--- title: Senior Regulatory Affairs Specialist at Stryker description: Stryker is hiring for the Senior Regulatory Affairs Specialist role in Redmond, WA. Full-time, hybrid role. See the full description and apply. type: job url: https://www.foundrole.com/jobs/senior-regulatory-affairs-specialist-at-stryker-01a1168d-3b8c-70fa-8e5e-6dad5ff74a85 date: 2026-11-15T01:26:44Z og_description: Join Stryker as Senior Regulatory Affairs Specialist in Redmond, WA. Pays $95.8K–$159.6K per year. Full-time, hybrid role. og_image: https://www.foundrole.com/og/m0nqv5.png breadcrumbs: - label: Home url: https://www.foundrole.com/ - label: Search url: https://www.foundrole.com/jobs --- | | | |---|---| | **Company** | [Stryker](https://www.foundrole.com/companies/stryker?utm_source=ai_markdown) | | **Location** | Redmond, WA (Hybrid) | | **Salary** | $95.8K/yr - $159.6K/yr | | **Type** | Full Time | | **Posted** | Oct 05, 2026 | ## Is this job real? **Ghost job check:** B · Low risk. Probably a real opening. ## Visa sponsorship - **H-1B:** Stryker sponsors H-1B visas. It filed 77 H-1B petitions (FY2026 Q1 – FY2026 Q4). - **E-Verify:** No E-Verify enrollment on record for Stryker. ## Pay for similar jobs Most similar jobs pay $92,000 – $136,000 a year (median $112,000). ## Description Work Flexibility: Hybrid Join Stryker's **Medical Division** supporting [**Emergency Care | Stryker**](https://www.stryker.com/us/en/emergency-care.html) as a **Senior Regulatory Affairs Specialist** based in **Redmond, Washington (Hybrid)**. In this role, you will support the continued compliance, registration, and market availability of medical devices throughout their lifecycle by partnering with cross-functional teams on product changes and regulatory activities. **What you will do** - Support R&D, Marketing and Manufacturing teams with regulatory assessments of proposed changes or product transfers. - Identify requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.). - Assist in the development of regulatory strategy and updates strategy based upon regulatory changes. - Evaluate proposed products for regulatory classification and jurisdiction. - Determine requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities. - Prepare and submit electronic and paper regulatory submissions according to applicable regulatory requirements and guidelines for required products. - Provide regulatory information and guidance for product development and planning throughout the product lifecycle to the regulatory groups and others within the organization. - Communicate and interact with regulatory authorities throughout the development and review process of a regulatory submission through appropriate communication tools. - Evaluate proposed pre-clinical, clinical, and manufacturing changes for regulatory filing solutions and propose plans/strategies (if appropriate) for changes that do not require submissions. - Identify, monitor, and submit applicable reports or notifications to regulatory authorities during the clinical research process. - Maintain current product registrations and assist with processing registration changes when required. **What you need** - Bachelor’s degree required. Preferred to be in Engineering, Science, Regulatory Affairs, or a related technical field. - Minimum of 2 years in a Regulatory Affairs role required. - Experience in an FDA or highly regulated industry required. **Preferred** - Experience supporting Software as a Medical Device (SaMD) products or software-enabled technologies within a regulated industry. - RAC certification or Advanced Degree (Masters in Regulatory Affairs). - Previous experience with Class II/III medical devices. - Experience authoring regulatory submissions for product approval. - Experience interacting with regulatory agencies. **US15**: $95,800 - $159,600 USD Annual View the [U.S. work location and transparency guide](https://view.stryker.com/viewer/fcd609f31e39eac44598615224ec7216?iid=69deda99678eb495e0710914#1) to find the pay range for your location. Travel Percentage: 0% 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. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. ## Skills - Market Access - Regulatory Filing - Planning - Purchasing - Medical Devices - Regulatory Submissions - New Product Development - Software as a Medical Device (SaMD) - Regulatory Affairs - Regulatory Strategy - FDA Regulations - Communication - Oracle Real Application Cluster RAC - Regulatory Compliance ## Related - [More jobs at Stryker](https://www.foundrole.com/companies/stryker?utm_source=ai_markdown) - [Legal & Compliance jobs](https://www.foundrole.com/careers/legal-and-compliance?utm_source=ai_markdown)- [Compliance & Regulatory jobs](https://www.foundrole.com/careers/legal-and-compliance/compliance-and-regulatory?utm_source=ai_markdown)- [Regulatory Affairs Specialist jobs](https://www.foundrole.com/careers/legal-and-compliance/compliance-and-regulatory/regulatory-affairs-specialist?utm_source=ai_markdown)- [Browse all companies](https://www.foundrole.com/companies?utm_source=ai_markdown) ## Explore this job market - [Washington](https://www.foundrole.com/locations/us/washington?utm_source=ai_markdown) — 61444 jobs - [Medical Equipment Manufacturing](https://www.foundrole.com/sectors/healthcare/medical-equipment-manufacturing?utm_source=ai_markdown) — 46981 jobs - [Redmond, WA](https://www.foundrole.com/locations/us/washington/redmond?utm_source=ai_markdown) — 3182 jobs - [Stryker](https://www.foundrole.com/companies/stryker?utm_source=ai_markdown) — 1225 jobs ## Related pages - [Washington](https://www.foundrole.com/locations/us/washington?utm_source=ai_markdown) — 61444 jobs - [Medical Equipment Manufacturing](https://www.foundrole.com/sectors/healthcare/medical-equipment-manufacturing?utm_source=ai_markdown) — 46981 jobs - [Redmond, WA](https://www.foundrole.com/locations/us/washington/redmond?utm_source=ai_markdown) — 3182 jobs - [Stryker](https://www.foundrole.com/companies/stryker?utm_source=ai_markdown) — 1225 jobs ## Browse - [Companies](https://www.foundrole.com/companies?utm_source=ai_markdown) - [Jobs by country](https://www.foundrole.com/locations?utm_source=ai_markdown) - [Jobs in the United States by state and city](https://www.foundrole.com/locations/us?utm_source=ai_markdown) - [H1B sponsors by location](https://www.foundrole.com/h1b-sponsors?utm_source=ai_markdown) - [H1B salaries](https://www.foundrole.com/h1b-salaries?utm_source=ai_markdown) - [Sectors and industries](https://www.foundrole.com/sectors?utm_source=ai_markdown) - [Jobs by career field](https://www.foundrole.com/careers?utm_source=ai_markdown) - [Latest jobs](https://www.foundrole.com/jobs/latest?utm_source=ai_markdown)