QA Documentation & Training Specialist (Veeva QMS)
Skyhawk Therapeutics, Inc.
Skyhawk Therapeutics, Inc. is seeking a Documentation Specialist, Quality Assurance to provide QA support across regulated operations, ensuring audit readiness and compliance with FDA, ICH and GxP. The role focuses on SOP development, training administration, and document control within Veeva QMS. Ideal candidates have a life sciences degree and at least five years in QA in a regulated environment, with hands-on Veeva Vault QMS experience, vendor qualification exposure, and strong written #J-18808-Ljbffr Skyhawk Therapeutics, Inc.
Vacancy posted 4 days ago
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