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Regulatory Affairs Specialist at Stryker - ApplyBlast

Regulatory Affairs Specialist

Stryker

4 months ago

4.0 on Glassdoor

Bloomington, Minnesota

Hybrid

Full Time

Junior

0 applicants

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About this role

As a Regulatory Affairs Specialist at Stryker, you will support the Trauma & Extremities unit by maintaining global product registrations and ensuring compliance across U.S. and international markets. The role involves preparing audit documentation, reviewing changes for regulatory impact, and coordinating submissions for medical device agencies.

Responsibilities

Maintain global product registrations and compliance documentation
Evaluate changes for regulatory impact on released products
Prepare technical documentation for internal and external audits
Coordinate regulatory submissions and agency packages
Develop and maintain regulatory procedures for the team

Skills

Qualifications

Bachelor's Degree in Engineering or Life SciencesMaster's Degree in Regulatory Science

About Stryker

stryker.com

Headquarters

Portage, Michigan, United States

Company Size

10001+ employees

Founded

1941

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Stryker is a global medical technology company that develops and sells a broad range of medical devices, equipment, and services. The company serves healthcare markets across the Americas, Asia Pacific, Europe, and the Middle East & Africa. Stryker's products span areas including surgical equipment, orthopedics, and medical instruments.