The role is responsible for ensuring product conformity to national and international pharmaceutical regulations through rigorous quality assurance processes
Job Summary
The role is responsible for ensuring product conformity to national and international pharmaceutical regulations through rigorous quality assurance processes.
Key duties include reviewing batch records, managing quality issues, and leading investigations to implement corrective and preventive actions.
Candidates will work in an inclusive environment at the Borgo San Michele production site in Latina, Italy, supporting life-saving treatments.
Matching Summary
The role is responsible for ensuring product conformity to national and international pharmaceutical regulations through rigorous quality assurance processes.
Skills & Requirements
Must-have
Batch Record Review
GMP Compliance Verification
Quality Issue Management
Corrective and Preventive Actions
Production Process Monitoring
Nice-to-have
Collaboration with International Teams
Process Improvement Identification
Field Intervention Experience
Key Requirements
Master's degree in Pharmacy, Chemistry, Biology, or Engineering
Minimum 6 months experience in pharmaceutical sector