Position Overview:
A QA intern should have basic knowledge of GMP regulations, quality documentation, laboratory practices, and pharmaceutical science coursework, along with strong attention to detail and compliance awareness.
Key Responsibilities:
• Documentation review & management — 30% SOP Review — 25% Shop Floor Quality Activities — 20% Data analysis & reporting — 15% Batch record review support — 10%.
Qualifications:
• Pharmaceutical Engineering, Chemical and Biochemical Engineering
What You'll Gain:
• During the internship, the intern will gain hands - on exposure to professional, technical, and business aspects of pharmaceutical Quality Assurance, including Cross - Functional Team Interaction, Leadership & Mentorship Exposure, Laboratory & Analytical Experience, Manufacturing Floor Experience, Regulatory & Compliance Understanding and Professional Skill Development.