On-site Full Time
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Pharco Corporation

Job Details

  • Support site readiness for regulatory and internal audits and inspections.

  • Manage and follow up on Deviations, CAPAs, Complaints, Recalls, and audit findings.

  • Conduct internal audits and self-inspections and support timely closure of observations.

  • Monitor compliance with cGMP, GDP, and internal procedures and identify improvement opportunities.

  • Support supplier and service provider qualification activities.

  • Ensure compliance of sterile manufacturing activities, where applicable.

  • Prepare and maintain quality and compliance documentation and reports.

  • Collaborate with cross-functional teams to resolve compliance issues and maintain a strong quality culture.

Requirements

  • Bachelor's degree in Pharmacy, Science, or a related field.

  • 3–5 years of relevant QA experience in the pharmaceutical industry.

  • Strong knowledge of cGMP, GDP, and pharmaceutical quality systems.

  • Experience in audits, inspections, Deviations, CAPA, and compliance activities.

  • Knowledge of sterile manufacturing and contamination control is preferred.

  • Strong analytical, communication, problem-solving, and organizational skills.

  • Good command of English.

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About Pharco Corporation
Egypt, Alexandria
Pharmaceuticals