Quality and Regulatory Affairs Specialist

Work Flexibility: Hybrid Join the team dedicated to ensuring the safety, quality, and compliance of life-saving medical devices. In this role, you will contribute directly to post-market surveillance and vigilance activities, helping to protect patients while supporting global regulatory compliance. This is an excellent opportunity for an early-career regulatory or quality professional looking to build expertise in medical device regulations and quality systems within a collaborative and mission-driven environment. What You Will Do Review product complaints and assess regulatory reportability within established timelines. Manage complaint handling activities, including documentation, tracking, and follow-up actions.…