Signant Health is seeking a Quality Specialist focused on Document Controls in Chile to oversee the lifecycle management of quality documentation.

This role is pivotal for ensuring compliance with regulatory requirements in clinical trials. The adecuado candidate will have experience in document control in a GCP‑regulated environment, possess strong organizational skills, and contribute to quality compliance culture across the organization.

Join Signant Health to be part of a collaborative team dedicated to improving lives through fast‑tracking clinical research.

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