Senior Regulatory Affairs Specialist; Hybrid

Join Stryker's Medical Division supporting Emergency Care | Stryker 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.

• 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.

• 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.

• 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

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• 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 Med Surg, 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.