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Associate Lead I - Biomanufacturing Compliance, Lead Investigator
CatalentMadison, WI
Posted Oct 8, 2026
What you’d do
Author and revise deviation records, preventive actions, and related cGMP documents with minimal supervision, track open investigations, and support audits and inspection readiness at a Madison biomanufacturing site. Full time. Found on the employer's careers page on Oct 21, 2026. Apply through the link.
You’ll need
- HS diploma/GED with 4+ years related experience, or STEM associate's with 1+ year, or STEM bachelor'
- Deviation writing experience
- Root Cause Analysis experience
- CAPA implementation experience
- cGMP documentation knowledge
Our summary of the listing. The full listing has the details.