Full time
Stryker
Irvine, CA
Work Flexibility: Hybrid or Onsite Senior Regulatory Affairs Specialist – Labeling Irvine, CA In this role, you will help shape and maintain accurate, compliant medical device labeling across global markets, supporting products from development through the post‑market lifecycle. If you are energized by global impact, cross‑functional collaboration, and meaningful work in a regulated environment, this role offers an opportunity to grow while making a difference. What You Will Do Evaluate medical device labeling to ensure compliance with global regulatory requirements and standards, supporting market access and patient safety. Prepare, review, and maintain labeling content across the full product lifecycle for multiple global markets. Support new product development by contributing labeling elements to regulatory submissions for global registrations. Maintain sustaining registrations through labeling updates, renewals, and post‑market changes. Analyze emerging...