Up to $7,000; duration: 6 months; not specified pm
Review and approve sops and batch records
Lead deviation investigations and capa implementation
Ensure gmp and gdocp compliance standards
This role supports day-to-day Quality Assurance activities in a multi-product pharmaceutical manufacturing facility while ensuring adherence to cGxP requirements
Job Summary
This role supports day-to-day Quality Assurance activities in a multi-product pharmaceutical manufacturing facility while ensuring adherence to cGxP requirements.
The specialist will lead deviation investigations, root cause analysis, and CAPA implementation to ensure timely closure and effectiveness.
Candidates must possess a minimum of five years of relevant experience in the pharmaceutical industry with a strong background in Quality Management Systems.
Matching Summary
Match Score: 85
This role supports day-to-day Quality Assurance activities in a multi-product pharmaceutical manufacturing facility while ensuring adherence to cGxP requirements.
Salary
Up to $7000; Duration: 6 months; Not specified
Skills & Requirements
Must-have
Review and approve SOPs and batch records
Lead deviation investigations and CAPA implementation