Science & ResearchOn site
Lead - Biomanufacturing Compliance - Investigator, Deviations
CatalentMadison, WI
Posted Oct 8, 2026
What you’d do
Author and revise complex deviation records, corrective actions, and other cGMP documents, tracking open investigations and supporting audits and inspection readiness. Full time role collaborating with manufacturing and quality systems. Found on the employer's careers page on Oct 21, 2026. Apply through the link.
You’ll need
- High School Diploma/GED with 7+ years related experience, or Associate's in STEM with 6+ years
- Bachelor's in STEM field with 3+ years related experience, or MS/PhD in technical discipline
- Experience authoring deviation records and cGMP documents
- Knowledge of upstream/downstream manufacturing and quality systems
- Full time
Our summary of the listing. The full listing has the details.