Roles & Responsibilities:GMP Experience.Minimum 8+ years in a GMP-regulated biopharmaceutical environment.Quality Assurance Experience .At least 2+ years specifically in a QA role.QA Compliance Knowledge.Strong knowledge of QA Compliance systems including.Quality Management Review (QMR).Annual Product Quality Review (APQR).Self-inspections.Audit readiness.In-depth understanding of FDA/ICH/EU cGMP regulations and guidelines.Data Integrity.Experience with Data Integrity principles (ALCOA+).
Job Details
| ID | #54150148 |
| Estado | Indiana |
| Ciudad | Indianapolis |
| Tipo de trabajo | Contract |
| Salario | USD TBD TBD |
| Fuente | Katalyst Healthcares & Life Sciences |
| Showed | 2025-07-11 |
| Fecha | 2025-07-11 |
| Fecha tope | 2025-09-09 |
| Categoría | Etcétera |
| Crear un currículum vítae | |
| Aplica ya | |
QA Compliance Specialist
Indiana, Indianapolis, 46201 Indianapolis USA