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Tracking Code 239-093 Job Description As a member of the Clinical, Regulatory & QA team you will be responsible for Regulatory Affairs support of submissions and on- going compliance for new and existing products. This involves the preparation of documents for submission to4/22/2016 Lexington, MA Save This Job
Job opening ID97 Posting titleSr. Regulatory Specialist Roles and responsibilitiesAs a member of our Regulatory Affairs team, you will play a key role in expediting the availability of our lifesaving products worldwide by ensuring that they meet all requirements for safety and4/25/2016 Alameda,, CA Save This Job
Menlo Park, CA, US Worker Category :Full Time Job ClassProfessional Earlens is looking for a regulatory professional who has experience with FDA and worldwide submissions to support a new technology hearing device. The title shall commensurate with candidate?s4/28/2016 Menlo Park, CA Save This Job