About the role
“Parkville is committed to diversity, equity, and inclusion, and all employees are expected to support these values in all aspects of their work”Perform in-process controls during manufacturing and packaging operations according to approved SOPs and specifications..Verify and monitor critical process parameters (CPPs) and critical quality attributes (CQAs).Conduct line clearance before batch start, product changeover, and after batch completion.Collect in-process samples according to approved sampling plans and SOPs.Perform in-process tests such as weight variation, hardness, friability, disintegration, pH, viscosity, and fill volume.Record all results accurately and in real time in Batch Manufacturing Records (BMR) and related documents.Ensure compliance with Good Documentation Practices (GDP).Ensure compliance with Data Integrity principles (ALCOA+).Ensure compliance with GMP, regulatory requirements, and company procedures.Perform AQL (Acceptance Quality Limit) inspection activities.Participate in supplier performance evaluation based on AQL results.Report deviations, Out-of-Specification (OOS), or Out-of-Trend (OOT) results to management.Support deviation investigations, CAPA, change control and customer complaint investigations activities.Participate in risk assessments when required.
Education:Bachelor’s degree in pharmacy, Chemistry or pharmaceutical sciences.Experience:0- 2 years of experience in pharmaceutical manufacturing, IPC, Quality Assurance, or Quality Control.Residency Requirement:Alexandria.
