Stryker Corporation in the United Kingdom is seeking a Senior Quality Systems Specialist to lead QMS integration activities, ensuring compliance with FDA 21 CFR Part 820, ISO 13485, and related global regulations. The role focuses on harmonizing processes, documentation, and controls across both organizations.
The successful candidate will map current-state processes, identify gaps, and define future-state ownership and interfaces while collaborating with Manufacturing, R&D, Quality and
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Senior Quality Systems Integrator — FDA & ISO Compliance employer: Stryker Corporation
At Stryker, we pride ourselves on being a leading employer in the medical technology sector, offering a dynamic work culture that fosters innovation and collaboration. Our Project Managers benefit from flexible working arrangements, comprehensive benefits, and ample opportunities for professional growth, all while contributing to meaningful projects that enhance healthcare outcomes. Join us in a supportive environment where your contributions are valued, and you can thrive both personally and professionally.
