Link-Worldwide is seeking a Quality Assistant for their QA team in Tijuana, Baja California, Mexico. This on-site role focuses on documentation management to ensure the proper release of products for sterilization or sale, detecting any deviations in the device history record.

The ideal candidate should have 1 to 3 years of experience in a similar role and knowledge of ISO standards and FDA regulations. Join us to help improve patient outcomes and enhance breast cancer diagnostics.