waypointjobs

Nesco Resource

Quality Control Assistant (Biotech/Biomedical)

indianapolis, IN

Check who can apply and the requirements below before continuing.

Availability awaiting confirmation

We are waiting for a fresh update from the source. This page preserves the last received job details; current availability is not confirmed.

Job description

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

Worksite address

indianapolis, IN, 46201, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.

Explore related searches

Current related jobs

Vitalcore Health Strategies

WhatJobs

Legal Counsel

topeka, KS

Salary not specified

Join the VitalCore Team in Kansas! We're people fueled by passion, not by profit! VitalCore Health Strategies (VCHS), an industry leader in Corre…

Listing review due 2026-10-08View job