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:
1- 2 years of experience in pharmaceutical manufacturing, IPC, Quality Assurance, or Quality Control.
Residency Requirement:
- Alexandria, Cairo, and Damietta.
