employer, offering a dynamic work environment in the heart of Minnesota where innovation meets collaboration. With a strong focus on employee growth and development, we provide comprehensive training and support to ensure our team members thrive in their roles. Our inclusive culture fosters teamwork and encourages diverse perspectives, making it a rewarding place for passionate individuals dedicated to transforming lives through advanced medical solutions.
