Be a key player in quality assurance for medical devices as a proactive Quality Engineer. Utilize your solid foundation in FDA regulations and validation processes to foster compliance and continuous improvement.

This role requires a commitment to quality within a regulated environment, supporting quality systems and leading CAPA initiatives. Engage in cross-functional collaborations to implement process improvements while ensuring adherence to regulatory standards during audits and documentation review.

Key Responsibilities: • Support quality systems for regulatory compliance • Lead CAPA investigations and conduct root cause analysis • Maintain, review, and update quality documentation • Collaborate with teams for effective process improvements • Assist in managing audits and resolving findings promptly

Requirements: • 3+ years of experience in Quality Engineering for medical devices • Strong knowledge in FDA regulatory frameworks and ISO 13485 • Experience ...