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Merit Medical Systems, Inc. is seeking a qualified professional in Utah to maintain and optimize the Global Adverse Event reporting system and related post-market surveillance activities.
You will lead recalls, coordinate with QA, Regulatory Affairs, Clinical, Manufacturing, and other teams, and ensure compliance with FDA/ISO requirements. Strong communication and project management skills are essential.
Merit Medical Systems, Inc. is seeking a qualified professional in Utah to maintain and optimize the Global Adverse Event reporting system and related post-market surveillance activities.
You will lead recalls, coordinate with QA, Regulatory Affairs, Clinical, Manufacturing, and other teams, and ensure compliance with FDA/ISO requirements. Strong communication and project management skills are essential.