Quality Assurance (IPQA / QMS / AQA / Process Validation)

Open Positions & Experience:
- IPQA: 2-4 Years
- QMS: 2–6 Years
- AQA: 6–10 Years
- Process Validation: 2–8 Years

Roles & Responsibilities:
- Perform IPQA activities, line clearance, and in-process inspections.
- Review BMR/BPR and ensure compliance with cGMP, GDP, and SOPs.
- Handle deviations, CAPA, change controls, incidents, and quality documentation.
- Execute and review process validation protocols and reports.
- Support internal, regulatory, and customer audits.
- Prepare, review, and maintain QA documentation and quality records.
- Coordinate with Production, QC, Engineering, and R&D; to ensure product quality and compliance.

Skills:
- Hands-on experience in QA activities for OSD (Pellets & Tablets).
- Strong knowledge of cGMP, GDP, SOPs, and pharmaceutical quality systems.
- Experience in IPQA, QMS, Process Validation, CAPA, Deviations, and Change Control.
- Valuable documentation, analytical, and problem-solving skills.
- Excellent communication and teamwork abilities.

📌 Walk-in || Quality Assurance (Hyderabad)
🏢 The Pharma Patashala
📍 Hyderabad