Join Stryker’s **Peripheral Vascular** division in **Irvine, CA** , where you’ll play a pivotal role in advancing life‑enhancing medical technologies. As a **Senior Regulatory Affairs Manager** - **International,** you will lead global regulatory strategies that accelerate patient access to innovative solutions and directly shape successful product launches across key international markets. This is an opportunity to make a measurable impact while developing a high‑performing team in a fast‑moving, mission‑driven environment. **What You Will Do** + **Lead** day‑to‑day global regulatory operations, ensuring activities are accurately evaluated, prioritized, and executed to meet business timelines. + **Oversee** preparation, review, and submission of regulatory filings supporting market access across **EMEA** , **EU** , **APAC** , and **Latin America** . + **Manage** regulatory processes for Patient‑Specific Solutions, including compassionate use and special access pathways. + **Interpret** global regulatory requirements and guide internal teams on submission strategies, labeling compliance, and product claims. + **Ensure** regulatory submissions, labeling, and marketing materials meet all applicable standards and internal quality expectations. + **Represent** Regulatory Affairs in internal and external audits with health authorities and Notified Bodies. + **Partner** with Quality, R&D, Supply Chain, Finance, Sales, and Marketing to drive cross‑functional alignment on regulatory deliverables. + **Lead and develop** a high‑performing Regulatory Affairs team, providing coaching, goal setting, issue resolution, and ongoing performance management. + **Establish** standardized regulatory processes with clear ownership and implement practical process improvements to reduce inefficiencies. + **Track and report** regulatory metrics, workload distribution, and submission timelines to support operational planning and budget management. **What You Will Need** **Required Qualifications** + Bachelor’s degree required. (Engineering, Science, or related field preferred). + Minimum **10 years** of experience in an FDA‑regulated industry. + Minimum **3 years** of people leadership experience. + Medical device industry experience required. **Preferred Qualifications** + Master’s degree and/or Regulatory Affairs Certification (RAC). + Experience with international submissions across EMEA, EU, APAC, Latin America, and Canada. + Experience leading geographically dispersed teams. $167,000-$278,600 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors. Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role. Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.