QA Specialist At Global Napi Pharmaceuticals 

🚨 We’re Hiring: QA Specialist – IPC 🚨

📩 To apply:

Send your CV to jobs@globalnapi.com

Subject line: QA IPC Specialist

📍 Location: 6th of October

🚌 Transportation Provided

We are seeking a QA Specialist – In-Process Control (IPC) to join our Quality Assurance team in a pharmaceutical manufacturing environment. The role focuses on ensuring in-process activities comply with GMP requirements and approved procedures.

Role Overview

The QA Specialist – IPC is responsible for monitoring and controlling manufacturing processes to ensure product quality, compliance, and adherence to GMP during all production stages.

Key Responsibilities

Perform in-process quality checks during manufacturing operations according to approved IPC plans and SOPs.

Monitor critical process parameters and ensure compliance with batch records and specifications.

Review and verify manufacturing documentation, logbooks, and IPC records.

Report, document, and follow up on deviations, non-conformities, and observations during production.

Ensure proper implementation of GMP, GDP, and safety requirements on the shop floor.

Participate in investigations, CAPA follow-up, and risk assessments related to IPC activities.

Coordinate with Production, QC, and QA teams to ensure smooth manufacturing flow.

Support internal and external audits and inspections.

Qualifications & Experience

Bachelor’s degree in Pharmaceutical Sciences or Science.

1–3 years of experience in the same field.

Good knowledge of GMP and in-process quality requirements.

Strong attention to detail and documentation accuracy.

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