Highlights
Prepare draft audit summaries and GQAAC audit reports for review/issuance by Lilly staff. - Assist with GQAAC compliance activities: training, CAPA, deviations, changes, self-inspections.
Numbers & Facts
| Location | Indianapolis, IN |
| Industry | Staffing/Employment Agencies |
| Company Size | 10,000 employees or more |
| Year Founded | 1956 |
| Website | https://nescoresource.com/ |
Description
Global Compliance Support Team Member
- Support 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 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
Education:
Bachelor's degree or equivalent experience
#EDS014
- Support 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 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
Education:
Bachelor's degree or equivalent experience
#EDS014
Benefits
Paid Sick Days, Parking, Performance Bonus, Employee Referral Program
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