A clinical-stage vaccine company located in San Carlos, CA is seeking a Document Control Specialist to manage GxP documentation as part of their Quality Management System. Responsibilities include maintaining electronic document control in Veeva, ensuring compliance with templates, and managing document workflows. The ideal candidate has at least 5 years of experience in the biopharmaceutical industry and familiarity with regulatory expectations. This full-time role offers a competitive salary range of $115,000 to $134,000, along with benefits.
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Senior GxP Document Control Specialist • San Carlos, CA, United States