Quality Data Management Specialist

About Stryker

Stryker 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 the #5 World’s Best Workplaces and a Best Workplace for Diversity by Fortune Magazine. Learn more about our award-winning organization by visiting stryker.com

Why regulatory affairs/quality assurance 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. If you are interested in working at one of the World’s Best Workplaces, apply now!

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-team

Who We Want

Data managers. People who enjoy compiling, organizing and consolidating large volumes of data and reports.

Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.

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.

This position can be based either in Mahwah NJ or Fort Lauderdale FL.

What you will do:

The Quality Data Management Specialist is primarily responsible for supporting the development of the quality management system in accordance with relevant regulatory requirements for medical devices. This is an entry level position which will allow you to gain experience in ERP systems, SAP, and quality data management.

• Lead and participate in local and global Master Data Governance projects, ensuring appropriate outcomes and compliance, particularly in those areas related to Quality Systems.
• Champion continuous process improvement throughout the Quality Systems/Master Data Governance and the rest of Stryker organization.
• Support QMS compliance with the appropriate internal and external regulatory requirements (including but not limited to Site, Division, Corporate, FDA, ISO, MDD, and individual country requirements).
• Engage in the development of optimum future state of QMS for business needs. Identify improvements and inputs in areas of responsibility.
• Execute development and/or modification of Stryker's QMS.
• Assess and quantify requirements for QMS requirements to optimize structure.

What you need:

• Bachelor's degree (Science, Engineering or business degree preferred)
• 0-3 years with ERP systems or SAP for materials data preferred
• Strong interpersonal and communication skills; ability to influence others
• Able to adapt to rapid changes

Our benefits

Our total rewards offering varies by country but often includes 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.

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/