Lead Post Market Surveillance Specialist EMEA (m/f/x)
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From Stryker’s original posting
Work Flexibility: Hybrid Why join Stryker? Looking for a place that values your unique talents? Discover Stryker's award-winning culture. Make a meaningful impact on patient safety and product quality across the EMEA region. In this role, you will help ensure medical devices remain safe, effective, and compliant throughout their lifecycle by supporting post-market surveillance activities and regulatory reporting processes. You will work across multiple countries and functions, partnering with regulatory, quality, commercial, and operational teams to drive compliance, continuous improvement, and business continuity. As this position is part of an international team, we kindly ask that you submit your CV in English. What You Will Do • Execute post-market surveillance activities in accordance with applicable regulations, quality requirements, and internal procedures. • Coordinate product field actions and commercial hold activities across the EMEA region, ensuring impacted products and customers are accurately identified and managed. • Manage regulatory notifications and submissions to competent authorities, including responses to requests for additional information. • Monitor…
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