DocumentControlandValidationSpecialist

**Career-defining. Life-changing.** At iRhythm, you’ll have the opportunity to grow your skills and your career while impacting the lives of people around the world. iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. Every day, we collaborate, create, and constantly reimagine what’s possible. We think big and move fast, driven by our commitment to put patients first and improve lives. We need builders like you. Curious and innovative problem solvers looking for the chance to meaningfully shape the future of cardiac health, our company, and your career **About This Role:** The Document Control and Validation Specialist is responsible for managing and implementing the process associated with creation and revision of iRhythm’s Marketing documents and develop and maintain validation documentation (test plans, test scripts, validation plan and reports). **Responsibilities:** * Responsible for coordination of controlled documents within iRhythm’s global Marketing system. * Maintain and improve processes associated with an electronic MLR system within the eQMS. * Work cross-functionally to ensure change orders are executed in a complaint and timely manner. * Responsible for the accuracy of documentation per approved Standard Operating Procedures, GMP and internal change control. * Supports internal and external audits in backrooms, and helps with the coordination of document requests. * Maintains quality records per applicable SOPs. * Responsible for coordinating document change orders, collaboration, approval, release, archival and retention. * Closely work with Training coordinator to ensure change orders are triggering training as required * Develop and maintain validation documentation (test plans, test scripts, validation plan and reports) * Support implementation of QMS systems, dashboards, or process changes through validation testing * Design, build, and maintain dashboards and recurring reports * Collabora