Quality Control Assistant (Biotech/Biomedical)

NESCO Inc

Global Compliance Support Team MemberSupport Auditable Unit (AU) Coordinator activities and TrackWise naming conventions. Process MyAccess requests and roster reviews for TrackWise Audit/Inspection systems. Prepare draft audit summaries and GQAAC audit reports for review/issuance by Lilly staff. Support regulatory inspection readiness and prep activities. Provide data entry, database updates, and SharePoint/Tableau access support. Assist with GQAAC compliance activities: training, CAPA, deviations, changes, self-inspections. Serve as QualityDocs Document Controller for select GQAAC Operations Documents. Collaborate with auditors, management, and customers to resolve questions.Qualifications: Minimum Requirements:Experience with TrackWise Audit/Inspection ModuleProficiency in MS Word, Excel, PowerPoint, SharePointExperience with document control in Veeva VaultExperience supporting regulatory inspections (e.g., FDA)1+ years of pharmaceutical industry experienceEducation: Bachelor's degree or equivalent experience NESCO Inc

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Vacancy posted 4 days ago

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