- Location
- Indianapolis
- Type
- Full-time
- Department
- Manufacturing
- Closing date
- Today
- Source
- CareersPage
Description
Quality Control Assistant needs 3- years' experience
MUST:
- Experience with TrackWise Audit/Inspection Module –
- Proficiency in MS Word, Excel, PowerPoint, SharePoint –
- Experience with document control in Veeva Vault –
- Experience supporting regulatory inspections (e.g., FDA) - 1+ years of pharmaceutical industry experience –
DUTIES:
- Process MyAccess requests and roster reviews for TrackWise Audit/Inspection systems
- Prepare draft audit summaries and GQAAC audit reports for review/
- Support regulatory inspection readiness and prep activities –
- Provide data entry, database updates, and SharePoint/Tableau access support
- Serve as Quality Docs Document Controller for select
- GQAAC Operations Documents
- Collaborate with auditors, management, and customers to resolve questions