This role ensures compliance with quality standards and regulatory requirements across manufacturing operations at the Mazères‑sur‑Salat site
Job Summary
This role ensures compliance with quality standards and regulatory requirements across manufacturing operations at the Mazères‑sur‑Salat site.
The successful candidate will lead investigations, analyze quality data, and implement corrective actions to maintain high product quality standards.
The position offers exposure to innovative technologies and the opportunity to directly impact patient care through quality oversight of critical products.
Matching Summary
This role ensures compliance with quality standards and regulatory requirements across manufacturing operations at the Mazères‑sur‑Salat site.
Skills & Requirements
Must-have
GMP/ISO regulated environments experience
Root cause analysis and CAPA implementation
Internal and external audit support
Nice-to-have
Statistical analysis tools proficiency
Project management and prioritization skills
Cross-functional collaboration abilities
Key Requirements
Bachelor's Degree plus 2 years QA experience or Advanced Degree
Experience in medical devices, pharmaceuticals, or biotechnology