Who we want
Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
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.
Goal-oriented developers. Keeping the customer and system requirements squarely in focus, people who deliver safe and robust solutions.
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 Senior QMS Specialist you will join the DRE (Digital, Robotics, and Enabling Technology) team which is an exciting and newly created organization in Stryker. DRE focuses on research and development of Digital, Robotics and Enabling Technology and works in close partnership with all Stryker commercial divisions. The role will align to the vision of DRE and will strengthen our QARA team to create, implement and maintain a new quality management system
As Senior QMS Specialist / technical writer you will develop, edit, and maintain Quality System Documentation to support DRE Quality System Management processes.
You will influence positive Quality outcomes across DRE by helping POs and SMEs navigate the Document Management Process, promoting improvements to processes where necessary and building strong relationships with POs, SMEs, and partners.
You will be participating in decision making and leading discussions on Quality Systems departmental issues.
This is an incredibly exciting position and will allow the incumbent to be involved in the creation and maintenance of a new QMS, enabling the success of Stryker's growing area of digital, robotics and enabling technologies!
What you need
Bachelor's degree in Technical Writing, Engineering or related field.
2+ years minimally required, technical writing or developing, editing and maintaining Quality System Documentation in the medical device or pharmaceutical industry environment.
Advanced working knowledge of MS Word, MS Excel, MS Visio and PowerPoint.
Ability to successfully interface with various departments and personnel
Excellent communication, time management, and organization skills with high emphasis on attention to detail.
Fluent in English
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