Quality Specialist III, Document Control and Training

Role: Support document control and training compliance activities within the Quality Assurance function for a biopharma developing RNAi-based therapeutics. Responsibilities: manage controlled documentation, quality records, and training records in eQMS and LMS systems; ensure regulatory compliance and audit readiness; assist with document formatting, approvals, and periodic reviews; support training administration including monitoring completion rates and maintaining training records. Requirements: BS/BA in chemistry, biology, or biochemistry; at least 5 years of experience in pharmaceutical/biotech or CRO environments with document management; strong organizational skills, attention to detail, and communication abilities. Preferred: experience with eQMS/eDMS platforms such as Veeva, knowledge of GMP/GCP/GLP regulations, proficiency in Adobe, Microsoft Office tools. HighValue: GxP compliance, document and training management in biopharma, regulated environment experience, support for audit activities. WorkSetup: not specified; location in Wisconsin, with competitive salary range.