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Regulatory Affairs Specialist

Company: Stryker
Location: Cary
Posted on: June 25, 2022

Job Description:

Why RA/QA at Stryker?Are you interested in working for a global company where you can work across functions and on a wide-variety of projects? As a member of Stryker's RA/QA team, that is exactly what you will do! Here, we provide our Regulatory Affairs team the opportunity to learn new things, as well as endless growth opportunities.Need another reason to apply? Here are 10 reasons to join our Regulatory Affairs team: https://www.strykercareersblog.com/post/10-reasons-to-join-strykers-regulatory-affairs-teamWe are proud to be named one of the World's Best Workplaces and a Best Workplace for Diversity by Fortune Magazine! Learn more about our award-winning organization by visiting stryker.comOur benefits include bonuses; commissions; healthcare; insurance benefits; retirement programs; stock based plans; paid time off plans; family and parenting leaves; tuition reimbursement; wellness programs; onsite fitness centers and cafeterias; discount purchase programs; and service and performance awards - not to mention various social and recreational activities.
Who We WantSelf-directed initiators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.What You Will DoAs the Regulatory Affairs Specialist, you will have the opportunity to support regulatory submissions for medical devices, pharmaceutical products, biocides and cosmetics which are developed and manufactured at Stryker's Cary IL site

  • Maintain files on local, regional, and global regulatory intelligence for products on the market
  • Monitor the regulatory environment for changes
  • Provide information used to evaluate proposed products for regulatory classification and jurisdiction
  • Research requirements for regulatory submissions, approval pathways, and compliance activitiesWhat You Need
    • Bachelors degree required, preferably in Science, Engineering or Law
    • 0+ yrs experience required, internship experience from an FDA regulated industry is preferable
    • Self-starter and team player
      Know someone at Stryker?Be sure to have them submit you as a referral prior to applying for this position. Learn more about our employee referral program at https://careers.stryker.com/referrals/About StrykerStryker is one of the world's leading medical technology companies and, together with our customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes.We are proud to be named one of the World's Best Workplaces and a Best Workplace for Diversity by Fortune Magazine! Learn more about our award-winning organization by visiting stryker.com

Keywords: Stryker, Elgin , Regulatory Affairs Specialist, Other , Cary, Illinois

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