Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Regulatory Affairs Specialist

Job

Stryker

Minneapolis, MN (In Person)

$101,500 Salary, Full-Time

Posted 3 weeks ago (Updated 3 weeks ago) • Actively hiring

Expires 7/14/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
74
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Join Stryker as a Regulatory Affairs Specialist in Bloomington, MN supporting Trauma & Extremities . This role provides hands-on exposure to sustaining regulatory activities, documentation, and global compliance across U.S. and international markets. You will support the ongoing maintenance of product registrations, evaluate changes, and contribute to regulatory systems and documentation. What you will do Collect, organize, and maintain regulatory intelligence and documentation for local, regional, and global requirements Research applicable regulations, guidance, and standards to support product classification, submission strategies, and compliance activities Support audit readiness activities by preparing technical documentation, ensuring traceability, and maintaining data accuracy across systems Assist in the development, review, and maintenance of regulatory procedures and standard operating procedures Review change documentation to assess regulatory impact on released products and document outcomes Support change control activities within PLM systems, including coordinating documentation updates, routing change orders, and ensuring appropriate reviewers and approvers are assigned Support preparation of regulatory submissions, including dossiers, pre-submissions, and agency packages Support the maintenance and alignment of product and regulatory data (e.g., UDI and registration data) to ensure compliance across global markets Provide regulatory input for audits, inspections, and nonconformance activities, and support follow-up actions What you will need Required Qualifications Bachelor's degree required. Preferred in Engineering, Life Sciences, or a related field 0+ years of experience Preferred Qualifications Master's degree in Regulatory Science or related field Demonstrated experience (academic, internship, or co-op) supporting regulatory documentation, submissions, or compliance activities in a regulated environment Exposure to
U.S. FDA
regulations or international medical device regulations Experience working with data or systems in a regulated environment preferred US5 : $76,100 - $126,900 USD Annual View the U.S. work location and transparency guide to find the pay range for your location.