IPC Specialist – New Capital

About the role

The In‑Process Quality Specialist ensures that all in‑process quality controls are executed and monitored during manufacturing at GEPD’s New Capital site. The role safeguards product quality and regulatory compliance in a highly regulated, aseptic environment.

Key responsibilities

• Perform in‑process checks, sampling, and testing according to approved procedures and regulatory guidelines.
• Maintain and verify sampling equipment cleanliness and segregation to avoid cross‑contamination.
• Conduct GEMBA and shop‑floor walkthroughs to confirm compliance with GMP, GEPD, and IPC requirements.
• Review IPC records, batch data, critical parameters, and equipment logs for accuracy.
• Support the Contamination Control Strategy by identifying gaps, reporting risks, and ensuring proper controls.
• Document IPC activities promptly and assist with batch record completion for release readiness.
• Monitor IPC results, flag deviations or trends, and trigger investigations as needed.
• Collaborate with production to maintain IPC frequencies and ensure availability of required materials and equipment.

Required profile

• Bachelor’s degree in health‑related sciences, preferably pharmacy.
• 2–3 years of experience in GMP pharmaceutical manufacturing with aseptic operations.
• Strong organizational, problem‑solving, and communication skills.
• Ability to work effectively in a regulated, labor‑intensive environment and follow SOPs.

Required skills

• Aseptic processing
• In‑process Quality Control
• cGMP knowledge
• eQMS proficiency
• ERP systems experience
• MS Office proficiency