CHEMIST, PHARMACEUTICAL

Responsibilities

• Review and approve GMP documentation and batch records to ensure accuracy and compliance with standards
• Manage deviations, CAPA, change controls, and customer complaints to resolve quality issues effectively
• Conduct GMP training sessions and internal audits to maintain staff competency and system integrity
• Support regulatory inspections and external audits by preparing documentation and facilitating processes
• Maintain document control and quality systems to ensure up-to-date and accessible records
• Perform supplier qualification and conduct quality risk assessments to ensure supplier reliability
• Support validation and qualification activities to verify process and equipment compliance
• Prepare Annual Product Reviews and analyze quality trends to identify improvement opportunities
• Ensure ongoing compliance with GMP, regulatory, and company requirements to uphold product quality