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Quality Control Assistant (BiotechBiomedical)
Job Location:
Job Location:
Indianapolis, IN - USA
Hourly Salary:
USD 21 - 25
Hourly Salary:
Posted:
11 October 2026 (13 hours ago)
Posted:
Application Deadline:
8 January 2027
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
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:
Bachelors degree or equivalent experience
- 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:
Bachelors degree or equivalent experience
Required Experience:
Junior IC
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