Regulatory Affairs Intern
Posted on 9/4/2023

10,001+ employees

Orthopedics technology products & services
Company Overview
Stryker’s mission is to make healthcare better together with their customers. Stryker is one of the world’s leading medical technology companies with their innovative products and services in medical and surgical, neurotechnology, orthopedics, and spine that can improve patient and hospital outcomes.
Tennessee, USA
Experience Level
Desired Skills
  • Learn about regulations within the medical device industry
  • Implement new ideas, be constantly challenged, and develop your skills
  • Network with key/high-level stakeholders and leaders of the business
  • Be a part of an innovative team and culture
  • Currently working on completion of a Bachelor's or Master's degree in related fieldor equivalent; we will only consider students who plan be enrolled in a degree-seekingprogram after the summer
  • Cumulative 3.0 GPA or above; must be the case at the date of hireand alsowill beverified during background check in the spring
  • Must be legally authorized to work in the U.S.and not require employment-basedsponsorship now or in the future
  • Excellent written and verbal communication skills
  • Strong organizational, problem-solving, and analytical skills; able to managepriorities and workflow
  • Versatility, flexibility, and a willingness to work within constantly changingpriorities with enthusiasm
  • Ability to exercise independent judgment
  • Proficient on basic computer programs: Microsoft Excel, Word, PowerPoint
  • Proven leadership and business acumen skills
  • Proven ability to handle multiple projects and meet deadlines
  • Strong interpersonal skills
  • Work cross functionally with different departments including R&D Engineering,Supplier Quality, Marketing, and Clinical Affairs to assist in regulatory decision-making and develop a broad understanding of the medical device industry
  • Perform Regulatory Intelligence activities to ensure divisional regulatory strategyremains optimally efficient amidst changing regulations and increasing liability
  • Prepare various regulatory submissions for registering products globally to ensureStryker products can reach our patients around the world
  • Shadow RA Specialists at new product development meetings to gain exposure tothe collaborative design and development process associated with bringing a newproduct to market
  • Support the Post Market Regulatory Reporting team on projects and initiatives thatallow the organization to monitor the performance of devices that have beenreleased to market and detect any potential safety and/or product quality issues
  • Help develop robust Regulatory assessments and strategy for proposed changenotifications in different regions to ensure minimal disruption to registrations orapprovals