In-Process Monitoring: Conduct regular inspections and quality checks on the production line. This includes verifying raw materials, components, and the final product to ensure they meet specified standards.
Documentation and Record-Keeping: Maintain meticulous records of all quality checks, test results, and production data. Ensure all batch records and logbooks are accurately filled out and signed.
Deviation Handling: Identify and report any deviations or non-conformances from the standard operating procedures (SOPs). Investigate the root cause of these deviations and collaborate with the production team to implement corrective actions.
Compliance: Ensure strict adherence to Good Manufacturing Practices (GMP), regulatory guidelines, and company quality policies.
Sampling and Testing: Collect samples of products at various stages for laboratory testing. Perform basic in-process tests (., tablet hardness, capsule weight variation, liquid volume).
Training: Provide guidance and training to production staff on quality procedures and GMP requirements to foster a culture of quality.