Regulatory Submissions & Quality Lead
Merck
Merck is seeking a Quality & Operations Specialist within the Clinical and Regulatory Strategic Communications (CRSC) team of Global Clinical Trial Operations. This role coordinates QA, document control, timelines, and regulatory submissions to ensure accuracy, compliance, and timely delivery of regulated content. The position requires an associate degree (life sciences or related) with extensive experience, strong Microsoft Office and document management skills, and ability to work #J-18808-Ljbffr Merck
Vacancy posted 7 hours ago
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