Quality Systems 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 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

Who we want

• Dedicated achievers. Relentless about quality, people who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
• Curious learners. Engineers who seek out cutting-edge research and information to expand and enhance their ability to design medical devices.
• Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.

What you will do

As a Quality System Specialist, you will be primarily responsible for the development support and maintenance of the quality management system processes in accordance with relevant regulatory requirements. You will ensure that an effective and efficient quality management system is supported through guiding Process Owners to the best solutions for presenting their processes. You will have the opportunity to be part of all regulated processes across the global Division

• You will research, organize, and draft business process maps and knowledge layer documents.
• You will work on cross-functional teams and collaborating with partners in the Organization to document and clarify processes.
• You will support updates to documentation when there are improvements to processes or changes to regulations/standards.
• You will coordinate documentation changes with impacted departments and sites to ensure accuracy.
• You will facilitate process mapping and documentation meetings and sessions.
• You will ensure documents conform to style and formatting standards and route documents through the site change control system coordinating with reviewers and affected sites to obtain appropriate approvals.
• You will help process owners and SMEs navigate the Document Management Process.
• You will build strong relationships with process owners, SMEs, and business partners.
• You will coordinate role and training updates with quality system training partners, process owners, and SMEs.
• You will assist with efforts to streamline training and to deliver engaging training to end users.
• You will create training materials for Quality System changes, including test materials, where applicable.

What you need

• Bachelor’s degree highly preferred
• 0-3 years of experience – preferred that individual has internship or experience in a regulated environment/quality system.

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.